Suppr超能文献

多糖基水凝胶药物传递技术与制剂设计。

Technologies and Formulation Design of Polysaccharide-Based Hydrogels for Drug Delivery.

机构信息

Department of Pharmacy, University of Salerno, Via Giovanni Paolo II 132, I-84084 Fisciano (SA), Italy.

Department of Pharmacy and Pharmaceutical Technology, University of Santiago de Compostela, 15782 Santiago de Compostela, Spain.

出版信息

Molecules. 2020 Jul 10;25(14):3156. doi: 10.3390/molecules25143156.

Abstract

Polysaccharide-based hydrogel particles (PbHPs) are very promising carriers aiming to control and target the release of drugs with different physico-chemical properties. Such delivery systems can offer benefits through the proper encapsulation of many drugs (non-steroidal and steroidal anti-inflammatory drugs, antibiotics, etc) ensuring their proper release and targeting. This review discusses the different phases involved in the production of PbHPs in pharmaceutical technology, such as droplet formation (SOL phase), sol-gel transition of the droplets (GEL phase) and drying, as well as the different methods available for droplet production with a special focus on prilling technique. In addition, an overview of the various droplet gelation methods with particular emphasis on ionic cross-linking of several polysaccharides enabling the formation of particles with inner highly porous network or nanofibrillar structure is given. Moreover, a detailed survey of the different inner texture, in xerogels, cryogels or aerogels, each with specific arrangement and properties, which can be obtained with different drying methods, is presented. Various case studies are reported to highlight the most appropriate application of such systems in pharmaceutical field. We also describe the challenges to be faced for the breakthrough towards clinic studies and, finally, the market, focusing on the useful approach of safety-by-design (SbD).

摘要

多糖水凝胶颗粒(PbHPs)是一种非常有前途的载体,旨在控制和靶向释放具有不同物理化学性质的药物。这种给药系统可以通过适当封装许多药物(非甾体和甾体抗炎药、抗生素等)来提供益处,确保它们的适当释放和靶向。本文讨论了制药技术中生产 PbHPs 的不同阶段,如液滴形成(SOL 相)、液滴的溶胶-凝胶转变(GEL 相)和干燥,以及用于液滴生产的不同方法,特别关注造粒技术。此外,还概述了各种液滴凝胶化方法,特别强调了几种多糖的离子交联,能够形成具有内部高度多孔网络或纳米纤维结构的颗粒。此外,还详细研究了不同的内部结构,即干凝胶、冷冻凝胶或气凝胶,每种都具有特定的排列和性质,可以通过不同的干燥方法获得。报告了各种案例研究,以突出此类系统在制药领域的最适应用。我们还描述了在向临床研究突破时面临的挑战,最后,我们还关注了安全设计(SbD)的有用方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/5ada/7397281/7c1b86e34731/molecules-25-03156-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验