Center for Advanced Biomedical Imaging and Photonics, Beth Israel Deaconess Medical Center, Harvard University, Boston, MA, 02215, USA.
Department of Pathology, Beth Israel Deaconess Medical Center, Harvard University, Boston, MA, 02215, USA.
Small. 2018 Nov;14(47):e1802392. doi: 10.1002/smll.201802392. Epub 2018 Oct 7.
The enormous increase of Raman signal in the vicinity of metal nanoparticles allows surface-enhanced Raman spectroscopy (SERS) to be employed for label-free detection of substances at extremely low concentrations. However, the ultimate potential of label-free SERS to identify pharmaceutical compounds at low concentrations, especially in relation to biofluid sensing, is far from being fully realized. Opioids are a particular challenge for rapid clinical identification because their molecular structural similarities prevent their differentiation with immunolabeling approaches. In this paper, a new method called quantitative label-free SERS (QLF-SERS) which involves the formation of halide-conjugated gold nanoclusters trapping the analyte of interest near the SERS hot spots is reported, and it is demonstrated that it yields a 10 fold improvement in the detection limit over previously reported results for the entire class of clinically relevant opioids and their metabolites. Measurements of opioid concentrations in multicomponent mixtures are also demonstrated. QLF-SERS has comparable detection limits as currently existing laboratory urine drug testing techniques but is significantly faster and inexpensive and, therefore, can be easily adapted as part of a rapid clinical laboratory routine.
金属纳米粒子附近拉曼信号的巨大增加使得表面增强拉曼光谱(SERS)能够用于极低浓度物质的无标记检测。然而,无标记 SERS 在低浓度下识别药物化合物的最终潜力,特别是在与生物流体传感相关方面,远未得到充分实现。阿片类药物是快速临床鉴定的一个特殊挑战,因为它们的分子结构相似,使得它们无法通过免疫标记方法进行区分。在本文中,报告了一种称为定量无标记 SERS(QLF-SERS)的新方法,该方法涉及形成卤化物共轭金纳米簇,将感兴趣的分析物捕获在 SERS 热点附近,并且证明它比以前报道的整个临床相关阿片类药物及其代谢物的检测限提高了 10 倍。还证明了多组分混合物中阿片类浓度的测量。QLF-SERS 的检测限与当前现有的实验室尿液药物检测技术相当,但速度更快、成本更低,因此可以很容易地作为快速临床实验室常规的一部分进行改编。