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Electrochemical genosensor array for the simultaneous detection of multiple high-risk human papillomavirus sequences in clinical samples

机译:电化学基因传感器阵列可同时检测临床样品中的多个高危人乳头瘤病毒序列

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摘要

An electrochemical genosensor array for the simultaneous detection of three high-risk human papillomavirus (HPV) DNA sequences, HPV16,18 and 45, exhibiting high sensitivity and selectivity is presented. The electrodes of a 4 x 4 array were modified via co-immobilization of a 1:100 (mol/mol) mixture of a thio-lated probe and an oligoethyleneglycol-terminated bipodal thiol. Detection of synthetic and PCR products was carried out in a sandwich type format, with the target hybridized between a surface immobilized probe and a horseradish peroxidase-labelled secondary reporter probe. The detection limits obtained in the detection of each individual target were in the pM range, allowing the application of this sensor for the detection of samples obtained from PCR amplification of cervical scrape samples. The results obtained exhibited an excellent correlation with the HPV genotyping carried out within a hospital Laboratory. Multiplexing and cross-reactivity studies demonstrated high selectivity over potential interfering sequences, facilitating application of the developed platform for the high-throughput screening of multiple high-risk DNA sequences.
机译:提出了一种电化学基因传感器阵列,用于同时检测三种高风险的人乳头瘤病毒(HPV)DNA序列HPV16、18和45,它们具有很高的灵敏度和选择性。通过将巯基化探针和低聚乙二醇封端的双足硫醇的1:100(mol / mol)混合物共固定化,可以对4 x 4阵列的电极进行修饰。合成和PCR产物的检测以夹心型进行,靶标在表面固定探针和辣根过氧化物酶标记的二级报告探针之间杂交。在检测每个单个靶标时获得的检测限在pM范围内,从而使得该传感器可用于检测从宫颈刮擦样品的PCR扩增获得的样品。获得的结果与医院实验室内进行的HPV基因分型具有极好的相关性。多重和交叉反应性研究证明了对潜在干扰序列的高度选择性,从而有利于开发平台用于多种高风险DNA序列的高通量筛选的应用。

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