赫拉
PEG比率
克隆形成试验
胶体金
癌细胞
分子生物学
体外
化学
生物物理学
材料科学
纳米颗粒
生物
生物化学
医学
癌症
纳米技术
内科学
经济
财务
作者
Hongge Ma,Wen‐Wen Lin,Panying Shi
出处
期刊:Chinese journal of radiological medicine and protection
日期:2015-11-25
卷期号:35 (11): 809-814
标识
DOI:10.3760/cma.j.issn.0254-5098.2015.11.003
摘要
Objective
To study the effects of AuNPs@PEG-AS1411 nanoparticles on radiosensitization of human uterine cervix cancer HeLa cells.
Methods
AuNPs were synthesized by citrate reduction method and then functioned with PEG and PEG-AS1411, respectively. CCK-8 assay and colon forming assay were used to detect the acute and chronic toxicity effects of AuNPs on HeLa cells, respectively. At the same time, clonogenic survival assay was applied to measure the cell survival rate of HeLa cells after exposure to AuNPs@PEG and AuNPs@PEG-AS1411 combined with X-ray radiation. The intracellular uptake of AuNPs@PEG and AuNPs@PEG-AS1411 in HeLa cells were detected by ICP-MS.
Results
The CCK-8 assay showed that AuNPs@PEG and AuNPs@PEG-AS1411 were not toxical on HeLa cells(P>0.05). But the clonogenic survival assay showed that AuNPs@PEG and AuNPs@PEG-AS1411 had toxicity on HeLa cells significantly after 10 d(t=4.38-11.60, P<0.05). AuNPs functioned with AS1411 could increase the cellular uptake of AuNPs. AuNPs@PEG and AuNPs@PEG-AS1411 both had significant radiosensitive effect on HeLa cells (F=7.90, 48.23, P<0.05). The values of SERDo for AuNPs@PEG and AuNPs@PEG-AS1411 were 1.12 and 1.20, respectively, when the concentration of Au was 10 mg/L.
Conclusions
AuNPs@PEG and AuNPs@PEG-AS1411 could cause chronic toxicity on HeLa cells instead of acute effect. PEGylated AuNPs functioned with AS1411 could enhance the radiosensitivity of HeLa cells in vitro.
Key words:
AS1411; Au nanoparticles; Radiosensitization
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