Suppr超能文献

探索布洛芬 L-氨基酸衍生物的烷基酯盐:理化特性和经皮潜力。

Exploring Alkyl Ester Salts of L-Amino Acid Derivatives of Ibuprofen: Physicochemical Characterization and Transdermal Potential.

机构信息

Department of Chemical Organic Technology and Polymeric Materials, Faculty of Chemical Technology and Engineering, West Pomeranian University of Technology in Szczecin, Piastów Ave. 42, 71-065 Szczecin, Poland.

Department of Cosmetic and Pharmaceutical Chemistry, Pomeranian Medical University in Szczecin, Powstańców Wielkopolskich Ave. 72, 70-111 Szczecin, Poland.

出版信息

Molecules. 2023 Nov 10;28(22):7523. doi: 10.3390/molecules28227523.

Abstract

This research presents novel ibuprofen derivatives in the form of alkyl ester salts of L-amino acids with potential analgesic, anti-inflammatory, and antipyretic properties for potential use in transdermal therapeutic systems. New derivatives of ()-2-[4-(2-methylpropyl)phenyl]propionic acid were synthesized using hydrochlorides of alkyl esters (ethyl, propyl, isopropyl, butyl, -butyl, -butyl, and pentyl) of L-glutamine. These were further transformed into alkyl esters of L-amino acid ibuprofenates through neutralization and protonation reactions. Characterization involved spectroscopic methods, including nuclear magnetic resonance and Fourier-transform infrared spectroscopy. Various physicochemical properties were investigated, such as UV-Vis spectroscopy, polarimetric analysis, thermogravimetric analysis, differential scanning calorimetry, X-ray diffraction, water solubility, octanol/water partition coefficient, and permeability through pig skin using Franz diffusion cells. The research confirmed the ionic structure of the obtained hydrochlorides of alkyl esters of L-amino acids and ibuprofenates of alkyl esters of L-glutamic acid. It revealed significant correlations between ester chain length and thermal stability, crystallinity, phase transition temperatures, lipophilicity, water solubility, skin permeability, and skin accumulation of these compounds. Compared to the parent ibuprofen, the synthesized derivatives exhibited higher water solubility, lower lipophilicity, and enhanced skin permeability. This study introduces promising ibuprofen derivatives with improved physicochemical properties, highlighting their potential for transdermal therapeutic applications. The findings shed light on the structure-activity relationships of these derivatives, offering insights into their enhanced solubility and skin permeation, which could lead to more effective topical treatments for pain and inflammation.

摘要

本研究提出了新型布洛芬衍生物,形式为 L-氨基酸的烷基酯盐,具有潜在的镇痛、抗炎和退热特性,可用于透皮治疗系统。使用 L-谷氨酰胺的烷基酯(乙酯、丙酯、异丙酯、丁酯、异丁酯、仲丁酯和戊酯)的盐酸盐合成了()-2-[4-(2-甲基丙基)苯基]丙酸的新衍生物。这些进一步通过中和和质子化反应转化为 L-氨基酸布洛芬的烷基酯。表征涉及光谱方法,包括核磁共振和傅里叶变换红外光谱。研究了各种物理化学性质,如紫外可见光谱、偏振分析、热重分析、差示扫描量热法、X 射线衍射、水溶解度、辛醇/水分配系数以及通过 Franz 扩散池的猪皮渗透性。该研究证实了所得到的 L-氨基酸烷基酯盐酸盐和 L-谷氨酸酸烷基酯布洛芬盐的离子结构。它揭示了酯链长度与热稳定性、结晶度、相变温度、亲脂性、水溶解度、皮肤渗透性和这些化合物在皮肤中的积累之间的显著相关性。与母体布洛芬相比,合成的衍生物表现出更高的水溶解度、更低的亲脂性和增强的皮肤渗透性。本研究介绍了具有改善的物理化学性质的有前途的布洛芬衍生物,强调了它们在透皮治疗应用中的潜力。研究结果阐明了这些衍生物的结构-活性关系,为它们增强的溶解度和皮肤渗透提供了深入了解,这可能导致更有效的局部疼痛和炎症治疗。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1743/10673250/01185cea3849/molecules-28-07523-g001.jpg

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验