Cwiertnia Barbara
Poznań University of Medical Sciences, Department of Inorganic and Analytical Chemistry 6 Grunwaldzka Street, 60-780 Poznań, Poland.
Acta Pol Pharm. 2006 Mar-Apr;63(2):135-9.
Pharmaceutical availability of diazepam, oxazepam and nitrazepam from solid dispersions of PEG 6000 have been studied in comparison with corresponding physical mixtures and pure benzodiazepines. Selected derivatives of 1,4-benzodiazepin-2-one are poorly water soluble drugs. The aim of this work was to report the properties of diazepam- and nitrazepam-PEG 6000 solid dispersions. Differential scanning calorimetry (DSC) and X-ray diffraction were used to characterize the solid dispersions. The effect of PEG 6000 on the dissolution of selected derivatives of 1,4-benzodiazepin-2-one was investigated. The dissolution of diazepam, oxazepam and nitrazepam from its solid dispersions increased in the presence of PEG 6000.
已对聚乙二醇6000(PEG 6000)固体分散体中地西泮、奥沙西泮和硝西泮的药物可利用性进行了研究,并与相应的物理混合物和纯苯二氮䓬类药物进行了比较。1,4-苯二氮䓬-2-酮的选定衍生物是水溶性较差的药物。这项工作的目的是报告地西泮-PEG 6000和硝西泮-PEG 6000固体分散体的性质。采用差示扫描量热法(DSC)和X射线衍射对固体分散体进行表征。研究了PEG 6000对1,4-苯二氮䓬-2-酮选定衍生物溶解的影响。在PEG 6000存在下,地西泮、奥沙西泮和硝西泮从其固体分散体中的溶出度增加。