UCEPR: Ultrafast localized CEST-spectroscopy with PRESS in phantoms and in vivo

Zheng Liu, Ivan E. Dimitrov, Robert E. Lenkinski, Asghar Hajibeigi, Elena Vinogradov

Research output: Contribution to journalArticlepeer-review

21 Scopus citations


Purpose Chemical exchange saturation transfer (CEST) is a contrast mechanism enhancing low-concentration molecules through saturation transfer from their exchangeable protons to bulk water. Often many scans are acquired to form a Z-spectrum, making the CEST method time-consuming. Here, an ultrafast localized CEST-spectroscopy with PRESS (UCEPR) is proposed to obtain the entire Z-spectrum of a voxel using only two scans, significantly accelerating CEST. Theory and Methods The approach combines ultrafast nonlocalized CEST spectroscopy with localization using PRESS. A field gradient is applied concurrently with the saturation pulse producing simultaneous saturation of all Z-spectrum frequencies that are also spatially encoded. A readout gradient during data acquisition resolves the spatial dependence of the CEST responses into frequency. UCEPR was tested on a 3T scanner both in phantoms and in vivo. Results In phantoms, a fast Z-spectroscopy acquisition of multiple pH-variant iopamidol samples was achieved with four- to seven-fold acceleration as compared to the conventional CEST methods. In vivo, amide proton transfer (APT) in white matter of healthy human brain was measured rapidly in 48 s and with high frequency resolution (≤ 0.2 ppm). Conclusion Compared with conventional CEST methods, UCEPR has the advantage of rapidly acquiring high-resolution Z-spectra. Potential in vivo applications include ultrafast localized Z-spectroscopy, quantitative, or dynamic CEST studies.

Original languageEnglish (US)
Pages (from-to)1875-1885
Number of pages11
JournalMagnetic resonance in medicine
Issue number5
StatePublished - May 1 2016


  • APT
  • broadband saturation
  • iopamidol
  • ultrafast localized CEST

ASJC Scopus subject areas

  • Radiology Nuclear Medicine and imaging


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