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细胞穿透肽的研究进展及其在聚合物纳米平台药物传递中的功能化。

Advances in cell penetrating peptides and their functionalization of polymeric nanoplatforms for drug delivery.

机构信息

School of Life Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, China.

Key Laboratory of Advanced Technologies of Materials, Ministry of Education, School of Materials Science and Engineering, Southwest Jiaotong University, Chengdu, Sichuan, China.

出版信息

Wiley Interdiscip Rev Nanomed Nanobiotechnol. 2021 Mar;13(2):e1668. doi: 10.1002/wnan.1668. Epub 2020 Sep 15.

Abstract

Cell penetrating peptides (CPPs), known as protein translocation domains, have emerged as efficient molecular transporters to overcome biological barriers and deliver cell-impermeable cargoes into cells. The conjugation of CPPs to polymeric nanoplatforms enhances the drug delivery efficiency thus increasing their therapeutic efficacy. However, conventional CPPs are generally lack of cell specificity and could be easily degraded in vivo. These limitations lead to the development of new CPPs with superior properties. To address the issue of cell specificity, activatable CPPs have been designed to be activated at desired site through different stimuli. On the other hand, macrocyclization has been used to constrain linear CPPs into their cyclic forms. This chemical optimization of peptides endows CPPs with enhanced stability and cell permeability. This brief review will cover recent advances in terms of different types of CPPs for enhanced cell penetration. In addition, the modification chemistry used to functionalize polymeric nanoplatforms with CPPs and their recent applications for drug delivery will also be discussed. This article is categorized under: Nanotechnology Approaches to Biology > Cells at the Nanoscale Therapeutic Approaches and Drug Discovery > Nanomedicine for Infectious Disease.

摘要

细胞穿透肽(CPPs),又称蛋白转导结构域,已成为有效的分子转运体,可克服生物屏障并将细胞不可渗透的载物递送至细胞内。CPPs 与聚合物纳米平台的缀合提高了药物递送效率,从而提高了治疗效果。然而,传统的 CPP 通常缺乏细胞特异性,并且在体内容易降解。这些限制导致了具有优越性能的新型 CPP 的开发。为了解决细胞特异性问题,设计了可通过不同刺激在所需部位激活的激活型 CPP。另一方面,大环化已被用于将线性 CPP 约束成其环状形式。这种对肽的化学优化赋予 CPP 增强的稳定性和细胞通透性。这篇简短的综述将涵盖不同类型 CPP 用于增强细胞穿透性的最新进展。此外,还将讨论用于对 CPP 进行功能化的聚合物纳米平台的修饰化学及其在药物递送中的最新应用。本文属于以下分类:纳米技术在生物学中的应用 > 纳米尺度下的细胞 治疗方法和药物发现 > 用于传染病的纳米医学。

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