• 동아시아식생활학회지
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• 제20권5호
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• pp.735-742
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• 2010

식품 중 잠재적 위험 물질로 작용할 수 있는 BAs의 신속 검출을 위하여 전기전도성이 우수하다고 알려진 MWCNTs의 개질, 작업 전극의 제작, 효소반응기 제작을 통해 바이오센서 시스템을 구성하고 hydrogen peroxide와 주요 BAs 물질에 대한 감응도를 측정하였다. MWCTS의 성질을 향상시키기 위해 아민기를 도입하였고, 이를 FT-IR 스펙트럼을 통해 확인하였다. 아민기를 도입한 MWCNTs를 GCE에 고착시키고 PB 막을 입힌 후 cyclic voltammetry 반응을 비교한 결과, PB/MWCNT-$NH_2$/GCE 전극이 GCE에 비해 산화 전류는 8배 이상, 전체 전류는 25배 이상의 높은 전류 흐름을 보였으며, 미세한 전류 흐름의 측정도 용이해진 것으로 나타났다. 또한, carrier buffer의 pH를 달리하여 제작된 전극의 감응 전류를 비교한 결과, pH 7.0에서 전류의 감응도가 가장 높게 측정되었다. 과산화수소를 주입하여 전극의 성능의 검증한 결과, $0.5 {\mu}M{\sim}100 {\mu}M$ 범위에서 선형관계를 보였으며, 검출 한계는 $0.5{\mu}M$로 측정되었다. Histamine 표준 용액 주입 시 $1{\mu}M{\sim}100{\mu}M$ 범위에서 선형 관계를 나타내었고, tyramine은 histamine에 비해 약 95%, 2-phenylethylamine과 tryptamine은 histamine에 비해 각각 75%, 70% 수준의 감응도를 이용하여 구성된 바이오센서 시스템이 낮은 검출 한계와 높은 수준의 반응 감도를 나타내어 BAs를 측정하는데 좋은 장치임이 확인되었다.

• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2005년도 생물공학의 동향(XVI)
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• pp.471-471
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• 2005

• 대한화학회지
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• 제48권6호
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• pp.654-658
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• 2004

• 대한화학회지
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• 제55권2호
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• pp.323-327
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• 2011

• 전기화학회지
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• 제10권3호
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• pp.229-232
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• 2007

An amperometric immunosensor for the determination of rabbit IgG is proposed. The immunoassay utilizes a screen-printed carbon electrode on which osmium redox polymer is electrodeposited. This immunoassay detects 0.1 ng/ml of rabbit IgG, which is ${\sim}10^2$ fold higher than the most sensitive enzyme amplified amperometric immunoassay. The assay utilizes a screen-printed carbon electrode which was pre-coated by a co-electrodeposited film of an electron conducting redox hydrogel and a rabbit IgG. The rabbit IgG in the electron conducting film conjugates captures, when present, the anti-rabbit IgG. The captured anti-rabbit-IgG is labeled with horseradish peroxidase (HRP) which catalyzes the two-electron reduction of $H_2O_2$ to water. Because the redox hydrogel electrically connects HRP reaction centers to the electrode, completion of the sandwich converts the film from non-electrocatalytic to electro-catalytic for the reduction of $H_2O_2$ to $H_2O$ when the electrode is poised at 200 mV vs. Ag/AgCl.

• 대한화학회지
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• 제41권7호
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• pp.343-350
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• 1997

과산화수소 정량을 위하여 닭의 간조직과 ferrocene을 탄소반죽에 혼입시켜 만든 전류법 바이오센서의 감응 특성이 조사되었다. 또한 조사된 전극 퍼텐샬 범위( - 0.5∼ + 0.05 V vs Ag/AgCl) 내에서 $t_{95%}$=13 sec의 빠른 감응시간과 $5.1{\times}10^{-5}$ M(S/N=3)의 검출한계를 보여 주었으며, 감응에 방해가 된다고 여겨지는 물질들에 대하여 좋은 선택성을 보여 주었다. 생촉매 안정성이 좋았으며, 이동매체를 사용하지 않는 전극의 제조 가능성을 제시하였다.

• Bulletin of the Korean Chemical Society
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• 제31권11호
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• pp.3259-3264
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• 2010

A label-free amperometric immunosensor has been proposed for the detection of myeloperoxidase (MPO) in human serum. To fabricate such an immunosensor, a composite film consisting of N,N-dimethylformamide (DMF), multiwall carbon nanotubes (MWCNTs) and 1-ethyl-3-methyl imidazolium tetrafluoroborate ($EMIMBF_4$) suspension was initially formed on a glassy carbon electrode (GCE). Then cerium dioxide ($CeO_2$) dispersed by chitosan was coated on the GCE. After that, MPO antibodies (anti-MPO) were attached onto the nano$CeO_2$ surface. With a noncompetitive immunoassay format, the antibody-antigen complex formed between the immobilized anti-MPO and MPO in sample solution. The immunosensor was characterized by cyclic voltammetry, transmission electron microscopy (TEM) and scanning electron microscopy (SEM). The factors influencing the performance of the immunosensor were studied in detail. Under optimal conditions, the current change before and after the immunoreaction was proportional to MPO concentration in the range of 5 to $300\;ng\;mL^{-1}$ with a detection limit of $0.2\;ng\;mL^{-1}$.

• 대한화학회지
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• 제17권2호
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• pp.126-129
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• 1973

회전백금전극을 지시전극으로하고 수은-요오드화수은(II)을 기준전극으로하여 암모니아수용액에서 2.5-dimercapto-1,3,4-thiadiazole에 의한 은의 전류적정법을 연구하였다. 암모니아수용액에서 EDTA를 은폐제로 사용하여 여러 가지 이온들의 존재 하에 미량의 은을 직접 적정할 수가 있었으며 백금과 금 이온만이 방해하였다. 이 방법으로 미량의 은을 상대 오차 ${\pm}3{\%}$이내 정량할 수 있다.

• Bulletin of the Korean Chemical Society
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• 제25권10호
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• pp.1499-1502
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• 2004

An amperometric biosensor based on carbon paste electrodes (CPEs) for the determination of urea was constructed by enzyme (urease/GL-DH)-modified method. Urea was hydrolyzed to ${NH_4}^+$ by catalyzing urease onto the enzyme-modified electrode surface in sample solution. In the presence of ${\alpha}$-ketoglutarate and reduced nicotinamide adenine dinucleotide(NADH), a liberated ${NH_4}^+$ produce to L-glutamate and $NAD^+$ by Lglutamate dehydrogenase (GL-DH). After the chemical reaction was proceeded, the electrochemical reaction was occurred that an excess of the NADH was oxidized to $NAD^+$. The oxidation current of NADH was monitored at +1.10 volt vs. Ag/AgCl. An optimum conditions of biosensor were investigated: The optimum pH range for catalyzed hydrolysis reaction of urea was pH 7.0-7.4. The linear response range and detection limit were $2.0\;{\times}\;10^{-5}{\sim}2.0\;{\times}\;10^{-4}M\;and\;5.0\;{\times}\;10^{-6}M$, respectively. Another physiological species did not interfere, except L-ascorbic acid.

• Bulletin of the Korean Chemical Society
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• 제30권12호
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• pp.2979-2983
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• 2009

Nanowires of polytetrakis(o-aminophenyl)porphyrin (PTAPPNW) were fabricated by electrochemical polymerization with the cyclic voltammetric method in anodic aluminum oxide (AAO) membranes. The glassy carbon electrode (GCE) modified by PTAPPNW, single-walled carbon nanotubes (SWNT) and Nafion as a binder was investigated with voltammetric methods in a phosphate buffer saline (PBS) solution at pH 7.4. The PTAPPNW + SWNT + Nafion/GCE exhibited strongly enhanced voltammetric and amperometric sensitivity towards hydrogen peroxide ($H_2O_2$), which shortened the response time and enhanced the sensitivity for $H_2O_2$ determination at an applied potential of 0.0 V by amperometric method. The PTAPPNW + SWNT + Nafion/GCE can be used to monitor $H_2O_2$ at very low concentrations in biological pH as an efficient electrochemical $H_2O_2$ sensor.