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壳聚糖-木质素磺酸盐超声化学制备纳米粒子:特性及潜在应用。

Chitosan-lignosulfonates sono-chemically prepared nanoparticles: characterisation and potential applications.

机构信息

Textile Engineering Department, University of Minho, Campus Azurém, 4800-058 Guimarães, Portugal.

出版信息

Colloids Surf B Biointerfaces. 2013 Mar 1;103:1-8. doi: 10.1016/j.colsurfb.2012.10.033. Epub 2012 Oct 30.

DOI:10.1016/j.colsurfb.2012.10.033
PMID:23178385
Abstract

Due to their recognised properties of biocompatibility, biodegradability and sustainability, chitosan nanocarriers have been successfully used as new delivery systems. In this work, nanoparticles combining chitosan and lignosulfonates were developed for the first time for cosmetic and biomedical applications. The ability of lignosulfonates to act as a counter polyion for stabilisation of chitosan particles, generated using high intensity ultrasound, was investigated. Several conditions for particles preparation were tested and optimised and the resulting nanoparticles were comprehensively characterised by measuring particle size, zeta potential and polydispersity index. The pH of chitosan solution, sonication time and the presence of an adequate surfactant, poloxamer 407, were determinant factors on the development of smaller particles with low polydispersity index (an average particle size of 230 nm was obtained at pH 5 after 8 min of sonication). The beneficial effects of lignosulfonates complex on chitosan nanoparticles were further characterised. Greater stability to lysozyme degradation, biocompatibility with human cells and antimicrobial activity was found upon lignosulfonates incorporation into chitosan nanoparticles. Furthermore, these particles were able to incorporate a hydrophilic model protein - RNase A. A burst release was observed when nanoparticles were loaded with low amount of protein while with high protein content, a sustained release was found, suggesting that the protein cargo maybe loaded both at the surface as in the bulk of the particle, depending on the concentration of drug incorporated.

摘要

由于壳聚糖纳米载体具有生物相容性、生物降解性和可持续性等特性,因此已被成功地用作新型递药系统。在这项工作中,首次开发了结合壳聚糖和木质素磺酸盐的纳米颗粒,用于化妆品和生物医学应用。研究了木质素磺酸盐作为抗衡离子稳定壳聚糖颗粒的能力,这些颗粒是使用高强度超声产生的。测试和优化了几种颗粒制备条件,并通过测量粒径、Zeta 电位和多分散指数对所得纳米颗粒进行了全面表征。壳聚糖溶液的 pH 值、超声时间以及适当的表面活性剂(泊洛沙姆 407)的存在是决定因素,可得到具有低多分散指数的较小颗粒(在 pH 5 下超声 8 分钟后,可得到平均粒径为 230nm 的颗粒)。进一步表征了木质素磺酸盐复合物对壳聚糖纳米颗粒的有益影响。发现木质素磺酸盐的掺入增加了壳聚糖纳米颗粒对溶菌酶降解的稳定性、与人细胞的生物相容性和抗菌活性。此外,这些颗粒能够包封亲水性模型蛋白 - RNase A。当纳米颗粒负载少量蛋白质时,观察到快速释放,而当蛋白质含量较高时,发现持续释放,表明蛋白质药物可能同时负载在颗粒表面和内部,这取决于所负载的药物浓度。

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