Jain Arvind K, Massey Ashley, Yusuf Helmy, McDonald Denise M, McCarthy Helen O, Kett Vicky L
School of Pharmacy, Medical Biology Centre, Queen's University Belfast, Belfast, Northern Ireland, UK ; Weatherall Institute of Molecular Medicine, MRC Molecular Haematology Unit, University of Oxford, John Radcliffe Hospital, Oxford, UK.
School of Pharmacy, Medical Biology Centre, Queen's University Belfast, Belfast, Northern Ireland, UK.
Int J Nanomedicine. 2015 Nov 24;10:7183-96. doi: 10.2147/IJN.S95245. eCollection 2015.
We report the formulation of novel composite nanoparticles that combine the high transfection efficiency of cationic peptide-DNA nanoparticles with the biocompatibility and prolonged delivery of polylactic acid-polyethylene glycol (PLA-PEG). The cationic cell-penetrating peptide RALA was used to condense DNA into nanoparticles that were encapsulated within a range of PLA-PEG copolymers. The composite nanoparticles produced exhibited excellent physicochemical properties including size <200 nm and encapsulation efficiency >80%. Images of the composite nanoparticles obtained with a new transmission electron microscopy staining method revealed the peptide-DNA nanoparticles within the PLA-PEG matrix. Varying the copolymers modulated the DNA release rate >6 weeks in vitro. The best formulation was selected and was able to transfect cells while maintaining viability. The effect of transferrin-appended composite nanoparticles was also studied. Thus, we have demonstrated the manufacture of composite nanoparticles for the controlled delivery of DNA.
我们报道了新型复合纳米颗粒的制备方法,该复合纳米颗粒结合了阳离子肽-DNA纳米颗粒的高转染效率以及聚乳酸-聚乙二醇(PLA-PEG)的生物相容性和延长递送特性。阳离子细胞穿透肽RALA用于将DNA凝聚成纳米颗粒,这些纳米颗粒被包裹在一系列PLA-PEG共聚物中。所制备的复合纳米颗粒表现出优异的物理化学性质,包括尺寸小于200 nm和包封率大于80%。用一种新的透射电子显微镜染色方法获得的复合纳米颗粒图像显示了PLA-PEG基质内的肽-DNA纳米颗粒。改变共聚物可调节体外DNA释放速率超过6周。选择了最佳配方,其能够在保持细胞活力的同时转染细胞。还研究了附加转铁蛋白的复合纳米颗粒的效果。因此,我们展示了用于DNA可控递送的复合纳米颗粒的制造。