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. Author manuscript; available in PMC: 2015 Nov 1.
Published in final edited form as: NMR Biomed. 2014 Sep 9;27(11):1313–1324. doi: 10.1002/nbm.3191

Fig. 8. In vivo amine-water proton exchange (APEX) signals measured with CEST and CESL.

Fig. 8

CEST and CESL MRI of rat brains were measured with RF offsets of ±2.5 ppm and ω1 of 500 Hz. (A–B) Data of a single pixel (inset in A) were examined with different flip angle error λ (=1 for CEST and 0 for CESL). The CEST signal intensity at −2.5 ppm and MTRasym (black lines) oscillate for short tirrad. Similar to the simulation and phantom studies, the in vivo results with flip angle error λ = 0.3 are already close to those of ideal spin-lock with λ = 0 and have higher sensitivity than saturation transfer with λ = 1. (C) In ischemic rats, the MTRasym and SLRasym maps with tirrad = 0.15 s show similar ischemic contrast, but the latter has about 20% higher sensitivity. While SLRasym maps are calculated from the difference of two normalized maps of S/S0 at ± 2.5 ppm, this ischemic contrast mostly originates from the APEX-weighted signal at 2.5 ppm. Note the difference gray scales of the maps. (D) The averaged MTRasym and SLRasym (n = 4) as a function of tirrad were obtained from the 2×2 mm2 ROIs in the ischemic ipsilateral (blue) and normal contralateral sides (red box). The CESL SLRasym signal (solid) has higher sensitivity and higher ischemic contrast (red vs. blue) than CEST MTRasym (dashed).