» Articles » PMID: 26666980

A Microperfusion and In-Bore Oxygenator System Designed for Magnetic Resonance Microscopy Studies on Living Tissue Explants

Overview
Journal Sci Rep
Specialty Science
Date 2015 Dec 16
PMID 26666980
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

Spectrometers now offer the field strengths necessary to visualize mammalian cells but were not designed to accommodate imaging of live tissues. As such, spectrometers pose significant challenges--the most evident of which are spatial limitations--to conducting experiments in living tissue. This limitation becomes problematic upon trying to employ commercial perfusion equipment which is bulky and--being designed almost exclusively for light microscopy or electrophysiology studies--seldom includes MR-compatibility as a design criterion. To overcome problems exclusive to ultra-high magnetic field environments with limited spatial access, we have designed microperfusion and in-bore oxygenation systems capable of interfacing with Bruker's series of micro surface-coils. These devices are designed for supporting cellular resolution imaging in MR studies of excised, living tissue. The combined system allows for precise control of both dissolved gas and pH levels in the perfusate thus demonstrating applicability for a wide range of tissue types. Its compactness, linear architecture, and MR-compatible material content are key design features intended to provide a versatile hardware interface compatible with any NMR spectrometer. Such attributes will ensure the microperfusion rig's continued utility as it may be used with a multitude of contemporary NMR systems in addition to those which are currently in development.

Citing Articles

Visualization of live, mammalian neurons during Kainate-infusion using magnetic resonance microscopy.

Flint J, Menon K, Hansen B, Forder J, Blackband S Neuroimage. 2020; 219:116997.

PMID: 32492508 PMC: 7510773. DOI: 10.1016/j.neuroimage.2020.116997.


Metabolic Support of Excised, Living Brain Tissues During Magnetic Resonance Microscopy Acquisition.

Flint J, Menon K, Hansen B, Forder J, Blackband S J Vis Exp. 2017; (128).

PMID: 29155793 PMC: 5752427. DOI: 10.3791/56282.


White matter biomarkers from fast protocols using axially symmetric diffusion kurtosis imaging.

Hansen B, Khan A, Shemesh N, Lund T, Sangill R, Eskildsen S NMR Biomed. 2017; 30(9).

PMID: 28543843 PMC: 5557696. DOI: 10.1002/nbm.3741.


Diffusion tensor microscopy data (15.6 μm in-plane) of white matter tracts in the human, pig, and rat spinal cord with corresponding tissue histology.

Flint J, Hansen B, Blackband S Data Brief. 2016; 9:271-4.

PMID: 27668273 PMC: 5024313. DOI: 10.1016/j.dib.2016.08.020.

References
1.
Flint J, Hansen B, Vestergaard-Poulsen P, Blackband S . Diffusion weighted magnetic resonance imaging of neuronal activity in the hippocampal slice model. Neuroimage. 2009; 46(2):411-8. PMC: 2719792. DOI: 10.1016/j.neuroimage.2009.02.003. View

2.
Schumacher K, Khong Y, Chang S, Ni J, Sun W, Yu H . Perfusion culture improves the maintenance of cultured liver tissue slices. Tissue Eng. 2007; 13(1):197-205. DOI: 10.1089/ten.2006.0046. View

3.
Choi Y, McClain M, LaPlaca M, Frazier A, Allen M . Three dimensional MEMS microfluidic perfusion system for thick brain slice cultures. Biomed Microdevices. 2006; 9(1):7-13. DOI: 10.1007/s10544-006-9004-8. View

4.
Mitchell R, CARMAN C, Severinghaus J, Richardson B, SINGER M, Shnider S . Stability of cerebrospinal fluid pH in chronic acid-base disturbances in blood. J Appl Physiol. 1965; 20(3):443-52. DOI: 10.1152/jappl.1965.20.3.443. View

5.
Pomper J, GRAULICH J, Kovacs R, Hoffmann U, Gabriel S, Heinemann U . High oxygen tension leads to acute cell death in organotypic hippocampal slice cultures. Brain Res Dev Brain Res. 2001; 126(1):109-16. DOI: 10.1016/s0165-3806(00)00132-2. View