墨西哥人口服氟康唑与伊曲康唑药代动力学比较。

Francisco J Flores-Murrieta, Miriam del C Carrasco-Portugal, Carlos Landa
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摘要

氟康唑和伊曲康唑是墨西哥广泛使用的抗真菌药物。然而,关于它们的药代动力学信息有限。据报道,这些化合物的理化特性是完全不同的,导致不同的药代动力学特征。此外,有研究表明,由于CYP3A4代谢降低,某些药物在墨西哥人体内的药代动力学可能与白种人不同。基于这些区别,重要的是开展当地研究,以便根据每个人群的特点制定给药方案。本研究的目的是比较氟康唑和伊曲康唑在墨西哥人的口服药代动力学,并将我们的结果与在其他人群中报道的结果进行比较。两组16名受试者自愿参加这项研究,该研究已得到机构研究和伦理委员会的批准。所有受试者均书面知情同意参与。禁食一夜后,志愿者口服100毫克氟康唑或伊曲康唑,并在96小时内的选定时间采集血液样本。取血浆,HPLC分析,获得药动学参数。正如预期的那样,氟康唑的血浆水平高于伊曲康唑,因为分布体积较小。此外,氟康唑的可变性较小。将墨西哥人获得的数据与其他人群获得的数据进行比较,没有观察到差异,这表明氟康唑和伊曲康唑的药代动力学没有种族间差异。
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Comparison of the oral pharmacokinetics of fluconazole and itraconazole in Mexicans.

Fluconazole and itraconazole are antimycotics widely used in Mexico. However, limited information about their pharmacokinetics is available. It has been reported that physicochemical characteristics of these compounds are disparate, leading to different pharmacokinetic profiles. Moreover, it has been suggested that pharmacokinetics of some drugs may vary in Mexicans when compared with Caucasians due to reduced metabolism by CYP3A4. Based on these distinctions, it is important to carry out local studies in order to establish dosage regimens according the characteristics of each population. The purpose of this study was to compare the oral pharmacokinetics of fluconazole and itraconazole in Mexicans and to compare our results with those reported in other populations. Two groups of 16 subjects volunteered for this study that was approved by the Institutional Research and Ethics Committees. All subjects gave written informed consent for participation. After an overnight fast, volunteers received an oral dose of 100 mg fluconazole or itraconazole and blood samples were obtained at selected times over 96 hr. Plasma was obtained and analyzed by HPLC and pharmacokinetic parameters were obtained. As expected, fluconazole plasma levels were higher than itraconazole due to a lower volume of distribution. Additionally, less variability was observed for fluconazole. When data obtained in Mexicans was compared with those obtained in other populations, no differences were observed, suggesting that there are not interethnic differences in the pharmacokinetics of fluconazole and itraconazole.

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