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Comparison of various pharmaceutical properties of clobetasol propionate cream formulations - considering stability of mixture with moisturizer-

机译:氯贝辛醇丙酸盐配方的各种药物性能的比较 - 考虑到润肤液混合物的稳定性 -

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Background:The clobetasol propionate cream formulations (CLB Cr ) belong to the "strongest" group, and are used widely. In addition, those formulations are often used as a mixture with moisturizer. Recently, we evaluated pharmaceutical properties of the CLB Cr using near infrared (NIR) spectroscopy, and characteristic NIR spectra depending on the formulation were observed. In the present study, we attempted to evaluate the more diverse pharmaceutical properties of CLB Cr , including the stability of mixture of CLB Cr and moisturizer.Method:Pharmaceutical properties of CLB Cr were evaluated using from rheological characteristics, microscopic observation, dye permeability observations, electrical conductivity method, thermogravimetry-differential thermal analysis (TG-DTA) and near infrared (NIR) spectroscopy. Stability of mixtures of CLB Cr and moisturizer were evaluated using from dye method and NIR spectroscopy.Results:The hardness of Dermovate? (DRM), Glydil? (GDL), and Myalone? (MYA) was greater than that of CLB Cr . High concentrations of white beeswax were considered the reason for the hardness of DRM and GDL. On the other hand, the hardness of MYA may be due to the presence of macrogol 6000. After storage of the cream formulations discharged from the tube at room temperature, mass reduction and attenuation of the peak reflecting water of NIR spectroscopy occurred in a time-dependent manner, except for GDL and MYA. Only GDL was shown to be a w/o-type formulation by dye and electric conductivity measurements, which suggested that this was the reason for the lack of changes in the mass or NIR spectrum of samples after storage. In the NIR spectrum of MYA, the peak reflecting water slightly increased in a time-dependent manner, suggesting the water absorption of macrogol 6000. TG-DTA provided curves indicating the presence of water in each formulation, except for MYA, which was consistent with water quantification previously reported. Finally, when mixing the CLB Cr with a moisturizer, in any CLB Cr , the stability of the mixture with w/o-type moisturizer varies greatly depending on the each CLB Cr .Conclusion:Thus, even for cream formulations with the same active pharmaceutical ingredient, pharmaceutical properties and stability of mixture with moisturizer may different significantly.? The Author(s). 2020.
机译:背景:Clobetasol丙酸盐膏制剂(CLB CR)属于“最强”组,广泛使用。此外,这些制剂通常用作与保湿剂的混合物。最近,我们使用近红外(NIR)光谱评估了CLB CR的药物特性,并且观察到根据制剂的特征NIR光谱。在本研究中,我们试图评估Clb Cr的更多样化的药物性质,包括Clb Cr和保湿剂的混合物的稳定性。方法:使用流变学特征,微观观察,染料渗透性观察来评估Clb Cr的药物性质,电导率法,热重分析差分热分析(TG-DTA)和近红外(NIR)光谱。使用染料方法和NIR光谱评估CLB CR和保湿剂混合物的稳定性。结果:皮肤陶醉的硬度? (DRM),Glydil? (gdl)和myalone? (Mya)大于CLB CR的大小。高浓度的白色蜂蜡被认为是DRM和GDL硬度的原因。另一方面,MyA的硬度可能是由于宏子醇6000的存在。在室温下从管排出的乳膏制剂后,在一次峰值光谱的峰值反射水中的质量降低和衰减发生后 - 依赖方式,除了GDL和Mya。仅通过染料和电导率测量显示GDL是W / O型制剂,这表明这是储存后样品缺乏变化的原因。在MyA的NIR光谱中,反射水的峰值以时间依赖性方式略微增加,表明宏子醇6000的吸水率。TG-DTA提供了表明每种配方中水的存在的曲线,除了mya,除了Mya之外,它们是符合的以前报道的水量化。最后,当将CLB Cr与保湿霜混合时,在任何CLBCR中,与W / O型保湿剂的混合物的稳定性取决于每个CLB Cr。结论,因此,即使用于具有相同活性药物的乳膏配方与保湿剂的混合物的成分,药物性能和稳定性显着不同。作者。 2020。

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