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Theoretical and experimental studies on manipulation of fluorescence by gold nanoparticle: Application for molecular imaging.

机译:金纳米粒子操纵荧光的理论和实验研究:在分子成像中的应用。

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摘要

Gold nanoparticles (GNPs) have shown beneficial properties for biomedical use, e.g., their non-toxic nature and surface properties for easy modification. Upon receiving light, they generate a strong surface plasmon field, which can alter the fluorescence of fluorophores. The level and type of the fluorescence alteration depend on the GNP size and shape, excitation (Ex)/emission (Em) wavelengths and quantum yield of the fluorophore, as well as the distance between the fluorophore and GNP.;Utilizing the quenching/enhancement ability of GNPs, a near-infrared (NIR) contrast agent that emits fluorescence at a higher level only at the particular cancer site was developed. Cypate, a safe NIR fluorophore, was selected as the fluorophore because NIR penetrates deeper into tissue and because Cypate is non-toxic. Cypate was conjugated to a GNP via two spacers. One is short for the quenching and with a substrate for a breast cancer-specific enzyme, urokinase-type plasminogen activator (uPA). The other is a long, biocompatible polymer chain for fluorescence enhancement. The fluorescence of the contrast agent was quenched by GNP by 93%. In the presence of uPA, the short spacer was cleaved and the remaining long spacer enhanced fluorescence 1.8 times.;The study results are beneficial for developing efficacious optical contrast agents. This novel contrast agent can detect and diagnose breast cancer with high specificity and sensitivity, as FRET or molecular beacon but with a higher sensitivity and without the restriction of using DNA/RNA segments.;In this dissertation, the effect of the properties listed above on the fluorescence output was theoretically analyzed for the fluorophores frequently used in biomedical studies. For fluorescence quenching, fluorophores with the Em wavelength near the GNP plasmon resonance peak (520 nm) are better suited. As the Em wavelength increases, a shorter distance is required for achieving the same level of quenching. A bigger GNP requires shorter distance for quenching. To obtain fluorescence enhancement, the Em wavelength of the fluorophore needs to be longer than the GNP plasmon resonance peak (e.g., > 650 nm). The fluorophore with lower intrinsic quantum yield tends to be enhanced more. The GNP needs to be sufficiently large (> 5 nm), and a bigger GNP provides a higher maximum enhancement.
机译:金纳米颗粒(GNP)已显示出对生物医学有益的特性,例如其无毒特性和易于修饰的表面特性。接收到光后,它们会产生很强的表面等离激元场,从而改变荧光团的荧光。荧光变化的水平和类型取决于GNP的大小和形状,荧光团的激发(Ex)/发射(Em)波长和量子产率以及荧光团与GNP之间的距离;利用猝灭/增强开发了GNP的功能,一种近红外(NIR)造影剂,仅在特定的癌症部位才会发出更高水平的荧光。 Cypate是一种安全的NIR荧光团,被选作荧光团是因为NIR可以更深入地渗透到组织中,并且Cypate无毒。经由两个间隔基将胞苷与GNP缀合。一种是淬灭的缩写,以乳腺癌特异性酶尿激酶型纤溶酶原激活剂(uPA)为底物。另一个是用于荧光增强的长生物相容性聚合物链。造影剂的荧光被GNP淬灭了93%。在存在uPA的情况下,短间隔子被切割,剩余的长间隔子被荧光增强1.8倍。该研究结果对于开发有效的光学造影剂是有益的。这种新型的造影剂可以像FRET或分子信标一样,以高特异性和高灵敏度检测和诊断乳腺癌,但具有更高的灵敏度,并且不受DNA / RNA片段使用的限制。从理论上分析了生物医学研究中常用的荧光团的荧光输出。对于荧光猝灭,更适合使用Em波长接近GNP等离子体共振峰(520 nm)的荧光团。随着Em波长的增加,实现相同水平的淬灭需要更短的距离。较大的GNP需要较短的淬火距离。为了获得荧光增强,荧光团的Em波长需要长于GNP等离子体激元共振峰(例如,> 650nm)。具有较低固有量子产率的荧光团趋于进一步增强。 GNP必须足够大(> 5 nm),并且更大的GNP会提供更高的最大增强。

著录项

  • 作者

    Wang, Jianting.;

  • 作者单位

    University of Louisville.;

  • 授予单位 University of Louisville.;
  • 学科 Chemistry Biochemistry.;Engineering Chemical.;Engineering Biomedical.
  • 学位 Ph.D.
  • 年度 2011
  • 页码 145 p.
  • 总页数 145
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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