"Petru Poni" Institute of Macromolecular Chemistry, Grigore Ghica Voda Alley, Iasi, Romania.
"Grigore T. Popa" University of Medicine and Pharmacy, Iasi, Romania.
Int J Biol Macromol. 2020 Nov 1;162:1323-1337. doi: 10.1016/j.ijbiomac.2020.06.218. Epub 2020 Jun 26.
The present paper focuses on the synthesis and characterization of new hydrogels and drug delivery systems, designed for local therapy. The hydrogels were obtained by reacting PEG-ylated chitosan derivatives with citral in different molar ratios of their functionalities. The drug delivery systems were obtained by the in situ hydrogelation of PEG-ylated chitosan derivatives with citral, in the presence of a hydrophilic anti-inflammatory drug, diclofenac sodium salt. The hydrogels and the drug delivery systems were characterized from the structural, supramolecular and morphological points of view by FTIR spectroscopy, wide angle X-ray diffraction, polarized optical microscopy and scanning electron microscopy. The in vitro release kinetics of the drug has been monitored in physiological conditions, while the in vivo release was evaluated by the somatic pain model on rats. The in vitro enzymatic degradability of the hydrogels was evaluated in the presence of lysozyme, leading to a significant mass loss of 47% in 21 days. All the findings, recommend the investigated materials as promising candidates for local drug delivery applications.
本文专注于新水凝胶和药物传递系统的合成与表征,旨在实现局部治疗。通过不同功能基摩尔比的聚乙二醇化壳聚糖衍生物与柠檬醛反应得到水凝胶,通过聚乙二醇化壳聚糖衍生物与柠檬醛在亲水性抗炎药物双氯芬酸钠盐存在下的原位水凝胶化得到药物传递系统。通过傅里叶变换红外光谱、广角 X 射线衍射、偏光显微镜和扫描电子显微镜从结构、超分子和形态学角度对水凝胶和药物传递系统进行了表征。在生理条件下监测了药物的体外释放动力学,通过大鼠躯体疼痛模型评估了体内释放情况。在溶菌酶存在下评估了水凝胶的体外酶降解性,导致 21 天内质量损失 47%。所有的研究结果均表明,所研究的材料有望成为局部药物传递应用的候选材料。