药品
生物相容性
MAPK/ERK通路
自愈水凝胶
解热药
信号转导
超分子化学
化学
药理学
药物发现
医学
天然产物
p38丝裂原活化蛋白激酶
环糊精
组合化学
药物输送
纳米技术
脚手架
药物开发
生物活性
作者
Penglong Wang,Xuemei Huang,Shaohui Geng,Guangrui Huang,Wenmin Pi,Nana Han,Yaozhi Zhang,Enfan Xiao,Zhimin Lin,Kai Yuan,Haimin Lei,Anlong Xu
标识
DOI:10.1016/j.mtbio.2025.102371
摘要
Numerous traditional Herbal medicine (THM) formulas have demonstrated their effectiveness during long-term clinical practices worldwide, offering a rich repository for the discovery of new drug and functional biomaterials. Consequently, the development of therapeutic supramolecular hydrogels based on plant-derived bioactive molecules has garnered significant attention in the field of new drug development. In this study, we developed a well-defined orally supramolecular drug derived from the classic Ma-Xing-Shi-Gan decoction (MXSGD) which has been widely used in China for the treatment of COVID-19 symptoms and acute infectious diseases. The four representative chemical components of MXSGD-pseudoephedrine, amygdalin, glycyrrhizic acid, and Ca2+-co-assembled into quaternary carrier-free supramolecular structure (Quad hydrogel) through non-covalent interactions. This Quad hydrogel exhibited well thermal reversibility, injectable performance, mechanical strength, sustained release, intestinal retention, enhanced drug absorption, and biocompatibility by oral administration. Moreover, Quad hydrogel significantly inhibited the activation of lipopolysaccharides (LPS)-induced MAPK and NF-κB signaling pathway, thereby synergistically relieving fever in rats more effectively than the original MXSG decoction, equivalent pseudoephedrine (PSE) monomer and the physical mixture four components (Quad mix). In summary, this study provides a novel strategy for developing new supramolecular drug based on classic THM formulas, as well as integrating THM with modern technologies.
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