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评估 Ceolus™ 微晶纤维素等级用于肠溶性微丸的直接压片。

Evaluation of Ceolus™ microcrystalline cellulose grades for the direct compression of enteric-coated pellets.

机构信息

Drug Dynamics Institute, The University of Texas at Austin, Austin, USA.

出版信息

Drug Dev Ind Pharm. 2012 Mar;38(3):341-50. doi: 10.3109/03639045.2011.604328. Epub 2011 Aug 26.

DOI:10.3109/03639045.2011.604328
PMID:21870908
Abstract

The preparation of multiparticulate tablets by direct compression of functionally coated pellets is technologically challenging. The objective was to investigate the influence of different grades of microcrystalline cellulose (Ceolus™ UF-711, PH-102, PH-200 and KG-802) as fillers on the properties of blends and tablets containing enteric pellets. Celphere™ spheres were drug-layered and then functionally coated with Eudragit(®) L 30 D-55/FS 30D dispersion. Tablets loaded with 50% pellets were prepared using pure or binary blends of microcrystalline cellulose fillers. The influence of the filler on the blend flow, segregation tendency, tablet hardness and enteric release properties were studied using a mixture design, and the optimum filler composition was determined. Rapidly disintegrating tablets, which yielded a drug release of less than 10% after 2 hours in acidic medium, could be successfully prepared. The blend composition had a significant effect on the flowability, but less on the tablet hardness which was influenced by the selection of lubricant. Blends containing celluloses with low bulk densities exhibited a reduced tendency to segregate. Pellet distribution uniformity was further improved when using Ceolus™ UF-711 blended with a high-density grade. As a conclusion, multiparticulate tablets containing enteric pellets with preserved delayed-release properties were successfully prepared using Ceolus™ microcrystalline celluloses as tableting excipients. The optimized filler blend for the direct compression of 50% enteric pellets into tablets contained Ceolus™ UF-711 as main component in combination with Ceolus™ PH-200.

摘要

采用直接压缩功能包衣丸的方法制备多颗粒片剂在技术上具有挑战性。目的是研究不同等级的微晶纤维素(Celphere™ UF-711、PH-102、PH-200 和 KG-802)作为填充剂对包含肠溶丸的混合物和片剂的特性的影响。Celphere™球被药物层涂,然后用 Eudragit(®)L 30 D-55/FS 30D 分散体进行功能包衣。用纯或二元混合物填充剂制备载有 50%丸的片剂。使用混合物设计研究了填充剂对混合物流动、分离倾向、片剂硬度和肠溶释放性能的影响,并确定了最佳填充剂组成。成功制备了快速崩解片剂,这些片剂在酸性介质中 2 小时后药物释放率低于 10%。混合物组成对流动性有显著影响,但对片剂硬度的影响较小,片剂硬度受润滑剂选择的影响。含有低堆密度纤维素的混合物表现出降低的分离倾向。当使用 Celosphere™ UF-711 与高密度等级混合时,丸剂的分布均匀性进一步提高。总之,使用 Celosphere™微晶纤维素作为压片赋形剂成功制备了保留延迟释放性能的肠溶丸多颗粒片剂。用于将 50%肠溶丸直接压片的优化填充剂混合物包含 Celosphere™ UF-711 作为主要成分,与 Celosphere™ PH-200 结合使用。

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