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首页> 外文期刊>Daru Journal of pharmaceutical sciences. >Obtainment of the spray-dried extracts of Peperomia pellucida L. (H.B.K.) using different atomization temperatures: physicochemical characterization and technological development for pharmaceutical applications
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Obtainment of the spray-dried extracts of Peperomia pellucida L. (H.B.K.) using different atomization temperatures: physicochemical characterization and technological development for pharmaceutical applications

机译:使用不同的雾化温度获得Peperomia pellucida L.(H.B.K.)的喷雾干燥提取物:药物化学表征和药物应用的技术开发

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Spray-dried extracts are prepared as powders or granules after solvent removal, which can be obtained in the presence or absence of pharmaceutical adjuvants. This work aimed to optimize the process of obtaining dried extracts of Peperomia pellucida L. (HBK) by spray drying. The characterization of the extract was performed by thermal analysis, specific surface area, particle size and high performance liquid chromatography (HPLC); then, capsules were developed for antimicrobial treatment, evaluating four bench lots by the determination of the angle of repose and time of flow, scanning electron microscopy, porosity and physicochemical quality control. There were no significant differences between the extracts obtained by spray drying at atomization temperatures of 140?°C, 160?°C and 180?°C, which was confirmed by thermal analysis. Specific surface area varied inversely with the mean particle size. Regarding the marker content by HPLC, no significant differences were found between the samples, although the flavonoid fraction was more stable at 160?°C. Bench lots (I to IV) were developed using the diluents Flowlac?, Starch? 1500, microcrystalline cellulose 250 and Cellactose? 80. Based on the results, the bench lot I, containing Flowlac?, was selected. The results of physicochemical quality control demonstrated that the selected formulation meets the pre-established parameters, and proving to be economically viable.
机译:在去除溶剂后,制备喷雾干燥的提取物作为粉末或颗粒,其可以在药物佐剂的存在或不存在中获得。这项工作旨在通过喷雾干燥优化获得甘草蛋白皮细胞干燥提取物的方法。提取物的表征通过热分析,比表面积,粒度和高性能液相色谱(HPLC)进行;然后,开发胶囊用于抗微生物处理,通过测定流动角度和流动时间,扫描电子显微镜,孔隙度和物理化学质量控制来评估四个台面批次。通过在140℃,160℃和180℃的雾化温度下喷雾干燥而获得的提取物之间没有显着差异,通过热分析确认。比表面积与平均粒径相同。关于HPLC的标记含量,样品之间没有发现显着的差异,尽管在160℃下黄酮级分数更稳定。使用稀释剂流动液(I至IV)开发了替补队(i至IV)? 1500,微晶纤维素250和细胞粘膜? 80.根据结果,选择了替补批次I,含流量的填料。物理化学质量控制的结果证明,所选配方符合预先建立的参数,并证明在经济上可行。

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