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作 者:潘运龙[1] 赵晓旭[1] 覃莉[2] 杜彬[3] 吕荣钊[1] 蔡继业[4]
机构地区:[1]暨南大学附属第一医院普外科,广州510632 [2]暨南大学医学院组织胚胎学教研室 [3]暨南大学医学院病理学教研室 [4]暨南大学生命科学技术学院纳米生物技术实验室
出 处:《中华实验外科杂志》2011年第4期533-535,共3页Chinese Journal of Experimental Surgery
基 金:基金项目:国家基础研究973计划资助项目(2010CB833603);国家自然科学基金资助项目(30772131);广东省自然科学基金资助项目(8151063201000034)
摘 要:目的观察纳米金对表阿霉素在抑制HepG2细胞增殖中如何发挥增敏作用。方法实验组分为纳米金预处理组和单纯表阿霉素组。常规消化HepG2细胞后种板,各组分别加入2μg/L的纳米金溶液和无血清培养液100μl,于设定的时间点(30、60、120和240min)加入1mg/L的表阿霉素溶液100山,继续培养24h后噻唑蓝(MTT)比色法检测两组药物对HepG2细胞的增殖抑制作用;紫外.可见分光光度计(uV—Vis)检测各组HepG2细胞内积聚的表阿霉素量;原子力显微镜(AFM)观察HepG2细胞表面形态及超微结构变化。结果纳米金预处理组各时间点HepG2细胞增殖抑制率[(50.53±1.38)%、(51.83±0.47)%、(48.66±2.21)%、(43.55±1.01)%]均明显高于对应的单纯表阿霉素组[(37.24±3.49)%、(39.42±2.28)%、(34.98±2.27)%、(28.92±3.80)%],P值〈0.01;纳米金预处理组(60min)表阿霉素在HepG2细胞内积聚的量最多,为(4.01±0.14)p,g;AFM检测到纳米金预处理组HepG2细胞膜内陷,粗糙度增加,表面孔径增大,细胞核的饱满程度减少。结论纳米金可通过增加表阿霉素在HepG2细胞内的积聚量来发挥增敏作用,纳米金预处理60rain对表阿霉素的增敏作用最大。Objective To observe the sensitization of gold nanoparticles on the epirubicin therapy of hepatocellular carcinoma cells (HepG2) and action mechanism. Methods The HepG2 ceils were divided into 2 experimental groups : gold nanoparticles pretreatment group and simple epirubicin group. After seeded in a 96-well plate and cultured for 24 h, HepG2 cells were treated with 100 ±xl of gold nanoparticles (2 μg/L) and serum-free medium respectively. Then 100 μl of epirubicin ( 1 mg/L) was added to both groups at different time points : 30, 60, 120 and 240 min. The inhibition effect of epirubicin on the HepG2 ceils was assessed by methyl thiazol tetrazolium (MTT) assay. Ultraviolet-visible spectrophotometer (UV-Vis) was applied to detect the epirubicin accumulation in HepG2 cells at different time points, and a- tomic force microscope (AFM) was used to examine the ultrastructural changes of HepG2 cell surface. Re- suits The inhibition rate of HepG2 cells in gold nanoparticles pretreatment group [ (50. 53 ± 1.38 ) % , (51.83 ±0. 47)%, (48.66 ±2.21 )%, (43.55 ± 1.01)% ] at different time points was higher than the simple epirubiein group remarkably [(37.24 ±3.49)%, (39.42 ±2.28)%, (34.98 ±2.27)%, (28.92 ± 3.80)% ] ,P 〈 0. 01. The gold nanoparticles pretreatment group (60 rain) had the maximal epi- rubiein accumulation: (4. 01 ± 0. 14) txg. AFM revealed that when treated with gold nanopartieles, the morphologie changes of HepG2 cells were significantly different: there appeared invagination, obvious shrinked cell membrane and much rougher surface. Conclusion Gold nanopartieles can sensitize epirubi- ein through the enhancement of epirubiein accumulation in HepG2 cells. The pretreatment of gold nanopar- tieles for 60 min has the maximum sensitization.
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