U.S. patent application number 12/638429 was filed with the patent office on 2013-11-21 for microelectrode array and method for modifying carbon nanotube electrode interface of the same array.
The applicant listed for this patent is Yen-Chung Chang, Wei-Lun Hsu, Huan-Chieh Su, Shih-Rung Yeh, Shiang-Jie YEN, Tri-Rung Yew. Invention is credited to Yen-Chung Chang, Wei-Lun Hsu, Huan-Chieh Su, Shih-Rung Yeh, Shiang-Jie YEN, Tri-Rung Yew.
Application Number | 20130307520 12/638429 |
Document ID | / |
Family ID | 49580801 |
Filed Date | 2013-11-21 |
United States Patent
Application |
20130307520 |
Kind Code |
A1 |
YEN; Shiang-Jie ; et
al. |
November 21, 2013 |
MICROELECTRODE ARRAY AND METHOD FOR MODIFYING CARBON NANOTUBE
ELECTRODE INTERFACE OF THE SAME ARRAY
Abstract
The present invention discloses a method for modifying a carbon
nanotube electrode interface, which modifies carbon nanotubes used
as a neuron-electrode interface by performing three stages of
modifications and comprises the steps of: carboxylating carbon
nanotubes to provide carboxyl functional groups and improve the
hydrophilicity of the carbon nanotubes; acyl-chlorinating the
carboxylated carbon nanotubes to replace the hydroxyl functional
groups of the carboxyl functional groups with chlorine atoms; and
aminating the acyl-chlorinated carbon nanotubes to replace the
chlorine atoms with a derivative having amine functional groups at
the terminal thereof. The modified carbon nanotubes used as the
neuron-electrode interface has lower impedance and higher adherence
to nerve cells. Thus is improved the quality of neural signal
measurement. The present invention also discloses a microelectrode
array, wherein the neuron-electrode interface uses carbon nanotubes
modified according to the method of the present invention.
Inventors: |
YEN; Shiang-Jie; (Penghu,
TW) ; Su; Huan-Chieh; (Changhua, TW) ; Yew;
Tri-Rung; (Hsinchu, TW) ; Chang; Yen-Chung;
(Hsinchu, TW) ; Hsu; Wei-Lun; (Taipei, TW)
; Yeh; Shih-Rung; (Hsinchu, TW) |
|
Applicant: |
Name |
City |
State |
Country |
Type |
YEN; Shiang-Jie
Su; Huan-Chieh
Yew; Tri-Rung
Chang; Yen-Chung
Hsu; Wei-Lun
Yeh; Shih-Rung |
Penghu
Changhua
Hsinchu
Hsinchu
Taipei
Hsinchu |
|
TW
TW
TW
TW
TW
TW |
|
|
Family ID: |
49580801 |
Appl. No.: |
12/638429 |
Filed: |
December 15, 2009 |
Current U.S.
Class: |
324/71.1 ;
564/142 |
Current CPC
Class: |
C01B 32/174 20170801;
B82Y 30/00 20130101; A61N 1/0551 20130101; B82Y 15/00 20130101;
B82Y 40/00 20130101; A61N 1/0502 20130101 |
Class at
Publication: |
324/71.1 ;
564/142 |
International
Class: |
C01B 31/02 20060101
C01B031/02; A61N 1/05 20060101 A61N001/05 |
Claims
1. A method for modifying a carbon nanotube electrode interface,
which modifies carbon nanotubes used as a neuron-electrode
interface and comprises the steps of: performing a carboxylation
process on the carbon nanotubes, performing an acyl-chlorination
process on the carbon nanotubes, and performing an amination
process on the carbon nanotubes, whereby surfaces of the carbon
nanotubes have amine functional groups.
2. The method for modifying a carbon nanotube electrode interface
according to claim 1, wherein the carboxylation process is a
H.sub.2O plasma process.
3. The method for modifying a carbon nanotube electrode interface
according to claim 2, wherein the H.sub.2O plasma process is
performed at a temperature of 25-150.degree. C., under a pressure
of 1-100 Torr, with a power of 25-100 W, for 10-300 seconds.
4. The method for modifying a carbon nanotube electrode interface
according to claim 1, wherein in the acyl-chlorination process, the
carbon nanotubes react with thionyl chloride in a reflux
system.
5. The method for modifying a carbon nanotube electrode interface
according to claim 4, wherein a microelectrode array using the
carbon nanotubes as the neuron-electrode interface thereof is
placed in the reflux system for a reaction, and wherein the
microelectrode array is placed on a carrier lest a magnet of the
reflux system interfere with the reaction.
6. The method for modifying a carbon nanotube electrode interface
according to claim 4, wherein the acyl-chlorination process is
performed at a temperature of 25-80.degree. C. for 10-20 hours.
7. The method for modifying a carbon nanotube electrode interface
according to claim 1, wherein in the amination process, the carbon
nanotubes react with a compound selected from a group consisting of
1,4-diaminobutane, ethylenediamine, and EDC
(1-ethyl-3-(3-dimethylaminopropyl)carbodiimide).
8. A microelectrode array comprising a base and at least one probe
connected to the base, wherein each the probe has at least one
electrode using carbon nanotubes as an interface thereof, and
wherein each the electrode is connected to the base via a wire, and
wherein the carbon nanotubes are modified to contain amine
functional groups according to any of claim 1.
9. The microelectrode array according to claim 8, wherein the
electrode includes a conductive layer and a catalytic layer, and
wherein the conductive layer is formed over a silicon wafer to
define a position and dimensions of the electrode, and wherein the
carbon nanotubes are catalyzed by the catalytic layer to form on
the catalytic layer.
10. The microelectrode array according to claim 9, wherein the
catalytic layer is made of a material selected from a group
consisting of iron, cobalt, and nickel.
Description
FIELD OF THE INVENTION
[0001] The present invention relates to a method for modifying a
carbon nanotube electrode interface, particularly to a method for
modifying a carbon nanotube electrode interface, which can increase
the affinity of neuron cells to the electrodes and improve the
quality of neural signals. The present invention also relates to a
microelectrode array using the carbon nanotube modified by the
abovementioned method.
BACKGROUND OF THE INVENTION
[0002] Since a planar multi-electrode array was proposed to study
the transmission mechanism of neural signals in 1972,
microelectrode arrays have been extensively used in the biomedical
engineering. The brain or a neural network is a complicated network
consisting of many neurons interconnecting each other.
Understanding the operation of the neural network is very important
to diagnose or treat neural diseases or fabricate neural
prostheses. A probe can easily puncture the skin to detect the
electrophysiological signals in vivo. A probe may also function as
an intermediary between analog physiological signals and digital
signal analysis.
[0003] FIG. 1 shows a microelectrode array 10 for detecting neural
signals. The microelectrode array 10 comprises a base 11 and a
plurality of probes 12 connected to the base 11. Each probe 12 has
a plurality of electrodes 13. For example, each probe 12 has four
electrodes 13 in FIG. 1. Each electrode 13 is electrically
connected to a metal pad 15 of the base 11 via a wire 14. Each wire
14 is insulated from the environment. The neural signals detected
by the electrode 13 is transmitted to the base 11 via the wire 14
and then processed by the succeeding devices.
[0004] Carbon nanotube, which was found by S. Iijima in 1991, has a
superior electric conductivity because of its special structure.
Thus, carbon nanotube has been widely used in the nanometric
electronic elements. The electrode interfaces of the conventional
probes are usually made of a metal having better biocompatibility,
such as gold, platinum, titanium, or platinum black. However, the
interfacial resistance of the metal electrode increases when the
size of a metal electrode is reduced to a very small scale. Thus,
the efficiency of the entire circuit decreases.
[0005] Carbon nanotube has very large surface area, high electrical
conductivity, better physicochemical properties, better chemical
inertness and better biocompatibility. Therefore, more and more
applications use carbon nanotube as the interface of neural
electrodes, for example, "Carbon Nanotubes for Neural Interfaces"
by David Ricci; "Carbon Nanotube Coating Improves Neuronal
Recording" by Edward, et al., Nature Nanotech., 2008; "Neural
Stimulation with a Carbon Nanotube Microelectrode Array" by Ke
Wang, Nano Lett., 2006; "Carbon Nanotube Substrates Boost Neuronal
Electrical Signaling" by Viviana Lovat, et al., Nano Lett., 2005;
"Carbon Nanotube Micro-Electrodes for Neuronal Interfacing" by E.
Ben-Jacob, et al., J. Mater. Chem., 2008.
[0006] The abovementioned technologies are only the rudimentary
carbon nanotube applications in the neural electrode interface. The
present invention further modifies the carbon nanotube electrode
interface and forms the functional groups, which neuron cells
prefer to adhere to. Therefore, neural signals were enhanced with
the use of this modified CNT electrode.
SUMMARY OF THE INVENTION
[0007] One objective of the present invention is to provide a
method for modifying a carbon nanotube electrode interface to
improve the adherence of neuron cells, decrease the impedance
between the electrode interface and the biological tissues, and
promote the signal intensity and quality of measurement.
[0008] To achieve the abovementioned objective, the present
invention proposes a method for modifying a carbon nanotube
electrode interface, which modifies carbon nanotubes used as a
neuron-electrode interface by performing three stages of
modifications, including a carboxylation process, an
acyl-chlorination process, and an amination process. Surfaces of
the carbon nanotubes have carboxyl functional groups after the
carboxylation process. Next, the hydroxyl functional groups of the
carboxyl functional groups are replaced by chlorine atoms of
thionyl chloride in the acyl-chlorination process. Next, the
amination process replaces the chlorine atoms with the amine
functional groups, which were favored by neuron cells.
[0009] In one embodiment, the carbon nanotubes of the
neuron-electrode interface are modified directly. In one
embodiment, the carboxylation process is carried out by a H.sub.2O
plasma process. In one embodiment, the acyl-chlorination and
amination are performed in a reflux system.
[0010] The present invention also provides a microelectrode array,
which comprises a base and at least one probe connected to the
base. Each probe has at least one electrode. The electrode uses the
carbon nanotubes as the neuron-electrode interface thereof, and the
carbon nanotubes is modified with the abovementioned method.
[0011] Below, the technical contents of the present invention are
described in detail with the embodiments and drawings.
BRIEF DESCRIPTION OF THE DRAWINGS
[0012] FIG. 1 is a diagram schematically showing a microelectrode
array for detecting neural signals according to the present
invention;
[0013] FIG. 2 is a flowchart of a method for modifying a carbon
nanotube electrode interface according to the present
invention;
[0014] FIG. 3 is a diagram schematically showing a method for
modifying a carbon nanotube electrode interface according to the
present invention;
[0015] FIG. 4 is a diagram schematically a reflux system according
to the present invention;
[0016] FIG. 5A is a diagram showing the impedance variation of a
neural electrode before and after the modification of carbon
nanotubes according to the present invention;
[0017] FIG. 5B is a diagram showing neural signals detected before
and after the modification of carbon nanotubes according to the
present invention; and
[0018] FIG. 6 is a cross-section view of a carbon nanotube
electrode interface according to one embodiment of the present
invention.
DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENTS
[0019] The present invention proposes a method for modifying a
carbon nanotube electrode interface, which modifies carbon
nanotubes used as a neuron-electrode interface to increase the
adherence of neuron cells to the carbon nanotube electrode
interface, improve the biocompatibility of neuronal, and promote
the quality of electrophysiological signals.
[0020] Refer to FIG. 2 and FIG. 3 respectively a flowchart and a
schematic diagram of a method for modifying a carbon nanotube
electrode interface according to the present invention.
[0021] The method of the present invention comprises a
carboxylation process (Step a), an acyl-chlorination process (Step
b) and an amination process (Step c).
[0022] In the Step a, the carbon nanotubes are carboxylated to form
a plurality of carboxyl functional groups "O.dbd.C--OH" on surfaces
of the carbon nanotubes (as shown in FIG. 3) to improve the
hydrophilicity of the carbon nanotubes. In one embodiment, a
microelectrode array used the carbon nanotubes as the
neuron-electrode interface is washed with deionized water and then
dried. Next, the microelectrode array is processed with a H.sub.2O
plasma to generate the carboxyl functional groups "O.dbd.C--OH" on
the carbon nanotubes. The H.sub.2O plasma process is performed at a
temperature of 25-150.degree. C., under a pressure of 1-100 Ton,
with a power of 25-100 W, for 10-300 seconds. The amount of the
carboxyl functional groups correlates with the processing time of
the H.sub.2O plasma. If the processing time is too short, it
results in insufficient carboxyl functional groups. If the
processing time is too long, the carbon nanotubes will be
damaged.
[0023] In other embodiment, the carboxylation process is carried
out by an O.sub.2 plasma process or via immersing the carbon
nanotubes into an acidic solution at an ambient temperature. The
acidic solutions include but are not limited to nitric acid
(HNO.sub.3), sulfuric acid (H.sub.2SO.sub.4), and hydrogen peroxide
(H.sub.2O.sub.2).
[0024] In the Step b, the carboxylated carbon nanotubes are further
acyl-chlorinated to replace the hydroxyl functional groups of the
carboxyl functional groups with chlorine atoms and form
"O.dbd.C--Cl" functional groups. In the acyl-chlorination process,
the carboxylated carbon nanotubes react with thionyl chloride
(SOCl.sub.2), phosphorus trichloride (PCl.sub.3), phosphorus
pentachloride (PCl.sub.5), Oxalyl dichloride (COCl).sub.2, or
cyanuric chloride (C.sub.3N.sub.3Cl.sub.3), and the hydroxyl
functional groups thereof are thus replaced by the chlorine
atoms.
[0025] In one embodiment, the acyl-chlorination process is carried
out with a chemical synthesis method, wherein the carboxylated
carbon nanotubes react with the thionyl chloride in a reflux
system, and the reaction formula thereof is expressed by Formula
(I).
R--COOH+SOCl.sub.2(l).fwdarw.R--COCl+SO.sub.2(g)+HCl.sub.(g)
(1)
[0026] Refer to FIG. 4 a diagram schematically shows a reflux
system. The microelectrode array 20 is immersed in the thionyl
chloride solution, and an inert gas, such as argon, is pumped into
the reflux system to implement the acyl-chlorination reaction. The
product gases sulfur dioxide (SO.sub.2) and hydrogen chloride (HCl)
are taken away via a condensation tube. The acyl-chlorination
process is undertaken at a temperature of 25-80.degree. C. for
10-20 hours. A magnet 21 is placed on the bottom of the reflux
system and used to agitate the solution to accelerate the reaction.
The microelectrode array 20 is placed on a supporter 22, whereby
the microelectrode array 20 is immersed in the thionyl chloride
solution and exempted from the interference of the magnet 21. After
the acyl-chlorination process, the microelectrode array 20 is dried
for the succeeding treatment.
[0027] In the Step c, the acyl-chlorinated nanotubes are aminated,
whereby the chlorine of the "O.dbd.C--Cl" functional groups are
replaced by an amine to form an amine derivative having
"O.dbd.C--.about.NH.sub.3.sup.+" functional groups at the terminals
thereof, as shown in FIG. 3. The "O.dbd.C--.about.NH.sub.3.sup.+"
functional group has very high affinity and excellent adherence to
the neuron cells and is exempt from the adherence of glial cells.
Therefore, the "O.dbd.C--.about.NH.sub.3.sup.+" functional groups
can prevent from the glial cells aggregation and inhibit the
formation of the sheaths, which will isolate the electrodes from
the biological tissue and impair the signal measurement. The amine
derivatives could be, but not limited to, 1,4-diaminobutane,
ethylenediamine and EDC (1-ethyl-3-(3-dimethylaminopropyl)
carbodiimide).
[0028] In one embodiment, the amination is realized with a chemical
synthesis method, wherein the acyl-chlorinated carbon nanotubes
react with 1,4-diaminobutane in a reflux system. The
1,4-diaminobutane is dissolved in a solvent by a concentration of
0.1-10 wt %. An appropriate amount of a basic compound is added
into the solution to neutralize the acidity. The solvent is, but
not limited to, toluene. Triethylamine may function as the basic
compound to neutralize the acidic products of the reaction, but the
basic compound is not limited to triethylamine. After the carbon
nanotubes are modified by 1,4-diaminobutane, the chlorine atom is
replaced by "--NH--C.sub.4--NH.sub.3.sup.+--", which has an amine
functional group at the terminal thereof.
[0029] Refer to FIG. 5A. The neural electrode containing the
modified carbon nanotubes has lower impedance than the neural
electrode containing the as-grown carbon nanotubes. In FIG. 5A, the
horizontal axis represents the concentration of 1,4-diaminobutane
in the Step c. With the increasing concentration of
1,4-diaminobutane, the amine functional groups also increase, and
the impedance of the electrode decreases. Refer to FIG. 5B, after
modifying the carbon nanotubes, the potential of the signals
detected by the neural electrodes is much greater than before the
modification. As shown in FIG. 5B, the electric potential and
signal-to-noise ratio also increase after the modification.
[0030] In the abovementioned embodiments, what are modified are the
carbon nanotubes that have been formed on the electrodes of a
microelectrode array. However, the present invention also includes
the case: independent carbon nanotubes are modified firstly, and
the modified carbon nanotubes are formed on the neural electrodes
via a coating method, a printing method, or another method.
[0031] The present invention also proposes a microelectrode array,
which comprises a base and at least one probe connected to the
base. Each probe has at least one electrode using the carbon
nanotubes as the interface thereof. Each electrode is connected to
the base via a wire. The carbon nanotubes are modified with the
above-mentioned method to contain amine functional groups.
[0032] The microelectrode array of the present invention is
fabricated from the combination of a silicon wafer and a
complementary metal-oxide-semiconductor (CMOS) in the semiconductor
processing techniques. Refer to FIG. 6 a sectional view
schematically showing an electrode 30 using the carbon nanotubes as
the interface thereof. The electrode 30 includes a carbon nanotube
layer 37, a conductive layer 34 and a catalytic layer 36. The
carbon nanotube layer 37 is the measurement interface of the
electrode 30. The conductive layer 34 (such as a gold layer shown
in FIG. 6) is deposited on a first adhesion layer 33 (such as a
chromium layer shown in FIG. 6) and over the silicon wafer 31, and
a position and dimensions of the electrode 30 are thus defined. In
one embodiment, an insulating layer 32 (such as a silicon dioxide
layer shown in FIG. 6) is formed between the conductive layer 34
and the wafer 31. The catalytic layer 36 is formed over the
conductive layer 34, and the carbon nanotube layer 37 is
catalytically formed on the catalytic layer 36. The catalytic layer
36 is made of iron, cobalt, or nickel. In FIG. 6, the catalytic
layer 36 is a nickel layer having a thickness of about 5 nm. In one
embodiment, the catalytic layer 36 is formed on a second adhesion
layer 35 and over the conductive layer 34, and the second adhesion
layer 35 is a titanium layer having a thickness of about 10-30 nm
in FIG. 6. In one embodiment, the carbon nanotube layer 37 is
synthesized at a temperature of 350-400.degree. C.
[0033] In the present invention, the modified carbon nanotube
interfaces of the electrodes of the microelectrode array can
obviously increase the adherence of neuron cells to the electrodes.
Thus, the microelectrode array can be implanted into the biological
tissue to perform a long-time measurement. Further, the
microelectrode array of the present invention can perform
intracellular recording to obtain higher-intensity signals.
[0034] The embodiments described above are only to exemplify the
present invention but not to limit the scope of the present
invention. Any equivalent modification or variation according to
the spirit of the present invention is to be also included within
the scope of the present invention.
* * * * *