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使用弹性蛋白样多肽对生物活性纳米颗粒进行空间稳定化。

Steric stabilization of bioactive nanoparticles using elastin-like polypeptides.

机构信息

Department of Pharmacology and Pharmaceutical Sciences, Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089, USA.

Department of Pharmacology and Pharmaceutical Sciences, Alfred E. Mann School of Pharmacy and Pharmaceutical Sciences, University of Southern California, Los Angeles, CA 90089, USA; Department of Biomedical Engineering, Viterbi School of Engineering, University of Southern California, Los Angeles, CA 90089, USA; Department of Ophthalmology, Keck School of Medicine, University of Southern California, Los Angeles, CA 90089, USA.

出版信息

Adv Drug Deliv Rev. 2024 Mar;206:115189. doi: 10.1016/j.addr.2024.115189. Epub 2024 Jan 26.


DOI:10.1016/j.addr.2024.115189
PMID:38281625
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11580827/
Abstract

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.

摘要

弹性蛋白样多肽(ELP)是一种多功能的热响应聚合物,可以与几乎任何治疗性有效载荷相连接。ELP 源自短的氨基酸序列,在人体中含量丰富,具有低免疫原性。作为内源性蛋白酶的底物,ELP 可生物降解,因此是候选生物材料。可以通过遗传工程将肽和蛋白质直接与 ELP 偶联,而其他聚合物和小分子可以通过共价生物偶联或非共价络合附加。在生理温度下相分离的 ELP 可以形成纳米组装体的核心;然而,保持可溶性的 ELP 可以使各种纳米颗粒的冠状物稳定。在冠状物上带有 ELP 的纳米颗粒促进胶体具有有利的药代动力学(PK)特性,使得间歇性给药具有治疗效果。本综述重点介绍了一系列广泛的 ELP 融合体,这些融合体能够稳定其有效载荷的溶解度,并且在某些情况下还能稳定其生物活性——重点介绍了构成其治疗效果的基础的生物物理特性。

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本文引用的文献

[1]
Biomimetic SARS-CoV-2 Spike Protein Nanoparticles.

Biomacromolecules. 2023-5-8

[2]
Dynamic Compartmentalization of Peptide-Oligonucleotide Conjugates with Reversible Nanovesicle-Microdroplet Phase Transition Behaviors.

ACS Appl Mater Interfaces. 2022-8-17

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Development of an enhanced immunoassay based on protein nanoparticles displaying an IgG-binding domain and luciferase.

Anal Bioanal Chem. 2022-3

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Int J Nanomedicine. 2021

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Formulation of stabilizer-free, nontoxic PLGA and elastin-PLGA nanoparticle delivery systems.

Int J Pharm. 2021-3-15

[6]
Sustained release of a GLP-1 and FGF21 dual agonist from an injectable depot protects mice from obesity and hyperglycemia.

Sci Adv. 2020-8

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Adaptable antibody Nanoworms designed for non-Hodgkin lymphoma.

Biomaterials. 2020-12

[8]
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Nanomedicine. 2020-10

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Virol J. 2020-6-9

[10]
Anti-FLT3 nanoparticles for acute myeloid leukemia: Preclinical pharmacology and pharmacokinetics.

J Control Release. 2020-8-10

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