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辊压压力对高载药量吡拉西坦颗粒和片剂性能的影响。

Effect of roll compaction pressure on the properties of high drug-loaded piracetam granules and tablets.

机构信息

School of Pharmacy, Queen's University Belfast, Belfast, UK.

出版信息

Drug Dev Ind Pharm. 2022 Sep;48(9):425-437. doi: 10.1080/03639045.2022.2123499. Epub 2022 Sep 16.

Abstract

OBJECTIVE

The aim of this study was to use an alternative granulation technique, solventless roll compaction, and to investigate the effect of the roll compaction pressure on the properties of granules and high-drug-loaded (80%, w/w) immediate release piracetam tablets.

SIGNIFICANCE

Piracetam is commonly manufactured as high drug-loaded tablets by wet granulation with an aqueous binder solution. Due to its high solubility in water, the wet granulation process is largely susceptible to processing methods and can induce the uncontrolled polymorphic transition of piracetam as well as convert it into mono- and di-hydrates.

METHODS

The blends, comprising piracetam, Kollidon 30, and Avicel PH-101 were roll compacted at 4, 5 and 13 MPa hydraulic pressure and calibrated using an industrial roll compactor. The resultant granules milled and raw piracetam was investigated with DSC. The resultant granules are mixed with Ac-Di-Sol, Aerosil 200 Pharma, and magnesium stearate to prepare tablets using an industrial tablet press at the same compression force and 25, 65, and 100 rpm. The obtained tablets were film coated with an aqueous dispersion of Opadry II using a pilot-scale solid-wall pan coater.

RESULTS

Roll compaction pressure influenced the polymorphic composition of piracetam, the granule properties and tablet mixture in relation to morphology, particle size, flowability, bulk and tapped density, as well as tablet hardness, tablet friability, disintegration, and dissolution.

CONCLUSION

This study showed that roll compaction can be successfully used for the preparation of highly water-soluble, highly drug-loaded piracetam film-coated tablets avoiding wet granulation pitfalls.

摘要

目的

本研究旨在使用替代制粒技术——无溶剂滚压法,并考察滚压压力对颗粒性质和高载药量(80%,w/w)即释型吡拉西坦片的影响。

意义

吡拉西坦通常采用湿法制粒,以水性粘合剂溶液制造高载药量的片剂。由于其在水中的高溶解度,湿法制粒过程在很大程度上容易受到处理方法的影响,并且会导致吡拉西坦不受控制的多晶型转变,以及将其转化为单水合物和二水合物。

方法

将包含吡拉西坦、共聚维酮 30 和 AVICEL PH-101 的混合物在 4、5 和 13 MPa 水压力下进行滚压,并使用工业滚压机进行校准。使用 DSC 研究所得颗粒的研磨和原始吡拉西坦。将所得颗粒与 Ac-Di-Sol、Aerosil 200 Pharma 和硬脂酸镁混合,在相同的压缩力和 25、65 和 100 rpm 下使用工业压片机制备片剂。使用小型固体壁盘式包衣机,用水性 OPADRY II 分散体对所得片剂进行薄膜包衣。

结果

滚压压力影响了吡拉西坦的多晶型组成、颗粒性质以及与形态、粒径、流动性、堆积密度和振实密度、片剂硬度、片剂脆碎度、崩解和溶解有关的片剂混合物。

结论

本研究表明,滚压可成功用于制备高水溶性、高载药量的吡拉西坦薄膜包衣片剂,避免了湿法制粒的缺陷。

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