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Oral Pharmacokinetics of Mirodenafil in Mexican Healthy Volunteers

机译:米罗地那非在墨西哥健康志愿者中的口服药代动力学

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Mirodenafil is a 5-phosphodiesterase inhibitor that is currently marketed in Korea for the treatment of erectile dysfunction; however, no information in other populations is available. It has been described that Mirodenafil is metabolized by CYP3A4, a metabolic pathway in which interethnic differences have been reported. The purpose of this study was to characterize the oral pharmacokinetics of Mirodenafil in Mexicans. Seventeen male healthy volunteers were enrolled in this study. After an overnight fast, volunteers received an oral 100 mg dose and blood samples were collected at selected times during 24 h. Plasma was stored frozen and analyzed by an HPLC method. Pharmacokinetic parameters obtained were: Cmax 331.129 ± 32.689 ng/mL, tmax 1.574 ± 0.293 h, AUC24h 883.293 ± 104.088 ng·h/mL, AUC¥ 976.477 ± 108.812 ng·h/mL and t1/2 1.807 ± 0.171 h. Parameter values observed in this study are similar to those reported in Koreans. Since efficacy and safety studies of Mirodenafil have been conducted in Koreans, it is expected that dosage regime to employ in Mexicans should be similar to the approved for Korean population.
机译:Mirodenafil是一种5-磷酸二酯酶抑制剂,目前在韩国销售,用于治疗勃起功能障碍。但是,没有其他人群的信息。已经描述了Mirodenafil被CYP3A4代谢,CYP3A4是一种代谢途径,据报道其中存在种族间差异。这项研究的目的是表征Mirodenafil在墨西哥人中的口服药代动力学。这项研究招募了十七名男性健康志愿者。过夜禁食后,志愿者口服100毫克剂量,并在24小时内的选定时间收集血液样本。将血浆冷冻保存并通过HPLC方法分析。获得的药代动力学参数为:Cmax 331.129±32.689 ng / mL,tmax 1.574±0.293 h,AUC24h 883.293±104.088 ng·h / mL,AUC ¥ 976.477±108.812 ng·h / mL和t1 / 2 1.807±0.171 h。在这项研究中观察到的参数值与韩国人报道的相似。由于Mirodenafil的功效和安全性研究已在韩国人中进行,因此预期在墨西哥人中使用的剂量方案应与韩国人批准的剂量方案相似。

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