Ren Yun-Hao, Song Feng-Yuan, Zhao Jing-Yu, Liang Bing-Wen, Peng Li-Hua
College of Pharmaceutical Sciences, Zhejiang University, Hangzhou 310058, China.
Jinhua Institute of Zhejiang University, Jinhua 321299, China.
Pharmaceutics. 2024 Dec 16;16(12):1600. doi: 10.3390/pharmaceutics16121600.
Cyclovirobuxine D, a natural compound derived from the medicinal plant Buxus sinica, demonstrates a diverse array of therapeutic benefits, encompassing anti-arrhythmic properties, blood pressure regulation, neuronal protection, and anti-ischemic activity. However, its limited solubility hinders the bioavailability of current oral and injectable formulations, causing considerable adverse reactions and toxicity. In this investigation, we embarked on an unprecedented exploration of the skin penetration potential of cyclovirobuxine D utilizing chemical penetration enhancers and niosomes as innovative strategies to enhance its dermal absorption. These strategies were rigorously tested and optimized. Among the tested chemical penetration enhancers, azone emerged as the most potent, achieving a 4.55-fold increase in skin penetration compared to the untreated group. Additionally, when encapsulated within niosomes, primarily composed of Span60 and cholesterol, the skin penetration of cyclovirobuxine D was notably enhanced by 1.50-fold. Furthermore, when both cyclovirobuxine D and azone were co-encapsulated within the niosomes, the skin penetration of cyclovirobuxine D was remarkably elevated by 8.10-fold compared to the solvent-dispersed group. This enhancement was corroborated through rigorous in vitro and in vivo experiments. Notably, the combination of other chemical penetration enhancers with niosome encapsulation also exhibited synergistic effects in enhancing the skin penetration of cyclovirobuxine D. These findings provide a compelling rationale for the administration of cyclovirobuxine D via skin-mediated transdermal delivery, offering superior safety, efficacy, and convenience. The innovative combination of niosomes and chemical penetration enhancers represents a novel system for the transdermal delivery of cyclovirobuxine D, holding immense promise for clinical applications in the treatment of brain, neuronal, and cardiovascular disorders.
环维黄杨星D是一种从药用植物黄杨中提取的天然化合物,具有多种治疗益处,包括抗心律失常特性、血压调节、神经保护和抗缺血活性。然而,其有限的溶解度阻碍了当前口服和注射制剂的生物利用度,导致相当多的不良反应和毒性。在本研究中,我们利用化学渗透促进剂和脂质体作为创新策略,以前所未有的方式探索环维黄杨星D的皮肤渗透潜力,以提高其经皮吸收。这些策略经过了严格的测试和优化。在测试的化学渗透促进剂中,氮酮表现出最强的效果,与未处理组相比,皮肤渗透率提高了4.55倍。此外,当环维黄杨星D包裹在主要由司盘60和胆固醇组成的脂质体中时,其皮肤渗透率显著提高了1.50倍。此外,当环维黄杨星D和氮酮共同包裹在脂质体中时,与溶剂分散组相比,环维黄杨星D的皮肤渗透率显著提高了8.10倍。通过严格的体外和体内实验证实了这种增强效果。值得注意的是,其他化学渗透促进剂与脂质体包裹的组合在提高环维黄杨星D的皮肤渗透率方面也表现出协同作用。这些发现为通过皮肤介导的透皮给药方式施用环维黄杨星D提供了令人信服的理由,具有更高的安全性、有效性和便利性。脂质体和化学渗透促进剂的创新组合代表了一种用于环维黄杨星D透皮给药的新型系统,在治疗脑、神经和心血管疾病的临床应用中具有巨大潜力。