Miyake Masateru, Kamada Naoki, Oka Yoshikazu, Mukai Tadashi, Minami Takanori, Toguchi Hajime, Odomi Masaaki, Ogawara Ken-ichi, Higaki Kazutaka, Kimura Toshikiro
Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka Okayama, Japan.
J Control Release. 2004 Sep 14;99(1):63-71. doi: 10.1016/j.jconrel.2004.06.007.
To develop the safe formulation that can safely improve bioavailability of poorly absorbable drugs and that is practically available, we prepared the suppositories of rebamipide, a poorly soluble and poorly absorbable antiulcer drug, by employing the combinatorial use of sodium laurate (C12), an absorption enhancer, with taurine (Tau) or L-glutamine (L-Gln), an adjuvant exerting the cytoprotective action. Although the dissolution of rebamipide from fatty base (FB) suppository prepared using Witepsol H-15 was very slow, it was remarkably improved by the addition of C12 and L-Gln or Tau into the suppository. On the other hand, the dissolution of rebamipide from water-soluble base (WB) suppository prepared using polyethylene glycol was very rapid and the addition of adjuvants did not influence its dissolution so much. Rectal absorption of rebamipide examined in rats was remarkably improved by FB suppository containing C12 or both C12 and Tau, while the enhancing effect of C12 was relatively small in the case of WB suppositories. Biochemical and histopathological studies have confirmed that FB suppository containing both C12 and Tau or L-Gln did not cause any serious local damage, while FB suppository containing C12 only caused the erosion and shrinkage for a lot of rectal epithelial cells. In conclusion, FB suppository employing the combinatorial use of C12 with Tau could be a promising formulation that is effective and safe enough for poorly absorbable drugs to be practically administered.
为了开发一种安全的制剂,能够安全地提高难吸收药物的生物利用度且切实可行,我们通过将吸收促进剂月桂酸钠(C12)与具有细胞保护作用的佐剂牛磺酸(Tau)或L-谷氨酰胺(L-Gln)联合使用,制备了瑞巴派特(一种难溶性和难吸收的抗溃疡药物)栓剂。尽管使用Witepsol H-15制备的脂肪酸基质(FB)栓剂中瑞巴派特的溶出非常缓慢,但通过在栓剂中添加C12和L-Gln或Tau,其溶出得到了显著改善。另一方面,使用聚乙二醇制备的水溶性基质(WB)栓剂中瑞巴派特的溶出非常迅速,添加佐剂对其溶出影响不大。在大鼠体内进行的瑞巴派特直肠吸收研究表明,含C12或同时含C12和Tau的FB栓剂能显著提高其吸收,而在WB栓剂中C12的增强作用相对较小。生化和组织病理学研究证实,同时含C12和Tau或L-Gln的FB栓剂不会引起任何严重的局部损伤,而仅含C12的FB栓剂会导致大量直肠上皮细胞出现糜烂和萎缩。总之,将C12与Tau联合使用的FB栓剂可能是一种有前景的制剂,对于难吸收药物的实际给药既有效又安全。