WO2009069846A1 - Method for manufacturing sensing unit made from nano-sized resist-derived carbon - Google Patents

Method for manufacturing sensing unit made from nano-sized resist-derived carbon Download PDF

Info

Publication number
WO2009069846A1
WO2009069846A1 PCT/KR2007/006802 KR2007006802W WO2009069846A1 WO 2009069846 A1 WO2009069846 A1 WO 2009069846A1 KR 2007006802 W KR2007006802 W KR 2007006802W WO 2009069846 A1 WO2009069846 A1 WO 2009069846A1
Authority
WO
WIPO (PCT)
Prior art keywords
sensor portion
nano
precursor
biomolecules
photo
Prior art date
Application number
PCT/KR2007/006802
Other languages
French (fr)
Inventor
Seung Seob Lee
Jung A Lee
Kwang Cheol Lee
Se Il Park
Original Assignee
Korea Research Institute Of Standards And Science
Korea Advanced Institute Of Science And Technology
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Korea Research Institute Of Standards And Science, Korea Advanced Institute Of Science And Technology filed Critical Korea Research Institute Of Standards And Science
Publication of WO2009069846A1 publication Critical patent/WO2009069846A1/en

Links

Classifications

    • BPERFORMING OPERATIONS; TRANSPORTING
    • B81MICROSTRUCTURAL TECHNOLOGY
    • B81CPROCESSES OR APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OR TREATMENT OF MICROSTRUCTURAL DEVICES OR SYSTEMS
    • B81C1/00Manufacture or treatment of devices or systems in or on a substrate
    • B81C1/00015Manufacture or treatment of devices or systems in or on a substrate for manufacturing microsystems
    • B81C1/00134Manufacture or treatment of devices or systems in or on a substrate for manufacturing microsystems comprising flexible or deformable structures
    • B81C1/00142Bridges
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B82NANOTECHNOLOGY
    • B82YSPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y15/00Nanotechnology for interacting, sensing or actuating, e.g. quantum dots as markers in protein assays or molecular motors
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B81MICROSTRUCTURAL TECHNOLOGY
    • B81BMICROSTRUCTURAL DEVICES OR SYSTEMS, e.g. MICROMECHANICAL DEVICES
    • B81B2201/00Specific applications of microelectromechanical systems
    • B81B2201/02Sensors
    • B81B2201/0214Biosensors; Chemical sensors
    • GPHYSICS
    • G01MEASURING; TESTING
    • G01NINVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
    • G01N33/00Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
    • G01N33/48Biological material, e.g. blood, urine; Haemocytometers
    • G01N33/483Physical analysis of biological material
    • G01N33/487Physical analysis of biological material of liquid biological material
    • G01N33/48707Physical analysis of biological material of liquid biological material by electrical means

Definitions

  • the present invention relates to a method for manufacturing a sensor portion of a biosensor used in detecting biomolecules and, more particularly, to a method for manufacturing a nano-size sensor portion of specified shape composed of pyrolyzed carbon.
  • MEMS micromachining-based semiconductor processing technology
  • the MEMS Micro-Electro-Mechanical System
  • the MEMS refers to a technology with which a sensor, an actuator and an electro-mechanical device each having an extremely small size in the order of microns are manufactured through a micromachining process derived from a semiconductor manufacturing process, particularly an integrated circuit technology.
  • the micro mechanical device manufactured by the micromachining process has a size and precision degree of several microns or less. Advantages of the micromachining process reside in that it can realize miniaturization, high performance, versatility and integration of a device through an extremely precise micromachining work while enhancing the stability and reliability of the device.
  • the micromachining technology can realize a unitary integrated system, thereby eliminating the need to perform an additional fabricating operation. This makes it possible to cost- effectively mass-produce micro structures through a series of process steps.
  • Bio-MEMS A MEMS used in the field of bio-engineering is referred to as Bio-MEMS.
  • the Bio-MEMS The Bio-MEMS
  • MEMS is a combination term of biotechnology and MEMS and means a micro device capable of analyzing biomolecules in vivo or in vitro.
  • One representative product using the Bio-MEMS is a biosensor.
  • the biosensor refers to an ultra-small sensor which includes a sensor portion for detecting biomolecules and a signal generating portion for generating an electrical or chemical signal corresponding to the biomolecules detected.
  • the biosensor is divided into a mechanical biosensor and an electrical biosensor.
  • the mechanical biosensor determines the kind and amount of biomolecules by measuring the resonant frequency or displacement of a cantilever having a pressure resistor, a piezoelectric material or a field-effect transistor formed thereon.
  • the resonant frequency or displacement of the cantilever varies when the pressure resistor, the piezoelectric material or the field-effect transistor reacts with biomolecules.
  • the electrical biosensor determines the kind and amount of biomolecules by measuring the change in electric resistance of a sensor portion made of a semiconductor nano wire, a carbon nano tube or a conductive polymer. The change in electric resistance occurs when the sensor portion makes a binding reaction with biomolecules.
  • the electrical biosensor offers an advantage in that it can accurately determine the biomolecules using a nano-sized sensor portion such as a carbon nano tube or a semiconductor nano wire.
  • a nano-sized sensor portion such as a carbon nano tube or a semiconductor nano wire.
  • the chirality of a nano-size material and the change in properties of the nano-size material occurring in a fabricating process make it difficult to freely manufacture a nano-size sensor portion of arbitrary shape.
  • additional process steps such as etching, deposition or the like, which makes it costly to produce the sensor portion in a nano size.
  • Another object of the present invention is to provide a method for cost-effectively manufacturing a sensor portion of a biosensor composed of pyrolyzed carbon.
  • a method for manufacturing a sensor portion of a biosensor used in detecting biomolecules including the steps of: applying a photo-sensitive material on a substrate; lithographically etching the photo-sensitive material to form a nano-size sensor portion precursor; and pyrolyzing the sensor portion precursor to form a sensor portion composed of conductive carbon.
  • the sensor portion has a center region and opposite end regions.
  • the width of the center region is smaller than that of the opposite end regions.
  • the sensor portion may have a width that grows smaller from the opposite end regions toward the center region.
  • Fig. 1 is a perspective view showing a biosensor manufactured in accordance with one embodiment of the present invention.
  • Fig. 2 illustrates a process for forming a sensor portion precursor using a lithography method.
  • Fig. 3 illustrates a process for forming a sensor portion by pyrolyzing the sensor portion precursor of specified pattern.
  • Fig. 4 shows one example of the sensor portion manufactured in accordance with the present invention.
  • FIG. 5 shows another example of the sensor portion manufactured in accordance with the present invention.
  • FIG. 6 shows a further example of the sensor portion manufactured in accordance with the present invention.
  • FIG. 7 shows a still further example of the sensor portion manufactured in accordance with the present invention. Best Mode for Carrying out the Invention
  • FIG. 1 is a perspective view showing a biosensor manufactured in accordance with one embodiment of the present invention.
  • an underlying insulation layer 2 is formed on the upper surface of a substrate 1.
  • electrodes 3 and alignment marks 4 On the upper surface of the underlying insulation layer 2, there are formed electrodes 3 and alignment marks 4.
  • a silicon, quartz or ceramic substrate may be used as the substrate 1.
  • a silicon oxide or silicon nitride film may be used as the underlying insulation layer 2.
  • a sensor portion 8 composed of pyrolyzed carbon is formed on the upper surface of the underlying insulation layer 2.
  • a covering insulation layer 10 is formed on the upper surface of the underlying insulation layer 2 on which the sensor portion 8 is formed.
  • the task of forming the covering insulation layer 10 on the underlying insulation layer 2 is performed by applying PMMA (polymethyl methacrylate), SOG (spin-on-glass), polyimide or the like on the upper surface of the underlying insulation layer 2 in a liquid or gas phase.
  • An exposure window 11 through which to expose the sensor portion 8 to biomolecules is formed in the covering insulation layer 10 to lie just above the sensor portion 8. If a test solution is allowed to flow over the covering insulation layer 10 of the biosensor, a part of the test solution enters the exposure window 11 and makes contact with the sensor portion 8. Thus the biomolecules contained in the test solution adhere to the sensor portion 8.
  • the electric resistance of the sensor portion 8 varies with the kind and amount of the biomolecules adhering to the sensor portion 8.
  • the electric resistance of the sensor portion 8 can be measured by supplying an electric current to the sensor portion 8 through the electrodes 3. Based on the electric resistance thus measured, it is possible to detect the kind and amount of the biomolecules adhering to the sensor portion 8.
  • Fig. 2 illustrates a process for lithographically forming a sensor portion precursor.
  • a photo-sensitive layer 5 composed of a polymer is applied on the upper surface of the underlying insulation layer 2 on which the electrodes 3 and the alignment marks 4 have been formed.
  • a polymer mask 6 having a sensor portion pattern pierced therethrough is attached to the upper surface of the photo-sensitive layer 5.
  • the alignment marks 4 are used in aligning the sensor portion pattern of the polymer mask 6 at a specified position on the underlying insulation layer 2.
  • the photo-sensitive layer 5 is lithographed using the polymer mask 6 having the sensor portion pattern pierced therethrough.
  • electron beams B are irradiated on the photo-sensitive layer 5 from above the polymer mask 6, at which time only the electron beams passed through the sensor portion pattern reach the photo-sensitive layer 5.
  • the photo-sensitive layer 5 is preferably made of a high molecular polymer. After the electron beams B are irradiated on the photo-sensitive layer 5 through the sensor portion pattern, the polymer mask 6 is separated from the photo-sensitive layer 5 and is then developed with a developer solution.
  • the portion of the photo-sensitive layer 5 irradiated with the electron beams is left intact, but the portion of the photo-sensitive layer 5 not irradiated with the electron beams is completely dissolved away in the developer solution.
  • a portion of the photo-sensitive layer 5 corresponding to the sensor portion pattern of the polymer mask 6, i.e., a sensor portion precursor is left on the upper surface of the underlying insulation layer 2.
  • Fig. 3 illustrates a process for forming a sensor portion by pyrolyzing the sensor portion precursor.
  • a sensor portion precursor 7 composed of a high molecular polymer is formed on the underlying insulation layer 2 after the photosensitive layer 5 is developed. Heat H is applied on the sensor portion precursor 7 to pyrolyze the same. The sensor portion precursor 7 thus pyrolyzed is converted to a sensor portion composed of conductive carbon.
  • the sensor portion precursor 7 is heated to an elevated temperature, nitrogen, oxygen and the like constituting the sensor portion precursor 7 are removed and only a carbon component is left as it is.
  • the carbon component has an amorphous structure.
  • the electric conductivity and residual stress of the pyrolyzed sensor portion precursor 7 varies depending on the heating temperature and time of the sensor portion precursor 7, the chemical components of the polymer constituting the sensor portion precursor 7 and the kind of additives added to the sensor portion precursor 7.
  • the sensor portion precursor 7 is pyrolyzed by heating the same to a temperature of from 500 0 C to 700 0 C for 0.5 to 2 hours in an oven. This produces a sensor portion 8 made from the pyrolyzed photo-sensitive sensor portion precursor.
  • Figs. 4 and 5 show examples of the sensor portion 8 manufactured in accordance with the present invention.
  • the width of the center region is smaller than that of the opposite end regions.
  • the width thereof grows smaller from the opposite end regions toward the center region. This makes it possible to detect biomolecules with increased sensitivity and within a shortened period of time. The reason is that the biomolecules tend to adhere to the center region in a greater quantity than to the opposite end regions.
  • Fig. 6 shows another example of the sensor portion 8 manufactured in accordance with the present invention.
  • the sensor portion 8 includes a plurality of parallel bars differing in length and width from one another. By changing the length and width of the bars constituting the sensor portion 8, it is possible to control the sensitivity of the sensor portion depending on the kinds of the biomolecules to be detected. Furthermore, it becomes possible to detect both the biomolecules with a lower concentration and the biomolecules with a higher concentration.
  • Fig. 7 shows a further example of the sensor portion 8 manufactured in accordance with the present invention.
  • the sensor portion 8 includes a plurality of parallel bars each having a gap of predetermined size.
  • the kinds of the biomolecules can be determined by measuring the change in electric resistance of the sensor portion 8.
  • the present invention provides a novel method for manufacturing a nano-size sensor portion of a biosensor having an arbitrary shape and composed of pyrolyzed carbon.

Landscapes

  • Engineering & Computer Science (AREA)
  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Physics & Mathematics (AREA)
  • Biochemistry (AREA)
  • Pathology (AREA)
  • Immunology (AREA)
  • Nanotechnology (AREA)
  • Food Science & Technology (AREA)
  • Medicinal Chemistry (AREA)
  • Manufacturing & Machinery (AREA)
  • Analytical Chemistry (AREA)
  • Molecular Biology (AREA)
  • General Physics & Mathematics (AREA)
  • Crystallography & Structural Chemistry (AREA)
  • Microelectronics & Electronic Packaging (AREA)
  • Biomedical Technology (AREA)
  • Hematology (AREA)
  • Urology & Nephrology (AREA)
  • Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
  • Apparatus Associated With Microorganisms And Enzymes (AREA)
  • Investigating Or Analyzing Materials By The Use Of Fluid Adsorption Or Reactions (AREA)

Abstract

Provided is a method for manufacturing a sensor portion of a biosensor used in detecting biomolecules. The method includes the steps of: applying a photo- sensitive material on a substrate; lithographically etching the photo- sensitive material to form a nano-size sensor portion precursor; and pyrolyzing the sensor portion precursor to form a sensor portion composed of conductive carbon.

Description

Description
METHOD FOR MANUFACTURING SENSING UNIT MADE FROM NANO-SIZED RESIST-DERIVED CARBON
Technical Field
[1] The present invention relates to a method for manufacturing a sensor portion of a biosensor used in detecting biomolecules and, more particularly, to a method for manufacturing a nano-size sensor portion of specified shape composed of pyrolyzed carbon. Background Art
[2] As a method for integrating a micro mechanical device, there is known a semiconductor processing technology using micromachining. The micromachining-based semiconductor processing technology, which is often referred to as "MEMS," has contributed to the development of a two-dimensional silicon processing technology represented by the conventional planar technology to a three-dimensional structure processing technology.
[3] The MEMS (Micro-Electro-Mechanical System) refers to a technology with which a sensor, an actuator and an electro-mechanical device each having an extremely small size in the order of microns are manufactured through a micromachining process derived from a semiconductor manufacturing process, particularly an integrated circuit technology. The micro mechanical device manufactured by the micromachining process has a size and precision degree of several microns or less. Advantages of the micromachining process reside in that it can realize miniaturization, high performance, versatility and integration of a device through an extremely precise micromachining work while enhancing the stability and reliability of the device. In addition, the micromachining technology can realize a unitary integrated system, thereby eliminating the need to perform an additional fabricating operation. This makes it possible to cost- effectively mass-produce micro structures through a series of process steps.
[4] A MEMS used in the field of bio-engineering is referred to as Bio-MEMS. The Bio-
MEMS is a combination term of biotechnology and MEMS and means a micro device capable of analyzing biomolecules in vivo or in vitro. One representative product using the Bio-MEMS is a biosensor. The biosensor refers to an ultra-small sensor which includes a sensor portion for detecting biomolecules and a signal generating portion for generating an electrical or chemical signal corresponding to the biomolecules detected.
[5] The biosensor is divided into a mechanical biosensor and an electrical biosensor. The mechanical biosensor determines the kind and amount of biomolecules by measuring the resonant frequency or displacement of a cantilever having a pressure resistor, a piezoelectric material or a field-effect transistor formed thereon. The resonant frequency or displacement of the cantilever varies when the pressure resistor, the piezoelectric material or the field-effect transistor reacts with biomolecules. In contrast, the electrical biosensor determines the kind and amount of biomolecules by measuring the change in electric resistance of a sensor portion made of a semiconductor nano wire, a carbon nano tube or a conductive polymer. The change in electric resistance occurs when the sensor portion makes a binding reaction with biomolecules.
Disclosure of Invention Technical Problem
[6] The electrical biosensor offers an advantage in that it can accurately determine the biomolecules using a nano-sized sensor portion such as a carbon nano tube or a semiconductor nano wire. However, the chirality of a nano-size material and the change in properties of the nano-size material occurring in a fabricating process make it difficult to freely manufacture a nano-size sensor portion of arbitrary shape. In order to manufacture the nano-size sensor portion using a semiconductor manufacturing process, there is a need to perform additional process steps such as etching, deposition or the like, which makes it costly to produce the sensor portion in a nano size.
[7] Therefore, it is an object of the present invention to provide a novel method for manufacturing a nano-size sensor portion of a biosensor having an arbitrary shape.
[8] Another object of the present invention is to provide a method for cost-effectively manufacturing a sensor portion of a biosensor composed of pyrolyzed carbon.
Technical Solution
[9] In accordance with the present invention, there is provided a method for manufacturing a sensor portion of a biosensor used in detecting biomolecules, including the steps of: applying a photo-sensitive material on a substrate; lithographically etching the photo-sensitive material to form a nano-size sensor portion precursor; and pyrolyzing the sensor portion precursor to form a sensor portion composed of conductive carbon.
[10] Preferably, the sensor portion has a center region and opposite end regions. The width of the center region is smaller than that of the opposite end regions. Alternatively, the sensor portion may have a width that grows smaller from the opposite end regions toward the center region.
Advantageous Effects
[11] With the present invention, it is possible to cost-effectively and easily manufacture a nano-size sensor portion having an arbitrary shape by forming a sensor portion precursor through a photolithography process and then pyrolyzing the sensor portion precursor to form a sensor portion composed of conductive carbon. Brief Description of Drawings [12] Fig. 1 is a perspective view showing a biosensor manufactured in accordance with one embodiment of the present invention.
[13] Fig. 2 illustrates a process for forming a sensor portion precursor using a lithography method.
[14] Fig. 3 illustrates a process for forming a sensor portion by pyrolyzing the sensor portion precursor of specified pattern.
[15] Fig. 4 shows one example of the sensor portion manufactured in accordance with the present invention.
[16] Fig. 5 shows another example of the sensor portion manufactured in accordance with the present invention.
[17] Fig. 6 shows a further example of the sensor portion manufactured in accordance with the present invention.
[18] Fig. 7 shows a still further example of the sensor portion manufactured in accordance with the present invention. Best Mode for Carrying out the Invention
[19] Hereinafter, a method for manufacturing a sensor portion of a biosensor in accordance with the present invention will be described in detail with reference to Figs. 1 through 7.
[20] Fig. 1 is a perspective view showing a biosensor manufactured in accordance with one embodiment of the present invention. Referring to Fig. 1, an underlying insulation layer 2 is formed on the upper surface of a substrate 1. On the upper surface of the underlying insulation layer 2, there are formed electrodes 3 and alignment marks 4. A silicon, quartz or ceramic substrate may be used as the substrate 1. A silicon oxide or silicon nitride film may be used as the underlying insulation layer 2. A sensor portion 8 composed of pyrolyzed carbon is formed on the upper surface of the underlying insulation layer 2.
[21] A covering insulation layer 10 is formed on the upper surface of the underlying insulation layer 2 on which the sensor portion 8 is formed. The task of forming the covering insulation layer 10 on the underlying insulation layer 2 is performed by applying PMMA (polymethyl methacrylate), SOG (spin-on-glass), polyimide or the like on the upper surface of the underlying insulation layer 2 in a liquid or gas phase.
[22] An exposure window 11 through which to expose the sensor portion 8 to biomolecules is formed in the covering insulation layer 10 to lie just above the sensor portion 8. If a test solution is allowed to flow over the covering insulation layer 10 of the biosensor, a part of the test solution enters the exposure window 11 and makes contact with the sensor portion 8. Thus the biomolecules contained in the test solution adhere to the sensor portion 8. In this case, the electric resistance of the sensor portion 8 varies with the kind and amount of the biomolecules adhering to the sensor portion 8. The electric resistance of the sensor portion 8 can be measured by supplying an electric current to the sensor portion 8 through the electrodes 3. Based on the electric resistance thus measured, it is possible to detect the kind and amount of the biomolecules adhering to the sensor portion 8.
[23] Fig. 2 illustrates a process for lithographically forming a sensor portion precursor.
Referring to Fig. 2, a photo-sensitive layer 5 composed of a polymer is applied on the upper surface of the underlying insulation layer 2 on which the electrodes 3 and the alignment marks 4 have been formed. A polymer mask 6 having a sensor portion pattern pierced therethrough is attached to the upper surface of the photo-sensitive layer 5. The alignment marks 4 are used in aligning the sensor portion pattern of the polymer mask 6 at a specified position on the underlying insulation layer 2.
[24] The photo-sensitive layer 5 is lithographed using the polymer mask 6 having the sensor portion pattern pierced therethrough. First, electron beams B are irradiated on the photo-sensitive layer 5 from above the polymer mask 6, at which time only the electron beams passed through the sensor portion pattern reach the photo-sensitive layer 5. The photo-sensitive layer 5 is preferably made of a high molecular polymer. After the electron beams B are irradiated on the photo-sensitive layer 5 through the sensor portion pattern, the polymer mask 6 is separated from the photo-sensitive layer 5 and is then developed with a developer solution. As the photo-sensitive layer 5 is developed with the developer solution, the portion of the photo-sensitive layer 5 irradiated with the electron beams is left intact, but the portion of the photo-sensitive layer 5 not irradiated with the electron beams is completely dissolved away in the developer solution. Thus only a portion of the photo- sensitive layer 5 corresponding to the sensor portion pattern of the polymer mask 6, i.e., a sensor portion precursor, is left on the upper surface of the underlying insulation layer 2.
[25] Fig. 3 illustrates a process for forming a sensor portion by pyrolyzing the sensor portion precursor. Referring to Fig. 3, a sensor portion precursor 7 composed of a high molecular polymer is formed on the underlying insulation layer 2 after the photosensitive layer 5 is developed. Heat H is applied on the sensor portion precursor 7 to pyrolyze the same. The sensor portion precursor 7 thus pyrolyzed is converted to a sensor portion composed of conductive carbon. In other words, if the sensor portion precursor 7 is heated to an elevated temperature, nitrogen, oxygen and the like constituting the sensor portion precursor 7 are removed and only a carbon component is left as it is. The carbon component has an amorphous structure. The electric conductivity and residual stress of the pyrolyzed sensor portion precursor 7 varies depending on the heating temperature and time of the sensor portion precursor 7, the chemical components of the polymer constituting the sensor portion precursor 7 and the kind of additives added to the sensor portion precursor 7. Preferably, the sensor portion precursor 7 is pyrolyzed by heating the same to a temperature of from 5000C to 7000C for 0.5 to 2 hours in an oven. This produces a sensor portion 8 made from the pyrolyzed photo-sensitive sensor portion precursor.
[26] Figs. 4 and 5 show examples of the sensor portion 8 manufactured in accordance with the present invention. In the sensor portion 8 shown in Fig. 4, the width of the center region is smaller than that of the opposite end regions. In the sensor portion 8 shown in Fig. 5, the width thereof grows smaller from the opposite end regions toward the center region. This makes it possible to detect biomolecules with increased sensitivity and within a shortened period of time. The reason is that the biomolecules tend to adhere to the center region in a greater quantity than to the opposite end regions.
[27] Fig. 6 shows another example of the sensor portion 8 manufactured in accordance with the present invention. In the example shown in Fig. 6, the sensor portion 8 includes a plurality of parallel bars differing in length and width from one another. By changing the length and width of the bars constituting the sensor portion 8, it is possible to control the sensitivity of the sensor portion depending on the kinds of the biomolecules to be detected. Furthermore, it becomes possible to detect both the biomolecules with a lower concentration and the biomolecules with a higher concentration.
[28] Fig. 7 shows a further example of the sensor portion 8 manufactured in accordance with the present invention. In the example shown in Fig. 7, the sensor portion 8 includes a plurality of parallel bars each having a gap of predetermined size. When the biomolecules to be detected are coupled with the gap of each of the bars, the kinds of the biomolecules can be determined by measuring the change in electric resistance of the sensor portion 8. Industrial Applicability
[29] The present invention provides a novel method for manufacturing a nano-size sensor portion of a biosensor having an arbitrary shape and composed of pyrolyzed carbon.
[30] With the present invention, it is possible to cost-effectively and easily manufacture a nano-size sensor portion having an arbitrary shape by forming a sensor portion precursor through a photolithography process and then pyrolyzing the sensor portion precursor to form a sensor portion composed of conductive carbon.
[31] The embodiments set forth hereinabove have been presented for illustrative purpose only and, therefore, the present invention is not limited to these embodiments. It will be understood by those skilled in the art that various changes and modifications may be made without departing from the scope of the invention defined in the claims.

Claims

Claims
[1] A method for manufacturing a sensor portion of a biosensor used in detecting biomolecules, comprising the steps of: applying a photo- sensitive material on a substrate; lithographically etching the photo-sensitive material to form a nano-size sensor portion precursor; and pyrolyzing the sensor portion precursor to form a sensor portion composed of conductive carbon. [2] The method as recited in claim 1, wherein the sensor portion precursor is pyrolyzed at a temperature of from 5000C to 7000C for 0.5 to 2 hours. [3] The method as recited in claim 1, wherein the sensor portion has a center region and opposite end regions, the center region having a width smaller than that of the opposite end regions. [4] The method as recited in claim 1, wherein the sensor portion has a center region and opposite end regions, the sensor portion having a width that grows smaller from the opposite end regions toward the center region. [5] The method as recited in claim 1, wherein the sensor portion includes a plurality of parallel bars differing in length and width from one another. [6] The method as recited in claim 1, wherein the sensor portion has a gap with which the biomolecules to be detected are coupled.
PCT/KR2007/006802 2007-11-26 2007-12-24 Method for manufacturing sensing unit made from nano-sized resist-derived carbon WO2009069846A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
KR1020070121048A KR100927617B1 (en) 2007-11-26 2007-11-26 Method of manufacturing a sensing part of a biosensor having nano size of pyrolysis carbon component
KR10-2007-0121048 2007-11-26

Publications (1)

Publication Number Publication Date
WO2009069846A1 true WO2009069846A1 (en) 2009-06-04

Family

ID=40678724

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/KR2007/006802 WO2009069846A1 (en) 2007-11-26 2007-12-24 Method for manufacturing sensing unit made from nano-sized resist-derived carbon

Country Status (2)

Country Link
KR (1) KR100927617B1 (en)
WO (1) WO2009069846A1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US9513555B2 (en) * 2013-03-29 2016-12-06 Sk Innovation Co., Ltd. Method for manufacturing a suspended single carbon nanowire and piled nano-electrode pairs
US10864159B2 (en) 2008-05-30 2020-12-15 Santen Pharmaceutical Co., Ltd. Method and composition for treating ocular hypertension and glaucoma

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101073518B1 (en) 2009-07-09 2011-10-17 한국표준과학연구원 Microelectromechanical device including pyrolyzed polymer structure and method for fabricating the same

Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020088521A (en) * 2001-05-18 2002-11-29 주식회사 아이센스 Biosensors with porous chromatographic membranes and enhanced sampling capability
KR20070033794A (en) * 2005-09-22 2007-03-27 전자부품연구원 Nanowire Device Manufacturing Method

Patent Citations (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR20020088521A (en) * 2001-05-18 2002-11-29 주식회사 아이센스 Biosensors with porous chromatographic membranes and enhanced sampling capability
KR20070033794A (en) * 2005-09-22 2007-03-27 전자부품연구원 Nanowire Device Manufacturing Method

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US10864159B2 (en) 2008-05-30 2020-12-15 Santen Pharmaceutical Co., Ltd. Method and composition for treating ocular hypertension and glaucoma
US9513555B2 (en) * 2013-03-29 2016-12-06 Sk Innovation Co., Ltd. Method for manufacturing a suspended single carbon nanowire and piled nano-electrode pairs

Also Published As

Publication number Publication date
KR100927617B1 (en) 2009-11-23
KR20090054268A (en) 2009-05-29

Similar Documents

Publication Publication Date Title
US9797860B2 (en) Manufacturing method of a graphene-based electrochemical sensor, and electrochemical sensor
US8557567B2 (en) Method for fabricating nanogap and nanogap sensor
KR101094870B1 (en) humidity sensor and manufacturing method thereof
EP1429992B1 (en) Flexible structure with integrated sensor/actuator
JP6778218B2 (en) Designs and methods for measuring analytes using nanomanufacturing devices
KR20090064693A (en) Micro gas sensor and manufacturing method thereof
US9768162B2 (en) Imprinted semiconductor multiplex detection array
EP1931978B1 (en) Polymer replicated interdigitated electrode array for (bio)sensing applications
WO2009069846A1 (en) Method for manufacturing sensing unit made from nano-sized resist-derived carbon
Shalabi et al. Switch mode capacitive pressure sensors
Wang et al. Nanofabrication, effects and sensors based on micro-electro-mechanical systems technology
WO2009069845A1 (en) Bio-sensor having sensing unit made from nano-sized resist-derived carbon
KR20110133352A (en) Micro structure, micro electro mechanical system therewith, and manufacturing method thereof
KR101339967B1 (en) Capillary Force Driven Nano-gap metal patterning
Huang et al. Silicone polymer chemical vapor sensors fabricated by direct polymer patterning on substrate technique (DPPOST)
Adam et al. Novel in-house fabrication of nano lab-on-chip devices
JP2004531720A (en) Biosensor matrix and method for producing the same
WO2008048209A2 (en) Functionalization of nanofluidic channels
Lee et al. Wafer-level fabrication of polymer microsensors with integrated heat control
EP1938364A1 (en) A method for fabricating nanogap and nanogap sensor
Chen Wearable RF Resonant Gaseous Chemical Sensor Array
KR101308010B1 (en) Sensor unit and manufacturing method the same
KR101073518B1 (en) Microelectromechanical device including pyrolyzed polymer structure and method for fabricating the same
Passi " Fabrication and characterization of silicon nanowires for electromechanical and gas sensing application
Toffoli Superhydrophobic BIOMEMS sensor arrays: development of actuation and readout electronic strategies

Legal Events

Date Code Title Description
121 Ep: the epo has been informed by wipo that ep was designated in this application

Ref document number: 07851761

Country of ref document: EP

Kind code of ref document: A1

NENP Non-entry into the national phase

Ref country code: DE

122 Ep: pct application non-entry in european phase

Ref document number: 07851761

Country of ref document: EP

Kind code of ref document: A1