Label-free electrochemical-based biosensor for gene-phosphatidylinositol mannosides detection in urine for the determination of multidrug-resistant tuberculosis.

IF 2.8 4区 材料科学 Q3 MATERIALS SCIENCE, MULTIDISCIPLINARY
Dinesh R Rotake, Jitendra B Zalke, Arpita Parakh, Shubham C Anjankar, Shiv Govind Singh, Ranjana Singh
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引用次数: 0

Abstract

Tuberculosis (TB) is a significant public health issue, and the existing diagnostic tests have shortcomings that cause delays in initiating treatment. In this study, we designed aGene-pimB-based biosensor for the determination of TB and tested it using an electrochemical technique. TheGene-pimBhas been reported to be upregulated in mannose-capped lipoarabinomannan (manLAM) in multidrug-resistant TB (MDR-TB). Due to its link with drug resistance,Gene-pimBholds promise as a biomarker for identifying MDR-TB strains. In this work, the biosensor is fabricated using graphite-zinc oxide nanofibers (GPH-ZnO NFs), which are generated using electrospinning and deposited on glassy carbon electrodes. The GPH-ZnO functionalized electrode were further functionalized with MSA/EDC/NHS protocol to provide efficient immobilization which enable the effective binding of pimB-sequences to the nanofibers on the electrodes. In addition, theGene-pimBhybridization on biosensors immobilized withGene-pimBprobe sequences was quantified using cyclic voltammetry (CV), differential pulse voltammetry (DPV), and electrochemical impedance spectroscopy (EIS) techniques. The experimental tests revealed that the limit of detection (LoD) for CV is 0.1482 pM ml-1, for DPV it is 0.196 pM ml-1, and for EIS it is 0.302 pM ml-1. Our findings suggest thatGene-pimBmay prove to be a useful technique in the creation of novel tests for TB prognosis. The efficacy of the developed biosensor was confirmed by a hybridization sensing assay including targeted short oligonucleotide sequences (probe) andGene-pimB(target) isolated from the urine sample. To assess its potential for clinical detection, urine samples were artificially spiked with the gene to simulate conditions encountered in clinical diagnostics. This approach allows for evaluating the feasibility of detectingGene-pimBin a non-invasive manner, which could aid in the early identification of drug-resistant TB cases and improve diagnostic strategies for effective disease management.

基于无标记电化学的基因生物传感器-尿中磷脂酰肌醇甘露糖检测多药耐药结核。
结核病(TB)是一个重大的公共卫生问题,现有的诊断测试存在导致延迟开始治疗的缺陷。在本研究中,我们设计了一种基于基因- pimb的生物传感器来检测结核病,并使用电化学技术对其进行了测试。据报道,在耐多药结核病(MDR-TB)中,甘露糖覆盖的脂阿拉伯甘露聚糖(manLAM)基因- pimb表达上调。由于基因- pimb与耐药性有关,它有望成为鉴定耐多药结核病菌株的生物标志物。在这项工作中,生物传感器是用石墨氧化锌纳米纤维(GPH-ZnO-NFs)制造的,这种纳米纤维是通过静电纺丝产生的,并沉积在玻碳电极(GCE)上。采用MSA/EDC/NHS协议对GPH-ZnO功能化电极进行了进一步功能化,以提供有效的固定,使pimb序列能够有效地结合到电极上的纳米纤维上。此外,利用循环伏安法(CV)、差分脉冲伏安法(DPV)和电化学阻抗谱法(EIS)技术,对固定化基因- pimb探针序列的生物传感器基因- pimb杂交进行了定量分析。实验结果表明,CV的检出限为0.1482pM/mL, DPV的检出限为0.196 pM/mL, EIS的检出限为0.302 pM/mL。我们的研究结果表明,Gene-pimB可能被证明是一种有用的技术,可用于创建新的结核病预后检测方法。该生物传感器的有效性通过从尿样中分离的靶向短寡核苷酸序列(探针)和基因- pimb(目标)的杂交传感实验得到证实。为了评估其临床检测的潜力,尿液样本被人为地加入了该基因,以模拟临床诊断中遇到的情况。这种方法可以评估以非侵入性方式检测基因- pimb的可行性,这可能有助于早期识别耐药结核病病例,并改善有效疾病管理的诊断策略。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Nanotechnology
Nanotechnology 工程技术-材料科学:综合
CiteScore
7.10
自引率
5.70%
发文量
820
审稿时长
2.5 months
期刊介绍: The journal aims to publish papers at the forefront of nanoscale science and technology and especially those of an interdisciplinary nature. Here, nanotechnology is taken to include the ability to individually address, control, and modify structures, materials and devices with nanometre precision, and the synthesis of such structures into systems of micro- and macroscopic dimensions such as MEMS based devices. It encompasses the understanding of the fundamental physics, chemistry, biology and technology of nanometre-scale objects and how such objects can be used in the areas of computation, sensors, nanostructured materials and nano-biotechnology.
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