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Surface-Enhanced, Spatially Offset Raman Spectroscopy (SESORS) in Tissue Analogues

机译:组织类似物中表面增强的空间偏移拉曼光谱(SESORS)

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Surface-enhanced, spatially offset Raman spectroscopy (SESORS) combines the remarkable enhancements in sensitivity afforded by surface-enhanced Raman spectroscopy (SERS) with the non-invasive, subsurface sampling capabilities of spatially offset Raman spectroscopy. Taken together, these techniques show great promise for in vivo Raman measurements. Herein, we present a step forward for this technique, demonstrating SESORS through tissue analogues of six known and varied thicknesses, with a large number of distinct spatial offsets, in a backscattering optical geometry. This is accomplished by spin-coating SERS-active nanoparticles (NPs) on glass slides and monitoring the relative spectral contribution from the NPs and tissue sections, respectively, as a function of both the tissue thickness and the spatial offset of the collection probe. The results show that SESORS outperforms SERS alone for this purpose, the NP signal can be attained at tissue thicknesses of >6.75 mm, and greater tissue thicknesses require greater spatial offsets to maximize the NP signal, all with an optical geometry optimized for utility. This demonstration represents a step forward toward the implementation of SESORS for non-invasive, in vivo analysis.
机译:表面增强的空间偏移拉曼光谱(SESORS)结合了表面增强拉曼光谱(SERS)的敏感性的显着增强,其具有空间偏移拉曼光谱的非侵入性,地下采样能力。在一起,这些技术在体内拉曼测量中表现出了很大的承诺。这里,我们向前展示了该技术的一步,通过六个已知的和变化厚度的组织类似物,在反向散射光学几何形状中,通过六个已知的和变化厚度的组织类似物的组织类似物。这是通过在玻璃载玻片上旋转涂覆的SERS-活性纳米颗粒(NPS)并分别从NPS和组织切片监测来自NPS和组织切片的相对光谱贡献来实现的。结果表明,SESORS为此目的优于单独的SERS,可以在组织厚度> 6.75mm的组织厚度下实现,并且更大的组织厚度需要更大的空间偏移以使NP信号最大化,并且具有针对实用的光学几何。该示范代表了对非侵入性的实施的前进,体内分析。

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