Functionalized 129Xe contrast agents for magnetic resonance imaging.

Functionalized 129Xe contrast agents for magnetic resonance imaging.
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DOI:
10.1016/j.cbpa.2009.10.009
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发表时间:
2010-02
影响因子:
7.8
通讯作者:
Dmochowski, Ivan J.
Dmochowski, Ivan J.
中科院分区:
生物学2区
文献类型:
--
作者:
Taratula, Olena;Dmochowski, Ivan J.

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2001年,伯克利大学的一个研究小组首次提出了用于磁共振成像的“氙气生物传感器”的概念,有证据表明,与生物素标记的隐巾结合的超极化129Xe可以在远低于对比剂增强磁共振实验的典型浓度(NM-μM)的情况下检测到链霉亲和素。129Xe生物传感器最近经历了许多发展,以应对分子成像方面的挑战。例如,已经合成了具有明显的~(129)Xe磁共振光谱的、具有10倍高的氙亲和力的隐形化合物。同样相关的还有树枝状隐形分子组装和无机沸石,它们将许多129Xe原子定位到稀有目标上。最后,本文考虑基于寡核苷酸、蛋白质或酶的活性在129Xe化学位移中产生可测量变化的生物传感器,并包括第一个细胞研究。
The concept of ‘xenon biosensor’ for magnetic resonance imaging (MRI) was first proposed by a Berkeley team in 2001, with evidence that hyperpolarized 129Xe bound to a biotin-labeled cryptophane can detect streptavidin at much lower concentrations (nM-μM) than is typical for contrast-enhanced MRI experiments. 129Xe biosensors have undergone many recent developments to address challenges in molecular imaging. For example, cryptophanes have been synthesized that exhibit 10-fold higher xenon affinity with distinct 129Xe magnetic resonance spectra. Also relevant are dendrimeric cryptophane assemblies and inorganic zeolites that localize many 129Xe atoms to rare targets. Finally, this article considers biosensors that produce measurable changes in 129Xe chemical shift based upon the activity of oligonucleotides, proteins, or enzymes, and includes the first cell studies.
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