Bhuiyan Mozammel Haque, Clarkson Andrew N, Ali M Azam
Center for Bioengineering and Nanomedicine, University of Otago, PO Box 56, Dunedin 9054, New Zealand; Department of Anatomy, Brain Health Research Centre and Brain Research New Zealand, University of Otago, PO Box 56, Dunedin 9054, New Zealand; Sir John Walsh Research Institute, Faculty of Dentistry, Division of Health Science, University of Otago, PO Box 56, Dunedin 9054, New Zealand.
Department of Anatomy, Brain Health Research Centre and Brain Research New Zealand, University of Otago, PO Box 56, Dunedin 9054, New Zealand.
Colloids Surf B Biointerfaces. 2023 Apr;224:113193. doi: 10.1016/j.colsurfb.2023.113193. Epub 2023 Feb 2.
Regeneration of neural tissue and recovery of lost functions following an accident or disease to the central nervous system remains a major challenge worldwide, with limited treatment options available. The main reason for the failure of conventional therapeutic techniques to regenerate neural tissue is the presence of blood-brain barrier separating nervous system from systemic circulation and the limited capacity of self-regeneration of the nervous system. Injectable hydrogels have shown great promise for neural tissue engineering given their suitability for minimally invasive in situ delivery and tunable mechanical and biological properties. Chitosan (CS)/β-glycerophosphate (β-GP) hydrogels have been extensively investigated and shown regenerative potential in a wide variety of tissues such as bone and cartilage tissue engineering. However, the potential of CS/β-GP hydrogels has never been tested for injectable neural tissue engineering applications. In the present study, CS/β-GP hydrogels, consisting of 0.5-2% CS and 2-3% β-GP, were prepared and characterized to investigate their suitability for injectable neural tissue engineering applications. The resulting CS/β-GP-hydrogels showed a varying range of properties depending on the CS/β-GP blend ratio. In particular, the 0.5%:3% and 0.75%:3% CS/β-GP hydrogels underwent rapid gelation (3 min and 5 min, respectively) at physiological temperature (37 °C) and pH (7.4). They also had suitable porosity, osmolality, swelling behavior and biodegradation for tissue engineering. The biocompatibility of hydrogels was determined in vitro using PC12 cells, an immortalized cell line with neuronal cell-like properties, revealing that these hydrogels supported cell growth and proliferation. In conclusion, the thermoresponsive 0.5%:3% and 0.75%:3% CS/β-GP hydrogels had the greatest potential for neural tissue engineering.
在中枢神经系统遭受意外事故或疾病后,神经组织的再生以及丧失功能的恢复仍是全球面临的一项重大挑战,可用的治疗选择有限。传统治疗技术在神经组织再生方面失败的主要原因是存在将神经系统与体循环分隔开的血脑屏障以及神经系统自我再生能力有限。可注射水凝胶因其适用于微创原位递送以及可调节的机械和生物学特性,在神经组织工程领域展现出了巨大潜力。壳聚糖(CS)/β-甘油磷酸酯(β-GP)水凝胶已得到广泛研究,并在多种组织如骨和软骨组织工程中显示出再生潜力。然而,CS/β-GP水凝胶在可注射神经组织工程应用方面的潜力从未得到过测试。在本研究中,制备了由0.5%-2% CS和2%-3% β-GP组成的CS/β-GP水凝胶,并对其进行了表征,以研究它们在可注射神经组织工程应用中的适用性。所得的CS/β-GP水凝胶根据CS/β-GP混合比例呈现出不同范围的特性。特别是,0.5%:3%和0.75%:3%的CS/β-GP水凝胶在生理温度(37℃)和pH(7.4)下分别在3分钟和5分钟内快速凝胶化。它们还具有适合组织工程的孔隙率、渗透压、溶胀行为和生物降解性。使用具有神经元样特性的永生化细胞系PC12细胞在体外测定了水凝胶的生物相容性,结果表明这些水凝胶支持细胞生长和增殖。总之,热响应性的0.5%:3%和0.75%:3% CS/β-GP水凝胶在神经组织工程方面具有最大潜力。