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基于负载人参皂苷 Rb1 的壳聚糖/海藻酸钠纳米复合膜的新型药物传递系统。

Novel Drug Delivery System Based on Ginsenoside Rb1 Loaded to Chitosan/Alginate Nanocomposite Films.

机构信息

Institute for Tropical Technology, VAST, 18, Hoang Quoc Viet, Cau Giay, Ha Noi, 100000, Vietnam.

Global Innovation Centre for Advanced Nanomaterials, The University of Newcastle, University Drive, Callaghan NSW 2308, Australia.

出版信息

J Nanosci Nanotechnol. 2019 Jun 1;19(6):3293-3300. doi: 10.1166/jnn.2019.16116.

Abstract

Recently, drug delivery using natural and biodegradable nanoparticles has attracted huge attention. This study focused to deliver an anti-cancer and anti-inflammatory drug Ginsenoside Rb1 through chitosan-Alginate nanocomposite film prepared by solution method. Ginsenoside Rb1 is a dammaran saponin group, which is extracted from an herbaceous plant . Ginsenoside loaded alginate-chitosan nanocomposite films were characterized by Fourier transform infrared spectroscopy (FT-IR), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) methods. The FTIR spectra of alginate/chitosan/ginsenoside Rb1 nanocomposite films show that chitosan, alginate, and ginsenoside Rb1 are linked through the hydrogen bonding and dipolar-dipolar interactions. The FESEM image indicates that the chitosan and ginsenoside Rb1 dispersed well in the alginate matrix. The DSC diagrams display that melting temperature of alginate/chitosan/ginsenoside Rb1 nanocomposite films higher than that of chitosan and lower than that of alginate. It means that alginate and chitosan interact together. Investigation of the ginsenoside Rb1 release from alginate/chitosan/ginsenoside Rb1 nanocomposite films at different pH solutions and different ginsenoside Rb1 content has been carried out by ultraviolet-visible spectroscopy method. The rate of drug release is proportional to the increase in pH solution and inversely proportional to the content of loaded ginsenoside Rb1. The Rb1 release process includes two stages: burst release in the first 10 hours, then constant release afterwards. The suitable ratio of alginate/chitosan to prepare the alginate/chitosan/ginsenoside Rb1 nanocomposite films for further investigations was found out to be 8:2. Ginsenoside Rb1 release process from alginate/chitosan/ginsenoside Rb1 nanocomposite films was believed to be first-order kinetics in the first stage, and then the Rb1 release complies with Higuchi kinetic model in the slow release stage. This study demonstrated the novel synthesis methodology to design drug delivery system based on ginsenoside Rb1 loaded to chitosan/alginate nanocomposite films.

摘要

最近,利用天然和可生物降解的纳米粒子进行药物输送引起了极大的关注。本研究专注于通过溶液法制备壳聚糖-海藻酸钠纳米复合材料膜来输送抗癌和抗炎药物人参皂苷 Rb1。人参皂苷 Rb1 是一种达玛烷皂苷组,从草本植物中提取而来。用人参皂苷 Rb1 负载的海藻酸钠-壳聚糖纳米复合材料膜的特征通过傅里叶变换红外光谱(FT-IR)、扫描电子显微镜(SEM)和差示扫描量热法(DSC)方法进行分析。海藻酸钠/壳聚糖/人参皂苷 Rb1 纳米复合材料膜的 FTIR 光谱表明壳聚糖、海藻酸钠和人参皂苷 Rb1 通过氢键和偶极-偶极相互作用连接。FESEM 图像表明壳聚糖和人参皂苷 Rb1 在海藻酸钠基质中分散良好。DSC 图显示,海藻酸钠/壳聚糖/人参皂苷 Rb1 纳米复合材料膜的熔融温度高于壳聚糖而低于海藻酸钠。这意味着海藻酸钠和壳聚糖相互作用。通过紫外可见光谱法研究了不同 pH 值溶液和不同人参皂苷 Rb1 含量下从海藻酸钠/壳聚糖/人参皂苷 Rb1 纳米复合材料膜中释放人参皂苷 Rb1 的情况。药物释放速率与 pH 值溶液的增加成正比,与负载的人参皂苷 Rb1 含量成反比。Rb1 释放过程包括两个阶段:前 10 小时内的快速释放,然后是随后的恒速释放。发现用于进一步研究的制备海藻酸钠/壳聚糖/人参皂苷 Rb1 纳米复合材料膜的合适的海藻酸钠/壳聚糖比例为 8:2。从海藻酸钠/壳聚糖/人参皂苷 Rb1 纳米复合材料膜中释放人参皂苷 Rb1 的过程在第一阶段被认为是一级动力学,然后在缓慢释放阶段,Rb1 释放符合 Higuchi 动力学模型。本研究证明了一种新的合成方法,用于设计基于负载有人参皂苷 Rb1 的壳聚糖/海藻酸钠纳米复合材料膜的药物输送系统。

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