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壳聚糖-酪蛋白酸钠聚电解质复合物的纳米粒子和胶体水凝胶用于药物控制释放应用。

Nanoparticles and Colloidal Hydrogels of Chitosan-Caseinate Polyelectrolyte Complexes for Drug-Controlled Release Applications.

机构信息

Laboratory for Sensors, Institute of Microsystems Engineering IMTEK, University of Freiburg, 79110 Freiburg, Germany.

Freiburg Materials Research Center FMF, University of Freiburg, 79104 Freiburg, Germany.

出版信息

Int J Mol Sci. 2020 Aug 5;21(16):5602. doi: 10.3390/ijms21165602.

Abstract

Chitosan-caseinate nanoparticles were synthesized by polyelectrolyte complex (PEC) formation. Caseinate is an anionic micellar nanocolloid in aqueous solutions, which association with the polycationic chitosan yielded polyelectrolyte complexes with caseinate cores surrounded by a chitosan corona. The pre-structuration of caseinate micelles facilitates the formation of natural polyelectrolyte nanoparticles with good stability and sizes around 200 nm. Such natural nanoparticles can be loaded with molecules for applications in drug-controlled release. In the nanoparticles processing, parameters such as the chitosan degree of acetylation (DA) and molecular weight, order of addition of the polyelectrolytes chitosan (polycation) and caseinate (polyanion), and added weight ratio of polycation:polyanion were varied, which were shown to influence the structure of the polyelectrolyte association, the nanoparticle size and zeta potential. Attenuated total reflection-Fourier transform infrared (ATR-FTIR) analyses revealed the chemical structure of hydrogel colloidal systems consisting of nanoparticles that contain chitosan and caseinate. Transmission electron microscopy (TEM) allowed further characterization of the spherical morphology of the nanoparticles. Furtherly, insulin was chosen as a model drug to study the application of the nanoparticles as a safe biodegradable nanocarrier system for drug-controlled release. An insulin entrapment efficiency of 75% was achieved in the chitosan-caseinate nanoparticles.

摘要

壳聚糖-酪蛋白纳米粒子通过聚电解质复合物(PEC)形成合成。酪蛋白是一种在水溶液中带负电荷的胶束纳米胶体,与带正电荷的壳聚糖结合,生成以酪蛋白为核心、壳聚糖为壳的聚电解质复合物。酪蛋白胶束的预结构化有利于形成具有良好稳定性和粒径约为 200nm 的天然聚电解质纳米粒子。这种天然纳米粒子可以负载分子,用于药物控制释放等应用。在纳米粒子的处理过程中,改变了壳聚糖的乙酰化度(DA)和分子量、聚电解质壳聚糖(聚阳离子)和酪蛋白(聚阴离子)的添加顺序以及添加的聚阳离子:聚阴离子的重量比等参数,这些参数影响聚电解质缔合的结构、纳米粒子的大小和zeta 电位。衰减全反射-傅里叶变换红外(ATR-FTIR)分析揭示了包含壳聚糖和酪蛋白的水凝胶胶体系统的化学结构。透射电子显微镜(TEM)进一步对纳米粒子的球形形态进行了表征。此外,胰岛素被选为模型药物,以研究纳米粒子作为安全可生物降解的载药控释纳米载体系统的应用。壳聚糖-酪蛋白纳米粒子的胰岛素包封效率达到 75%。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/14a2/7460567/3cc48ea38384/ijms-21-05602-g001.jpg

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