An Integrated Raman Spectroscopy and Mass Spectrometry Platform to Study Single-Cell Drug Uptake, Metabolism, and Effects

被引:2
|
作者
Ali, Ahmed [1 ,2 ]
Abouleila, Yasmine [1 ,2 ]
Germond, Arno [1 ]
机构
[1] RIKEN, Biodynam Res Ctr BDR, Wako, Saitama, Japan
[2] Misr Int Univ, Res Ctr, Cairo, Egypt
来源
关键词
Biochemistry; Issue; 155; single-cell analysis; Raman spectroscopy; mass spectrometry; drug discovery; tamoxifen; nanospray ionization; HETEROGENEITY;
D O I
10.3791/60449
中图分类号
O [数理科学和化学]; P [天文学、地球科学]; Q [生物科学]; N [自然科学总论];
学科分类号
07 ; 0710 ; 09 ;
摘要
Cells are known to be inherently heterogeneous in their responses to drugs. Therefore, it is essential that single-cell heterogeneity is accounted for in drug discovery studies. This can be achieved by accurately measuring the plethora of cellular interactions between a cell and drug at the single-cell level (i.e., drug uptake, metabolism, and effect). This paper describes a single-cell Raman spectroscopy and mass spectrometry (MS) platform to monitor metabolic changes of cells in response to drugs. Using this platform, metabolic changes in response to the drug can be measured by Raman spectroscopy, while the drug and its metabolite can be quantified using mass spectrometry in the same cell. The results suggest that it is possible to access information about drug uptake, metabolism, and response at a single-cell level.
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页数:7
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