中华放射医学与防护杂志
中華放射醫學與防護雜誌
중화방사의학여방호잡지
Chinese Journal of Radiological Medicine and Protection
2013年
3期
265-268
,共4页
倪昕晔%钱农%林涛%聂斌%孙志强%孙苏平
倪昕曄%錢農%林濤%聶斌%孫誌彊%孫囌平
예흔엽%전농%림도%섭빈%손지강%손소평
甘氨双唑钠%纳米金%放射增敏%肺腺癌细胞/A549
甘氨雙唑鈉%納米金%放射增敏%肺腺癌細胞/A549
감안쌍서납%납미금%방사증민%폐선암세포/A549
Sodium glycididazole%Gold nanoparticles%Radiosensitization%Lung adenocarcinoma cell/AS49
目的 探讨甘氨双唑钠修饰纳米金制备及放射增敏效果.方法 把甘氨双唑钠修饰到已连接聚乙二醇的纳米金上,纳米金粒径18 nm.利用扫描电镜观察肺腺癌(A549)细胞吞噬甘氨双唑钠-纳米金的现象.将培养的肺腺癌细胞分为甘氨双唑钠组、纳米金组、甘氨双唑钠·纳米金组、对照组(不加药组).用四甲基偶氮唑盐比色法和克隆形成实验对肺腺癌(A549)细胞进行放射增敏的研究.结果 甘氨双唑钠-纳米金能进入细胞质和细胞核;浓度为0.003 mg/ml纳米金和甘氨双唑钠-纳米金没有明显的细胞毒性;甘氨双唑钠-纳米金组相对于甘氨双唑钠组、纳米金组、对照组,D0、Dq出现了下调;接受2、4、6和8 Gy剂量照射后,甘氨双唑钠-纳米金组肺腺癌细胞的存活率与其他3组相比,均明显下降(F=4.8、14.5、5.7、7.6,P<0.05).结论 甘氨双唑钠修饰的纳米金能增加肺腺癌细胞的辐射敏感性.
目的 探討甘氨雙唑鈉脩飾納米金製備及放射增敏效果.方法 把甘氨雙唑鈉脩飾到已連接聚乙二醇的納米金上,納米金粒徑18 nm.利用掃描電鏡觀察肺腺癌(A549)細胞吞噬甘氨雙唑鈉-納米金的現象.將培養的肺腺癌細胞分為甘氨雙唑鈉組、納米金組、甘氨雙唑鈉·納米金組、對照組(不加藥組).用四甲基偶氮唑鹽比色法和剋隆形成實驗對肺腺癌(A549)細胞進行放射增敏的研究.結果 甘氨雙唑鈉-納米金能進入細胞質和細胞覈;濃度為0.003 mg/ml納米金和甘氨雙唑鈉-納米金沒有明顯的細胞毒性;甘氨雙唑鈉-納米金組相對于甘氨雙唑鈉組、納米金組、對照組,D0、Dq齣現瞭下調;接受2、4、6和8 Gy劑量照射後,甘氨雙唑鈉-納米金組肺腺癌細胞的存活率與其他3組相比,均明顯下降(F=4.8、14.5、5.7、7.6,P<0.05).結論 甘氨雙唑鈉脩飾的納米金能增加肺腺癌細胞的輻射敏感性.
목적 탐토감안쌍서납수식납미금제비급방사증민효과.방법 파감안쌍서납수식도이련접취을이순적납미금상,납미금립경18 nm.이용소묘전경관찰폐선암(A549)세포탄서감안쌍서납-납미금적현상.장배양적폐선암세포분위감안쌍서납조、납미금조、감안쌍서납·납미금조、대조조(불가약조).용사갑기우담서염비색법화극륭형성실험대폐선암(A549)세포진행방사증민적연구.결과 감안쌍서납-납미금능진입세포질화세포핵;농도위0.003 mg/ml납미금화감안쌍서납-납미금몰유명현적세포독성;감안쌍서납-납미금조상대우감안쌍서납조、납미금조、대조조,D0、Dq출현료하조;접수2、4、6화8 Gy제량조사후,감안쌍서납-납미금조폐선암세포적존활솔여기타3조상비,균명현하강(F=4.8、14.5、5.7、7.6,P<0.05).결론 감안쌍서납수식적납미금능증가폐선암세포적복사민감성.
Objective To study the radioseusitization effect of gold nanoparticles modified by sodium glycididazole.Methods The sodium glycididazole was connected to gold nanoparticle,in dimension of about 18 nm,that had been modified with polyethylene glycol.The nanoparticle-swallowing efficiency of lung adenocarcinoma A549 cells was observed by a scanning electron microscope.Cells were divided into four groups:sodium glycididazole group,gold nanoparticles group,sodium glycididazole-gold nanoparticles group,and no drug control group.The radiosensitivity was detected by MTT and colony formation assays.Results Sodium glycididazole-gold nanoparticles could enter the cell cytoplasm and nucleus.The concentration of 0.003 mg/ml gold nanoparticles and sodium glycididazole-gold nanoparticles had no obvious cytotoxic effect.After irradiation of 2,4,6,8 Gy,the cell survival of the sodium glycididazole-gold nanoparticle group was significantly lower than that of the other three groups (F =4.8,14.5,5.7,7.6,P <0.05) and the D0 and Dq values of the sodium glycididazole-gold nanoparticle group were significantly lower than those of other three groups.Conclusion Sodium glycididazole-gold nanoparticles can enhance the radiosensitivity of lung adenocarcinoma cells.