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首页> 外文期刊>International Journal of Pharmaceutics >Evaluation of drug-carrier interactions in quaternary powder mixtures containing perindopril tert-butylamine and indapamide
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Evaluation of drug-carrier interactions in quaternary powder mixtures containing perindopril tert-butylamine and indapamide

机译:含有培哚普利叔丁胺和吲达帕胺的四元粉末混合物中药物-载体相互作用的评价

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摘要

Interactions occurring between components in the quaternary powder mixtures consisting of perindopril tert-butylamine, indapamide (active pharmaceutical ingredients), carrier substance and hydrophobic colloidal silica were examined. Two grades of lactose monohydrate: Spherolac (R) 100 and Granulac (R) 200 and two types of microcrystalline cellulose: M101D+ and Vivapur (R) 102 were used as carriers. We determined the size distribution (laser diffraction method), morphology (scanning electron microscopy) and a specific surface area of the powder particles (by nitrogen adsorption-desorption). For the determination of the surface energy of powder mixtures the method of inverse gas chromatography was applied. Investigated mixtures were characterized by surface parameters (dispersive component of surface energy, specific interactions parameters, specific surface area), work of adhesion and cohesion as well as Flory-Huggins parameter chi(23). Results obtained for all quaternary powder mixtures indicate existence of interactions between components. The strongest interactions occur for both blends with different types of microcrystalline cellulose (PM-1 and PM-4) while much weaker ones for powder mixtures with various types of lactose (PM-2 and PM-3). Published by Elsevier B.V.
机译:检查了由培哚普利叔丁胺,吲达帕胺(活性药物成分),载体物质和疏水性胶体二氧化硅组成的季粉末混合物中各组分之间的相互作用。两种等级的乳糖一水合物:Spherolac(R)100和Granulac(R)200以及两种类型的微晶纤维素:M101D +和Vivapur(R)102被用作载体。我们确定了粉末颗粒的尺寸分布(激光衍射法),形态(扫描电子显微镜)和比表面积(通过氮吸附-脱附)。为了测定粉末混合物的表面能,使用了反相气相色谱法。所研究的混合物的特征在于表面参数(表面能的分散成分,比相互作用参数,比表面积),附着力和内聚功以及Flory-Huggins参数chi(23)。所有四元粉末混合物获得的结果表明组分之间存在相互作用。两种混合物与不同类型的微晶纤维素(PM-1和PM-4)的相互作用最强,而与各种乳糖(PM-2和PM-3)的粉末混合物的相互作用则弱得多。由Elsevier B.V.发布

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