RESUMO
Solid inclusion complex between hydroxypropyl-ß-cyclodextrin (HP-ß-CD) and minoxidil (MXD) was prepared by freeze-drying and characterized by yield, drug loading and dissolution rate. Moreover, the complex was formulated as alginate gel (GEL HP-ß-CD)/MXD 3.5% w/w). The efficacy of the novel GEL HP-ß-CD)/MXD 3.5% w/w and of MXD 3.5% w/w ethanolic/propylene-glycol solution (MXD solution) were evaluated by monitoring the hair growth of dorsal skin 1-4 weeks after depilation followed by histological analysis and gene expression in skin biopsies in male rat. Patch-clamp experiments and cell-dehydrogenase activity (CDA) were performed to evaluate the capability of the formulations to activate "in vitro" the ATP-sensitive K+-channels (KATP) and their effects on cell viability in skin fibroblasts. After 3 weeks, the MXD solution and MXD/HP-ß-CD GEL enhanced the hair growth, respectively, of 80.1⯱â¯2% and 84.3⯱â¯4% vs controls. After 4 weeks, the MXD/HP-ß-CD GEL significantly enhanced the hair length and bulb diameter vs others groups. The MXD/HP-ß-CD GEL significantly enhanced the mRNA levels of the SUR2 and Kir6.1 subunits of the KATP channels and AKT2 vs other groups. The AR gene was down-regulated vs controls following the treatment with either MXD formulations. Either MXD (10-4â¯M) formulations were effective in potentiating the KATP currents. The MXD solution and its vehicle after 9â¯h of incubation time, but not MXD/HP-ß-CD, reduced CDA in fibroblasts. In sum, the MXD/HP-ß-CD GEL shows a favorable profile following topical long-term use.