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http://ir.lib.ncu.edu.tw/handle/987654321/49929
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| 題名: | Development of a label-free impedance biosensor for detection of antibody-antigen interactions based on a novel conductive linker |
| 作者: | Chen,CS;Chang,KN;Chen,YH;Lee,CK;Lee,BYJ;Lee,ASY |
| 貢獻者: | 化學工程與材料工程學系 |
| 關鍵詞: | POLARIZATION INTERFEROMETRIC BIOSENSOR;SURFACE-PLASMON RESONANCE;SELF-ASSEMBLED MONOLAYERS;GOLD ELECTRODES;BIOMOLECULAR INTERACTIONS;REAL-TIME;ELECTROCHEMICAL BIOSENSORS;DNA-SENSORS;SPECTROSCOPY;IMMUNOSENSOR |
| 日期: | 2011 |
| 上傳時間: | 2012-03-27 16:26:43 (UTC+8) |
| 出版者: | 國立中央大學 |
| 摘要: | We developed a label-free impedance biosensor based on an innovative conductive linker for detecting antibody-antigen interactions. As the often used conventional long chain thiol is a poor conductor, it is not a suitable material for use in a faradaic biosensor. In this study, we adopted a thiophene-based conductive bio-linker to form a self-assembled monolayer and to immobilize the bio-molecules. We used cyclic voltammetry and impedance spectroscopy to verify the enhanced conductivity properties. Results showed that the electron transfer resistance of this new conductive linker was 3 orders of a magnitude lower than for a case using a conventional long chain thiol linker. With the decreased impedance (i.e. increased faradaic current), we can obtain a higher signal/noise ratio such that the detection limit is improved. Using fluorescence microscopy, we verified that our new conductive linker has a protein immobilization capability similar to a conventional long chain thiol linker. Also, using S100 proteins, we verified the protein interaction detection capability of our system. Our obtained results showed a linear dynamic range from 10 ng/ml to 10 mu g/ml and a detection limit of 10 ng/ml. With our new conductive linker, an electrochemical impedance biosensor shows great potential to be used for point-of-care applications. (C) 2010 Elsevier B.V. All rights reserved. |
| 關聯: | BIOSENSORS & BIOELECTRONICS |
| 顯示於類別: | [化學工程與材料工程學系 ] 期刊論文
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