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构建脂质体递药系统的基石。

Building Blocks to Design Liposomal Delivery Systems.

机构信息

Department of Cytobiochemistry, Faculty of Biotechnology, University of Wroclaw, 50-383 Wroclaw, Poland.

Research and Development Center, Regional Specialist Hospital, Kamieńskiego 73a, 51-124 Wroclaw, Poland.

出版信息

Int J Mol Sci. 2020 Dec 15;21(24):9559. doi: 10.3390/ijms21249559.

Abstract

The flexibility of liposomal carriers does not just simply rely on their capability to encapsulate various types of therapeutic substances, but also on the large array of components used for designing liposome-based nanoformulations. Each of their components plays a very specific role in the formulation and can be easily replaced whenever a different therapeutic effect is desired. It is tempting to describe this by an analogy to Lego blocks, since a whole set of structures, differing in their features, can be designed using a certain pool of blocks. In this review, we focus on different design strategies, where a broad variety of liposomal components facilitates the attainment of straightforward control over targeting and drug release, which leads to the design of the most promising systems for drug delivery. The key aspects of this block-based architecture became evident after its implementation in our recent works on liposomal carriers of antisense oligonucleotides and statins, which are described in the last chapter of this review.

摘要

脂质体载体的灵活性不仅取决于其封装各种类型治疗物质的能力,还取决于用于设计基于脂质体的纳米制剂的大量成分。它们的每个成分在制剂中都起着非常特定的作用,并且只要需要不同的治疗效果,就可以轻松更换。用乐高积木来描述这一点很诱人,因为可以使用特定的积木池设计出一套结构不同的结构。在这篇综述中,我们重点介绍了不同的设计策略,其中广泛的脂质体成分有助于直接控制靶向和药物释放,从而设计出最有前途的药物传递系统。在最后一章中,我们描述了反义寡核苷酸和他汀类药物的脂质体载体的最近研究工作,这一基于积木的架构的关键方面在这些工作中得到了体现。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ce48/7765547/7cf83b37af01/ijms-21-09559-g001.jpg

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