Floriano Pierre N, Christodoulides Nick, Romanovicz Dwight, Bernard Bruce, Simmons Glennon W, Cavell Myles, McDevitt John T
Department of Chemistry and Biochemistry, The University of Texas at Austin, Austin, TX 78712, USA.
Biosens Bioelectron. 2005 Apr 15;20(10):2079-88. doi: 10.1016/j.bios.2004.08.046.
We report here the adaptation of our electronic microchip technology towards the development of a new method for detecting and enumerating bacterial cells and spores. This new approach is based on the immuno-localization of bacterial spores captured on a membrane filter microchip placed within a flow cell. A combination of microfluidic, optical, and software components enables the integration of staining of the bacterial species with fully automated assays. The quantitation of the analyte signal is achieved through the measurement of a collective response or alternatively through the identification and counting of individual spores and particles. This new instrument displays outstanding analytical characteristics, and presents a limit of detection of approximately 500 spores when tested with Bacillus globigii (Bg), a commonly used simulant for Bacillus anthracis (Ba), with a total analysis time of only 5 min. Additionally, the system performed well when tested with real postal dust samples spiked with Bg in the presence of other common contaminants. This new approach is highly customizable towards a large number of relevant toxic chemicals, environmental factors, and analytes of relevance to clinical chemistry applications.
我们在此报告将我们的电子微芯片技术应用于开发一种检测和计数细菌细胞及孢子的新方法。这种新方法基于对捕获在置于流通池内的膜过滤微芯片上的细菌孢子进行免疫定位。微流体、光学和软件组件的组合使得细菌物种的染色与全自动检测得以整合。分析物信号的定量通过测量集体响应或通过识别和计数单个孢子及颗粒来实现。这台新仪器具有出色的分析特性,在用球形芽孢杆菌(Bg,炭疽芽孢杆菌(Ba)的常用模拟物)进行测试时,检测限约为500个孢子,总分析时间仅为5分钟。此外,当在存在其他常见污染物的情况下用添加了Bg的真实邮政灰尘样本进行测试时,该系统表现良好。这种新方法对于大量相关有毒化学品、环境因素以及与临床化学应用相关的分析物具有高度可定制性。