Lin Yunfeng, Hamme Ashton T
Department of Chemistry and Biochemistry, Jackson State University, 1400 J R Lynch street, Jackson, MS 39217, USA.
J Mater Chem B. 2015 May 7;3(17):3573-3582. doi: 10.1039/C5TB00223K. Epub 2015 Mar 23.
Bacteria such as and present a great challenge in public health care in today's society. Protection of public safety against bacterial contamination and rapid diagnosis of infection require simple and fast assays for the detection and elimination of bacterial pathogens. After utilizing as an example bacterial strain for our investigation, we report a rapid and sensitive assay for the qualitative and quantitative detection of bacteria by using antibody affinity binding, popcorn shaped gold nanoparticle (GNPOPs) labeling, surfance enchanced Raman spectroscopy (SERS), and inductively coupled plasma mass spectrometry (ICP-MS) detection. For qualitative analysis, our assay can detect within 10 min by Raman spectroscopy; for quantitative analysis, our assay has the ability to measure as few as 100 in a 1 mL sample (100 CFU/mL) within 40 min. Based on the quantitative detection, we investigated the quantitative destruction of , and the assay's photothermal efficiency in order to reduce the amount of GNPOPs in the assay to ultimately to eliminate any potential side effects/toxicity to the surrounding cells . Results suggest that our assay may serve as a promising candidate for qualitative and quantitative detection and elimination of a variety of bacterial pathogens.
诸如[具体细菌名称1]和[具体细菌名称2]之类的细菌在当今社会的公共卫生保健中构成了巨大挑战。保护公众安全免受细菌污染以及快速诊断感染需要用于检测和消除细菌病原体的简单快速检测方法。在以[具体细菌名称3]作为我们研究的示例菌株后,我们报告了一种通过抗体亲和结合、爆米花形状的金纳米颗粒(GNPOPs)标记、表面增强拉曼光谱(SERS)和电感耦合等离子体质谱(ICP-MS)检测对细菌进行定性和定量检测的快速灵敏检测方法。对于定性分析,我们的检测方法可在10分钟内通过拉曼光谱检测到[具体细菌名称3];对于定量分析,我们的检测方法能够在40分钟内对1 mL样品中低至100个[具体细菌名称3](100 CFU/mL)进行测量。基于定量检测,我们研究了[具体细菌名称3]的定量破坏以及该检测方法的光热效率,以便减少检测中GNPOPs的量,最终消除对周围细胞的任何潜在副作用/毒性。结果表明,我们的检测方法可能是用于定性和定量检测及消除多种细菌病原体的有前景的候选方法。