溶解
聚乙二醇
溶解度
肺表面活性物质
化学
硝苯地平
色谱法
PEG比率
聚合物
剂型
钠
水溶液
溶解试验
核化学
有机化学
钙
生物制药分类系统
生物化学
经济
财务
作者
Sangalli Me,Paolo Giunchedi,Paolo Colombo,Ubaldo Conte,A. Gazzaniga,La Manna A
出处
期刊:PubMed
日期:1989-07-01
卷期号:128 (7-8): 242-7
被引量:17
摘要
The dissolution rate is often the limiting step in gastrointestinal absorption of water insoluble drugs from solid oral dosage forms. The aim of this work was to use a swellable polymer chosen among superdisintegrants, for improving the dissolution rate of a sparingly soluble drug, loaded on its surface. Nifedipine, which has a very low water solubility, was chosen as a model drug, while cross-linked sodium carboxymethylcellulose (Ac-Di-Sol) was chosen as the swellable polymer. The Nifedipine/Ac-Di-Sol systems were prepared using two different techniques: evaporation and spraying; in some preparations polyethylene glycol (PEG 1500), or sucrose palmitate (Sucrodet), or dioctyl sodium sulfosuccinate (Aerosol OT) were added. The results of the dissolution tests showed that the dissolution rate of Nifedipine from the systems prepared increases, particularly in the case of the preparation composed of Ac-Di-Sol plus surfactant agents.
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