Simpson Fiona C, Islam Mohammed Mirazul, Buznyk Oleksiy, Edin Elle, Groleau Marc, Kozak-Ljunggren Monika, Magrelli Federica M, AbuSamra Dina B, Argüeso Pablo, Chodosh James, Liszka Aneta, Fagerholm Per, Griffith May
Department of Clinical and Experimental Medicine, Linköping University, Linköping, Sweden.
Maisonneuve-Rosemont Hospital Research Centre, Montréal, QC, Canada.
Front Bioeng Biotechnol. 2022 Jun 13;10:883977. doi: 10.3389/fbioe.2022.883977. eCollection 2022.
Sterilization of biodegradable, collagen-based implants is challenging as irradiation sterilization methods can alter their mechanical properties. Electron beam (EB) irradiation is a terminal sterilization method that has been used for biologically-derived implants. Here, recombinant human collagen type III-phosphorylcholine (RHCIII-MPC) hydrogels were irradiated with EB doses of 17, 19, or 21 kGy and their subsequent biocompatibility and ability to promote regeneration in rabbit corneas was evaluated. Unirradiated hydrogels stored in 1% chloroform in phosphate-buffered saline (C-PBS) were the controls. There were no significant differences between irradiated and non-irradiated samples in optical or physical properties (tensile strength, modulus, elasticity), or the ability to support cell growth. However, irradiated implants were more sensitive to high levels of collagenase than unirradiated controls and the C-PBS implants had increased cell growth compared to EB and controls at 72 h. Corneal implants e-beamed at 17 kGy or e-beamed and subsequently frozen (EB-F) to increase shelf-life showed no adverse biological effects of the irradiation. EB, EB-F, and C-PBS implanted corneas all rapidly re-epithelialized but showed mild neovascularization that resolved over 6 months. The regenerated neo-corneas were transparent at 6 months post-operation. confocal microscopy confirmed normal morphology for the epithelium, stroma, sub-basal nerves and unoperated endothelium. Histology showed that all the regenerated corneas were morphologically similar to the normal. Immunohistochemistry indicated the presence of a differentiated corneal epithelium and functional tear film. In conclusion, the e-beamed corneal implants performed as well as non-irradiated control implants, resulting in fully regenerated neo-corneas with new nerves and without blood vessels or inflammation that may impede vision or corneal function. Therefore, a complete validation study to establish EB irradiation as an effective means for corneal implant sterilization prior to clinical application is necessary as a next step.
对基于胶原蛋白的可生物降解植入物进行灭菌具有挑战性,因为辐照灭菌方法会改变其机械性能。电子束(EB)辐照是一种终端灭菌方法,已用于生物衍生的植入物。在此,用17、19或21 kGy的EB剂量辐照重组人III型胶原蛋白-磷酰胆碱(RHCIII-MPC)水凝胶,并评估其随后的生物相容性以及促进兔角膜再生的能力。储存在磷酸盐缓冲盐水(C-PBS)中的1%氯仿中的未辐照水凝胶作为对照。辐照和未辐照样品在光学或物理性质(拉伸强度、模量、弹性)或支持细胞生长的能力方面没有显著差异。然而,辐照后的植入物比未辐照的对照对高水平的胶原酶更敏感,并且在72小时时,C-PBS植入物的细胞生长比EB和对照有所增加。以17 kGy进行电子束辐照或电子束辐照后冷冻(EB-F)以延长保质期的角膜植入物未显示出辐照的不良生物学效应。EB、EB-F和C-PBS植入的角膜均迅速重新上皮化,但显示出轻度新生血管形成,在6个月内消退。术后6个月再生的新角膜是透明的。共聚焦显微镜检查证实上皮、基质、基底膜下神经和未手术的内皮形态正常。组织学显示所有再生角膜在形态上与正常角膜相似。免疫组织化学表明存在分化的角膜上皮和功能性泪膜。总之,电子束辐照的角膜植入物与未辐照的对照植入物表现相同,产生了具有新神经的完全再生的新角膜,没有可能妨碍视力或角膜功能的血管或炎症。因此,下一步有必要进行一项完整的验证研究,以确定EB辐照作为角膜植入物临床应用前有效灭菌手段的有效性。