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Direct quantitative C-filtered H magnetic resonance imaging of PEGylated biomacromolecules in vivo.

作者信息

Alvares Rohan D A, Lau Justin Y C, Macdonald Peter M, Cunningham Charles H, Prosser R Scott

机构信息

Department of Chemistry, University of Toronto, Mississauga, Ontario, Canada.

Department of Medical Biophysics, University of Toronto, Toronto, Ontario, Canada.

出版信息

Magn Reson Med. 2017 Apr;77(4):1553-1561. doi: 10.1002/mrm.26237. Epub 2016 Apr 15.

Abstract

PURPOSE

H MRI is an established diagnostic method that generally relies on detection of water. Imaging specific macromolecules is normally accomplished only indirectly through the use of paramagnetic tags, which alter the water signal in their vicinity. We demonstrate a new approach in which macromolecular constituents, such as proteins and drug delivery systems, are observed directly and quantitatively in vivo using H MRI of C-labeled poly(ethylene glycol) ( C-PEG) tags.

METHODS

Molecular imaging of C-PEG-labeled species was accomplished by incorporating a modified heteronuclear multiple quantum coherence filter into a gradient echo imaging sequence. We demonstrate the approach by monitoring the real-time distribution of C-PEG and C-PEGylated albumin injected into the hind leg of a mouse.

RESULTS

Filtering the H PEG signal through the directly coupled C nuclei largely eliminates background water and fat signals, thus enabling the imaging of molecules using H MRI.

CONCLUSION

PEGylation is widely employed to enhance the performance of a multitude of macromolecular therapeutics and drug delivery systems, and C-filtered H MRI of C-PEG thus offers the possibility of imaging and quantitating their distribution in living systems in real time. Magn Reson Med 77:1553-1561, 2017. © 2016 International Society for Magnetic Resonance in Medicine.

摘要

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