z-logo
Premium
In vivo oximetry using a nitroxide‐liposome system
Author(s) -
Glockner James F.,
Chan HsiaoChang,
Swartz Harold M.
Publication year - 1991
Publication title -
magnetic resonance in medicine
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.696
H-Index - 225
eISSN - 1522-2594
pISSN - 0740-3194
DOI - 10.1002/mrm.1910200113
Subject(s) - nitroxide mediated radical polymerization , liposome , chemistry , electron paramagnetic resonance , spin probe , oxygen , in vivo , aqueous solution , limiting oxygen concentration , nuclear magnetic resonance , analytical chemistry (journal) , chromatography , biochemistry , polymerization , radical polymerization , physics , microbiology and biotechnology , organic chemistry , biology , polymer
Liposomes containing the deuterated, charged, aqueous soluble nitroxide 4‐trimethylammonium‐2,2,6,6‐tetramethylpiperidine‐d 16 ‐1‐oxyl (d‐Cat 1 ) were used as probes to measure oxygen concentrations in vivo . Following intramuscular or intraperitoneal injection of the liposome suspension, ICR mice were placed over the surface probe of a low frequency (1.1 GHz) electron paramagnetic resonance (EPR) spectrometer. The linewidth of the deuterated nitroxide is sensitive to changes in the dissolved oxygen concentration: this parameter was calibrated separately so that linewidths measured in the injected mice could be converted into oxygen tensions. This technique detected substantial changes in pO 2 as the oxygen content of the breathing gas was changed from 21 to 85 to 0%. Intravenous injection of the liposomes also is possible, and the liposomes accumulate in the liver and spleen, where detectable, oxygen‐sensitive EPR signals can be measured. © 1991 Academic Press, Inc.

This content is not available in your region!

Continue researching here.

Having issues? You can contact us here
Accelerating Research

Address

John Eccles House
Robert Robinson Avenue,
Oxford Science Park, Oxford
OX4 4GP, United Kingdom