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An integrated microfluidic system for automatic and self-validated analysis of cervical extracellular vesicle markers PD-L1 and ERBB3.

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Analytical sciences : the international journal of the Japan Society for Analytical Chemistry 2026 Vol.42(5) p. 299-312 OA Extracellular vesicles in disease
TL;DR An integrated, self-validated microfluidic system for the rapid, on-chip isolation and multiplexed identification of the gynecological EV markers PD-L1 and ERBB3 is presented, holding prospective potential for the early screening and personalized therapy guidance of gynecological tumor detection.
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PubMed DOI PMC OpenAlex Semantic 마지막 보강 2026-04-28
OpenAlex 토픽 · Extracellular vesicles in disease Nanoplatforms for cancer theranostics Advanced Biosensing Techniques and Applications

Lu Y, Qin H, Zhang W, Shi Q, Hui J, Wu Z

📝 환자 설명용 한 줄

An integrated, self-validated microfluidic system for the rapid, on-chip isolation and multiplexed identification of the gynecological EV markers PD-L1 and ERBB3 is presented, holding prospective pote

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APA Yunxing Lu, Han Qin, et al. (2026). An integrated microfluidic system for automatic and self-validated analysis of cervical extracellular vesicle markers PD-L1 and ERBB3.. Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, 42(5), 299-312. https://doi.org/10.1007/s44211-026-00871-8
MLA Yunxing Lu, et al.. "An integrated microfluidic system for automatic and self-validated analysis of cervical extracellular vesicle markers PD-L1 and ERBB3.." Analytical sciences : the international journal of the Japan Society for Analytical Chemistry, vol. 42, no. 5, 2026, pp. 299-312.
PMID 41838284 ↗

Abstract

The early and precise diagnosis of gynecological malignancies, such as cervical cancer, is critical for improving patient treatments. Extracellular vesicles (EVs), such as exosomes, which carry molecular signals from their parental cells, offer a promising method for non-invasive liquid biopsy, however, conventional detection methods are often complex, high in reagent consumption, and susceptible to environmental fluctuations. To address this, we present an integrated, self-validated microfluidic system for the rapid, on-chip isolation and multiplexed identification of the gynecological EV markers PD-L1 and ERBB3. The chip achieved simultaneous on-chip processing of test and positive samples for parallel analysis within 1 h, enabling synchronous detection under the same conditions and thereby significantly enhancing the reliability of the assay. Additionally, a deep learning YOLOv8-based self-validated detection strategy facilitates automated and precise fluorescence identification. Validation with four cell lines (SiHa, C33A, HeLa, and H8) revealed remarkable EV protein signatures, achieving a limit of detection (LOD) of 15.56 particles/μL. This platform provides an integrated tool for sensitive and precise EV marker analysis, holding prospective potential for the early screening and personalized therapy guidance of gynecological tumor detection.

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🏷️ 같은 키워드 · 무료전문 — 이 논문 MeSH/keyword 기반

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