首页> 美国卫生研究院文献>International Journal of Nanomedicine >Detection of Mycobacterium tuberculosis based on H37Rv binding peptides using surface functionalized magnetic microspheres coupled with quantum dots – a nano detection method for Mycobacterium tuberculosis
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Detection of Mycobacterium tuberculosis based on H37Rv binding peptides using surface functionalized magnetic microspheres coupled with quantum dots – a nano detection method for Mycobacterium tuberculosis

机译:使用表面功能化的磁性微球和量子点结合基于H37Rv结合肽的结核分枝杆菌的检测–结核分枝杆菌的纳米检测方法

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摘要

Despite suffering from the major disadvantage of low sensitivity, microscopy of direct smear with the Ziehl–Neelsen stain is still broadly used for detection of acid-fast bacilli and diagnosis of tuberculosis. Here, we present a unique detection method of Mycobacterium tuberculosis (MTB) using surface functionalized magnetic microspheres (MMSs) coupled with quantum dots (QDs), conjugated with various antibodies and phage display-derived peptides. The principle is based upon the conformation of the sandwich complex composed of bacterial cells, MMSs, and QDs. The complex system is tagged with QDs for providing the fluorescent signal as part of the detection while magnetic separation is achieved by MMSs. The peptide ligand H8 derived from the phage display library Ph.D.-7 is developed for MTB cells. Using the combinations of MMS-polyclonal antibody+QD-H8 and MMS-H8+QD-H8, a strong signal of 103 colony forming units (CFU)/mL H37Rv was obtained with improved specificity. MS-H8+QD-H8 combination was further optimized by adjusting the concentrations of MMSs, QDs, and incubation time for the maximum detection signal. The limit of detection for MTB was found to reach 103 CFU/mL even for the sputum matrices. Positive sputum samples could be distinguished from control. Thus, this novel method is shown to improve the detection limit and specificity of MTB from the sputum samples, and to reduce the testing time for accurate diagnosis of tuberculosis, which needs further confirmation of more clinical samples.
机译:尽管存在灵敏度低的主要缺点,但用Ziehl-Neelsen染色剂直接涂片显微镜检查仍广泛用于检测抗酸杆菌和诊断结核病。在这里,我们提出了一种独特的结核分枝杆菌(MTB)检测方法,该方法使用表面功能化的磁性微球(MMS)与量子点(QD)偶联,并结合了各种抗体和噬菌体展示衍生肽。该原理基于由细菌细胞,MMS和QD组成的三明治复合物的构象。复杂的系统标记有QD,用于在检测通过MMS实现磁分离的同时提供荧光信号作为检测的一部分。衍生自噬菌体展示文库Ph.D.-7的肽配体H8是为MTB细胞开发的。使用MMS多克隆抗体+ QD-H8和MMS-H8 + QD-H8的组合,可以提高特异性,获得10 3 集落形成单位(CFU)/ mL H37Rv的强信号。通过调整MMS,QD的浓度和最大检测信号的孵育时间,进一步优化了MS-H8 + QD-H8组合。即使对痰液基质,MTB的检出限也达到了10 3 CFU / mL。阳性痰样本可与对照区分开。因此,该新方法显示出可提高痰标本中MTB的检出限和特异性,并减少了准确诊断结核病的检测时间,这需要进一步确认更多的临床标本。

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