Department of Pharmaceutics, School of Pharmaceutical Science, Hebei Medical University, ShiJiaZhuang, PR China.
J Pharm Sci. 2010 Jan;99(1):186-95. doi: 10.1002/jps.21810.
The purpose of the study was to (i) prepare the chitosan/Kollicoat SR 30D film-coated pellets for colonic drug delivery, and (ii) evaluate the colonic delivery and efficacy of these coated pellets in the rat. The pellets were coated to different film thickness with chitosan/Kollicoat SR 30D formulations. In vitro drug release was assessed in simulated gastrointestinal (GI) tract conditions. Biodistribution of aminosalicylates (5-ASA) in GI tract and plasma was measured after oral administration of coated or uncoated 5-ASA pellets. Efficacy of the coated or uncoated 5-ASA pellets was tested in 2,4,6-trinitrobenzene sulfonic acid (TNBS)-induced rat colitis model. Healing of induced colitis was assessed by measuring the myeloperoxidase activities, colon wet weight/body weight, and damage score. The coating was susceptible to bacteria digestion, resulting in an increase in the release of 5-ASA from the coated pellets. After administration of the coated pellets, the drug concentration in the large intestine was higher than those of uncoated pellets. In plasma, the observed mean C(max) from the coated pellets was significantly lower than that of the uncoated pellets. Chitosan/Kollicoat SR 30D film-coated pellets could deliver the 5-ASA to the targeted site, providing effective treatment for inflammatory bowel disease.
(i)制备壳聚糖/ Kollicoat SR 30D 薄膜包衣微丸用于结肠递药,以及(ii)评估这些包衣微丸在大鼠中的结肠递药和疗效。用壳聚糖/ Kollicoat SR 30D 制剂将微丸包衣至不同的膜厚。在模拟胃肠道(GI)条件下评估体外药物释放。口服包衣或未包衣的 5-ASA 微丸后,测量氨基水杨酸盐(5-ASA)在 GI 道和血浆中的分布。在 2,4,6-三硝基苯磺酸(TNBS)诱导的大鼠结肠炎模型中测试包衣或未包衣的 5-ASA 微丸的疗效。通过测量髓过氧化物酶活性、结肠湿重/体重和损伤评分来评估诱导性结肠炎的愈合情况。包衣易受细菌消化,导致包衣微丸中 5-ASA 的释放增加。给予包衣微丸后,大肠中药物浓度高于未包衣微丸。在血浆中,从包衣微丸观察到的平均 C(max)显著低于未包衣微丸。壳聚糖/ Kollicoat SR 30D 薄膜包衣微丸可将 5-ASA 递送至靶向部位,为炎症性肠病提供有效治疗。