Kuang Yu, Yuan Tun, Zhang Zhongwei, Li Mingyuan, Yang Yuan
West China School of Preclinical and Forensic Medicine, Sichuan University, Chengdu, Sichuan 610041, China.
J Drug Deliv. 2012;2012:920764. doi: 10.1155/2012/920764. Epub 2012 Dec 27.
New approaches to improve the traditional gene carriers are still required. Here we explore Fe(3)O(4) modified with degradable polymers that enhances gene delivery and target delivery using permanent magnetic field. Two magnetic Fe(3)O(4) nanoparticles coated with chitosan (CTS) and polyethylene glycol (PEG) were synthesized by means of controlled chemical coprecipitation. Plasmid pEGFP was encapsulated as a reported gene. The ferriferous oxide complexes were approximately spherical; surface charge of CTS-Fe(3)O(4) and PEG-Fe(3)O(4) was about 20 mv and 0 mv, respectively. The controlled release of DNA from the CTS-Fe(3)O(4) nanoparticles was observed. Concurrently, a desired Fe(3)O(4) concentration of less than 2 mM was verified as safe by means of a cytotoxicity test in vitro. Presence of the permanent magnetic field significantly increased the transfection efficiency. Furthermore, the passive target property and safety of magnetic nanoparticles were also demonstrated in an in vivo test. The novel gene delivery system was proved to be an effective tool required for future target expression and gene therapy in vivo.
仍需要改进传统基因载体的新方法。在此,我们探索用可降解聚合物修饰的Fe(3)O(4),其可利用永久磁场增强基因递送和靶向递送。通过可控化学共沉淀法合成了两种分别包覆壳聚糖(CTS)和聚乙二醇(PEG)的磁性Fe(3)O(4)纳米颗粒。将质粒pEGFP作为报告基因进行包封。铁氧化物复合物近似球形;CTS-Fe(3)O(4)和PEG-Fe(3)O(4)的表面电荷分别约为20 mV和0 mV。观察到CTS-Fe(3)O(4)纳米颗粒中DNA的控释。同时,通过体外细胞毒性试验证实,低于2 mM的理想Fe(3)O(4)浓度是安全的。永久磁场的存在显著提高了转染效率。此外,在体内试验中还证明了磁性纳米颗粒的被动靶向特性和安全性。新型基因递送系统被证明是未来体内靶向表达和基因治疗所需的有效工具。