Enhanced dissolution of poorly soluble antiviral drugs from nanoparticles of cellulose acetate based solid dispersion matrices

被引:0
|
作者
Sonal Mazumdera [1 ]
Ashish Kumar Dewangan [1 ]
Naresh Pavurala [2 ]
机构
[1] Department of Chemical Engineering, Birla Institute of Science and Technology
[2] Oak Ridge Associated Universities, Food and Drug Administration
关键词
Solid dispersions; Ritonavir; Efavirenz; Nanoparticles; Precipitation; Solubility;
D O I
暂无
中图分类号
R943 [制剂学];
学科分类号
100602 ; 100702 ;
摘要
Polysaccharide-based polymers were used to produce nanoparticles of poorly soluble antiviral drugs using a rapid precipitation process. The structure-property relationships of four novel cellulose acetate-based polymers were studied for their solubility enhancement of poorly soluble drugs. Particles were purified by dialysis, and dried powders were recovered after freeze-drying. The particle diameters were 150–200 nm. The target drug loading in the particles was 25 wt%, and the drug loading efficiencies were 80–96%. The effects of the formulation process and nanoparticle properties on drug solubility were investigated. All nanoparticles afforded increased solubility and faster release compared to pure drugs. Drug release was a function of the relative hydrophobicity (or solubility parameters) of the polymers.Production and hosting by Elsevier B.V. on behalf of Shenyang Pharmaceutical University.
引用
收藏
页码:532 / 541
页数:10
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