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用于骨软骨修复的支架介导基因递送

Scaffold-Mediated Gene Delivery for Osteochondral Repair.

作者信息

Madry Henning, Venkatesan Jagadeesh Kumar, Carballo-Pedrares Natalia, Rey-Rico Ana, Cucchiarini Magali

机构信息

Center of Experimental Orthopaedics, Saarland University Medical Center, Kirrbergerstr. Bldg 37, D-66421 Homburg, Germany.

Cell Therapy and Regenerative Medicine Unit, Centro de Investigacións Científicas Avanzadas (CICA), Universidade da Coruña, S-15071 A Coruña, Spain.

出版信息

Pharmaceutics. 2020 Sep 29;12(10):930. doi: 10.3390/pharmaceutics12100930.

Abstract

Osteochondral defects involve both the articular cartilage and the underlying subchondral bone. If left untreated, they may lead to osteoarthritis. Advanced biomaterial-guided delivery of gene vectors has recently emerged as an attractive therapeutic concept for osteochondral repair. The goal of this review is to provide an overview of the variety of biomaterials employed as nonviral or viral gene carriers for osteochondral repair approaches both in vitro and in vivo, including hydrogels, solid scaffolds, and hybrid materials. The data show that a site-specific delivery of therapeutic gene vectors in the context of acellular or cellular strategies allows for a spatial and temporal control of osteochondral neotissue composition in vitro. In vivo, implantation of acellular hydrogels loaded with nonviral or viral vectors has been reported to significantly improve osteochondral repair in translational defect models. These advances support the concept of scaffold-mediated gene delivery for osteochondral repair.

摘要

骨软骨缺损涉及关节软骨和下方的软骨下骨。如果不进行治疗,可能会导致骨关节炎。先进的生物材料引导基因载体递送最近已成为一种有吸引力的骨软骨修复治疗概念。本综述的目的是概述在体外和体内用于骨软骨修复方法的各种生物材料,这些材料用作非病毒或病毒基因载体,包括水凝胶、固体支架和混合材料。数据表明,在无细胞或细胞策略的背景下,治疗性基因载体的位点特异性递送能够在体外对骨软骨新生组织组成进行空间和时间控制。在体内,据报道,植入负载非病毒或病毒载体的无细胞水凝胶可显著改善转化缺陷模型中的骨软骨修复。这些进展支持了支架介导的基因递送用于骨软骨修复的概念。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/9a07/7601511/9d4794a49290/pharmaceutics-12-00930-g001.jpg

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