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利用表面增强拉曼光谱(SERS)研究美法仑作为烷化剂与核苷酸的相互作用。

Investigation of Melphalan interaction as an alkylating agent with nucleotides by using surface enhanced Raman spectroscopy (SERS).

机构信息

Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.

Department of Medical Nanotechnology, School of Advanced Technologies in Medicine, Tehran University of Medical Sciences, Tehran, Iran.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2024 Sep 5;317:124359. doi: 10.1016/j.saa.2024.124359. Epub 2024 Apr 26.

Abstract

SERS (Surface Enhanced Raman Spectroscopy) is a new Raman spectroscopy which relies on Surface Plasmon Resonance (SPR) of metal nanoparticles. We have applied colloidal silver and gold nanoparticles as amplifier agents to enhance nucleotide Raman signals. It is observed that without these enhancing agents, it is impossible to investigate nucleotide spectrum due to weak Raman signals. Interaction mechanism of Melphalan, an anticancer drug with four nucleotides (Adenine, Cytosine, Guanine, Thymine) was investigated using SERS to detect and identify changes due to alkylating process in Raman spectra. After incubating Melphalan drug with nucleotides for 24 h at 37 °C, some changes occurred in SERS spectrum and interpretation of SERS spectra revealed the influence of the alkyl substitution on peaks and Raman shifts. After incubation of Melphalan with each nucleotide, intensity of relevant SERS signals assigned to Amid III group of Cytosine and Amid I of Thymine decreased significantly, confirming alkylating taking place. In this study, we also investigated the effect of nanoparticles type on nucleotide spectrum. We could not obtain useful information in the cases of guanine nucleotide. The SERS spectrum of Cytosine as an example of nucleotides in aqueous solution compared to solid state and results demonstrated that in solid state better signals were obtained than in liquid state.

摘要

SERS(表面增强拉曼光谱)是一种新的拉曼光谱技术,依赖于金属纳米粒子的表面等离子体共振(SPR)。我们已经应用胶体银和金纳米粒子作为放大剂来增强核苷酸拉曼信号。可以观察到,如果没有这些增强剂,由于拉曼信号较弱,就不可能研究核苷酸光谱。我们使用 SERS 研究了一种抗癌药物美法仑(包含腺嘌呤、胞嘧啶、鸟嘌呤和胸腺嘧啶四种核苷酸)与四种核苷酸的相互作用机制,以检测和识别由于烷化过程在拉曼光谱中引起的变化。在 37°C 下孵育美法仑药物与核苷酸 24 小时后,SERS 光谱中发生了一些变化,对 SERS 光谱的解释表明了烷基取代对峰和拉曼位移的影响。在与每个核苷酸孵育后,与胞嘧啶的酰胺 III 基团和胸腺嘧啶的酰胺 I 相关的 SERS 信号强度显著降低,证实了烷化反应的发生。在这项研究中,我们还研究了纳米粒子类型对核苷酸光谱的影响。在鸟嘌呤核苷酸的情况下,我们无法获得有用的信息。以胞嘧啶核苷酸为例,比较了水溶液和固态的 SERS 光谱,结果表明在固态下比在液态下获得了更好的信号。

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