Kim In-Sook, Lee Soo-Kyung, Park Yu-Mi, Lee Yong-Bok, Shin Sang-Chul, Lee Kang Choon, Oh In-Joon
College of Pharmacy and Research Institute of Drug Development, Chonnam National University, Yongbong-dong, Bug-gu, Gwangju 500-757, Republic of Korea.
Int J Pharm. 2005 Jul 14;298(1):255-62. doi: 10.1016/j.ijpharm.2005.04.017.
Polymer nanoparticles have been used as non-viral gene delivery systems and drug delivery systems. In this study, biodegradable poly(L-lactic acid) (PLA)/polyethylenimine (PEI) and poly(D,L-lactide-co-glycolide) (PLGA)/PEI nanoparticles were prepared and characterized as gene delivery systems. The PLA/PEI and PLGA/PEI nanoparticles, which were prepared by a diafiltration method, had spherical shapes and smooth surface characteristics. The size of nanoparticles was controlled by the amount of PEI, which acted as a hydrophilic moiety, which effectively reduced the interfacial energy between the particle surface and the aqueous media. The nanoparticles showed an excellent dispersive stability under storage in a phosphate-buffered saline solution for 12 days. The positive zeta-potentials for the nanoparticles decreased and changed to negative values with increasing plasmid DNA (pDNA) content. Agarose gel electrophoresis showed that the complex formation between the nanoparticles and the pDNA coincided with the zeta-potential results. The results of in vitro transfection and cell viability on HEK 293 cells indicated that the nanoparticles could be used as gene delivery carriers.
聚合物纳米颗粒已被用作非病毒基因递送系统和药物递送系统。在本研究中,制备了可生物降解的聚(L-乳酸)(PLA)/聚乙烯亚胺(PEI)和聚(D,L-丙交酯-共-乙交酯)(PLGA)/PEI纳米颗粒,并将其表征为基因递送系统。通过渗滤法制备的PLA/PEI和PLGA/PEI纳米颗粒呈球形,表面光滑。纳米颗粒的尺寸由作为亲水部分的PEI的量控制,这有效地降低了颗粒表面与水性介质之间的界面能。纳米颗粒在磷酸盐缓冲盐溶液中储存12天时表现出优异的分散稳定性。随着质粒DNA(pDNA)含量的增加,纳米颗粒的正ζ电位降低并变为负值。琼脂糖凝胶电泳表明,纳米颗粒与pDNA之间的复合物形成与ζ电位结果一致。体外转染和对HEK 293细胞的细胞活力结果表明,纳米颗粒可作为基因递送载体。