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近红外照射下金纳米链及Anti-EGFR/Au共轭物对人喉癌Hep-2细胞的抑制*☆
引用本文:丛林海,彭淑昆,何晓光,杨一兵. 近红外照射下金纳米链及Anti-EGFR/Au共轭物对人喉癌Hep-2细胞的抑制*☆[J]. 中国组织工程研究, 2012, 16(12): 2145-2148. DOI: 10.3969/j.issn.1673-8225.2012.12.013
作者姓名:丛林海  彭淑昆  何晓光  杨一兵
作者单位:昆明医学院第一附属医院耳鼻咽喉科,云南省昆明市 650031
基金项目:国家自然科学基金项目(81160324/H1625),课题名称: EGFR-mAb功能化修饰金纳米棒光热诱导Hep-2细胞凋亡分子机制研究。
摘    要:背景:金纳米颗粒在近红外激光照射下对肿瘤细胞具有杀伤效应。目的:评价金纳米链及anti-EGFR/Au共轭物近红外照射对人喉癌Hep-2细胞的生长抑制和热杀伤作用。方法:取对数生长期的Hep-2细胞,随机分为空白对照组、单纯照射组、金纳米链照射组和anti-EGFR/Au照射组,加入不同培养液后,各照射组进行近红外激光照射。观察照射后细胞凋亡情况和凋亡程度。结果与结论:倒置显微镜下观察显示空白对照组和单纯照射组Hep-2细胞仍具有活性,金纳米链照射组有明显的损伤,但anti-EGFR/Au照射组损伤程度更重。流式细胞分析显示金纳米链照射组及anti-EGFR/Au靶向照射组均有不同程度的Hep-2细胞凋亡,且照射时间越长,凋亡细胞越多。说明金纳米链近红外照射可以杀伤人喉鳞癌Hep-2细胞,anti-EGFR/Au靶向照射比金纳米链照射效果更好,并呈现一定照射时间的依赖性。关键词:金纳米链;Hep-2细胞;流式细胞分析;照射;生物材料与纳米技术doi:10.3969/j.issn.1673-8225.2012.12.013

关 键 词:金纳米链  Hep-2细胞  流式细胞分析  照射  生物材料与纳米技术  
收稿时间:2011-11-19

Apoptosis of human laryngeal cancer cells induced by gold nanochain and anti-epidermal growth factor receptor/Au conjugate under near-infrared hyperthermia
Cong Lin-hai,Peng Shu-kun,He Xiao-guang,Yang Yi-bing. Apoptosis of human laryngeal cancer cells induced by gold nanochain and anti-epidermal growth factor receptor/Au conjugate under near-infrared hyperthermia[J]. Chinese Journal of Tissue Engineering Research, 2012, 16(12): 2145-2148. DOI: 10.3969/j.issn.1673-8225.2012.12.013
Authors:Cong Lin-hai  Peng Shu-kun  He Xiao-guang  Yang Yi-bing
Affiliation:Department of Otolaryngology, the First Affiliated Hospital of Kunming Medical College, Kunming  650031, Yunnan Province, China
Abstract:BACKGROUND: The gold nanoparticles have a killing effect on tumor cells under the near-infrared laser irradiation.OBJECTIVE: To evaluate the growth inhibition and heat killing effect of gold nanochain and anti-epidermal growth factor receptor (EGFR)/Au conjugate on human laryngeal cancer Hep-2 cells under near-infrared hyperthermia.METHODS: The Hep-2 cells in the logarithmic growth phase were collected and divided into blank control group, irradiation group, gold nanochain irradiation group and anti-EGFR/Au irradiation group. After added with different culture medium, the near-infrared laser irradiation was performed in each group. Then the apoptosis of Hep-2 cells in different experimental groups was observed after the near-infrared laser irradiation. RESULTS AND CONCLUSION: Inverted microscope observation showed that the Hep-2 cells in the blank control and irradiation groups were still active and the Hep-2 cells in the gold nanochain irradiation group were damaged significantly, while the Hep-2 cells in anti-EGFR/Au irradiation group were damaged more serious. Flow cytometry analysis showed that the Hep-2 cells in the gold nanochain irradiation and anti-EGFR/Au irradiation groups had a varying degree of apoptosis and the increasingly heavy damage with the time. The gold nanochain irradiation can kill Hep-2 cells and the anti-EGFR/Au irradiation has a better effect in a time-depended manner.
Keywords:
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