Serunai - leaf提取物(Chromolaena - L)的纳米胶囊的特性,通过采用不同的吹气方法进行分化

Roosma Hatmayana, Noval Noval, Dede Mahdiyah, R. Ramadhani, Nurul Auliyani
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摘要

龙葵(Chromolaena odorata L.)是一种具有广泛药用价值的植物,其抗糖尿病作用是其中之一。但是使用植物提取物治疗在活性物质的溶解度和体内的生物利用度方面存在缺点。纳米胶囊是粒子技术中的一种系统,它可以利用一种聚合物来封装活性物质,并将其缓慢地释放到预定的目标上,从而解决这个问题。为了实现这一目标,纳米胶囊的制造必须满足几个特性要求,如粒径、潜在ζ、吸收效率和乳液稳定性。本研究通过壳聚糖-海藻酸盐的变化,确定了丝蚕叶提取物纳米胶囊的特性,并确定了壳聚糖-海藻酸盐的变化对纳米胶囊特性的影响。本研究为单组后测设计的实验室实验研究。采用乳化液扩散法制备白叶提取物纳米胶囊,并对其进行了粒径测定、电位zeta测定、吸收效率(%EE)测试和乳化液稳定性测试。公式I的粒径为196.4 nm,公式II为264.2 nm,公式III为207.4 nm,电势为zeta,公式I为-36.1 mV,公式II为-40.1 mV,公式III为-36.5 mV,公式I %EE值为99.7%,公式II为99.8%,公式III为99.7%,所有公式均表示乳液类型为m/a。三种配方均满足纳米胶囊特性要求。当壳聚糖浓度为0.3%,海藻酸盐浓度为0.6%时,得到的配方最佳,因此壳聚糖和海藻酸盐的变化会影响表征结果。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Karakterisasi Nanokapsul Ekstrak Daun Serunai (Chromolaena odorata L.) dengan Variasi Kitosan-Alginat Menggunakan Metode Emulsi-Difusi
Serunai (Chromolaena odorata L.) is a plant that has been widely used in medicine, one of which is as an antidiabetic. But treatment using plant extracts has drawbacks to the solubility of the active substance and its bioavailability in the body. Nanocapsules are one of the systems in particle technology that can solve this problem by utilizing a polymer that will encapsulate the active substance and release it slowly at the intended target. To achieve this, the manufacture of nanocapsules must meet several characteristic requirements such as particle size, potential zeta, absorption efficiency, and emulsion stability. This study was conducted to identify the nanocapsules characteristics of Serunai leaf extract (Chromolaena odorata L.) with chitosan-alginate variations and identify the influence of chitosan-alginate variations on the characteristics of nanocapsules. This study is a laboratory experimental study with a one-group posttest-only design. The manufacture of Serunai leaf extract nanocapsules using the emulsion-diffusion method, which is then characterized including particle size determination, potential zeta determination, absorption efficiency test (%EE), and emulsion stability test. The results obtained from the determination of the particle size of Formula I 196.4 nm, Formula II 264.2 nm, and Formula III 207.4 nm, potential zeta Formula I -36.1 mV, Formula II -40.1 mV, and Formula III -36.5 mV, the formula I %EE values 99.7%, Formula II 99.8%, and Formula III 99.7%, as well as all formulas indicating the emulsion type m/a. Three formulas have met the requirements of nanocapsules characteristics. The formula is best obtained in Formula II with a chitosan concentration of 0.3% and alginate of 0.6%, so chitosan-alginate variations influence the characteristic results.
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