U.S. patent application number 10/791974 was filed with the patent office on 2004-09-16 for cutaneous administration system.
Invention is credited to Lo, Clement C., Noonan, William D., Pickup, Ray L..
Application Number | 20040181196 10/791974 |
Document ID | / |
Family ID | 25513036 |
Filed Date | 2004-09-16 |
United States Patent
Application |
20040181196 |
Kind Code |
A1 |
Pickup, Ray L. ; et
al. |
September 16, 2004 |
Cutaneous administration system
Abstract
Bioactive agents are cutaneously delivered by a jet dispenser
using inkjet technology, such as that used in printing. The
dispenser propels precise volumes of bioactive agent toward the
skin, where they exert a local or topical effect, or move through
the skin for transdermal systemic delivery. Drugs are either
delivered directly to the skin, or are introduced into a
transdermal patch, which may receive repeated dosages. A controller
in the dispenser may control delivery of multiple different drugs,
timing of drug administration, or change drug regimens in response
to a changing medical condition of a patient, such as those
monitored by a sensor in communication with the controller, for
example to prevent an overdose. The dispenser may act as an
electromechanical patch, capable of long term administration of
drugs to the skin, to achieve local or systemic pharmaceutical
effects. Administration methods are also provided, along with
replacement kits.
Inventors: |
Pickup, Ray L.; (Brush
Prairie, WA) ; Lo, Clement C.; (Lake Oswego, OR)
; Noonan, William D.; (Sherwood, OR) |
Correspondence
Address: |
HEWLETT-PACKARD COMPANY
Intellectual Property Administration
P.O. Box 272400
Fort Collins
CO
80527-2400
US
|
Family ID: |
25513036 |
Appl. No.: |
10/791974 |
Filed: |
March 3, 2004 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
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10791974 |
Mar 3, 2004 |
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09967603 |
Sep 28, 2001 |
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6723077 |
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Current U.S.
Class: |
604/305 |
Current CPC
Class: |
A61M 37/00 20130101;
B41J 3/36 20130101; A61M 5/14248 20130101; A61M 31/002 20130101;
B41J 2/16535 20130101; A01K 11/005 20130101; B41J 2/16505 20130101;
B41J 3/407 20130101; A61M 35/003 20130101; A61M 37/0084 20130101;
A01K 13/003 20130101 |
Class at
Publication: |
604/305 |
International
Class: |
A61F 013/00; A61K
009/70 |
Claims
We claim:
1. An applicator for cutaneous delivery of a bioactive composition
to a cutaneous target, comprising: a jet dispenser comprising an
orifice, and a container which holds and delivers the bioactive
composition to said orifice for ejection therethrough; and a spacer
positioned between the dispenser orifice and the target during
ejection of the bioactive composition to the target.
2. An applicator according to claim 1, wherein the spacer is
supported by the dispenser.
3. An applicator according to claim 1, wherein the spacer is
attached to the cutaneous target.
4. An applicator according to claim 1, further comprising an
adhesive applicator patch for application to the cutaneous
target.
5. An applicator according to claim 1, wherein the applicator is an
applicator for transdermal delivery of a bioactive composition
capable of transdermal flux.
6. An applicator according to claim 1, further comprising a
bioactive composition in the container.
7. An applicator according to claim 6, wherein the bioactive
composition is a pharmaceutical composition.
8. An applicator according to claim 7, wherein the pharmaceutical
composition is capable of transdermal delivery.
9. An applicator according to claim 1, wherein the dispenser is a
thermal droplet jet dispenser.
10. An applicator according to claim 1, wherein the dispenser is a
piezoelectric droplet jet dispenser.
11. An applicator according to claim 1, further comprising a
controller which automatically ejects the bioactive composition
from the dispenser orifice at selected times.
12. An applicator according to claim 11, wherein the controller is
a microprocessor programmed to dispense the bioactive composition
at predetermined intervals.
13. An applicator according to claim 1, wherein the container
comprises multiple container modules.
14. An applicator according to claim 13, wherein the multiple
container modules are removable from the dispenser.
15. An applicator according to claim 13, wherein at least two of
the container modules contain a bioactive substance.
16. An applicator according to claim 15, wherein at least one of
the container modules contains a bioactive agent in powder
form.
17. An applicator according to claim 15, wherein at least two of
the container modules contain different bioactive substances that
combine after ejection to produce a bioactive effect.
18. An applicator according to claim 17, wherein at least one of
the bioactive substances is a penetration enhancer that improves
cutaneous penetration of another bioactive substance.
19. An applicator according to claim 18, wherein the penetration
enhancer is dimethyl sulfoxide (DMSO).
20. An applicator according to claim 15, wherein the bioactive
composition is a nitrate, an anti-hypertensive drug, an analgesic,
a hormone or an analogue thereof, or nicotine or an analogue
thereof.
21. An applicator according to claim 20, wherein: the dispenser is
a piezoelectric droplet jet dispenser; and the nitrate is
nitroglycerin.
22. An applicator according to claim 20, wherein the
anti-hypertensive drug is clonidine or minoxidil, the analagesic is
fentanyl, or the hormone is estrogen or testosterone.
23. An applicator according to claim 1, further comprising an
attachment member that selectively retains the dispenser in
prolonged contact with the cutaneous target.
24. An applicator according to claim 23, wherein the attachment
member comprises a strap.
25. An applicator according to claim 23, wherein the attachment
member comprises an adhesive.
26. An applicator according to claim 1, wherein: the cutaneous
target comprises skin covering a subject; and the spacer comprises
a sealing member that selectively substantially seals the dispenser
against the skin to form a substantially closed chamber when the
dispenser is in contact with the skin.
27. An applicator according to claim 26, wherein the sealing member
is a continuous elastomeric seal.
28. An applicator according to claim 1, further comprising an
indicator which indicates a degree of depletion of the bioactive
composition in the dispenser.
30. An applicator according to claim 1 wherein: the cutaneous
target comprises skin covering a subject having a measurable
parameter; and the applicator further comprises: a bio-sensor which
monitors said parameter of the subject and generates a signal in
response thereto; and a controller which automatically dispenses
the bioactive composition from the dispenser orifice in response to
said signal.
31. An applicator according to claim 30 wherein the bio-sensor
comprises a pulse oximetry device.
32. An applicator according to claim 31 wherein said parameter
comprises pulse rate.
33. An applicator according to claim 31 wherein said parameter
comprises blood oxygenation levels.
34. An applicator according to claim 31 wherein said bio-sensor
communicates said signal to the controller by infrared
communication.
35. An applicator according to claim 31 wherein said bio-sensor
communicates said signal to the controller by radiowave
communication.
36. An applicator according to claim 1, further comprising a
display which displays information about said composition.
37. An applicator according to claim 1, further comprising an
interface which receives a memory storage device containing dosage
information concerning administration of said composition.
38. An applicator according to claim 1, further comprising a keypad
input which receives dosage information concerning administration
of said composition.
39. An applicator according to claim 1, further comprising: a
display which displays information about said composition,
including various dosages; and a keypad input including scroll keys
which when activated cause the display to selectively show said
various dosages.
40. An applicator according to claim 1, further comprising a
controller which is programmable.
41. An applicator according to claim 40, wherein said controller is
programmable from a remote computer in communication with said
controller.
42. An applicator according to claim 1, further comprising: a main
body which supports said container; and a dispensing head which
supports said orifice.
43. An applicator according to claim 42, wherein said dispensing
head supports plural orifices each fluidically coupled to said
container.
44. An applicator according to claim 42, further comprising a
flexible link which couples together said main body and said
dispensing head.
45. An applicator according to claim 43, wherein said flexible link
is hollow and contains a fluid conduit which fluidically couples
said container to said orifice.
46. An applicator according to claim 1, further comprising a main
body which supports said container and said orifice.
47. An applicator according to claim 46, wherein said container is
removable from the main body.
48. An applicator according to claim 1, further comprising a
sensor.
49. An applicator according to claim 48, further comprising a
controller in communication with said sensor.
50. An applicator according to claim 49, wherein: said sensor
comprises an optical sensor; said target changes color following
delivery of the bioactive composition; and said optical sensor
detects said color change and in response thereto, the controller
ceases ejection of said composition.
51. An applicator according to claim 49, wherein: said sensor
comprises an optical sensor; said target changes color following
absorption of the bioactive composition; and said optical sensor
detects said color change and in response thereto, the controller
causes said orifice to eject said composition.
52. An applicator according to claim 49, wherein: said sensor
comprises an optical sensor; the container comprises two container
modules each containing different bioactive substances; the target
has indicia detectable by said optical sensor indicative of one of
said different bioactive substances; and the controller causes said
orifice to eject said one of said different bioactive
substances.
53. An applicator according to claim 1, further comprising a dermal
patch between said orifice and said target.
54. An applicator according to claim 53, wherein the dermal patch
is of an absorbent material which receives said delivery of said
composition.
55. A kit for filling an applicator having a jetting orifice with a
bioactive composition for cutaneous delivery through ejection from
said orifice to a subject, the kit comprising: a container which
contains the bioactive substance, with the container having an
interface to fluidically couple the container with the applicator
to deliver said composition to the orifice; and a dermal patch for
placement on the subject to receive said composition from said
orifice when spaced a selected distance therefrom.
56. A kit according to claim 55, further comprising instructions
for dispensing the bioactive composition from the applicator on to
the patch.
57. A kit according to claim 55, further comprising a bioactive
composition in the container.
58. A kit according to claim 55, further comprising plural
containers.
59. A kit according to claim 58, wherein at least two of the plural
containers contain the same bioactive composition.
60. A kit according to claim 58, wherein at least two of the plural
containers contain different bioactive compositions.
61. A kit according to claim 60, wherein said different bioactive
compositions combine after ejection to produce a bioactive
effect.
62. A kit according to claim 60, wherein at least one of the
bioactive compositions is a penetration enhancer that improves
cutaneous penetration of another bioactive composition.
63. A kit according to claim 62, wherein the penetration enhancer
is dimethyl sulfoxide (DMSO).
64. A kit according to claim 58, wherein at least one of the plural
containers contains a bioactive composition in powder form.
65. A kit according to claim 55, wherein the bioactive composition
is suitable for cutaneous administration.
66. A kit according to claim 55, wherein the bioactive composition
is suitable for transdermal administration.
67. A kit according to claim 55, wherein the bioactive composition
is a pharmaceutical composition.
68. A kit according to claim 55, wherein said bioactive composition
is capable of transdermal flux.
69. A kit according to claim 55, wherein the bioactive composition
is a nitrate, an anti-hypertensive drug, an analgesic, a hormone or
an analogue thereof, or nicotine or an analogue thereof.
70. A kit according to claim 69, wherein the nitrate is
nitroglycerin.
71. A kit according to claim 69, wherein the anti-hypertensive drug
is clonidine or minoxidil, the analagesic is fentanyl, or the
hormone is estrogen or testosterone.
72. A kit according to claim 55, wherein the patch has an adhesive
portion for application to the subject.
73. A kit according to claim 72, further comprising a removable
release sheet overlying the adhesive portion during shipment.
74. A kit according to claim 55, wherein the patch has a
replaceably removable moisture impervious cover layer.
75. A kit according to claim 55 for filling an applicator having a
programmable controller which controls said ejection from said
orifice in response to programming instructions, and the kit
further contains said programming instructions.
76. A kit according to claim 75 for filling an applicator having an
interface, wherein said programming instructions are stored on a
memory storage device which is received by said interface to supply
said instructions to said controller.
77. A kit according to claim 76, wherein said memory storage device
is supported by said container.
78. A kit according to claim 76, wherein said interface comprises a
slot, and said memory storage device is received within said
slot.
79. A kit according to claim 55, wherein said container is
refillable with said bioactive composition.
80. A kit for administering a bioactive composition to a subject,
the kit comprising: a jet dispenser comprising an orifice, and a
container which delivers the bioactive composition to said orifice
for ejection therethrough; and a retainer for retaining the
dispenser in contact with skin of a subject.
81. A kit according to claim 80, further comprising a controller
which controls said ejection through the orifice in response to
information about a physiological condition of the subject
82. A kit according to claim 82, further comprising a sensor which
senses a physiological condition of the subject, and provides
information about said condition to the controller.
83. A method of administering a bioactive composition to a subject,
the method comprising: applying to a cutaneous surface of the
subject a jet dispenser comprising a container holding the
bioactive composition; dispensing the bioactive composition from
the dispenser through at least one orifice toward the cutaneous
surface; and retaining the bioactive composition in prolonged
contact with the cutaneous surface.
84. A method according to claim 83, wherein retaining the bioactive
composition in prolonged contact with the cutaneous surface
comprises dispensing the bioactive composition on to a dermal patch
that is retained on the cutaneous surface.
85. A method according to claim 84, wherein the dermal patch is an
adhesive dermal patch that is applied to the cutaneous surface
prior to dispensing the bioactive composition from the
dispenser.
86. A method according to claim 85, wherein the dermal patch
comprises a selectively removable cover that is removed prior to
dispensing the bioactive composition into the patch, and is
subsequently replaced on the patch to improve retention of the
bioactive composition in the patch.
87. A method according to claim 83, wherein retaining the bioactive
composition in prolonged contact with the cutaneous surface
comprises providing a seal between the dispenser and cutaneous
surface, to form a substantially sealed chamber between the
dispenser and the cutaneous surface, and retaining the dispenser in
prolonged contact with the seal.
88. A method according to claim 83, further comprising repeatedly
dispensing the bioactive composition toward the cutaneous
surface.
89. A method according to 88, further comprising resupplying the
dispenser with the bioactive substance.
90. A method according to claim 89, wherein resupplying the
dispenser comprises replacing a container in the dispenser.
91. A method of administering a bioactive composition to a subject,
the method comprising: applying a cutaneous patch to skin of the
subject; and dispensing the bioactive composition from a jet
dispenser by ejection through an orifice to the patch using inkjet
technology.
92. A method according to claim 91, further comprising dispensing
the bioactive composition to the patch at intervals to provide
sustained dosages of the bioactive composition from the patch to
the subject.
93. A method according to claim 92, wherein the intervals are
preselected intervals.
94. A method according to claim 91 further comprising dispensing
the bioactive composition from the dispenser to the patch when an
amount of the bioactive composition in the patch falls below a
desired level.
95. A method according to claim 91: wherein said dispensing further
comprises dispensing a second substance from the dispenser to the
patch; and the method further comprises mixing the bioactive
composition with dispensing.
96. A method according to claim 95 wherein said mixing occurs
between said orifice and said patch.
97. A method according to claim 95 wherein said mixing occurs
within said patch.
98. A method according to 91 further comprising containing said
bioactive composition a container portion of said jet dispenser
prior to said dispensing.
99. A method according to claim 98 further comprising refilling
said container with said bioactive composition.
100. A method according to claim 99 further comprising removing
said container from the jet dispenser prior to said refilling, and
after said refilling, replacing said container for further
dispensing.
101. An applicator according to claim 1, wherein the dispenser
comprises a silicon electrostatic actuated droplet jet
dispenser.
102. A method according to claim 83, wherein said dispensing
comprises using a thermal droplet jet dispenser.
103. A method according to claim 83, wherein said dispensing
comprises using a piezoelectric droplet jet dispenser.
104. A method according to claim 83, wherein said dispensing
comprises using a silicon electrostatic actuated droplet jet
dispenser.
105. A method according to claim 91, wherein said inkjet technology
used in said dispensing comprises thermal inkjet technology.
106. A method according to claim 91, wherein said inkjet technology
used in said dispensing comprises piezoelectric inkjet
technology.
107. A method according to claim 91, wherein said inkjet technology
used in said dispensing comprises silicon electrostatic actuated
inkjet technology.
108. A method according to claim 83, further comprising: optically
reading subject identification information with an optical reading
device of said jet dispenser; correlating said subject
identification information with prescribed dosage information; and
wherein said dispensing comprises dispensing the bioactive
composition according to said prescribed dosage information.
109. A method according to claim 91, further comprising: optically
reading subject identification information with an optical reading
device of said jet dispenser; correlating said subject
identification information with prescribed dosage information; and
wherein said dispensing comprises dispensing the bioactive
composition according to said prescribed dosage information.
110. An applicator according to claim 28, wherein said indicator
comprises an indicator light.
111. An applicator according to claim 28, wherein said indicator
comprises an audible signal.
112. An applicator according to claim 28, wherein said indicator
comprises a tactile signal.
113. An applicator according to claim 112, wherein said tactile
signal comprises a vibratory signal.
114. An applicator according to claim 48, wherein said sensor
comprises an optical sensor.
115. An applicator according to claim 48, wherein said sensor
comprises a mechanical sensor which monitors a physical parameter
of a subject.
116. An applicator according to claim 115, wherein said mechanical
sensor comprises an accelerometer.
117. An applicator according to claim 116, wherein said
accelerometer monitors activity of a subject bearing said cutaneous
target and adjusts said delivery in response to said
monitoring.
118. A method according to claim 83, further comprising: monitoring
a physical parameter of the subject; and in response to said
monitoring, adjusting said dispensing.
119. A method according to claim 118, wherein said physical
parameter comprises heartbeats.
120. A method according to claim 118, wherein said physical
parameter comprises breathing.
121. A method according to claim 118, wherein said physical
parameter comprises an activity in which the subject is
engaged.
122. A method according to claim 121, wherein: said activity
comprises participating in a sport; and said adjusting comprises
dispensing an additional amount of said bioactive composition.
123. A method according to claim 118, wherein said monitoring
comprises using a monitor portion of the jet dispenser.
124. A method according to claim 123, wherein said monitor portion
comprises a mechanical sensor.
125. A method according to claim 124, wherein said mechanical
sensor comprises an accelerometer.
126. A method according to claim 91, further comprising: monitoring
a physical parameter of the subject; and in response to said
monitoring, adjusting said dispensing.
127. A method according to claim 126, wherein said physical
parameter comprises heartbeats.
128. A method according to claim 126, wherein said physical
parameter comprises breathing.
129. A method according to claim 126, wherein said physical
parameter comprises an activity in which the subject is
engaged.
130. A method according to claim 129, wherein: said activity
comprises participating in a sport; and said adjusting comprises
dispensing an additional amount of said bioactive composition.
131. A method according to claim 126, wherein said monitoring
comprises using a monitor portion of the jet dispenser.
132. A method according to claim 131, wherein said monitor portion
comprises a mechanical sensor.
133. A method according to claim 132, wherein said mechanical
sensor comprises an accelerometer.
134. A kit according to claim 80, further comprising a bioactive
agent.
135. A kit according to claim 134, wherein said bioactive agent
comprises a bioactive composition attracting agent selected from
the group comprising a cream, a paste, or a salve.
136. A method according to claim 83, further comprising: applying a
bioactive composition attracting agent to a treatment location on
the cutaneous surface of the subject; pulling the bioactive
composition toward said agent; and penetrating said agent with the
bioactive composition to treat the treatment location with the
bioactive composition.
137. An applicator according to claim 1, further including an
activation device which may be manually triggered to eject said
bioactive composition from the jet dispenser.
138. An applicator according to claim 137, further including plural
activation devices each bearing a label corresponding to an event,
with different dosages of the bioactive composition being ejected
from the jet dispenser according to which of the plural activation
devices is triggered.
139. An applicator according to claim 137, wherein the jet
dispenser contains plural bioactive compositions, and the
applicator further includes plural activation devices with
different bioactive compositions being ejected from the jet
dispenser according to which of the plural activation devices is
triggered.
140. A method according to claim 83, further comprising manually
triggering an activation device after said applying and before said
dispensing, with said dispensing occurring in response to said
triggering.
141. A method according to claim 91, further comprising manually
triggering an activation device after said applying and before said
dispensing, with said dispensing occurring in response to said
triggering.
142. An applicator according to claim 1, further including a
reservoir containing said bioactive composition and a fluid conduit
to convey the bioactive composition from the reservoir to the jet
dispenser.
143. An applicator according to claim 142, wherein said fluid
conduit comprises tubing.
144. An applicator according to claim 142, wherein said reservoir
comprises a collapsible bladder.
145. A kit according to claim 55, wherein said container comprises
a collapsible bladder, and said interface comprises tubing.
146. A kit according to claim 80, wherein said container comprises
a collapsible bladder, and the kit further includes a fluid conduit
to convey the bioactive composition from the bladder to the jet
dispenser.
147. An applicator according to claim 146, wherein said fluid
conduit comprises tubing.
148. A method according to claim 83, further comprising: storing
the bioactive composition in a collapsible bladder; and conveying
the bioactive composition from the collapsible bladder to the jet
dispenser.
149. A method according to claim 148 wherein said conveying
comprises conveying the bioactive composition through tubing.
150. A method according to claim 91, further comprising: storing
the bioactive composition in a collapsible bladder; and conveying
the bioactive composition from the collapsible bladder to the jet
dispenser through tubing.
Description
INTRODUCTION
[0001] This invention relates generally to the administration of
compositions (such as pharmaceutical compositions) for cutaneous
administration, including transdermal absorption through the skin.
In particular, this invention combines the previously unrelated
technologies of pharmaceutical administration and inkjet
technology.
[0002] Pharmaceutical compositions provide effective treatments for
a variety of illnesses. Unfortunately, there are many obstacles to
the administration of therapeutically effective doses of many
medications. For example, some drugs (particularly peptide based
drugs such as insulin) are partially or totally inactivated
following oral ingestion, by the highly acidic environment of the
stomach. Another problem is the "first pass" effect, which refers
to the partial inactivation of orally ingested drugs in the liver,
after they have been absorbed from the gastrointestinal system, but
before they have exerted their full therapeutic effect. Even when
these problems are overcome, patients often fail to take their
medications at the proper prescribed intervals, or for the
necessary period of time, to achieve an optimal therapeutic
response.
[0003] Inhalational and intranasal administration have been used as
alternative routes of drug delivery. Inhaled drugs can be absorbed
directly through the mucous membranes and epithelium of the
respiratory tract, thereby minimizing initial inactivation of
bioactive substances by the liver. Inhalational delivery can also
provide drugs directly to therapeutic sites of action (such as the
lungs or the sinuses). This mode of administration has been
particularly effective for the delivery of pulmonary drugs (such as
asthma medications) and peptide based drugs (usually via intranasal
administration), using metered dose inhalers (MDIs). However, MDIs
often require coordinating inspiration with actuation of the MDI,
and some patients are not able to master this technique. Moreover,
patients still often forget to take the medication at prescribed
times, or for the necessary period of time to achieve clinical
goals. Other patients inadvertently or inappropriately use
medications, leading to hospitalizations, morbidity, and even
death.
[0004] In an effort to overcome such problems, some drugs are
administered by passive cutaneous routes, such as transdermal
delivery of drugs from a patch applied to the skin. Examples of
drugs that are routinely administered by this route are
nitroglycerin, steroid hormones, and some analgesics (such as
fentanyl). Transdermal administration avoids initial inactivation
of drugs in the gastrointestinal tract, and provides continuous
dosages usually over a relatively short period of time (such as a
day), without requiring active participation by the patient.
Continuous sustained administration provides better bioavailability
of the drug, without peaks and troughs, and eliminates the problem
of the patient forgetting to take multiple doses of the drug
throughout the day. However the patch must be changed regularly,
usually each day, to provide a necessary drug concentration in the
patch to establish the correct concentration gradient for delivery
of the appropriate dose of the drug across the skin.
[0005] In addition to transdermal systemic delivery of drugs,
topical delivery of drugs to the surface of the skin is also used
for treating many skin conditions. For example, antibiotics are
topically administered to the skin to treat infection, anesthetics
to treat pain, retinoids to treat acne, and minoxidil to treat hair
loss. These drugs must be repeatedly applied to the skin to achieve
their effect, and much of the dosage may be lost by drainage of
liquid from the application site, or being inadvertently wiped
away. Moreover, excess drug is usually applied to the skin, which
can lead to undesired toxic effects particularly if the drug is
absorbed through the skin.
[0006] Devices and methods are disclosed herein for improving the
cutaneous delivery of drugs, by using inkjet-like applicators for
transdermal and other cutaneous delivery of drugs. Kits and systems
for administrating drugs in this fashion are also described.
BRIEF DESCRIPTION OF THE DRAWINGS
[0007] FIG. 1 is a perspective, fragmented, and partially
schematic, view of one form of a transdermal application system
illustrated herein, having a dispenser and a transdermal patch
applied to a human arm.
[0008] FIG. 2 is an enlarged, side elevational view of the
transdermal application system of FIG. 1, shown in place over a
transdermal patch for dispensing.
[0009] FIG. 3 is an enlarged, front elevational view of the
dispenser of FIG. 1, showing a container module removed from the
applicator and a protective cap for placement on the droplet head
during periods of inactivity. This figure also schematically
illustrates how the applicator may be connected to a remote control
device, such as a computer.
[0010] FIG. 4 is a top plan view of another form of a transdermal
patch, which may be used in conjunction with the transdermal
application system of FIG. 1.
[0011] FIG. 5 is a perspective, fragmented, and partially
schematic, view of a more compact alternative form of a transdermal
application system illustrated herein, having a compact dispenser
which may be used with or without a patch, here shown retained
against a human arm.
[0012] FIG. 6 is a cross-sectional, side elevational view of a
removable module of the dispenser of FIG. 5.
[0013] FIG. 7 is a bottom plan view of the module of FIG. 7.
[0014] FIG. 8 is a schematic view, partially in cross-section, of
an alternative embodiment, in which a bioactive agent is
administered from a thermal jet dispenser to a cutaneous target,
such as a pad, acting as a substitute for conventional intravenous
("IV") administration of the bioactive agent.
[0015] FIG. 9 is a side elevational view, partially in
cross-section, of the transdermal application system of FIG. 5,
taken along lines 9-9 thereof, showing application of a
bioactive-composition-attracting agent, such as a cream, a paste,
or a salve to the skin, here on a skin blemish, such as a wart.
DETAILED DESCRIPTION OF PARTICULAR EXAMPLES
[0016] Unless otherwise noted, technical terms are used according
to conventional usage. Definitions of common terms in pharmacology
may be found in Remington: The Science and Practice of Pharmacy,
19.sup.th Edition, published by Mack Publishing Company, 1995 (ISBN
0-912734-04-3). Transdermal delivery is discussed in particular at
page 743 and pages 1577-1584.
[0017] The singular forms "a," "an," and "the" refer to one or more
than one, unless the context clearly dictates otherwise. The term
"comprising" means "including."
[0018] An "array" refers to a predetermined pattern, which can be
either regular or irregular. Examples of arrays are linear
distributions or two-dimensional matrices.
[0019] A "bioactive" composition, substance or agent is a
composition which affects a biological function of a subject to
which it is administered. An example of a bioactive composition is
a pharmaceutical substance, such as a drug, which is given to a
subject to alter a physiological condition of the subject, such as
a disease. Bioactive substances, compositions and agents also
include other biomolecules, such as proteins and nucleic acids, or
liposomes and other carrier vehicles that contain bioactive
substances.
[0020] "Cutaneous" refers to the skin, and "cutaneous delivery"
means application to the skin. This form of delivery can include
either delivery to the surface of the skin to provide a local or
topical effect, or transdermal delivery, in which a drug diffuses
through the skin surface and into the underlying microvasculature,
often for systemic administration of the drug.
[0021] The present disclosure concerns an applicator for cutaneous
delivery of a bioactive composition using a jet dispenser, such as
a piezoelectric or thermal jet dispenser, for instance of a
construction used in the inkjet printing arts. The dispenser
includes a container for holding the bioactive agent and delivering
it to a dispenser orifice, or an array of dispenser orifices. The
thermal or piezoelectric jet propels precise amounts of droplets
from the dispenser toward a cutaneous target. In one embodiment, a
spacer is also provided between the dispenser orifice and a
cutaneous target, to space the dispenser a desired distance away
from the cutaneous target during delivery of the bioactive agent.
This spacer may be attached to either the skin or the dispenser, or
merely be interposed between them, to provide an interface across
which the bioactive substance may be distributed from the orifice,
or from an array of orifices, to a cutaneous target. The target may
include skin or a skin patch, such as a transdermal drug delivery
patch, which acts as a reservoir for subsequent prolonged
transdermal delivery of the agent.
[0022] In certain embodiments, the dispenser includes the bioactive
agent in the container. Examples of agents that can be included in
the container include pharmaceutical compositions that are capable
of transdermal delivery. Such agents include drugs having
sufficient lipophilicity or hydrophilicity to move through the skin
surface and stratum corneum. Certain of these agents are designed
to reach the microvasculature of the skin, for subsequent systemic
absorption and distribution. Examples of agents that are suitable
for transdermal delivery include scopolamine, nitrates such as
nitroglycerine, an antihypertensive or anti-adrenergic drug such as
clonidine, steroid hormones such as 17-beta-estradiol and
testosterone, analgesics, such as the opioid analgesic fentanyl,
and treatments for nicotine withdrawal, such as nicotine. Many
analogues of these drugs retain their biological activity, and are
also suitable for transdermal delivery. Although the disclosed
dispenser is particularly suited for transdermal delivery of drugs,
it can also be used for topical surface application of drugs, such
as antibiotics, corticosteroids, minoxidil or retinoids (such as
Retin A).
[0023] The dispenser may also include a controller for manually or
automatically dispensing the bioactive substance from the dispenser
at selected times. The controller may take the form of an actuator
that is manually depressed to activate the dispenser and dispense
the agent. Alternatively, the controller may be a microprocessor
which is programmed to dispense the bioactive substance at
predetermined intervals, for example several times a day, directly
on to the skin or on to a patch. Alternatively, the controller can
be used to adjust dosages of drug administered, for example for a
particular time of day, an event (such as an activity that will
require a dosage modification), or detection of a physiological
condition (such a an adverse drug reaction that requires reduction
or cessation of drug administration). When the dispenser is used
with a patch, the dispenser may be used to recharge the patch and
avoid the necessity of changing the patch as often. Either with or
without a patch, complex administration protocols may be followed,
for example applying different drugs at different times throughout
the day or longer period, for example as long as a week, a month,
or even longer.
[0024] In certain examples, the container may carry multiple
container modules, such as removable and replaceable modules that
contain the bioactive agent(s). Several modules may contain the
same or different agents, for example different agents that combine
before or at the time of delivery to modify one or both of the
agents, or to produce a desired bioactive effect. An example of a
modifying substance that may be combined at the point of ejection
is a penetration enhancer that improves cutaneous penetration of
the other bioactive substance. Penetration enhancers that may be
mixed with a bioactive agent at the time of delivery include
solvents such as water; alcohols (such as methanol, ethanol and
2-propanol); alkyl methyl sulfoxides (such as dimethyl sulfoxide,
decylmethyl sulfoxide and tetradecylmethyl sulfoxide); pyrrolidones
(such as 2-pyrrolidone, N-methyl-2-pyrroloidone and
N-(2-hydroxyethyl)pyrrolidone); laurocapram; and miscellaneous
solvents such as acetone, dimethyl acetamide, dimethyl formamide,
and tetrahyrdofurfuryl alcohol. Other penetration enhancers include
amphiphiles such as L-amino acids, anionic surfactants, cationic
surfactants, amphoteric surfactants, nonionic surfactants, fatty
acids and alcohols. Additional penetration enhancers are disclosed
in Remington: The Science and Practice of Pharmacy, 19.sup.th
Edition (1995) on page 1583. Of course agents such as penetration
enhancers can also be premixed with the bioactive agent prior to
the point of ejection, for example the bioactive agent and
modifying substance can be present together in the container.
[0025] The bioactive agent may be any flowable fluid (for example a
liquid, gel or powder), although liquids are particularly of use in
the dispenser. In some embodiments, at least one of the container
modules may contain a bioactive agent in powder or other dry form.
The powder or other agent is dispensed from the container, and may
be combined with a liquid (such as a penetration enhancer) en route
to the cutaneous delivery site. The interface provided by a spacer
between the orifice plate and the target allows chemical reactions
to occur, as well as phase changes to stabilize (such as a change
from a solid to a liquid state). This interface may also provide
flexibility in the distribution of the drug across a larger target
area, as compared to application of the agent from an orifice that
abuts the target. Using existing inkjet technology, distribution of
the drug to the target may be carefully controlled, and exact
dosing of the drug may be achieved. Controllers may be used to
dispense simple or complex drug regimens, which is of particular
advantage in patients who require numerous daily medications.
Computerized control of medication dosing, which may be programmed
by medical personnel for subsequent automated delivery, can help
avoid toxic drug interactions, overdosages, and deaths.
[0026] The applicator is suitable for use in a variety of ways. For
example, the applicator may be intermittently applied to the skin
to administer a dosage of a drug directly to the skin.
Alternatively, the applicator may be applied to a transdermal patch
to recharge it with medication, instead of replacing the patch. In
another embodiment, the applicator may be selectively retained in
prolonged contact with the cutaneous target, for example by
securing the applicator to the skin with an attachment member, such
as a strap or adhesive. In this manner, the active agent may be
administered from the dispenser for a prolonged period of time into
a transdermal patch, or directly onto the skin. A replaceable
container module may be removed from the applicator and replaced,
to avoid the necessity of removing the applicator from the
patient.
[0027] In some embodiments, the applicator forms a substantially
sealed chamber directly against the skin, without an intervening
transdermal patch, and effectively become a direct cutaneous or
transdermal applicator. In particularly effective embodiments, an
elastomeric seal (such as a continuous seal) is provided between
the applicator and the skin to form the sealed chamber in which the
drug can be maintained until it is absorbed. Conditions in the
sealed chamber may be altered to enhance absorption of the drug,
for example by increasing humidity in the chamber by dispensing
water droplets, or intermittently applying a penetration enhancer
to the skin from the dispenser.
[0028] One particularly disclosed embodiment of the device includes
a piezoelectric or thermal jet dispenser that includes a plurality
of removable modules in fluid communication with one or more fluid
orifices (such as an array of orifices) ejecting and directing a
pharmaceutical fluid from the modules toward a cutaneous target. A
spacer may be carried by the dispenser and positioned to be
disposed against the cutaneous target while the dispenser ejects
the pharmaceutical fluid from the dispenser. A programmable
microprocessor in the dispenser may control ejection of the
pharmaceutical fluid from the orifice plate at pre-selected
intervals, such as every three or four hours, or even every few
minutes or seconds, or ejection can be triggred by a sensor or
other feedback mechanism.
[0029] The device may further include a programming module, such as
a keyboard for entering dosage information, a display screen for
showing what information has been entered, and indicators (such as
one or more lights or a display screen on the exterior of the
device) that provide information about how much drug remains in the
device. Display screens may also provide information about
medications in the device, and provide an interface through which
other information about the medications or their administration can
be entered and/or obtained.
[0030] The following detailed description of the device is
illustrated in the accompanying figures.
Embodiment of FIGS. 1-3
[0031] The medication dispensers disclosed herein may be similar to
liquid dispensers known as inkjet printheads used in inkjet
printing mechanisms, such as printers, plotters, facsimile machines
and the like, some of which are described for example in Durbeck
and Sherr, Output Hardcopy Devices, Academic Press Inc., 1987 (ISBN
0-12-225040-0), particularly in chapter 13, pages 311-370. These
technologies have in common the extraction of small quantities of a
fluid from a reservoir, which are converted into fine droplets, and
transported through the air to a target medium by appropriate
application of physical forces. This technology has been
implemented in a variety of ways, but one of the common approaches
has been thermal inkjet technology, in which liquids are heated
using resistors to form drops and propel them from a chamber
through an orifice toward a target. Another approach is
piezoelectric inkjet technology, in which movement of a
piezoelectric transducer changes a chamber volume to generate the
drop. An additional approach is known as silicon electrostatic
actuator ("SEA") inkjet technology, such as that disclosed in U.S.
Pat. No. 5,739,831 to Nakamura (assigned to Seiko Epson
Corporation).
[0032] A typical jet printing mechanism uses cartridges (often
called "pens") which shoot drops of liquid colorant (generally
referred to as "ink") onto a page. Each cartridge has a printhead
formed with very small nozzles through which the ink drops are
fired. Most often, the printhead is held in a carriage which slides
back and forth along a guide rod in a reciprocating printhead
system, with a target or print media, such as paper, being advanced
in steps between each pass of the printhead. To print an image on
media, the printhead is scanned back and forth across the page,
shooting drops of ink in a desired pattern as it moves. Other
printing systems known as "page-wide array" printers, extend the
printhead across the entire page in a stationary location, and
print as the media advances under the printhead. The particular
liquid ejection mechanism within either type of printhead may take
on a variety of different forms known to those skilled in the art,
such as the piezoelectric or thermal printhead technology.
[0033] For instance two thermal ink ejection mechanisms are shown
in U.S. Pat. Nos. 5,278,584 and 4,683,481, both assigned to the
present assignee Hewlett-Packard Company. In a thermal system, a
barrier layer containing fluid channels and vaporization chambers
is located between a nozzle orifice plate and a substrate layer.
The substrate layer typically contains linear arrays of heater
elements, such as resistors, which are energized to heat ink within
the vaporization chambers. Upon heating, an ink droplet is ejected
from a nozzle associated with the energized resistor. By
selectively energizing the resistors as the printhead moves across
the page, the ink is expelled in a pattern on the print media to
form a desired image (e.g., picture, chart or text).
[0034] In piezoelectric inkjet technology, an activating pulse is
applied to a piezoelectric plate or member attached to a plate,
which then responds by flexing to propel an ink drop out of a
nozzle. Several examples of piezoelectric inkjet printheads are
described in U.S. Pat. Nos. 4,992,808; 6,186,619; and 6,149,968
(assigned to Xaar Technology Ltd.) and U.S. Pat. No. 6,193,343 and
WO 00/16981 (assigned to Seiko Epson Corporation)
[0035] Some printhead designs use "snapper" reservoir systems, in
which permanent or semi-permanent printheads are used in
conjunction with a detachable reservoir carrying a fresh liquid
supply, with the reservoir being snapped into place on the
printhead. Another design uses permanent or semi-permanent
printheads in what is known in the industry as an "off-axis"
printer. In an off-axis system, the printheads carry only a small
liquid supply reciprocally back and forth across the printzone,
with this on-board supply being replenished through tubing that
delivers liquid from an "off-axis main reservoir" placed at a
remote, stationary location within or near the printhead. In both
the snapper and off-axis systems, rather than purchasing an entire
new cartridge which includes a costly new printhead, the consumer
buys only a new supply of liquid for the main reservoir.
[0036] In striving to duplicate the quality of photographic film
images, the inkjet industry has focused on decreasing the size of
ink droplets ejected from the nozzles, as well as accurately
placing these droplets on the print media. For instance, some of
the more recent inkjet print cartridges are able to deliver
droplets of a size on the order of 0.5-6 picoliters, although
larger droplets can also be generated, for example droplets of 10,
50, 100 or more picoliters. The resolution within which currently
commercially available inkjet printing mechanisms may place ink
droplets on a page is on the order of 1200-4800 dots per inch
(known in the industry as a "dpi" rating). Thus, while striving to
achieve photographic print quality, inkjet printing technology has
become very adept at accurately metering and dispensing fluids. The
ability to dispense very small and accurate amounts of fluids
(including liquids and powders) is taken advantage of in
constructing the transdermal cutaneous application systems
illustrated herein.
[0037] While these inkjet printheads may be used in the cutaneous
application systems illustrated here, rather than using a printing
analogy,. the printhead will instead be referred to in a more
general nature as a "dispenser head" or "applicator head."
[0038] FIGS. 1-3 illustrate one embodiment of a transdermal
application system 20, constructed in accordance with the present
invention, for applying a bioactive substance to a subject, such as
to a forearm of an animal or person 22, through the skin 24. While
the bioactive agent, which is typically dispensed as a fluid, may
be applied directly to skin 24, the illustrated embodiment shows
applying the agent to an absorbent member, such as a patch 25 of a
fabric or other absorbent material which is adhered to skin 24.
Patch 25 has an upper exposed surface 26, and an opposing under
surface 27 which is in contact with skin 24. A removable protective
layer 28, such as a layer of a liquid impermeable thin polyester,
may be selectively removed and reapplied to patch 25. In one
particular embodiment, the fluid is applied to patch 25, which then
allows skin 24 to gradually absorb the fluid from patch 25.
[0039] Any of the many types of transdermal patches may be used, or
modified for use with the dispenser. For example the Testoderm.RTM.
transdermal system (Alza Pharmaceuticals) uses a flexible backing
of transparent polyester, and a testosterone containing film of
ethylene-vinyl acetate copolymer membrane that contacts the skin
surface and controls the rate of release of active agent from the
system. The surface of the drug containing film is partially
covered by thin adhesive stripes of polyisobutylene and colloidal
silicon dioxide, to retain the drug film in prolonged contact with
the skin. In the present system, adhesive can be provided on both
surfaces of the drug containing film, for example on both upper
face 26 and under face 27 of patch 25, so that the flexible
polyester backing 28 may be selectively removed to provide access
to the drug-containing layer without removing the patch. An
adhesive release layer with openings in it can be provided between
the patch and backing 28, to help protect upper face 26 of patch 25
during repeated removals of backing 28. Alternatively, the patch
may be removed, recharged with the drug, and then reapplied, in
which event the impermeable backing 28 may be permanently applied
to patch 25. In this case, adhesive need only be present on under
surface 27 of patch 25. In yet other embodiments, there may be no
impermeable backing, such as layer 28, over patch 25, so, for
instance the selected drug may be continually administered, or the
absorbency of the patch is sufficient to retain the drug in the
patch without an impermeable backing. Further examples of
transdermal patches that may be used or modified for use in the
present system and method include the Nicoderm.RTM. and
Duragesic.RTM. patch.
[0040] The transdermal application system 20 illustrated in FIG. 1
includes an applicator or dispenser 30, which is illustrated as an
applicator for dispensing a fluidic chemical composition either
directly to skin 24, or to patch 25. The applicator 30 includes a
main body 32 which may be coupled to a rectangular application head
34 via a linkage, such as a hollow ball and socket linkage 35 which
allows applicator head 34 to pivot with respect to main body 32. To
assure even and controlled application of a chemical composition to
skin 24 or patch 25, the illustrated applicator head 34 is provided
with a pair of spacer bars 36 and 38 at opposing edges of
applicator head 34. Alternatively, a series of discrete spacer
protrusions or bumps, or roller or wheel assemblies (not shown) may
be used. As further alternative embodiments, one or more spacers
may be formed on the patch 25, or a separate spacer unit (not
shown) may be positioned between the dispenser head 34 and the
patch upper surface 26 during delivery of the bioactive agent.
While the illustrated applicator 30 includes a separate body 32 and
applicator head 34, it is apparent that in some embodiments a
simpler design may eliminate linkage 35, such that the applicator
is a one-piece member.
[0041] As shown in FIG. 3, applicator head 34 includes one or more
ejection heads, such as fluid ejection heads 40, 42, 44 and 46.
Ejection heads 40-46 may be constructed according to principles in
the thermal inkjet technology, using piezoelectric ejection
techniques, or other manners of fluid ejection known to those
skilled in the inkjet arts. Indeed, the ejection of some chemicals
may be benefited by a thermal ink ejection technology, in which
elevated temperature can activate the agent. In contrast, other
agents may chemically degrade and lose some or all bioactivity when
heated in a thermal system, and such compositions would preferably
be dispensed using a piezoelectric or other non-thermal ejecting
head technology. Preferably, the spacer bars 36, 38 maintain a
spacing between the ejection heads 40-46 and the upper exposed
surface 26 of the patch 25 or skin 24 of greater than about 30 mil
(30.times.10.sup.-3 inch), for example 1-3 mm, or even 3-5 mm or
more. One preferred spacing of 0.2-2.0 mm after the patch has
swollen from soaking up the applied fluid permits a smooth even
application of fluid over patch 25. Additionally, this ejection
head to receiving surface spacing advantageously protects ejection
heads 40-46 from unnecessarily coming into contact with the patch
25, which avoids forcing fibers or other debris from the surface of
the patch into the printhead nozzles. Adequate spacing between the
nozzles and patch also avoids capillary wicking of drug from the
nozzles, than can result in inadvertent or unwanted administration
of drug to the patch. Such debris or other fibers in the nozzles
could potentially damage the ejection head nozzles, leading to
fully or partially blocked nozzles that dispense less fluid than
intended. Such debris could also lead to misdirected droplets which
would miss the target area on patch 25. Applicator head 34 may also
include a feedback mechanism, for instance such as a mechanical
sensor or an optical sensor 48 which may be used by applicator 30
in a closed-loop system, as described further below.
[0042] The fluid dispensed by ejection heads 40, 42, 44 and 46 may
be stored in replaceable fluid reservoirs 50, 52, 54 and 56,
respectively. As shown in the specific example of FIG. 3, the
reservoirs 50-56 may be inserted into receptacles formed within
main body 32. Following insertion of the reservoirs 50-56 into the
main body 32, a multi-conduit fluid tubing system 58 delivers fluid
from the reservoirs 50-56, through the hollow ball and socket
linkage 35, into applicator head 34. As shown in FIG. 3, a
multi-conduit system 58 may include four discrete fluid conduits,
such as tubing running through applicator head 34, or conduits
molded, bored or otherwise formed therein, such as conduits 60, 62,
64 and 66. In the illustrated embodiment, the conduits 60, 62, 64
and 66 deliver fluid from the respective reservoirs 50, 52, 54 and
56 to their respective associated ejection heads 40, 42, 44 and
46.
[0043] To maintain ejection heads 40-46 relatively moist and free
of clogs during periods of applicator inactivity, the application
system 20 may include a protective ejection head storage and/or
servicing member 68, which in the illustrated embodiment is
rectangularly shaped to mate with the open face of rectangular
application head 34. Head storage member 68 has four ejection head
sealing members, for example elastomeric or foam caps 70, 72, 74
and 76, which are positioned to seal ejection heads 40, 42, 44 and
46 respectively, for instance, using various printhead cap designs
known to those skilled in the inkjet arts. To maintain caps 70-76
against their respective ejection heads 40-46, the storage member
68 may include a securement means, such as a pair of clips 78 that
mate with applicator head 34 to selectively connect member 68 to
applicator head 34.
[0044] In a more sophisticated embodiment, storage member 68 may
also include one or more ejection head wipers, such as elastomeric
wipers 80, 82, 84 and 86. In one embodiment of the storage member
68 having only caps 70-76, the storage member 68 may be positioned
over applicator head 34 by movement in a direction parallel with
the Z-axis, with securement member 78 being formed with a snap-fit
feature to hold member 68 securely in place, with each of the
ejection heads 40-46 resting securely against their respective caps
70-76. Such a capping system having foam caps may be constructed as
described in U.S. Pat. No. 5,635,965 currently assigned to the
Hewlett-Packard Company. A more sophisticated combination storage
and servicing member 68 may have securement member 78 formed so
that member 68 is applied over the applicator head 34 in a
direction parallel to the negative Y axis, and removed in a
direction parallel to the positive Y axis. Such a lateral
application of the storage and service member 68 over applicator
head 34 allows elastomeric wipers 80-86 to wipe liquid or other
residue from ejection heads 40-46 as member 68 is applied, as well
as upon removal of the service member after uncapping. When the
storage/service member 68 has wiping capability, it may be
desirable to have a back wall portion 88 of the service member
hinged or otherwise retractable to fold downwardly, so upon
installation of member 68 the heads 40-46 first contact wiper
blades 80-86, and upon removal of member 68, the last items which
contact the heads 40-46 are the wipers 80-86.
[0045] As illustrated in FIG. 1, the applicator 30 includes an
onboard ejection head controller 100, illustrated schematically for
convenience. Controller 100 and ejection heads 40-46 receive power
either from an onboard battery storage system, which may be located
in either main body 32, applicator head 34, or both. Alternatively,
power may be supplied from an external source, such as a standard
electrical outlet. Of course, rechargeable or replaceable batteries
may be preferred in some embodiments for ease of portability and
use. Controller 100 operates to apply firing signals to the
ejection heads 40-46, which respond by ejecting fluid from
reservoirs 50-56, respectively. In a simple embodiment, applicator
30 may include an ON/OFF power switch 102, to which controller 100
responds by beginning and/or ending a fluid ejection sequence.
Alternatively, switch 102 may simply serve as an ON switch, with
controller 100 determining the precise amount of fluid to be
ejected from heads 40-46, and then stopping ejection automatically
after the selected metered amount has been dispensed.
[0046] In a more sophisticated embodiment, applicator 30 may
include an input keypad 104, such as an alpha or alpha numeric
keypad. Using keypad 104, a physician, nurse, pharmacist or other
health professional, or the subject 22 to which the fluid will be
applied, may input variations in the amount of and types of fluids
dispensed by applicator head 34. Applicator 30 may also include a
display screen, such as liquid crystal display 105, to indicate
which selections have been made using keypad 104. Alternatively,
keypad 104 may be eliminated, and the controller 100 programmed to
display various selections on screen 105. Use of a pair of
scrolling buttons 106 and 108 may allow different instructions or
selections to be scrolled across, or up and down along, screen 105,
including such information such as desired dosages, frequency, and
potential side effects.
[0047] Display screen 105 may also indicate various selections
along an upper portion of the screen, adjacent buttons 102, 110
and/or 112, allowing a user to then select a particular drug or
dosage by depressing one or more of these buttons. Alternatively,
depressing one of the buttons could indicate the occurrence of a
particular event, such as an adverse medication response that would
alter (for example decrease) a subsequent dosage administration, or
an event (such as physical exertion) than can signal a need to
alter a medication dosage. The controller can also be programmed to
prevent unauthorized alteration of dosages, for example an increase
in a dosage of a controlled substance above that authorized by the
prescribing physician. Alternatively, the controller can permit
certain ranges of dosages to be administered, for example various
doses of an opioid pain reliever in response to fluctuating
pain.
[0048] As shown in FIG. 3, a more expedient method of initially
programming controller 100, or supplying dosage and other
information, may be to use a computer input conductor 114,
selectively attachable to a receptacle on main body 32, to couple
an external computer, microcomputer or other input device 115 to
controller 100. It is apparent that other linkage devices may be
used to communicate between external computing device 115 and
controller 100, such as by using infrared signals, radio waves,
modems, and the like. For example, a patient can download
information stored in the device about self-regulated dosage
administrations or symptoms experienced (as indicated for example
by which buttons have been depressed on the device, and/or the
pattern and frequency of the buttons that are pushed). This
information can be transmitted over a modem to a physician's or
other health care provider's office, where it can be displayed (in
electronic or other form) to a health care professional, and
appropriate action can be taken. For example, if symptoms are noted
to be increasing in spite of administration of a therapeutic amount
of a particular drug, consideration can be given to providing a new
drug or reconsidering the diagnosis for which the drug has been
administered.
[0049] Alternatively, as shown in FIG. 2, main body 32 may define
an input slot 116 which is sized to receive an input device, such
as a flash memory card 118, which carries input data for controller
100. Indeed, use of the flash memory card 118 in conjunction with
the controller 100 may result in the only other input device of
applicator 30 being the ON/OFF switch 102. Alternatively, the
switch may only be an ON switch, with the controller 100 ceasing
fluid application after a selected dosage has been
administered.
[0050] Thus, in one embodiment applicator 30 may only have an ON
switch 102, and be completely preprogrammed via an external
computer 115, such as at a doctor's office or pharmacy, prior to
giving the applicator 30 to a patient. In another embodiment, the
applicator 30 may be sold with only an ON switch 102, and with the
physician or pharmacy supplying one or more of the fluid reservoirs
50-56 in a kit with a flash memory card 118. In such an example,
the kit includes one or more reservoirs 50-56, a flash memory card
118, and may also include a supply of patches 25, or the patches
may be purchased separately. Alternatively, any combination of the
components can be provided in the kit.
[0051] While each of the fluid reservoirs 50-56 may carry different
bioactive agents, it may also be convenient to have each reservoir
carry the same agent, with controller 100 applying fluid from first
reservoir 50 until empty, followed by fluid from a second reservoir
52, and so forth. In such a same-fluid embodiment, it would be
preferable for applicator 30 to indicate to the person 22, or an
attendant, when fluid is being dispensed from the last reservoir,
such as reservoir 56. This indication may take the form of
displaying a message on screen 105, or simply by having an
indicator light or a series of indicator lights mounted on the main
body 32. For example, switch 102 may be back lighted to turn a red
color when the supply of active agent in the containers 50-56 is
low. Alternatively, the indicator may be an audible signal, such as
a beeping sound or a buzzer, or a tactile signal, such as a
vibratory or vibrating signal similar to those used on pager
devices.
[0052] As mentioned briefly above, applicator head 34 may also
include an optical sensor 48 constructed to have a variety of
different uses. For example, optical sensor 48 may be able to
determine whether the storage/service member 68 is in place
protecting applicator head 34. When so engaged, it may be practical
for the controller 100 to periodically purge fluid from the
ejection heads 40-46, to keep the caps 70-76 moist and to purge any
blockages of dried or partially drying fluid from the ejection head
nozzles, or to prevent any inadvertent or undesired administration
of the bioactive agent. Additionally, optical sensor 48 may
indicate to controller 100 whether ejection heads 40-46 are located
over bare skin 24, or over the exposed surface 26 of patch 25. In
some embodiments, to distinguish patch 25 from clothing or other
fabric, patch 25 has its exposed surface 26 treated with a visual
indicator, such as a coating of infrared or ultraviolet ink which
is detectable by the sensor 48.
Embodiment of FIG. 4
[0053] Furthermore, the optical sensor 48 may be used in
conjunction with a segmented pad 120 shown in FIG. 4. The pad 120
is divided into regions, here shown as four regions 122, 124, 126
and 128, separated from one another by a non-absorbing region 130,
shown in this symmetrical embodiment as a plus (+) sign. Each of
the four absorbent regions 122, 124, 126 and 128 has an identifying
indicia 132, 134, 136 and 138, respectively. The patch 120 may be
covered with a moisture impervious layer, such as layer 28
described above. The optical sensor 48 may be used to recognize
various identifying indicia 132-138, and apply a selected
corresponding fluid from one of reservoirs 50-56 to a selected
region 122-128 associated with each of indicia 132-138. For
instance, optical sensors which can distinguish the colors of
black, cyan, magenta and yellow from one another are disclosed in
U.S. Pat. No. 6,036,298. Each of the indicia 132-138 may be a
different one of these colors, and controller 100 recognizes each
of the different indicia, and dispenses a corresponding fluid agent
from ejection heads 40, 42, 44 or 46 to a selected area of the
patch associated with the appropriate color. Moreover, if a tint,
pigment or other colorant is added to the fluids in reservoirs
50-56, optical sensor 48 may be used to distinguish which agent has
previously been applied by applicator 30 to patch 120, allowing the
controller to apply more of the same fluid over this area, a
different fluid over another area, or no fluid over previously
applied areas. Alternatively, changes in color of the substrate may
be sensed by optical sensor 48 as a drug leaves patch 120, and this
color change may be used to indicate to the controller 100 that
additional drug must be dispensed to patch 120.
[0054] In some embodiments of patch 120, such as shown in FIG. 4,
patch 120 may be constructed of a non-woven material which has
selected regions which may be made absorbent, and other regions
which may be made non-absorbent. In the illustrated example, patch
120 is divided into four absorbent quadrants 122, 124, 126 and 128
by the non-absorbent border region 130. While a circular patch is
illustrated, it is apparent that the patch 120 may have other
shapes, and each of the regions 122-128 need not be symmetrical,
but may be of differing sizes and/or shapes. One manner of making
absorbent and non-absorbent regions in the non-woven fabric arts is
to form pad 120 as a multi-layer pad, with the layers bonded
together by applying heat along the border region 130. Typically
non-woven fabrics, such as those of polyethylene and polyurethane,
are moisture impervious when manufactured, with moisture pervious
or absorbent regions being formed by applying surfactants in
regions 122, 124, 126 and 128.
[0055] It may be preferable in some embodiments to provide various
indicia or markings on pad 120, such as indicia 132, 134, 136 and
138 appearing within the absorbent quadrants 122, 124, 126 and 128,
respectively. Indicia 132-138 may be fashioned to change color
after administration of the bioactive agent to the pad 120. Thus, a
user of a single agent system may apply the agent at different
times of the day. Rather than continually tearing off a depleted
patch and replacing it with a new one, a situation which may be
bothersome, time consuming and irritating or painful, a single
patch 120 may be used throughout the day, with fluid applied at
various intervals (such as prescribed intervals) to the different
quadrants 122-128. The patch 120 may be replenished daily or at
even longer intervals, to prolong the effective life of the patch.
In some embodiments, a single patch might be retained in place for
days or even months.
[0056] Moreover, by allowing indicia 132-138 to change color, or
otherwise change appearance after application of the bioactive
agent, a patient 22 would have a clear visual indicator or reminder
as to whether or not a certain dosage had been administered.
Alternatively, indicia 132-138 may be color coded, or otherwise
provided with indicia displayed on the various fluid reservoirs
50-56. For example, each indicium may be a color that corresponds
to a color of a fluid reservoir 50, 52, 54 or 56, or a distinctive
shape cut in a release layer on top of pad 120, such as the letters
A, B, C and D, each of which may correspond to a particular fluid
reservoir. An external surface of each reservoir can also be
provided with identifiers, such as bar codes, that are recognized
by an optical sensor in the dispenser, to assure that the correct
prescribed agent it being dispensed from each reservoir.
[0057] Furthermore, while the illustrated applicator 30 has been
shown as a rather large box like device capable of dispensing at
least four different types of fluids, it is apparent that the
configuration of the housing may be simplified and modified to
provide a more compact unit, particularly for application of a
single fluid. Such a more compact unit may easily be concealed
within the palm of one's hand, allowing for more discrete
application of the composition, such as when a dosage is required
while shopping, in a meeting, or otherwise in public, particularly
if the patch is positioned in an accessible location beneath loose
fitting clothing.
[0058] In use, transdermal patch 25 or 120 is applied to the skin
of a subject 22. Impermeable backing 28 is peeled away from patch
25, 120 and applicator 20 is applied to the patch, with spacers 36,
38 resting on the skin. Applicator 20 is then actuated, either
manually by pressing switch 102 or automatically by sensors in
applicator 20, to apply a bioactive agent from applicator 20 to
patch 25, 120. This application can occur several times a day, or
at longer intervals. The applicator may be programmed to remind the
user (for example by an audible beep) to use the applicator to
replenish the supply of drug in the patch 25, 120.
Embodiment of FIGS. 5-7
[0059] An example of a more compact dispenser 200 is shown in FIGS.
5-7, in which the dispenser applies a bioactive agent directly to
the skin of a subject, without the necessity of an intervening
patch. Dispenser 200 is applied to forearm 202 of a subject to
whole a bioactive substance is to be administered. In the
illustrated example, dispenser 200 is retained in place by a strap
204 which wraps around forearm 202. An elastomeric seal 205 extends
around the base of dispenser 200, to simultaneously act as a spacer
and form a substantially closed chamber between the ejection head
and the skin. Although dispenser 200 is shown attached to an arm
202, it may also be applied to many other parts of the body (such
as the torso or leg) which have sufficient permeability to receive
the bioactive agent. Many different attachment devices can also be
substituted for the strap 204, such as a suction device or
adhesive. For example, a relative vacuum can be created within seal
205 to hold dispenser 200 in place, for instance if the seal is
formed to act as a suction cup device.
[0060] Dispenser 200 includes a removable, replaceable, and/or
refillable module 206, which includes a container 208 and an
enlarged endplate 210 (or other means to facilitate removal) which
may be grasped to manipulate, insert and remove module 206 from
dispenser 200. As particularly shown in FIG. 6, container 208 has
an upper storage chamber 212 for holding a bioactive liquid (such
as a drug), and a lower piezoelectric dispenser portion 214 that
includes an array of piezoelectric chambers 215 that communicate
with storage chamber 212 through small openings 216. Droplet
orifices are also provided through the lower face of dispenser 200,
as shown in FIG. 7, to form an array of dispenser orifices 218. At
least a portion of one or more walls of each chamber is a
piezoelectric member that expands when electrical current is passed
through it. The chambers 215 are sufficiently small so that liquid
supplied to the chambers 215 from storage chamber 212 remains in
each of the chambers 215 (for example by surface tension or back
pressure) until the liquid is expelled as a droplet by the
expansion of the piezoelectric member. Expansion of the
piezoelectric member reduces a volume of the chamber 215 to expel a
carefully regulated volume of the liquid.
[0061] A controller 220, such as one in the form of a programmable
microchip, is attached to an interior wall of dispenser 200.
Information may be pre-programmed into controller 220, or
controller 220 may be activated by pressing a switch 222 on the
exterior of dispenser 200. Alternatively, controller 220 may be
programmed by a computer (not illustrated) which communicates with
controller 220 through a port (not illustrated) on the exterior of
dispenser 200. Controller 220 is capable of selectively activating
different piezoelectric members to expel liquid from each chamber,
and may also precisely modulate a volume of liquid that is
expelled, by regulating a drive signal that passes through the
piezoelectric member. Controller 220 may also communicate with one
or more remote bio-sensors which monitor one or more parameters of
a subject's condition, such as a pulse oximetry device 224 (FIG. 5)
shown clipped on a finger of the subject. The pulse oximetry device
224 may provide information about pulse rate and blood oxygenation
levels to controller 220 by an electrical lead (not illustrated) or
other remote communication device, such as infrared or radiowave
communication.
[0062] In operation, module 206 is placed in dispenser 200, and
dispenser 200 is applied to the skin of the subject and secured in
place by latching strap 204 around forearm 202. The elastomeric
seal 205 provides a substantially liquid impermeable seal that
helps form a closed chamber between dispenser 200 and the skin.
Switch 222 is then depressed to activate controller 220, which
sends one or more electrical signals to selected piezoelectric
members to change shape or other feature a selected number of
times, and induce a vibration that discharges one or more droplets
of liquid from corresponding piezoelectric chambers 215. The
pattern of discharge may be controlled by selectively activating
different piezoelectric members, but in one embodiment all the
piezoelectric members are simultaneously activated to expel small
droplets from all of dispenser orifices 218. Very small liquid
droplet sizes may be dispensed in this manner to provide a fine
mist of droplets that adhere to the skin, for example by surface
tension. The applied liquid then moves through the skin by
transdermal flux, to deliver a bioactive agent.
[0063] Expulsion of liquid droplets may be repeated at selected
intervals, for example every few seconds, minutes, hours or days,
to provide a concentration gradient of the drug on the skin surface
sufficient to provide transdermal flux across the cutaneous
barrier. Generally, the amount of liquid applied is not sufficient
to causing a pooling of liquid on the surface of the skin, although
such pooling is certainly an option in some embodiments. In this
manner, the dispenser can replace a transdermal patch 25, 120,
which avoids problems of patch degradation and dislodgment (for
example caused by bathing or sweating). Dispenser 200 effectively
becomes an electromechanical patch that may in some embodiments be
removed for short periods (such as for bathing) and replaced,
unlike traditional patches which degrade or become non-adhesive
following prolonged use or exposure to moisture. Dispenser 200 may
also provide very prolonged administration of a drug, for days,
weeks, months, or even years. All that is required is that module
206 be replaced or refilled when depleted.
[0064] The electromechanical patch may also be programmed to
administer multiple different drugs at different times. In such an
embodiment, module 206 may contain multiple liquid sub-compartments
that contain different drugs to be administered. The different
sub-compartments supply different liquids to different
piezoelectric chambers 215, which can be selectively activated to
dispense different drugs either simultaneously or at different
times. Patients who require complex drug regimens, for example
taking multiple different drugs at many different times of day,
will benefit from the ability of controller 220 to track and
administer the drugs. Moreover, controller 220 may be repeatedly
reprogrammed as pharmaceutical dosage regimens are changed in
response to a changing medical condition of a subject. Dosage
regimens may even be automatically and/or remotely changed in
response to varying clinical parameters, such a the results of
laboratory tests.
[0065] The electromechanical patch 200 provides even greater
versatility for substantially immediately responding to the
changing medical status of the wearer. Sensors applied to the
subject, such as pulse oximetry sensor 224 (FIG. 5), may provide
real time feedback to the controller 220 to alter dosage regimens.
For example, if one of the drugs to be dispensed is clonidine
(which reduces adrenergic stimulation), then sensor 224 provides
continuous feedback about pulse rate, which often correlates with a
degree of adrenergic stimulation. In a clinically correct
situation, the dosage of clonidine administered may be correlated
to the pulse rate detected by sensor 224, such that the dosage is
increased as pulse rate rises and decreased as pulse rate declines.
Alternatively, if the medication being dispensed is an opiate
analgesic that has a potential adverse effect on respiratory rate,
then further administration of the drug would be halted if blood
oxygenation levels fall below a predetermined value, for example
94%.
[0066] Although the electromechanical patch dispenser 200 has been
described as a substitute for a conventional transdermal patch, it
may also be used in conjunction with such a patch 25, 120. In such
an embodiment, dispenser 200 is used to apply drug to the patch 25
or 120, which retains the drug against the skin until transdermal
flux of the drug occurs. Drug in the patch may be repeatedly
replenished by dispenser 200.
[0067] In yet other embodiments, the dispenser may be an
iontophoretic dispenser, in which ionized drugs are moved through
the skin under the influence of an applied electric current.
Alternatively, drug movement through the skin can be enhanced by
phonophoresis or sonophoresis, in which drug molecules are moved
through the skin under the influence of sonic energy, such as
ultrasound waves applied to the cutaneous target. Iontophoretic and
phonophoretic drug delivery are disclosed in greater detail in
Remington: The Science and Practice of Pharmacy at page 1584.
[0068] While the illustrated embodiment of applicator 200 is shown
as being attached to the subject by the strap 204, in other
implementations it may be more advantageous to have the applicator
200, perhaps in a smaller or disposable form, attached to the
subject by an adhesive tape, for instance under a blouse or a shirt
for discrete use. As mentioned above, the applicator 200 may be
coupled to a remote sensor, or may include a sensor, such as the
optical sensor 48 of FIG. 3, or a mechanical sensor, as mentioned
briefly above. For example, a mechanical sensor such as an
accelerometer 225 may be used, for instance to monitor physical
parameters of a subject, such as a mechanical sensor positioned to
monitor heartbeats, breathing for
shortness-of-breath/excessively-fast- -breathing, or, in a more
practical daily application, to monitor a subject's activity. For
instance, those jogging or involved in playing sports may need a
boost of medication over the dosage used when they are working at a
desk, watching television, or sleeping, with the mechanical
accelerator sensor 225 monitoring the change in inertia of the
individual (bouncing more when active). In response to increased
activity signals generated by the mechanical sensor 225, the
controller 220 in most instances, administers more medication
during these periods of increased activity.
[0069] In other embodiments, the applicator 200 may be activated by
depressing the button or switch 222, or additional switches, for
instance in response to an event to administer an additional dosage
or a booster dosage. In such an implementation, the button 222 may
be labeled with the event or symptom for which the booster dose is
required. For example, the button 222 may be labeled "pain" for
addressing pain symptoms, such as chest pains, headaches or nausea,
or perhaps "relief" may be a more optimistic label. Examples of
events may be eating, strenuous physical activity such as manual
labor, playing sports or jogging. Indeed, several buttons may be
provided to indicate a variety of events, each of which may
administer different dosages or types of medication. As another
example, the bioactive composition may not only be one to treat a
symptom, but for various physical events, the bioactive composition
may be a performance enhancing composition, such as one designed to
provide a boost of energy.
Embodiment of FIG. 8
[0070] FIG. 8 shows another embodiment of a transdermal application
system 300, constructed in accordance with the present invention,
for applying a bioactive substance or agent 301 to a skin surface
302 of a subject or patient 304, preferably using a patch 305,
which may be constructed as described above for patch 25. The
bioactive agent 301 is stored in a remote reservoir, here shown as
a flexible bladder 306, such as a plastic bag similar or identical
to the containers which are used to administer intravenous ("IV")
fluids to patients in hospitals, ambulances, nursing homes, and the
like. The illustrated container 306 preferably includes a fixture,
such as eyelet 308, which may be used to hang the container from a
conventional IV stand, allowing easy substitution of the system 300
for conventional IV's.
[0071] The transdermal application system 300 illustrated in FIG. 8
includes an applicator or dispenser 310, which may be constructed
as described above for applicators 30 and 200. The applicator 310
in FIG. 8 shows one form of the internal workings of thermal fluid
ejecting system, similar to that used in thermal inkjet printheads
in the printing arts, for instance of the construction described in
U.S. Pat. No. 5,420,627, which is assigned to the present assignee,
Hewlett-Packard Company. The applicator 310 includes a main body
312 that defines a feed chamber 314, which receives the bioactive
fluid 301 (labeled "bioagent" in FIG. 8) from the ink reservoir 306
by way of a fluid conduit, such as tubing 315, illustrated
partially schematically in FIG. 8. A fluid ejection mechanism 316
is preferably located centrally within the chamber 314, and held in
place through attachment by an adhesive or other bonding agent to a
flexible polymer tape 318, such as Kapton.RTM. tape, available from
the 3M Corporation, Upilex.RTM. tape, or other equivalent materials
known to those skilled in the inkjet arts. The illustrated tape 318
serves as a nozzle orifice plate by defining at least one, but
preferably more, fluid ejection nozzle hole or orifice 320 formed
in tape 318 by, for example, laser ablation technology. The
adhesive between the body 312 and the tape 318 may be of an epoxy,
a hot-melt, a silicone, a UV curable compound, mixtures thereof, or
their structural equivalents.
[0072] The ink ejection mechanism 316 includes a silicon substrate
322 that contains for each nozzle 320 an individually energizable
thin film firing resistor 324, each located generally behind an
associated single nozzle 320. The firing resistors 324 act as ohmic
heaters when selectively energized by one or more enabling signals
or firing pulses 325, which are delivered from a controller 326
through conductors (omitted for clarity) carried by the polymer
tape 318. The controller 326 may operate as described above for
controllers 100 and 220 of FIGS. 1 and 5. In the illustrated
embodiment of FIG. 8, the controller 326 receives a patient
condition input signal 328 from a patient monitoring device 330,
which may be a remote bio-sensor monitoring one or more parameters
of a subject's condition, similar to the pulse oximetry device 224
of FIG. 5, or a conventional hospital patient monitoring device for
gathering information concerning a patient's blood pressure, oxygen
level, respiration, etc.
[0073] The ink ejection mechanism 316 also includes a barrier layer
332 which may be formed on a surface of the substrate 322 using
conventional photolithographic techniques. The barrier layer 332
may be a layer of photoresist or some other polymer, which in
cooperation with tape 318 defines a vaporization chamber 334
surrounding an associated firing resistor 324. The barrier layer
332 is bonded to the tape 318 by a thin adhesive layer, such as an
uncured layer of polyisoprene photoresist. Fluid 301 from the feed
chamber 314 flows through one or more feed channels 336, around the
edges of the substrate 322, and into the vaporization chamber 334.
When the firing resistor 324 is energized, fluid 301 within the
vaporization chamber 334 is ejected, as illustrated by an emitted
bioactive fluid droplet 338. In the illustrated embodiment, the
fluid droplet 338 is shown traveling through an air gap between the
orifice plate tape 318 and the patch 305, with this air gap being
defined by spacer members, such as spacers 340 and 342 shown
extending from the applicator body 312, for instance in the same
manner as described above for spacers 36 and 38 in FIGS. 1-3.
Alternatively, an elastomeric lip, such as lip 205 in FIG. 5, may
be used instead of spacers 340 and 342, with or without the patch
305.
[0074] In operation, the dispenser 310 supplies accurate, metered
doses of the bioactive fluid 301 received via tubing 315 at
intervals (such as controlled or selected intervals) to the patch
305 when used. The patch 305 absorbs the fluid 301 and retains the
fluid against the patient's skin 302 to achieve transcutaneous
delivery of the bioactive liquid 301. In this manner, long term
administration of the agent 301 to the patch 305 may be achieved,
without the necessity of repeatedly applying a dispenser to the
patch.
[0075] The transdermal application system 300 illustrated in FIG. 8
is particularly suitable for drug administration in a hospital,
clinic, or other health care delivery facility in which medication
is administered for a prolonged period to a subject. Furthermore,
anyone who has had an IV knows it is painful to have a needle
inserted into their vein, followed by the pain and annoyance of
dealing with the needle remaining taped to their hand while the IV
fluid is administered. Emergency medical personal often have to
deal with trying to insert an IV needle into a trauma patient with
low blood pressure, where locating a viable vein is often
difficult. Medical personal treating the elderly or infirm often
encounter the same difficulties, with their patients suffering the
pain of the needle probing for a vein. Clearly, the transdermal
application system 300 alleviates these problems for both patients
and medical personal alike by providing a non-invasive method of
administering medications or other bioactive agents.
Embodiment of FIG. 9
[0076] FIG. 9 shows an alternate embodiment a transdermal
application system using the applicator 200 of FIG. 5, for
instance, in conjunction with a bioactive composition attracting
agent, such as a cream, a paste, or a salve 400 applied to the skin
402 of a subject 404, here on a skin blemish, such as a wart 405.
The applicator 200 is shown by way of illustration, and it is
apparent that applicators 30 and 310 may also be used with cream
400, shown here without use of a patch 25, 120, 305. Here we see
the applicator 200 ejecting bioactive fluid droplets 406 into a
chamber 408 defined between the ejection head defining nozzles 218
(see FIGS. 6 and 7), the patient's skin 402, and the sealing lip
205. The droplets 406 accumulate in a puddle 406' which is drawn
toward the wart 405 as indicated by arrows 408, 410 by the fluid's
affinity with the cream 400. The fluid 406' and the cream 400 mix
together so the fluid travels through the cream to contact and
treat the wart 405. In this manner, the bioactive-agent-attracting
cream 400 assists in drawing or pulling the treatment fluid 408
toward the location to be treated, here, wart 405. Examples of
bioactive-agent-attracting creams, pastes or salves include a
product sold under the trade name Recepta-gel.RTM., as well as
dimethyl sulfoxide ("DMSO"). Such a bioactive composition
attracting agent 400 may also enhance the penetration of the
bioactive composition 406', for instance, in the same manner as
DMSO or glycerin works to enhance transcutaneous flux of the
bioactive agent 406' that is delivered to wart 405. Thus, when
provided as a refill kit, the a fresh module carrying the treatment
fluid 406 may be supplied with a container of the cream 400, for
instance in a tear-away container(s), similar to those in which
single servings of mustard and ketchup are supplied, or in a
resealable tube.
Conclusion
[0077] Many other variations of devices and methods are within the
scope of this disclosure. For example, instead of mixing a
bioactive agent with another agent (such as another bioactive
agent, for example a penetrant such as DMSO) at the time of
ejection from a jet dispenser, the agents can be mixed prior to
ejection (for example, as illustrated in U.S. Pat. No. 5,980,014
assigned to Sony Corporation). Also, instead of mixing bioactive
agents prior to delivery, one of the bioactive agents can be
applied to the cutaneous surface, or the penetrant can be present
in the pad itself. For example, DMSO or other agents can be applied
to the skin, or can be present in the patch, to enhance
transcutaneous flux of a bioactive agent that is delivered to the
skin or pad. Another variation uses the optical sensor 48 to read
patient identification, such as a bar code on a patient's hospital
identification bracelet, with this patient information then being
used by controller 100 to adjust the dosage and/or type of
medication administered. Such a system avoids accidentally
administering the wrong medication to a patient. As another
example, the embodiments shown in the drawings are given to
illustrate the principles and concepts covered by the claims below,
and it is apparent that the applicator may be constructed larger or
smaller than those shown here.
[0078] This specification has described several detailed examples,
which are not intended to be limiting. Rather, these examples are
provided to illustrate some of the embodiments which come within
the scope of the following claims.
* * * * *