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Intermittent lysis on a single paper-based device to extract exosomal nucleic acid biomarkers from biological samples for downstream analysis.
Vu, Van-Truc; Vu, Cao-An; Huang, Chun-Jen; Cheng, Chao-Min; Pan, Shin-Chen; Chen, Wen-Yih.
Afiliación
  • Vu VT; Department of Chemical and Materials Engineering, National Central University, Taoyuan, 320317, Taiwan.
  • Vu CA; Department of Chemical and Materials Engineering, National Central University, Taoyuan, 320317, Taiwan.
  • Huang CJ; Department of Chemical and Materials Engineering, National Central University, Taoyuan, 320317, Taiwan.
  • Cheng CM; R&D Center for Membrane Technology, Chung Yuan Christian University, Taoyuan, 32023, Taiwan.
  • Pan SC; Institute of Biomedical Engineering, National Tsing Hua University, Hsinchu, 300044, Taiwan.
  • Chen WY; Department of Surgery, Section of Plastic and Reconstructive Surgery, National Cheng Kung University Hospital, National Cheng Kung University, Tainan, 704, Taiwan. pansc@mail.ncku.edu.tw.
Mikrochim Acta ; 191(8): 501, 2024 08 02.
Article en En | MEDLINE | ID: mdl-39093424
ABSTRACT
As the role of exosomes in physiological and pathological processes has been properly perceived, harvesting them and their internal components is critical for subsequent applications. This study is a debut of intermittent lysis, which has been integrated into a simple and easy-to-operate procedure on a single paper-based device to extract exosomal nucleic acid biomarkers for downstream analysis. Exosomes from biological samples were captured by anti-CD63-modified papers before being intermittently lysed by high-temperature, short-time treatment with double-distilled water to release their internal components. Exosomal nucleic acids were finally adsorbed by sol-gel silica for downstream analysis. Empirical trials not only revealed that sporadically dropping 95 °C ddH2O onto the anti-CD63-modified papers every 5 min for 6 times optimized the exosomal nucleic acids extracted by the anti-CD63 paper but also verified that the whole deployed procedure is applicable for point-of-care testing (POCT) in low-resource areas and for both in vitro (culture media) and in vivo (plasma and chronic lesion) samples. Importantly, downstream analysis of exosomal miR-21 extracted by the paper-based procedure integrated with this novel technique discovered that the content of exosomal miR-21 in chronic lesions related to their stages and the levels of exosomal carcinoembryonic antigen originated from colorectal cancer cells correlated to their exosomal miR-21.
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Texto completo: 1 Base de datos: MEDLINE Asunto principal: Papel / MicroARNs / Exosomas / Tetraspanina 30 Idioma: En Revista: Mikrochim Acta Año: 2024 Tipo del documento: Article

Texto completo: 1 Base de datos: MEDLINE Asunto principal: Papel / MicroARNs / Exosomas / Tetraspanina 30 Idioma: En Revista: Mikrochim Acta Año: 2024 Tipo del documento: Article