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pharmaceutical compositions derived from microemulsion-based gels, method for their preparation and new gels based on microemulsions.

机译:源自微乳液的凝胶的药物组合物,其制备方法和基于微乳液的新凝胶。

摘要

The invention relates to a composition PHARMACEUTICAL INCLUDING ONE MADE microemulsion a hydrophilic component, a lipophilic component, a surfactant and a drug, so that the hydrophilic component, the lipophilic component and surfactant form, when EXAMINE ON A SCALE macroscopic, a solution of a phase. The hydrophilic component is dispersed as droplets COLLOIDAL in the lipophilic component or lipophilic COMPONENT COLLOIDAL as droplets dispersed IN hydrophilic component. In another alternative Hydrophilic Lipophilic COMPONENTS AND FORMING A microemulsion with bicontinuous structure so SUCH COMPONENTS ADJACENT CHANNELS ARE EXTENDED. The drug is dissolved in the component dispersed OR, IN THE CASE OF AN bicontinuous microemulsion structure, hydrophilic or lipophilic COMPONENT. The microemulsion is stabilized by the surfactant. Characteristically ADD A gelling AND WATER EMULSION TO GIVING WELL TO THIS FORM OF GEL.
机译:本发明涉及一种药物组合物,其包含一种微乳液,其包含亲水性成分,亲脂性成分,表面活性剂和药物,从而当在宏观上进行考察时,亲水性成分,亲脂性成分和表面活性剂形成相溶液。 。亲水性组分以液滴COLLOIDAL的形式分散在亲脂性组分中或亲脂性COMPONENT COLLOIDAL以液滴形式分散在亲水性组分中。在另一个替代方案中,亲水亲脂性组分和形成具有双连续结构的微乳液,因此延伸了此类组分相邻的通道。药物溶解在分散的成分中,或者在双连续微乳液结构的情况下,溶解在亲水性或亲脂性成分中。微乳液被表面活性剂稳定。特征性地添加凝胶和水乳液以很好地形成这种形式的凝胶。

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