SERS study of different configurations of pharmaceutical and natural product molecules ginsenoside Rg3 under the interaction with human serum albumin on simple self-assembled substrate
文献类型: 外文期刊
第一作者: Zhang, Wei
作者: Zhang, Wei;Wang, Yingping;Hou, Wei;Jin, Yinping;Bai, Xueyuan;Zhao, Yu;Zhao, Daqing;Zhao, Bing
作者机构:
关键词: Ginsenoside Rg3;Human serum albumin;Surface-enhanced Raman scattering;Interaction
期刊名称:SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY ( 影响因子:4.098; 五年影响因子:3.464 )
ISSN:
年卷期:
页码:
收录情况: SCI
摘要: Surface-enhanced Raman scattering (SERS) and fluorescence spectroscopy were employed to probe the interaction of the pharmaceutical and natural product molecules,20(R) and 20(S)-ginsenoside Rg3,with human serum albumin (HSA).Normal Raman spectra of 20(R) and 20(S)-ginsenoside Rg3 were obtained from solid powder on glass slide.Based on the splitting peaks near 1440 cm~(-1),the stacking modes of 20(R) and 20(S)-ginsenoside Rg3 were quite different.SERS spectra of both R and S configurations were obtained from a colloidal silver surface on a self-assembled SERS substrate,the most enhanced modes of 20(R) and 20(S)-ginsenoside Rg3 were those with certain motions perpendicular to the metal surface.The SERS spectra were used to predict a common orientation geometry for the alkyl chain portion of the drugs on the colloidal surface with a minor difference in the carbocyclic rings.Nevertheless,once combined with HSA,the flexible portion of alkyl chains assumes a collectively similar conformation on the Ag surface with the glucose rings perpendicularly plugging into the hydrophobic site of HSA.
分类号: O657.3
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