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Study of intracellular anabolism of 5-fluorouracil and incorporation in nucleic acids based on an LC-HRMS method

机译:基于LC-HRMS方法的5-氟尿嘧啶细胞内合成的研究及核酸掺入

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摘要

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 separationwas 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.

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  • 来源
    《药物分析学报(英文)》 |2021年第001期|77-87|共11页
  • 作者单位

    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 Benite 69495 France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

    Laboratoire de Biochimie et de Pharmaco-toxicologie Centre Hospitalier Lyon -Sud-HCL Pierre Benite 69495 France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

    Laboratoire de toxicologie Faculté de pharmacie de Lyon 8 avenue Rockefeller F-69373 Lyon France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

    Laboratoire de Biochimie et de Pharmaco-toxicologie Centre Hospitalier Lyon -Sud-HCL Pierre Benite 69495 France;

    Laboratoire de Biochimie et de Pharmaco-toxicologie Centre Hospitalier Lyon -Sud-HCL Pierre Benite 69495 France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

    Institut des Biomolécules Max Mousseron (IBMM) UMR 5247 CNRS Université de Montpellier ENSCM Campus Triolet Montpellier France;

    Inserm U1052 CNRS UMR5286 Centre de Recherche en Cancérologie de Lyon F-69000 Lyon France. Centre Léon Bérard F-69008 Lyon France Universitéde Lyon 1 F-69000 Lyon France;

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  • 入库时间 2022-08-19 04:56:32
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