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Label-Free Surface-Enhanced Raman Scattering Imaging to Monitor the Metabolism of Antitumor Drug 6-Mercaptopurine in Living Cells

机译:无标签的表面增强拉曼散射成像,以监测活细胞中抗肿瘤药物6-巯基嘌呤的代谢

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The molecular processes of drugs from cellular uptake to intracellular distribution as well as the intracellular interaction with the target molecule are critically important for the development of new antitumor drugs. In this work, we have successfully developed a label-free surface-enhanced Raman scattering (SERS) technique to monitor and visualize the metabolism of antitumor drug 6-mercaptopurine in living cells. It has been clearly demonstrated that Au@Ag NPs exhibit an excellent Raman enhancement effect to both 6-mercaptopurine and its metabolic product 6-mercaptopurine-ribose. Their different ways to absorb at the surface of Au@Ag NPs lead to the obvious spectral difference for distinguishing the antitumor drug and its metabolite by SERS spectra. The Au@Ag NPs can easily pass through cell membranes in a large amount and sensitively respond to the biological conversion of 6-mercaptopurine in tumor cells. The Raman imaging can visualize the real-time distribution of 6-mercaptopurine and its biotransformation with the concentrations in tumor cells. The SERS-based method reported here is simple and efficient for the assessments of drug efficacy and the understanding of the molecular therapeutic mechanism of antitumor drugs at the cellular level.
机译:从细胞吸收到细胞内分布以及与靶分子的细胞内相互作用的药物分子过程对于开发新的抗肿瘤药物至关重要。在这项工作中,我们已经成功开发了无标记的表面增强拉曼散射(SERS)技术,以监测和可视化抗肿瘤药物6-巯基嘌呤在活细胞中的代谢。清楚地表明,Au @ Ag NPs对6-巯基嘌呤及其代谢产物6-巯基嘌呤-核糖均表现出优异的拉曼增强作用。它们在Au @ Ag NPs表面的吸收方式不同,导致通过SERS光谱区分抗肿瘤药及其代谢物存在明显的光谱差异。 Au @ Ag NPs可以很容易地大量通过细胞膜,并对肿瘤细胞中6-巯基嘌呤的生物转化敏感。拉曼成像可以可视化6-巯基嘌呤的实时分布及其随肿瘤细胞浓度的生物转化。此处报道的基于SERS的方法简单有效,可用于评估药物功效以及在细胞水平上了解抗肿瘤药物的分子治疗机制。

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