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水溶性载体对双氯芬酸钠溶出曲线的影响。

Effect of water soluble carrier on dissolution profiles of diclofenac sodium.

作者信息

Cwiertnia Barbara

机构信息

Poznan University of Medical Sciences, Department of Inorganic and Analytical Chemistry, 6 Grunwaldzka St., 60-780 Poznań, Poland.

出版信息

Acta Pol Pharm. 2013 Jul-Aug;70(4):721-6.

Abstract

Pharmaceutical aviailability of diclofenac sodium from solid dispersions of PEG 6000 have been studied in comparison to those of the corresponding physical mixtures and pure diclofenac sodium. The diclofenac sodium is poorly water soluble drug. The properties of diclofenac sodium-PEG 6000 solid dispersions have been determined by the methods of differential scanning calorimetry (DSC), X-ray diffraction and scanning electron microscopy (SEM). The effect of PEG 6000 on the solubility of selected diclofenac sodium dispersions has been studied. The solubility of diclofenac sodium from its solid dispersion has been found to increase in the presence of PEG 6000.

摘要

已对双氯芬酸钠在聚乙二醇6000固体分散体中的药物可利用性进行了研究,并与相应的物理混合物和纯双氯芬酸钠进行了比较。双氯芬酸钠是一种水溶性较差的药物。采用差示扫描量热法(DSC)、X射线衍射法和扫描电子显微镜(SEM)等方法对双氯芬酸钠-聚乙二醇6000固体分散体的性质进行了测定。研究了聚乙二醇6000对所选双氯芬酸钠分散体溶解度的影响。发现在聚乙二醇6000存在下,双氯芬酸钠从其固体分散体中的溶解度增加。

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