Machon Christelle, Catez Frédéric, Venezia Nicole Dalla, Vanhalle Floriane, Guyot Laetitia, Vincent Anne, Garcia Maxime, Roy Béatrice, Diaz Jean-Jacques, Guitton Jérôme
Laboratoire de Chimie Analytique, Faculté de Pharmacie de Lyon, Université Lyon 1, 8 Avenue Rockefeller, Lyon, 69373, France.
Laboratoire de Biochimie et de Pharmaco-toxicologie, Centre Hospitalier Lyon -Sud-HCL, Pierre Bénite, 69495, France.
J Pharm Anal. 2021 Feb;11(1):77-87. doi: 10.1016/j.jpha.2020.04.001. Epub 2020 Apr 7.
5-Fluorouracil (5-FU) is an anticancer drug extensively used for different cancers. Intracellular metabolic activation leads to several nucleoside and nucleotide metabolites essential to exert its cytotoxic activity on multiple cellular targets such as enzymes, DNA and RNA. In this paper, we describe the development of a method based on liquid chromatography coupled with high resolution mass spectrometry suitable for the simultaneous determination of the ten anabolic metabolites (nucleoside, nucleotide and sugar nucleotide) of 5-FU. The chromatographic separation was optimized on a porous graphitic carbon column allowing the analysis of the metabolites of 5-FU as well as endogenous nucleotides. The detection was performed on an Orbitrap® tandem mass spectrometer. Linearity of the method was verified in intracellular content and in RNA extracts. The limit of detection was equal to 12 pg injected on column for nucleoside metabolites of 5-FU and 150 pg injected on column for mono- and tri-phosphate nucleotide metabolites. Matrix effect was evaluated in cellular contents, DNA and RNA extracts for nucleoside and nucleotides metabolites. The method was successfully applied to i) measure the proportion of each anabolic metabolite of 5-FU in cellular contents, ii) follow the consequence of inhibition of enzymes on the endogenous nucleotide pools, iii) study the incorporation of metabolites of 5-FU into RNA and DNA, and iv) to determine the incorporation rate of 5-FUrd into 18 S and 28 S sub-units of rRNA.
5-氟尿嘧啶(5-FU)是一种广泛用于治疗多种癌症的抗癌药物。细胞内的代谢激活会产生几种核苷和核苷酸代谢物,这些代谢物对于在多个细胞靶点(如酶、DNA和RNA)上发挥其细胞毒性活性至关重要。在本文中,我们描述了一种基于液相色谱与高分辨率质谱联用的方法的开发,该方法适用于同时测定5-FU的十种合成代谢物(核苷、核苷酸和糖核苷酸)。在多孔石墨化碳柱上对色谱分离进行了优化,从而能够分析5-FU的代谢物以及内源性核苷酸。检测在Orbitrap®串联质谱仪上进行。该方法的线性在细胞内含量和RNA提取物中得到了验证。5-FU核苷代谢物的柱上检测限为12 pg,单磷酸和三磷酸核苷酸代谢物的柱上检测限为150 pg。对细胞内容物、DNA和RNA提取物中的核苷和核苷酸代谢物评估了基质效应。该方法成功应用于:i)测量细胞内容物中5-FU各合成代谢物的比例;ii)跟踪酶抑制对内源性核苷酸池的影响;iii)研究5-FU代谢物掺入RNA和DNA的情况;iv)确定5-氟尿苷掺入rRNA的18 S和28 S亚基的掺入率。