积雪草叶乙醇提取物聚乳酸凝胶的体外释放性能

Mardiyanto, E. F. Apriani, Pandu Kalingga Jati
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引用次数: 0

摘要

背景:积雪草(Centella asiatica L.)叶被证明含有高浓度的黄酮类化合物作为抗氧化剂。黄酮类化合物是一种不稳定的化合物,受光照、湿度、pH值和氧气等环境影响。pegagan提取物的稳定性已被证明通过将提取物制成纳米颗粒制剂来提高。目的:本研究旨在将聚乙二醇纳米颗粒配制成凝胶制剂,并使用玻璃纸膜进行Franz扩散试验,与未配制成纳米颗粒的聚乙二醇凝胶相比,测定其释放能力。方法:用聚乳酸-乙醇酸聚合物制备纳米颗粒,然后将其配制成不同浓度的Carbopol 934凝胶,即1%、1.5%和2%。然后对凝胶纳米粒子进行制剂的表征、稳定性测试和释放测试。结果:1%Carbopol 934的浓度提供了凝胶制剂的最佳评价,其中产生的凝胶是均匀的,pH约为6.2,粘度为3417.12cPs,铺展性为5.1cm,粘附力为209.33秒。稳定性试验表明,在感官和pH值方面没有显著变化(p>0.05)。释放动力学模型为零级。F1具有比其他制剂更高的反应动力学常数(k),因此药物释放发生得更快。结论:筛选出的聚乙二醇(F1)纳米粒子凝胶具有良好的物理稳定性和释放性能。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
In Vitro Release Ability of Nanoparticles Poly-Lactic-Co-Glycolic-Acid (PLGA) Gel Containing Pegagan Leaves Ethanolic Extract (Centella asiatica L.)
Background: Pegagan (Centella asiatica L.) leaves are proven to contain high concentrations of flavonoid compounds as antioxidants. Flavonoids are unstable compounds due to environmental influences such as light, humidity, pH, and oxygen. The stability of pegagan extract was proven to be improved by making the extract into nanoparticle preparations. Objective: This study aims to formulate nanoparticles of pegagan into gel preparations and determine their release ability with the Franz diffusion test using a cellophane membrane compared to pegagan gel not formulated into nanoparticles. Methods: Nanoparticles were made using poly-lactic-co-glycolic acid polymers and then formulated into gels with various concentrations of Carbopol 934, namely 1, 1.5 and 2%. The gel nanoparticles were then subjected to the characterization of the preparation, stability test and release test of the preparation. Results: A concentration of 1% Carbopol 934 provides the best evaluation of gel preparations where the gel produced was homogeneous, pH was around 6.2, viscosity was 3417.12 cPs, spreadability was 5.1 cm, and adhesion was 209.33 seconds. The stability test showed no significant organoleptic and pH changes (p>0.05). The release kinetics model occurs at zero order. F1 has a higher reaction kinetics constant (k) than the other formulations, so drug release occurs faster. Conclusion: The best formula of pegagan (F1) nanoparticle gel was proven to have good physical stability and release ability.
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