IN VITRO STUDIES FURTHER DETAILS
In Vitro Study No: 170
METHODS
Chemical
Conc. (mg/ml)
Volume (ml)
Loading (mg/cm2)
Vehicle
Species
Membrane
Site
Area (cm2)
Cell Type
Receptor Fluid
Temp. (oC)
Temp. Measured
Exposure Time (h)
Study Length (h)
Occluded
Analytical Method
2-Phenoxyethanol
73
0.01
1.14
Methanol
Rat
Dermatomed to 0.244mm
Dorsal
0.64
Flow-through
MEM & penicilllin/streptomycin + CO2
37
Receptor Fluid
24
24
2
Radiolabelled (14C)
RESULTS
% Recovery
+/-
% In Stratum Corneum
+/-
% in Viable Skin
+/-
% Penetrated
+/-
% Absorbed
+/-
s-s-flux (mcrg/cm2/h)
+/-
kp (cm/h)
n
Lag Time (h)
51
2.9
0.3
1.6
0.4
47.5
43
3.7
0.001764
6
0
NOTES
Only 51% of the applied dose was accounted for 24h post dose. The loss is expected to be due to evaporation.
REFERENCE
Percutaneous Penetration Of 2-Phenoxyethanol Through Rat And Human Skin (1997) Food Chem.Toxicol., 35 :1009-1016