Development of a gene-activated scaffold platformfor tissue engineering applications using chitosan-pDNA nanoparticles on collagen-based scaffolds

被引:79
|
作者
Raftery, Rosanne M. [1 ,2 ,3 ,4 ]
Tierney, Erica G. [1 ,2 ,3 ,4 ]
Curtin, Caroline M. [1 ,2 ,3 ,4 ]
Cryan, Sally-Ann [1 ,2 ,5 ]
O'Brien, Fergal J. [1 ,2 ,3 ,4 ]
机构
[1] Royal Coll Surgeons Ireland, Dept Anat, Tissue Engn Res Grp, Dublin 2, Dublin, Ireland
[2] Univ Dublin Trinity Coll, Trinity Ctr Bioengn, Dublin 2, Dublin, Ireland
[3] RCSI, Adv Mat & Bioengn Res Ctr AMBER, Dublin, Ireland
[4] TCD, Dublin, Ireland
[5] Royal Coll Surgeons Ireland, Sch Pharm, Dublin 2, Dublin, Ireland
基金
爱尔兰科学基金会; 欧洲研究理事会;
关键词
Chitosan nanoparticles; Gene delivery; Mesenchymal stem cells (MSCs); Gene-activated scaffold; Tissue engineering; IN-VIVO; TRANSFECTION EFFICIENCY; MOLECULAR-WEIGHT; DNA NANOPARTICLES; DELIVERY-SYSTEM; GAG SCAFFOLDS; BONE REGENERATION; NONVIRAL VECTORS; PROTON SPONGE; THERAPY;
D O I
10.1016/j.jconrel.2015.05.005
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Biomaterial scaffolds that support cell infiltration and tissue formation can also function as platforms for the delivery of therapeutics such as drugs, proteins, and genes. As burst release of supraphysiological quantities of recombinant proteins can result in adverse side effects, the objective of this study was to explore the potential of a series of collagen-based scaffolds, developed in our laboratory, as gene-activated scaffold platforms with potential in a range of tissue engineering applications. The potential of chitosan, a biocompatible material derived from the shells of crustaceans, as a gene delivery vector was assessed using mesenchymal stem cells (MSCs). A transfection efficiency of >45% is reported which is similar to what is achieved with polyethyleneimine (PEI), a non-viral gold standard vector, without causing cytotoxic side effects. When the optimised chitosan nanoparticles were incorporated into a series of collagen-based scaffolds, sustained transgene expression from MSCs seeded on the scaffolds was maintained for up to 28 days and interestingly the composition of the scaffold had an effect on transfection efficiency. These results demonstrate that by simply varying the scaffold composition and the gene (or combinations thereof) chosen; the systemhas potential for amyriad of therapeutic applications. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:84 / 94
页数:11
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