Mussel inspired sequential protein delivery based on self-healing injectable nanocomposite hydrogel

自愈水凝胶 纳米复合材料 药物输送 壳聚糖 牛血清白蛋白 控制释放 共价键 化学 智能聚合物 聚电解质 纳米技术 化学工程 生物物理学 聚合物 材料科学 高分子化学 色谱法 有机化学 生物 工程类
作者
Xiao Han,Peng Cheng Li,Heng Tao Song,Yuan He,Jian Hui Li,Yang Yang,Hao-Peng Li,Hideyuki Miyatake,Yoshihiro Ito
出处
期刊:International Journal of Biological Macromolecules [Elsevier BV]
卷期号:264: 130568-130568 被引量:6
标识
DOI:10.1016/j.ijbiomac.2024.130568
摘要

Polysaccharide based self-healing and injectable hydrogels with reversible characteristics have widespread potential in protein drug delivery. However, it is a challenge to design the dynamic hydrogel for sequential release of protein drugs. Herein, we developed a novel mussel inspired sequential protein delivery dynamic polysaccharide hydrogel. The nanocomposite hydrogel can be fabricated through doping polydopamine nanoparticles (PDA NPs) into reversible covalent bond (imine bonds) crosslinked polymer networks of oxidized hyaluronic acid (OHA) and carboxymethyl chitosan (CEC), named PDA NPs@OHA-l-CEC. Besides multiple capabilities (i.e., injection, self-healing, and biodegradability), the nanocomposite hydrogel can achieve sustained and sequential protein delivery of vascular endothelial growth factor (VEGF) and bovine serum albumin (BSA). PDA NPs doped in hydrogel matrix serve dual roles, acting as secondary protein release structures and form dynamic non-covalent interactions (i.e., hydrogen bonds) with polysaccharides. Moreover, by adjusting the oxidation degree of OHA, the hydrogels with different crosslinking density could control overall protein release rate. Analysis of different release kinetic models revealed that Fickian diffusion drove rapid VEGF release, while the slower BSA release followed a Super Case II transport mechanism. The novel biocompatible system achieved sequential release of protein drugs has potentials in multi-stage synergistic drug deliver based on dynamic hydrogel.
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