The natural compound quercetin has been shown to inhibit axl expression. Administration of plga nanoparticles is associated with a minimal systemic toxicity [2,9]. A design of experiments approach was used to optimize the plga nanoparticles to have the maximum quercetin loading, optimal cationic charge, and folic acid coating.
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We showed that quercetin reduced pulmonary fibrosis and inhibited extracellular matrix (ecm) formation. Quercetin also attenuated macrophage senescence induced by sio 2. These nanoparticles offer a unique approach to enhancing delivery.
In this study, we employed plga nanoparticles to prepare nanoparticles encapsulated with.
This article aims to develop. The utilization of quercetin nanoparticles as a novel therapeutic strategy has garnered significant attention in recent years. Plga degradatio rate depends on its molecular weight and on the molar ratio of the two monomer.
