Quantitative Evaluation of Cisplatin Uptake in Sensitive and Resistant Individual Cells by Single-Cell ICP-MS (SC-ICP-MS)

化学 细胞内 顺铂 电感耦合等离子体质谱法 流式细胞术 单细胞分析 细胞培养 癌细胞 感应耦合等离子体 细胞 色谱法 质谱法 癌症 生物化学 分子生物学 等离子体 化疗 内科学 外科 物理 生物 医学 量子力学 遗传学
作者
Mario Corte‐Rodríguez,Roberto Álvarez-Fernández García,Elisa Blanco,Jörg Bettmer,María Montes‐Bayón
出处
期刊:Analytical Chemistry [American Chemical Society]
卷期号:89 (21): 11491-11497 被引量:123
标识
DOI:10.1021/acs.analchem.7b02746
摘要

One of the main limitations to the Pt-therapy in cancer is the development of associated drug resistance that can be associated with a significant reduction of the intracellular platinum concentration. Thus, intracellular Pt concentration could be considered as a biomarker of cisplatin resistance. In this work, an alternative method to address intracellular Pt concentration in individual cells is explored to permit the evaluation of different cell models and alternative therapies in a relatively fast way. For this aim, total Pt analysis in single cells has been implemented using a total consumption nebulizer coupled to inductively coupled plasma mass spectrometric detection (ICP-MS). The efficiency of the proposed device has been evaluated in combination with flow cytometry and turned out to be around 25% (cells entering the ICP-MS from the cells in suspension). Quantitative uptake studies of a nontoxic Tb-containing compound by individual cells were conducted and the results compared to those obtained by bulk analysis of the same cells. Both sets of data were statistically comparable. Thus, final application of the developed methodology to the comparative uptake of Pt-species in cisplatin resistant and sensitive cell lines (A2780cis and A2780) was conducted. The results obtained revealed the potential of this analytical strategy to differentiate between different cell lines of different sensitivity to the drug which might be of high medical interest.

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