Rational Design of Zwitterionic Nanosystems to Overcome Biological Barriers for Drug Delivery by Various Administration Routes.

IF 8.2
Jiahui Ma, Dongyue Ding, Rui Xu, Shuxian Ma, Yinan Zhong, Wei Liu, Liqing Gao, Wei Chen
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Abstract

The drug delivery nanosystems (DDNS) have demonstrated excellent potential in numerous drug modifications reliant on the physical and chemical properties. However, the main challenge in the clinical application transformation of DDNS lies in the biological barriers between the administration site and the target site, which hinders efficient drug transport. The polyethylene glycol (PEG)-modified stealth strategies that have been clinically approved have also been questioned due to inherent defects such as accelerated blood clearance and specific immune responses. As an alternative to PEG, zwitterion polymers with characteristics including forming a strong hydration layer, extremely low immunogenicity, and ultra-delayed blood circulation time have stood out in the surface modification of DDNS for various administration routes. This review introduces the biological barriers faced by drugs in various administration routes, elaborates on the advantages of the inherent properties of zwitterions in overcoming these barriers, and focuses on the latest progress in how zwitterions can flexibly modify DDNS to achieve superior delivery efficiency and efficacy in various administration routes. Finally, the rational design of zwitterion-modified DDNS for future disease treatment is envisioned. This article is categorized under: Therapeutic Approaches and Drug Discovery > Emerging Technologies.

合理设计两性离子纳米系统以克服不同给药途径给药的生物障碍。
药物传递纳米系统(DDNS)在许多依赖于物理和化学性质的药物修饰方面显示出优异的潜力。然而,DDNS临床应用转化的主要挑战在于给药部位与靶点之间存在生物屏障,阻碍了药物的高效转运。经临床批准的聚乙二醇(PEG)修饰的隐形策略也因其固有缺陷(如加速血液清除和特异性免疫反应)而受到质疑。两性阴离子聚合物作为PEG的替代品,具有形成强水合层、极低免疫原性、超延迟血液循环时间等特点,在各种给药途径的DDNS表面改性中脱颖而出。本文介绍了药物在各种给药途径中面临的生物屏障,阐述了两性离子的固有特性在克服这些屏障方面的优势,并重点介绍了两性离子如何灵活修饰DDNS以在各种给药途径中获得优异的给药效率和疗效的最新进展。最后,对两性离子修饰DDNS的合理设计进行了展望。本文分类如下:治疗方法和药物发现>新兴技术。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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CiteScore
17.60
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