纳米纤维素
明胶
材料科学
形态学(生物学)
纤维素
细菌纤维素
生物材料
复合数
粘附
脚手架
纳米技术
复合材料
胶粘剂
化学工程
纳米纤维
自愈水凝胶
组织工程
化学
表面改性
纳米复合材料
作者
Janet V. Reid,Niki Hazelton,Stefan Hill,Marie-Joo Le Guen,Lyn M. Wise
出处
期刊:Tissue Engineering Part A
[Mary Ann Liebert, Inc.]
日期:2025-12-30
标识
DOI:10.1177/19373341251410203
摘要
Nanocellulose has emerged as a promising biomaterial for development of scaffolds for tissue engineering. Incorporation of nanocellulose into a polymer scaffold can increase its stiffness, allowing it to better mimic the mechanical properties of native extracellular matrix. Plant-derived nanocellulose is classified as either cellulose nanofibrils (CNFs) or cellulose nanocrystals (CNCs) depending on particle characteristics and extraction methods. Although both materials have been used in hydrogel composites, the impact of nanocellulose source and morphology on scaffold properties remains unclear. Here, we isolated high aspect ratio CNFs from two macroalgae species and compared them with conventional wood pulp-derived CNFs and CNCs in the preparation of composite gelatin hydrogels. All nanocellulose types increased hydrogel stiffness in a concentration-dependent manner; however, the greatest increase was achieved using brown algae CNF, where the addition of 1.25 wt.% nanocellulose resulted in a 5.2-fold increase in compression modulus relative to neat gelatin. Bioassays showed that nanocellulose improved keratinocyte adhesion and spreading on gelatin scaffolds, with a positive correlation between nanocellulose concentration and surface coverage and inverse with cell circularity. These findings demonstrate the influence of nanocellulose source and morphology on the mechanical and biological properties of composite scaffolds and highlight the potential of novel nanocellulose sources for scaffold development.
科研通智能强力驱动
Strongly Powered by AbleSci AI