Haas Jochen, Ravi Kumar M N V, Borchard Gerrit, Bakowsky Udo, Lehr Claus-Michael
Department of Biopharmaceutics and Pharmaceutical Technology, Saarland University, Building 8.1, 66123 Saarbrücken, Germany.
AAPS PharmSciTech. 2005 Aug 10;6(1):E22-30. doi: 10.1208/pt060106.
The purpose of this research was to prepare poly-(epsilon-caprolactone) (PCL) particles by an emulsion-diffusion-evaporation method using a blend of poly-(vinyl alcohol) and chitosan derivatives as stabilizers. The chitosan derivatives used were chitosan hydrochloride and trimethyl chitosans (TMC) with varying degrees of quaternization. Particle characteristics-size, zeta potential, surface morphology, cytotoxicity, and transfection efficiency-were investigated. The developed method yields PCL nanoparticles in the size range of 250 to 300 nm with a positive surface charge (2.5 to 6.8 mV). The cytotoxicity was found to be moderate and virtually independent of the stabilizers' concentration with the exception of the highly quaternized TMC (degree of substitution 66%) being significantly more toxic. In immobilization experiments with gel electrophoresis, it could be shown that these cationic nanoparticles (NP) form stable complexes with DNA at a NP:DNA ratio of 3:1. These nanoplexes showed a significantly higher transfection efficiency on COS-1 cells than naked DNA.
本研究的目的是使用聚乙烯醇和壳聚糖衍生物的混合物作为稳定剂,通过乳液扩散蒸发法制备聚(ε-己内酯)(PCL)颗粒。所使用的壳聚糖衍生物为盐酸壳聚糖和不同季铵化程度的三甲基壳聚糖(TMC)。研究了颗粒特性——尺寸、zeta电位、表面形态、细胞毒性和转染效率。所开发的方法可产生尺寸范围为250至300nm且表面带正电荷(2.5至6.8mV)的PCL纳米颗粒。除了高度季铵化的TMC(取代度66%)毒性明显更大外,细胞毒性被发现为中等且几乎与稳定剂浓度无关。在凝胶电泳固定实验中,可以表明这些阳离子纳米颗粒(NP)在NP:DNA比例为3:1时与DNA形成稳定的复合物。这些纳米复合物在COS-1细胞上显示出比裸DNA显著更高的转染效率。