化学
微流控
赫拉
多路复用
多重聚合酶链反应
微流控芯片
聚合酶链反应
单细胞分析
细胞
人乳头瘤病毒
荧光
计算生物学
纳米技术
基因
生物化学
生物信息学
光学
物理
内科学
材料科学
生物
医学
作者
Yizheng Huang,Linjun Sun,Wenwen Liu,Ling Yang,Zhigang Song,Xin Ning,Weijun Li,Manqing Tan,Yude Yu,Li Zhao
标识
DOI:10.1016/j.aca.2023.341050
摘要
High-risk human papillomavirus (HPV) testing can significantly decline the incidence and mortality of cervical cancer. Microfluidic technology provides an effective method for accurate detection of high-risk HPV by utilizing multiplex single-cell droplet polymerase chain reaction (PCR). However, current strategies are limited by low-integration microfluidic chip, complex reagent system, expensive detection equipment and time-consuming droplet identification. Here, we developed a novel multiplex droplet PCR method that directly detected high-risk HPV sequences in single cells. A multiplex microfluidic chip integrating four flow-focusing structures was designed for one-step and parallel droplet preparation. Using single-cell droplet PCR, multi-target sequences were detected simultaneously based on a monochromatic fluorescence signal. We applied machine learning to automatically identify the large populations of single-cell droplets with 97% accuracy. HPV16, 18 and 45 sequences were sensitively detected without cross-contamination in mixed CaSki and Hela cells. The approach enables rapid and reliable detection of multi-target sequences in single cells, making it powerful for investigating cellular heterogeneity related to cancer diagnosis and treatment.
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