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空气传播细菌检测:使用游离抗体的比色检测进行物种特异性浓度测量。

Airborne bacteria detection: Species-specific concentration measurement using colorimetric detection of free antibodies.

作者信息

Park Sungjae, Shin Dongmin, Lee Sojeong, Park Jungwoo, Haam Seungjoo, Hwang Jungho

机构信息

Department of Mechanical Engineering, Yonsei University, Republic of Korea.

Department of Chemical & Biomolecular Engineering, Yonsei University, Republic of Korea.

出版信息

J Hazard Mater. 2025 Aug 15;494:138761. doi: 10.1016/j.jhazmat.2025.138761. Epub 2025 May 27.

DOI:10.1016/j.jhazmat.2025.138761
PMID:40450995
Abstract

This study presents a novel colorimetric detection method for species-specific quantification of airborne bacteria. Using a filtration-based approach combined with antibody-conjugated horseradish peroxidase (HRP), this method enhanced the detection of target bacteria (Escherichia coli and Staphylococcus aureus) collected via an aerosol-to-hydrosol sampler. Bacteria-antibody-HRP complexes were captured on a membrane by filtration, and the free antibody-conjugated HRP in the filtrate was subsequently quantified. Experimental results demonstrated that the absorbance increased as the airborne bacterial concentration decreased. Absorbance values were obtained for bacterial samples at varying concentrations, ranging from 10 to 10 colony-forming unit (CFU) per 1 mL of liquid. A correlation between the absorbance and CFU·mL was established for each bacterial species, resulting in a limit of detection (LOD) of 21.5 CFU·mL for E. coli and 246 CFU·mL for S. aureus. The absorbance values were measured for the bacteria collected using a commercial air-to-liquid sampler with an experimental setup that generated airborne bacteria in a controlled laboratory environment. The liquid bacterial concentrations (CFU·mL) were converted to airborne bacterial concentrations in CFU·m air by dividing by enrichment ratio of the air sampler, yielding an LOD of 545 CFU·m air for E. coli and an LOD of 953 CFU·m air for S. aureus.

摘要

本研究提出了一种用于对空气中细菌进行物种特异性定量的新型比色检测方法。该方法采用基于过滤的方法并结合抗体偶联辣根过氧化物酶(HRP),增强了通过气溶胶 - 水溶胶采样器收集的目标细菌(大肠杆菌和金黄色葡萄球菌)的检测。细菌 - 抗体 - HRP复合物通过过滤捕获在膜上,随后对滤液中游离的抗体偶联HRP进行定量。实验结果表明,随着空气中细菌浓度的降低,吸光度增加。获得了不同浓度细菌样品的吸光度值,范围为每1 mL液体中10至10个菌落形成单位(CFU)。为每种细菌建立了吸光度与CFU·mL之间的相关性,大肠杆菌的检测限(LOD)为21.5 CFU·mL,金黄色葡萄球菌的检测限为246 CFU·mL。使用商业气液采样器收集细菌,并在可控实验室环境中生成空气中细菌的实验装置测量吸光度值。通过将液体细菌浓度(CFU·mL)除以空气采样器的富集率,将其转换为空气中细菌浓度(CFU·m³空气),大肠杆菌的检测限为545 CFU·m³空气,金黄色葡萄球菌的检测限为953 CFU·m³空气。

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