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基于纤维素或吡咯烷酮衍生物聚合物的阿托伐他汀固体分散体的口服吸收。

Oral absorption of atorvastatin solid dispersion based on cellulose or pyrrolidone derivative polymers.

机构信息

Department of Pharmaceutical Engineering, Inje University, Gimhae, Gyeongnam 621-749, Republic of Korea.

出版信息

Int J Biol Macromol. 2013 Aug;59:138-42. doi: 10.1016/j.ijbiomac.2013.03.068. Epub 2013 Apr 6.

Abstract

The objectives of this study were to investigate the effects of hydrophilic polymer on the supersaturation and oral absorption of amorphous atorvastatin calcium. Solid dispersions of atorvastatin calcium were prepared by a supercritical antisolvent (SAS) process. The solid dispersion with polyvinylpyrrolidone vinyl acetate (PVP VA64) achieved a higher degree and extent of supersaturation than the dispersions prepared with water-soluble polymers such as hydroxypropylmethyl cellulose (HPMC) and polyvinylpyrrolidone (PVP K30). The absorption of atorvastatin in rats was markedly increased when atorvastatin was orally administered in a PVP VA64 solid dispersion due to enhanced supersaturation and dissolution properties. Therefore, the oral absorption of atorvastatin calcium increased with the degree of supersaturation of solid dispersions prepared using an SAS process.

摘要

本研究旨在探讨亲水性聚合物对无定形阿托伐他汀钙的过饱和度和口服吸收的影响。阿托伐他汀钙固体分散体通过超临界抗溶剂(SAS)工艺制备。与水溶性聚合物(如羟丙甲纤维素(HPMC)和聚乙烯吡咯烷酮(PVP K30))制备的分散体相比,具有聚维酮醋酸乙烯酯(PVP VA64)的固体分散体实现了更高的过饱和度和程度。由于增强了过饱和度和溶解性能,当阿托伐他汀以 PVP VA64 固体分散体口服给予时,大鼠中阿托伐他汀的吸收明显增加。因此,口服吸收阿托伐他汀钙随着使用 SAS 工艺制备的固体分散体的过饱和度的增加而增加。

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