Dissolution rate enhancement of Alprazolam by Solid Dispersion

被引:0
作者
Roul, L. K. [1 ]
Manna, N. K. [1 ]
Parhi, R. N. [2 ]
Sahoo, S. [2 ]
Suresh, P. [2 ]
机构
[1] Coll Pharmaceut Sci, Berhampur, Orissa, India
[2] GITAM Univ, GITAM Inst Pharm, Visakhapatnam 530045, Andhra Pradesh, India
关键词
Solid dispersion; Similarity factor; Alprazolam; SOLUBILITY; SYSTEM;
D O I
暂无
中图分类号
G40 [教育学];
学科分类号
040101 ; 120403 ;
摘要
Solid dispersions were prepared by both solvent evaporation and physical mixing method for poorly water soluble model drug Alprazolam using carriers such as polyethylene glycol-6000 (PEG-6000) and polyvinylpyrrolidone-K30 (PVP-K30) at different proportions (Drug:carriers-1:1, 1:2, 1:4). The solid dispersions were characterized by solubility, drug content uniformity, dissolution rate, similarity factor analysis and stability after 2 months at 30 degrees C/75%RH and 40 degrees C/75%RH. More than 80% of Alprazolam was released within 30 minutes of dissolution and the release was more with PVP-K30 when prepared by solvent evaporation method than prepared by physical mixing. The dissolution data's were fitted in Zero order, First order, Higuchi model and Korsmeyer-peppas equation. All the formulations followed Higuchi model (r(2)>0.96) and the 'n' values were within 0.5 to 0.95, which indicates anomalous transport. The formulations containing drug and PEG-6000 and PVP-K30 at 1:1 revealed similar dissolution profile with theoretical dissolution. The stability study indicates condition of 30 degrees C/75%RH as suitable for solid dispersion storage. Tablets were prepared from selected solid dispersions and subjected to various quality control tests.
引用
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页码:38 / 44
页数:7
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