Citryl-imine-PEG-ylated chitosan hydrogels - Promising materials for drug delivery applications

被引:25
|
作者
Ailincai, Daniela [1 ]
Mititelu-Tartau, Liliana [2 ]
Marin, Luminita [1 ]
机构
[1] Petro Poni Inst Macromol Chem, Grigore Ghica Voda Alley, Iasi, Romania
[2] Grigore T Popa Univ Med & Pharm, Iasi, Romania
基金
欧盟地平线“2020”;
关键词
PEG-ylation; Chitosan hydrogels; Local drug delivery; Sustained drug release; Antinociceptive effect; Biocompatibility; INJECTABLE HYDROGELS; ANIMAL-MODELS; POLY(ETHYLENE GLYCOL); ANTIFUNGAL ACTIVITY; SYSTEMS; ISOPROPYLACRYLAMIDE; DERIVATIVES; DICLOFENAC; RELEASE; PAIN;
D O I
10.1016/j.ijbiomac.2020.06.218
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
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. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页码:1323 / 1337
页数:15
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