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纳米金-表阿霉素复合体的体外抗肿瘤作用[J]. 中山大学学报(医学科学版), 2012,33(2).
The In Vitro Antitumour effects of epirubicin-nanogold compounds[J]. Journal of Sun Yat-sen University (Medical Sciences), 2012, 33(2).
摘 要:【目的】 观察纳米金-表阿霉素复合体(epirubicin-nanogold compounds
EPI- AuNP)能否抑制人脐静脉内皮细胞(human umbilical vein endothelial cells
HUVECs)、人肝癌细胞(HepG2)的增殖。【方法】 采用化学合成法制备EPI-AuNP,通过紫外-可见吸收光谱、荧光淬灭实验、动态光散射及Zeta电位变化对其进行鉴定。体外实验分为AuNP处理组、EPI处理组、EPI- AuNP处理组和空白对照组。将HUVECs、HepG2细胞分别接种于96孔板,培养24h后各组分别加入AuNP溶液、EPI溶液、EPI-AuNP溶液和无血清培养液200?l,继续培养24h后:MTT比色法检测HUVECs、HepG2细胞生存率;紫外-可见分光光度法检测各细胞内EPI的积聚量。【结果】 紫外-可见吸收光谱显示:AuNP的最大吸收峰在520nm处,而EPI-AuNP在525nm处。EPI (100mg/L)荧光强度为195.2±7.5;EPI-AuNP为16.4±5.0,P=0.000。AuNP的平均粒径及Zeta电位分别为:(14.34?0.75) nm、(-21.19?0.64)mV;EPI-AuNP为:(18.54?1.84)nm、(-15.34?0.72)mV,P<0.01。体外实验:MTT比色法结果显示EPI处理组HUVECs、HepG2细胞的生存率分别为(29.25? 1.59)%、(71.10?4.16)%;EPI-AuNP处理组:(21.29?1.51)%、(43.82?2.21)%,P=0.000。【结论】 成功合成EPI-AuNP复合体,体外实验证实其对HUVECs、HepG2细胞均具有增殖抑制作用。
Abstract : 【Objective】 To observe the in vitro antitumour effects of epirubicin-nanogold compounds(EPI-AuNP). 【Methods】 EPI-AuNP was prepared by chemosynthesis and investigated using UV-Vis spectrophotometer
fluorescence studies
dynamic light scattering and zeta potential. Human umbilical vein endothelial cells (HUVECs) and HepG2 cells were divided into 4 groups: AuNP treatment group
EPI treatment group
EPI-AuNP treatment group and control group. After seeded in 96-well plate and cultured for 24h separately
HUVECs and HepG2 cells were treated with 200?l of AuNP
EPI
EPI-AuNP and serum-free medium respectively. Inhibition effect of each group on the HUVECs and HepG2 cells was assessed using MTT colorimetric method. UV-Vis spectrophotometer was applied to detect the cells epirubicin accumulation of different groups. 【Results】 A red shift in the SPR band maxima in the EPI-AuNP spectrum (λmax?525 nm) as compared with the spectrum of AuNP alone(λmax?520 nm) ; The fluorescence intensity of EPI (100mg /L) was (195.2±7.5) and EPI-AuNP was (16.4± 5.0)
P=0.000; The hydrodynamic diameter of AuNP was (14.34?0.75) nm while EPI-AuNP was (18.54?1.84) nm; meanwhile
the zeta potential of AuNP was (-21.19?0.64) mV while EPI- AuNP was (-15.34?0.72)mV
P<0.01. The HUVECs survival rate of EPI-AuNP treatment group [(21.29 ?1.51)%] was lower than the EPI group[(29.25?1.59)%]; The HepG2 cells survival rate of EPI-AuNP treatment group[(43.82?2.21)%] was lower than the EPI group[(71.10?4.16)%]
P<0.01. 【Conclusions】 EPI-AuNP has been synthesized and indicated enhanced drug potency in vitro by MTT assay.
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