Developing transdermal patch from Momordica charantia L. fruit using polyvinyl alcohol and ethyl cellulose potentially as anti-inflammatory dosage form

Teti Indrawati, Zainur Rahman Hakim, Fiqi Fatimah
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Abstract

Introduction: Anti-inflammatory medication is currently sufficiently developed for the ease of application and effectiveness of therapy. Development of natural ingredients that are applied through the skin is needed to get a profitable product. This study aimed to develop bitter melon (Momordica charantia L.) fruit as an anti-inflammatory agent using transdermal patch preparations. Materials and Methods: Dried bitter melon powder was macerated using 96% ethanol, followed by evaporation until a viscous extract was obtained. Bitter melon fruit extract (BMFE) 30% was prepared into three patch transdermal preparations using combinations of polyvinyl alcohol (PVA) and ethyl cellulose (EC) as bases. A mixture of BMFE, propylene glycol, and glycerin was added to the bases and mixed until homogeneous. The entire mass was poured into a mold, coated with aluminum foil, allowed to stand for 24 h, and dried in an oven at 40 °C for 30 min. All preparations of the transdermal patch were evaluated for their physical and chemical characteristics as well as their anti-inflammatory effects Results: All transdermal patch preparations had solid form, visible brown, weight 0.424 -0.432 g, thickness 0.344 – 0.320 mm, folding endurance of more than 300, pH 4.84 – 4.87, and hygroscopicity 6.50 - 6.99 %. All preparations showed a decrease in the diameter of the edema, but this was not significant; after the 90th minute, the edema diameter was significantly reduced. Conclusion: This study showed that BMFE can be used for anti-inflammatory patch preparation and has the potential to be developed as a transdermal anti-inflammatory dosage form.
用聚乙烯醇和乙基纤维素制备苦瓜果透皮贴剂
导读:目前,抗炎药物的应用和治疗效果都得到了充分的发展。需要开发通过皮肤涂抹的天然成分,以获得有利可图的产品。本研究旨在利用透皮贴剂制备苦瓜(Momordica charantia L.)果实。材料与方法:用96%乙醇浸渍苦瓜干粉,蒸发至粘性浸出物。以30%的苦瓜果提取物(BMFE)为基料,以聚乙烯醇(PVA)和乙基纤维素(EC)为基料,配制成3种贴片透皮制剂。将BMFE、丙二醇和甘油的混合物加入到碱中并混合至均匀。整个质量注入模具,涂有铝箔,允许代表24小时,在烤箱和干30分钟40°C。皮肤药贴的所有准备工作的人都有各种各样的物理和化学特征以及它们的抗炎作用结果:所有皮肤药贴制剂固体形态,可见棕色,体重0.424 - -0.432 g,厚度0.344 - 0.320毫米,超过300的耐折度,pH值4.84 - 4.87,吸湿性6.50 - 6.99%。所有制剂均显示水肿直径减小,但不显著;90分钟后,水肿直径明显减小。结论:本研究表明BMFE可用于抗炎贴剂的制备,具有开发经皮抗炎剂型的潜力。
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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