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作 者:成杰伟 黄赛朋[1] 温惠云[1] 许宁侠[1,2] 刘先宁 肖湘华 李文帅 薛伟明[1] CHENG Jie-wei;HUANG Sai-peng;WEN Hui-yun;XU Ning-xia;L;XIAO Xiang-hua;LI Wen-shuai;XUE Wei-ming(School of Chemical Engineering,Northwest University,Xi'an 710069,China;Xi'an International University,Xi'an 710077,China;Shaa~xi Institute of Ophthalmology,Xi'an 710002,China)
机构地区:[1]西北大学化工学院,陕西西安710069 [2]西安外事学院,陕西西安710077 [3]陕西省眼科研究所,陕西西安710002
出 处:《高校化学工程学报》2018年第4期893-901,共9页Journal of Chemical Engineering of Chinese Universities
基 金:陕西省教育厅专项科研计划项目(16JK1770);陕西省自然科学基金(2015JM2044;2014JQ2067);中国博士后科学基金第61批面上项目(2017M613190)
摘 要:以反式白藜芦醇(resveratrol,RES)为还原剂,硝酸银(AgNO_3)为前驱体,十六烷基三甲基溴化铵(cetyltrimethylammonium bromide,CTAB)为表面活性剂和相转移催化剂,采用原位液相还原工艺制备了负载RES的银基纳米载体(RES-AgNPs)。当AgNO_3、RES和CTAB摩尔比为1:1:0.5、40℃反应13 h时,制得平均粒径(45.5±2)nm、zeta电位-21 mV的RES-AgNPs。红外光谱和紫外吸收光谱分析结果表明,RES成功负载在纳米银表面,负载量达到0.0883 mg?mg^(-1)。体外释放实验表明,RES-AgNPs具有过氧化氢(H_2O_2)敏感响应的释放特性,当p H=5.4且CH_2O_2=25μmol?L^(-1)时RES释放率为89%。以人乳腺癌细胞MCF-7为肿瘤细胞模型,MTT实验结果显示,当样品剂量均为15μg?mL^(-1)时,与RES、AgNPs和RES+AgNPs联合给药相比,RES-AgNPs对细胞的生长抑制率分别提高了62.6%、68.2%和55.1%,体现了纳米载体中银纳米粒子与负载药物RES对肿瘤细胞的协同杀伤效应。Silver nanoparticles(RES-AgNPs) were prepared by in-situ reduction using resveratrol(RES) as a reducing agent, silver nitrate as a precursor and cetyltrimethylammonium bromide(CTAB) as a dispersing agent and phase transfer catalyst. When studied with RES, AgNO3 and CTAB molar mass ratio of 1:1:0.5 at 40 for ℃13 h, the optimum RES-AgNPs prepared has an average size of 45.5 nm ± 2 nm and zeta value of-21 mV. Moreover, the infrared spectroscopy(IR) and ultraviolet visible(UV) spectrum results show that RES is successfully loaded on the surface of AgNPs with high loading efficiency of 0.0883 mg?mg^(-1). Drug release measurement in vitro shows that RES-AgNPs is responsive to hydrogen peroxide H2 O2, and the release ratio is 89 % when hydrogen peroxide concentration is 25 μmol?L^(-1) at p H 5.4. Further evaluation of the therapeutic efficacy of RES-AgNPs was carried out in vitro by evaluating MCF-7 cell viability using MTT method. Compared with cell inhibition effects of RES, AgNPs and RES + AgNPs, RES-AgNPs exhibits excellent synergistic antitumor effects with an improvement of 62.6 %, 68.2 % and 55.1 %, respectively.
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