Andrade Jayanaraian F M, Rocho Rafael V, Matos Breno N, Barbalho Geisa N, Nunes Kariane M, Cunha-Filho Marcilio, Gelfuso Guilherme M, Gratieri Tais
Laboratory of Food, Drugs, and Cosmetics (LTMAC), University of Brasilia (UnB), Brasília 70910-900, DF, Brazil.
Pharmaceutical and Cosmetic Research and Development Laboratory, Institute of Public Health, Federal University of Western Pará (UFOPA), Santarem 68040-255, PA, Brazil.
Pharmaceutics. 2025 Jun 17;17(6):786. doi: 10.3390/pharmaceutics17060786.
Treatment options for androgenic alopecia are still very limited and lack long-term efficacy. Dutasteride (DUT) has gained interest as a potent inhibitor of 5α-reductase, allowing for spaced applications, but DUT oral intake can cause serious adverse effects. Herein, we developed, characterized, and assessed the potential of DUT-loaded ethosomes with increasing ethanolic concentrations for hair follicle (HF) targeting to treat androgenic alopecia, hypothesizing that ethanol's interaction with HFs' sebum might increase DUT targeting to the HFs. Ethosomes were obtained using the water-dropping method. After a hydrodynamic size screening, a 30% ethanol concentration was fixed. Ethosomes with 30% ethanol were also prepared and had their ethanolic content removed by rotary evaporation for the evaluation of ethanol in targeting DUT to the HFs. The targeting factor (Tf) was calculated as the ratio between the DUT amount in HFs and the total DUT amount recovered from all skin layers after in vitro porcine skin penetration tests for 12 and 24 h. The ethanolic concentration affected the vesicles' size and the targeting potential. While the dried ethosomes could not increase DUT accumulation in the HFs at both time points (Tf: 0.27 in 12 h and Tf: 0.28 in 24 h), the presence of 30% ethanol in the vesicles increased the Tf from 0.28 (12 h) to 0.34 (24 h), significantly superior ( < 0.05) than the dried ethosome and control (Tf: 0.24) in 24 h. Ethosomes with a 30% ethanolic concentration were slightly more efficient in targeting HFs for dutasteride delivery.
雄激素性脱发的治疗选择仍然非常有限,且缺乏长期疗效。度他雄胺(DUT)作为一种强效的5α-还原酶抑制剂受到关注,可间隔使用,但口服DUT会引起严重的不良反应。在此,我们开发、表征并评估了乙醇浓度递增的载DUT乙醇脂质体靶向毛囊(HF)治疗雄激素性脱发的潜力,推测乙醇与HF皮脂的相互作用可能会增加DUT对HF的靶向性。乙醇脂质体采用水滴法制备。经过流体动力学尺寸筛选后,确定乙醇浓度为30%。还制备了含30%乙醇的乙醇脂质体,并通过旋转蒸发去除其乙醇含量,以评估乙醇在将DUT靶向HF中的作用。靶向因子(Tf)计算为体外猪皮肤渗透试验12小时和24小时后HF中DUT量与从所有皮肤层回收的总DUT量之比。乙醇浓度影响囊泡大小和靶向潜力。虽然干燥的乙醇脂质体在两个时间点都不能增加HF中DUT的积累(12小时时Tf为0.27,24小时时Tf为0.28),但囊泡中30%乙醇的存在使Tf从0.28(12小时)增加到0.34(24小时),在24小时时显著优于(<0.05)干燥的乙醇脂质体和对照组(Tf为0.24)。乙醇浓度为30%的乙醇脂质体在将度他雄胺递送至HF方面效率略高。