Salètes Margaux, Vartin Marta, Mocquot Caroline, Chevalier Charlène, Grosgogeat Brigitte, Colon Pierre, Attik Nina
CPE Lyon, Université Claude Bernard Lyon 1, CEDEX 08, 69372 Lyon, France.
Laboratoire des Multimatériaux et Interfaces, UMR CNRS 5615, Université de Lyon-Université Claude Bernard Lyon 1, CEDEX 08, 69372 Lyon, France.
Biomimetics (Basel). 2021 Jan 23;6(1):9. doi: 10.3390/biomimetics6010009.
Thanks to their high porosity and surface area, mesoporous bioactive glasses (MBGs) have gained significant interest in the field of medical applications, in particular, with regards to enhanced bioactive properties which facilitate bone regeneration. The aim of this article is to review the state of the art regarding the biocompatibility evaluation of MBGs and provide a discussion of the various approaches taken. The research was performed using PubMed database and covered articles published in the last five years. From a total of 91 articles, 63 were selected after analyzing them according to our inclusion and exclusion criteria. In vitro methodologies and techniques used for biocompatibility assessment were investigated. Among the biocompatibility assessment techniques, scanning electron microscopy (SEM) has been widely used to study cell morphology and adhesion. Viability and proliferation were assessed using different assays including cell counting and/or cell metabolic activity measurement. Finally, cell differentiation tests relied on the alkaline phosphatase assay; however, these were often complemented by specific bimolecular tests according to the exact application of the mesoporous bioactive glass. The standardization and validation of all tests performed for MBG cytocompatibility is a key aspect and crucial point and should be considered in order to avoid inconsistencies, bias between studies, and unnecessary consumption of time. Therefore, introducing standard tests would serve an important role in the future assessment and development of MBG materials.
由于其高孔隙率和表面积,介孔生物活性玻璃(MBG)在医学应用领域引起了极大的关注,特别是在促进骨再生的增强生物活性方面。本文的目的是回顾关于MBG生物相容性评估的最新进展,并对所采用的各种方法进行讨论。研究使用了PubMed数据库,并涵盖了过去五年发表的文章。在总共91篇文章中,根据我们的纳入和排除标准进行分析后,选择了63篇。研究了用于生物相容性评估的体外方法和技术。在生物相容性评估技术中,扫描电子显微镜(SEM)已被广泛用于研究细胞形态和粘附。使用包括细胞计数和/或细胞代谢活性测量在内的不同检测方法评估细胞活力和增殖。最后,细胞分化测试依赖于碱性磷酸酶检测;然而,根据介孔生物活性玻璃的具体应用情况,这些检测通常会辅以特定的双分子检测。对MBG细胞相容性进行的所有测试的标准化和验证是一个关键方面和要点,为避免研究之间出现不一致、偏差以及不必要的时间消耗,应予以考虑。因此,引入标准测试将在MBG材料的未来评估和开发中发挥重要作用。