Rapid duplex immunoassay for wound biomarkers at the point-of-care

被引:40
|
作者
Worsley, G. J. [1 ]
Attree, S. L. [1 ]
Noble, J. E. [1 ]
Horgan, A. M. [1 ]
机构
[1] Natl Phys Lab, Biotechnol Grp, Qual Life Div, Teddington TW11 0LW, Middx, England
来源
BIOSENSORS & BIOELECTRONICS | 2012年 / 34卷 / 01期
关键词
Diagnosis; Lateral flow; Multiplexing; Interleukin; 6; Tumour necrosis factor alpha; LATERAL FLOW ASSAY; LEG ULCERS; CYTOKINES; LABELS; SERS;
D O I
10.1016/j.bios.2012.02.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
In this study we describe a novel method of sampling and quantifying wound biomarkers for clinical settings. We believe the chosen format will allow rapid assessments of wound healing and provide biomarker evidence-based decision points for treatment of the wound at the time of presentation. The wound monitoring principle uses a proprietary sample collection tool (a thermally reversible hydrogel) to sample and isolate biomarkers within a wound environment without further sample extraction/preparation steps. We show how gel samples can be analysed in a lateral flow assay format utilising fluorescent microspheres with optically discrete emission characteristics and demonstrate quantitative detection of two analytes (duplexing) achieved in a single test line. As a model assay, the chronic wound biomarkers interleukin 6 (IL6) and tumour necrosis factor alpha (TNF alpha) are used. Limits of detection of 48.5 pg/mL and 55.5 pg/mL respectively in hydrogel samples and 7.15 pg/mL and 10.7 pg/mL respectively in plasma are reported. We believe this is the first literature example of quantitative detection of multiple analytes within a single test line using spectral separation to distinguish the analytes. Crown Copyright (c) 2012 Published by Elsevier B.V. All rights reserved.
引用
收藏
页码:215 / 220
页数:6
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