Follicle-Targeted Delivery of Betamethasone and Minoxidil Co-Entrapped in Polymeric and Lipid Nanoparticles for Topical Alopecia Areata Treatment

Alopecia areata is managed with oral corticosteroids, which has known side effects for patients. Given that a topical application of formulations containing a corticoid and a substance controlling hair loss progression could reduce or eliminate such adverse effects and increase the patient's adherence to the treatment, this study prepares polymeric and lipidic nanoparticles (PNPs and NLCs) to co-entrap minoxidil and betamethasone and compares the follicular drug delivery provided by topical application of these nanoparticles. The prepared PNPs loaded 99.1 +/- 13.0% minoxidil and 70.2 +/- 12.8% betamethasone, while the NLCs entrapped 99.4 +/- 0.1 minoxidil and 80.7 +/- 0.1% betamethasone. PNPs and NLCs presented diameters in the same range, varying from 414 +/- 10 nm to 567 +/- 30 nm. The thermal analysis revealed that the production conditions favor the solubilization of the drugs in the nanoparticles, preserving their stability. In in vitro permeation studies with porcine skin, PNPs provided a 2.6-fold increase in minoxidil penetration into the follicular casts compared to the control and no remarkable difference in terms of betamethasone; in contrast, NLCs provided a significant (specifically, a tenfold) increase in minoxidil penetration into the hair follicles compared to the control, and they delivered higher concentrations of betamethasone in hair follicles than both PNPs and the control. Neither PNPs nor NLCs promoted transdermal permeation of the drugs to the receptor solution, which should favor a topical therapy. Furthermore, both nanoparticles targeted approximately 50% of minoxidil delivery to the follicular casts and NLCs targeted 74% of betamethasone delivery to the hair follicles. In conclusion, PNPs and NLCs are promising drug delivery systems for enhancing follicular targeting of drugs, but NLCs showed superior performance for lipophilic drugs.

Automated summary

This study prepared polymeric and lipidic nanoparticles (PNPs and NLCs) co-entrapping minoxidil and betamethasone for follicular drug delivery. The nanoparticles showed suitable size and thermal stability, significantly increasing the penetration of minoxidil and betamethasone into the hair follicles and delivering higher concentrations of betamethasone. The nanoparticles are suitable for topical therapy and effectively target the hair follicles.