Liu Guang, Fang Zhiwei, Yuan Minglu, Li Weimin, Yang Yunqi, Jiang Mier, Ouyang Yuanming, Yuan Weien
Department of Vascular Surgery, Shanghai Ninth People's Hospital, Shanghai Jiao Tong University School of MedicineShanghai, China.
School of Pharmacy, Shanghai Jiao Tong UniversityShanghai, China.
Front Pharmacol. 2017 Aug 9;8:528. doi: 10.3389/fphar.2017.00528. eCollection 2017.
The safe and efficient delivery of therapeutic nucleic acid is a prerequisite for an effective DNA therapy. In this study, we condensed the low molecular weight polyethylenimine (PEI, 1.8k Da) with 2,6-pyridinedicarboxaldehyde (PDA), both of which are degradable , to synthesize a biodegradable polycationic material (PDAPEI) to deliver vascular endothelial growth factor (VEGF) plasmid DNA (pDNA). Particle size and zeta potential of this novel degradable PEI derivatives-pDNA nanoparticle were investigated and cytotoxicity was estimated on human umbilical vein endothelial cells (HUVECs). Using pDNA-encoding VEGF-A and green fluorescence protein (GFP), we also checked transfection efficiency of the vector (PDAPEI) and found its excellent performance at 40 w/w ratio. We successfully established peripheral ischemia animal model on C57/BL6J mice to evaluate the therapeutic effect of PDAPEI/pVEGF-A polyplex system on ischemic disease and a conclusion was made that PDAPEI is a promising gene vector in the treatment of peripheral ischemic artery disease (PAD).
治疗性核酸的安全有效递送是有效的DNA治疗的前提条件。在本研究中,我们将低分子量聚乙烯亚胺(PEI,1.8k Da)与均可降解的2,6-吡啶二甲醛(PDA)缩合,以合成一种可生物降解的聚阳离子材料(PDAPEI)来递送血管内皮生长因子(VEGF)质粒DNA(pDNA)。研究了这种新型可降解PEI衍生物-pDNA纳米颗粒的粒径和zeta电位,并评估了其对人脐静脉内皮细胞(HUVECs)的细胞毒性。使用编码VEGF-A和绿色荧光蛋白(GFP)的pDNA,我们还检测了载体(PDAPEI)的转染效率,发现其在40 w/w比例下具有优异的性能。我们成功地在C57/BL6J小鼠上建立了外周缺血动物模型,以评估PDAPEI/pVEGF-A多聚体系统对缺血性疾病的治疗效果,并得出结论:PDAPEI是治疗外周缺血性动脉疾病(PAD)的一种有前景的基因载体。