A Compact Immunoassay Platform Based on a Multicapillary Glass Plate

A highly sensitive, rapid immunoassay performed in the multi-channels of a micro-well array consisting of a multicapillary glass plate (MCP) and a polydimethylsiloxane (PDMS) slide is described. The micro-dimensions and large surface area of the MCP permitted the diffusion distance to be decreased a...

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Main Authors: Shuhua Xue, Hulie Zeng, Jianmin Yang, Hizuru Nakajima, Katsumi Uchiyama
Format: Article
Language:English
Published: MDPI AG 2014-05-01
Series:Sensors
Subjects:
Online Access:http://www.mdpi.com/1424-8220/14/5/9132
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spelling doaj-0adb4e305a0e49ffaf3be83683da037a2020-11-24T21:06:33ZengMDPI AGSensors1424-82202014-05-011459132914410.3390/s140509132s140509132A Compact Immunoassay Platform Based on a Multicapillary Glass PlateShuhua Xue0Hulie Zeng1Jianmin Yang2Hizuru Nakajima3Katsumi Uchiyama4Department of Applied Chemistry, Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, 1-1 Minamiohsawa, Hachioji, Tokyo 192-0397, JapanDepartment of Applied Chemistry, Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, 1-1 Minamiohsawa, Hachioji, Tokyo 192-0397, JapanDepartment of Applied Chemistry, Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, 1-1 Minamiohsawa, Hachioji, Tokyo 192-0397, JapanDepartment of Applied Chemistry, Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, 1-1 Minamiohsawa, Hachioji, Tokyo 192-0397, JapanDepartment of Applied Chemistry, Graduate School of Urban Environmental Sciences, Tokyo Metropolitan University, 1-1 Minamiohsawa, Hachioji, Tokyo 192-0397, JapanA highly sensitive, rapid immunoassay performed in the multi-channels of a micro-well array consisting of a multicapillary glass plate (MCP) and a polydimethylsiloxane (PDMS) slide is described. The micro-dimensions and large surface area of the MCP permitted the diffusion distance to be decreased and the reaction efficiency to be increased. To confirm the concept of the method, human immunoglobulin A (h-IgA) was measured using both the proposed immunoassay system and the traditional 96-well plate method. The proposed method resulted in a 1/5-fold decrease of immunoassay time, and a 1/56-fold cut in reagent consumption with a 0.05 ng/mL of limit of detection (LOD) for IgA. The method was also applied to saliva samples obtained from healthy volunteers. The results correlated well to those obtained by the 96-well plate method. The method has the potential for use in disease diagnostic or on-site immunoassays.http://www.mdpi.com/1424-8220/14/5/9132multicapillary glass platecompact immunoassayenzyme-linked immunosorbent assay
collection DOAJ
language English
format Article
sources DOAJ
author Shuhua Xue
Hulie Zeng
Jianmin Yang
Hizuru Nakajima
Katsumi Uchiyama
spellingShingle Shuhua Xue
Hulie Zeng
Jianmin Yang
Hizuru Nakajima
Katsumi Uchiyama
A Compact Immunoassay Platform Based on a Multicapillary Glass Plate
Sensors
multicapillary glass plate
compact immunoassay
enzyme-linked immunosorbent assay
author_facet Shuhua Xue
Hulie Zeng
Jianmin Yang
Hizuru Nakajima
Katsumi Uchiyama
author_sort Shuhua Xue
title A Compact Immunoassay Platform Based on a Multicapillary Glass Plate
title_short A Compact Immunoassay Platform Based on a Multicapillary Glass Plate
title_full A Compact Immunoassay Platform Based on a Multicapillary Glass Plate
title_fullStr A Compact Immunoassay Platform Based on a Multicapillary Glass Plate
title_full_unstemmed A Compact Immunoassay Platform Based on a Multicapillary Glass Plate
title_sort compact immunoassay platform based on a multicapillary glass plate
publisher MDPI AG
series Sensors
issn 1424-8220
publishDate 2014-05-01
description A highly sensitive, rapid immunoassay performed in the multi-channels of a micro-well array consisting of a multicapillary glass plate (MCP) and a polydimethylsiloxane (PDMS) slide is described. The micro-dimensions and large surface area of the MCP permitted the diffusion distance to be decreased and the reaction efficiency to be increased. To confirm the concept of the method, human immunoglobulin A (h-IgA) was measured using both the proposed immunoassay system and the traditional 96-well plate method. The proposed method resulted in a 1/5-fold decrease of immunoassay time, and a 1/56-fold cut in reagent consumption with a 0.05 ng/mL of limit of detection (LOD) for IgA. The method was also applied to saliva samples obtained from healthy volunteers. The results correlated well to those obtained by the 96-well plate method. The method has the potential for use in disease diagnostic or on-site immunoassays.
topic multicapillary glass plate
compact immunoassay
enzyme-linked immunosorbent assay
url http://www.mdpi.com/1424-8220/14/5/9132
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