共 87 条
In vitro and in vivo investigation of chitosan/silk fibroin injectable interpenetrating network hydrogel with microspheres for cartilage regeneration
被引:12
作者:

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Shamloo, Amir
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机构:
Sharif Univ Technol, Sch Mech Engn, Azadi Ave, Tehran, Iran
Sharif Univ Technol, Stem Cell & Regenerat Med Inst, Tehran, Iran Sharif Univ Technol, Sch Mech Engn, Azadi Ave, Tehran, Iran

Akbarnataj, Kazem
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h-index: 0
机构:
Sharif Univ Technol, Sch Mech Engn, Azadi Ave, Tehran, Iran
Isfahan Univ Technol, Dept Mech Engn, Esfahan, Iran Sharif Univ Technol, Sch Mech Engn, Azadi Ave, Tehran, Iran

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机构:
[1] Sharif Univ Technol, Sch Mech Engn, Azadi Ave, Tehran, Iran
[2] Sharif Univ Technol, Stem Cell & Regenerat Med Inst, Tehran, Iran
[3] Isfahan Univ Technol, Dept Mech Engn, Esfahan, Iran
关键词:
Thermosensitive hydrogel;
Interpenetrating polymer network;
Tissue engineering;
SILK FIBROIN;
TISSUE;
SCAFFOLDS;
FABRICATION;
REPAIR;
ACID;
BONE;
BIOMATERIALS;
SIMULATION;
SYSTEM;
D O I:
10.1016/j.ijbiomac.2024.132126
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:
Articular cartilage is an avascular and almost acellular tissue with limited self-regenerating capabilities. Although injectable hydrogels have garnered a lot of attention as a promising treatment, a biocompatible hydrogel with adequate mechanical properties is yet to be created. In this study, an interpenetrating network hydrogel comprised of chitosan and silk fibroin was created through electrostatic and hydrophobic bonds, respectively. The polymeric network of the scaffold combined an effective microenvironment for cell activity with enhanced mechanical properties to address the current issues in cartilage scaffolds. Furthermore, microspheres (MS) were utilized for a controlled release of methylprednisolone acetate (MPA), around similar to 75 % after 35 days. The proposed scaffolds demonstrated great mechanical stability with similar to 0.047 MPa compressive moduli and similar to 145 kPa compressive strength. Moreover, the degradation rate of the samples (similar to 45 % after 35 days) was optimized to match neo-cartilage formation. Furthermore, the use of natural biomaterials yielded good biocompatibility with similar to 76 % chondrocyte viability after 7 days. According to gross observation after 12 weeks the defect site of the treated groups was filled with minimally discernible boundary. These results were confirmed by histopathology assays were the treated groups showed higher chondrocyte count and collagen type II expression.
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