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用于免疫抑制药物他克莫司结肠递送的pH敏感微球设计

Design of pH-sensitive microspheres for the colonic delivery of the immunosuppressive drug tacrolimus.

作者信息

Lamprecht Alf, Yamamoto Hiromitsu, Takeuchi Hirofumi, Kawashima Yoshiaki

机构信息

Laboratory of Pharmaceutical Engineering, Gifu Pharmaceutical University, Gifu, Japan.

出版信息

Eur J Pharm Biopharm. 2004 Jul;58(1):37-43. doi: 10.1016/j.ejpb.2004.01.003.

Abstract

Recently, tacrolimus was shown to be effective in mitigating inflammatory bowel disease (IBD). In the treatment of IBD, oral drug delivery using pH-dependent polymers is one of the most successful therapeutic strategies. Eudragit P-4135F, a pH-sensitive polymer for colonic delivery was used to prepare tacrolimus microparticles using an oil/oil emulsification or an oil/water emulsification technique combined with a solvent extraction or evaporation step. Although the pH-dependent drug release was similar for all types of microspheres, it was generally found that encapsulation rates of oil/water systems (extraction 38.8 +/- 9.4%; evaporation 56.3 +/- 1.9%) were superior to the oil/oil emulsification (4.8 +/- 0.4%). Eudragit P-4135F was found to limit drug leakage at pH 6.8 to levels lower than 10% within 6 h. At pH 7.4, almost immediate release (within 30 min) was observed. From differential scanning calorimetry and X-ray analyses, the drug inside the polymeric microsphere matrix was concluded to be present in a molecular dispersion. Generally, all formulations proved their applicability in vitro as a promising device for pH-dependent colonic delivery of tacrolimus, however, the oil/water technique was found to be superior to the oil/oil approach and among them solvent evaporation seemed to be more advisable, due to the higher encapsulation rate.

摘要

最近,已证明他克莫司在减轻炎症性肠病(IBD)方面有效。在IBD的治疗中,使用pH依赖性聚合物的口服给药是最成功的治疗策略之一。Eudragit P - 4135F是一种用于结肠给药的pH敏感聚合物,采用油/油乳化或油/水乳化技术结合溶剂萃取或蒸发步骤来制备他克莫司微粒。尽管所有类型微球的pH依赖性药物释放相似,但通常发现油/水系统的包封率(萃取法为38.8±9.4%;蒸发法为56.3±1.9%)优于油/油乳化法(4.8±0.4%)。发现Eudragit P - 4135F可将pH 6.8时的药物泄漏限制在6小时内低于10%的水平。在pH 7.4时,观察到几乎立即释放(30分钟内)。通过差示扫描量热法和X射线分析得出,聚合物微球基质内的药物以分子分散形式存在。总体而言,所有制剂在体外均证明其作为他克莫司pH依赖性结肠给药的有前景装置的适用性,然而,发现油/水技术优于油/油方法,并且在它们之中,由于包封率更高,溶剂蒸发似乎更可取。

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