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.

Rosali Maria Ferreira da Silva, Thays Cristiane Barbosa Lucena Gomes, Adriana Fernandes Campos, Williana Tôrres Vilela, Pollyne Amorim Silva, Victor de Albuquerque Wanderley Sales, Giovanna Christinne Rocha de Medeiros Schver, Keyla Emmanuelle Ramos da Silva, Salvana Priscylla Manso Costa, Fábio Santos de Souza, Manolo Cleiton Costa de Freitas, Mara Sílvia Pinheiro Arruda, Milton Nascimento da Silva, Pedro José Rolim Neto
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引用次数: 2

Abstract

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.

不同雾化温度下透明胡椒喷雾干燥提取物的制备:理化性质及制药应用技术研究。
喷雾干燥提取物经溶剂去除后制成粉末或颗粒,可在存在或不存在药物佐剂的情况下获得。本研究旨在优化喷雾干燥法制备透明胡椒(Peperomia pellucida L., HBK)提取物的工艺条件。采用热分析法、比表面积法、粒径法和高效液相色谱法对提取物进行表征;然后开发抗菌胶囊,通过静息角、流动时间、扫描电镜、孔隙度和理化质量控制等指标对4批样品进行评价。在雾化温度为140°C、160°C和180°C时,喷雾干燥得到的提取物无显著差异,热分析证实了这一点。比表面积与平均粒径成反比。HPLC法测定的标记物含量差异不显著,但黄酮类成分在160℃时更为稳定。使用稀释剂Flowlac®,Starch®1500,微晶纤维素250和Cellactose®80开发工作台批次(I至IV)。根据结果,选择了含有Flowlac®的第1批样品。理化质量控制结果表明,所选配方符合预先设定的参数,经济上可行。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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