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[The golden hour of sepsis: initial therapy should start in the prehospital setting].[脓毒症的黄金一小时:初始治疗应在院前环境中开始]
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磁驱动、珠增强硅光子免疫传感器。

Magnetically-actuated, bead-enhanced silicon photonic immunosensor.

作者信息

Valera Enrique, McClellan Melinda S, Bailey Ryan C

机构信息

Department of Chemistry, University of Illinois at Urbana-Champaign 600 South Matthews Avenue, Urbana, IL 61801, USA.

出版信息

Anal Methods. 2015 Oct 21;7(20):8539-8544. doi: 10.1039/C5AY01477H. Epub 2015 Jun 26.

DOI:10.1039/C5AY01477H
PMID:26528374
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4627713/
Abstract

Magnetic actuation has been introduced to an optical immunosensor technology resulting in improvements in both rapidity and limit of detection for an assay quantitating low concentrations of a representative protein biomarker. For purposes of demonstration, an assay was designed for monocyte chemotactic protein 1 (MCP-1), a small cytokine which regulates migration and infiltration of monocytes and macrophages, and is an emerging biomarker for several diseases. The immunosensor is based on arrays of highly multiplexed silicon photonic microring resonators. A one-step sandwich immunoassay was performed and the signal was further enhanced through a tertiary recognition event between biotinylated tracer antibodies and streptavidin-coated magnetic beads. By integrating a magnet under the sensor chip, magnetic beads were rapidly directed towards the sensor surface resulting in improved assay performance metrics. Notably, the time required in the bead binding step was reduced by a factor of 11 (4 vs 45 min), leading to an overall decrease in assay time from 73 min to 32 min. The magnetically-actuated assay also lowered the limit of detection (LOD) for MCP-1 from 124 pg mL down to 57 pg mL. In sum, the addition of magnetic actuation into bead-enhanced sandwich assays on a silicon photonic biosensor platform might facilitate improved detection of biomarkers in point-of-care diagnostics settings.

摘要

磁驱动已被引入光学免疫传感器技术,这在检测一种代表性蛋白质生物标志物的低浓度时,提高了检测速度和检测限。为了进行演示,设计了一种针对单核细胞趋化蛋白1(MCP-1)的检测方法,MCP-1是一种小型细胞因子,可调节单核细胞和巨噬细胞的迁移和浸润,并且是几种疾病的新兴生物标志物。该免疫传感器基于高度复用的硅光子微环谐振器阵列。进行了一步夹心免疫测定,并通过生物素化示踪抗体与链霉亲和素包被的磁珠之间的三级识别事件进一步增强了信号。通过在传感器芯片下方集成一块磁铁,磁珠被快速引导至传感器表面,从而改善了检测性能指标。值得注意的是,磁珠结合步骤所需的时间减少了11倍(从45分钟减少到4分钟),导致检测总时间从73分钟减少到32分钟。磁驱动检测还将MCP-1的检测限从124 pg/mL降至57 pg/mL。总之,在硅光子生物传感器平台上的磁珠增强夹心检测中加入磁驱动,可能有助于在即时诊断环境中更好地检测生物标志物。