Milano Fiona, Chevrier Anik, De Crescenzo Gregory, Lavertu Marc
Biomedical Engineering Institute, Polytechnique Montreal, Montréal, QC H3T 1J4, Canada.
Chemical Engineering Department, Polytechnique Montreal, Montréal, QC H3T 1J4, Canada.
Polymers (Basel). 2023 Jun 30;15(13):2919. doi: 10.3390/polym15132919.
Freeze-dried chitosan formulations solubilized in platelet-rich plasma (PRP) are currently evaluated as injectable implants with the potential for augmenting the standard of care for tissue repair in different orthopedic conditions. The present study aimed to shorten the solidification time of such implants, leading to an easier application and a facilitated solidification in a wet environment, which were direct demands from orthopedic surgeons. The addition of thrombin to the formulation before lyophilization was explored. The challenge was to find a formulation that coagulated fast enough to be applied in a wet environment but not too fast, which would make handling/injection difficult. Four thrombin concentrations were analyzed (0.0, 0.25, 0.5, and 1.0 NIH/mL) in vitro (using thromboelastography, rheology, indentation, syringe injectability, and thrombin activity tests) as well as ex vivo (by assessing the implant's adherence to tendon tissue in a wet environment). The biomaterial containing 0.5 NIH/mL of thrombin significantly increased the coagulation speed while being easy to handle up to 6 min after solubilization. Furthermore, the adherence of the biomaterial to tendon tissues was impacted by the biomaterial-tendon contact duration and increased faster when thrombin was present. These results suggest that our biomaterial has great potential for use in regenerative medicine applications.
目前正在评估溶解于富血小板血浆(PRP)中的冻干壳聚糖制剂作为可注射植入物,其有可能提高不同骨科病症中组织修复的护理标准。本研究旨在缩短此类植入物的凝固时间,以实现更便捷的应用,并在潮湿环境中促进凝固,这是骨科医生的直接需求。研究探讨了在冻干前向制剂中添加凝血酶的方法。面临的挑战是找到一种凝固速度足够快以适用于潮湿环境但又不会太快的制剂,因为太快会使操作/注射变得困难。体外分析了四种凝血酶浓度(0.0、0.25、0.5和1.0 NIH/mL)(使用血栓弹性描记法、流变学、压痕、注射器注射性和凝血酶活性测试)以及离体分析(通过评估植入物在潮湿环境中对肌腱组织的粘附性)。含有0.5 NIH/mL凝血酶的生物材料显著提高了凝固速度,同时在溶解后长达6分钟内易于操作。此外,生物材料与肌腱组织的接触持续时间会影响生物材料对肌腱组织的粘附性,并且当存在凝血酶时,粘附性增加得更快。这些结果表明,我们的生物材料在再生医学应用中具有巨大潜力。