Optimization of Suppository Preparation Containing Sodium Laurate and Taurine That Can Safely Improve Rectal Absorption of Rebamipide(Biopharmacy)
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概要
- 論文の詳細を見る
We previously reported that the fatty base suppository containing sodium laurate (C12) and taurine (Tau) (C12-Tau suppository) could enhance the colonic absorption of rebamipide, a poorly water-soluble and poorly absorbable drug, without any serious mucosal damages in rats. In the preset study, in order to make C12-Tau suppositories available for practical use, the scaling-up studies of animal and formulation size were performed, compared with the suppositories containing sodium caprate (C10) (C10 suppository) at the same amounts as those contained in the commercial products. Twenty-mg C12 improved the dissolution of rebamipide from suppository remarkably and the addition of 30-mg Tau only slightly decreased the dissolution rate. The absorption of rebamipide from rabbit rectum was more markedly improved by suppositories containing C12 than C10 suppositories. Although Tau tended to attenuate the absorption-enhancing effect of C12, several C12-Tau suppositories kept high bioavailability values, which were much higher than control. Histopathological studies showed that Tau exerted the cytoprotective action and that C12-Tau suppositories were better than C10 suppositories in safety. Considering the balance between efficacy and safety, the suppository containing 10- or 20-mg C12 with 30-mg Tau is better than C10 suppositories as commercial products and could be promising for practical use in human.
- 公益社団法人日本薬学会の論文
- 2006-02-01
著者
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HIGAKI Kazutaka
Department of Basic Pharmaceutics, Faculty of Pharmaceutical Sciences, Kyoto University
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KIMURA Toshikiro
Department of Pharmaceutics, Okayama University Graduate School of Medicine, Dentistry and Pharmaceu
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MUKAI Tadashi
Formulation Research Institute, Otsuka Pharmaceutical Co., Ltd.
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ODOMI Masaaki
Formulation Research Institute, Otsuka Pharmaceutical Co., Ltd.
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Kimura Toshikiro
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Okayama University
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Kamada Naoki
Formulation Development 1 Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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Odomi Masaaki
Formulation Development 1 Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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Oka Yoshikazu
Formulation Development 1 Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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MIYAKE Masateru
Formulation Development 1, Formulation Research Institute, Otsuka Pharmaceutical Co., Ltd.
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MINAMI Takanori
Histopathology Research Office, Department of Toxicology, Tokushima Research Institute, Otsuka Pharm
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YAMAZAKI Hiroyuki
Formulation Development 1, Formulation Research Institute, Otsuka Pharmaceutical Co., Ltd.
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KATO Yusuke
Formulation Development 1, Formulation Research Institute, Otsuka Pharmaceutical Co., Ltd.
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TOGUCHI Hajime
Formulation Development 1, Formulation Research Institute, Otsuka Pharmaceutical Co., Ltd.
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OGAWARA Ken-ichi
Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Okayama University
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Toguchi Hajime
Formulation Development 1 Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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Ogawara Ken-ichi
Department Of Pharmaceutics Faculty Of Pharmaceutical Sciences Okayama University
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Miyake Masateru
Formulation Development 1 Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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Minami Takanori
Histopathology Research Office Department Of Toxicology Tokushima Research Institute Otsuka Pharmace
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Higaki Kazutaka
Okayama Univ. Graduate School Of Medicine Dentistry And Pharmaceutical Sci.
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Mukai Tadashi
Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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Kato Yusuke
Formulation Development 1 Formulation Research Institute Otsuka Pharmaceutical Co. Ltd.
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Yamazaki Hiroyuki
Department Of Pharmacokinetics And Biopharmaceutics Subdivision Of Biopharmaceutical Sciences Instit
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