相关实验视频
Updated: Jun 28, 2026

11:43
Hyperpolarized 13C Metabolic Magnetic Resonance Spectroscopy and Imaging
Published on: December 30, 2016
为13C-MRI使用的新型高极化对比剂来自对氧基乙烯基基的化
Francesca Reineri1, Alessandra Viale, Giovanbattista Giovenzana
1Dipartimento di Chimica IFM, Università di Torino, Via P. Giuria 7, 10125 Torino, Italy.
Journal of the American Chemical Society
|October 17, 2008
概括
两个新型的基因衍生物是对化有效的基质,产生高极化基. 由此产生的对称衍生物是水溶性的,可以在体内进行MRI应用.
科学领域:
- 超极化MRI对比剂是一种超极化的MRI对比剂.
- 有机合成 有机合成
- 量子化学是一种量子化学.
背景情况:
- 准化是一种生产高极化化合物的方法.
- 超极化分子增强MRI的灵敏度.
- 基基底被探索,因为它们在产生新型超极化剂方面的潜力.
研究的目的:
- 合成和评估基因衍生物作为对化基质.
- 开发一个理论框架来解释准化机制.
- 评估所得到的超极化化合物对于MRI应用的适用性.
主要方法:
- 基因衍生物与氧乙烯链的合成.
- 使用ALTADENA和PASADENA技术进行准化反应.
- 理论建模对诱导效应的理论建模.
- 在不同溶剂中进行体外 (13) C-MR成像.
- 现场循环用于增强信号采集.
主要成果:
- 两种基因衍生物在准化中表现出良好的基质性能.
- 实现了对应的高极化基的高产量.
- 开发了一个理论来解释对称和不对称的基因中的准化效应.
- 对称的化产品表现出良好的水溶性.
- 在水溶液中进行了成功的体外 (13) C-MR成像.
结论:
- 橄氧乙烯链赋予了对化基衍生物的水溶性.
- 溶于水的产品有助于分离和准备体内MRI.
- 这些发现支持开发新的超极化对比剂用于医学成像.
相关概念视频
Nuclear Overhauser Enhancement (NOE)
Irradiation of a spin-active nucleus causes an increase or decrease in the signal intensity of neighboring nuclei that are not necessarily chemically bonded or involved in J-coupling. This phenomenon, called the nuclear Overhauser enhancement (NOE), results from through-space interactions between the nuclear spins. The NOE effect decreases with increasing internuclear distance and is generally not observed beyond 4 angstroms. In NOE, dipole-dipole interactions between neighboring spin-active...
Magnetic Resonance Imaging
Magnetic resonance imaging (MRI) is a noninvasive medical imaging technique based on a phenomenon of nuclear physics discovered in the 1930s, in which matter exposed to magnetic fields and radio waves was found to emit radio signals. In 1970, a physician and researcher named Raymond Damadian noticed that malignant (cancerous) tissue gave off different signals than normal body tissue. He applied for a patent for the first MRI scanning device in clinical use by the early 1980s. The early MRI...
¹³C NMR: ¹H–¹³C Decoupling
The probability of having two carbon-13 atoms next to each other is negligible because of the low natural abundance of carbon-13. Consequently, peak splitting due to carbon-carbon spin-spin coupling is not observed in spectra. However, protons up to three sigma bonds away split the carbon signal according to the n+1 rule, resulting in complicated spectra.
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
A broadband decoupling technique is used to simplify these complex, sometimes overlapping, signals. Broadband decoupling relies on a...
Insensitive Nuclei Enhanced by Polarization Transfer (INEPT)
Insensitive Nuclei Enhanced by Polarization Transfer (INEPT) is an advanced Nuclear Magnetic Resonance (NMR) technique specifically designed to detect and enhance the signals of low-abundance nuclei, such as carbon-13 and nitrogen-15, in small molecules. The fundamental principle behind INEPT is the transfer of polarization from a more abundant and highly polarizable nucleus, typically hydrogen-1, to the low-abundance nucleus of interest. This process effectively boosts the NMR signal of the...
Reduction of Alkenes: Asymmetric Catalytic Hydrogenation
Catalytic hydrogenation of alkenes is a transition-metal catalyzed reduction of the double bond using molecular hydrogen to give alkanes. The mode of hydrogen addition follows syn stereochemistry.
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
The metal catalyst used can be either heterogeneous or homogeneous. When hydrogenation of an alkene generates a chiral center, a pair of enantiomeric products is expected to form. However, an enantiomeric excess of one of the products can be facilitated using an enantioselective reaction or an...
π Electron Effects on Chemical Shift: Overview
An applied magnetic field causes loosely bound π-electrons in organic molecules to circulate, producing a local or induced diamagnetic field over a large spatial volume. As the molecules tumble in solution, the field generated by π-electrons in spherical substituents results in a zero net field. However, the net field generated by π-electrons in non-spherical substituents is not zero. The effect of this induced field depends on the orientation of the molecule with respect to B0, resulting in...

