Enhanced Bioavailability of Acetohexamide by β-Cyclodextrin Complexation
Bibliographic Information
- Other Title
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- β-シクロデキストリン複合体化によるアセトヘキサミドのバイオアベイラビリティの向上
- ベータ シクロデキストリン フクゴウタイカ ニヨル アセトヘキサミド ノ バイ
- Enhanced Bioavailability of Acetohexamide by β-Cyclodextrin Complexation
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Abstract
An inclusion complex of acetohexamide (AHA) with β-cyclodextrin (β-CyD) in the molar ratio of 1 : 2 was prepared, and its permeation behavior through a cellophane membrane, in situ absorption behavior in rabbit small intestinal tract, and in vivo extent of bioavailability in rabbit were examined in comparison with those of AHA alone. The membrane permeation constant and in situ absorption rate of AHA in solution were found to decrease by the addition of β-CyD. However, the lesser permeability and absorptivity of the complex were significantly overcome by an improved solubility of AHA. The inclusion complexation of AHA with β-CyD was also effective in releasing drug from a hydrophobic suppository base such as Witepsol W35. The complex increased highly the levels of plasma concentration and cumulative urinary excretion of AHA and hydroxyhexamide, one of the metabolites of AHA, after oral or rectal administration to rabbits. The increase of bioavailability of AHA by means of the inclusion complexation suggested the possibility of smaller doses and fewer side effects in sulfonylurea therapy.
Journal
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- YAKUGAKU ZASSHI
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YAKUGAKU ZASSHI 100 (9), 903-909, 1980
The Pharmaceutical Society of Japan
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Details 詳細情報について
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- CRID
- 1390282681105628160
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- NII Article ID
- 130007274882
- 110003650864
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- NII Book ID
- AN00284903
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- ISSN
- 13475231
- 00316903
- http://id.crossref.org/issn/00316903
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- NDL BIB ID
- 2225445
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- Data Source
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- JaLC
- NDL
- Crossref
- CiNii Articles
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- Abstract License Flag
- Disallowed