...
首页> 外文期刊>Biosensors & Bioelectronics: The International Journal for the Professional Involved with Research, Technology and Applications of Biosensers and Related Devices >Fast and continuous microorganism detection using aptamer-conjugated fluorescent nanoparticles on an optofluidic platform
【24h】

Fast and continuous microorganism detection using aptamer-conjugated fluorescent nanoparticles on an optofluidic platform

机译:使用适体偶联的荧光纳米颗粒在光流体平台上快速连续地检测微生物

获取原文
获取原文并翻译 | 示例

摘要

Fast and accurate pathogen detection in aquatic environments is challenging in many biomedical studies and microbial diagnostic applications. In this study, we developed a real-time, continuous, and non-destructive single cell detection method using target specific aptamer-conjugated fluorescent nanopartides (A-FNPs) and an optofluidic particle-sensor platform. A-FNPs selectively bound to the surfaces of target bacteria (Escherichia coli) and labeled them with high affinity and selectivity so that target bacteria can be countable particles in an optofluidic particle-sensor. A-FNP-labeled target bacterial complexes were detected by the optofluidic particle-sensing system, which provides rapid and continuous single-cell detection. A-FNPs selectively bound to E. coil with a dissociation constant of 0.83 nM, but did not bind Enterobacter aerogenes or Citrobacter freundii strains, which lacked affinity for the aptamer used. We demonstrated that our optofluidic device achieves a detection throughput of similar to 100 particles per second with high accuracy (similar to 85%) in detecting single bacterial cells conjugated with A-FNPs. This approach can be immediately extended to the real-time, high-throughput detection of other microorganisms such as viruses that are selectively conjugated with A-FNPs. Collectively, these data suggest that optofluidic systems are widely applicable for the fast and continuous detection of microbial cells. (C) 2014 Elsevier B.V. All rights reserved.
机译:在许多生物医学研究和微生物诊断应用中,在水生环境中快速准确地检测病原菌是一项挑战。在这项研究中,我们开发了一种实时,连续,无损的单细胞检测方法,使用靶标特异性适体缀合的荧光纳米粒子(A-FNP)和光电流体粒子传感器平台。 A-FNP选择性结合至目标细菌(大肠杆菌)的表面,并以高亲和力和选择性对其进行标记,因此目标细菌可以成为光流体颗粒传感器中的可数颗粒。 A-FNP标记的目标细菌复合物通过光流体颗粒传感系统进行检测,该系统可进行快速,连续的单细胞检测。 A-FNPs以0.83 nM的解离常数选择性结合大肠杆菌,但不结合产气肠杆菌或弗氏柠檬酸杆菌菌株,这些菌株对所用的适体缺乏亲和力。我们证明了我们的光流控设备在检测与A-FNPs偶联的单个细菌细胞中的检测吞吐量达到了每秒约100个颗粒,并且具有很高的准确度(约85%)。这种方法可以立即扩展到实时,高通量检测其他微生物(例如与A-FNP选择性结合的病毒)。总体而言,这些数据表明光流体系统广泛适用于微生物细胞的快速和连续检测。 (C)2014 Elsevier B.V.保留所有权利。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号