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Bioequivalence of oral candesartan cilexetil capsules in healthy volunteers |
GUO Zhe1, QIANG LieYing1, ZHU Zhe1, WANG Hui1,BI Jingfeng1,and WEI Zhenman2 |
1. Department of Pharmacy, Second Hospital of Beijing Municipal Corps; Chinese People’s Armed Police Force, Beijing 100037, China; 2. The Center of New Drug Clinical Trial, No.302 Hospital of PLA, Beijing 100039, China |
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Abstract Objective To study the bioequivalence of the tested and reference oral candesartan Cilexetil in healthy male volunteers. Methods According to the crossover design,each volunteer was orally given 8 mg candesartan cilexetil capsules or tablets. Their plasma concentrations were determined by LC/MS/MS. Pharmacokinetic parameters were obtained using DAS program. Results Cmax were(79.62±29.99) ng/ml and (77.74±28.46) ng/ml,AUC0-t were (850.17±249.52) ng/(ml· h)and (837.26±243.26)ng/(ml· h),AUC0-∞ were (908.96±249.64) ng/(ml· h) and(896.94±241.53) ng/(ml· h),respectively. Two-way unilateral t-test results showed that the test preparation did not exceed the prescribed upper limit and lower limit of the reference preparation, rejected null hypothesis (P<0.05). The 90% confidence intervals of Cmax,AUC0-t and AUC0-∞were between the standard of reference tablets (80%-125%). Conclusions Candesartan cilexetil capsules and candesartan cilexetil tablets are bioequivalent.
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Received: 12 February 2015
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徐 戎, 斯陆勤, 顾世芬, 等. 国产和进口坎地沙坦酯片人体生物等效性评价[J]. 中国药学杂志, 2008, 43(6): 455-458.
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[10] |
朱燕妮, 傅潞仙, 徐飞瑶, 等. 高效液相色谱法对坎地沙坦酯固体分散体颗粒溶出度的测定[J].中国医药导报, 2013, 10(3): 127-129.
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[11] |
朱余兵, 于翠霞, 程俊霖, 等. 复方坎地沙坦酯片在健康受试者体内的生物等效性研究[J]. 中国药师,2011,14(6):775-778.
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[12] |
徐 戎, 斯陆勤, 顾世芬, 等. 国产和进口坎地沙坦酯片人体生物等效性评价[J]. 中国药学杂志, 2008, 43(6): 455-458.
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