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凝聚体:作为治疗性生物分子纳米结构递药载体的最新进展。

Coacervates: Recent developments as nanostructure delivery platforms for therapeutic biomolecules.

机构信息

College of Pharmacy, CHA University, Seongnam 13488, Republic of Korea.

College of Pharmacy, CHA University, Seongnam 13488, Republic of Korea.

出版信息

Int J Pharm. 2022 Aug 25;624:122058. doi: 10.1016/j.ijpharm.2022.122058. Epub 2022 Jul 26.

Abstract

Coacervation is a liquid-liquid phase separation that can occur in solutions of macromolecules through self-assembly or electrostatic interactions. Recently, coacervates composed of biocompatible macromolecules have been actively investigated as nanostructure platforms to encapsulate and deliver biomolecules such as proteins, RNAs, and DNAs. One particular advantage of coacervates is that they are derived from aqueous solutions, unlike other nanoparticle delivery systems that often require organic solvents. In addition, coacervates achieve high loading while maintaining the viability of the cargo material. Here, we review recent developments in the applications of coacervates and their limitations in the delivery of therapeutic biomolecules. Important factors for coacervation include molecular structures of the polyelectrolytes, mixing ratio, the concentration of polyelectrolytes, and reaction conditions such as ionic strength, pH, and temperature. Various compositions of coacervates have been shown to deliver biomolecules in vitro and in vivo with encouraging activities. However, major hurdles remain for the systemic route of administration other than topical or local delivery. The scale-up of manufacturing methods suitable for preclinical and clinical evaluations remains to be addressed. We conclude with a few research directions to overcome current challenges, which may lead to successful translation into the clinic.

摘要

凝聚作用是一种液-液相分离,可以通过自组装或静电相互作用在大分子溶液中发生。最近,由生物相容性大分子组成的凝聚物作为纳米结构平台被积极研究,用于封装和输送生物分子,如蛋白质、RNA 和 DNA。凝聚物的一个特别的优势是它们源自水溶液,与其他纳米颗粒输送系统不同,后者通常需要有机溶剂。此外,凝聚物在保持货物材料活力的同时实现高负载。在这里,我们综述了凝聚物在治疗性生物分子输送方面的应用及其局限性的最新进展。凝聚作用的重要因素包括聚电解质的分子结构、混合比、聚电解质的浓度以及反应条件,如离子强度、pH 和温度。已经显示出各种组成的凝聚物可以在体外和体内输送生物分子,具有令人鼓舞的活性。然而,除了局部或局部给药之外,对于全身给药途径仍然存在主要障碍。适合临床前和临床评估的制造方法的扩大规模仍然是一个待解决的问题。我们以克服当前挑战的几个研究方向结束,这可能会导致成功转化为临床应用。

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