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Preparation and physicochemical characterization of 5 niclosamide solvates and 1 hemisolvate

机译:5种烟酰胺和1种半溶剂化物的制备及理化性质

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摘要

The purpose of the study was to characterize the physicochemical, structural, and spectral properties of the 1∶1 niclosamide and methanol, diethyl ether, dimethyl sulfoxide, N,N' dimethylformamide, and tetrahydrofuran solvates and the 2∶1 niclosamide and tetraethylene glycol hemisolvate prepared by recrystallization from these organic solvents. Structural, spectral, and thermal analysis results confirmed the presence of the solvents and differences in the structural properties of these solvates. In addition, differences in the activation energy of desolvation, batch solution calorimetry, and the aqueous solubility at 25°C, 24 hours, showed the stability of the solvates to be in the order: anhydrate > diethyl ether solvate > tetraethylene glycol hemisolvate > methanol solvate > dimethyl sulfoxide solvate > N,N' dimethylformamide solvate. The intrinsic and powder dissolution rates of the solvates were in the order: anhydrate > diethyl ether solvate > tetraethylene glycol hemisolvate > N,N' dimethylformamide solvate > methanol solvate > dimethyl sulfoxide solvate. Although these nonaqueous solvates had higher solubility and dissolution rates than the monohydrous forms, they were unstable in aqueous media and rapidly transformed to one of the monohydrous forms.
机译:该研究的目的是表征1∶1的新洛氨酰胺和甲醇,乙醚,二甲基亚砜,N,N'二甲基甲酰胺和四氢呋喃溶剂化物以及21:1的新洛氨酰胺和四甘醇半溶剂化物的物理化学,结构和光谱性质通过从这些有机溶剂中重结晶制备。结构,光谱和热分析结果证实了溶剂的存在以及这些溶剂化物的结构性质差异。另外,去溶剂化的活化能,分批溶液量热法和在25°C,24小时的水溶解度的差异表明溶剂化物的稳定性依次为:无水物>乙醚溶剂化物>四甘醇半溶剂化物>甲醇溶剂化物>二甲基亚砜溶剂化物> N,N'二甲基甲酰胺溶剂化物。溶剂化物的本征和粉末溶解速率的顺序为:无水物>乙醚溶剂化物>四乙二醇半溶剂化物> N,N'二甲基甲酰胺溶剂化物>甲醇溶剂化物>二甲基亚砜溶剂化物。尽管这些非水溶剂化物的溶解度和溶解度均高于一水形式,但它们在水性介质中不稳定并迅速转变为一水形式。

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