共加工片剂辅料组成,其制备及用途:US10071059 B2:专利聚光灯。

IF 1.8 Q3 PHARMACOLOGY & PHARMACY
Sajal Jain, Ritu Rathi, Upendra Nagaich, Inderbir Singh
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引用次数: 0

摘要

协同加工包括将一种赋形剂结合到其他赋形剂的颗粒结构中,以克服每种赋形剂的缺陷。目前的专利描述了通过流化床团聚的微晶纤维素和甘露醇的协同加工,目的是限制润滑剂在片剂组合物中的使用。将共制辅料与物理共制辅料进行了比较,并对共制辅料进行了扫描电镜、崩解和硬度表征。共加工辅料的平均粒径小于0.55 mm,具有较大的单个乳糖包被颗粒,而物理共加工辅料颗粒无包被,形状不规则。比较了物理混合和共加工辅料制成的片剂。硬度和崩解研究表明,随着辅料混合时间的增加,硬度和崩解时间均减小。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Co-processed tablet excipient composition, its preparation and use: US10071059 B2: patent spotlight.

Co-processing involves the incorporation of one excipients into the particle structure of other excipients to overcome the deficiencies of each excipients. The current patent describes the co-processing of microcrystalline cellulose and mannitol via fluid bed agglomeration with an aim to limit the use of lubricant in tablet composition. The co-processed excipients blend was compared with the physical blend of excipients and characterized for scanning electron microscopy, disintegration and hardness. The average particle size of co-processed excipients was less than 0.55 mm, characterized by large individual lactose-coated particles whereas, the physical blend particles are uncoated and irregular in shape. Tablets made from both physical blend and co-processed excipients were compared. As per the hardness and disintegration studies, with increase in mixing time of excipients both hardness and disintegration time decreases.

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来源期刊
Pharmaceutical patent analyst
Pharmaceutical patent analyst PHARMACOLOGY & PHARMACY-
CiteScore
1.80
自引率
0.00%
发文量
22
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