Mukaizawa Fuyuki, Taniguchi Koji, Miyake Masateru, Ogawara Ken-ichi, Odomi Masaaki, Higaki Kazutaka, Kimura Toshikiro
Department of Pharmaceutics, Faculty of Pharmaceutical Sciences, Okayama University, 1-1-1 Tsushima-naka, Okayama 700-8530, Japan.
Int J Pharm. 2009 Feb 9;367(1-2):103-8. doi: 10.1016/j.ijpharm.2008.09.027. Epub 2008 Sep 25.
The combinatorial use of spermine (SPM), a typical polyamine, and sodium taurocholate (STC), a typical bile salt, was found to be a promising safe preparation for improving the oral absorption of poorly water-soluble and/or poorly absorbable drug in our previous studies utilizing rats and dogs. To clarify the mechanisms behind the synergistic enhancement effect of the polyamine and bile salt, the transport of rebamipide, which is classified into Biopharmaceutics Classification System Class IV, was investigated in Caco-2 cell monolayers. The synergistic enhancement of rebamipide transport by SPM and STC was certainly observed in Caco-2 cells as well, while the separate use of either SPM or STC did not significantly improve the transport of rebamipide. The combinatorial use of SPM and STC significantly decreased the transepithelial electrical resistance (TEER) in Caco-2 cell monolayers, suggesting that the opening of paracellular pathway. On the other hand, it was also confirmed that the decrease in TEER was transient and reversible after removal of SPM and STC and that cell viability was maintained. Voltage-clamp study clearly showed that their combinatorial use improved rebamipide transport via both paracellular and transcellular pathways, and that the contribution of transcellular route could be larger than paracellular route.
在我们之前利用大鼠和犬类进行的研究中,发现典型的多胺精胺(SPM)与典型的胆盐牛磺胆酸钠(STC)联合使用,是一种有前景的安全制剂,可用于改善难溶性和/或难吸收药物的口服吸收。为了阐明多胺和胆盐协同增强作用背后的机制,在Caco-2细胞单层中研究了被归类为生物药剂学分类系统IV类的瑞巴派特的转运。在Caco-2细胞中也确实观察到了SPM和STC对瑞巴派特转运的协同增强作用,而单独使用SPM或STC均未显著改善瑞巴派特的转运。SPM和STC联合使用显著降低了Caco-2细胞单层的跨上皮电阻(TEER),表明细胞旁途径开放。另一方面,还证实去除SPM和STC后TEER的降低是短暂且可逆的,并且细胞活力得以维持。电压钳研究清楚地表明,它们联合使用可通过细胞旁和跨细胞途径改善瑞巴派特的转运,并且跨细胞途径的贡献可能大于细胞旁途径。