マイクロ流体チップ統合による迅速な現場病原体検出(Rapid On-Site Pathogen Detection Enabled by Integrated Microfluidic Chip)

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2026-04-08 合肥物質科学研究院(HFIPS)

中国科学院合肥物質科学研究院と安徽省第二人民医院の共同研究チームは、分子診断と免疫診断を統合したマイクロ流体チップによる迅速な病原体検出技術を開発した。等温増幅(LAMP)と比色・蛍光の二重モード免疫クロマト法を組み合わせることで感度と信頼性を向上し、検査は約30分で完了する。密閉構造により汚染リスクを低減し、操作は試料投入後1ステップのみで現場利用に適する。黄色ブドウ球菌やレジオネラ菌などに対し82~140 CFU/mLの高感度検出を達成し、コストも低廉(2ドル未満)。院内感染対策や迅速診断に有効な技術として期待される。

マイクロ流体チップ統合による迅速な現場病原体検出(Rapid On-Site Pathogen Detection Enabled by Integrated Microfluidic Chip)
Integrated “Isothermal Amplification–Immunochromatography” Detection Platform (Image by DAI Liping)

<関連情報>

医療現場における医療関連感染病原体の高感度検出のための、デュアルシグナルナノプローブを備えたプッシュボタン式マイクロ流体プラットフォーム Push-Button Microfluidic Platform with Dual-Signal Nanoprobes for Enhanced Sensitivity Detection of Healthcare-Associated Infection Pathogens at Point-of-Care

Liping Dai,Yun Wang,Xiaosong Wu,Qian Wang,Zhigang Li,Yong Liu,Long Zhang,Shuai Zheng,and Shu Wang
Analytical Chemistry  Published: February 9, 2026
DOI:https://doi.org/10.1021/acs.analchem.5c05437

Abstract

Healthcare-associated infection (HAI) pathogens cause severe nosocomial outbreaks, jeopardizing patient safety and straining healthcare systems. Conventional loop-mediated isothermal amplification–lateral flow immunoassay (LAMP-ICA) allows rapid pathogen detection but is constrained by low sensitivity, a high false-positive rate, and an extended detection time. To address these limitations, we present a dual-mode (colorimetric/fluorescent) microfluidic biosensing platform based on silicon–gold/quantum dot core–shell nanoprobes (Si@Au/DQD NPs). The platform incorporates two key innovations: (1) The colorimetric/fluorescent dual-signal Si@Au/DQD nanoprobe enhances detection reliability and sensitivity through dual-signal complementary verification and multilayered QD design, halving the LAMP amplification time compared to traditional colloidal gold systems, and (2) a modular microfluidic chip integrates LAMP amplification and ICA detection within a closed system, effectively preventing leakage and contamination of amplification products. Performance evaluation showed that the fluorescence detection limit of this system for Staphylococcus aureus (S. aureus), Legionella pneumophila (L. pneumophila), and Klebsiella pneumoniae (K. pneumoniae) reaches 82–140 CFU/mL, with the entire process completed within 30 min. In addition, the detection of 25 clinical environmental samples verifies the practicality of the designed integrated detection platform. With high sensitivity, strong specificity, and dual-mode capability for qualitative colorimetric screening and quantitative fluorescence analysis, this technology offers an efficient solution for point-of-care testing (POCT) of HAI pathogens, particularly in resource-limited settings and in on-site emergency diagnostics.

医療・健康
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