Pharmacokinetics and Relative Bioavalability of Glipizide Tablet
Yuanda Zhou, Gaoqiong Yao
Abstract
Yuanda Zhou, Gaoqiong Yao
Abstract
OBJECTIVE:To determine the pharmacokinetics and bioavalability of glipizide tablet,and to compare Chongqing glipizide tablet with that produced in Hainan.METHODS:The drug concentrations in plasma were assayed by HPLC after administration of a single oral dose of 5mg Chongqing or Hainan glipizide to each of 12 healthy male volunteers in a randomized crossover study.RESUITS:The peak plasma levels averaged (267 26±64 35)ng/ml and (260 14±43 89)ng/ml,times to reach the peak level were (2 86±0 56)h and (2 92±0 7)h,and the areas under the drug concentration curves were (1 721 53±505 17)ng/(h·ml) and (1 714 00±266 29)ng/(h·ml) for Chongqing and Hainan glipizide,respectively.CONCLUSION:The result sh_owed that the two tablets were bioequivalent.
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OBJECTIVE:To determine the pharmacokinetics and bioavalability of glipizide tablet,and to compare Chongqing glipizide tablet with that produced in Hainan.METHODS:The drug concentrations in plasma were assayed by HPLC after administration of a single oral dose of 5mg Chongqing or Hainan glipizide to each of 12 healthy male volunteers in a randomized crossover study.RESUITS:The peak plasma levels averaged (267 26±64 35)ng/ml and (260 14±43 89)ng/ml,times to reach the peak level were (2 86±0 56)h and (2 92±0 7)h,and the areas under the drug concentration curves were (1 721 53±505 17)ng/(h·ml) and (1 714 00±266 29)ng/(h·ml) for Chongqing and Hainan glipizide,respectively.CONCLUSION:The result sh_owed that the two tablets were bioequivalent.
Key concepts: Glipizide, Bioequivalence, Pharmacokinetics, Crossover study, Pharmacology, Plasma concentration, Plasma levels, Chemistry