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Improved shellac mediated nanoscale application drug release effect in a gastric-site drug delivery system

机译:虫胶介导的纳米级应用在胃部位给药系统中的释药效果

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The development of biocompatible nanocomposites for biomedical applications such as drug release has attracted increasing attention in recent years. Shellac/sodium shellac nanofibers and nanoparticles were produced for drug delivery applications. Ketoprofen was loaded on the drug delivery system (DDS), and three schemes based on shellac/sodium shellac were chosen. The biocompatibility and nontoxicity of shellac and the promising results of the nanofibers and nanoparticles highlighted their challenging potential for controlled drug delivery applications. A significant increase of drug release rate can be observed at the gastric site. The prepared drug-loaded nanofibers and nanoparticles were characterized by scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The results show that the above-mentioned drug delivery system is able to support high-efficiency encapsulation. A new drug delivery system was designed and studied through shellac and sodium shellac. The application scope of shellac to DDSs is extended.
机译:近年来,用于生物医学应用如药物释放的生物相容性纳米复合材料的发展引起了越来越多的关注。紫胶/紫胶钠纳米纤维和纳米颗粒被生产用于药物递送应用。将酮洛芬装入药物递送系统(DDS)上,并选择了三种基于虫胶/虫胶钠的方案。虫胶的生物相容性和无毒性以及纳米纤维和纳米颗粒的有希望的结果凸显了其在受控药物递送应用中的挑战性潜力。在胃部位可以观察到药物释放速率的显着增加。通过扫描电子显微镜(SEM),傅立叶变换红外光谱(FTIR)和X射线衍射(XRD)对制备的载药纳米纤维和纳米颗粒进行表征。结果表明,上述药物递送系统能够支持高效封装。通过紫胶和紫胶钠设计并研究了一种新的药物递送系统。虫胶在DDS上的应用范围得到了扩展。

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