Verdoliva Valentina, Muzio Giuliana, Autelli Riccardo, De Luca Stefania
Institute of Crystallography, National Research Council, Caserta, Italy.
Department of Clinical and Biological Sciences, University of Turin, Turin, Italy.
Chem Biodivers. 2025 Apr;22(4):e202402495. doi: 10.1002/cbdv.202402495. Epub 2024 Nov 30.
Herein, a sustainable solid-state procedure is employed for the synthesis of a water-soluble molecule obtained by linking hyaluronic acid to the hydrophobic quercetin (HA-QCT). The micellar self-aggregation of the developed conjugate suggested its employment as a drug delivery nano-system, considering the numerous biological activities of QCT. Indeed, the spectroscopic characterization (ultraviolet-visible and Fourier transform infrared) ensured that the QCT maintained its chemical integrity. In addition, a cytotoxicity test revealed that HA-QCT can be employed as a biocompatible drug vehicle for pharmacological purposes. A preliminary colorimetric test also confirmed that QCT retained its anti-oxidant activity.
在此,采用一种可持续的固态方法合成了一种通过将透明质酸与疏水性槲皮素(HA-QCT)连接而获得的水溶性分子。考虑到槲皮素的多种生物活性,所开发的共轭物的胶束自聚集表明其可作为药物递送纳米系统。实际上,光谱表征(紫外可见光谱和傅里叶变换红外光谱)确保了槲皮素保持其化学完整性。此外,细胞毒性测试表明HA-QCT可作为用于药理学目的的生物相容性药物载体。初步比色测试也证实了槲皮素保留了其抗氧化活性。