Purpose: To assess the feasibility and accuracy of 3D ultrashort echo time (UTE) magnetic resonance (MR) thermometry of frozen tissue during cryoablation on a clinical 3T MR system.
Materials And Methods: Ex vivo porcine muscle specimens (n = 4) were imaged during two cycles of 10:3 minutes freeze-thaw on a 3T clinical MR scanner. Continuous MR monitoring was performed using a 3D radial ramp-sampled UTE sequence with a shortest TE of 70 μs. Fiber optic sensors were used for temperature reference. Data of three experiments were used as reference sets. Signal intensity values were normalized to baseline before cooling and related to temperature. Data for subzero temperatures were fit to a monoexponential function. In the separate validation set, the obtained fit was used to generate 3D MR temperature maps of frozen tissue at each imaging timepoint. Statistical analysis was performed to assess accuracy of the MR temperature maps.
Results: With 3D UTE imaging, MR signal was measured from frozen tissue down to temperatures as low as -40°C. Temperatures predicted from the MR temperature maps strongly correlated with sensor recorded values (r = 0.977, P < 0.001). Bland-Altman analysis demonstrated a mean difference between MR-estimated temperatures and sensor readings of -1.2 ± 2.7°C with upper and lower limits of agreement of +4.1 and -6.5°C, respectively.
Conclusion: 3D MR thermometry of frozen tissue using UTE signal intensity was feasible during cryoablation on a clinical 3T MR system. Down to temperatures as low as -40°C, accuracy of the MR temperature maps was within clinically acceptable limits. J. Magn. Reson. Imaging 2016;44:1572-1579.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1002/jmri.25301 | DOI Listing |
Methods Mol Biol
January 2025
Sorbonne Université, Institut du Cerveau (Paris Brain Institute) ICM, Inserm, CNRS, Hôpital de la Pitié Salpêtrière, Paris, France.
Somatic mosaic variants, and especially somatic single nucleotide variants (sSNVs), occur in progenitor cells in the developing human brain frequently enough to provide permanent, unique, and cumulative markers of cell divisions and clones. Here, we describe an experimental workflow to perform lineage studies in the human brain using somatic variants. The workflow consists in two major steps: (1) sSNV calling through whole-genome sequencing (WGS) of bulk (non-single-cell) DNA extracted from human fresh-frozen tissue biopsies, and (2) sSNV validation and cell phylogeny deciphering through single nuclei whole-genome amplification (WGA) followed by targeted sequencing of sSNV loci.
View Article and Find Full Text PDFZhongguo Shi Yan Xue Ye Xue Za Zhi
December 2024
Blood Disease Institute, Xuzhou Medical University,Xuzhou 221000, Jiangsu Province, China.
Objective: To harvest the primary Philadelphia chromosome-positive (Ph) cells of B-acute lymphoblastic leukemia (B-ALL) and to establish the B-ALL mouse model.
Methods: The plasmid carrying fusion gene was transferred into the bone marrow(BM) cells of C57BL/6J mice by retrovirus. Syngeneic mice irradiated with 9 Gy of Co γ-ray were injected with the transfected BM cells as the first generation (G1), and then the primary cells from the spleen and BM of the diseased mice were obtained and frozen.
EBioMedicine
December 2024
Translational & Clinical Research Institute, Faculty of Medical Sciences, Newcastle University, Newcastle upon Tyne, United Kingdom; Department of Gastroenterology, The Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle upon Tyne, United Kingdom. Electronic address:
Background: Large-scale multicentre studies are needed to understand complex relationships between the gut microbiota, health and disease. Interrogating the mucosal microbiota may identify important biology not captured by stool analysis. Gold standard tissue cryopreservation ('flash freezing') limits large-scale study feasibility.
View Article and Find Full Text PDFAm J Sports Med
January 2025
Department of Orthopedics and Traumatology, Medical University of Innsbruck, Innsbruck, Austria.
Background: It is still unknown if the double-femoral tunnel technique (Arciero [ARC]) provides better stability as compared with the single-femoral tunnel technique (modified Larson [LAR]) in posterolateral corner reconstruction. The ideal angle of fixation of the popliteofibular strand in ARC is also unknown.
Hypotheses: The ARC provides greater external rotation (ER) stability than the LAR (hypothesis 1); there is no difference in varus rotation (VR) stability between LAR and ARC (hypothesis 2); and femoral fixation of the popliteofibular strand at 60° during the ARC leads to greater ER stability than fixation at 30° or 90° of knee flexion (hypothesis 3).
Sci Rep
December 2024
Department of Health Science and Technology, Aalborg University, Gistrup, 9260, Denmark.
Cryopreservation enhances the availability of "off-the-shelf" cell therapies. However, the choice between tissue culture polystyrene (TCP) and hollow fiber system (HFB) system for adipose-derived stem cell (ASC) production remains a critical decision, with implications for scalability, reproducibility, and the clinical efficacy. Therefore, the characteristics of ASCs expanded in TCP and HFB and cryopreserved were compared.
View Article and Find Full Text PDFEnter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!