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首页> 外文期刊>Materials science & engineering >The physicochemical and biological characterization of a 24-month-stored nanocomplex based on gold nanoparticles conjugated with cetuximab demonstrated long-term stability, EGFR affinity and cancer cell death due to apoptosis
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The physicochemical and biological characterization of a 24-month-stored nanocomplex based on gold nanoparticles conjugated with cetuximab demonstrated long-term stability, EGFR affinity and cancer cell death due to apoptosis

机译:基于金纳米颗粒与西妥昔单抗缀合的24个月存储的纳米复合物的理化和生物学特性显示出长期稳定性,EGFR亲和力和凋亡导致的癌细胞死亡

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摘要

Nanotechnology is one of the most promising tools for future diagnosis and therapy. Thus, we have produced gold nanoparticles coated with cetuximab at a dose-range from 5 mu g up to 200 mu g, and prolonged stable nanocomplexes were obtained. The nanocomplexes were characterized by UV-Vis, zeta potential, TEM, fluorometry, infrared regions, XPS and atomic absorption spectrometry. For biological characterization the A431 cell line was used. Cellular uptake, target affinity and cell death were assessed using ICP-OES, immunocytochemistry and flow cytometry, respectively. The immobilization of cetuximab on the AuNPs surfaces was confirmed. The nanocomplex with 24 months of manufacturing promoted efficient EGFR binding and induced tumour cell death due to apoptosis. Significant (p < 0.05) cell death was achieved using relatively low cetuximab concentration for AuNPs coating compared to the antibody alone. Therefore, our results provided robust physicochemical and biological characterization data corroborating the cetuximab-bioconjugate AuNPs as a feasible nanocomplex for biomedical applications.
机译:纳米技术是未来诊断和治疗的最有前途的工具之一。因此,我们制备了用西妥昔单抗包被的金纳米颗粒,其剂量范围为5微克至200微克,并获得了稳定的纳米复合物。通过UV-Vis,ζ电势,TEM,荧光法,红外区,XPS和原子吸收光谱对纳米复合物进行了表征。为了生物学表征,使用A431细胞系。分别使用ICP-OES,免疫细胞化学和流式细胞仪评估细胞摄取,靶标亲和力和细胞死亡。证实西妥昔单抗固定在AuNPs表面上。具有24个月制造时间的纳米复合物促进有效的EGFR结合并诱导由于凋亡引起的肿瘤细胞死亡。与单独的抗体相比,使用相对较低浓度的AuNPs涂层西妥昔单抗可实现显着(p <0.05)细胞死亡。因此,我们的结果提供了可靠的理化和生物学表征数据,证实了西妥昔单抗-生物共轭物AuNPs作为生物医学应用中可行的纳米复合物。

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