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Immunomagnetic separation and rapid detection of bacteria using bioluminescence and microfluidics

机译:免疫磁分离和使用生物发光和微流控技术快速检测细菌

摘要

This paper describes an immunomagnetic separation of target bacterial cells from others by using magnetic bead. The surface of bead was coated with antibodies which can capture specific organism. The binding efficiency of immunomagnetic bead (IMB) capturing target bacterial cells was higher than 98% when the concentrations of target and interferent bacterial cells were at the same level. The concentration of bacteria was determined indirectly by detecting adenosine 5'-triphosphate (ATP) employing bioluminescence (BL) reaction of firefly luciferin-ATR Benzalkonium chloride (BAC) was used as an ATP extractant from living bacterial cells. We found that BAC could enhance the light emission when the concentration of BAC was less than 5.3 x 10(-2)% (w/v) and the BL intensity reached its maximum at the concentration of BAC was 2.7 x 10(-2)%, which was 10-fold stronger than that without BAC. Based on the principle of the IMB, a microfluidic chip combined with immunofluorescence assay for separating and detecting bacteria simultaneously was also developed. The IMBs were magnetically fixed in the bead-beds of chip channels with a 3-mm diameter of NdFeB permanent magnet. The target bacterial cells can be captured magnetically and observed by a fluorescent microscope. (C) 2009 Elsevier B.V. All rights reserved.
机译:本文介绍了使用磁珠对靶细菌细胞进行免疫磁分离的方法。珠的表面涂有可以捕获特定生物的抗体。当目标细菌和干扰细菌细胞的浓度处于相同水平时,捕获目标细菌细胞的免疫磁珠(IMB)的结合效率高于98%。通过使用萤火虫荧光素的生物发光(BL)反应检测A5'-三磷酸腺苷(ATP)间接确定细菌的浓度-苯扎氯铵(BAC)被用作从活细菌细胞中提取的ATP。我们发现当BAC的浓度小于5.3 x 10(-2)%(w / v)且BL强度在BAC的浓度为2.7 x 10(-2)时达到最大值时,BAC可以增强发光。 %,比没有BAC的强度高10倍。基于IMB的原理,还开发了一种微流控芯片结合免疫荧光检测法同时分离和检测细菌。 IMB用3毫米直径的NdFeB永磁体磁性固定在芯片通道的珠床上。目标细菌细胞可以被磁性捕获并通过荧光显微镜观察。 (C)2009 Elsevier B.V.保留所有权利。

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