Suppr超能文献

实验设计的冻干干乳剂片剂增强阿托伐他汀钙的抗高血脂活性:制备、体外评价和体内评价。

Experimentally designed lyophilized dry emulsion tablets for enhancing the antihyperlipidemic activity of atorvastatin calcium: Preparation, in-vitro evaluation and in-vivo assessment.

机构信息

Department of Pharmaceutical Technology, National Research Centre, Cairo 12622, Egypt.

Department of Pharmaceutical Technology, National Research Centre, Cairo 12622, Egypt.

出版信息

Eur J Pharm Sci. 2018 Jan 15;112:52-62. doi: 10.1016/j.ejps.2017.11.003. Epub 2017 Nov 5.

Abstract

This article presents the development of lyophilized orally disintegrating tablets prepared with the dry emulsion technique to enhance the in-vitro dissolution and in-vivo performance of the poorly bioavailable drug atorvastatin calcium (ATV). Tablets were fabricated by freeze-drying o/w emulsions of ATV. The Emulsions were prepared using a matrix former solution (alginate or gelatin, 2 or 4%) containing a sugar alcohol (mannitol) and a collapse protectant (glycine) as the water phase and Labrafac® as the oil phase in the presence of surfactant (synperonic® PE/P 84 or synperonic® F108) under proper homogenization. The influence of formulation parameters on friability of the prepared tablets, disintegration time and in-vitro dissolution of the drug from these tablets were investigated. Results showed the significant influence of the matrix former and emulsifier type on the disintegration time. In-vitro dissolution study revealed the enhanced dissolution rate of ATV from the lyophilized dry emulsion tablets (LDET) compared to the plain drug. DSC and XRD studies of the optimized ATV-loaded LDET proved the presence of the drug in the amorphous form. SEM images showed the intact, porous and non-collapsible structure of the prepared LDET with complete loss of ATV crystallinity. Administration of ATV-loaded LDET to high fat diet-induced hyperlipidemic rats demonstrated a significant decrease (p<0.05) in the serum and tissue levels of the tested parameters compared to the market product used. The obtained results suggest a promising, easy-to-manufacture and effective dosage form for the treatment of hyperlipidemia.

摘要

本文介绍了通过冻干法制备口服即溶片的方法,以提高疏水性药物阿托伐他汀钙(ATV)的体外溶出度和体内性能。该片剂是通过冻干 o/w 乳剂制备而成的,其中 ATV 是油相,乳化剂(Synperonic® PE/P84 或 Synperonic® F108)是水相。处方中还含有海藻酸钠或明胶(2%或 4%)、山梨醇和甘氨酸等基质形成剂、甘露醇等糖醇和甘氨酸等塌陷保护剂。在适当的均质条件下,将油相和水相混合制备乳液。考察了处方参数对冻干片脆碎度、崩解时间和药物体外溶出度的影响。结果表明,基质形成剂和乳化剂类型对崩解时间有显著影响。体外溶出度研究表明,与原料药相比,冻干干乳片(LDET)中 ATV 的释放速率更快。对优化的 ATV-LDET 的 DSC 和 XRD 研究表明,药物以无定形形式存在。SEM 图像显示,所制备的 LDET 具有完整的、多孔的、不可塌陷的结构,ATV 结晶度完全丧失。将 ATV-LDET 给予高脂饮食诱导的高血脂大鼠,与市售产品相比,血清和组织中检测参数的水平显著降低(p<0.05)。结果表明,LDET 是一种有前途的、易于制备的、有效的治疗高血脂症的药物剂型。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验