Kaushal Ankur, Singh Swati, Kumar Ashok, Kumar Dinesh
Shoolini University of Biotechnology and Management Sciences, Solan, 173212 India.
CSIR-Institute of Genomics and Integrative Biology, Mall Road, Delhi, 110007 India.
Indian J Microbiol. 2017 Mar;57(1):121-124. doi: 10.1007/s12088-016-0636-y. Epub 2017 Jan 3.
A specific 5' NH labeled DNA probe of gene was immobilized onto the gold nanoparticles/carboxylated multi walled carbon nanotubes (Nano-Au/cMWCNT) screen printed electrode using EDC/NHS cross linking chemistry. This was followed by hybridization with 0.5-50 ng/6 µl of single stranded genomic DNA infected patient throat swab samples. Electrochemical amperometric assay was deciphered by using cyclic voltammetry (CV) with methylene blue a redox indicator. The sensor had a sensitivity of 104.7 µA cm ng using CV with a R of 0.907 and 0.01 ng/6 µl as the limit of detection (LOD). The modified electrode surface morphology was characterized using scanning electron microscopy. The stability of the electrode was seen at 4 °C for 180 days having 6% loss in the initial current. The sensor is gene specific and can detect the pathogen within 30 min.
使用EDC/NHS交联化学方法,将基因的特定5' NH标记DNA探针固定在金纳米颗粒/羧基化多壁碳纳米管(Nano-Au/cMWCNT)丝网印刷电极上。随后,将其与0.5 - 50 ng/6 µl的感染患者咽喉拭子样本单链基因组DNA进行杂交。使用亚甲基蓝作为氧化还原指示剂,通过循环伏安法(CV)进行电化学安培分析。该传感器使用CV时的灵敏度为104.7 µA cm ng,相关系数R为0.907,检测限(LOD)为0.01 ng/6 µl。使用扫描电子显微镜对修饰电极的表面形态进行了表征。电极在4°C下可稳定保存180天,初始电流损失6%。该传感器具有基因特异性,可在30分钟内检测到病原体。