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用于肠溶包衣和人回肠靶向的包衣聚合物的体外评价

In vitro evaluation of coating polymers for enteric coating and human ileal targeting.

作者信息

Huyghebaert Nathalie, Vermeire An, Remon Jean Paul

机构信息

Laboratory of Pharmaceutical Technology, Ghent University, Faculty of Pharmaceutical Science, Harelbekestraat 72, B-9000, Ghent, Belgium.

出版信息

Int J Pharm. 2005 Jul 14;298(1):26-37. doi: 10.1016/j.ijpharm.2005.03.032.

Abstract

Recombinant interleukin-10 producing Lactococcus lactis is an alternative therapy for Crohn's disease. For in vivo interleukin-10 production, thymidine, the essential feed component of these recombinant bacteria should be coadministered. Different coating polymers were evaluated in vitro for enteric properties and targeting suitability to the ileum, the major site of inflammation in Crohn's disease. To guarantee ileal delivery, the polymer must dissolve from pH 6.8 and allow complete release within 40 min. Aqoat AS-HF coated pellets (15%) showed poor enteric properties and thymidine was released below pH 6.8. Eudragit FS30D coated pellets (15%) showed good enteric properties, but no thymidine was released within 40 min at pH 6.8. Eudragit S coated pellets (15%) showed good enteric properties after curing at elevated temperature while no thymidine was released within 40 min at pH 6.8. In another approach to pass the proximal small intestine intact, pellets were coated with 30% Eudragit L30D-55. At pH 6.0, they showed a lag-phase of 20 min. No influence of layer thickness was seen above pH 6.5. Alternatively, pellets were coated with a mixture of Eudragit FS30D/L30D-55 but they showed poor enteric properties and thymidine was released below pH 6.8. In conclusion, none of the tested polymers/mixtures ensured enteric properties and ileal targeting.

摘要

产重组白细胞介素-10的乳酸乳球菌是克罗恩病的一种替代疗法。为了在体内产生白细胞介素-10,这些重组细菌的必需营养成分胸苷应同时给药。在体外评估了不同的包衣聚合物的肠溶性能以及对回肠(克罗恩病炎症的主要部位)的靶向适用性。为确保在回肠释放,聚合物必须在pH 6.8时溶解并在40分钟内完全释放。Aqoat AS-HF包衣微丸(15%)表现出较差的肠溶性能,胸苷在pH 6.8以下释放。Eudragit FS30D包衣微丸(15%)表现出良好的肠溶性能,但在pH 6.8时40分钟内无胸苷释放。Eudragit S包衣微丸(15%)在高温固化后表现出良好的肠溶性能,但在pH 6.8时40分钟内无胸苷释放。在另一种使近端小肠完整通过的方法中,微丸用30%的Eudragit L30D-55包衣。在pH 6.0时,它们表现出20分钟的延迟期。在pH 6.5以上未观察到层厚度的影响。或者,微丸用Eudragit FS30D/L30D-55混合物包衣,但它们表现出较差的肠溶性能,胸苷在pH 6.8以下释放。总之,所测试的聚合物/混合物均未确保肠溶性能和回肠靶向性。

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