纳米生物聚合物药物递送载体的制备与表征

S. S. Sagiri, S. Nayak, S. Lakshmi, K. Pal
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摘要

近年来,生物聚合物纳米颗粒作为药物递送载体的使用呈指数增长。本研究分别采用离子凝胶法和脱溶法制备壳聚糖和明胶纳米颗粒。以水杨酸为模型药。采用扫描电镜(SEM)、x射线衍射(XRD)和红外光谱(FTIR)对纳米颗粒进行了表征。通过体外释药实验了解其释药机制。SEM显微图显示球形纳米颗粒的形成。XRD研究表明,壳聚糖纳米颗粒比明胶纳米颗粒具有更高的结晶性。红外光谱研究表明,水杨酸存在于载药纳米颗粒中。药物释放研究表明,所制备的纳米颗粒可作为多种生物活性药物的载体。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Preparation and Characterization of Biopolymeric Nanoparticles as Drug Delivery Vehicles
In recent years, the use of biopolymeric nanoparticles as vehicles for drug delivery has increased exponentially. In the present study, chitosan and gelatin nanoparticles were prepared by ionic gelation and desolvation methods, respectively. Salicylic acid was used as the model drug. The nanoparticles were characterized using SEM, XRD analysis and FTIR spectrophotometric studies. In vitro drug release experiments were carried out to understand the mechanism of drug release. SEM micrographs showed the formation of spherical nanoparticles. XRD studies indicated a higher crystalline nature of the chitosan nanoparticles as compared to the gelatin nanoparticles. FTIR studies indicated the presence of salicylic acid within the drug- loaded nanoparticles. Drug release studies indicated that the developed nanoparticles may be used as carriers for various bioactive agents.
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