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机构地区:[1]南华大学研究生院,湖南衡阳421001 [2]长沙市第四医院消化内科,湖南长沙410004
出 处:《现代生物医学进展》2009年第19期3669-3672,3695,共5页Progress in Modern Biomedicine
摘 要:目的:探讨羟基磷灰石-聚乙烯亚胺(nHA-PEI 10KD)纳米颗粒的癌细胞基因转染效率。方法:通过透射电子显微镜(TEM)观察HA-PE(I10KD)纳米颗粒的形态及粒径,Zeta电位仪测定nHA-PEI和HA在酸、碱、中性环境中的电位,用琼脂糖凝胶电泳检测nHAP-PE(I10KD)与DNA结合的能力,MTT比色法检测nHAP-PE(I10KD)对HepG2细胞的毒性,选用增强型绿色荧光蛋白质粒pEGFP1与nHA-PEI结合后,分别转染真核细胞HepG2、Hela、SW620,计算其转染率。结果:nHA-PE(I10KD)分散程度好,粒径60-80nm,在PH7.2时,Zeta电位42.87mV,能转染实验中的细胞,转然效果最好的是HepG2细胞,其次Hela、SW620,转染率高于PEI(10KD)、nHA,但低于脂质体。结论:通过阳离子PEI修饰HA,可有效将增强型绿色荧光蛋白质粒转入HepG2细胞,HA-PE(I10KD)纳米颗粒复合物有望成为基因传递的有效载体。Objective:To investigate the efficiency of gene transfection mediated by hydroxyapatite-polyethyleneimine(nHA-PEI 10KD) nanoparticles in cancer cells.Methods: The shape and size of HA-PEI nano-particle were observed by Transmission Electron Microscopy(TEM),The potential of nHA-PEI and HA in acid,alkaliand neutral conditions were measured by Zeta Potential Instrument.DNA binding capacity of nHAP-PEI(10KD) was detected by agarose gel electrophoresis,MTT assy was performed to evaluate the toxicity ofnHAP-PEI (10KD) to HepG2 cells. The combinations of enhanced green fluorescent protein plasmid pE(3FP1 and nHA-PEI were transfected into HepG2, Hela and SW620 cells, and the transfection efficiency was evaluated by Flow Cytomea'y. Remtlts: nHA-PEI (10KD) are in high dispersion and the size of particle is 60 - 80nm. At PH of 7.2, Zeta Potential of 42.87mV, nHA-PEI transfects into experiment cells, especially in HepG2 cells, followed by Hela, SW620.The transfection efficiency ofnHA-PEI was higher than PEI (10) and nHA, but lower than liposomes. Conclusions: The modified HA by PEI cation can potentiate the transfection of enhanced green fluorescent protein plasmid into HepG2 cells. HA-PEI (10KD) composite nanoparticles are expected to become an effective gene delivery vector.
分 类 号:R318[医药卫生—生物医学工程]
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