CRP detection from serum for chip-based point-of-care testing system

被引:56
|
作者
Kim, Chang-Hoon [1 ]
Ahn, Jae-Hyuk [1 ]
Kim, Jee-Yeon [1 ]
Choi, Ji-Min [1 ]
Lim, Kyung-Choon [2 ]
Park, Tae Jung [3 ]
Heo, Nam Su [4 ]
Lee, Hee Gu [5 ]
Kim, Jong-Wan [6 ]
Choi, Yang-Kyu [1 ]
机构
[1] Korea Adv Inst Sci & Technol, Dept Elect Engn, Taejon 305701, South Korea
[2] Sungshin Womens Univ, Coll Nursing, Dept Nursing, Seoul 142732, South Korea
[3] Chung Ang Univ, Dept Chem, Seoul 156756, South Korea
[4] Korea Adv Inst Sci & Technol, BioProc Engn Res Ctr, Taejon 305701, South Korea
[5] Korea Res Inst Biosci & Biotechnol, Med Genom Res Ctr, Taejon 305806, South Korea
[6] DanKook Univ, Dept Lab Med, Cheonan 330714, South Korea
来源
BIOSENSORS & BIOELECTRONICS | 2013年 / 41卷
关键词
C-reactive protein; CRP; Nanogap-embedded FET; FET-based biosensor; Point-of-care testing (POCT); C-REACTIVE PROTEIN; SURFACE-PLASMON RESONANCE; FIELD-EFFECT TRANSISTOR; BIOSENSORS; ELISA;
D O I
10.1016/j.bios.2012.08.047
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Most of point-of-care testing (POCT) to improve facilitates in diagnosis, treatment, and monitoring of patients. POCT technique has still remained a quantitatively and accurately detective effect. In this article, we demonstrated that real human C-reactive protein (CRP) in serum was detected for a chip-based point-of-care testing application based on a nanogap-embedded field effect transistor (FET), and the results were compared with those obtained via the enzyme-linked immunosorbent assay (ELISA) method. The limit of detection (LOD), determined from the standard curve, was 0.1 ng/ml, which is comparable to that of commercialized ELISAs. We evaluated that an improved detection range (0.1 ng/ml to 100 ng/ml) was achieved by comparing with commercialized ELISA. Control experiments to determine selectivity and to discern false-positive/false-negative rates were also performed. This report is the first description of the detection of CRP in human serum using a silicon-based biosensor. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:322 / 327
页数:6
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