Development of an open stand-alone platform for regenerable automated microarrays

被引:42
作者
Kloth, Katrin [1 ]
Niessner, Reinhard [1 ]
Seidel, Michael [1 ]
机构
[1] Tech Univ Munich, Inst Hydrochem & Chair Analyt Chem, D-81377 Munich, Germany
关键词
Chemiluminescence; Analytical microarray; Multiplex immunoassay; Microfluidic; Automated microarray reader; ARRAY BIOSENSOR; BACTERIAL; TECHNOLOGY; SYSTEM;
D O I
10.1016/j.bios.2008.11.005
中图分类号
Q6 [生物物理学];
学科分类号
071011 ;
摘要
A novel automated chemiluminescence (CL) read-out system for analytical flow-through microarrays based on multiplexed immunoassays has been developed. The microarray chip reader (MCR 3) is designed as a stand-alone platform, with the goal to quantify multiple analytes in complex matrices of food and liquid samples for field analysis or for routine analytical laboratories. The CL microarray platform is a self-contained system for the fully automated multiplexed immunoanalysis: the microarray chip, the fluidic system and the software module enable automated calibration and determination of analyte concentrations during a whole working day. The detection of antibiotics in milk was demonstrated to validate this device. There are few quantitative multi-residue detection methods for routine analysis although the EU has defined maximum residue limits (MRLs) for a number of antibacterial reagents. Therefore, an automated multianalyte detection instrument is needed quantifying simultaneously antibiotics within some minutes. Also regeneration is required to avoid replacing the assay surface. The MCR 3 uses a microarray chip, which consists of two channels for parallel measurement and regeneration. The microarray chip is designed for parallel analysis of up to 13 different antibiotics in milk applying an indirect competitive microarray immunoassay (MIA). Microspotted antibiotics are directly coupled to epoxylated PEG surfaces. As an initial example, penicillin G is quantified in milk on the MCR 3. The penicillin G surface is regenerable for 47 measurement cycles per channel. A limit of detection (LOD) of 1.1 mu g/L is achieved by an assay time of 6 min. (C) 2008 Elsevier B.V. All rights reserved.
引用
收藏
页码:2106 / 2112
页数:7
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