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Rapid and field-deployable biological and chemical Raman-based identification

机译:快速和可现场部署的基于拉曼的生化识别

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Pathogen detection using Raman spectroscopy is achieved through the use of a sandwich immunoassay. Antibody-modified magnetic beads are used to capture and concentrate target analytes in solution and surface-enhanced Raman spectroscopy (SERS) tags are conjugated with antibodies and act as labels to enable specific detection of biological pathogens. The rapid detection of biological pathogens is critical to first responders, thus assays to detect E.Coli and Anthrax have been developed and will be reported. The problems associated with pathogen detection resulting from the spectral complexity and variability of microorganisms are overcome through the use of SERS tags, which provide an intense, easily recognizable, and spectrally consistent Raman signal. The developed E. coli assay has been tested with 5 strains of E. coli and shows a low limit of detection, on the order of 10 and 100 c.f.u. per assay. Additionally, the SERS assay utilizes magnetic beads to collect the labeled pathogens into the focal point of the detection laser beam, making the assay robust to commonly encountered white powder interferants such as flour, baking powder, and corn starch. The reagents were also found to be stable at room temperature over extended periods of time with testing conducted over a one year period. Finally, through a specialized software algorithm, the assays are interfaced to the Raman instrument, StreetLab Mobile, for rapid-field-deployable biological identification.
机译:使用拉曼光谱法的病原体检测是通过使用三明治免疫测定法实现的。抗体修饰的磁珠用于捕获溶液中的目标分析物并将其浓缩,表面增强拉曼光谱(SERS)标签与抗体结合在一起,并用作标记,以实现对生物病原体的特异性检测。快速检测生物病原体对于急救人员至关重要,因此已经开发出检测大肠杆菌和炭疽的方法,并将进行报道。通过使用SERS标签可以克服由微生物的光谱复杂性和可变性引起的病原体检测相关问题,该标签可提供强烈,易于识别且光谱一致的拉曼信号。已开发的大肠杆菌测定法已用5株大肠杆菌进行了测试,并显示出较低的检出限,约为10和100 c.f.u.。每个测定。此外,SERS分析利用磁珠将标记的病原体收集到检测激光束的焦点中,从而使该分析对常见的白色粉末干扰物(如面粉,发酵粉和玉米淀粉)具有较强的抵抗力。还发现,该试剂在室温下可长时间稳定,并且在一年的时间内进行了测试。最后,通过专门的软件算法,将测定法连接到拉曼仪器StreetLab Mobile,以进行快速现场可生物识别。

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