Electrical signaling of enzyme-linked immunosorbent assays with an ion-sensitive field-effect transistor

被引:50
作者
Jang, Hyun-June [1 ,2 ]
Ahn, Junhyoung [3 ]
Kim, Min-Gon [4 ]
Shin, Yong-Beom [5 ]
Jeun, Minhong [1 ,2 ]
Cho, Won-Ju [6 ]
Lee, Kwan Hyi [1 ,2 ]
机构
[1] Korea Inst Sci & Technol, Biomed Res Inst, Seoul 136791, South Korea
[2] Asan Med Ctr, AMC KIST Translat Res Ctr TRC, Seoul 138736, South Korea
[3] Korea Inst Machinery & Mat, Dept Nano Mfg Technol, Nano Convergence Mech Syst Res Div, Taejon 305343, South Korea
[4] Gwanyju Inst Sci & Technol, Dept Chem, Kwangju 500712, South Korea
[5] Korea Res Inst Biosci & Biotechnol, Res Ctr Integrat Cellul, Taejon 305806, South Korea
[6] Kwangwoon Univ, Dept Elect Mat Engn, Seoul 139701, South Korea
基金
新加坡国家研究基金会;
关键词
Immunosensor; Point-of-care device; ISFET; ELISA; ALP; SILVER NANOPARTICLES; AMYLOID-BETA; HUMAN SERUM; THIN-FILM; IMMUNOSENSOR; ENHANCEMENT; PERFORMANCE; BIOMARKERS; BIOSENSOR; GRAPHENE;
D O I
10.1016/j.bios.2014.09.020
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
Optical laboratory-based immunoassays, such as enzyme-linked immunosorbent assay (ELISA) give a high sensitivity and specificity of various fatal diseases. However, these assays are no longer efficient in on-spot diagnostics of wide-spreading and contagious infections. At this point in time, portable and handhold devices play a pivotal role in infectious diseases with quick diagnostics at or near the site of the disease propagation. In this paper, we demonstrated a novel electrical immunoassay of ELISA that was not based on optical signaling but on electrical signaling. This was done by combining an ion-sensitive field-effect transistor (ISFET) with ELISA. By harnessing the catalytic reaction of alkaline phosphatase that precipitated silver particles, we effectively overcame the chronic Debye screening length issue of the ISFET. Ultimately, small signal ranging from 1 pg/mL to 10 ng/mL was immensely amplified with the ALP label, regardless of buffer conditions. The sensor platform herein surpassed a sensing capability of conventional ELISA that is considered to have a LOD on the order of similar to 1 ng/mL. The results were compared with those of horseradish peroxidase label, which is generally used for optical analyses in ELISA. Our newly developed ISFET-based portable sensor holds a large potential for point-of-care tools in a variety of diseases, without being limited by the need for expensive equipment such as spectro-photometers. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:318 / 323
页数:6
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