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Simultaneous measurement of intracellular and extracellular oxygen concentrations using a nitroxide-liposome system

✍ Scribed by James F. Glockner; Shong-Wan Norby; Harold M. Swartz


Publisher
John Wiley and Sons
Year
1993
Tongue
English
Weight
695 KB
Volume
29
Category
Article
ISSN
0740-3194

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✦ Synopsis


Abstract

The concentration of oxygen within cells is important in many physiological and pathological processes, but such oxygendependent phenomena are generally studied as a function of the concentration of extracellular oxygen, due to a lack of suitable methods. Electron parmamagnetic resonance (EPR) oximetric techniques offer an attractive alternative to make such measurements. Previous EPR oximetric studies of extracellular‐intracellular oxygen gradients have been hindered, however, by the fact that separate samples, prepared in slightly different ways, were required for individual measurements of extracellular and intracellular oxygen concentrations. In this study we demonstrate a technique that allows simultaneous measurement of intracellular and extracellular oxygen concentrations in a single sample: extracellular measurement is achieved using positively charged nitroxides encapsulated in liposomes, while intracellular oxygen is determined using a membrane‐permeable nitroxide along with an extracellular broadening agent. Application of this system to the measurement of oxygen concentrations in suspensions of rat myoblast cells gave results which are consistent with nonsimultaneous measurements and which show substantial extracellular‐intracellular oxygen gradients in these rapidly respiring cells.


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## Abstract [O~2~] was measured in the embedding material (alginate) in a typical apparatus for conducting studies of viable cells with NMR, using low frequency EPR. In suspension cultures respiration was independent of [O~2~] in the perfusing media down to about 1 μM while in alginate beads, the c