Jiyu Wu, Renai Xu, Xiaowei Xu, Shiyuan Ye, Aifang Huang
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引用次数: 0
摘要
本研究旨在设计和评估Huperzine A乙素体凝胶的体外透皮性。研究人员采用注射法制备了Huperzine A乙硫体,并对其物理和化学特性进行了表征。比较了 Huperzine A 乙素体凝胶、普通凝胶和乳膏。在小鼠腹部皮肤上进行了弗朗兹扩散细胞试验,并使用 LC-MS/MS 测定了 Huperzine A 的浓度。透皮量、皮肤保留率和透皮率用于评估三种制剂的经皮渗透性。结果表明,与普通凝胶和乳膏相比,Huperzine A ethosomes 凝胶的累积渗透率、透皮率和皮肤保留率明显更高。研究结果表明,Huperzine A ethosomes 凝胶具有可控的质量和良好的透皮吸收特性,有望成为临床用药的安全选择。
Preparation and evaluation of transdermal permeation of Huperzine A ethosomes gel in vitro
This study aimed to design and evaluate the transdermal permeation of Huperzine A ethosomes gel in vitro. Huperzine A ethosomes were prepared using the injection method, and their physical and chemical properties were characterized. A comparison was made between Huperzine A ethosomes gel, ordinary gel, and cream. The Franz diffusion cell test on mouse abdominal skin was conducted, and Huperzine A concentration was determined using LC-MS/MS. Transdermal volume, skin retention, and transdermal rate were used to assess the percutaneous permeability of the three preparations. Results demonstrated that Huperzine A ethosomes gel exhibited significantly higher accumulative permeation, transdermal rate, and skin retention compared to ordinary gel and cream. The findings suggest that Huperzine A ethosomes gel, with its controllable quality and favorable transdermal absorption properties, holds potential as a safe option for clinical administration.