透皮
自愈水凝胶
布洛芬
溶解度
药品
化学
药理学
卡拉胶
剂型
药物输送
水溶液
渗透
毒品携带者
药剂学
色谱法
医学
有机化学
生物化学
膜
作者
Sónia Pedro,Maria S.M. Mendes,Bruno Miguel Neves,Isabel F. Almeida,Paulo Costa,Inês Correia‐Sá,Carla Vilela,Mara G. Freire,Armando J. D. Silvestre,Carmen S. R. Freire
出处
期刊:Pharmaceutics
[MDPI AG]
日期:2022-04-10
卷期号:14 (4): 827-827
被引量:18
标识
DOI:10.3390/pharmaceutics14040827
摘要
The transdermal administration of nonsteroidal anti-inflammatory drugs (NSAIDs) is a valuable and safer alternative to their oral intake. However, most of these drugs display low water solubility, which makes their incorporation into hydrophilic biopolymeric drug-delivery systems difficult. To overcome this drawback, aqueous solutions of bio-based deep eutectic solvents (DES) were investigated to enhance the solubility of ibuprofen, a widely used NSAID, leading to an increase in its solubility of up to 7917-fold when compared to its water solubility. These DES solutions were shown to be non-toxic to macrophages with cell viabilities of 97.4% (at ibuprofen concentrations of 0.25 mM), while preserving the anti-inflammatory action of the drug. Their incorporation into alginate-based hydrogels resulted in materials with a regular structure and higher flexibility. These hydrogels present a sustained release of the drug, which is able, when containing the DES aqueous solution comprising ibuprofen, to deliver 93.5% of the drug after 8 h in PBS. Furthermore, these hydrogels were able to improve the drug permeation across human skin by 8.5-fold in comparison with the hydrogel counterpart containing only ibuprofen. This work highlights the possibility to remarkably improve the transdermal administration of NSAIDs by combining new drug formulations based on DES and biopolymeric drug delivery systems.
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