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In vivo photoacoustic imaging of breast cancer tumor with HER2-targeted nanodiamonds

机译:在乳腺癌肿瘤的体内光声成像与Her2目标纳米金刚石

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Radiation-damaged nanodiamonds (NDs) are ideal optical contrast agents for photoacoustic (PA) imaging in biological tissues due to their good biocompatibility and high optical absorbance in the near-infrared (NIR) range. Acid treated NDs are oxidized to form carboxyl groups on the surface, functionalized with polyethylene glycol (PEG) and human epidermal growth factor receptor 2 (HER2) targeting ligand for breast cancer tumor imaging. Because of the specific binding of the ligand conjugated NDs to the HER2-overexpressing murine breast cancer cells (4T1.2 neu), the tumor tissues are significantly delineated from the surrounding normal tissue at wavelength of 820 nm under the PA imaging modality. Moreover, HER2 targeted NDs (HER2-PEG-NDs) result in higher accumulation in HER2 positive breast tumors as compared to non-targeted NDs after intravenous injection (i.v.). Longer retention time of HER-PEG-NDs is observed in HER2 overexpressing tumor model than that in negative tumor model (4T1.2). This demonstrates that targeting moiety conjugated NDs have great potential for the sensitive detection of cancer tumors and provide an attractive delivery strategy for anti-cancer drugs.
机译:由于其近红外(NIR)范围内的良好的生物相容性和高光学吸光度,辐射损坏的纳米二胺(NDS)是生物组织中的光声(PA)成像的理想光学造影剂。酸处理的ND被氧化以在表面上形成羧基,用聚乙二醇(PEG)和人表皮生长因子受体2(HER2)靶向配体的乳腺癌肿瘤成像。由于配体缀合的NDS对HER2-过表达鼠乳腺癌细胞(4T1.2 NEU)的特异性结合,肿瘤组织在PA成像模态下从820nm的周围正常组织显着描绘。此外,与静脉注射后(I.V.)之后的非靶向ND相比,HER2靶向NDS(HER2-PEG-NDS)导致HER2阳性乳腺肿瘤中的累积较高。在HER2过表达肿瘤模型中观察到HER-PEG-NDS的更长的保留时间而不是阴性肿瘤模型(4T1.2)。这证明靶向部分缀合的ND具有敏感性癌症肿瘤的敏感性潜力,并为抗癌药物提供有吸引力的交付策略。

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