1. Field of the Invention
One or more embodiments relate to microfluidics, and more particularly, to a microfluidic chip and a method of fabricating the microfluidic chip.
2. Description of the Related Art
Microfluidic chips, that is, chip-shaped devices, are used in microfluidics to perform various biochemical reactions using a small amount of biochemical fluid or to process a biochemical fluid for biochemical reactions. In general, a microfluidic chip includes an inlet hole for injecting a biochemical fluid into the microfluidic chip, an outlet hole for discharging the biochemical fluid out of the microfluidic chip, a channel through which the biochemical fluid can flow, and a chamber in which the biochemical fluid is received.
Microfluidic chips could have the organic thin films on an inner surface of the chamber using an organosilane-based material in order to capture the cells present in a biochemical fluid or to purify DNA extracted from the cells, which are well known. Such a conventional microfluidic chip includes a lower substrate formed of silicon (Si) and an upper substrate formed of a transparent glass material, and the lower substrate and the upper substrate are attached to each other using an anodic bonding method. The anodic bonding may destroy an organosilane-based material since it requires a high temperature condition of 400° C. or higher. Therefore, after attaching the lower substrate and the upper substrate using the anodic bonding method, the organic thin film is formed through the holes on inner surfaces of the chamber and the channel using a chemical vapor deposition (CVD) method.
Microfluidic devices are used in various fields. For example, the microfluidic device may be used as an analyzing apparatus of a high throughput. The microfluidic device includes microfluidic structures such as channels and chambers. The microfluidic device may be fabricated in various ways. Microfluidic fabricating technologies such as lithography, etching, depositing, micromachining, and Lithographie, Galvanoformung, and Abformung (LIGA) processes may be used to fabricate the microfluidic devices.
The microfluidic device may be fabricated by forming microfluidic structures on two substrates and coupling the substrates to each other. For example, the microfluidic structures may be formed on two glass substrates, and the glass substrates are coupled to each other to fabricate the microfluidic device. Each of the two substrates includes entire or a part of the microfluidic structures.
The conventional microfluidic chip uses the expensive inorganic materials such as silicon or glass, and the lower substrate and the upper substrate are attached to each other using the anodic bonding method that requires the high temperature condition. In addition, since the organic thin film should be formed through the holes after attaching the lower substrate and the upper substrate to each other, the fabrication costs of the conventional microfluidic chip increase and the uniformity of generated organic thin film is not guaranteed. In addition, a method for effectively forming the microfluidic structures on the substrate and coupling the substrates on which the microfluidic structures are formed, and a microfluidic device fabricated by the above method are required.
One or more embodiments provide a microfluidic chip including a lower substrate and an upper substrate attached to each other using a novel bonding method instead of an anodic bonding, and including an organic thin film formed on an inner surface of a chamber, and a method of fabricating the microfluidic chip.
According to an aspect, there is provided a microfluidic chip including: a lower substrate including a channel, through which a biochemical fluid can flow, and a chamber, in which the biochemical fluid can be received, formed on an upper surface of the lower substrate; an upper substrate formed of a silicon resin, and having a lower surface attached to the upper surface of the lower substrate; and an organic thin film formed on the upper surface of the lower substrate except for portions on which the lower substrate and the upper substrate are attached to each other, wherein the lower surface of the upper substrate is activated by an O2-plasma process, and the lower surface of the upper substrate is adhered to the upper surface of the lower substrate so that the lower substrate and the upper substrate can be attached to each other.
The microfluidic chip may further include: a unit for enlarging a contact surface area with the biochemical fluid in the chamber.
The unit for enlarging the contact surface area may include a plurality of pillars protruding from the lower substrate so that they contact the lower surface of the upper substrate, and they are separately arranged from one another.
The organic thin film may be formed on a surface of the unit for enlarging the contact surface area.
The silicon resin of the upper substrate may be PDMS (polydimethylsiloxane).
The lower substrate may include Si, SiO2, SiN, or a polymer.
The organic thin film may be a SAM (self-assembled monolayer).
The organic thin film may include an organosilane-based material.
The organosilane-based material may have an alkoxysilane group or a chlorosilane group.
A photocatalyst layer including a photocatalyst material may be disposed between the lower substrate and the organic thin film.
The photocatalyst material may be TiO2, ZnO, SnO2, SrTiO3, WO3, B2O3, or Fe2O3.
The lower substrate may include a photocatalyst material.
The photocatalyst material may be TiO2.
An oxide layer or a nitride layer may be formed on portions of the upper surface of the lower substrate, which contact the lower surface of the upper substrate.
The oxide layer may include SiO2 or TiO2.
The nitride layer may include SiN.
According to another aspect, there is provided a method of fabricating a microfluidic chip, the method including: forming a lower substrate including a channel, through which a biochemical fluid can flow, and a chamber, in which the biochemical fluid can be received, on an upper surface of the lower substrate; forming an upper substrate including a silicon resin; forming an organic thin film on the upper surface of the lower substrate; removing the organic thin film that is formed on portions of the lower substrate, which will be attached to the upper substrate; and activating a lower surface of the upper substrate using an O2-plasma process, and adhering the upper substrate to the lower substrate to attach the upper and lower substrates to each other.
The formation of the organic thin film may include: coating the lower substrate with a solution including the material forming the organic thin film.
The removal of the organic thin film may include: forming a photo mask including a flat transparent plate, a photoresist layer including a pattern corresponding to the portions, from which the organic thin film will be removed, on the transparent plate, and a photocatalyst layer including a photocatalyst material formed on a lower surface of the transparent plate; arranging the photo mask on the upper surface of the lower substrate so that the photocatalyst layer can contact the organic thin film; and irradiating ultraviolet (UV) rays to the photo mask so that the organic thin film that contacts the photocatalyst layer and is exposed to the UV rays can be decomposed.
The removal of the organic thin film may include: placing a flat photocatalyst plate including a photocatalyst material on the lower substrate on which the organic thin film is formed; and irradiating the UV rays to the photocatalyst plate to decompose the organic thin film that contacts the photocatalyst plate and is exposed to the UV rays.
The method may further include: forming a photocatalyst layer including a photocatalyst material on the upper surface of the lower substrate before forming of the organic thin film, and forming the organic thin film on the photocatalyst layer in the process of forming the organic thin film, wherein the removal of the organic thin film includes: forming a photo mask including a flat transparent plate and a photoresist layer including a pattern corresponding to portions, from which the organic thin film will be removed, on the transparent plate; arranging the photo mask on the upper surface of the lower substrate; and irradiating the UV rays to the photo mask so that the organic thin film that contacts the photocatalyst layer and is exposed to the UV rays can be decomposed.
One or more embodiments may include a microfluidic structure including a polysiloxane layer.
One or more embodiments may include a method of fabricating a microfluidic structure by using a polysiloxane layer.
According to one or more embodiments, the microfluidic structure includes: a first substrate; a second substrate; and a polysiloxane layer disposed between the first and second substrates, wherein the polysiloxane layer is coupled to the first and second substrates via an SiO2 layer.
According to one or more embodiments, the method of fabricating a microfluidic structure includes: providing a first substrate and a second substrate on which micro-structures are formed; depositing an SiO2 layer on surfaces of the first and second substrates; and coupling the first and second substrates to each other by interposing a polysiloxane layer between the surfaces, on which the SiO2 layer is deposited, of the first and second substrates.
The above and other features and advantages will become more apparent by describing in detail exemplary embodiments thereof with reference to the attached drawings in which:
Hereinafter, a microfluidic chip and a method of fabricating the same will be described with reference to accompanying drawings.
Referring to
The surface of the lower substrate 101 formed of the Si material is oxidized by oxygen in the air, and thus, an oxide layer 109 including SiO2 is formed. The oxide layer 109 has a function of attaching the upper substrate 115 and the lower substrate 101 to each other. On the other hand, the lower substrate 101 may be formed of a polymer resin such as PDMS (polydimethylsiloxane), PMMA (polymethylmetaacrylate), PC (polycarbonate), and PE (polyethylene). If the lower substrate 101 is formed of the polymer resin, the oxide layer 109 is not formed. Therefore, an oxide layer including SiO2 or TiO2 or a nitride layer including SiN should be specifically formed. In order to form the oxide layer or the nitride layer, a CVD method or a physical vapor deposition (PVD) method can be used. In addition, the lower substrate 101 may be formed of SiO2 or SiN. In this case, since the lower substrate 101 is formed of the oxide material or the nitride material, an additional oxide layer or a nitride layer is not required.
An organic thin film 110 is formed on the upper surface of the lower substrate 101. The organic thin film 110 is coated to capture in the chamber 105 certain cells such as bacteria included in a biochemical fluid injected into the microfluidic chip 100 or to purify DNA extracted from the cells in the chamber 105. The organic thin film may include an organosilane based material, and can be stacked as a self-assembled monolayer. The organic thin film 110 is also formed on surfaces of the plurality of pillars 107. The organosilane-based material can be an alkoxysilane group material or a chlorosilane group material. The alkoxysilane group material can be octadecyldimethyl(3-trimethoxysilyl propyl) ammonium chloride, polyethyleneiminertrimethoxysilane, and aminopropyltriethoxysilane, and the chlorosilane group material can be octadecyltrichlorosilane.
The organic thin film 110 is mostly formed of a hydrophobic material, and thus, interferes with the attachment between the lower substrate 101 and the upper substrate 115. Therefore, the organic thin film formed on areas 112 on the upper surface of the lower substrate 101, which are attached to the upper substrate 115, is removed. Hereinafter, the area 112 will be referred to as an attaching area.
The upper substrate 115 is formed of a silicon resin, for example, PDMS (polydimethylsiloxane). The upper substrate 115 includes an inlet hole 116 connected to a side of the channel 102 of the chamber 105 so as to inject the biochemical fluid into the microfluidic chip 100, and an outlet hole 117 connected to the other side of the channel 102 of the chamber 105 so as to exhaust the biochemical fluid out of the microfluidic chip 100. The method of attaching the lower substrate 101 and the upper substrate 115 will be described later.
The method of fabricating the microfluidic chip 100 may include into a first process (refer to
Referring to
The surface of the lower substrate 101, on which the channel 102, the chamber 105, and the pillars 107 are formed, is oxidized by the oxygen in the air, and the oxide layer 109 including SiO2 is formed. The oxide layer 109 helps the attachment between the upper substrate 115 and the lower substrate 101. Meanwhile, the lower substrate 101 can be formed of a polymer resin such as PDMS (polydimethylsiloxane), PMMA (polymethylmetaacrylate), PC (polycarbonate), and PE (polyethylene). If the lower substrate 101 is formed of the polymer resin, the oxide layer 109 is not formed, and thus, the oxide layer including SiO2 or TiO2 or the nitride layer including SiN should be specifically formed. The oxide layer or the nitride layer can be formed using the CVD method or the PVD method.
In the second process, a mixed solution including the PDMS resin and a linking agent is injected into a mold (not shown) corresponding to the shape of the upper substrate 115 and is cured, and then, the cured shape is separated from the mold to form the upper substrate 115 (refer to
The inlet hole 116 and the outlet hole 117 can be formed using a general machining process such as a pressing process or a drilling process. Otherwise, a structure corresponding to the inlet hole 116 and the outlet hole 117 is disposed in the mold, and the mixed solution of the PDMS resin and the linking agent is injected into the mold to form the inlet hole 116 and the outlet hole 117.
Referring to
The fourth process includes forming of a photomask 10 (refer to
Referring to
The photocatalyst layer 15 is formed of a photocatalyst material. The photocatalyst material is a material causing a reaction of decomposing the organic thin film 110 when it is exposed to ultraviolet rays when contacting the organic thin film 110. For example, the photocatalyst material can be TiO2, ZnO, SnO2, SrTiO3, WO3, B2O3, or Fe2O3. The photocatalyst layer 15 can be formed by spin coating TiO2-sol solution on the lower surface of the transparent plate 11, and baking the coated layer. The TiO2-sol solution can be formed by mixing titanium isopropoxide, isopropanol, and HCl of 0.1N, and stabilizing the mixed solution. Otherwise, the photocatalyst layer 15 can be formed using the CVD method or the PVD method.
Referring to
Referring to
Referring to
The first process and the third process are the same as the first and third processes for fabricating the microfluidic chip 100 described with reference to
The fourth process includes placing a flat photocatalyst plate 20 on the lower substrate 201 and irradiating UV rays onto the photocatalyst plate 20 (refer to
When the UV rays are irradiated onto the photocatalyst plate 20, the photocatalyst plate 20 is exposed, and at the same time, some parts of the organic thin film 210 contacting the photocatalyst plate 20 are decomposed by the photocatalyst material. Referring to
On the other hand, according to the method of removing the organic thin film 210 shown in
The fifth process includes activating a lower surface of the upper substrate 215 by performing an O2-plasma process, in order to collide O2-plasma with the lower surface of the upper substrate 215, as shown in
Referring to
The surface of the lower substrate 301 formed of Si is oxidized by the oxygen in the air, and thus, an oxide layer 309 including SiO2 is formed. On the other hand, if the lower substrate 301 is formed of a polymer such as PDMS (polydimethylsiloxane), PMMA (polymethylmetaacrylate), PC (polycarbonate), and PE (polyethylene), an oxide layer including SiO2 or TiO2 or a nitride layer including SiN can be specifically formed.
A photocatalyst layer 311 including a photocatalyst material is deposited on the oxide layer 309. The photocatalyst material can be TiO2, ZnO, SnO2, SrTiO3, WO3, B2O3, or Fe2O3. An organic thin film 310 is formed on the photocatalyst layer 311. The organic thin film 310 is the same as the organic thin film 110 included in the microfluidic chip 100 of
The upper substrate 315 is formed of PDMS (polydimethylsiloxane) that is a silicon resin. The upper substrate 315 includes an inlet hole 316 and an outlet hole 317.
Referring to
Referring to
The fourth process includes forming a photo mask 30 (refer to
Referring to
Referring to
Referring to
Referring to
Since TiO2 is an oxide material that can help the attachment between the upper substrate 415 and the lower substrate 401, the lower substrate 401 does not require an additional oxide layer like the oxide layer 109 shown in
The upper substrate 415 is formed of a silicon resin, for example, PDMS (polydimethylsiloxane), and includes an inlet hole 416 and an outlet hole 417. As described with reference to
On the other hand, cell capture experiments and polymerase chain reaction (PCR) experiments were performed using the microfluidic chip 100 of the present invention and the conventional microfluidic chip having the lower substrate formed of Si and the upper substrate formed of a glass material, and the results of the experiments were compared. Since equivalent results were obtained within an acceptable error range, and thus, it could be determined that the microfluidic chip 100 can be used instead of the conventional microfluidic chip in microfluidics.
The microfluidic chip, in which the organic thin film is formed on the inner surfaces of the chamber, can be fabricated using silicon resin that can be easily formed and is cheaper than the glass material. Therefore, the costs for fabricating the microfluidic chip can be reduced, and a defect rate can be reduced and a production yield can be improved by generating the organic thin film before the bonding process.
According to another embodiment, a microfluidic structure includes a first substrate, a second substrate, and a polysiloxane layer disposed between the first and second substrates, wherein the polysiloxane layer is coupled to the first and second substrates via a SiO2 layer.
The SiO2 layer may be deposited on the first and second substrates. The first and second substrates may be formed of a solid support, for example, a material selected from the group consisting of plastic, silicon, and glass. The plastic may have a hydrophilic or a hydrophobic surface, for example, may be one of selected from the group consisting of polyethylene, polypropylene, polystyrene, polyurethane, polysulfone, PTFE, PVC, polycarbonate, and PMMA, however, the embodiments of the present invention are not limited thereto.
One or more of the first and second substrates may include a micro-structure. The micro-structure may not be in micro-meter level, but may have a small structure. For example, at least one cross-section of the micro-structure, that is, a diameter, an width, and a height of the micro-structure may be in ranges of about 10 nm to about 1000 mm, from about 10 nm to about 100 mm, or from about 10 nm to about 10 mm. The micro-structure may provide the fluid with a path. For example, the micro-structure may be selected from the group consisting of a channel, a chamber, an inlet, and an outlet. A part of the micro-structure may be formed on the surface or inner space of the substrate, or on the surface and in the inner space of the substrate.
The microfluidic structure includes a polysiloxane layer disposed between the first substrate and the second substrate, and the polysiloxane layer is coupled to the first and second substrates via the SiO2 layer.
The polysiloxane may be one of PDMS and diphenylsiloxane.
The polysiloxane layer may be formed as a film. The film may have a thickness of about 10 to about 500 μm, or about 100 to about 300 μm.
The polysiloxane layer may be coupled to entire surfaces of the first and second substrates. The polysiloxane layer may be simple membrane without including the micro-structure. Otherwise, the polysiloxane layer may be coupled to a part of the surfaces of the first and second substrates.
The SiO2 layer is strongly adhered to the polysiloxane. Therefore, the SiO2 layer may be deposited onto the first and second substrates and fixed on the substrates, and then, may be adhered to the polysiloxane layer. The deposition of SiO2 layer onto the first and second substrates may be performed using a method selected from the group consisting of the liquid phase deposition, evaporation, and sputtering method.
The microfluidic structure is a device including one or more micro-structures. The micro-structure is described above. The microfluidic structure may be a microfluidic apparatus, an inlet and an outlet of which are connected to each other through one or more channels. The microfluidic apparatus may further include an additional structure of a valve, a pump, or a chamber.
The microfluidic structure includes the first substrate having a surface on which a pneumatic channel is formed, and the second substrate having a surface on which a fluid channel is formed. In addition, the polysiloxane layer is disposed between the above surfaces of the first and second substrates so that the polysiloxane layer is deflected to control the flow of the fluid in the fluid channel when a pressure or vacuum is applied to the pneumatic channel. The polysiloxane layer generally blocks the flow of the fluid in the fluid channel, and when a pressure or vacuum is applied to the pneumatic channel, the polysiloxane layer may be deflected to flow the fluid in the fluid channel. The microfluidic structure may further include an additional surface and a layer. The additional surface may be an additional channel for providing the fluid with a flow path. The second substrate may include a plurality of bias channels for providing the fluid with flow paths. The microfluidic structure may include a plurality of valves realized by the polysiloxane layer, which are disposed as parts of the pumps.
The microfluidic structure may include the first substrate having a surface on which a pneumatic channel is formed, and the second substrate having a surface on which a fluid channel is formed. In addition, the polysiloxane layer is disposed between the above surfaces of the first and second substrates so that the polysiloxane layer is deflected to activate a plurality of valves which may be switched pneumatically when a pressure or vacuum is applied to the pneumatic channel. In addition, the valves which may be pneumatically switched may control the flow of the fluid in the microfluidic apparatus. Here, the first substrate may include a plurality of etched channels, and the etched channels may distribute the pressure applied to the polysiloxane layer. In the microfluidic structure, three successive valves which may be pneumatically switched may form a pump. The three valves may include an input valve, a diaphragm valve, and an output valve.
According to another embodiment of the present invention, a method of fabricating a microfluidic structure includes providing a first substrate and a second substrate, on which micro-structures are formed, depositing a SiO2 layer on surfaces of the first and second substrates, and coupling the first substrate and the second substrate by interposing polysiloxane between the surfaces of the first and second substrates on which SiO2 layer is deposited.
The above method includes an operation of providing the first and second substrates on which micro-structures are formed. The micro-structures on the first and second substrates may be formed of a well-known method, for example, an injection molding, a photolithography, or a LIGA method.
The substrates may be formed of a solid support, for example, one selected from the group consisting of plastic, silicon, and glass. The plastic may include a hydrophilic surface or a hydrophobic surface, for example, may be one of selected from the group consisting of polyethylene, polypropylene, polystyrene, polyurethane, polysulfone, PTFE, PVC, polycarbonate, and PMMA.
The micro-structure may not be in micro-meter level, but may have a small structure. For example, at least one cross-section of the micro-structure, that is, a diameter, an width, and a height of the micro-structure may be in ranges of about 10 nm to about 1000 mm, from about 10 nm to about 100 mm, or from about 10 nm to about 10 mm. The micro-structure may provide the fluid with a path. For example, the micro-structure may be selected from the group consisting of a channel, a chamber, an inlet, and an outlet. A part of the micro-structure may be formed on the surface or inner space of the substrate, or on the surface and in the inner space of the substrate.
The above method also includes an operation of depositing SiO2 on the surfaces of the first and second substrates. The depositing process may be performed by the method selected from the group consisting of the liquid phase deposition (LPD), evaporation method, sputtering method, and chemical vapor deposition (CVD) method. The LPD method includes an operation of forming hydrofluosilicic acid aqueous solution which is saturated at a room temperature by dissolving silicon dioxide powder in an aqueous solution including 34% of hydrofluosilicic acid (H2SiF6). The silicon dioxide powder which is not dissolved in the solution may be removed from the aqueous solution of hydrofluosilicic acid by using a filter paper. The saturated hydrofluosilicic acid solution may be changed into a supersaturated solution by adding water, boric acid aqueous solution, or ammonium hydroxide in the saturated aqueous solution. In addition, the substrates are dipped into the supersaturated solution to grow a silicon dioxide film on the surfaces of the substrates. The deposition may be performed in a temperature range of about 10° C. to about 50° C. The above deposition is a method of depositing the silicon dioxide film on the plastic substrates in a previously evacuated chamber by a glow discharge, and includes forming an air flow on outer portion of the chamber by evaporating organic silicon component and mixing the evaporated organic silicon component with an oxidizing agent and an inert gas; flowing the air flow to the chamber to be adjustable; establishing glow discharge plasma in the chamber from the air flow; flowing the air flow in the plasma to be adjustable while locking a part of the plasma therein; depositing a first coating of silicon dioxide on the substrates; removing and/or redistributing external surface particles from the substrates; and repeatedly performing the above operations to deposit a second coating of silicon dioxide on the substrates. The oxidizing agent may be oxygen. The organic silicon may be selected from the group consisting of 1,1,3,3-tetramethyldisiloxane, hexamethyldisiloxane, vinyltrimethylsilane, methyltrimethoxysilane, vinyltrimethoxysilane, and hexamethyldisilazane. However, the above method of depositing SiO2 layer is an example, and other well known deposition methods may be used in one or more embodiments of the present invention. The operation of depositing SiO2 layer may be performed before providing the substrates. That is, before forming the micro-structures on the substrates, the SiO2 layer may be deposited, and then, the micro-structures may be formed.
The above method also includes an operation of coupling the first and second substrates to each other by interposing the polysiloxane between the surfaces, on which the SiO2 layer is deposited, of the first and second substrates.
The operation of coupling the first and second substrates may include arranging the surface of the first substrate, the polysiloxane layer, and the surface of the second substrate to correspond to each other, and coupling them by compressing the first and second substrates.
The polysiloxane may be selected from the group consisting of PDMS and diphenylsiloxane.
The polysiloxane layer may be formed as a film. For example, the polysiloxane layer may have a thickness of about 10 μm to about 500 μm, or about 100 μl in to about 300 μm.
The polysiloxane layer may be coupled to entire surfaces of the first and second substrates. That is, the polysiloxane layer may not include the micro-structure. Otherwise, the polysiloxane layer may be coupled to a part of the surfaces of the first and second substrates.
The microfluidic structure is a device including one or more micro-structures. The micro-structure is described above. The microfluidic structure may be a microfluidic apparatus, an inlet and an outlet of which are connected to each other through one or more channels. The microfluidic apparatus may further include an additional structure of a valve, a pump, or a chamber.
The microfluidic structure includes the first substrate having a surface on which a pneumatic channel is formed, and the second substrate having a surface on which a fluid channel is formed. In addition, the polysiloxane layer is disposed between the above surfaces of the first and second substrates so that the polysiloxane layer is deflected to control the flow of the fluid in the fluid channel when a pressure or vacuum is applied to the pneumatic channel. The polysiloxane layer generally blocks the flow of the fluid in the fluid channel, and when a pressure or vacuum is applied to the pneumatic channel, the polysiloxane layer may be deflected to flow the fluid in the fluid channel. The microfluidic structure may further include an additional surface and a layer. The additional surface may be an additional channel for providing the fluid with a flow path. The second substrate may include a plurality of bias channels for providing the fluid with flow paths. The microfluidic structure may include a plurality of valves realized by the polysiloxane layer, which are disposed as parts of the pumps.
The microfluidic structure may include the first substrate having a surface on which a pneumatic channel is formed, and the second substrate having a surface on which a fluid channel is formed. In addition, the polysiloxane layer is disposed between the above surfaces of the first and second substrates so that the polysiloxane layer is deflected to activate a plurality of valves which may be switched pneumatically when a pressure or vacuum is applied to the pneumatic channel. In addition, the valves which may be pneumatically switched may control the flow of the fluid in the microfluidic apparatus. Here, the first substrate may include a plurality of etched channels, and the etched channels may distribute the pressure applied to the polysiloxane layer. In the microfluidic structure, three successive valves which may be pneumatically switched may form a pump. The three valves may include an input valve, a diaphragm valve, and an output valve.
Hereinafter, one or more embodiments will be described in more detail. However, one or more embodiments of the present invention are exemplary embodiments, and the scope of the invention is not limited thereto.
Referring to
Referring to
In the microfluidic structure fabricated by the method illustrated in
The valve illustrated in
The film valve may form various modes of controlling the fluid.
According to the microfluidic structure of one or more embodiments, the microfluidic structure may be fabricated in a simple way. Therefore, the microfluidic structure including various micro-structures on the substrates of various materials may be fabricated efficiently.
According to the method of fabricating the microfluidic structure of one or more embodiments, the microfluidic structure may be fabricated effectively and easily.
While the present invention has been particularly shown and described with reference to exemplary embodiments thereof, it will be understood by those of ordinary skill in the art that various changes in form and details may be made therein without departing from the spirit and scope of the present invention as defined by the following claims.
Number | Date | Country | Kind |
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10-2007-0055716 | Jun 2007 | KR | national |
10-2008-110004 | Nov 2008 | KR | national |
This application is a continuation-in-part application of U.S. patent application Ser. No. 11/934,811 filed on Nov. 5, 2007, which claims the benefit of Korean Patent Application No. 10-2007-0055716, filed on Jun. 7, 2007; this application claims the benefit of Korean Application No. 10-2008-110004, filed on Nov. 6, 2008, in the Korean Intellectual Property Office, the disclosures of which are incorporated herein in their entirety by reference.
Number | Date | Country | |
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Parent | 11934811 | Nov 2007 | US |
Child | 12613847 | US |