U.S. patent application number 16/791518 was filed with the patent office on 2020-06-11 for system for monitoring body chemistry.
The applicant listed for this patent is Sano Intelligence, Inc.. Invention is credited to Matthew Chapman, Michael Gifford, Dominic Pitera, Ashwin Pushpala.
Application Number | 20200178853 16/791518 |
Document ID | / |
Family ID | 59723142 |
Filed Date | 2020-06-11 |
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United States Patent
Application |
20200178853 |
Kind Code |
A1 |
Pushpala; Ashwin ; et
al. |
June 11, 2020 |
SYSTEM FOR MONITORING BODY CHEMISTRY
Abstract
A system and method for monitoring body chemistry of a user, the
system comprising: a housing supporting: a microsensor comprising a
first and second working electrode, a reference electrode, and a
counter electrode, and configured to access interstitial fluid of
the user, and an electronics subsystem comprising a signal
conditioning module that receives a signal stream, from the
microsensor, wherein the electronics subsystem is configured to
detect an impedance signal derived from two of the first working
electrode, the second working electrode, the reference electrode,
and the counter electrode; and a processing subsystem comprising: a
first module configured to generate an analysis indicative of an
analyte parameter of the user and derived from the signal stream
and the impedance signal, and a second module configured to
transmit information derived from the analysis to the user, thereby
facilitating monitoring of body chemistry of the user.
Inventors: |
Pushpala; Ashwin; (San
Francisco, CA) ; Pitera; Dominic; (San Francisco,
CA) ; Chapman; Matthew; (San Francisco, CA) ;
Gifford; Michael; (San Francisco, CA) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
Sano Intelligence, Inc. |
San Francisco |
CA |
US |
|
|
Family ID: |
59723142 |
Appl. No.: |
16/791518 |
Filed: |
February 14, 2020 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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15601204 |
May 22, 2017 |
10595754 |
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16791518 |
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15412229 |
Jan 23, 2017 |
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15601204 |
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14657973 |
Mar 13, 2015 |
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15412229 |
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61952594 |
Mar 13, 2014 |
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62012874 |
Jun 16, 2014 |
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62025174 |
Jul 16, 2014 |
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Current U.S.
Class: |
1/1 |
Current CPC
Class: |
A61B 5/1473 20130101;
A61B 5/7285 20130101; G16H 40/67 20180101; A61B 5/6849 20130101;
A61B 5/0537 20130101; A61B 5/14532 20130101; A61B 5/0022 20130101;
A61B 5/6833 20130101; A61B 5/1451 20130101; A61B 5/685 20130101;
A61B 2562/0214 20130101; A61B 5/7275 20130101; A61B 5/746 20130101;
A61B 5/14546 20130101; A61B 5/688 20130101; A61B 2562/164 20130101;
A61B 5/0002 20130101; A61B 5/6885 20130101; A61B 2562/028 20130101;
A61B 5/7278 20130101; A61B 2562/046 20130101; A61B 5/0538
20130101 |
International
Class: |
A61B 5/145 20060101
A61B005/145; A61B 5/00 20060101 A61B005/00; A61B 5/1473 20060101
A61B005/1473; A61B 5/053 20060101 A61B005/053; G16H 40/67 20060101
G16H040/67 |
Claims
1. A system for sensing body chemistry of a user, the system
comprising: a first housing portion supporting a sensor operable to
access interstitial fluid of the user upon coupling of the first
housing to the user, the sensor exposed through a base surface of
the first housing portion, and the first housing including an
opening into an electrical interface with the sensor; an adhesive
region coupled to the base surface and surrounding the sensor; a
covering for the adhesive region; and a second housing portion
supporting an electronics subsystem comprising a signal
conditioning portion and a data transmission portion comprising an
antenna, wherein the system is operable between: a loaded mode
wherein the second housing portion is seated within the opening of
the first housing portion with the electronics subsystem coupled to
the electrical interface and the covering is coupled to the
adhesive region, a released mode wherein the sensor and the
adhesive region are coupled to a user with the electronics
subsystem of the second housing portion transmitting signals from
the sensor through the antenna and the covering is uncoupled from
the adhesive region, and an uncoupled mode wherein the second
housing portion is released from the first housing portion.
Description
CROSS-REFERENCE TO RELATED APPLICATIONS
[0001] This application is a continuation of U.S. patent
application Ser. No. 15/601,204, filed 22 May 2017, which is a
continuation-in-part of U.S. patent application Ser. No.
15/412,229, filed 23 Jan. 2017, which is a continuation of U.S.
patent application Ser. No. 14/657,973, filed 13 Mar. 2015, which
claims the benefit of U.S. Provisional Application Ser. No.
61/952,594, filed on 13 Mar. 2014, U.S. Provisional Application
Ser. No. 62/012,874, filed on 16 Jun. 2014, and U.S. Provisional
Application Ser. No. 62/025,174, filed on 16 Jul. 2014, which are
each incorporated herein in its entirety by this reference.
TECHNICAL FIELD
[0002] This invention relates generally to the biometric device
field, and more specifically to a new and useful system for
monitoring body chemistry in the biometric device field.
BACKGROUND
[0003] Biomonitoring devices are commonly used, particularly by
health-conscious individuals and individuals diagnosed with
ailments, to monitor body chemistry. Such biomonitoring devices
perform the tasks of determining an analyte level in a user's body,
and providing information regarding the analyte level to a user;
however, these current biomonitoring devices typically convey
information to users that is limited in detail, intermittent, and
prompted by the command of the user. Such biomonitoring devices,
including blood glucose meters, are also inappropriate for many
applications outside of intermittent use, and place significant
burdens on users (e.g., in requiring finger sticks, in requiring
lancing, etc.) due to design and manufacture considerations.
Additionally, current devices are configured to analyze one or a
limited number of analytes contributing to overall body chemistry,
due to limitations of sensors used in current biomonitoring
devices.
[0004] There is thus a need in the biometric device field to create
a new and useful system for monitoring body chemistry. This
invention provides such a new and useful system.
BRIEF DESCRIPTION OF THE FIGURES
[0005] FIG. 1 depicts elements of an embodiment of a system for
monitoring body chemistry;
[0006] FIGS. 2A and 2B depict embodiments of a microsensor patch, a
transmitting unit, a housing, and an array of filaments in an
embodiment of a system for monitoring body chemistry;
[0007] FIG. 2C depict a variation of electrodes in an embodiment of
a system for monitoring body chemistry;
[0008] FIGS. 3A-3H depict examples of filament variations in an
embodiment of a system for monitoring body chemistry;
[0009] FIG. 4 depicts an embodiment of an electronics subsystem in
an embodiment of a system for monitoring body chemistry;
[0010] FIGS. 5A-5C depict examples of a portion of an electronics
subsystem in an embodiment of a system for monitoring body
chemistry;
[0011] FIGS. 6A-6B depict examples of power management modules in
an embodiment of a system for monitoring body chemistry;
[0012] FIG. 7 depicts a variation of an impedance detection module
in an embodiment of a system for monitoring body chemistry;
[0013] FIG. 8 depicts an example of an applied voltage waveform in
an embodiment of a system for monitoring body chemistry;
[0014] FIG. 9 depicts a variation of a housing in an embodiment of
a system for monitoring body chemistry;
[0015] FIGS. 10A-10B depict specific examples of a housing in an
embodiment of a system for monitoring body chemistry;
[0016] FIG. 10C depicts a specific portion of a housing in an
embodiment of a system for monitoring body chemistry;
[0017] FIGS. 10D and 10E depict specific portions of a housing in
an embodiment of a system for monitoring body chemistry;
[0018] FIGS. 11A-11B depict examples of user interfaces implemented
using a software module in an embodiment of a system for monitoring
body chemistry;
[0019] FIG. 12A depicts a notification module of an embodiment of a
system for monitoring body chemistry;
[0020] FIGS. 12B-12C depict specific examples of notifications in
an embodiment of a system for monitoring body chemistry;
[0021] FIG. 13 depicts communication between a processing subsystem
and a storage module in an embodiment of a system for monitoring
body chemistry;
[0022] FIGS. 14A-14C depict examples of an arch application method
and an end-to-end application method, respectively, in an
embodiment of a system for monitoring body chemistry;
[0023] FIG. 15 depicts an embodiment of an applicator system in an
embodiment of a system for monitoring body chemistry;
[0024] FIGS. 16A and 16B depict a first specific example of an
applicator system in an embodiment of a system for monitoring body
chemistry;
[0025] FIGS. 17A and 17B depict a second specific example of an
applicator system in an embodiment of a system for monitoring body
chemistry;
[0026] FIGS. 18A-18B depict variations of a applicator system in an
embodiment of a system for monitoring body chemistry;
[0027] FIGS. 19A-19D depict a first specific example of a
applicator system in an embodiment of a system for monitoring body
chemistry;
[0028] FIG. 20 depicts a second specific example of a applicator
system in an embodiment of a system for monitoring body
chemistry;
[0029] FIGS. 21A-21B depict a specific example of a base station in
an embodiment of a system for monitoring body chemistry;
[0030] FIG. 22 depicts operation modes of components of an
embodiment of a system for monitoring body chemistry;
[0031] FIG. 23 depicts an embodiment of a method for monitoring
body chemistry;
[0032] FIG. 24 depicts a portion of a variation of a system for
monitoring body chemistry;
[0033] FIG. 25 depicts an example of a portion of an electronics
subsystem in a system for monitoring body chemistry;
[0034] FIGS. 26A and 26B depict an example of a portion of a system
for monitoring body chemistry;
[0035] FIG. 27 depicts an example of a liner in an embodiment of a
system for monitoring body chemistry; and
[0036] FIGS. 28A-28B depict examples of liners in an embodiment of
a system for monitoring body chemistry.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0037] The following description of the preferred embodiments of
the invention is not intended to limit the invention to these
preferred embodiments, but rather to enable any person skilled in
the art to make and use this invention.
1. System
[0038] As shown in FIG. 1, an embodiment of the system 100 for
monitoring body chemistry of a user comprises a housing 190 that
supports a microsensor 116 and an electronics subsystem 120 in
communication with the microsensor 116; and a processing subsystem
160 configured to generate an analysis indicative of an analyte
parameter of the user, wherein the analysis is derived from a
signal stream of the microsensor and an impedance signal from the
electronics subsystem. In more detail, the housing 190, microsensor
116, and the electronics subsystem 120 can be configured as a
microsensor patch 110 configured to sense analyte levels in a
user's body, wherein the electronics subsystem includes a signal
conditioning module 122, a power management module 124, a storage
module 127, and a transmitting unit 130 in communication with the
processing subsystem 160 and/or an electronic device (e.g., mobile
computing device 150) associated with the user.
[0039] In some variations, the system 100 can further include a
applicator system 180 configured to facilitate application of the
microsensor patch 110 onto the body of a user in a reliable manner.
The system 100 functions to provide continuous monitoring of a
user's body chemistry through reception and processing of signals
associated with one or more analytes present in the body of the
user, and to provide an analysis of the user's body chemistry to
the user and/or an entity (e.g., health care professional,
caretaker, relative, friend, acquaintance, etc.) associated with
the user. Alternatively, the system 100 can function to detect a
user's body chemistry upon the user's request or sporadically,
and/or can provide an analysis of the user's body chemistry only to
the user.
[0040] The system 100 is configured to be worn by the patient
outside of a clinical (e.g., hospital) or research (e.g.,
laboratory) setting, such that the patient can be in a
non-contrived environment as he or she is interfacing with the
microsensor patch 110 for monitoring of body chemistry.
Furthermore, elements of the system 100 can be reusable or
disposable (e.g., based upon modularity of the system 100), or the
entire system 100 can be configured to be disposable. In one
specific example, the system 100 adheres to the patient (thus not
compelling the patient to hold any part of the system 100 by hand),
has a low profile that conforms to the patient, and is configured
to receive and transmit signals indicative of body chemistry
parameters of the user, for downstream analysis and information
transfer to the user. Alternatively, the system 100 can be
substantially non-portable, non-wearable, and/or intended for use
in a clinical or research setting.
[0041] As indicated above and further below, elements of the system
can be implemented on one or more computer networks, computer
systems, or applications servers, etc. The computer system(s) can
comprise one or more of: a cloud-based computer, a mainframe
computer system, a grid-computer system, or any other suitable
computer system, and the computer system can support collection of
data from a wearable device and/or a base station, processing of
these data, and transmission of alerts, notifications, and/or user
interface updates to one or more electronic computing devices
(e.g., mobile computing device, wrist-borne mobile computing
device, head-mounted mobile computing device, etc.) linked to or
affiliated with an account of the user. For example, the computer
system can receive signals indicative of one or more analyte
parameters of the user and distribute alerts and notifications over
a distributed network, such as over a cellular network or over an
Internet connection. In this example, the computer system can
upload alerts and notifications to a native body chemistry
monitoring application including the user interface and executing
on a mobile computing device associated with the user.
[0042] Additionally or alternatively, an electronic computing
device (e.g., a laptop computer, a desktop computer, a tablet, a
smartphone, a smart watch, a smart eyewear accessory, a personal
data assistant, etc.) associated with the system (e.g., with the
account of the user) can maintain the account of the user, create
and maintain a user-specific model within the account, and execute
a native body chemistry monitoring application (including the user
interface) with functions including one or more of: generating
alerts or notifications, receiving alerts or notifications,
displaying alerts or notifications, updating predictions of changes
in state of the user, and any other suitable function that enhances
body chemistry monitoring of the user. The system 100 is preferably
configured to implement at least a portion of the method 200
described in Section 2 below; however, the system 100 can
additionally or alternatively be configured to implement any other
suitable method.
1.1 System--Microsensor Patch
[0043] As shown in FIG. 1, the microsensor patch 110 comprises a
microsensor 116 and an electronics subsystem 120 in communication
with the microsensor 116, wherein the microsensor 116 and the
electronics subsystem 120 are supported by a housing 190. The
microsensor patch 110 can be configured to detect and sense only a
single analyte; however, the microsensor patch 110 can
alternatively be configured to detect and sense multiple analytes
in order to provide an analysis based on multiple analytes.
Preferably, the microsensor patch 110 is configured to be
disposable; however, the microsensor patch 110 can alternatively be
configured to be reusable for any suitable duration or number of
uses. In one variation, the microsensor patch 110 is configured to
be a semi-permanent component (e.g., wearable for a week before
replacement, wearable for a month before replacement, etc.)
configured to sense the user's body chemistry with minimal signal
degradation for at a least a week post-coupling of the microsensor
patch 110 to the body of the user. However, in another variation,
the microsensor patch 110 can be configured to be a permanent
component configured to permanently couple to a user. Modularity of
the microsensor patch 110 is described in further detail below.
1.1.1 System--Microsensor
[0044] The microsensor 116 of the microsensor patch 110 preferably
comprises an array of filaments 117, as shown in FIGS. 1 and 2A,
and functions to penetrate skin of the user in order to sense one
or more analytes characterizing the user's body chemistry.
Preferably, the array of filaments 117 is configured to penetrate
the user's stratum corneum (i.e., an outer skin layer) in order to
sense analytes within interstitial (extracellular) fluid, which is
throughout the body; however, the array of filaments 117 can be
configured to penetrate the user's skin to any other suitable
depth. For instance, the microsensor 116 can alternatively be
configured to penetrate deeper layers, or various depth layers of a
user's skin in order to sense analytes within any appropriate
bodily fluid of the user. The microsensor 116 can be configured to
sense analytes/ions characterizing a user's body chemistry using a
potentiometric measurement (e.g., for small analytes including
potassium, sodium calcium, etc.), using an amperometric measurement
(e.g., for large analytes including glucose, lactic acid,
creatinine, etc.), using a conductometric measurement, and/or using
any other suitable measurement.
[0045] Preferably, sensed analytes result in a signal (e.g.,
voltage, current, resistance, capacitance, impedance, gravimetric,
etc.) detectable by the electronics subsystem 120 in communication
with the microsensor 116; however, analyte sensing can comprise any
other appropriate mechanism using the microsensor 116. As mentioned
earlier, the microsensor 116 is also preferably integrated with the
electronics subsystem 120. In a first variation, the microsensor
116 is coupled to the semiconductor architecture of the electronics
subsystem 120 (e.g., the microsensor 116 is coupled to an
integrated circuit comprising the electronics subsystem 120), in a
second variation, the microsensor 116 is more closely integrated
into the semiconductor architecture of the electronics subsystem
120 (e.g., there is closer integration between the microsensor 116
and an integrated circuit including the electronics subsystem 120),
and in a third variation, the microsensor 116 and the electronics
subsystem 120 are constructed in a system-on-a-chip fashion (e.g.,
all components are integrated into a single chip). As such, in some
variations, filaments the array of filaments 117 of the microsensor
116 can be directly or indirectly integrated with electronics
components, such that preprocessing of a signal from the
microsensor 116 can be performed using the electronics components
(e.g., of the array of filaments 117, of the electronics subsystem
120) prior to or after transmitting signals to the electronics
subsystem 120 (e.g., to an analog front end, to an analog to
digital converter). The electronics components can be coupled to a
filament substrate, or otherwise integrated with the filaments in
any suitable fashion (e.g., wired, using a contact pad, etc.).
Alternatively, the electronics components can be fully integrated
into the electronics subsystem 120 and configured to communicate
with the microsensor 116, or the electronics components can be
split between the microsensor and the electronics subsystem 120.
The microsensor 116 can, however, comprise any other suitable
architecture or configuration.
[0046] The microsensor 116 preferably senses analyte parameters
using the array of filaments 117, such that absolute values of
specific analytes/ions can be detected and analyzed. The
microsensor 116 can additionally be configured to sense analyte
parameters using the array of filaments 117, such that changes in
values of specific analyte/ion parameters or derivatives thereof
(e.g., trends in values of a parameter, slopes of curves
characterizing a trend in a parameter vs. another parameter, areas
under curves characterizing a trend, a duration of time spent
within a certain parameter range, etc.) can be detected and
analyzed. In one variation, sensing by the microsensor 116 is
achieved at a low frequency at discrete time points (e.g., every
minute, or every hour), and in another variation, sensing by the
microsensor 116 is achieved substantially continuously at a high
frequency (e.g., every picosecond, every millisecond, every
second). In one specific example for blood chemistry analysis, the
array of filaments 117 of the microsensor 116 is configured to
sense one or more of: electrolytes, glucose, bicarbonate,
creatinine, body urea nitrogen (BUN), sodium, iodide, iodine and
potassium of a user's blood chemistry. In another specific example,
the array of filaments 117 of the microsensor 116 is configured to
sense at least one of biomarkers, cell count, hormone levels,
alcohol content, gases (e.g. carbon dioxide, oxygen, etc.), drug
concentrations/metabolism, pH and analytes within a user's body
fluid.
[0047] As shown in FIG. 2A, the array of filaments 117 is
preferably located at the base surface of the microsensor patch
110, and functions to interface directly with a user in a
transdermal manner (e.g., in accessing interstitial fluid) in order
to sense at least one analyte/ion characterizing the user's body
chemistry. The array of filaments 117 is preferably arranged in a
uniform pattern with a specified density optimized to effectively
penetrate a user's skin and provide an appropriate signal, while
minimizing pain to the user. Additionally, the array of filaments
117 can be arranged in a manner to optimize coupling to the user,
such that the microsensor firmly couples to the user over the
lifetime usage of the system. For example, the filaments 118 can
comprise several pieces and/or be attached to a flexible base to
allow the array of filaments 117 to conform to a user's body. In
one variation, the array of filaments 117 is arranged in a
rectangular pattern, and in another variation, the array of
filaments 117 is arranged in a circular or ellipsoid pattern.
However, in other variations, the array of filaments 117 can be
arranged in any other suitable manner (e.g., a random arrangement).
The array of filaments 117 can also be configured to facilitate
coupling to a user, by comprising filaments of different lengths or
geometries. Having filaments 118 of different lengths can further
function to allow measurement of different ions/analytes at
different depths of penetration (e.g., a filament with a first
length can sense one analyte at a first depth, and a filament with
a second length can sense another analyte at a second depth). The
array of filaments 117 can also comprise filaments 118 of different
geometries (e.g., height, diameter) to facilitate sensing of
analytes/ions at lower or higher concentrations. In one specific
example, the array of filaments 117 is arranged at a density of 100
filaments per square centimeter and each filament 118 in the array
of filaments 117 has a length of 250-350 microns, which allows
appropriate levels of detection, coupling to a user, and pain
experienced by the user.
[0048] Each filament 118 in the array of filaments 117 preferably
functions to sense a single analyte; however, each filament 118 in
the array of filaments 117 can additionally be configured to sense
more than one analyte. Furthermore, the array of filaments 117 can
be further configured, such that a subarray of the array of
filaments 117 functions as a single sensor configured to sense a
particular analyte or biomarker, as shown in FIG. 2B. Furthermore,
any configuration of subarrays of the array of filaments 117 can
additionally or alternatively be configured as one or more of: a
working electrode, a counter electrode (i.e., auxiliary electrode),
and a reference electrode, for instance, in a two-electrode cell, a
three-electrode cell, or a more-than-three-electrode cell. In one
variation, as shown in FIG. 2C, the array of filaments 117 of the
microsensor 116 is configured as a first working electrode 11
(corresponding to a first subarray of filaments), a second working
electrode 12 (corresponding to a second subarray of filaments), a
counter electrode 13 (corresponding to a third subarray of
filaments), and a reference electrode 14 (corresponding to a fourth
subarray of filaments). In a specific example of this variation,
each subarray associated with the first working electrode 11, the
second working electrode 12, the counter electrode 13, and the
reference electrode 14, respectively, is substantially identical in
morphology (e.g., area of the microsensor). Furthermore, in the
specific example, each subarray has a square footprint, and the
subarrays are configured in a 2.times.2 arrangement to define a
larger square footprint. However, the array of filaments 117 can be
configured as one or more of: a working electrode, a counter
electrode, and a reference electrode in any other suitable manner,
and can furthermore have any other suitable morphology(ies) and/or
configuration relative to each other.
[0049] Additionally or alternatively, any subarray of the array of
filaments 117 can be configured to release biomaterials (e.g.,
therapeutic substances, drugs) for treating a medical condition of
a user (e.g., as facilitated by biomaterial dissolution in
interstitial fluid). Multiple subarrays of the array of filaments
can then be configured to sense different analytes/biomarkers, or
the same analyte/biomarker. Furthermore, a subarray or a single
filament 118 of the array of filaments 117 can be configured as a
ground region of the microsensor 116, such that signals generated
by the microsensor 116 in response to analyte detection can be
normalized by the signals generated by the subarray or single
filament 118 serving as a ground region. Preferably, all subarrays
of the array of filaments 117 are substantially equal in size and
density; however, each subarray of the array of filaments 117 can
alternatively be optimized to maximize signal generation and
detection in response to a specific analyte. In an example,
analytes that are known to have a lower concentration within a
user's body fluid can correspond to a larger subarray of the array
of filaments 117. In another example, analytes that are known to
have a higher concentration within a user's body fluid can
correspond to a smaller subarray of the array of filaments 117. In
one extreme example, an entire array of filaments can be configured
to sense a single analyte, such that the microsensor 116 and
microsensor patch 110 is configured to sense and detect only one
analyte. In another extreme example, each single filament in an
array can be configured to detect a single analyte allowing for
detection of multiple analytes within a single array (e.g., for a
100-filament array, 100 analytes can be tested).
[0050] In other variations, a subarray of the array of filaments
117 can also be used to detect other physiologically relevant
parameters, such as electrophysiological signals (e.g.,
electrocardiogram, electroencephalogram), body temperature,
respiration, and skin impedance change (e.g., to measure hydration
state or inflammatory response). In these other variations, the
subarray can be dedicated to measuring these physiologically
relevant parameters, which could be combined with analyte/ion
parameter measurements in order to provide meaningful information
to a user. As an example, the simultaneous measurement of potassium
levels and electrocardiogram measurements, enabled by subarrays of
the array of filaments 117, can provide a more complete diagnosis
of cardiovascular problems or events than either measurement by
itself.
[0051] A filament 118 of the array of filaments can comprise one or
more of: a substrate core, the substrate core including a base end
coupled to the substrate, a columnar protrusion having a proximal
portion coupled to the base end and a distal portion, and a tip
region coupled to the distal portion of the columnar protrusion and
that facilitates access to the body fluid of the user; a conductive
layer, isolated to the tip region of the substrate core and
isolated away from the base end and the columnar protrusion as an
active region that enables transmission of electronic signals
generated upon detection of an analyte; an insulating layer
ensheathing the columnar protrusion and base end of the substrate
core and exposing a portion of the conductive layer, thereby
defining a boundary of the active region; a sensing layer, in
communication with the active region, characterized by reversible
redox behavior for transduction of an ionic concentration of the
analyte into an electronic signal; an intermediate selective layer
superficial to the conductive layer and deeper than the sensing
layer, relative to a most distal point of the tip region of the
filament, that facilitates detection of the analyte; an
intermediate protective layer, superficial to the intermediate
selective layer, including a functional compound that promotes
generation of a protective barrier; and a selective coating
superficial to the intermediate protective layer, having a
distribution of molecules that respond to presence of the analyte,
superficial to the sensing layer. Thus, a filament can comprise one
or more regions, morphologies (examples of which are shown in FIGS.
3A-3H, with elements 118a-118h), compositions, and/or
configurations as described in U.S. Pub. No. 2014/0275897, entitled
"On-Body Microsensor for Biomonitoring" and filed on 14 Mar. 2014
and/or U.S. App. No. 62/025,174, and entitled "System for
Monitoring Body Chemistry" and filed on 16 Jul. 2014, which are
each incorporated herein in their entirety by this reference.
However, the filament can additionally or alternatively comprise
any other suitable region, composition, morphology, and/or
configuration.
[0052] In general, the system 100 can include components configured
to protect portions of the microsensor 116 during manufacturing,
packaging, and/or use of the system 100. For instance, a mold of
impact-absorbing material 17 can be positioned about the edge
regions of the microsensor 116, in order to protect edges of the
microsensor 116 from damage (e.g., as a barrier). The mold of
impact-absorbing material 17 can additionally or alternatively
function to protect skin of the user from irritation caused by
edge-regions of the microsensor. The mold can comprise a continuum
of material (e.g., polymeric material), or can include a set of
bumpers or spacers of material (e.g., polymeric material) to
protect the microsensor 116, an example of which is shown in FIG.
24. Additionally or alternatively, the material of the
edge-protecting portion can be dispensed (e.g., as a gel, as an
epoxy) during manufacture. However, the system 100 can additionally
or alternatively include any other suitable microsensor 116
supporting elements.
1.1.2 System--Electronics Subsystem
[0053] The electronics subsystem 120 functions to receive analog
signals from the microsensor 116 and to convert them into digital
signals to be processed by a microprocessor 113 of the electronics
subsystem 120. In receiving signals, processing signals, regulating
function, storing data, and/or transmitting data, the electronics
subsystem 120 preferably includes a microprocessor 113 interfacing
with one or more of: a signal conditioning module 122, a power
management module 124, an impedance detection module 126, a storage
module 127, and a transmitting unit 130, as shown in FIG. 4.
However, the electronics subsystem 120 can additionally or
alternatively include any other suitable modules configured to
facilitate signal reception, signal processing, and data transfer
in an efficient manner.
[0054] The microprocessor 113 preferably includes memory and/or is
coupled to a storage module 127 (e.g., flash storage). The
microprocessor 113 can also include and/or be coupled to a
clock/watchdog module (which can be incorporated into a
microcontroller unit) for control of timing between different
functions of the electronics subsystem 120. The microprocessor 113
functions to process received signals, enable power distribution,
enable impedance monitoring, and enable data transmission from the
electronics subsystem 120, in relation to other portions of the
electronics subsystem 120 described below; however, the
microprocessor 113 can alternatively or additionally be configured
to perform any other suitable function.
[0055] The signal conditioning module 122 functions to preprocess
signals detected and received using the microsensor 116, thereby
producing conditioned data prior to processing at the processing
subsystem 160. The signal conditioning module 122 can include one
or more of: a signal multiplexer, an analog front end, an amplifier
(e.g., a variable gain amplifier), a filter (e.g., low pass filter,
high pass filter, band pass filter, etc.), an analog-to-digital
converter (ADC), and a digital-to-analog converter (DAC). In one
variation, as shown in FIG. 4, the signal conditioning module 122
comprises a multiplexer 22 in communication with the microsensor
116, wherein the multiplexer 22 is configured to communicate an
output to an analog front end 23 that interfaces the microsensor
116 with an ADC 24 by way of a variable gain amplifier 25 coupled
to a filter 26. In a specific example of this variation, the analog
front end 23 circuitry is configured with a shifted potential
different than a reference potential of the reference electrode 14
of the microsensor 116, wherein the shifted potential is different
(e.g., -2V to 2V different) from the reference potential of the
reference electrode 14. The configuration involving a difference
between the shifted potential and the reference potential can allow
the system 100 to drive redox reactions at the surface of the
microsensor 110. However, in alternative variations of the specific
example, the analog front end (or any other element of the signal
conditioning module 122) can be configured with any other suitable
potential relative to potentials of electrodes of the microsensor
116.
[0056] In more detail, the multiplexer 22 of the signal
conditioning module 122 is preferably configured to receive
multiple signals from the microsensor 116 (e.g., from subarrays of
the array of filaments 117) and to forward the multiple signals
received at multiple input lines in a single line at the analog
front end. The multiplexer 22 thus increases an amount of data that
can be transmitted within a given time constraint and/or bandwidth
constraint. The number of input channels to the multiplexer 22 is
preferably greater than or equal to the number of output channels
of the microsensor 116, and can have any suitable relationship
between the number of input lines into the multiplexer 22, select
lines of the multiplexer, and output lines from the multiplexer 22.
In some variations, the multiplexer 22 can include a
post-multiplexer gain in order to reduce capacitance values of the
analog front end 23 coupled to the multiplexer 22, and which can
also be used to limit a number of amplifiers of the electronics
120, such that a single amplifier is coupled to the multiplexer 22
(as opposed to amplifiers coupled to each individual sensor);
however, the multiplexer 22 can alternatively not include any gain
producing elements. In some variations, the multiplexer 22 can
additionally or alternatively include high frequency and/or low
frequency limiting elements. However, the multiplexer 22 can
additionally or alternatively be configured in any other suitable
manner. Furthermore, in alternative variations, the signal
conditioning module 122 can omit a multiplexer and/or comprise or
omit any other suitable element.
[0057] In variations, an interface between the microsensor 116 and
other elements of the electronics subsystem 120 can be configured
in a manner that prevents or otherwise reduces leakage current
effects due to a redox potential of the microsensor 16 in relation
to other elements electronics subsystem 120. In a first
configuration, a leakage current effect can result when a diode to
ground (e.g., an ESD-diode to ground) is configured at an interface
between the microsensor 116 and a multiplexer 22, as shown in FIG.
5A. To prevent or otherwise reduce the leakage current effect, a
set of diodes 70, comprising a first diode 71 (e.g., a first
EST-diode) and a second diode 72 (e.g., a second ESD-diode),
configured at an interface between the microsensor 116 and the
multiplexer 22 can be coupled to an element 73 (e.g., inductor,
ferrite bead, resistor, etc.) that provides a high resistance to
transient voltage spikes and directs any discharge through the
second diode 72 to ground (instead of damaging the electronics
subsystem 120), as shown in FIG. 5B. The multiplexer 22 can also
comprise a switch 75, as shown in FIG. 5C, that allows altering of
potentials within the analog front end 23. As shown in FIG. 5C,
eliminating a voltage difference (i.e., between Vs and V2)
eliminates or otherwise reduces leakage currents that can affect
readings from the microsensor 110.
[0058] The power management module 124 functions to provide dynamic
modulation of power transfer to and from elements of the
microsensor patch 110, in a manner that enables efficient operation
of the system 100. Preferably, the power management module 124
interfaces with a battery 138 and elements of the transmitting unit
130 requiring power (e.g., by way of a microprocessor 113, as shown
in FIG. 4), as described in further detail below. Additionally, the
power management module 124 can further interface with an external
processing element of the processing subsystem 160, such that the
power management module 124 can be at least partially implemented
in firmware. In one such variation of the power management module
124, wherein power management is achieved in firmware, the power
management module 124 can be configured to anticipate power
requirements of one or more elements, and to automatically operate
at the highest demanded power mode (e.g., voltage) required, while
never dropping below a minimum power level required by the
elements. The power management module 124 can also facilitate
efficient switching of components to an "off" state when not
needed, in order to contribute to lower current consumption.
Additionally or alternatively, the power management module 124 can
be configured to dynamically trigger high current draw sensing
components (e.g., the impedance detection module 126) to an "on"
state, only when needed, by monitoring other system components
(e.g., voltage of a counter electrode 13).
[0059] In an example, as shown in FIG. 6A, a group of elements
requiring different operating power levels can be coupled to the
power management module 124, and the power management module 124
can output power at the highest operating power level anticipated
among the elements. Disparate elements can also set a minimum level
of power they require, and as elements vary their power
requirements, the power management module 124 can then
automatically adjust power output such that a power level provided
never drops below the lowest power level required. In this
variation, elements of the microsensor patch 110 requiring power
are thus dynamically provided with their highest demanded power
level, to substantially limit energy wasted by the system 100 and
to satisfy power level requirements of all running elements. In
another variation of the power management module 124, wherein power
management is achieved in firmware, the power management module 124
can be configured to detect elements requiring power, and to
automatically operate at the highest demanded power mode (e.g.,
voltage) required. In an example, a group of elements requiring
different operating voltages can be detected, and the power
management module 124 can output power at the highest operating
voltage detected. As elements vary their voltage requirements, the
power management module 124 can then automatically adjust voltage
output to meet the highest demanded voltage. In this variation,
elements of the microsensor patch 110 requiring power are thus
dynamically provided with their highest demanded voltage, to
substantially limit energy wasted by the system 100.
[0060] In other variations, power management can be achieved by the
power management module 124 without implementation in firmware,
such that power management occurs in circuitry. In these other
variations, an example of which is shown in FIG. 6B, power
management can comprise providing a set amount of power to elements
requiring power, and completely eliminating power transfer to
elements not requiring power. The system 100 can, however, comprise
any other suitable variation of the power management modules
124.
[0061] In relation to the power management module 124, the
electronics subsystem 120 can comprise a battery 138, which
functions to serve as a power source for the electronics subsystem
120. The battery 138 is preferably coupled to a fuel gage 38 and a
charging detection module 39, each of which is coupled to the
microprocessor 113 (described in further detail below). The battery
138 is preferably a lithium-ion battery that is configured to be
rechargeable, but can be any appropriate rechargeable battery
(e.g., nickel-cadmium, nickel metal hydride, or lithium-ion
polymer). Alternatively, the battery 138 may not be a rechargeable
battery. Preferably, the battery 138 is configured to have a
profile with a low aspect ratio, contributing to a thin form factor
of the microsensor patch 110. However, the battery 138 can be
configured to have any appropriate profile such that the battery
130 provides adequate power characteristics (e.g., cycle life,
charging time, discharge time, etc.) for the system 100. In some
variations, a thin-film battery can be integrated with the
microsensor patch 110 in order to facilitate substantially
continuous analyte detection by the system 100, independent of the
microprocessor 113 and digital electronics of the electronics
subsystem 120.
[0062] In embodiments where the battery 138 is rechargeable, the
electronics subsystem 120 can also comprise a charging coil 140
that functions to provide inductive charging for the battery 138,
and a charging detection module 39, in communication with the
microprocessor 113, that enable detection of charging of the
battery 138. The charging coil 140 is preferably coupled to the
battery 138 and converts energy from an electromagnetic field
(e.g., provided by an element of a base station, as described in
further detail below), into electrical energy to charge the battery
138. Inductive charging provided by the charging coil 140 thus
facilitates user mobility while interacting with the system 100. In
alternative variations, however, the charging coil 140 can
altogether be omitted (e.g., in embodiments without a rechargeable
battery), or replaced by a connection configured to provide wired
charging of a rechargeable battery.
[0063] Additionally or alternatively, in some variations, the
microsensor patch 110 can comprise a semi-active or fully-active
power cell (e.g., implementing microelectromechanical system
elements) that functions to absorb and/or release generated energy
from any one or more of: body heat of the user, body movement of
the user (e.g., with piezoelectric elements, with capacitive
elements), static voltage from the environment of the user, light
in the environment of the user (e.g., using solar cells), magnetic
energy flux, galvanic differentials, and any other suitable energy
source to provide secondary backup energy for the system 100.
[0064] The impedance detection module 126 is in communication with
the signal conditioning module 122 and the power management module
124, and functions to enable detection of a proper interface
between the microsensor 116 and body fluid (e.g., interstitial
fluid) of the user. In facilitating monitoring of impedance, the
impedance detection module 126 can thus provide signals that
indicate that the microsensor patch 110 is properly coupled to the
user (e.g., interfacing with interstitial fluid and experiencing an
.about.80% moisture environment) or improperly coupled to the user
(e.g., not interfacing properly with interstitial fluid and
experiencing a low-moisture environment). Signals from the
impedance detection module 126 can further be used to trigger an
error correction action (e.g., notification for the user to reapply
the microsensor patch 110, automatic manipulation of the
microsensor patch 110 to re-establish interface with body fluid,
etc.). In one variation, as shown in FIG. 4, the impedance
detection module can comprise electronic circuitry configured to
communicate with the multiplexer 22, the ADC 24, and the power
management module 124, in receiving an impedance signal from the
microsensor 116. However, the impedance detection module 126 can
additionally or alternatively be configured relative to other
elements of the electronics subsystem 120 in any other suitable
manner.
[0065] In generating the impedance signal, the impedance detection
module 126 can be configured to detect impedance between two
electrodes of the array of filaments 117 in response to an applied
voltage provided in cooperation with the power management module
126 and the microprocessor 113. In one variation, wherein the
microsensor 116 comprises a first working electrode 11, a second
working electrode 12, a counter electrode 13, and a reference
electrode, the impedance detection module 126 can be configured to
detect impedance from two of the first working electrode 11, the
second working electrode 12, the counter electrode 13, and the
reference electrode 14, examples of which are shown in FIG. 7. In a
specific example, an applied signal can be injected into the system
in a working electrode and detected in the reference electrode 14.
However in other configurations of the microsensor 116, the
impedance detection module 126 can be configured to detect
impedance from electrodes of the microsensor 116 in any other
suitable manner.
[0066] In relation to the applied voltage used for generation and
reception of the impedance signal (i.e., for purposes of
perturbation), the electronics subsystem 120 is preferably
configured to provide an applied voltage waveform having a
characteristic value (e.g., average value) near the operating
potential of the signal conditioning module 122 of the electronics
subsystem 120. In a variation wherein the signal conditioning
module 122 (e.g., an analog front end 23 of the signal conditioning
module 122) operates at a shifted potential relative to a potential
of an electrode of the microsensor 116 (e.g., a reference potential
of a reference electrode), the applied voltage waveform preferably
has a characteristic value (e.g., average value) near or equal to
that of the shifted potential, in order to improve stability of the
microsensor 110 when switching back to a current sensing mode
(i.e., the primary detection mode). The offset (i.e., shifted
potential) is configured to reduce or minimize any disruption to
signal integrity when the microsensor 110 is switched from a
current sensing mode to an impedance detection mode, and then back
to a current sensing mode. In a specific example, as shown in FIG.
8, the applied voltage waveform is shifted about a characteristic
value and has a frequency from 50-200 kHz, in relation to a shifted
potential of the analog front end 23 relative to the reference
electrode 14. However, the applied voltage can alternatively have
any other suitable characteristics (e.g., characteristic voltage
values, frequencies, etc.) defined in relation to the operating
potential(s) of any other suitable element of the electronic
subsystem 120 related to the microsensor 116.
[0067] In relation to triggering of a measurement using the
impedance detection module 126, triggering can occur with any
suitable frequency (e.g., in relation to the lifespan of usage of
the system 100), any suitable regularity (e.g., at regular time
intervals, at irregular time intervals, etc.), and/or upon any
suitable triggering event. In one variation, the impedance
detection module 126 can be configured to provide an impedance
signal in association with monitoring of an electrode (e.g.,
monitoring voltage of the counter electrode 13) of the microsensor
116, wherein detection of an out-of-range parameter (e.g., voltage)
of the electrode triggers the applied voltage waveform and
generation of an impedance signal. As such, the electronics
subsystem 120 and the processing subsystem 160 (described further
below) can be configured to cooperate in continuously detecting a
voltage parameter of the counter electrode 13, and the electronics
subsystem 120 can be configured to apply the applied voltage
waveform and detect the impedance signal when the voltage parameter
of the counter electrode satisfies a voltage threshold
condition.
[0068] Additionally or alternatively, in another variation, the
impedance detection module 126 can be configured to provide an
impedance signal upon initial application of the system 100 to the
body of the user. Additionally or alternatively, in another
variation, the impedance detection module 126 can be configured to
provide impedance signals at regular time intervals (e.g., once
every hour) over the course of use of the system 100 by the user.
Additionally or alternatively, in relation to other sensors (e.g.,
of a mobile computing device associated with the user and the
system 100, of a wearable computing device associated with the user
and the system 100, of the system 100, etc.) the impedance
detection module 126 can be configured to provide an impedance
signal in response to a sensor signal that indicates performance of
an action by the user. For instance, monitoring of signals provided
by an accelerometer and/or gyroscope can be used to indicate that
the user is exercising, and that an impedance measurement should be
taken (e.g., during exercise, after exercise, etc.) to ensure
proper coupling of the system 100 to the user. In another example,
monitoring of body temperature of the user can be used to indicate
that the user is showering, and that an impedance measurement
should be to ensure proper coupling of the system 100 to the user.
The impedance detection module 126 can, however, be configured in
any other suitable manner.
[0069] The impedance detection module 126 can further be used to
generate notifications pertaining to impedance signal measurements
that indicate improper coupling. For instance, a notification can
be generated (and transmitted to a mobile computing device of the
user) in response to detection of unsuitable impedance derived from
comparison between the impedance signal and an impedance threshold
condition. However, use of the impedance signal in performing an
error correction action can be performed in any other suitable
manner.
[0070] The transmitting unit 130 functions to receive signals
generated by the microsensor patch 110 (e.g., by way of the
microprocessor 113), and to interface with at least one of a mobile
computing device 500, a data processing and/or storage module
(e.g., a module external to an on-board storage module, a
cloud-based computing module, etc.) by outputting signals based on
at least one analyte parameter. The transmitting unit 130 thus
cooperates with other elements of the electronics subsystem 120 to
transmit signals based on sensed analyte parameters, which can be
used to facilitate analyses of the user's body chemistry. In
variations, the transmitting unit 130 includes an antenna 132, a
radio 134 coupling the antenna to the microprocessor 113, and can
additionally or alternatively include a linking interface 136
(e.g., wireless or wired interface, as described in further detail
below).
[0071] Preferably, the transmitting unit 130 and the microsensor
patch 110 are integrated as a cohesive unit; however, the
transmitting unit 130 and the microsensor patch 110 can
alternatively form a modular unit, wherein one of the transmitting
unit 130 and the microsensor patch 110 is disposable, and wherein
one of the transmitting unit 130 and the microsensor patch 110 is
reusable. In variations of the microsensor patch 110 and the
transmitting unit 130, elements of the microsensor patch 110 aside
from the microsensor 116 can alternatively be integrated with the
transmitting unit 130, such that the transmitting unit 130 is
configured to be reusable and the microsensor 116 of the
microsensor patch 110 is configured to be disposable. Modularity in
the system 100 is described in further detail in relation to the
housing 190 below.
[0072] Additionally, the transmitting unit 130 is preferably
configured to output signals based on at least one analyte
parameter characterizing body chemistry continuously over the
lifetime usage of the transmitting unit 130; however, the
transmitting unit 130 can alternatively be configured to output
signals based on at least one analyte parameter at a set of time
points (e.g., minutes, hours, days). Still alternatively, the
transmitting unit 130 can be configured to output signals in a
manner that does not interfere with other operations (e.g., signal
collection operations) of the electronics subsystem 120. In one
such example, the transmitting unit 130 can be configured to stop
signal transmission whenever the ADC 24 is collecting signal data
from the microsensor 116, in coordination with timing enabled by a
clock/watchdog module associated with the microprocessor 113. In
variations, the transmitting unit 130 can be further configured to
output signals upon a user prompt, and/or can comprise a variable
sampling rate. For example, the sampling rate can be lower when
user is asleep, higher during activity (e.g., exercise), higher
when there is a sudden change in a value, higher in response to
other stimuli (e.g., if glucose spikes, sampling rate increases for
all analytes).
[0073] The antenna 132 of the transmitting unit 130 functions to
convert electrical signals from the microsensor patch 110 into
radio waves, to facilitate communication with one or more devices
external to the microsensor patch 110 and/or transmitting unit 130
assembly (e.g., by a Bluetooth Low Energy connection). The antenna
132 preferably interfaces with a radio 134 coupled to the
microprocessor 113, as shown in FIG. 4, but can additionally or
alternatively interface with other elements of the transmitting
unit 130. The antenna is preferably an omnidirectional antenna that
radiates radio wave power uniformly primarily in one plane, with
the power decreasing with elevation angle relative to the plane;
however, the antenna can alternatively be an isotropic antenna that
has a spherical radiation pattern. Other variations of the antenna
can include any appropriate antenna that can be integrated with the
form factor of the transmitting unit, while providing appropriate
communication with external devices.
[0074] Because the system 100 can transmit in configurations where
the system 100 is proximal/near/coupled to the body of the user,
the antenna 132 can be configured, with other components of the
transmitting unit 130, in order to promote undisrupted signal
transmission due to signal interactions with the body of the user.
For instance, one or more of the following can be implemented: the
antenna 132 can be decoupled from the ground plane of the printed
circuit board of the electronics subsystem, the antenna 132 can be
positioned near an edge region of the housing 190 described below,
the antenna/transmitting unit 130 can have a configuration of DC
coupling to skin of the user (e.g., thereby providing an offset and
using the body of the user as an RF ground), and any other suitable
antenna design can be implemented to reduce signal disruption.
[0075] The radio 134 functions to transmit and receive signals from
the antenna 132, and also facilitates communication with elements
of the transmitting unit 130 and external devices. The radio 134
and the antenna 132 can additionally or alternatively be
supplemented with a linking interface 136, as described in further
detail below, but can additionally or alternatively interface with
other elements of the electronics subsystem 120.
[0076] The linking interface 136 functions to transmit an output of
at least one element of the microsensor patch 110/transmitting unit
130 assembly to a mobile computing device 150. Additionally, the
linking interface 136 can function to transmit and output of at
least one element of the microsensor patch 110 and transmitting
unit 130 assembly to another element external to the microsensor
patch 110 and transmitting unit 1300. Preferably, the linking
interface 136 is a wireless interface; however, the linking
interface 136 can alternatively be a wired connection. In a first
variation, the linking interface 136 can include a first module
that interfaces with a second module included in a mobile computing
device 150 or other external element (e.g., wrist-borne mobile
computing device, head-mounted mobile computing device), wherein
data or signals (e.g., microsensor or transceiver outputs) are
transmitted from the transmitting unit 130 to the mobile computing
device 150 or external element over non-wired communications. The
linking interface 136 of the first variation can alternatively
implement other types of wireless communications, such as 3G, 4G,
radio, or Wi-Fi communication. In the first variation, data and/or
signals are preferably encrypted before being transmitted by the
linking interface 136. For example, cryptographic protocols such as
Diffie-Hellman key exchange, Wireless Transport Layer Security
(WTLS), or any other suitable type of protocol can be used. The
data encryption can also comply with standards such as the Data
Encryption Standard (DES), Triple Data Encryption Standard (3-DES),
or Advanced Encryption Standard (AES). In variations with data
encryption, data can be unencrypted upon transmission to the mobile
computing device 150 associated with the user. However, in an
alternative variation, data can remain encrypted throughout
transmission to a mobile computing device (associated with the
user, not associated with the user) and unencrypted at another
module of a processing subsystem 160 (e.g., unencrypted in the
cloud), wherein information derived from analysis of the data can
then be transmitted back to the mobile computing device associated
with the user in a secure manner. In this variation, a user can
thus pair his/her microsensor patch 110 with a mobile computing
device unassociated with the user for transmission of encrypted
data, and then later receive personalized body information at
his/her own mobile computing device 150 after processing in the
cloud.
[0077] In a second variation, the linking interface 136 is a wired
connection, wherein the linking interface 136 includes a wired jack
connector (e.g., a 1/8'' headphone jack, a USB connection, a
mini-USB connection, a lightning cable connection, etc.) such that
the transmitting unit 130 can communicate with the mobile computing
device 150 and/or an external element through a complementary jack
of the mobile device and/or external element. In one specific
example of the linking interface 136 that includes a wired jack,
the linking interface is configured only to transmit output signals
from the transmitting unit 130/microsensor patch 110. In another
specific example, the linking interface 136 is configured to
transmit data to and from at least one element of transmitting unit
130/transdermal path 110 assembly and a mobile computing device
150. In this example, the linking interface 136 can transmit output
signals into the mobile computing device 150 through an input of
the jack of the mobile computing device 150 and can retrieve data
from an output of the jack of the mobile computing device 150. In
this example, the linking interface 136 can communicate with the
mobile computing device 150 via inter-integrated circuit
communication (I2C), one-wire, master-slave, or any other suitable
communication protocol. However, the linking interface can transmit
data in any other way and can include any other type of wired
connection that supports data transfer between the transmitting
unit 130 and/or microsensor patch 110, and the mobile computing
device 150.
[0078] The electronics subsystem 120 can further include a
thermistor/potentiostat component 20, which functions to enable
temperature monitoring of skin of the user, in order to improve
signal processing by accounting for thermal fluctuations of the
body of the user. The thermistor/potentiostat component 20 can
further function to enable detection of proper application of the
system 100 at the body of the user, based upon monitoring of the
temperature of the body of the user. As shown in FIG. 25, in one
variation, the thermistor/potentiostat component 20 can interface
components of the microsensor 116/first housing portion (e.g.,
patch coupled to the user) and components of the second housing
portion 196 (e.g., pod for signal acquisition and transmission).
However, variations of the thermistor/potentiostat component 20 can
additionally or alternatively be configured in any other suitable
manner. For instance, measurement of temperature using the
thermistor/potentiostat component 20 can be additionally or
alternatively used to assist with measurement of analyte readings
(e.g., glucose readings), in relation to other biological or
physiological phenomena of the user (e.g., fertility, fever,
diurnal variations in temperature, etc.).
[0079] As noted above, the electronics subsystem 120 can include
any other suitable module(s) and/or be configured in any other
suitable manner. For instance, the electronics subsystem 120 can
include or be in communication with an actuator configured to
automatically perform an action (e.g., vibration, provision of a
biasing force) that biases the microsensor into communication with
interstitial fluid of the user, in response to detection of
unsuitable impedance derived from comparison between an impedance
signal and an impedance threshold condition.
1.1.3 System--Housing
[0080] The housing 190 supports the microsensor 116 and the
electronics subsystem 120, and functions to facilitate robust
coupling of the microsensor patch 110 to the user in a manner that
allows the user to wear the microsensor patch 110 for a sufficient
period of time (e.g., one week, one month, etc.). The housing 190
can also function to protect elements of the microsensor patch 110
from physical damage over the lifetime usage of the microsensor
patch 110. Preferably, at least one portion of the housing 190 is
flexible to facilitate adhesion to the user and compliance with
skin of the user as the user moves in his/her daily life; however,
at least a portion of the housing 190 can alternatively be rigid in
order to provide more robust protection against physical damage. In
an embodiment where a portion of the housing 190 is flexible, other
elements of the microsensor patch 110 can also be flexible (e.g.,
using a thin film battery, using flexible electronics, etc.) to
facilitate adhesion to the user and compliance as the user moves
about in his/her daily life. In one variation, the housing 190 can
comprise a single unit that entirely houses the microsensor 116 and
the electronics subsystem 120. In this variation, the housing 190
can be configured to couple to the user using any suitable coupling
mechanism (e.g., adhesive coupling mechanism, strap-based coupling
mechanism, etc.). However, in other variations, the housing 190 can
alternatively be modular and comprise a set of portions, each
portion configured to enable coupling of the microsensor 116 to the
user and/or to house elements of the electronics subsystem 120.
Modularity of the housing 190 can thus allow portions of the system
100 to be disposable and/or reusable.
[0081] In some variations, modularity of the housing 190 can
include housing components that are configured to break or
otherwise prevent future recoupling after separation. For instance,
with multiple housing portions, the system 100 can comprise coupled
operation modes, wherein the multiple housing portions are coupled
together during use (e.g., body chemistry monitoring), but once the
system needs to be decoupled from the user and/or the housing
portions need to be decoupled from each other (e.g., for charging
of a module of the system, etc.), one or more of the multiple
housing portions can break in a way that prevents re-coupling. In a
first example, microsensor-supporting portions of the housing 190
can be configured to break apart (e.g., an opening of a first
housing portion can comprise a perforation or other stress
concentration region operable to break apart) after other
electronics/power management/signal transmission components of the
system 100 are separated from the microsensor-supporting portions
of the housing 190. However, the system 100 can additionally or
alternatively be configured in any other suitable manner in
relation to modularity/reusability.
[0082] In one modular variation of the housing 190, as shown in
FIG. 9, the housing can comprise a first housing portion 191 and a
second housing portion 196, wherein the first housing portion 191
is configured to facilitate coupling of filaments of the
microsensor 116 to the user, and the second housing portion 196 is
configured to house elements of the electronics subsystem 120 and
to couple the electronics subsystem 120 to the microsensor 116 by
way of the first housing portion 191. As such, the first housing
portion 191 and the second housing portion 196 of this variation
are preferably configured to mate with each other in a
complementary manner (e.g., with a male-female coupling mechanism,
with a magnetic coupling mechanism, with a latch-based coupling
mechanism, with a lock-and-key based coupling mechanism, etc.). In
a specific example, as shown in FIGS. 10A-10B, the first housing
portion 191' includes an opening 192', and a second housing portion
196' is insertable into the opening of the first housing portion in
a first configuration, wherein coupling between the first housing
portion 191' and the second housing portion 196' provides a
hermetic seal between the first housing portion 191 and the second
housing portion 196 (e.g., in a manner that prevents water or other
fluids from passing into a region between the second housing
portion 196 and the first housing portion 191). In more detail, as
shown in FIG. 10C, the first housing portion 191 can include an
o-ring 193 (e.g., an o-ring co-molded onto the material of the
first housing portion) at a perimeter of the opening 192, and a
perimeter region of the second housing portion 196 can include a
recessed region 197 that interfaces with the o-ring 193 in a manner
that provides a hermetic seal. As such, the o-ring 193 can be
physically coextensive with the material of the first housing
portion 191 near the opening 192 in order to facilitate coupling
between the first housing portion 191 and the second housing
portion 196. Alternatively, the o-ring 193 can be physically
coextensive (e.g., go-molded) on material of the second housing
portion) at a region configured to interface with the opening 192,
or can be coupled to one or more of the first housing portion 191
and the second housing portion 196 in any other suitable
manner.
[0083] In an alternative example, as shown in FIGS. 10D and 10E,
the second housing portion 196 can include an o-ring 193 internal
to the outer diameter of the second housing portion 196, wherein
the second housing portion 196 is configured in a manner that
produces a crush seal when the second housing portion 196 is
inserted into the opening of the first housing portion 191 (e.g.,
as in FIG. 10E). In this example, the first housing portion 191 can
thus be manufactured (e.g., molded) without undercuts, in order to
facilitate manufacturability with respect to reduced tooling
complexity and cycle time.
[0084] Additionally or alternatively, the interface between the
first housing portion 191 and the second housing portion 196 can be
sealed using a covering 96 that adequately spans the
interface/opening 192 between the first housing portion 191 and the
second housing portion 196, in order to prevent water or any other
undesired material from entering the interface. In variations, the
covering 96 can be flexible or rigid, and can be comprised of any
suitable material or composite of materials. Furthermore, the
covering 96 can be coupled to one or more of the first housing
portion 191 and the second housing portion 196 using an adhesive
coupling mechanism or any other suitable coupling mechanics that
promotes sealing of the opening/interface. In a specific example,
the system 100 can include a covering 96 comprising a flexible
polymer layer that is coupled to surfaces of both the first housing
portion 191 and the second housing portion 196 proximal the opening
192, wherein the flexible polymer layer is coupled to the housing
portions with an adhesive backing. However, variations of the
covering 96 can be configured in any other suitable manner, or some
variations of the system 100 can entirely omit a covering 96.
[0085] The first housing portion 191 preferably exposes the
microsensor 116 through a base surface of the first housing portion
191, an example of which is shown in FIGS. 26A and 26B, such that
portions of the microsensor 116 for accessing body fluid of the
user are exposed at the base surface of the first housing portion
191. In a first variation, only microsensor filament portions
operable to penetrate the body of the user may be exposed through
the base surface of the first housing portion 191. In another
variation, the entire microsensor 116, including portions that do
not penetrate the body of the user can be exposed at the base
surface of the first housing portion. However, portions of the
microsensor 116 can be exposed through the base surface of the
first housing portion 191 in any other suitable manner. In
variations wherein at least a portion of the microsensor 116 is
exposed at the base surface of the first housing portion 191, the
system 100 can include a cap that is temporarily coupled to the
base surface, wherein the cap protects the microsensor 116 from
damage (e.g., in packaging, during shipping, etc.).
[0086] The first housing portion 191 can additionally or
alternatively include an adhesive substrate 91 that substantially
surrounds the microsensor 116 and is coupled to the base surface of
the first housing portion 191, wherein the adhesive substrate 91
facilitates coupling of the first housing portion to the user and
facilitates retention of a state of coupling between the
microsensor 116 and the user after portions of the microsensor have
been inserted into the user's body.
[0087] Prior to application of the system 100 onto the user's body,
the adhesive substrate 91 of the first housing portion 191 can be
covered with or otherwise coupled to a liner 911, as shown in FIG.
27, wherein the liner 911 prevents the adhesive substrate 91 from
prematurely sticking to objects and/or prevents the adhesive
substrate 91 from losing its tack. The liner 911 can additionally
or alternatively be designed to be easily separated from the
adhesive substrate 91 by the user, such that removal of the liner
911 by the user does not interfere with application of the system
100 onto the body of the user. In some variations, the liner 911
can include multiple parts. For instance, the liner 911 can include
overlapping or non-overlapping leaves, each leaf configured to be
separated from the adhesive substrate 91 independently of the other
leaves. Alternatively, the liner 911 can be a single liner designed
to be separated from the adhesive substrate along a path that does
not interfere with a process for applying the system 100 onto the
body of the user. The liner 911 is preferably configured to be
separated in a central-to-peripheral direction, in relation to the
adhesive substrate 91. In another variation, the liner 911 can be
configured to be separated in a peripheral-to-central direction in
relation to the adhesive substrate 91. However, in still other
variations, the liner 911 can be configured to be released from the
adhesive substrate 91 in any other suitable direction or along any
other suitable path.
[0088] In a first example, as shown in FIG. 28A, the liner 911'
includes two overlapping leaves, wherein the two overlapping leaves
includes 1) a first leaf spanning a first portion of the adhesive
substrate 91 and including a first valley fold configured to be
used as a pull-tab, and 2) a second leaf spanning a second portion
of the adhesive substrate 91 and including a second valley fold
overlapping the first valley fold configured to be used as a
pull-tab. As such, in this example, each of the first leaf and the
second leaf is configured to be pulled away in a
central-to-peripheral direction in relation to the adhesive
substrate 91. In relation to the cap described above, the first
leaf and the second leaf can each include cutaways, such that the
leaves do not touch exposed portions of the microsensor 116;
however, the first leaf and the second leaf can alternatively be
configured in any other suitable manner.
[0089] In a second example, as shown in FIG. 28B, the liner 911'
can include a single liner having a spiral path initiating at a
central region of the adhesive substrate and terminating at a
peripheral region of the adhesive substrate, wherein the central
region portion of the liner has a pull-tab to indicate that this is
where separation should initiate. As such, in this example, the
liner is configured to be pulled away in a central-to-peripheral
direction in relation to the adhesive substrate 91. In relation to
the cap described above, the liner can include a cutaway, such that
the liner does not touch exposed portions of the microsensor 116;
however, the liner can alternatively be configured in any other
suitable manner.
[0090] The opening 192 of the first housing portion 191 and the
second housing portion 196 can each have substantially circular
footprints; however, the opening 192 and the second housing portion
196 can additionally or alternatively have any other suitable
footprints or be configured in any other suitable manner.
[0091] In the specific example, as shown in FIGS. 10A-10B, the
first housing portion 191' can comprise an adhesive substrate 91
having a microsensor opening 92, a microsensor interface substrate
93 superior to the adhesive substrate and configured to pass the
microsensor 92 through the microsensor opening 92, a coupling ring
94 configured to retain the position of the microsensor interface
substrate 93 relative to the adhesive substrate 91 and to provide
an interface for mating with the second housing portion 196, and a
flexible cover 95 ensheathing the coupling ring 94, coupled to the
adhesive substrate 91, and configured to maintain coupling between
the adhesive substrate 191, the microsensor interface substrate 93,
and the coupling ring 94. In relation to the configuration
described above, the adhesive substrate 91 is configured to
facilitate adhesion of the microsensor patch 110 to the user at an
inferior surface of the adhesive substrate, and the flexible cover
95 is configured to provide the opening 192' that receives the
second housing portion 192.
[0092] The second housing portion 196 of the specific example is
rigid, and configured to form a shell about the electronics
subsystem 120, while including openings that provide access for a
set of contacts 98 that interface the electronics subsystem 120
with the microsensor interface substrate 93 when the first housing
portion 191 is coupled to the second housing portion 196. In
relation to the microsensor interface substrate 93 of the first
housing portion 191, and in relation to a circular (or otherwise
axially symmetric) configuration of an interface between the second
housing portion 196 and the opening 192 of the first housing
portion 191, the microsensor interface substrate 93 of the specific
example can include a circular printed circuit board comprising a
set of concentric ring contacts 97, as shown in FIG. 10A, that
interface electronics of the second housing portion 196 with
filaments of the microsensor 116. As such, the set of contacts 98
(e.g., digital contacts) of electronics of the second housing
portion 196 can properly interface with the microsensor 116 in any
rotational position of the second housing portion 196 within the
first housing portion 191, as shown in FIG. 10B. In alternative
variations of this specific example however, orientation-unspecific
coupling between the first housing portion 191 and the second
housing portion 196 can be achieved in any other suitable manner.
In still alternative variations of this specific example, the first
housing portion 191 and the second housing portion 196 can be
configured to couple with a set orientation in order to ensure
proper communication between the microsensor 116 and the
electronics subsystem 120.
[0093] Some variations of the housing 190 can additionally or
alternatively include a coating that prevents water permeation
(and/or other liquid permeation), but allows electrical contact
(e.g., for current passage) to be made between the set of
concentric ring contacts 97 of the first housing portion 191 and
contacts 98 of the second housing portion 196. In variations, the
coating can include a nanocoating of colloidal suspension of
silicon oxide, which allows current passage through a waterproof
layer that protects electronic components from shorting; however,
the housing 190 can additionally or alternatively include any other
suitable coating. For instance, waterproofing of electronics with
coatings can additionally or alternatively be achieved using an
adhesive coating (e.g., thin film) applied to circuit board
components prior to assembly. Additionally or alternatively, the
coating can include a nanocoating of another suitable material
(e.g., paralene, etc.).
[0094] Furthermore, in relation to coupling between printed circuit
board (PCB) components and components of either or both the first
and the second housing portions 191, 196, coupling can be achieved
using an adhesive process (e.g., using a glue or other adhesive).
Additionally or alternatively, coupling can be achieved using a
thermal process (e.g., a heat staking process) to couple PCB(s) to
portions of the first housing portion 191 and/or the second housing
portion 196.
[0095] In variations of the housing 190 comprising a first housing
portion 191 and a second housing portion 196, the first housing
portion 191 and the second housing portion 196 can be coupled
together and/or coupled to the user by way of a applicator system
180, as described in further detail below. Furthermore, other
variations of modularity can comprise any other suitable
distribution of the microsensor 116 and elements of the electronics
subsystem 120 across portions of the housing in any other suitable
manner. For instance, in one such variation, the microsensor 116,
the multiplexer 22, and the analog front end 93 of the electronics
subsystem 120 can be coupled to a separate battery (e.g., a thin
film battery) within a disposable portion of the housing 190, and
other elements of the electronics subsystem 120 can be supported by
a reusable portion of the housing 190. The system 100 can, however,
comprise any other suitable distribution of elements across the
housing 190 in a modular fashion.
1.2 System--Processing Subsystem
[0096] The processing subsystem 160 is in communication with the
electronics subsystem 120 and functions to generate analyses
pertaining to the user's body chemistry, and to transmit
information derived from the analyses to the user at an electronic
device associated with the user. As shown in FIG. 1, the processing
subsystem 160 can be implemented in one or more of: a computer
machine, a remote server, a cloud computing system, a
microprocessor, processing hardware of a mobile computing device
(e.g., smartphone, tablet, head-mounted mobile computing device,
wrist-borne mobile computing device, etc.) and any other suitable
processing system. In one variation, the processing subsystem 160
comprises a first module 161 configured to generate an analysis
indicative of an analyte parameter of the user and derived from a
signal stream from the microsensor 116 and an impedance signal from
the electronics subsystem 120. Additionally, in this variation, the
processing subsystem 160 comprises a second module 162 configured
to render information derived from the analysis at an electronic
device (e.g., mobile computing device 150) associated with the
user, thereby facilitating monitoring of body chemistry of the
user. In this variation, the modules of the processing subsystem
160 can be implemented in a hardware module and/or a software
module. In variations, a software module 163 can be implemented, at
least in part, as a native software application executing on a
mobile computing device 150 associated with the user, wherein the
user has a user account associated with the native software
application.
[0097] In more detail, the software module 163 functions to analyze
an output provided by the transmitting unit 130 of the electronics
subsystem 120, and to communicate an analysis of the output back to
the user, so that the user can monitor his/her body chemistry.
Preferably, the software module 163 analyzes at least one analyte
parameter in order to determine a metric providing information
about a user's body chemistry. In one variation, the software
module can determine that a body analyte parameter (e.g., glucose
level) of the user is too low or less than ideal, and facilitate a
behavior change in the user by providing a body chemistry metric
indicating a hypoglycemic state. In this variation, the software
module can additionally determine that the body analyte parameter
(e.g., glucose level) of the user is within a proper range based on
a determined metric. The software module of this variation can
additionally determine that the body analyte parameter (e.g.,
glucose level) of the user is too high and facilitate a behavior
change in the user by providing a body chemistry metric indicating
a hyperglycemic state.
[0098] In another example, the software module can analyze an
output provided by the transmitting unit 130 based on a set of
parameters for multiple analytes characterizing a user's body
chemistry, at a set of time points, and determine at least one
metric based on the set of parameters at the set of time points.
The software module can then determine and output at least one of a
temporal trend in a metric, a temporal trend in an analyte
parameter, absolute values of a metric, changes in value of a
metric, absolute values of an analyte parameter, and changes in
value of an analyte parameter. The software module 163 in this
example can further be configured to communicate a suggestion to
the user based on an analysis determined from the set of parameters
for multiple analytes.
[0099] The software module preferably incorporates at least one of
user health condition, user characteristics (e.g., age, gender,
ethnicity), and user activity in analyzing an output provided by
the transmitting unit 130. In one specific example, if a user sets
a desired body glucose level range, which is entered into the
software module, the software module can be configured to
facilitate provision of alerts notifying the user of short-term
risks (e.g., diabetic crash), long-term risks (e.g., worsening
diabetic condition), and risk of exiting the desired body glucose
level range. In another specific example, the software module can
compare analyte parameters and/or a metric characterizing the
user's body chemistry to other users with similar health conditions
or characteristics (e.g., age, gender, ethnicity). In yet another
example, the software module can be able to correlate at least one
analyte parameter or metric to a user activity, such that the user
is provided with information relating a value of the analyte
parameter and/or metric to an activity that he or she has
performed. The software module can additionally or alternatively
provide an analysis that includes any other health- and/or
user-related information that can be useful in treating,
maintaining, and/or improving a health condition of a user.
[0100] As shown in FIGS. 1, 11A, and 11B, the software module can
be implemented, at least in part, as an application executable on a
mobile computing device 150. As described above, the mobile
computing device 150 is preferably a smartphone but can also be a
tablet, laptop computer, PDA, e-book reader, head-mounted computing
device, smart-watch, or any other mobile device. The software
module can alternatively be an application executable on a desktop
computer or web browser. The software module preferably includes an
interface that accepts inputs from the user (e.g., user health
condition, user characteristics, user activity), and uses these
inputs in analyzing an output provided by the transmitting unit
1300. Preferably, the software module also includes an interface
that renders an analysis based on sensed analytes and/or user
inputs in some form. In an example, the software module includes an
interface that summarizes analyte parameter values in some manner
(e.g., raw values, ranges, categories, changes), provides a trend
(e.g., graph) in at least one analyte parameter or body chemistry
metric, provides alerts or notifications, provides additional
health metrics, and provides recommendations to modify or improve
body chemistry and health metrics. In another example, the software
module can implement two interfaces: a first interface accessible
by a user, and a second interface accessible by a health care
professional servicing the user. The second interface can provide
summarized and detailed information for each user that the health
care professional interacts with, and can further include a message
client to facilitate interactions between multiple users and the
health care professional. The software module can additionally or
alternatively access a remote network or database containing health
information of the user. The remote network can be a server
associated with a hospital or a network of hospitals, a server
associated with a health insurance agency or network of health
insurance agencies, a server associated with a third party that
manages health records, or any other user- or heath-related server
or entity. The software module can additionally or alternatively be
configured to accept inputs from another entity, such as a
healthcare professional, related to the user.
[0101] The software module 163 can additionally or alternatively
execute fully or in part on a remote server. In a first variation,
the software module can be a cloud-computing-based application that
performs data analysis, calculations, and other actions remotely
from the mobile computing device 150. In one example of the first
variation, the mobile computing device 150 can receive an output of
the transmitting unit 130 via the linking interface 136 and then
transfer the output to the remote server upon which the software
module executes. In the first variation, signals are preferably
transferred via a wireless connection, such as a Bluetooth
connection, 3G or 4G cellular connection, and/or via a Wi-Fi
internet connection. In another example of the first variation, a
mobile computing device 150 can function to transmit data to and/or
receive data from the software module. In a second variation, the
software module can include a first software component executable
on a mobile computing device 150, such as an application that
manages collection, transmission, retrieval, and/or display of
data. In the second variation, the software module can further
include a second software component that executes on the remote
server to retrieve data, analyze data, and/or manage transmission
of an analysis back to the mobile computing device 150, wherein the
first software component manages retrieval of data sent from the
second software component and/or renders of a form of the analysis
on a display of the mobile computing device 150. However, the
software module can include any number of software components
executable on any mobile computing device 150, computing device,
and/or server and can be configured to perform any other function
or combination of functions.
[0102] As shown in FIG. 12A, the software module 163 can further be
integrated with a notification module 165 configured to provide an
alert or notification to a user and/or health care professional
based on the analysis of the output. The notification module 165
functions to access an analysis provided by the software module and
to control transmission of a notification 166 to at least one of a
user and a healthcare profession interacting with the user. In one
variation, the notification module 165 receives an analysis of the
software module being executed on a mobile computing device 150,
and generates a notification 166 based upon the analysis. In this
variation, a form of the analysis is preferably transmitted from
the software module, executing on the mobile computing device 150,
to the notification module 165, wherein the mobile computing device
150 accesses the analysis either from the software module executing
on the mobile computing device 150 or from the software module
executing on a remote server and in communication with the mobile
computing device 150. The notification module 165 preferably
controls transmission of the notification 166 to the user, such as
by triggering a display of the mobile computing device 150 to
display a form of the notification, or by generating and/or
transmitting an email, SMS, voicemail, social media platform (e.g.,
Facebook or Twitter) message, or any other message accessible by
the user and which contains the notification 166. The notification
module 165 can also convey the notification 166 by triggering a
vibration of the mobile device 160, and/or by altering the state
(i.e., ON or OFF) of one or more light sources (e.g., LEDs) of the
mobile computing device 150. However, the notification module 165
can alternatively manage the transmission of any other information
and function in any appropriate manner.
[0103] The notification 166 preferably contains information
relevant to a body chemistry status of the user. The notification
166 can additionally include an explicit directive for the user to
perform a certain action (e.g., eat, rest, or exercise) that
affects the body chemistry of the user. Therefore, the notification
166 preferably systematically and repeatedly analyzes a body
chemistry status of the user based on at least one analyte
parameter of the user and provides and alert and/or advice to
manage and monitor a user's body chemistry substantially in real
time. In one example, the notification 166 can further include
information related to what or how much to eat, where and how long
to run, level of exertion, and/or how to rest and for how long in
order to appropriately adjust body chemistry. In other examples,
the notification 166 can include any appropriate information
relevant to monitoring a body chemistry metric of the user.
[0104] In still other examples, as shown in FIG. 12B, the
notification 166 can indicate one or more of: a current level of a
measured analyte (e.g., represented in hue, represented in
saturation, represented in intensity, etc. of a graphical
rendering); a trending direction for the level of the measured
analyte (e.g., represented in a feature gradient within a graphical
rendering); a lower bounding level and an upper bounding level
between which the level of the measured analyte is traversing; a
trending direction of a level of a measured analyte (e.g.,
represented in an arrow of a graphical rendering); a quantification
of a level of a measured analyte (e.g., represented as rendered
text); a summary of a level of a measured analyte (e.g.,
represented as rendered text); a percent of time within a time
duration (e.g., one day) that the level of the measured analyte is
within a target range (e.g., healthy range); and historical
behavior of a level of a measured analyte (e.g., represented as
historical "ghosting" of a rendering based upon a previous analyte
level).
[0105] Additionally or alternatively, in still other examples, as
shown in FIG. 12C, the notification 166 can include a graphical
rendering that shows analyte data from past to present using a line
graph representation, wherein an amount (e.g., concentration) of
the analyte is represented along a first axis and time is
represented along a second axis. In these examples, the graphical
rendering can further include a "predicted region" based upon the
analysis of the processing subsystem 160, wherein the predicted
region 66 depicts a prediction of where the analyte level will be
at a future time point, and a width of the predicted region 66
indicates confidence in the prediction.
[0106] In relation to the processing subsystem 160 and analyses
generated at the processing subsystem 160, the processing subsystem
160 can be coupled to or comprise a data storage unit 170, as shown
in FIG. 13. The data storage unit 170 functions to retains data,
such as an analysis provided by a software module, a notification
166, and/or any other output of any element of the system 100. The
data storage unit 170 can be implemented with the microsensor patch
110, transmitting unit 130, mobile computing device 150, personal
computer, web browser, external server (e.g., cloud), and/or local
server, or any combination of the above, in a network configured to
transmit, store, and receive data. Preferably, data from the data
storage unit 170 is automatically transmitted to any appropriate
external device continuously; however, data from the data storage
unit 170 can alternatively be transmitted only semi-continuously
(e.g., every minute, hourly, daily, or weekly). In one example,
data generated by any element can be stored on a portion of the
data storage unit 170 when the linking interface 136 is not coupled
to an element external to the microsensor patch 110/transmitting
unit 130 assembly. However, in the example, when a link is
established between the linking interface 136 and an external
element, data can then be automatically transmitted from the
storage unit 170. In other examples, the data storage unit 170 can
alternatively be prompted to transmit stored data by a user or
other entity. Operation modes related to device pairing and
information transfer are further described in relation to the base
station of Section 1.4 below.
1.3 System--Applicator
[0107] As shown in FIG. 1, the system 100 can further comprise a
applicator system 180, which functions to facilitate application of
at least one of the microsensor patch 110 and the transmitting unit
130 onto a body region of the user. The applicator system 180
preferably accelerates the a portion of the housing with the
microsensor 116 toward skin of the user, thereby causing the
microsensor 116 to penetrate skin of the user and sensing regions
of the microsensor to access interstitial fluid of the user.
However, the applicator system 180 can additionally or
alternatively facilitate coupling of the microsensor 116 to the
user using one or more of: skin stretching, skin permeabilization,
skin abrasion, vibration, and/or any other suitable mechanism,
variations of which are shown in FIGS. 14A-14C.
[0108] In variations, as shown in FIG. 15, the applicator system
180 can include a first applicator portion 81 comprising a coupling
interface 811; a second applicator portion 82 comprising a retainer
821; an elastic coupler 83 between the first applicator portion 81
and the second applicator portion 82; and a trigger 84 operable
between a loaded mode 84aa and a released mode 84b; wherein, in the
loaded mode, the elastic coupler is in a first compressed state
between the first applicator portion and the second applicator
portion, the first applicator portion is retained by the retainer
of the second applicator portion, and the coupling interface is
coupled to the second housing portion; and wherein, in the released
mode, the elastic coupler is in a second compressed state (e.g., a
state of lower compression or non-compression) between the first
applicator portion and the second applicator portion, the first
applicator portion is released from the retainer of the second
applicator portion, and the coupling interface is uncoupled from
the second housing portion, with the microsensor portions coupled
to the user.
[0109] These variations of the applicator system 180 function to
provide a mechanism that promotes proper application of the
microsensor patch 110 at the body of the user. As such, these
variations are configured for ease of use and/or error-preventing
use in relation to one or more of: transitioning the applicator
system into a loaded mode; initial positioning of the microsensor
patch 110 at portions of the applicator system; positioning the
applicator system 180 with the microsensor patch 110 at a body
region prior to insertion of microsensor portions into the body;
transitioning the applicator system from the loaded mode to the
released mode, thereby properly inserting microsensor into the body
of the user; and moving the applicator system 180 away from the
body of the user.
1.3.1 Applicator--First Applicator Portion
[0110] The first applicator portion 81 functions to reversibly
retain the microsensor patch 110 prior to coupling of the
microsensor patch 110 to the user. The first applicator portion 81
can thus function to retain the microsensor patch as the
microsensor patch is loaded and then accelerated toward the body of
the user for microsensor insertion. Then, the first applicator
portion 81 can release the microsensor patch 110 such that the
microsensor patch 110 can be left at the body of the user.
[0111] As such, the first applicator portion 81 can include a
coupling interface 811 that couples to one or more portions of the
microsensor patch 110 prior to insertion. The coupling interface
811 can include: a suction interface operable to temporarily retain
a surface of the microsensor patch 100 using negative pressure and
by forming a temporary seal with the surface of the microsensor
patch 100. Additionally or alternatively, the coupling interface
811 can interface with the microsensor patch 110 by any any one or
more of: an adhesive interface formed by an adhesive region of the
first applicator portion and/or the microsensor patch 110; a
magnetic interface between magnetic regions of the first applicator
portion and the microsensor patch 110; a locking interface between
the first applicator portion and the microsensor patch 110, a
press-fit interface between the first applicator portion and the
microsensor patch 110; and any other suitable interface between the
first applicator portion and the microsensor patch.
[0112] The coupling interface 811 preferably couples to the second
housing portion 196, which as described above, supports the
electronics subsystem 120 and is insertable into an opening of the
first housing portion 191. However, the coupling interface 81 can
alternatively couple to the first housing portion 191 and/or to
both the first housing portion 191 and the second housing portion.
In a specific example, the coupling interface 811 comprises a
suction interface that couples to a surface of the second housing
portion 196 opposing a second surface of the second housing portion
196 that interfaces with electronics of the first housing portion
191; however, variations of the specific example can be configured
in any other suitable manner.
[0113] In variations of the coupling interface 811 including a
suction interface, the coupling interface 811 can further include a
venting channel having a first opening into a concave portion of
the suction interface (that couples to the microsensor patch) and a
second opening at a distal end. The venting channel facilitates
release of the microsensor patch 110 from the applicator system 180
during and/or after acceleration of the microsensor patch toward
the body of the user. The venting channel preferably has a shaft,
an example of which is shown in FIGS. 16A and 16B, and a pathway
through the shaft that connects the first opening to the second
opening. As described below, the second opening of the venting
channel preferably interfaces with a sealing interface at one or
more of the second applicator portion 82 and the trigger 84 of the
applicator system 180 in order to provide 1) a sealed state that
supports coupling between the microsensor patch 110 and the
applicator system 180 and 2) an unsealed state that supports
uncoupling between the microsensor patch 110 and the applicator
system 180. However, the venting channel 86 can alternatively be
configured in any other suitable manner.
1.3.2 Applicator--Second Applicator Portion
[0114] The second applicator portion 82 functions to support the
first applicator portion 81, the elastic coupler 83, and the
trigger 84, and functions to cooperate with one or more portions of
the applicator system 110 to reversibly lock the first applicator
portion 81 into place and to release the first applicator portion
81 to accelerate a microsensor patch 110 coupled to the first
applicator portion 81 along a path toward the body of the user. The
second applicator portion 82 can thus circumscribe or otherwise
surround the first applicator portion 81 in a manner that controls
a path of motion of the first applicator portion 81 within the
second applicator portion 82. However, any other suitable
relationship can exist between the first applicator portion 81 and
the second applicator portion 82, such that acceleration of the
microsensor patch 110 toward the body of the user occurs as
desired.
[0115] In relation to retention of the first applicator portion 81
(with the coupled microsensor patch 110) by the second applicator
portion 82, the second applicator portion 82 can include or be
coupled to a retainer 821 that provides a mechanism for reversibly
locking the first housing portion 81 with the second housing
portion 82 (e.g., during the loading mode described below).
[0116] The retainer 821 can include a mechanical latching
mechanism, that, when engaged by the first housing portion 81,
retains the position of the first housing portion in a loaded mode;
then, with activation of the trigger 84 described below disengages
the latching mechanism to release the first housing portion 81. In
specific examples, the retainer can thus include one or more of: a
wedge-shaped protrusion biased laterally toward a corresponding
recessed region of the first housing portion 81, whereby the
wedge-shaped protrusion engages the recessed region as the first
housing portion 81 transitions into the loaded mode; a
ram-and-catch mechanism whereby twisting of at least one of the
second housing portion 82 and the first housing portion 81 engages
a retaining region of the retainer 821; and any other suitable
mechanical latching mechanism. In more detail, a ram-and-catch
mechanism (or other twisting mechanism) can be used, in combination
with a elastic component (as described below), to adjust the
acceleration of the first applicator portion 81, with the
microsensor patch 110, toward the body of the user. Such an
adjustment can be based upon an amount of potential energy stored
in a spring that is compressed by the rotation mechanism, or any
other suitable mechanism, and can be used to ensure proper
insertion of the microsensor for a variety of skin types or user
demographics.
[0117] The retainer 821 can additionally or alternatively include a
magnetic retention mechanism that reversibly retains a position of
the first housing portion 81 relative to the second housing portion
82. The magnetic retention mechanism can include a magnet of a
first polarity coupled to the second applicator portion 82 that
interfaces with a magnet of a second polarity coupled to the first
applicator portion 81, such that the two magnets provide a
configuration that reversibly retains the first housing portion 81
in position relative to the second housing portion 82.
Alternatively, at least one magnet of the magnetic retention
mechanism can include an electromagnetic element. In a specific
example, as shown in FIGS. 17A and 17B, the magnetic retention
mechanism can interface with a coil element that passes current in
a manner where the current magnitude affects an acceleration
profile of the first housing portion 81, with the coupled
microsensor patch 110, toward the body of the user. This mechanism
is described in further detail in relation to the elastic coupler
83 below.
[0118] In variations, the second applicator portion 81 can be
composed of a polymeric material (e.g., plastic), a metallic
material, and/or any other suitable material. In variations of the
applicator system 180 incorporating mechanical mechanisms, the
second applicator portion 81 can be at least partially composed of
plastic. In variations of the applicator system 180 incorporating
magnetic and/or electromagnetic mechanisms, the second applicator
portion 81 can be at least partially composed of a metal (e.g.,
steel, etc.). However, any applicator portion can additionally or
alternatively be composed of any other suitable material.
1.3.3 Applicator--Support Elements and Other Elements
[0119] The applicator system 180 can also include an elastic
coupler 83 between the first applicator portion 81 and the second
applicator portion 82, wherein the elastic coupler 83 functions to
store potential energy in the loaded mode of the trigger, which can
be released to accelerate the first housing portion 81, with the
microsensor patch 110, toward the body of the user. In variations
wherein the first applicator portion 81 is situated within the
second applicator portion 82, the elastic coupler 83 can be
positioned such that translation of the first applicator portion 81
within the second applicator portion 82 adjusts a state of
compression of the elastic coupler, thereby transitioning between a
state of high potential energy in the loaded mode and a state of
low potentially in the released mode, as described below. In a
specific example, as shown in FIGS. 15, 16A, and 16B, the elastic
coupler 83 can reside within a space laterally between a venting
channel 86 of the first applicator portion 81 and an interior wall
of the second housing portion, wherein the elastic coupler 83 is
retained in position at either a base surface of the venting
channel 86 of the first applicator portion 81 or a base surface of
the second applicator portion 82; however, the elastic coupler 83
can additionally or alternatively be configured relative to the
first applicator portion 81 and the second applicator portion 82 in
any other suitable manner.
[0120] The elastic coupler 83 can include a spring with a suitable
spring force in relation to storage of a maximum amount of
potential energy to provide proper acceleration of the microsensor
patch 110 toward the body of the user. Additionally or
alternatively, the elastic coupler 83 can comprise any other
suitable material that can transition between a state of high
potential energy and low potential energy. In other variations, the
elastic coupler 83 can include a pair of magnets with like polarity
oriented toward each other, an elastomeric element, or any other
suitable component that stores and releases potential energy.
[0121] As indicated above, in some variations wherein the second
applicator portion 82 includes or is coupled to a magnet, the
applicator system 180 can further include a coil of conductive
material that passes current in a manner that causes an interaction
between a magnetic field formed by the current and the magnet. In a
specific example, as shown in FIGS. 17A and 17B, the elastic
coupler 83 can be replaced or in some manner supplemented by a coil
of wire (e.g., voice coil) coupled to a current source and operable
to pass a desired amount of current, thereby affecting acceleration
parameters (e.g., a velocity profile) of the first applicator
portion 81, with the microsensor patch 110, toward the body of the
user. As such, the second applicator portion can be operable
between different modes, each mode associated with a different
amount of current passage, wherein the current magnitude changes
acceleration parameters of the first applicator portion 81, with
the microsensor patch 110, toward the body of the user.
[0122] In still other variations, however, the elastic coupler 83
can additionally or alternatively include or replaced with any
other suitable element that promotes an acceleration of the first
applicator portion 81, with the microsensor patch 110, toward the
body of the user. In one alternative example, the first applicator
portion can be pneumatically driven using compressed air; however,
any other suitable mechanism can be incorporated.
[0123] As indicated above, in some variations, the applicator
system 180 can include a trigger 84 operable between a loaded mode
84aa and a released mode 84b, wherein the trigger 84 functions to
enable release of the first applicator portion 81 to accelerate the
microsensor patch 110 toward the body of the user. The trigger 84
can be mechanically controlled or electrically controlled. For
instance, in a first variation, the trigger 84 can be entirely
mechanical and used to transition the retainer 821 of the second
applicator portion 82 into a configuration that unlatches the first
applicator portion 81 from the second applicator portion 82,
allowing the compressed elastic coupler 83 to be released and
accelerate the first applicator portion 81, with the microsensor
patch 110, toward the user. In a second variation, the trigger 84
can be electronic and, when activated, allow current to pass
through a conductive coil about a magnet of the second applicator
portion 82, thereby generating a magnetic field that interacts with
the magnet and creating a driving force to accelerate the first
applicator portion 81, with the microsensor patch 110, toward the
user. However, other variations of the trigger 84 can be configured
in any other suitable manner, some examples of which are described
in Sections 1.3.4 and 1.3.5 below.
[0124] The applicator system 180 can additionally or alternatively
include any other suitable support elements. For instance, the
applicator system 180 can include components that support the
microsensor patch 110 and/or the applicator system 180 against the
skin of the user prior to coupling of the microsensor to the user.
In one variation, the applicator system 180 can include a
compressible support material situated behind the coupling
interface/suction interface of the first applicator portion 81,
wherein the compressible support material complies with the user's
body during the process of coupling the microsensor patch 110 to
the user's body. The applicator system 180 can additionally or
alternatively include structures that obscure the microsensor patch
110 from the user's view during the insertion process, in order to
prevent apprehension of the user during the insertion process.
Additionally or alternatively the applicator system 180 can include
noise-dampening elements operable to prevent apprehension of the
user during the insertion process. Additionally or alternatively,
the applicator system 180 can include an audio detection element
(e.g., a microphone coupled to an element of the applicator system)
operable to detect a sound output from the elastic coupler 83
during a transition from the loaded mode to the released mode,
thereby facilitating assessment of proper The system can, however,
include any other suitable element(s).
1.3.4 Applicator--Specific Examples
[0125] In a first specific example, as shown in FIGS. 16A and 16B,
the applicator system 180' includes a first applicator portion 81'
including a suction interface 811' coupled to a venting channel 86'
with an opening 87'; a second applicator portion 82' including a
retainer; a spring 83' between the first applicator portion 81' and
the second applicator portion 82'; and a trigger 84' including a
sealing interface 88', the trigger 84' operable between a loaded
mode 84a' and a released mode 84b'; wherein, in the loaded mode, as
shown in FIG. 16A, the elastic coupler is in a first compressed
state between the first applicator portion and the second
applicator portion, the first applicator portion is retained by the
retainer of the second applicator portion, and the suction
interface is coupled to the second housing portion with the opening
of the venting channel sealed by the sealing interface. As shown in
FIG. 16A, transitioning to the loaded mode 84a' can be facilitated
using an example of the base station 5 described in section 1.4 and
shown in FIGS. 1 and 16A, wherein the base station 5 includes a
recessed platform for receiving and positioning the first housing
portion 191 within a substantially horizontal plane. In this
example, the recessed platform includes a central opening into a
cavity, wherein the cavity provides clearance for portions of the
microsensor 116 coupled to the first housing portion 191, and
wherein the cavity includes a charging slot that can accept units
of the second housing portion 196 for charging (e.g., even when the
first housing portion 191 is positioned at the recessed platform).
As such, the base station 5 can include a charging station within
the cavity and a platform, such that the base station 5 facilitates
loading of a patch assembly and charging of a battery of the second
housing portion. Then, as shown in FIG. 16A, pressing the second
applicator portion 82' downward can transition the applicator 180'
to the loaded mode 84a' by way of a trigger ring 2 of the second
applicator portion 82' that translates upon being compressed by a
recessed ring in the base station 5 that is concentric with the
trigger ring 2.
[0126] After the applicator 180' is in the loaded mode 84a', it can
then be transitioned to the released mode 84b', wherein, in the
released mode, as shown in FIG. 16B, the spring 83' is in a second
compressed state (e.g., a state of low compression) between the
first applicator portion 81' and the second applicator portion 82',
the first applicator portion is released from the retainer 821' of
the second applicator portion, the suction interface 811' is
released from the second housing portion with the opening 87' of
the venting channel 86' unsealed by the sealing interface 88', and
microsensor portions of the body chemistry monitor are coupled to
the user. In the specific example, pressing the second applicator
portion 82' downward against the user's skin can transition the
applicator 180' to the released mode 84b' by way of the trigger
ring 2 of the second applicator portion 82' that translates upon
being compressed against the user's skin. In variations of this
specific example, the trigger ring can have an adjustable set
position that affects a travel distance between the loaded patch
assembly and skin of the user, such that the acceleration profile
of the applicator 180' can be adjusted depending on specific needs
of the user. However, the trigger ring can alternatively be
adjusted in any other suitable manner. In the specific example, the
velocity of the microsensor 116 upon impact can be between 3 and 15
m/s; however, the velocity can alternatively be any other suitable
velocity to provide coupling between the microsensor 116 and skin
of the user.
[0127] In a broader use case for the applicator system 180'
described above, the microsensor patch 110 can be loaded into the
applicator system 180 with the second housing portion 196 coupled
to a suction interface of the first housing portion, wherein in the
loaded mode the venting channel 86 is sealed by a sealing interface
of the second applicator portion 82/trigger 84. An adhesive portion
of the first housing portion 191 can then be exposed, and the
applicator system 180 can be positioned, in the loaded mode 84a and
with the microsensor exposed and facing the body of the user. Then,
the trigger 84 can be activated to transition the applicator system
180 to the released mode 84, thereby using converted potential
energy from the compressed spring of the loaded mode 84a to
accelerate portions of the microsensor into the body of the user.
However, variations of the use case described above can be
configured in any other suitable manner.
[0128] In a second specific example, as shown in FIGS. 17A and 17B,
the applicator system 180'' includes a first applicator portion
81'' including a coupling interface 811'' that couples to the
microsensor patch by suction; a second applicator portion 82''
composed of steel and including a magnet 89''; a spring 83''
between the first applicator portion 81'' and the second applicator
portion 82''; a coil 88'' operable to pass current and interact
with the magnet 89''; and a trigger 84'' operable between a loaded
mode 84a'' and a released mode 84b''; wherein, in the loaded mode,
as shown in FIG. 17A, the elastic coupler is in a first compressed
state between the first applicator portion and the second
applicator portion, the first applicator portion is retained by the
retainer of the second applicator portion, and the coupling
interface is coupled to the microsensor patch; and wherein in the
released mode, as shown in FIG. 17B, the spring 83'' is in a second
compressed state (e.g., a state of low compression) between the
first applicator portion 81'' and the second applicator portion
82'', the first applicator portion is released from the retainer
821' of the second applicator portion with passage of current
through the coil 88'', the coupling interface 811'' is released
from the second housing portion 82'', and microsensor portions of
the body chemistry monitor are accelerated into to the user.
[0129] In a use case for the applicator system 180'' described
above, the microsensor patch 110 can be loaded into the applicator
system 180'' with the second housing portion 196 coupled to the
coupling interface of the first housing portion. An adhesive
portion of the first housing portion 191 can then be exposed, and
the applicator system 180'' can be positioned, in the loaded mode
84a and with the microsensor exposed and facing the body of the
user. Then, the trigger 84 can be activated to transition the
applicator system 180 to the released mode 84 with passage of
current through the coil 88'', thereby using electromagnetic
interactions between the magnet 89'' and the coil 88 to accelerate
portions of the microsensor into the body of the user. However,
variations of the use case described above can be configured in any
other suitable manner
[0130] However, variations of the specific examples and/or use
cases described above can be configured in any other suitable
manner. For instance, some variations of the applicator system 180
can include speaker components (or other components) operable to
generate audible signals (or other signals, such as light signals,
haptic signals, etc.) indicative of correct or incorrect
application of the microsensor at the user's body.
1.3.5 Applicator--Other Variations
[0131] In another variation, as shown in FIG. 18A, the applicator
system 180' can be incorporated into a first housing portion 191 of
a housing 190 of the system 100 and can comprise an elastic pin 181
(e.g., spring-loaded pin) configured to complement a recess of a
second housing portion 196. In this variation, a normal force
applied to a broad surface of the second housing portion 196
initially causes the elastic pin 181 to retract, and rebounding of
the elastic pin 181 into the recess of the second housing portion
196 biases and accelerates the microsensor 116 into the skin of the
user.
[0132] In another variation, as shown in FIG. 18B, the applicator
system 180'' implements elastic portions of the housing 190, which
can be used to retract a housing portion with the microsensor 116
and to release the housing portion, thereby accelerating the
microsensor 116 into skin of the user.
[0133] In another variation, the applicator system cooperates with
a first housing portion 191 and a second housing portion 196,
wherein the applicator system comprises a first applicator portion
configured to surround the housing 190 and interface with the
second housing portion 196, and a second applicator portion
configured to accelerate the second housing portion toward skin of
the user. In a first specific example of this variation, as shown
in FIG. 19A, the applicator system 180a comprises a ram-and-catch
mechanism, wherein twisting of a rotatable component 83 of the
applicator system 180a transitions a plunger 84 of the applicator
system 180a from a resting configuration 84a to a loaded
configuration 84b, as shown in FIGS. 19B and 19C, and pushing of
the rotatable component 83 of the applicator system 180a releases
the plunger 84 back to the resting configuration 84a (as shown in
FIG. 19D), thereby accelerating the microsensor 116 toward skin of
the user during application of the microsensor patch 110 to the
user. In more detail, in the first specific example, twisting of
the rotatable component 83 transitions the plunger 84 along ramped
surfaces 85 of the applicator system 180a to the loaded
configuration 84a, where the plunger 84 rests on triggers 86 of the
applicator system 180a. Then, as shown in FIG. 19D, pressing of the
rotatable component 83 provides an outward biasing force on the
triggers 86 (e.g., due to wedge-shaped morphology of the triggers
that interacts with a complementary portion of the rotatable
component 83), thereby releasing the plunger 84 to the resting
configuration 84a. In this specific example, a set of ribs 87
coupled to a wall of the applicator system 180 surrounding the
plunger 84 maintain plunger alignment.
[0134] In a second specific example of this variation, as shown in
FIG. 20, the applicator system 180b comprises an elastic component
89 housed within and coupled to a translating component 88 of the
applicator system 180b, wherein the translating component 88
comprises a plunger 84' and is configured to translate along a
first axis. The applicator system 180b further comprises a trigger
188 coupled to a biasing spring 189 and configured to translate
along a second axis perpendicular to the first axis, between a
holding position 188a and a releasing position 188b. In the second
specific example, the translating component 88 is biased in holding
position 188a, and pushing of the translating component 88 places a
lateral biasing force on the trigger 188 against the biasing spring
189 (e.g., due to wedge-shaped morphology of the trigger 188 that
interacts with a complementary portion of the translating component
88), thereby releasing the plunger 84' to accelerate the
microsensor 116 toward skin of the user. In pushing the translating
component 88, compression of the elastic component 89 creates a
reverse biasing force that automatically releases the translating
component 88 toward the resting configuration 88a.
[0135] The applicator system 180 can alternatively be configured to
receive the microsensor patch 110, to stretch the skin of the user
isotropically in two dimensions to facilitate application, and to
push the microsensor patch 110/transmitting unit 130 assembly onto
the user's stretch skin. Still alternatively, the applicator system
180 can include any other suitable applicator, variations and
examples of which are described in U.S. App. No. 62/025,174
entitled "System for Monitoring Body Chemistry" and filed on 16
Jul. 2014. Still other variations of the system 100 can entirely
omit a applicator system 180.
1.4 System--Base Station
[0136] As shown in FIG. 1, the system can include a base station 5
that functions to receive the microsensor patch 110 (e.g., within a
second housing portion 196). In receiving the microsensor patch
110, the base station 5 can include alignment elements 6 (e.g.,
protrusions, recesses, magnetic alignment elements, etc.) that
facilitate alignment of the microsensor patch 110 within the base
station, as shown in FIG. 18A. The base station 5 can additionally
or alternatively facilitate charging of a rechargeable battery of
the microsensor patch 110 by including elements that generate an
electromagnetic field that interacts with a charging coil coupled
to the battery, thereby charging the battery 138. In more detail,
as described above, the base station 5 can include a cavity with a
slot that accepts the second housing portion 196 (or any other
portion of the system 100 containing the battery) for charging,
where by contacts of the charging unit can detect a feedback loop
between the an analog front end (AFE) circuit of the second housing
portion 196 and charging contacts, in order to initiate charging.
The base station 5 can additionally or alternatively be used to
transition the microsensor patch between different operational
states, in relation to data transfer between the microsensor patch
110, a mobile computing device 150 associated with the user, and
modules of a processing subsystem 160 (e.g., cloud module) as shown
in FIGS. 21A and 21B. In a first operation mode 5a, the
transmitting unit 130 of the microsensor patch 110 and the mobile
computing device 150 can pair/bond only when the second housing
portion 196 of the microsensor patch 110 is in communication with
the base station 5 (e.g., aligned within the base station 5). Thus,
in the first operation mode 5a, the microsensor patch 110 can
transmit and receive data (e.g., compact raw data compounded into a
plurality of bits over Bluetooth communication). In a second
operation mode 5b wherein the microsensor patch 110 is not in
communication with the base station 5, the microsensor patch 110
can be configured to only transmit data (but not receive data),
thereby reducing energy usage, preventing man-in-the-middle attack,
and preventing tampering. As such, the second operation mode 5b
prevents reading of data from the microsensor patch 110 by a
fraudulent entity, without gaining physical access to the
microsensor patch 110.
[0137] The operation modes of the system 100 enabled by the
microsensor patch, the base station 5, the mobile computing device
150, and the processing subsystem 160 are further detailed in FIGS.
21A and 21B and 22. In relation to pairing with the microsensor
patch 110 in the first operation mode 5a, the mobile computing
device 150 functions to provide one or more of: data relay, data
visualization, data storage, notification, and action functions
(e.g., as described in relation to the software module 163
described above). In communicating information between the mobile
computing device 150 and a cloud module of the processing subsystem
160, the mobile computing device 150 can be configured to transmit
raw data in Javascript Object Notation (JSON) format (or any other
suitable format) to be processed in the cloud, and analyte data,
notifications, and alerts (e.g., as derived from an analysis) can
be transmitted back to the mobile computing device 150 in JSON
format (or any other suitable format). The cloud module of the
processing subsystem 160 can thus serve to enable authentication of
the user (e.g., in association with a user account of a native
application) and/or data, data storage, data processing,
notification, and prediction functions, as described in relation to
the processing subsystem 160 described above. Thus, the system 100
is configured for fault tolerance, wherein the microsensor patch
110 stores data when faulty operation of the mobile computing
device 150 occurs, and failure of the processing subsystem 100
results in data storage at the mobile computing device. The system
100 can, however, be configured in any other suitable manner.
[0138] As shown in FIG. 21B, the base station 5 and the applicator
system 180 can be configured to couple together, thus facilitating
portability of the base station 5 and applicator system 180.
However, the base station 5, applicator system 180, and microsensor
110 can alternatively be configured to couple or not couple
together in any other suitable manner.
1.5 System--Calibration
[0139] The microsensor patch 110 is preferably calibrated to
prevent signal degradation and to mitigate the effects of transient
effects experienced during analyte sensing. The primary sensing
mechanism is potentiometric for small analytes (e.g., potassium,
sodium, calcium), and amperometric for large molecules (e.g.,
glucose, lactic, creatinine). In a first variation, the microsensor
patch 110 passively detects analytes by detecting an impedance
and/or capacitance change, as well as a voltage change when an
analyte or analyte concentration contacts the microsensor 116.
Calibration can occur by normalizing sensing measurements relative
to a grounded portion of the microsensor 116, such as a reference
electrode.
[0140] In a second variation, the microsensor patch 110 can
implement active impedance calibration, wherein a drive voltage is
implemented by the electronics subsystem 111 of the microsensor
patch 110, and voltage and impedance and/or capacitance changes are
detected. The drive voltage is preferably applied in a sinusoidal
pattern, but can alternatively be applied in any appropriate
pattern. In the second variation, sensed analytes or analyte
concentrations are characterized by changes in impedance, and noise
is characteristically distinguished from analyte detection by
monitoring changes in voltage unaccompanied by changes in impedance
or capacitance. The second variation thus employs a conductometric
measurement to calibrate the microsensor patch 110. Impedance
measurements can also be used to address shift in a reference
electrode (e.g., in the first variation described above).
[0141] In a third variation, the microsensor patch 110 can employ
injection of a volume of a calibration solution with a known
concentration of at least one analyte, in order to calibrate the
microsensor patch 110. In an example of the third variation, the
calibration solution can have a known concentration of at least one
analyte, such that changes (e.g., changes in electrical parameters)
detected by the microsensor patch 110 in response to the
calibration solution can be used to normalize measurements
resulting from sensed analytes or analyte concentrations occurring
after injection of the volume of calibration solution. In the third
variation, the calibration solution can be injected automatically
and periodically over the lifetime usage of the transdermal patch;
however, the calibration solution can alternatively be injected
when prompted by a user or other entity.
[0142] In a fourth variation, the microsensor patch 110 can include
a membrane comprising a known concentration and/or release profile
of at least one analyte, in order to calibrate the microsensor
patch 110. In an example of the fourth variation, the membrane can
have a known concentration and release profile of at least one
analyte, such that changes (e.g., changes in electrical parameters)
detected by the microsensor patch 110 in response to the membrane
can be used to normalize measurements resulting from sensed
analytes or analyte concentrations. In the fourth variation, the
membrane can be a degradable membrane, such that degradation of the
membrane over time releases analytes from the membrane.
Alternatively, the membrane can be manufactured with specific
porosity, contributing to a certain analyte release profile.
[0143] In a fifth variation, the microsensor patch 110 can include
a coating or a cap comprising a soluble species (e.g., analyte/ion)
with a well-known solubility, in order to calibrate the microsensor
patch 110. In an example of the fifth variation, the soluble
species maintains a known concentration of the species within the
vicinity of a filament that can be used to normalize and/or
calibrate a signal. Examples of soluble species include low
solubility, biocompatible calcium salts, such as calcium carbonate,
calcium phosphate, and dicalcium phosphate for calcium sensing.
Other suitable soluble species can be used to calibrate other
analytes.
[0144] In alternative variations, the microsensor patch 110 can use
any other suitable calibration method. For instance, the
transdermal patch can be pre-staged, prepped, loaded, or activated
to have a set calibration state enabling calibration of the system
after application to the user within a desired period of time
(e.g., an 85 mg/dl calibration state equilibrated after insertion
within a period of 2 hours).
[0145] As a person skilled in the art will recognize from the
previous detailed description and from the figures and claims,
modifications and changes can be made to the described embodiments,
variations, and examples of the system 100 without departing from
the scope of the system 100.
2. Method
[0146] As shown in FIG. 23, a method 200 for monitoring body
chemistry of a user comprises: receiving a second housing portion
into an opening of a first housing portion S210, the first housing
portion supporting a microsensor including a first working
electrode, a second working electrode, a reference electrode, and a
counter electrode, and the second housing portion supporting an
electronics subsystem configured to receive a signal stream from
the microsensor; after interfacing with the second housing portion,
accelerating the second housing portion toward skin of the user
S220, thereby delivering sensing regions of the microsensor into
interstitial fluid of the user; generating an impedance signal,
from two of the first working electrode, the second working
electrode, the reference electrode, and the counter electrode, in
response to applying a voltage, near a shifted potential different
than a reference potential of the reference electrode S230, wherein
the shifted potential is associated with a signal conditioning
module of the electronics subsystem; at a processing system in
communication with the electronics subsystem, receiving the signal
stream and the impedance signal S240; at the processing system,
generating an analysis indicative of an analyte parameter of the
user and derived from the signal stream and the impedance signal
S250; and transmitting information derived from the analysis to an
electronic device associated with the user, thereby facilitating
monitoring of body chemistry of the user S260.
[0147] The method 200 functions to provide continuous monitoring of
a user's body chemistry through reception and processing of signals
associated with of one or more analytes present in the body of the
user, and to provide an analysis of the user's body chemistry to
the user and/or an entity (e.g., health care professional,
caretaker, relative, friend, acquaintance, etc.) associated with
the user. Alternatively, the method 200 can function to detect a
user's body chemistry upon the user's request or sporadically,
and/or can provide an analysis of the user's body chemistry only to
the user. The method is preferably implemented, at least in part,
using an embodiment, variation, or example of elements of the
system 100 described in Section 1 above; however, the method 200
can additionally or alternatively be implemented using any other
suitable system.
[0148] Variations of the system 100 and method 200 include any
combination or permutation of the described components and
processes. Furthermore, various processes of the preferred method
can be embodied and/or implemented at least in part as a machine
configured to receive a computer-readable medium storing
computer-readable instructions and/or in the cloud. The
instructions are preferably executed by computer-executable
components preferably integrated with a system and one or more
portions of a control module and/or a processor. The
computer-readable medium can be stored on any suitable computer
readable media such as RAMs, ROMs, flash memory, EEPROMs, optical
devices (CD or DVD), hard drives, floppy drives, or any suitable
device. The computer-executable component is preferably a general
or application specific processor, but any suitable dedicated
hardware device or hardware/firmware combination device can
additionally or alternatively execute the instructions.
[0149] The FIGURES illustrate the architecture, functionality and
operation of possible implementations of systems, methods and
computer program products according to preferred embodiments,
example configurations, and variations thereof. In this regard,
each block in the flowchart or block diagrams may represent a
module, segment, step, or portion of code, which comprises one or
more executable instructions for implementing the specified logical
function(s). It should also be noted that, in some alternative
implementations, the functions noted in the block can occur out of
the order noted in the FIGURES. For example, two blocks shown in
succession may, in fact, be executed substantially concurrently, or
the blocks may sometimes be executed in the reverse order,
depending upon the functionality involved. It will also be noted
that each block of the block diagrams and/or flowchart
illustration, and combinations of blocks in the block diagrams
and/or flowchart illustration, can be implemented by special
purpose hardware-based systems that perform the specified functions
or acts, or combinations of special purpose hardware and computer
instructions.
[0150] As a person skilled in the art will recognize from the
previous detailed description and from the figures and claims,
modifications and changes can be made to the preferred embodiments
of the invention without departing from the scope of this invention
defined in the following claims.
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