Release Rate Enhancement of Lurasidone Hydrochloride from Orally Disintegrating Tablets using Lyophilisation

被引:1
|
作者
Skocibusic, J. [1 ]
Barbaric, J. [1 ]
Zizek, K. [1 ]
机构
[1] Univ Zagreb, Fac Chem Engn & Technol, Marulicev Trg 19, Zagreb 10000, Croatia
关键词
Lurasidone hydrochloride; solid dispersion; lyophilisation; orally disintegrating tablet; drug release; POLYMER; PEG;
D O I
10.15255/KUI.2020.023
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
This paper investigates the possibilities for release rate enhancement of lurasidone hydrochloride, a second-generation antipsychotic, by preparing solid dispersions via lyophilisation process. FTIR, DSC, and XRPD measurements have been performed in order to detect potential interactions between lurasidone hydrochloride and polymer matrices that might significantly increase drug solubility and provide faster release from the dosage form. Such solid dispersions and excipients have been used in the preparation of tablets that disintegrate in less than 3 min. In vitro dissolution profiles indicate a higher drug release rate from disintegrating tablets in comparison to pure LRS HCl.
引用
收藏
页码:P11 / P20
页数:10
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