Abstract
Precise knowledge of the oxygen diffusion coefficient (D) in tissue is essential for the analysis of oxygen transport. The PO2 profile in a tissue can be measured with a deeply recessed (L/d > 5), Polarographic microelectrode (Linsenmeier, 1986; Haugh et al., 1990). By contrast, one with a shallow recess (L/d < 1) is affected by D in the tissue. It is possible to utilize this feature to determine the tissue D from the polarization transient when the electrode is turned on (i.e., the imposed voltage is changed). The faster the approach to steady state, the larger the value of D must be. Previous attempts to utilize a microelectrode turn-on transient to give local values of D in tissue (Erdmann and Krell, 1976; Buerk, 1980; Buerk and Goldstick, 1990) were plagued by the problem that initially the extremely large current saturated the amplifier. In the present study, the amplifier saturation was eliminated by open-circuiting the amplifier for a few ms initially. All of the data recorded after the initial delay, including those at very early times, were used for the calculation of D by a nonlinear regression analysis. Apparently there have been no reliable previous measurements of D in the mammalian retina or cornea in situ. The usual previous approach has been to make the measurement on a slice of excised tissue in vitro. The measurements in the present study are therefore novel because they are local and made in situ in the intact tissue of a living animal.
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© 1990 Plenum Press, New York
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Roh, HD., Goldstick, T.K., Linsenmeier, R.A. (1990). Spatial Variation of the Local Tissue Oxygen Diffusion Coefficient Measured in situ in the Cat Retina and Cornea. In: Piiper, J., Goldstick, T.K., Meyer, M. (eds) Oxygen Transport to Tissue XII. Advances in Experimental Medicine and Biology, vol 277. Springer, Boston, MA. https://doi.org/10.1007/978-1-4684-8181-5_17
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DOI: https://doi.org/10.1007/978-1-4684-8181-5_17
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