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Methylprednisolone acetate–Eudragitsup?/sup RS100 electrospuns: Preparation and physicochemical characterization

机译:醋酸甲基泼尼松龙-Eudragit ? RS100电纺丝:制备和理化特性

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Abstract The aim of the present study was to formulate methylprednisolone acetate -Eudragit? RS100 nanofibers and nanobeads by the electrospinning method. The physicochemical characteristics of the prepared electrospuns were assessed as well. The particle size and morphology were evaluated using scanning electron microscopy. The crystallinity of the drug in the nanofibers and nanobeads obtained was also studied by X-ray crystallography and differential scanning calorimetry (DSC) thermograms. In addition, FT-IR spectroscopy was applied to investigate any possible chemical interaction between the drug and carrier during the preparation process. The drug release kinetics were considered, to predict the release mechanism. Increasing the concentration of the injected solution resulted in the production of more nanofibers and less nanobeads, with the particle size ranging from 100 to 500 nm. The drug crystallinity was decreased during the electrospinning process; however, no interaction between drug and polymer was observed. The electrospuns showed faster drug release pattern compared to the pure drug. The release data were best fitted to the Weibull model, in which the corresponding shape factor values of the model were less than 0.75 indicating the diffusion mechanism of drug release. In conclusion, electrospinning could be considered as a simple and cost effective method for fabricating the drug: polymer nanofibers and nanobeads.
机译:摘要本研究的目的是制备乙酸甲泼尼龙-Eudragit? RS100纳米纤维和纳米珠通过静电纺丝法制成。还评估了制备的电纺丝的理化特性。使用扫描电子显微镜评估粒度和形态。还通过X射线晶体学和差示扫描量热法(DSC)热谱图研究了所得药物在纳米纤维和纳米珠中的结晶度。此外,FT-IR光谱学被用于研究在制备过程中药物与载体之间任何可能的化学相互作用。考虑药物释放动力学,以预测释放机理。增加注入溶液的浓度导致产生更多的纳米纤维和更少的纳米珠,其粒径范围为100至500 nm。在静电纺丝过程中,药物结晶度降低;然而,没有观察到药物和聚合物之间的相互作用。与纯药物相比,电纺丝显示出更快的药物释放模式。释放数据最适合Weibull模型,其中模型的相应形状因子值小于0.75,表明药物释放的扩散机制。总之,静电纺丝可以被认为是一种简单且经济高效的制造药物的方法:聚合物纳米纤维和纳米珠。

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