Muranushi N, Yoshida M, Kinoshita H, Hirose F, Fukuda T, Doteuchi M, Yamada H
Shionogi Research Laboratories, Osaka, Japan.
Nihon Yakurigaku Zasshi. 1988 Jun;91(6):377-83. doi: 10.1254/fpj.91.377.
Benexate.CD, a new orally active antiulcer agent, is an inclusion compound of benexate and beta-cyclodextrin (beta-CD). The present report investigated the significance of complex formation on the antiulcer activity of benexate, the effective ingredient of benexate.CD. To evaluate the improvement of solubility, the dissolution properties of benexate from various pharmaceutical forms into the 1st fluid of the Pharmacopoeia of Japan, a model of gastric juice, were compared. Benexate itself was hardly soluble, but the physical mixture of benexate and beta-CD showed a solubility increase of benexate. On the other hand, benexate.CD showed a supersaturated dissolution curve and its peak concentration was 8 times higher than the solubility of the physical mixture. When benexate.CD was administered orally to pylorus ligated rats in the powder formulation, the similar supersaturated dissolution behavior was observed in the stomach, and the benexate level in gastric tissue was higher than that in benexate or the physical mixture administration. Benexate.CD extremely inhibited the ulcer formation caused by HCl-ethanol ingestion, but there was no significant inhibition after treatment with benexate or the physical mixture. These results indicated that it is necessary for benexate to form an inclusion compound in order to exert a strong antiulcer activity.
贝奈酯-CD是一种新型口服活性抗溃疡药物,是贝奈酯与β-环糊精(β-CD)的包合物。本报告研究了包合物形成对贝奈酯-CD有效成分贝奈酯抗溃疡活性的意义。为评估溶解性的改善情况,比较了贝奈酯从各种剂型在日本药典第一液(一种胃液模型)中的溶解特性。贝奈酯本身几乎不溶,但贝奈酯与β-CD的物理混合物显示贝奈酯的溶解度增加。另一方面,贝奈酯-CD呈现过饱和溶解曲线,其峰值浓度比物理混合物的溶解度高8倍。当将粉末制剂的贝奈酯-CD口服给予幽门结扎大鼠时,在胃中观察到类似的过饱和溶解行为,胃组织中的贝奈酯水平高于给予贝奈酯或物理混合物后的水平。贝奈酯-CD极大地抑制了因摄入盐酸-乙醇引起的溃疡形成,但用贝奈酯或物理混合物处理后没有明显抑制作用。这些结果表明,贝奈酯形成包合物对于发挥强大的抗溃疡活性是必要的。