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Self-Assembly of Peptide Amphiphiles Designed as Imaging Probes for 19F and Relaxation-Enhanced 1H imaging.

机译:肽两亲物的自组装设计为19F和增强弛豫1H成像的成像探针。

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摘要

This work incorporates whole-body imaging functionality into peptide amphiphile (PA) nanostructures used for regenerative medicine to facilitate magnetic resonance imaging (MRI). Two strategies were employed: 1. Conjugation of gadolinium chelates to peptide nanostructures to monitor biomaterial degradation in vivo with MRI and inductively-coupled plasma-mass spectroscopy (ICP-MS) 2. Synthesis of perfluorinated moiety-bearing peptide amphiphiles for 19F-MRI. The Gd(III) chelate gadoteridol was conjugated by copper-catalyzed "click" chemistry to a series of PAs known to form cylindrical nanostructures. By fitting nuclear magnetic resonance dispersion (NMRD) profiles to the Solomon-Bloembergen-Morgan (SBM) equations, it was observed that the water exchange parameter (tauM) depended on thermal annealing or calcium ion cross-linking. The sequence C16V 3A3E3G(Gd) exhibited an acceleration of nearly 100 ns after thermal annealing and calcium addition. These gadolinium-labeled PAs were used to track in vivo degradation of gels within the tibialis anterior muscle in a murine model. The half-life of biomaterial degradation was determined to be 13.5 days by inductively coupled plasma mass spectrometry (ICP-MS) of Gd(III). Gel implants could be monitored by MRI for eight days before the signal dispersed due to implant degradation and dilution.;Additionally, nanostructures incorporating highly fluorinated domains were investigated for use as MRI contrast agents. Short, perfluoroalkyane tails of seven or eight carbon atoms in length were grafted to PA sequences containing a V2A2 beta-sheet forming sequence. The V2A2 sequence is known to drive 1D nanostructure assembly. It was found that the sequences C7F13V2A 2E2 and C7F13V2A 2K3 formed 1D assemblies in water which transition from ribbon-like to cylindrical shape as pH increases from 4.5 to 8.0. Ribbon-like nanostructures had reduced magnetic resonance signal by T 2 relaxation quenching, whereas their cylindrical counterparts exhibited strong signals with signal-to-noise ratios greater than 100. In addition to pH, the effect of divalent calcium ions on NMR signal was probed. C7 V2A2E2 was shown to exhibit the highest sensitivity to calcium in the 1.5 to 6 mM regime. This range corresponded to widening of the C7V2A2E2 nanostructure from 16+/-4 to 22+/-5 nm. It is speculated that increasing ribbon thickness is tied to magnetic resonance signal quenching due to higher local viscosity of the perfluorinated moiety.
机译:这项工作将全身成像功能整合到用于再生医学的两亲肽(PA)纳米结构中,以促进磁共振成像(MRI)。采用了两种策略:1.将ado螯合物与肽纳米结构缀合,以通过MRI和电感耦合等离子体质谱(ICP-MS)监测体内生物材料的降解。2.合成用于19F-MRI的带有全氟部分的肽两亲物。通过铜催化的“喀哒”化学将Gd(III)螯合物加德替多偶联到一系列已知可形成圆柱形纳米结构的PA上。通过将核磁共振扩散(NMRD)曲线拟合到Solomon-Bloembergen-Morgan(SBM)方程,可以观察到水交换参数(tauM)取决于热退火或钙离子交联。在热退火和添加钙后,序列C16V 3A3E3G(Gd)表现出近100 ns的加速度。这些g标记的PA用于在鼠模型中追踪胫骨前肌内凝胶的体内降解。通过电感耦合等离子体质谱法(ICP-MS)测定Gd(III)的生物材料降解的半衰期为13.5天。由于植入物的降解和稀释,在信号分散之前,可以通过MRI监测凝胶植入物八天。此外,研究了掺入高度氟化域的纳米结构作为MRI造影剂。将长度为七个或八个碳原子的短的全氟烷烃尾部接枝到含有V2A2β-折叠形成序列的PA序列上。已知V2A2序列可驱动一维纳米结构组装。已经发现,序列C7F13V2A 2E2和C7F13V2A 2K3在水中形成了一维组件,随着pH从4.5从8.0增加到8.0,该组件从带状过渡到圆柱状。带状纳米结构通过T 2弛豫淬灭降低了磁共振信号,而其圆柱状对应结构则显示出强信噪比大于100的信号。除了pH值外,还探究了二价钙离子对NMR信号的影响。已显示C7 V2A2E2在1.5至6 mM的方案中表现出对钙的最高敏感性。此范围对应于C7V2A2E2纳米结构从16 +/- 4 nm扩展到22 +/- 5 nm。据推测,由于全氟化部分的较高局部粘度,增加的带厚度与磁共振信号猝灭有关。

著录项

  • 作者

    Preslar, Adam Truett.;

  • 作者单位

    Northwestern University.;

  • 授予单位 Northwestern University.;
  • 学科 Materials science.;Medical imaging.
  • 学位 Ph.D.
  • 年度 2016
  • 页码 235 p.
  • 总页数 235
  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类
  • 关键词

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