Minoxidil has been proposed as a potential topical inhibitor of wound
contraction and proliferative scarring. Suggestions for this applicati
on are derived from in vitro investigations demonstrating inhibition o
f various fibroblastic functions, The purpose of this study was to att
empt to establish in vivo support of these effects using an establishe
d animal model of wound contraction, Standardized cutaneous wounds wer
e created on the dorsum of Sprague-Dawley rats, which were divided equ
ally into six treatment groups. Wounds were treated daily after tracin
g their unhealed areas, On complete closure of the wounds, analyses of
the contraction rates and tensile strength were performed for compari
son among groups, Minoxidil did not demonstrate significant inhibition
of wound contraction rates relative to either an inert vehicle, an ac
tive vehicle, or no treatment, Contrarily, as previously demonstrated
in this animal model, silver sulfadiazine did demonstrate significant
inhibition of wound contraction rates relative to both vehicles. No si
gnificant difference in tensile strength was demonstrated among groups
. These observations do not support the proposed use of minoxidil as a
n ''antifibrotic'' agent.