Salimi Anayatollah, Jafarian Soroush, Salimi Arghavan, Mohammad Soleymani Saeed
Department of Pharmaceutics, Faculty of Pharmacy, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
Nanotechnology Research Center, Ahvaz Jundishapur University of Medical Sciences, Ahvaz, Iran.
J Cosmet Dermatol. 2025 Feb;24(2):e16685. doi: 10.1111/jocd.16685. Epub 2024 Nov 20.
Valproic acid (VPA) is used to treat various neurological and psychiatric conditions. While oral VPA can cause hair loss, topical application has shown potential for hair regeneration. This study aimed to develop and evaluate microemulsion (ME) formulations of VPA for enhanced transfollicular delivery.
VPA-loaded MEs were prepared using oleic acid, Transcutol P, Tween 80, Labrasol, and Capryol 90. The MEs were characterized for physicochemical properties, stability, in vitro release, and ex vivo permeation through the hairy abdominal and nonhairy ear skin of guinea pigs.
Eight stable ME formulations were developed with droplet sizes ranging from 10 to 24 nm, pH 4.6 to 5.2, and viscosity 77 to 85 cps. In vitro release studies showed controlled release profiles over 24 h. Permeation studies revealed enhanced drug delivery through both follicular and nonfollicular pathways compared with aqueous VPA solution. Formulations with higher surfactant/cosurfactant ratios showed increased permeation through the follicular pathway.
The ME formulations significantly enhanced VPA penetration into both epidermal and follicular pathways compared with aqueous solution. The composition of the MEs, particularly the oil content, water content, and surfactant/cosurfactant ratio, played a crucial role in determining the physicochemical properties and skin permeation parameters of VPA.
丙戊酸(VPA)用于治疗各种神经和精神疾病。虽然口服VPA会导致脱发,但局部应用已显示出促进毛发生长的潜力。本研究旨在开发和评估用于增强经毛囊递送的VPA微乳剂(ME)制剂。
使用油酸、Transcutol P、吐温80、Labrasol和辛酸癸酸甘油三酯制备载有VPA的微乳剂。对微乳剂的理化性质、稳定性、体外释放以及通过豚鼠腹部有毛皮肤和耳部无毛皮肤的离体渗透进行了表征。
开发了8种稳定的微乳剂制剂,液滴尺寸范围为10至24纳米,pH值为4.6至5.2,粘度为77至85厘泊。体外释放研究显示在24小时内具有控释曲线。渗透研究表明,与VPA水溶液相比,通过毛囊和非毛囊途径的药物递送均有所增强。具有较高表面活性剂/助表面活性剂比例的制剂通过毛囊途径的渗透增加。
与水溶液相比,微乳剂制剂显著增强了VPA对表皮和毛囊途径的渗透。微乳剂的组成,特别是油含量、水含量以及表面活性剂/助表面活性剂比例,在决定VPA的理化性质和皮肤渗透参数方面起着关键作用。