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Plasmon resonance coupling of metal nanoparticles for molecular imaging of carcinogenesis in vivo

机译:金属纳米粒子的等离子体共振耦合用于体内致癌分子成像

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An effective cancer control strategy requires improved early detection methods, patient-specific drug selection, and the ability to assess response to targeted therapeutics. Recently, plasmon resonance coupling between closely spaced metal nanoparticles has been used to develop ultrasensitive bioanalytical assays in vitro. We demonstrate the first in vivo application of plasmon coupling for molecular imaging of carcinogenesis. We describe molecular-specific gold bioconju-gates to image epidermal growth factor receptor (EGFR); these conjugates can be delivered topically and imaged noninvasively in real time. We show that labeling with gold bioconjugates gives information on the overexpression and nanoscale spatial relationship of EGF receptors in cell membranes, both of which are altered in neoplasia. EGFR-mediated aggregation of gold nanoparticles in neoplastic cells results in more than a 100-nm color shift and a contrast ratio of more than tenfold in images of normal and precahcerous epithelium in vivo, dramatically increasing contrast beyond values reported previously for antibody-targeted fluorescent dyes.
机译:有效的癌症控制策略需要改进的早期检测方法,针对患者的药物选择以及评估针对靶向疗法的反应的能力。近来,紧密间隔的金属纳米颗粒之间的等离振子共振耦合已被用于体外开发超灵敏生物分析测定。我们证明了等离激元偶联的首次体内应用为致癌分子成像。我们描述了分子特异性金生物缀合物来成像表皮生长因子受体(EGFR);这些结合物可以局部递送并实时进行无创成像。我们表明,用金生物共轭物标记可提供关于EGF受体在细胞膜中过度表达和纳米级空间关系的信息,两者在赘生物中均发生改变。 EGFR介导的肿瘤细胞中金纳米颗粒的聚集导致体内正常和癌前上皮图像中超过100 nm的色移和超过十倍的对比度,从而大大提高了对比度,超出了以前针对抗体靶向的荧光报告的值染料。

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