Pedro Sónia N, Mendes Maria S M, Neves Bruno M, Almeida Isabel Filipa, Costa Paulo, Correia-Sá Inês, Vilela Carla, Freire Mara G, Silvestre Armando J D, Freire Carmen S R
Department of Chemistry and CICECO-Aveiro Institute of Materials, University of Aveiro, 3810-193 Aveiro, Portugal.
Department of Medical Sciences and Institute of Biomedicine-iBiMED, University of Aveiro, 3810-193 Aveiro, Portugal.
Pharmaceutics. 2022 Apr 10;14(4):827. doi: 10.3390/pharmaceutics14040827.
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.
非甾体抗炎药(NSAIDs)的经皮给药是口服给药的一种有价值且更安全的替代方式。然而,这些药物大多水溶性较低,这使得将它们纳入亲水性生物聚合物药物递送系统变得困难。为克服这一缺点,研究了基于生物的低共熔溶剂(DES)水溶液以提高布洛芬(一种广泛使用的NSAIDs)的溶解度,与在水中的溶解度相比,其溶解度提高了高达7917倍。这些DES溶液对巨噬细胞无毒,细胞活力为97.4%(布洛芬浓度为0.25 mM时),同时保留了药物的抗炎作用。将它们掺入基于藻酸盐的水凝胶中得到了结构规则且柔韧性更高的材料。这些水凝胶呈现药物的持续释放,当含有包含布洛芬的DES水溶液时,在PBS中8小时后能够释放93.5%的药物。此外,与仅含有布洛芬的水凝胶相比,这些水凝胶能够使药物透过人体皮肤的能力提高8.5倍。这项工作突出了通过结合基于DES的新药物制剂和生物聚合物药物递送系统来显著改善NSAIDs经皮给药的可能性。