Pharmaceutics Research Projects Laboratory, Department of Pharmaceutical Sciences, Dr. Hari Singh Gour Central University, Sagar, MP, India.
J Drug Target. 2010 Sep;18(8):589-601. doi: 10.3109/10611860903572933.
The treatment of ulcerative colitis (inflammatory bowel disease, IBD) has been achieved by using colon specific drug delivery system bearing 5-ASA and Camylofine dihydrochloride. Chitosan microspheres were prepared separately for both the drugs using emulsion method followed by enteric coating with EudragitS-100. The in vitro drug release was investigated in different simulated GIT medium. The drug release in PBS (pH7.4) and simulated gastric fluid has shown almost similar pattern and rate, whereas a significant increase in drug release (70.3 +/- 1.36 and 72.5 +/- 1.33% of 5-ASA and Camylofine, respectively) was observed in medium containing 3% rat caecal matter, after 24 h. In control study, 57.1 +/- 1.13% of 5-ASA and 59.2 +/- 1.2% of Camylofine release was observed in 24 h. For enzyme induction, rats were orally administered with 1 mL of 1% w/v dispersion of chitosan for 5 days and release rate studies were conducted in SCF with 3% w/v of caecal matter. An enhanced drug release (i.e., 92.3 +/- 3.81 and 95.5 +/- 3.52% 5-ASA and Camylofine, respectively) was observed after 24 h in dissolution medium containing 3% caecal content obtained from enzyme induced animals. In vivo data showed that microspheres delivered most of its drug load (76.55 +/- 2.13%) to the colon after 9 h, which reflects its targeting potential to the colon. It is concluded that orally administered microspheres of both drugs can be used together for the specific delivery of drug to the colon and reduce symptoms of ulcerative colitis.
溃疡性结肠炎(炎症性肠病,IBD)的治疗方法是使用载有 5-ASA 和 Camylofine 二盐酸盐的结肠特异性药物递送系统。分别使用乳化法制备两种药物的壳聚糖微球,然后用 EudragitS-100 进行肠溶包衣。在不同的模拟胃肠道介质中研究了体外药物释放。在 PBS(pH7.4)和模拟胃液中的药物释放表现出几乎相似的模式和速率,而在含有 3%大鼠盲肠物质的介质中,药物释放显著增加(5-ASA 和 Camylofine 分别为 70.3 +/- 1.36%和 72.5 +/- 1.33%),在 24 小时后。在对照研究中,在 24 小时内观察到 5-ASA 的 57.1 +/- 1.13%和 Camylofine 的 59.2 +/- 1.2%释放。对于酶诱导,大鼠口服给予 1 毫升 1%w/v 壳聚糖分散体 5 天,并在含有 3%w/v 盲肠物质的 SCF 中进行释放率研究。在含有 3%盲肠内容物的溶解介质中,在 24 小时后观察到药物释放增强(即 5-ASA 和 Camylofine 分别为 92.3 +/- 3.81%和 95.5 +/- 3.52%)。体内数据表明,微球在 9 小时后将其大部分药物负荷(76.55 +/- 2.13%)递送到结肠,这反映了其对结肠的靶向潜力。结论是,口服给予两种药物的微球可以一起用于将药物特异性递送到结肠并减轻溃疡性结肠炎的症状。