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作 者:李永盛[1] 贺思佳 江翰[1] 边睿[1] 王硕[1] 郝袁 王雪峰[1] 刘颖斌[1] 徐雷鸣[2] 施伟斌[1]
机构地区:[1]上海交通大学医学院附属新华医院普通外科/胆道研究所,上海200092 [2]上海交通大学医学院附属新华医院消化内科,上海200092
出 处:《中国普通外科杂志》2015年第2期206-210,共5页China Journal of General Surgery
基 金:上海市科学技术委员会纳米科技专项课题资助项目(11nm0503700)
摘 要:目的:探讨聚己内酯载5-氟尿嘧啶(5-FU)纳米粒子对人胆管癌细胞株的体外杀伤作用、安全性及机制。方法:超声乳化法制备载5-FU聚己内酯纳米粒子(5-FU-PCL-NP),观察空载纳米粒子的体外溶血及5-FU-PCL-NP的体外药物释放情况,检测5-FU-PLA-NP对人胆管癌细胞株Hccc-9810增殖抑制及凋亡诱导作用。结果:5-FU-PCL-NP成功合成,其载药率为15.1%,包封率为41.9%,溶血试验阴性,5-FU-PCL-NP体外释放5-FU缓慢,其72 h释放率为62.9%。与单纯5-FU比较,5-FU-PCL-NP对Hccc-9810细胞的增殖抑制作用明显增强,IC50明显降低[(1.32±0.12)μg/m L vs.(2.5±0.39)μg/m L],促Hccc-9810细胞凋亡作用明显增强(均P<0.05)。空载纳米粒对Hccc-9810细胞凋亡无明显影响(P>0.05)。结论:载5-FU聚己内酯纳米粒子5-FU-PCL-NP具有良好的药物缓释效应,可延长5-FU的作用时间窗,对胆管癌细胞有较好的体外杀伤作用,且生物安全性好。Objective: To investigate the killing effect of 5-fluorouracil(5-FU) loaded polycaprolactone nanoparticles on human cholangiocarcinoma cells in vitro, and its safety and mechanism.Methods: The 5-FU loaded polycaprolactone nanoparticles(5-FU-PCL-NPs) were prepared by ultrasonic emulsification. In vitro hemolysis of the empty nanoparticles and drug release of 5-FU-PCL-NPs was observed, and the inhibition of proliferation and induction of apoptosis of 5-FU-PCL-NPs in human cholangiocarcinoma Hccc-9810 cells were determined.Results: The 5-FU-PCL-NPs were successfully synthesized, with drug loading rate of 15.1% and encapsulation efficiency of 41.9%. The empty nanoparticles showed a negative result in hemolysis test. 5-FU-PCL-NPs exhibited a sustained 5-FU release and the 72-h release rate was 62.9%. Compared with pure 5-FU, 5-FU-PCL-NPs had a significantly increased inhibitory effect on proliferation in Hccc-9810 cells, significantly decreased IC50 value [(1.32±0.12) μg/mL vs.(2.5±0.39) μg/mL ], and significantly enhanced effect on apoptosis in Hccc-9810 cells(all P〈0.05). The empty nanoparticles exerted no obvious effect on apoptosis in Hccc-9810 cells(P〉0.05).Conclusion: The 5-FU loaded polycaprolactone nanoparticles(5-FU-PCL-NPs) possess a sustainedrelease property that prolongs the suppressive effect of 5-FU, and have enhanced killing effect on human cholangiocarcinoma cells in vitro, with a satisfactory biological safety profile.
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