不同胶凝剂对香豆醇提物天然凝胶的制备及评价

Dyera Forestryana, Annisa Hayati, Aristha Novyra Putri
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引用次数: 0

摘要

香莲花叶乙醇提取物中含有槲皮素,具有抗炎作用。凝胶剂型非常适合伤口愈合治疗,因为它给皮肤一种冷的感觉。本研究的目的是通过改变胶凝剂来制备香檀凝胶,比较天然胶凝剂、半合成胶凝剂和合成胶凝剂对香檀凝胶物理特性的影响。凝胶配方分为三种配方。评价包括感官,均匀性,铺展性,附着力,pH值和粘度。用溶出仪对最佳凝胶配方进行了释放研究。利用零阶、一阶、Higuchi和Korsmeyer-Peppas动力学方法确定释放动力学模型。感官检测结果显示,凝胶呈墨绿色,具有香桐香气,均匀性好。凝胶配方的pH值符合凝胶的物理质量标准。F1、F2和F3的展布性试验数据分别为12.16、14.66和10.75 g.cm/sec。F1、F2、F3粘附试验结果分别为11.66、10、47.33。F1的粘度为15750 cps, F2为4807 cps, F3为19380 cps。本研究得出了以Na-CMC为胶凝剂的最佳配方。F2的槲皮素释放量为42.76%,释放动力学模型符合Higuchi动力学。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Formulation and Evaluation of Natural Gel Containing Ethanolic Extract of Pandanus amaryllifolius R. Using Various Gelling Agents
Ethanol extract of Pandanus amaryllifolius leaves contains quercetin has anti-inflammatory properties. The gel dosage form is very appropriate for wound healing therapy because it gives a cold sensation to the skin. This study aims to formulate a P. amaryllifolius gel by variation of a gelling agent to compare the effect of a natural gelling agent, semi-synthetic gelling agent, and synthetic gelling agent on the physical characteristics of the gel. The gel formulation was made in three formulas. Evaluations include organoleptic, homogeneity, spreadability, adhesion, pH, and viscosity. The optimum gel formula was tested for release study using a dissolution apparatus 5. Determination of release kinetics model using the kinetics approach of zero-order, first-order, Higuchi, and Korsmeyer-Peppas. The organoleptic shows the gel's dark green color, P. amaryllifolius aromas, and good homogeneity. The gel formulas had pH values that matched the physical quality criteria of the gel. Data obtained for the spreadability test for F1, F2, and F3 were 12.16, 14.66, and 10.75 g.cm/sec, respectively. The F1, F2, and F3 adhesion test results were 11.66, 10, and 47.33, respectively. The viscosity of F1 was 15750 cps, F2 was 4807 cps, and F3 was 19380 cps. This study concludes that the optimum formula is obtained from the gelling agent of Na-CMC as a gelling agent. The number of quercetins released from F2 was 42.76%, and the release kinetics model followed the kinetics of Higuchi.
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