透皮
动态光散射
傅里叶变换红外光谱
离子液体
微乳液
化学工程
化学
材料科学
分析化学(期刊)
色谱法
纳米技术
药理学
纳米颗粒
医学
有机化学
生物化学
肺表面活性物质
工程类
催化作用
作者
Isabel R. Nichols,Christine M. Hamadani,Claylee M. Chism,Alysha N. Hunter,Humayun Ahmad,Kendall Wontor,Ashley E. Williams,Priyavrat Vashisth,Nathan I. Hammer,Santanu Kundu,Eden E. L. Tanner
标识
DOI:10.1002/adtp.202200096
摘要
Abstract Ionic liquids (ILs) have been shown to be effective transdermal penetrants of pharmaceutically active ingredients, including small molecules and proteins. The presence of water within ionic liquids has been demonstrated to play a critical role in their structural organization on the molecular level. However, the impact of water on IL transdermal transport efficacy has yet to be investigated. Herein, a water concentration gradient (0%–100% v/v) is tested to evaluate choline trans‐2‐octenoic (CA2OE)‐mediated transport of a hydrophilic model drug dextran (10000 Da) in an ex vivo porcine skin model.Compared to 2:1, 1:1, 1:4, and 1:5 ionic ratio formulations, 50% v/v CA2OE 1:2‐water evidences the greatest success at transporting dextran to the acceptor fluid. Physicochemical characterization (dynamic light scattering (DLS), scanning electron microscopy (SEM), optical density (O.D.), Fourier transform infrared spectroscopy (FTIR), fluorescent microscopy, and rheology) is conducted to test both bulk and nanoscale‐level CA2OE 1:2–water interactions. It is hypothesized that the presence of microemulsions in the CA2OE 1:2 75% v/v formulation accounted for the severely decreased transport compared to the 50%. It is thus critical to comprehensively consider interactions between IL components, co‐solvents, anddrug molecules when formulating ILs for transdermal transport applications.
科研通智能强力驱动
Strongly Powered by AbleSci AI