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Hypoxia is a feature of most solid tumors and a key determinant of cancer growth and propagation. Sensing hypoxia effectively could lead to more favorable clinical outcomes. Here, we report a molecular antenna-based bimodal probe designed to exploit the complementary advantages of magnetic resonance (MR)- and optical-based imaging. Specifically, we describe the synthesis and evaluation of a dual-action probe () that permits hypoxia-activated chemical exchange saturation transfer (CEST) MR and optical imaging. In CT26 cells, this probe not only provides an enhanced CEST MRI signal but also turns "on" the optical signal under hypoxic conditions. Time-dependent CEST imaging in a hypoxic CT26 tumor xenograft mouse model revealed probe-dependent tumor detection by CEST MRI contrast in the tumor area. We thus suggest that dual-action hypoxia probes, like that reported here, could have a role to play in solid tumor diagnosis and monitoring.
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http://dx.doi.org/10.1021/acs.jmedchem.1c01745 | DOI Listing |
Magn Reson Imaging
September 2025
Physikalisch-Technische Bundesanstalt (PTB), Berlin and Braunschweig, Germany.
Unlabelled: A novel steady-state CEST sequence design, based on the underlying physical model of longitudinal magnetization development during CEST saturation and data acquisition is presented and validated in-silico, in vitro and in vivo. This design ensures consistent data acquisition in the pure CEST steady-state, leading to high MTR scores and image quality, both in vitro and in vivo, when compared to contemporary sequential and steady-state CEST sequences.
Purpose: The aim of this study was to enhance CEST sequences by utilizing the pure CEST steady-state in order to deliver higher CEST effects and better sensitivity.
IEEE Access
May 2025
Department of Electrical and Computer Engineering, University of Nebraska-Lincoln, Omaha, NE 68182, USA.
Chemical exchange saturation transfer (CEST) magnetic resonance imaging (MRI) is an emerging non-invasive molecular imaging technique offering significant potential for biomedical research and clinical applications. However, CEST MRI data acquisition requires prolonged scanning times, as data need to be collected at multiple frequency offsets to capture necessary information for accurate analysis of biological compounds. Faster CEST MRI will improve molecular imaging, advancing biomedical pre-clinical research studies and clinical applications.
View Article and Find Full Text PDFMagn Reson Med
August 2025
Department of Diagnostic Radiology, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Purpose: EPI is a fast acquisition sequence, but suffers from geometric distortion because of B field inhomogeneity. This study aims to evaluate the effectiveness of using ΔB map generated from single-shot CEST-EPI to achieve distortion self-correction (DISC).
Methods: CEST MRI usually requires B correction during postprocessing, and the ΔB map can be calculated directly from Z-spectra without extra scan.
NMR Biomed
September 2025
Biomedical Imaging Research Institute, Cedars-Sinai Medical Center, Los Angeles, California, USA.
To assess lower back pain using quantitative chemical exchange saturation transfer (qCEST) imaging in a porcine model by comparing exchange rate maps obtained from multitasking qCEST with conventional qCEST. Use a permuted random forest (PRF) model trained on CEST-derived magnetization transfer ratio (MTR) and exchange rate (k) features to predict Glasgow pain scores. Six Yucatan minipigs were scanned at baseline and at four post-injury time points (weeks 4, 8, 12, and 16) following intervertebral disc injury.
View Article and Find Full Text PDFCancers (Basel)
August 2025
Department of Medical Physics and Engineering, Division of Health Sciences, Graduate School of Medicine, The University of Osaka, Suita 560-0871, Osaka, Japan.
: This study aimed to examine the changes in brain metabolites and water molecule diffusion using chemical exchange saturation transfer (CEST) imaging and diffusion-weighted imaging (DWI) after 15 Gy of X-ray irradiation in a rat model of glioma. : The glioma-derived cell line, C6, was implanted into the striatum of the right brain of 7-week-old male Wistar rats. CEST imaging and DWI were performed on days 8, 10, and 17 after implantation using a 7T-magnetic resonance imaging.
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