U.S. patent application number 13/567158 was filed with the patent office on 2012-11-29 for microfluidic system and method for creating an encapsulated droplet with a removable shell.
This patent application is currently assigned to NATIONAL CHIAO TUNG UNIVERSITY. Invention is credited to CHIUN-HSUN CHEN, SHIH-KANG FAN, YAO-WEN HSU.
Application Number | 20120301564 13/567158 |
Document ID | / |
Family ID | 44149567 |
Filed Date | 2012-11-29 |
United States Patent
Application |
20120301564 |
Kind Code |
A1 |
FAN; SHIH-KANG ; et
al. |
November 29, 2012 |
MICROFLUIDIC SYSTEM AND METHOD FOR CREATING AN ENCAPSULATED DROPLET
WITH A REMOVABLE SHELL
Abstract
A microfluidic system for creating encapsulated droplets whose
shells can be further removed comprises: two electrode plates and a
spacing structure disposed between the two electrode plates. One of
the electrode plates has three reservoir electrodes and a plurality
of channel electrodes. The three electrodes are respectively used
for accommodating a shell liquid, a core liquid, and a removing
liquid which is able to remove the shell liquid. The channel
electrodes are used for communicating droplets among the three
reservoir electrodes. Via these arrangements, the microfluidic
system can create a quantitative shell droplet and a quantitative
core droplet, and then merge the shell and core droplets to form an
encapsulated droplet. Moreover, the shell of the encapsulated
droplet can be removed by mixing it with the removing liquid. This
invention is further provided with a method for creating an
encapsulated droplet with a removable shell.
Inventors: |
FAN; SHIH-KANG; (HSINCHU,
TW) ; HSU; YAO-WEN; (TAIPEI COUNTY, TW) ;
CHEN; CHIUN-HSUN; (HSINCHU CITY, TW) |
Assignee: |
NATIONAL CHIAO TUNG
UNIVERSITY
HSINCHU
TW
|
Family ID: |
44149567 |
Appl. No.: |
13/567158 |
Filed: |
August 6, 2012 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
|
|
12815580 |
Jun 15, 2010 |
8287708 |
|
|
13567158 |
|
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Current U.S.
Class: |
425/5 |
Current CPC
Class: |
B01J 13/04 20130101;
Y10T 436/2575 20150115 |
Class at
Publication: |
425/5 |
International
Class: |
B01J 13/02 20060101
B01J013/02 |
Foreign Application Data
Date |
Code |
Application Number |
Dec 18, 2009 |
TW |
98143595 |
Claims
1. A microfluidic system for creating an encapsulated droplet with
a removable shell comprising: a first electrode plate having a
first substrate and a first electrode layer, the first electrode
layer being disposed on a surface of the first substrate, the first
electrode layer having a first reservoir electrode, a second
reservoir electrode, a third reservoir electrode, a plurality of
first channel electrodes being sequent and adjacent to one another,
and a plurality of second channel electrodes being sequent and
adjacent to one another, one of the first channel electrodes being
adjacent to the first reservoir electrode, another one of the first
channel electrodes being adjacent to the second reservoir
electrode, one of the second channel electrodes being adjacent to
the third reservoir electrode, another one of the second channel
electrodes being adjacent to the first channel electrodes, the
first reservoir electrode being used for accommodating a shell
liquid, the second reservoir electrode being used for accommodating
a core liquid, and the third reservoir electrode being used for
accommodating a removing liquid capable of removing the shell
liquid; a second electrode plate having a second substrate and a
second electrode layer, the second electrode layer being disposed
on a surface of the second substrate and opposite to the first
electrode layer; and a spacing structure disposed between the first
and the second electrode plates, wherein a space is formed between
the first and the second electrode plates.
2. The microfluidic system according to claim 1, wherein the shell
liquid or the core liquid is a dielectric fluid.
3. The microfluidic system according to claim 1, wherein the shell
liquid or the core liquid is a conductive fluid.
4. The microfluidic system according to claim 1, wherein the first
electrode plate includes a dielectric layer disposed on the first
electrode layer.
5. The microfluidic system according to claim 4, wherein the first
electrode plate includes a hydrophobic layer disposed on the
dielectric layer.
6. The microfluidic system according to claim 1, wherein the second
electrode plate includes a hydrophobic layer disposed on the second
electrode layer.
7. The microfluidic system according to claim 1, wherein the first
channel electrodes and the second channel electrodes are arranged
in forms of letters "T", ".lamda." or "E".
8. The microfluidic system according to claim 1, wherein the first
and the second substrates are made of glass materials.
9. A microfluidic system for creating an encapsulated droplet with
a removable shell comprising: a first electrode plate having a
first substrate and a first electrode layer, the first electrode
layer being disposed on a surface of the first substrate, the first
electrode layer having a first reservoir electrode, a second
reservoir electrode, a plurality of first channel electrodes being
sequent and adjacent to one another, one of the first channel
electrodes being adjacent to the first reservoir electrode, another
one of the first channel electrodes being adjacent to the second
reservoir electrode, the first reservoir electrode being used for
accommodating a shell liquid, the second reservoir electrode being
used for accommodating a core liquid; a second electrode plate
having a second substrate and a second electrode layer, the second
electrode layer being disposed on a surface of the second substrate
and opposite to the first electrode layer; and a spacing structure
disposed between the first and the second electrode pates, wherein
a space is formed between the first and the second electrode
plates.
Description
RELATED APPLICATIONS
[0001] This application is a Divisional patent application of
co-pending application Ser. No. 12/815,580, filed on 15 Jun. 2010,
now pending. The entire disclosure of the prior application, Ser.
No. 12/815,580, from which an oath or declaration is supplied, is
considered a part of the disclosure of the accompanying Divisional
application and is hereby incorporated by reference.
BACKGROUND OF THE INVENTION
[0002] 1. Field of the Invention
[0003] The present invention relates to an encapsulated droplet, in
particular, to a microfluidic system and a method for creating an
encapsulated droplet with a removable shell.
[0004] 2. Description of Related Art
[0005] The microfluidic system, which is also called the
microfluidic chip, now is widely studied and highly valued. It has
many advantages, such as, high response rate, high sensitivity,
high reproducibility, low cost, and low pollution, so as to be
applied to biology, medicine, optoelectronics and other fields.
[0006] For the latest technology of the droplet-based microfluidic
system, the volume of the driven droplet has been decreased to the
level of sub-micro liter, or even to the level of pico liter. The
rapid evaporation is consequently an issue to the shrunk
droplets.
[0007] Then, possible solutions to this rapid-evaporation issue
include enhancement of packaging and sealing of the microfluidic
system or precise control of the environmental humidity and
temperature. However, the straight forward solutions may increase
the systems cost or limit the applicable situations and
environments.
[0008] Therefore, some scholars have proposed the concept of
encapsulated droplet by encapsulating the original
ease-of-evaporating droplet with another immiscible droplet. For
example, the original one is a water droplet; the immiscible one is
an oil droplet. The oil droplet will wrap all around the water
droplet in order to form an oil shell, preventing the water drop
from evaporation. However, making the oil-shell with a controlled
and reproducible volume by manually dispensing is difficult.
SUMMARY OF THE INVENTION
[0009] In view of the above-mentioned issues, a microfluidic system
and a method for creating an encapsulated droplet with a removable
shell are disclosed, in which volume of the encapsulated droplet is
able to be precisely controlled, and the shell droplet of the
encapsulated droplet is able to be removed if necessary.
[0010] To achieve the above-mentioned objectives, the present
invention provides a microfluidic system for creating an
encapsulated droplet with a removable shell, which includes a first
electrode plate, a second electrode plate and a spacing structure.
The first electrode plate has a first substrate and a first
electrode layer. The first electrode layer is disposed on a surface
of the first substrate. The first electrode layer has a first
reservoir electrode, a second reservoir electrode, a third
reservoir electrode, a plurality of first channel electrodes being
sequent and adjacent to one another, and a plurality of second
channel electrodes being sequent and adjacent to one another. A
respective one of the first channel electrodes is adjacent to the
first reservoir electrode, while another respective one of those is
adjacent to the second reservoir electrode. A respective one of the
second channel electrodes is adjacent to the third reservoir
electrode, while another respective one of those is adjacent to the
first channel electrodes. The first reservoir electrode
accommodates a shell liquid, the second reservoir electrode
accommodates a core liquid, and the third reservoir electrode
accommodates a removing liquid that is able to remove the shell
liquid. The second electrode plate has a second substrate and a
second electrode layer. The second electrode layer is disposed on a
surface of the second substrate and opposite to the first electrode
layer. The spacing structure is disposed between the first and the
second electrode plates to induce a space formed between the first
and the second electrode plates.
[0011] To achieve the above-mentioned objectives, a method for
creating an encapsulated droplet with a removable shell is
provided. The method includes steps as follows: providing a
microfluidic system having a first electrode layer and a second
electrode layer opposite to each other; arranging a shell liquid
onto a first reservoir electrode of the first electrode layer;
arranging a core liquid onto a second reservoir electrode of the
first electrode layer; arranging a removing liquid onto a third
reservoir electrode of the first electrode layer; moving part of
the shell liquid from the first reservoir electrode to one of
channel electrodes of the first electrode layer by applying an
electric potential across the first and the second electrode
layers, so as to form a shell droplet; moving part of the core
liquid from the second reservoir electrode to another one of the
channel electrodes of the first electrode layer by applying an
electric potential across the first and the second electrode
layers, so as to form a core droplet; moving the shell droplet and
the core droplet to contact each other by applying an electric
potential across the first and the second electrode layers, the
shell droplet wrapping around the core droplet to form an
encapsulated droplet; moving the encapsulated droplet on the
channel electrodes to approach the third reservoir electrode by
applying an electric potential across the first and the second
electrode layers; and removing the shell droplet of the
encapsulated droplet by contacting the removing liquid and the
encapsulated droplet.
[0012] The present invention further provides a microfluidic system
for individually manipulating multiple liquids to create
encapsulated droplets. The system includes a first electrode plate,
a second electrode plate and a spacing structure. The first
electrode plate has a first substrate and a first electrode layer.
The first electrode layer is disposed on a surface of the first
substrate. The first electrode layer has at least two reservoir
electrodes (i.e., first reservoir electrode and second reservoir
electrode), and a plurality of first channel electrodes being
sequent and adjacent to one another. A respective one of the first
channel electrodes is adjacent to one of the reservoir electrodes,
while another respective one of those is adjacent to the other
reservoir electrode. The first reservoir electrode accommodates a
shell liquid, and the second reservoir electrode accommodates a
core liquid. The second electrode plate has a second substrate and
a second electrode layer. The second electrode layer is disposed on
a surface of the second substrate and opposite to the first
electrode layer. The spacing structure is disposed between the
first and the second electrode plates to induce a space formed
between the first and the second electrode plates.
[0013] It is worth mentioning that there are some advantages as
follows:
[0014] 1. Each volume of the shell droplet and the core droplet can
be determined by the size of the first channel electrode and the
distance between the first and second electrode plates, so that the
volume thereof can be precisely calculated and experimentally
obtained with high predictability and repeatability.
[0015] 2. The shell droplet of the encapsulated droplet can be
easily removed by merging it with the removing,
[0016] in order to further understand the techniques, means and
effects the present invention takes for achieving the prescribed
objectives, the following detailed descriptions and appended
drawings are hereby referred, such that, through which, the
purposes, features and aspects of the present invention can be
thoroughly and concretely appreciated; however, the appended
drawings are merely provided for reference and illustration,
without any intention to he used for limiting the present
invention.
BRIEF DESCRIPTION OF THE DRAWINGS
[0017] FIG. 1 is a cross-sectional view of a microfluidic system
for creating an encapsulated droplet with a removable shell in
accordance with a preferred embodiment of the present
invention;
[0018] FIG. 2 is a top view of a first electrode layer of the
microfluidic system in accordance with the preferred embodiment of
the present invention;
[0019] FIG. 3 is a top view of a first electrode layer of a
microfluidic system in accordance with another embodiment of the
present invention;
[0020] FIG. 4 is a top view of a first electrode layer of a
microfluidic system in accordance with an additional embodiment of
the present invention;
[0021] FIG. 5 is a schematic view illustrating droplets controlled
by the microfluidic system in accordance with the preferred
embodiment of the present invention;
[0022] FIG. 6 is another schematic view illustrating an
encapsulated droplet controlled by the microfluidic system in
accordance with the preferred embodiment of the present
invention;
[0023] FIG. 7 is a flowchart of a method for creating an
encapsulated droplet with as removable shell in accordance with a
preferred embodiment of the present invention;
[0024] FIGS. 8A to 8F are schematic views illustrating sequential
steps of the method in accordance with the preferred embodiment of
the present invention;
[0025] FIG. 9 is a flowchart of a method in accordance with another
embodiment of the present invention;
[0026] FIGS. 10A and 10B are schematic views illustrating
sequential steps of the method in accordance with the other
embodiment of the present invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0027] Referring now to FIGS. 1 and 2, in which a microfluidic
system for creating an encapsulated droplet with a removable shell
in accordance with a preferred embodiment of the present invention
is disclosed. For conciseness of illustration, the "microfluidic
system for creating an encapsulated droplet with a removable shell"
is called "microfluidic system" for short. The microfluidic system
1 includes a first electrode plate 11, a second electrode plate 12,
and a spacing structure 13. After detailed descriptions for the
technical feature of the microfluidic system 1, method for using
the microfluidic system 1 will be introduced thereby.
[0028] The first electrode plate 11 includes a first substrate 111,
a first electrode layer 112, a dielectric layer 113 and a first
hydrophobic layer 114.
[0029] The first substrate 111 can be a rectangular substrate,
which is made of glass materials, silicon materials,
poly-dimethylsiloxane (PDMS), polyethylene terephthalate (PET),
polyethylene naphthalate (PEN), flexible polymer materials or
insulating materials. The glass materials would be better
selections because the low surface roughness thereof may reduce the
driving voltage of the microfluidic system 1.
[0030] The first electrode layer 112 is disposed on a surface, a
top surface, of the first substrate 111. The first electrode layer
112 is made of conductive materials, conductive polymeric materials
or conductive oxides, such as Cr, Cu metal, PEDOT: PSS
(poly(3,4-ethylenedioxythiophene)polystyrenesulfonate) or Indium
Tin Oxide (ITO). The first electrode layer 112 includes a plurality
of electrodes 1121 to 1125, which are sequent and adjacent to one
another. According to their functional or dimensional requirements,
the electrodes 1121 to 1125 can be divided into a first reservoir
electrode 1121, a second reservoir electrode 1122, a third
reservoir electrode 1123, a plurality of first channel electrodes
1124, and a plurality of second channel electrodes 1125.
[0031] The first reservoir electrode 1121 is used for reserving a
shell liquid 2 (shown in FIG. 8). The second reservoir electrode
1122 is used for reserving a core liquid 3, which is immiscible to
the shell liquid 2 (shown in FIG. 8). The third reservoir electrode
1123 is used for reserving a removing liquid 4, which is able to
dissolve the shell liquid 2 but unable to or hard to mix with the
core liquid 3 (shown in FIG. 8). The first and second channel
electrodes 1124 and 1125 are used for communicating the droplets
among the three reservoir electrodes 1121 to 1123.
[0032] The first channel electrodes 1124 could be adjacent to one
another in a sequential order, i.e. there would he a gap among
them, and be arranged in a horizontal line. Likely, the second
channel electrodes 1125 also are adjacent to one another in a
sequential order, and arranged in a vertical line. A respective one
of the first channel electrodes 1124, the extreme left one, is
adjacent to the first reservoir electrode 1121. Another respective
one of the first channel electrodes 1124, the extreme right one, is
adjacent to the second reservoir electrode 1122. A respective one
of the second channel electrodes 1125, the extreme bottom one, is
adjacent to the third reservoir electrode 1123. Another respective
one of the second channel electrodes 1125, the extreme top one, is
adjacent to another respective one of the first channel electrodes
1124, the one next to the extreme right one.
[0033] In accordance with the top view of the channel electrodes,
the first channel electrodes 1124 and the second channel electrodes
1125 are arranged in a form of letter "T". With respect to FIGS. 3
and 4, the first channel electrodes 1124 and the second channel
electrodes 1125 could also be arranged in forms of letters "E" and
".lamda.".
[0034] With respect to FIG. 2, the top view of each electrode
1121-1125 could he rectangular. Moreover, the dimensions of the
first, the second and the third reservoir electrodes 1121-1123 are
larger than the dimensions of the first and the second channel
electrodes 1124 and 1125. The respective three of the first channel
electrodes 1124, which are close to the first reservoir electrode
1121, are denoted as 1124A. Another respective three of the first
channel electrodes 1124, which are close to the second reservoir
electrode 1122, are denoted as 1124B. The dimension of each first
channel electrode 1124A could be designed to differ from that of
each first channel electrode 1124B. For example, the dimension of
each first channel electrode 1124A is smaller than that of each
first channel electrode 1124B, so as to change the ratio of shell
droplet to core droplet of the encapsulated droplet mentioned
below.
[0035] Here are descriptions of other components of the
microfluidic system 1. The dielectric layer 113 is disposed on the
first electrode layer 112 to cover the electrodes 1121-1125. The
dielectric layer 113 could be made of Parylene, positive
photoresist materials, negative photoresist materials, high
dielectric constant materials, and low dielectric constant
materials.
[0036] The first hydrophobic layer 114 is disposed on the top of
the dielectric layer 113 to cover all over the dielectric layer
113. The first hydrophobic layer 114 is made of hydrophobic
materials, such as Teflon, Cytop, and fluoropolymers; and its
purpose is to ease the driving of the shell droplet 21 and core
droplet 31, (shown in FIG. 5), mentioned below. The first
hydrophobic layer 114 is also called a low friction layer, because
of to coefficient of friction between the fluid and itself, so that
the fluid can easily flow over the first hydrophobic layer 114.
[0037] The above description is for the first electrode plate 11,
and here is description for the second electrode plate 12. The
second electrode plate 12 is disposed over and parallel to the
first electrode plate 11. The second electrode plate 12 has a
second substrate 121, a second electrode layer 122 and a second
hydrophobic layer 123.
[0038] Similarly, the second substrate 121 is a rectangular
substrate, which could he also made of glass materials, silicon
materials, PDMS, PET, PEN, flexible polymer materials or isolating
materials. The glass materials could be better selections due to
the low surface roughness thereof, which may reduce the driving
voltage of the microfluidic system 1.
[0039] The second electrode layer 122 is disposed on a surface, a
bottom surface, of the second substrate 121, and is opposite to the
first electrode layer 112. The second electrode layer 122 is made
of conductive materials, conductive, polymeric materials or
conductive oxides, such as Cr, Cu, PEDOT: PSS, metal or ITO.
[0040] The second hydrophobic layer 123 is disposed on the bottom
of the second electrode layer 122 to cover all over the second
electrode layer 122. The second hydrophobic layer 123, similar to
the first hydrophobic layer 114, is made of hydrophobic materials,
such as Teflon, Cytop, and fluoropolymers, for easing the driving
of the shell droplet 21 and core droplet 31 (shown in FIG. 5,
mentioned below). The second hydrophobic layer 123 could be also
called it low friction layer.
[0041] The above description is for the second electrode plate 12,
and here is description for the spacing structure 13. The spacing
structure 13 is disposed between the first and the second electrode
plates 11, 12 to induce a space 14 formed between the first and the
second electrode plates for accommodating liquid. The spacing
structure 13 may be a continuous frame structure or several
separated pillar structures.
[0042] The fluid in the microfluidic system 1 is controlled through
physical phenomena, such as Dielectrophoresis (DEP),
Electrowetting-on-dielectric (EWOD), in accordance with the
properties of the liquid, such as dielectric fluid or conductive
fluid. Usually, dielectric fluid is non-polar liquids; the
conductive fluid is polar liquids. If the liquid is a dielectric
fluid, it may be driven by the phenomenon of DEP. If the liquid is
a conductive fluid, the liquid may be driven by the phenomenon of
EWOD or DEP.
[0043] With respect to FIGS. 5 and 6, more details regarding how
the microfluidic system 1 controls the fluid or droplet and creates
the encapsulated droplet are described below. A shell droplet 21
and a core droplet 31 are taken as an example.
[0044] The shell droplet 21 is a dielectric fluid, such as an oil
droplet, arranged in the space 14 and on a respective one of the
first channel electrodes 1124A. The core droplet 31 is a conductive
fluid, such as a water droplet, arranged in the space 14 and on a
respective one of the first channel electrodes 1124B. The shell
droplet 21 and the core droplet 31 are individually surrounded by
environmental fluid, such as air.
[0045] With respect to FIG. 5, a direct current (DC) is applied
between the second electrode layer 122 and a respective one of the
first channel electrodes 1124A, which is just at the right hand
side of the shell droplet 21. Due to the difference of the
dielectric constant between the shell droplet 21 and the air,
different electric forces on the interface will generate a pressure
difference, which leads the shell droplet 21 to move toward the
right hand side. The phenomenon is called DEP. An alternating,
current (AC)is applied between the second electrode layer 122 and a
respective one of the first channel electrodes 1124B, which is just
at the left hand side of the core droplet 31. Due to the decrease
of the contact angle between the core droplet 31 and the dielectric
layer and/or hydrophobic layer, a pressure difference is generated
so as to lead the core droplet 31 to move forward the left-hand
side, where the liquid pressure is smaller. The phenomenon is
called EWOD.
[0046] FIG. 6 illustrates the encapsulated droplet, which is formed
by the core droplet 31 wrapped in the shell droplet 21
spontaneously due to different surface tensions when they contact.
Because the encapsulated droplet possesses dielectric and
conductive fluids. DEP and EWOD would he chosen for the movement of
the encapsulated droplet. The EWOD phenomenon is selected to
implement in the preferred embodiment. Moreover, the core droplet
31 in FIG. 5 can also be driven through the DEP phenomenon, which
is usually induced by a DC signal. However, the DEP phenomenon can
also be induced by an AC signal.
[0047] Referring to FIGS. 7 and 8, a method for creating an
encapsulated droplet with a removable shell according to a
preferred embodiment of the present invention is described below,
which is performed by the microfluidic system 1 mentioned
above.
[0048] Referred in step S101: a microfluidic system 1 is provided,
and a shell liquid 2, a core liquid 3 and a removing liquid 4 are
selected to use in the microfluidic system 1. The shell liquid 2
and the core liquid 3 may be respectively dielectric fluid and
conductive fluid depending on the specific function that the
microfluidic system 1 meets. In this embodiment, the dielectric
fluid, such as silicone oil, which is beneficial to the biomedical
field very well, is selected as the shell liquid 2; the conductive
fluid, such as water, is selected as the core liquid 3; and the
volatile solvent, such as Hexane, which can mix with and dissolve
the silicone oil very well, is selected as the removing liquid.
[0049] Referred in steps S103 to S107: shown in FIG. 8A, the shell
liquid 2 is arranged in the space 14 and on the first reservoir
electrode 1121, the core liquid 3 is arranged in the space 14 and
on the second reservoir electrode 1122, and the removing liquid 4
is arranged in the space 14 and on the third reservoir electrode
1123. Proper electric potentials are applied to the first, second
and the third reservoir electrodes 1121, 1122 and 1123 to hold
liquid 2, 3, and 4 thereon respectively.
[0050] Referred in step S109: shown in FIG. 8B, the electric
potential is applied to the second electrode layer 122 and a
respective one of the first channel electrodes 1124A, which is
closest to the first reservoir electrode 1121. Part of the shell
liquid 2 can be moved by DEP to the one of the first channel
electrodes 1124A, to which electric potential is applied, so as to
form a shell droplet 21.
[0051] Referred in step S111: shown in FIG. 8C, the electric
potential is applied to the second electrode layer 122 and a
respective one of the first channel electrodes 1124B, which is
closest to the second reservoir electrode 1122. Part of the core
liquid 3, can be moved by EWOD to the one of the first channel
electrodes 1124B, to which electric potential is applied, so as to
form a core droplet 31.
[0052] Referred in step S113: shown in FIGS. 8D and 5, the electric
potential is applied to the first channel electrodes 1124A and the
second electrode layer 122: and the electric potential is applied
to the first channel electrodes 1124B and the second electrode
layer 122. Therefore, the shell droplet 31 and the core droplet 21
move respectively on the first channel electrodes 1124A and 1124B
so as to contact or merge with each other. The shell droplet 21
wraps around the core droplet 31 to form an encapsulated
droplet.
[0053] Referred in step S115: shown in FIG. 8E, the electric
potential is applied to the second channel electrodes 1125 and the
second electrode layer 122, so as to move the encapsulated droplet
on the second channel electrodes 1125 until it approaches the third
reservoir electrode 1123.
[0054] Referred in step S117: shown in FIG. 8F, the removing liquid
4 on the third reservoir electrode 1123 contacts the shell droplet
21 of the encapsulated droplet. The removing liquid 4 mixes with
the shell liquid 21, and dissolves the shell liquid 21, so that the
encapsulated droplet is returned to the core droplet 31. Then, the
electric potential is applied to the second channel electrodes 1125
and the second electrode layer 122 again, making the core droplet
31 leave the third reservoir electrode 1123 to one of the second
channel electrodes 1125. A part of the removing liquid 4 is also
moved to the second channel electrode 1125 with core droplet 31,
and wraps around the core droplet 31. However, the removing liquid
4 evaporates in a short period of time, leaving the core droplet 31
alone on the second channel electrode 1125.
[0055] The procedures of steps S101 to S117 can be adjusted. For
example, the step S107 can be set following the step S115, and the
step S109 can be set following the step S111. The result of the
adjusted steps is as same as the previous one.
[0056] Moreover, after the step S113, a second shell droplet (not
shown) can be further formed, to be immiscible with the shell
droplet 21. The second shell droplet contacts the encapsulated
droplet to create a second shell thereon. To repeat this step, the
encapsulated droplet could have multiple shells thereon.
[0057] By the method of creating the encapsulated droplet, the
volume of shell droplet 21 or the core droplet 31 can be calculated
precisely. The volume is obtained in response to the dimension of
each first channel electrode 1124A, 1124B and the distance between
the first and the second electrode plates 11 and 12. When the
dimension of each first channel electrode 1124A and 1124B is
larger, the volume of the shell droplet 21 and the core droplet 31
become greater.
[0058] In addition to increasing the dimension of the first channel
electrodes 1124A and 1124B, the volume of the shell droplet 21 and
the core droplet 31 could be increased further by the steps
mentioned below. With respect to FIGS. 9 and 10, the shell droplet
21 is taken as an example.
[0059] Referred in step S201: with respect to FIG. 10A, the shell
droplet 21 has been formed on a respective one of the first channel
electrodes 1124A, which is remote from the first reservoir
electrode 1121. Then electric potential is applied to the second
electrode layer 122 and another respective one of the first channel
electrodes 1124A, which is close to the first reservoir electrode
1121. Another partial part of the shell liquid 2 can move to the
first channel electrode 1124A, to which the electric potential is
applied, so as to form another shell droplet 21A.
[0060] Referred in step S203: with respect with FIG. 10B, the
electric potential is applied to the first channel electrodes 1124A
and the second electrode layer 122. Then the two shell droplets 21
and 21A move on the first channel electrode 1124A to contact each
other. The two shell droplets 21, 21A merge with each other to
create a lamer shell droplet 21B.
[0061] After the step S203, the step S113 may be performed to form
the encapsulated droplet having a larger quantitative shell droplet
21B. Moreover, it is noteworthy that the steps S201 and S203 can be
repeated more than once, so as to further increase the volume of
shell droplet 21B.
[0062] Here are descriptions for real applications of the
microfluidic system 1, such as extraction, purification, protein
crystallization, and artificial cell membrane formation. Take
extraction fur instance, while the user injects the blood sample
into the shell liquid 2, the core liquid 3 attracts a specific
molecule of the blood sample. When the shell droplet 21 containing
the specific molecule of the blood sample contacts the core droplet
31 to create an encapsulated droplet, the specific molecule of the
blood sample will move into the core droplet 31. Alter the shell
droplet 21 is removed by the removing liquid 4, the core droplet 31
only includes one specific molecule of the blood sample, so as to
achieve the extraction. In addition, the volume of the shell
droplet 21 and the core droplet 31 could be calculated, so that the
concentration of the extracted molecule is calculated thereby.
[0063] Take purification for instance, while the user injects the
blood sample into the core liquid 3, the shell liquid 2 attracts a
specific molecule of the blood sample. When the core droplet 31
containing the specific molecule of the blood sample contacts the
shell droplet 21 to create an encapsulated droplet, the specific
molecule of the blood sample will be moved into the shell droplet
21. After the shell droplet 21 is removed by the removing liquid 4,
the core droplet 31 would not include the specific molecule of the
blood sample, so as to achieve the purification.
[0064] Take protein crystallization for instance, while the user
injects the protein molecules into the core liquid 3, the core
droplet 31 merges with the shell droplet 21 to create an
encapsulated droplet including the protein molecules. Because the
vaporization velocity of core droplet 31 could be controlled in the
encapsulated droplet, which is adjusted by the types and volume of
the shell droplet 21, the protein crystal growth and nucleation
would be controlled in accordance with the vaporization velocity.
Therefore, the protein molecules arrange in order slowly for
crystallization.
[0065] Take artificial cell membrane formation for instance, while
the user injects lipid molecules into the core liquid 3 or the
shell liquid 2, the core droplet 31 merges with the shell droplet
21 to create an encapsulated droplet with a monolayer of lipid
molecules self-assembled at the core-shell liquid interface. When
contact two or more encapsulated droplets, artificial cell
membrane(s) can be formed between two encapsulated droplets.
[0066] Other embodiments of the microfluidic system 1 are detailed
below. If the shell liquid 2 or the core liquid 3 possesses
sufficient hydrophobic property or surface energy, or the
dielectric layer 113 and the second electrode layer 122 are
hydrophobic to the shell liquid 21 or the core liquid 3, the first
hydrophobic layer 114 and the second hydrophobic 123 are not
necessary to be set.
[0067] Moreover, if the shell liquid 21 and the core liquid 31 are
both controlled through the DEP phenomenon, and the dielectric
property of the shell liquid 2 and the core liquid 3 has met usage
requirements, the dielectric layer 113 are not necessary to be
set.
[0068] Moreover, the second electrode layer 122 may include
individual sequential electrodes, and the dimension and arrangement
of each electrode would correspond to the electrodes 1221 to 1125
of the first electrode layer 112.
[0069] Furthermore, the shell liquid 2 and the core liquid 3 could
he the conductive fluid or polar liquid. For example, the shell
liquid 2 can be high-carbon aliphatic alcohol, such as octanol or
decanol alcohol, while the core liquid 2 is water.
[0070] In conclusion, it is worth mentioning that there are some
advantages as follows:
[0071] 1. Each volume of the shell droplet 21 and the core droplet
31 is determined in response to the size of the first channel
electrode 1124 and the distance between the first and second
electrode plates 11, 12, so that the volume thereof can be
calculated precisely and obtained with high predictability and
repeatability.
[0072] 2. The shell droplet 21 of the encapsulated droplet can be
easily removed by merging with the removing liquid 4.
[0073] The above-mentioned descriptions represent merely the
preferred embodiment Of the present invention, without any
intention to limit the scope of the present invention thereto.
Various equivalent changes, alternations or modifications based on
the claims of present invention are all consequently viewed as
being embraced by the scope of the present invention.
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