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Screening CEST contrast agents using ultrafast CEST imaging.

Xiang Xu1, Nirbhay N Yadav1, Xiaolei Song1

  • 1Russell H. Morgan Department of Radiology and Radiological Science, The Johns Hopkins University School of Medicine, Baltimore, MD, United States; F.M. Kirby Research Center for Functional Brain Imaging, Kennedy Krieger Institute, Baltimore, MD, United States.

Journal of Magnetic Resonance (San Diego, Calif. : 1997)
|March 13, 2016
PubMed
Summary
This summary is machine-generated.

Ultrafast chemical exchange saturation transfer (CEST) imaging accelerates sample screening. This method enables rapid quantification of exchange rates for high-throughput screening of CEST contrast agents.

Keywords:
CESTContrast agentMRIUltrafast spectroscopy

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Area of Science:

  • Magnetic Resonance Imaging
  • Chemical Exchange Saturation Transfer (CEST)
  • Biomedical Imaging

Background:

  • Chemical Exchange Saturation Transfer (CEST) is a powerful MRI technique for detecting low-concentration metabolites.
  • Traditional CEST experiments can be time-consuming, limiting their application in high-throughput screening.
  • Developing faster CEST methods is crucial for broader clinical and research applications.

Purpose of the Study:

  • To present a novel, ultrafast method for chemical exchange saturation transfer (CEST) imaging.
  • To enable simultaneous screening of multiple samples using this accelerated CEST approach.
  • To facilitate rapid quantification of exchange rates for CEST contrast agents.

Main Methods:

  • Implementing a gradient field simultaneously with the saturation pulse for ultrafast CEST acquisition.
  • Developing a method for simultaneous multi-sample screening.
  • Interleaving saturation and readout periods within the repetition time (TR) to acquire images with varying saturation times.
  • Utilizing the variable saturation time (QUEST) approach for accelerated exchange rate quantification.

Main Results:

  • Demonstrated the feasibility of ultrafast CEST for various applications, including dia- and paramagnetic CEST agents, hyperpolarized Xe gas, and in vivo spectroscopy.
  • Successfully implemented a simple method for simultaneous screening of multiple samples.
  • Achieved accelerated quantification of exchange rates, significantly reducing acquisition time.

Conclusions:

  • The presented ultrafast CEST method offers a significant acceleration of imaging and analysis.
  • This technique enables high-throughput screening of CEST contrast agents and other applications.
  • The simultaneous multi-sample screening capability further enhances the efficiency of CEST-based investigations.