利用弹性蛋白样多肽对生物活性纳米粒子进行立体稳定化处理

IF 15.2 1区 医学 Q1 PHARMACOLOGY & PHARMACY
Alvin Phan , J. Andrew MacKay
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引用次数: 0

摘要

弹性蛋白样多肽(ELP)是一种用途广泛的热响应聚合物,几乎可以与任何治疗药物连接。某些 ELP 源自短氨基酸序列,在人体中含量丰富,免疫原性低。作为内源性蛋白酶的底物,ELPs 可生物降解,因此是一种候选生物材料。肽和蛋白质可通过基因工程直接与 ELPs 结合,而其他聚合物和小分子则可通过共价生物结合或非共价复合物添加到 ELPs 中。在生理温度下发生相分离的ELP可形成纳米组合体的核心;然而,保持可溶性的ELP可在立体上稳定各种纳米粒子的电晕。具有ELPs电晕的纳米颗粒可形成具有良好药代动力学(PK)特性的胶体,从而实现间歇给药的疗效。本综述重点介绍了各种ELP融合物,这些融合物能稳定货物的溶解度,有时还能稳定货物的生物活性,重点介绍了这些融合物的生物物理特性,这些特性是其治疗效果的基础。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Steric stabilization of bioactive nanoparticles using elastin-like polypeptides

Steric stabilization of bioactive nanoparticles using elastin-like polypeptides

Steric stabilization of bioactive nanoparticles using elastin-like polypeptides

Elastin-like polypeptides (ELP) are versatile, thermo-responsive polymers that can be conjugated to virtually any therapeutic cargo. Derived from short amino-acid sequences and abundant in humans, certain ELPs display low immunogenicity. Substrates for endogenous proteases, ELPs are biodegradable and thus, are candidate biomaterials. Peptides and proteins can be directly coupled with ELPs through genetic engineering, while other polymers and small molecules can be appended through covalent bioconjugation or non-covalent complexation. ELPs that phase separate at physiological temperatures can form the core of nano assemblies; however, ELPs that remain soluble can sterically stabilize the corona of a variety of nanoparticles. Nanoparticles with ELPs at their corona promote colloids with favorable pharmacokinetic (PK) properties that enables therapeutic efficacy with intermittent administration. This review highlights a comprehensive spectrum of ELP fusions shown to stabilize the solubility, and sometimes bioactivity, of their cargo – with a focus on biophysical properties that underlie their therapeutic effects.

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来源期刊
CiteScore
28.10
自引率
5.00%
发文量
294
审稿时长
15.1 weeks
期刊介绍: The aim of the Journal is to provide a forum for the critical analysis of advanced drug and gene delivery systems and their applications in human and veterinary medicine. The Journal has a broad scope, covering the key issues for effective drug and gene delivery, from administration to site-specific delivery. In general, the Journal publishes review articles in a Theme Issue format. Each Theme Issue provides a comprehensive and critical examination of current and emerging research on the design and development of advanced drug and gene delivery systems and their application to experimental and clinical therapeutics. The goal is to illustrate the pivotal role of a multidisciplinary approach to modern drug delivery, encompassing the application of sound biological and physicochemical principles to the engineering of drug delivery systems to meet the therapeutic need at hand. Importantly the Editorial Team of ADDR asks that the authors effectively window the extensive volume of literature, pick the important contributions and explain their importance, produce a forward looking identification of the challenges facing the field and produce a Conclusions section with expert recommendations to address the issues.
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