首页> 外文期刊>Journal of biomedical nanotechnology >Hypoxic Radiosensitizer-Lipid Coated Gold Nanoparticles Enhance the Effects of Radiation Therapy on Tumor Growth
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Hypoxic Radiosensitizer-Lipid Coated Gold Nanoparticles Enhance the Effects of Radiation Therapy on Tumor Growth

机译:缺氧放射胶酶 - 脂质涂覆的金纳米颗粒增强了放射治疗对肿瘤生长的影响

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摘要

Radiotherapy (RT) has become one of the most effective treatments for malignant tumor. Intra-tumoral hypoxia is recognized as a chief reason that induces resistance to radiation. Moreover, the toxicities of RT to normal tissues limits the usage of high doses of radiation to eliminate cancer cells. Therefore, developing an effective radiosensitizer is critical for improving the curative effects of RT. In the present study, we developed angiopep-2 (A2) modified hypoxic lipid radiosensitizer (HLR) coated gold nanoparticles (GNPs) (referred to as A2-HRGNPs) to increase the RT sensitivity of tumors. The A2-HRGNPs are comprised of the following two functional components: (1) HLR enhances the RT sensitivity on hypoxic tumor cells; (2) alkylthiol modified GNPs (DGNPs) increase radiation effects by a dose enhancing effect in RT. Our findings suggest that the synergistic radiosensitizing effects of A2-HRGNPs can significantly enhance radiosensitization effects and thus, inhibit tumor growth in vivo.
机译:放射疗法(RT)已成为恶性肿瘤最有效的治疗之一。肿瘤内缺氧被认为是诱导对辐射抗性的主要原因。此外,RT至正常组织的毒性限制了高剂量辐射以消除癌细胞的使用。因此,开发有效的辐射敏化剂对于改善室温的疗效至关重要。在本研究中,我们开发了Angiopep-2(A2)改性的缺氧脂质放射剂(HLR)涂覆的金纳米颗粒(GNP)(称为A2-HRGNP)以增加肿瘤的RT敏感性。 A2-HRGNPS由以下两种功能组分组成:(1)HLR增强了缺氧肿瘤细胞的RT敏感性; (2)烷硫醇改性的GNPS(DGNPS)通过在室温中的剂量增强作用增加辐射效应。我们的研究结果表明,A2-HRGNPS的协同放射敏化效应可以显着增强放射敏化效应,从而抑制体内肿瘤生长。

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