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

被引:63
作者
Han, Guangmei [1 ]
Liu, Renyong [1 ]
Han, Ming-Yong [2 ]
Jiang, Changlong [1 ]
Wang, Jianping [1 ]
Du, Shuhu [3 ]
Liu, Bianhua [1 ]
Zhang, Zhongping [1 ]
机构
[1] Chinese Acad Sci, Inst Intelligent Machines, Hefei 230031, Anhui, Peoples R China
[2] ASTAR, Inst Mat Res & Engn, Singapore 117602, Singapore
[3] Nanjing Med Univ, Sch Pharm, Nanjing 210029, Jiangsu, Peoples R China
关键词
DENSITY-FUNCTIONAL THEORY; IN-VIVO; IDENTIFICATION; SPECTROSCOPY; ADSORPTION; NANOTAGS;
D O I
10.1021/ac503539w
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
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.
引用
收藏
页码:11503 / 11507
页数:5
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