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ISO 10993-5在磷酸钙生物材料评估中的适用性挑战:迈向更准确的体外细胞毒性评估

Challenging applicability of ISO 10993-5 for calcium phosphate biomaterials evaluation: Towards more accurate in vitro cytotoxicity assessment.

作者信息

Kovrlija Ilijana, Menshikh Ksenia, Abreu Hugo, Cochis Andrea, Rimondini Lia, Marsan Olivier, Rey Christian, Combes Christèle, Locs Janis, Loca Dagnija

机构信息

Institute of Biomaterials and Bioengineering, Faculty of Natural Sciences and Technology, Riga Technical University, Pulka 3, Riga LV-1007, Latvia; Baltic Biomaterials Centre of Excellence, Headquarters at Riga Technical University, Riga, Latvia.

Center for Translational Research on Autoimmune and Allergic Disease-CAAD, Department of Health Sciences, Università del Piemonte Orientale, 28100 Novara, Italy.

出版信息

Biomater Adv. 2024 Jun;160:213866. doi: 10.1016/j.bioadv.2024.213866. Epub 2024 Apr 18.

Abstract

Research on biomaterials typically starts with cytocompatibility evaluation, using the ISO 10993-5 standard as a reference that relies on extract tests to determine whether the material is safe (cell metabolic activity should exceed 70 %). However, the generalized approach within the standard may not accurately reflect the material's behavior in direct contact with cells, raising concerns about its effectiveness. Calcium phosphates (CaPs) are a group of materials that, despite being highly biocompatible and promoting bone formation, still exhibit inconsistencies in basic cytotoxicity evaluations. Hence, in order to test the cytocompatibility dependence on different experimental setups and material-cell interactions, we used amorphous calcium phosphate, α-tricalcium phosphate, hydroxyapatite, and octacalcium phosphate (0.1 mg/mL to 5 mg/mL) with core cell lines of bone microenvironment: mesenchymal stem cells, osteoblast-like and endothelial cells. All materials have been characterized for their physicochemical properties before and after cellular contact and once in vitro assays were finalized, groups identified as 'cytotoxic' were further analyzed using a modified Annexin V apoptosis assay to accurately determine cell death. The obtained results showed that indirect contact following ISO standards had no sensitivity of tested cells to the materials, but direct contact tests at physiological concentrations revealed decreased metabolic activity and viability. In summary, our findings offer valuable guidelines for handling biomaterials, especially in powder form, to better evaluate their biological properties and avoid false negatives commonly associated with the traditional standard approach.

摘要

生物材料的研究通常始于细胞相容性评估,以ISO 10993-5标准为参考,该标准依靠提取物测试来确定材料是否安全(细胞代谢活性应超过70%)。然而,该标准中的通用方法可能无法准确反映材料与细胞直接接触时的行为,这引发了对其有效性的担忧。磷酸钙(CaPs)是一类材料,尽管具有高度的生物相容性并能促进骨形成,但在基本细胞毒性评估中仍表现出不一致性。因此,为了测试细胞相容性对不同实验设置和材料-细胞相互作用的依赖性,我们使用了无定形磷酸钙、α-磷酸三钙、羟基磷灰石和八钙磷酸钙(0.1mg/mL至5mg/mL)与骨微环境的核心细胞系:间充质干细胞、成骨样细胞和内皮细胞。所有材料在细胞接触前后都已对其物理化学性质进行了表征,一旦体外试验完成,被鉴定为“细胞毒性”的组将使用改良的膜联蛋白V凋亡试验进行进一步分析,以准确确定细胞死亡情况。获得的结果表明,按照ISO标准进行的间接接触对测试细胞对材料没有敏感性,但在生理浓度下的直接接触试验显示代谢活性和活力降低。总之,我们的研究结果为处理生物材料提供了有价值的指导方针,特别是对于粉末形式的材料,以更好地评估其生物学特性,并避免通常与传统标准方法相关的假阴性结果。

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