期刊
ANALYTICA CHIMICA ACTA
卷 1252, 期 -, 页码 -出版社
ELSEVIER
DOI: 10.1016/j.aca.2023.341050
关键词
Multiplex microfluidic chip; Single-cell droplet PCR; Machine learning; High-risk HPV detection
High-risk human papillomavirus (HPV) testing can greatly reduce the incidence and mortality of cervical cancer. Microfluidic technology combined with multiplex single-cell droplet polymerase chain reaction (PCR) provides an efficient and accurate method for detecting high-risk HPV. A novel multiplex droplet PCR method was developed in this study to directly detect high-risk HPV sequences in single cells. A multiplex microfluidic chip with four flow-focusing structures was designed for one-step and parallel droplet preparation. Machine learning was applied to automatically identify the single-cell droplets with a high accuracy of 97%. This approach enables rapid and reliable detection of multiple target sequences in single cells, which is valuable for studying cellular heterogeneity in cancer diagnosis and treatment.
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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