Development of Ethosomes for the Topical Treatment of Androgenic Alopecia: Ethanol Effect on Dutasteride Targeting to the Hair Follicles.

IF 5.5 3区 医学 Q1 PHARMACOLOGY & PHARMACY
Jayanaraian F M Andrade, Rafael V Rocho, Breno N Matos, Geisa N Barbalho, Kariane M Nunes, Marcilio Cunha-Filho, Guilherme M Gelfuso, Tais Gratieri
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Abstract

Background/Objectives: 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. Methods: 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. Results: 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 (p < 0.05) than the dried ethosome and control (Tf: 0.24) in 24 h. Conclusion: Ethosomes with a 30% ethanolic concentration were slightly more efficient in targeting HFs for dutasteride delivery.

局部治疗雄激素性脱发的溶酶体的研制:乙醇对靶向毛囊的杜他雄胺的影响。
背景/目的:雄激素性脱发的治疗选择仍然非常有限,缺乏长期疗效。Dutasteride (DUT)是一种有效的5α-还原酶抑制剂,可以间隔使用,但Dutasteride口服可引起严重的不良反应。在此,我们开发、表征并评估了负载DUT的酶体在增加乙醇浓度的情况下对毛囊(HF)靶向治疗雄激素性脱发的潜力,并假设乙醇与HF皮脂的相互作用可能会增加DUT对HF的靶向。方法:采用水滴法提取脂质体。经过水动力粒度筛选后,固定30%的乙醇浓度。还制备了含30%乙醇的酶体,并通过旋转蒸发去除其乙醇含量,以评估乙醇靶向DUT到hf的效果。靶因子(targeting factor, Tf)计算为体外猪皮透皮试验12和24 h后,hf中DUT量与各皮肤层回收的总DUT量之比。结果:乙醇浓度影响囊泡大小和靶电位。虽然干燥的醇质体在两个时间点(12 h和24 h的Tf分别为0.27和0.28)均不能增加DUT在HFs中的积累,但30%乙醇的存在使其在24 h的Tf从0.28 (12 h)增加到0.34 (24 h),显著优于干燥的醇质体和对照组(Tf: 0.24) (p < 0.05)。结论:30%乙醇浓度的醇质体靶向HFs递送du他雄胺的效率略高。
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来源期刊
Pharmaceutics
Pharmaceutics Pharmacology, Toxicology and Pharmaceutics-Pharmaceutical Science
CiteScore
7.90
自引率
11.10%
发文量
2379
审稿时长
16.41 days
期刊介绍: Pharmaceutics (ISSN 1999-4923) is an open access journal which provides an advanced forum for the science and technology of pharmaceutics and biopharmaceutics. It publishes reviews, regular research papers, communications,  and short notes. Covered topics include pharmacokinetics, toxicokinetics, pharmacodynamics, pharmacogenetics and pharmacogenomics, and pharmaceutical formulation. Our aim is to encourage scientists to publish their experimental and theoretical details in as much detail as possible. There is no restriction on the length of the papers. The full experimental details must be provided so that the results can be reproduced.
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