核酸
核酸检测
微流控
实时聚合酶链反应
检出限
化学
灵敏度(控制系统)
计算机科学
纳米技术
生物化学
材料科学
色谱法
电子工程
工程类
基因
作者
Shaolei Huang,Yiquan An,Bangchao Xi,Xianglian Gong,Zhongfu Chen,Shan Shao,Shengxiang Ge,Jun Zhang,Dongxu Zhang,Ningshao Xia
出处
期刊:Lab on a Chip
[Royal Society of Chemistry]
日期:2023-01-01
卷期号:23 (11): 2611-2622
被引量:11
摘要
Nucleic acid detection directly identifies the presence of pathogenic microorganisms and has various advantages, such as high sensitivity, commendable specificity and a short window period, and has been widely used in many fields, such as early tumor screening, prenatal diagnosis and infectious disease detection. Real-time PCR (polymerase chain reaction) is the most commonly used method for nucleic acid detection in clinical practice, but it always takes about 1-3 hours, severely limiting its application in particular scenarios such as emergency testing, large-scale testing and on-site testing. To solve the time-consuming problem, a real-time PCR system based on multiple temperature zones was proposed, which realized the speed of temperature change of biological reagents from 2-4 °C s-1 to 13.33 °C s-1. The system integrates the advantages of fixed microchamber-type and microchannel-type amplification systems, including a microfluidic chip capable of fast heat transfer and a real-time PCR device with a temperature control strategy based on the temperature difference. The detection of HCMV biological samples using the real-time PCR system in this research took only 15 min, which was 75% shorter compared to the commercial qPCR instrument such as BIO-RAD, and the detection sensitivity remained essentially the same. The system could complete nucleic acid detection within 9 min under extreme conditions, characterized by fast detection speed and high sensitivity, providing a promising solution for ultra-fast nucleic acid detection.
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