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In Vitro Study No: 681

METHODS

Chemical Conc. (mg/ml)Volume (ml)Loading (mg/cm2)VehicleSpeciesMembraneSiteArea (cm2)Cell TypeReceptor FluidTemp. (oC)Temp. MeasuredExposure Time (h)Study Length (h)OccludedAnalytical Method
Propoxur7.50.20.1560% aq. EthanolPigFull Thickness SkinEar10Perfused Pig EarWhole Pigs Blood30Incubator442Radiolabelled (14C)

RESULTS

% Recovery+/-% In Stratum Corneum+/-% in Viable Skin+/-% Penetrated+/-% Absorbed+/-s-s-flux (mcrg/cm2/h)+/-kp (cm/h)nLag Time (h)
        5.333.22.5 0.00033361

NOTES

The integrity of the skin was tested with [3H]labelled water. The Potential absorbed dose was calculated from the applied dose minus the dose left on the surface at the end of the experiment this was 26.1 mcrg/cm2. The absorbed dose after 4h was 8mcrg/cm2. The permeability coefficient was calculated by dividing the steady state flux by the concentration applied.

REFERENCE

Comparative In Vitro-In Vivo Percutaneous Absorption Of The Pesticide Propoxur (2000) Toxicol. Sci., 58 :15-22