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含潘那生丁 W/O 微乳的三七总皂苷透皮给药系统,以泛醇作为助表面活性剂以降低皮肤刺激性用于脱发治疗。

Panax notoginseng saponins loaded W/O microemulsion for alopecia therapy with panthenol as cosurfactant to reduce skin irritation.

机构信息

School of Pharmaceutical Sciences, Sun Yat-sen University, University Town, Guangzhou 510006, PR China.

School of Traditional Dai-Thai Medicine, West Yunnan University of Applied Sciences, Jinghong 666100, PR China.

出版信息

Int J Pharm. 2024 Sep 30;663:124585. doi: 10.1016/j.ijpharm.2024.124585. Epub 2024 Aug 13.

DOI:10.1016/j.ijpharm.2024.124585
PMID:39147248
Abstract

The etiology of alopecia is so complex that current therapies with single-mechanism and attendant side-effects during long-term usage, are insufficient for treatment. Panax notoginseng saponins (PNS) is supposed to treat alopecia with multiple mechanisms, but difficult to penetrate skin efficiently due to water-solubility. Here, we designed water-in-oil microemulsion (PNS ME) using jojoba oil, fractioned coconut oil, RH 40 + Span 80 and cosurfactant D-panthenol, to help PNS penetrating the skin. Particularly, D-panthenol not only enlarges the microemulsion area, reduces the usage amounts of surfactants thus relieves skin irritation, but stimulates the migration of dermal papilla cells (DPCs), displaying cooperative effects on anti-alopecia. PNS ME penetrates through sebum-rich corneum via high-affinity lipid fusion, targets to hair follicles (HFs), where it resides in skin for sustained drug release, accelerates angiogenesis to build well-nourished environment for HFs, and facilitates the proliferation and migration of DPCs in vitro. PNS ME markedly improved hair density, skin pigmentation, new hair weight, skin thickness, and collagen generation of telogen effluvium mice. Moreover, PNS also took outstanding curative effects on androgenetic alopecia mice. Upon further exploration, PNS ME caused dramatic upregulations of β-catenin, VEGF and Ki67, suggesting it might function by triggering Wnt/β-catenin pathway, accelerating vessels formation, and activating the hair follicle stem cells. Notably, PNS ME indicated longer-term safety than minoxidil tincture. Together, PNS ME provides a comprehensive strategy for alopecia, especially it avoids defects by high-proportioned surfactants in traditional microemulsion, exhibiting milder and safer, which shows bright prospect of applying microemulsion in hair growth promotion.

摘要

脱发的病因非常复杂,目前的单一机制治疗方法和长期使用带来的副作用,都不足以治疗这种疾病。三七总皂苷(PNS)被认为可以通过多种机制治疗脱发,但由于其水溶性,很难有效地穿透皮肤。在这里,我们使用霍霍巴油、分馏椰子油、RH 40+Span 80 和助表面活性剂 D-泛醇设计了水包油型微乳(PNS ME),以帮助 PNS 穿透皮肤。特别是,D-泛醇不仅可以扩大微乳液的区域,减少表面活性剂的用量,从而减轻皮肤刺激,还可以刺激真皮乳头细胞(DPC)的迁移,对防治脱发具有协同作用。PNS ME 通过与高亲和力的脂质融合穿透富含皮脂的角质层,靶向毛囊(HFs),在皮肤中持续释放药物,促进血管生成,为 HFs 提供营养丰富的环境,并促进 DPC 的体外增殖和迁移。PNS ME 显著改善了休止期脱发小鼠的毛发密度、皮肤色素沉着、新毛重量、皮肤厚度和胶原蛋白生成。此外,PNS 对雄激素性脱发小鼠也有显著的疗效。进一步研究发现,PNS ME 引起β-catenin、VEGF 和 Ki67 的显著上调,提示其可能通过触发 Wnt/β-catenin 通路、加速血管形成和激活毛囊干细胞来发挥作用。值得注意的是,PNS ME 比米诺地尔酊显示出更长的安全性。总之,PNS ME 为脱发提供了一种全面的治疗策略,特别是它避免了传统微乳液中高比例表面活性剂的缺陷,表现出更温和、更安全的特点,这表明微乳液在促进毛发生长方面具有广阔的应用前景。

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