Kim You-Kyoung, Cho Chong-Su, Cho Myung-Haing, Jiang Hu-Lin
State Key Laboratory of Natural Medicines, Department of Pharmaceutics, China Pharmaceutical University, Nanjing, 210009, People's Republic of China.
J Biomed Mater Res A. 2014 Jul;102(7):2230-7. doi: 10.1002/jbm.a.34905. Epub 2013 Aug 13.
The clinical success of gene therapy critically depends upon the safety and efficiency of delivery system used. Although polyethylenimine (PEI) has been commonly used as an efficient cationic polymeric gene carrier due to its high transfection efficiency, its cytotoxicity and nondegradability limit the polymer's therapeutic applications in clinical trials. In this study, biocompatible polyspermine based on spermine (SPE) and poly(ethylene glycol) (PEG) diacrylate (SPE-alt-PEG) was synthesized using a Michael-type addition reaction, and its ability as an alternative gene carrier for lung cancer therapy was evaluated. SPE-alt-PEG polyspermine was complexed with plasmid DNA, and the resulting complexes were characterized by particle size and surface charge by dynamic light scattering, complex formation and DNA protection ability by gel retardation, and complex shape by energy-filtering transmission electron microscopy. The SPE-alt-PEG copolymer showed low cytotoxicity, and SPE-alt-PEG/DNA complexes showed efficacious transfection efficiency compared with 25 kDa PEI (PEI 25K). Also SPE-alt-PEG/GFP complexes were efficiently transferred into the lungs after aerosol administration without toxicity, and delivery of Pdcd4 gene as a therapeutic gene with SPE-alt-PEG polyspermine greatly reduced tumor size as well as tumor numbers in K-ras(LA1) lung cancer model mice compared relative to the effect observed for PEI 25K. These results suggest that SPE-alt-PEG has potential as a gene carrier for lung cancer gene therapy.
基因治疗的临床成功与否关键取决于所使用的递送系统的安全性和效率。尽管聚乙烯亚胺(PEI)因其高转染效率而一直被广泛用作一种高效的阳离子聚合物基因载体,但其细胞毒性和不可降解性限制了该聚合物在临床试验中的治疗应用。在本研究中,通过迈克尔型加成反应合成了基于精胺(SPE)和聚乙二醇(PEG)二丙烯酸酯的生物相容性聚精胺(SPE-alt-PEG),并评估了其作为肺癌治疗替代基因载体的能力。将SPE-alt-PEG聚精胺与质粒DNA复合,通过动态光散射对所得复合物的粒径和表面电荷进行表征,通过凝胶阻滞分析复合物的形成和DNA保护能力,通过能量过滤透射电子显微镜观察复合物的形状。SPE-alt-PEG共聚物显示出低细胞毒性,与25 kDa PEI(PEI 25K)相比,SPE-alt-PEG/DNA复合物显示出有效的转染效率。此外,气溶胶给药后,SPE-alt-PEG/GFP复合物可有效转移至肺部且无毒性,在K-ras(LA1)肺癌模型小鼠中,用SPE-alt-PEG聚精胺作为治疗基因递送Pdcd4基因,相对于PEI 25K所观察到的效果,可显著减小肿瘤大小并减少肿瘤数量。这些结果表明,SPE-alt-PEG有潜力作为肺癌基因治疗的基因载体。