Purpose
To characterize qualitatively and quantitatively the absorption of
metronidazole solution, in greater concentrations and for longer periods,
when applied topically to an experimental open skin wound model.
Methods
An open skin wound, 2 cm in diameter and total skin thickness was prepared,
under anesthetic, in the dorsal region of 108 Wistar rats weighing between
300 and 350 grams. The animals were allocated to groups of 18 animals in
accordance with the concentration of metronidazole in the solution to be
applied daily to the wound. In the control group (CG), 0.9% sodium chloride
solution was used for application, and in the experimental groups (GI, GII,
GIII, GIV and GV) metronidazole solution at 4%, 6%, 8%, 10% and 12%,
respectively, was applied. After 3, 7 and 14 days of treatment. Blood
samples collected through cardiac puncture were examined for the existence
or non-existence of metronidazole, using high performance liquid
chromatography (HPLC). Detected metronidazole values were compared
statistically within each group (temporal analysis 3 days X 7 days X 14
days) and between the groups that used topical metronidazole (4% X 6% X 8% X
10% and 12%) using the Kruskal-Wallis test, considering a statistical
significance of 95% (p<0.05).
Results
Metronidazole was detected in all the samples at all times in all the groups
in which topical metronidazole was applied to the wounds.
Characteristically, there was no significant difference between the doses
obtained within each group over time (3 days X 7 days X 14 days) GI=0.461;
GII=0.154; GIII=0.888; GIV= 0.264 and GV=0.152. In the evaluation between
groups, a similar degree of absorption was found after 3 days (p=0.829) and
14 days (p=0.751).
Conclusion
The serum concentration of metronidazole that was achieved was not influenced
by the concentration of the solution applied to the skin wound, with similar
extend, or by the duration of the application.