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

作者：Raftery Rosanne M; Tierney Erica G; Curtin Caroline M; Cryan Sally Ann; O' Brien Fergal J

来源：Journal of Controlled Release, 2015, 210: 84-94.

DOI：10.1016/j.jconrel.2015.05.005

• Chitosan nanoparticles
• Gene delivery
• Mesenchymal stem cells (MSCs)
• Gene-activated scaffold
• Tissue engineering

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.

• 出版日期2015-7-28