Injectable 3D Hydrogel Scaffold with Tailorable Porosity Post-Implantation

被引:43
作者
Al-Abboodi, Aswan [1 ]
Fu, Jing [2 ]
Doran, Pauline M. [3 ]
Tan, Timothy T. Y. [4 ]
Chan, Peggy P. Y. [5 ,6 ]
机构
[1] Monash Univ, Dept Chem Engn, Clayton, Vic 3800, Australia
[2] Monash Univ, Dept Mech & Aerosp Engn, Clayton, Vic 3800, Australia
[3] Swinburne Univ Technol, Fac Life & Social Sci, Hawthorn, Vic 3122, Australia
[4] Nanyang Technol Univ, Sch Chem & Biomed Engn, Singapore 637459, Singapore
[5] RMIT Univ, Sch Appl Sci, MicroNanoPhys Res Lab, Melbourne, Vic 3000, Australia
[6] Australian Natl Fabricat Facil, Melbourne Ctr Nanofabricaton, Clayton, Vic 3168, Australia
基金
澳大利亚研究理事会;
关键词
injectable hydrogels; tissue engineering; porous scaffolds; in vivo implantation; tunable porosity; PORE-SIZE; POROUS HYDROGELS; PROLIFERATION; DIFFERENTIATION; RESISTANCE; ADHESION; SOFT;
D O I
10.1002/adhm.201300303
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
Since rates of tissue growth vary significantly between tissue types, and also between individuals due to differences in age, dietary intake, and lifestyle-related factors, engineering a scaffold system that is appropriate for personalized tissue engineering remains a significant challenge. In this study, a gelatin-hydroxyphenylpropionic acid/carboxylmethylcellulose-tyramine (Gtn-HPA/CMC-Tyr) porous hydrogel system that allows the pore structure of scaffolds to be altered in vivo after implantation is developed. Cross-linking of Gtn-HPA/CMC-Tyr hydrogels via horseradish peroxidase oxidative coupling is examined both in vitro and in vivo. Post-implantation, further alteration of the hydrogel structure is achieved by injecting cellulase enzyme to digest the CMC component of the scaffold; this treatment yields a structure with larger pores and higher porosity than hydrogels without cellulase injection. Using this approach, the pore sizes of scaffolds are altered in vivo from 32-87 m to 74-181 m in a user-controled manner. The hydrogel is biocompatible to COS-7 cells and has mechanical properties similar to those of soft tissues. The new hydrogel system developed in this work provides clinicians with the ability to tailor the structure of scaffolds post-implantation depending on the growth rate of a tissue or an individual's recovery rate, and could thus be ideal for personalized tissue engineering.
引用
收藏
页码:725 / 736
页数:12
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