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首页> 外文期刊>Analytical Biochemistry: An International Journal of Analytical and Preparative Methods >Immunomagnetic capture and colorimetric detection of malarial biomarker Plasmodium falciparum lactate dehydrogenase
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Immunomagnetic capture and colorimetric detection of malarial biomarker Plasmodium falciparum lactate dehydrogenase

机译:疟原虫疟原虫乳酸脱氢酶的免疫磁捕获和比色性检测

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摘要

We report a sensitive, magnetic bead-based colorimetric assay for Plasmodium falciparum lactate dehydrogenase (PfLDH) in which the biomarker is extracted from parasitized whole blood and purified based on antigen binding to antibody-functionalized magnetic particles. Antigen-bound particles are washed, and PfLDH activity is measured on-bead using an optimized colorimetric enzyme reaction (limit of detection [LOD] = 21.1 +/- 0.4 parasites/mu l). Enhanced analytical sensitivity is achieved by removal of PfLDH from the sample matrix before detection and elimination of nonspecific reductases and species that interfere with the optimal detection wavelength for measuring assay development. The optimized assay represents a simple and effective diagnostic strategy for P. falciparum malaria with time-to-result of 45 min and detection limits similar to those of commercial enzyme-linked immunosorbent assay (ELISA) kits, which can take 4-6 h. This method could be expanded to detect all species of malaria by switching the capture antibody on the magnetic particles to a pan-specific Plasmodium LDH antibody. (C) 2015 The Authors. Published by Elsevier Inc.
机译:我们报告了一种敏感的磁珠基比色测定疟原虫乳酸脱氢酶(PFLDH),其中生物标志物从寄生的全血中提取,并基于与抗体官能化磁性颗粒的抗原结合纯化。洗涤抗原结合的颗粒,使用优化的比色酶反应(检测极限= 21.1 +/- 0.4寄生虫/μl)测量PFLDH活性。通过在检测和消除干扰测量测定发育的最佳检测波长的非特异性还原酶和物种之前通过从样品基质中除去PFLDH来实现增强的分析敏感性。优化的测定代表了45分钟的疟原虫疟疾的简单有效诊断策略,并且检测限与商业酶联免疫吸附测定(ELISA)试剂盒类似的检测限,这可能需要4-6小时。通过将磁性颗粒上的捕获抗体切换到泛特异性疟原虫LDH抗体,可以扩展该方法以检测所有物种的疟疾。 (c)2015年作者。 elsevier公司发布

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