Pedro Dorado, Esther Machín, Fernando de Andrés, María-Eugenia Naranjo, Eva M Peñas-Lledó, Adrián Llerena
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引用次数: 8
摘要
背景:氯沙坦被多态细胞色素CYP2C9代谢为氯沙坦羧酸(E-3174)。本研究的目的是建立高效液相色谱(HPLC)荧光检测同时测定尿中氯沙坦及其代谢物E-3174的方法,评估氯沙坦尿代谢比(MR: losartan/E-3174)对人CYP2C9表型的影响。方法:采用反相色谱柱分离,荧光检测,激发波长为250 nm,发射波长为370 nm。结果:内源化合物对分析无干扰,提取回收率在88%以上。氯沙坦和E-3174分别获得了2 ng mL-1和5 ng mL-1的定量限,且变异系数重复性好。结论:所建立的方法简便、经济、mr计算灵敏、可靠,可用于不同等位基因组合人群(如西班牙裔)中氯沙坦作为药物试验的CYP2C9表型分析。
Development of a HPLC method for the determination of losartan urinary metabolic ratio to be used for the determination of CYP2C9 hydroxylation phenotypes.
Background: Losartan is metabolized to losartan carboxylic acid (E-3174) by the polymorphic cytochrome CYP2C9. The aim of the study was to develop a high-performance liquid chromatographic (HPLC) method with fluorescence detection for simultaneously measuring losartan and its metabolite E-3174 in urine to evaluate the losartan urinary metabolic ratio (MR: losartan/E-3174) for CYP2C9 phenotyping in humans.
Methods: The compounds were separated in a reversed-phase chromatographic column and detected by fluorescence at a wavelength of 250 nm for excitation and of 370 nm for emission.
Results: No analytical interferences with endogenous compounds were found, and the extraction recoveries were over 88%. Limits of quantification of 2 ng mL-1 for losartan and 5 ng mL-1 for E-3174 were achieved, as well as good reproducibility with coefficients of variation of <9% in all cases. Analyses with the present HPLC method show significant differences (p<0.05) in losartan MRs between the four CYP2C9 genotype groups in 13 Spanish healthy volunteers.
Conclusions: The method developed is simple and affordable, as well as sensitive and reliable to calculate the MR. Therefore, it appears to be useful for CYP2C9 phenotyping using losartan as a drug test in populations, such as Hispanics with different allele combinations.