生物等效性
最大值
皮塔伐他汀
药代动力学
高脂血症
血脂异常
药理学
医学
餐后
生物利用度
餐食
化学
他汀类
内科学
内分泌学
胰岛素
糖尿病
肥胖
作者
Dewei Shang,Shuhua Deng,Zhenhong Yao,Zhanzhang Wang,Xiaojia Ni,Ming Zhang,Jinqing Hu,Haoyang Lu,Xiuqing Zhu,Wencan Huang,Chang Qiu,Wen Yu-guan
出处
期刊:PubMed
[National Institutes of Health]
日期:2016-01-01
卷期号:46 (1): 34-9
被引量:7
标识
DOI:10.3109/00498254.2015.1046153
摘要
1. Pitavastatin is an effective treatment for primary hyperlipidemia and mixed dyslipidemia. The aim of the present study was to investigate the effect of food on the pharmacokinetic properties and bioequivalence of the original, branded, formulation of pitavastatin calcium and a new generic formulation in healthy Chinese male subjects under fasting and fed conditions. 2. Under fasting and fed conditions, 90% CIs of the geometric mean of generic/branded AUC0-48 h ratios were 92.2-102.4%, 93.1-104.5%, the ratios of ln(AUC0-∞) were 92.6-103.7%, 93.2-103.5%, and ln(Cmax) ratios were 90.7-110.3%, 84.7-100.8%, respectively. The generic and branded formulations were bioequivalent in terms of rate and extent of absorption under both the conditions. The average values of AUC0-48 h, AUC0-∞ and Cmax decreased noticeably following a high-fat breakfast. Values for AUC0-48 h were 87.69% and 83.7%, values for AUC0-∞ were 87.5% and 84.6%, and values for Cmax were 45.0% and 50.4% in subjects given the generic and branded preparations, respectively. The absorption of pitavastatin calcium tablets was delayed following a high-fat meal, with Tmax increasing by up to 2.43-fold. 3. Both formulations were generally well tolerated, with no serious adverse reactions reported. The newly developed generic formulation may provide a reliable alternative to the branded tablets for patients with primary hyperlipidemia or mixed dyslipidemia.
科研通智能强力驱动
Strongly Powered by AbleSci AI