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Polybutylcyanoacrylate nanoparticles as novel vectors in cancer gene therapy

机译:聚氰基丙烯酸丁酯纳米颗粒在癌症基因治疗中的新载体

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To make progress toward an efficient gene vector for cancer gene therapy,a novel nonviral vector of polybutylcyanoacrylate nanoparticles(PBCA NPs)was developed.Cetyltrimethyl ammonium bromide(CTAB)was used to modify the surface of PBCA NPs,and then the plasmid DNA(pDNA)of pAFP-TK was wrapped into PBCA-CTAB NPs.Atomic force microscopy and zeta potential demonstrated that PBCA-CTAB NPs were 80-200 nm in diameter and had +15.6 mV positive surface charges.Assay using 3-(4,5-dimethyl-2-thiazolyl)-2,5-diphenyl-2H-tetrazolium bromide showed that PBCA-CTAB NPs had less cytotoxicity to 3T3 cells than HepG2 cells.The analysis of PBCA-CTAB-DNA complexes could not only protect DNA from degradation by DNase I,it could also transfer pDNA into targeted cells with high transfection efficiency.Furthermore,when PBCA-CTAB NPs combined with suicide gene pAFP-TK,alpha-fetoprotein-positive cells transfected by it were highly sensitive to ganciclovir treatment,and cell survival declined precipitously.Therefore,this target strategy using a pAFP-TK/GCV suicide gene therapy system in which PBCA-CTAB NPs serve as gene delivery vectors explores a promising area for alpha-fetoprotein-positive hepatocellular carcinoma and associated carcinoma therapy.
机译:为了向癌症基因治疗的有效基因载体发展,开发了一种新型的聚氰基丙烯酸丁酯纳米粒子(PBCA NPs)非病毒载体。用十六烷基三甲基溴化铵(CTAB)修饰PBCA NPs的表面,然后构建质粒DNA pAFP-TK)包裹在PBCA-CTAB NPs中。原子力显微镜和zeta电位表明PBCA-CTAB NPs直径为80-200 nm,并具有+15.6 mV正表面电荷。使用3-(4,5-二甲基-2-噻唑基)-2,5-二苯基-2H-溴化四氮唑表明,PBCA-CTAB NPs对3T3细胞的杀伤力比HepG2细胞小.PBCA-CTAB-DNA复合物的分析不仅能保护DNA免受降解DNase I还可以将pDNA转移到目标细胞中,具有较高的转染效率。此外,当PBCA-CTAB NPs与自杀基因pAFP-TK结合后,被其转染的甲胎蛋白阳性细胞对更昔洛韦治疗和细胞存活高度敏感急剧下降。再次,使用PBCA-CTAB NPs作为基因传递载体的pAFP-TK / GCV自杀基因治疗系统的这一靶策略探索了甲胎蛋白阳性肝细胞癌及相关癌治疗的广阔前景。

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