Bhatia Sujata K, Yetter Ann B
Biochemical Sciences and Engineering, Central Research and Development, DuPont Experimental Station, Wilmington, DE 19880, USA.
Cell Biol Toxicol. 2008 Aug;24(4):315-9. doi: 10.1007/s10565-007-9040-z. Epub 2007 Oct 12.
Medical devices and implanted biomaterials are often assessed for biological reactivity using visual scores of cell-material interactions. In such testing, biomaterials are assigned cytotoxicity ratings based on visual evidence of morphological cellular changes, including cell lysis, rounding, spreading, and proliferation. For example, ISO 10993 cytotoxicity testing of medical devices allows the use of a visual grading scale. The present study compared visual in vitro cytotoxicity ratings to quantitative in vitro cytotoxicity measurements for biomaterials to determine the level of correlation between visual scoring and a quantitative cell viability assay. Biomaterials representing a spectrum of biological reactivity levels were evaluated, including organo-tin polyvinylchloride (PVC; a known cytotoxic material), ultra-high molecular weight polyethylene (a known non-cytotoxic material), and implantable tissue adhesives. Each material was incubated in direct contact with mouse 3T3 fibroblast cell cultures for 24 h. Visual scores were assigned to the materials using a 5-point rating scale; the scorer was blinded to the material identities. Quantitative measurements of cell viability were performed using a 3-(4,5-dimethylthiozol-2-yl)-2,5-diphenyltetrazolium bromide (MTT) colorimetric assay; again, the assay operator was blinded to material identities. The investigation revealed a high degree of correlation between visual cytotoxicity ratings and quantitative cell viability measurements; a Pearson's correlation gave a correlation coefficient of 0.90 between the visual cytotoxicity score and the percent viable cells. An equation relating the visual cytotoxicity score and the percent viable cells was derived. The results of this study are significant for the design and interpretation of in vitro cytotoxicity studies of novel biomaterials.
医疗设备和植入生物材料通常使用细胞与材料相互作用的视觉评分来评估其生物反应性。在这种测试中,根据细胞形态变化的视觉证据,包括细胞裂解、变圆、铺展和增殖,为生物材料指定细胞毒性等级。例如,医疗器械的ISO 10993细胞毒性测试允许使用视觉分级量表。本研究将生物材料的体外视觉细胞毒性等级与定量体外细胞毒性测量进行了比较,以确定视觉评分与定量细胞活力测定之间的相关程度。评估了代表一系列生物反应性水平的生物材料,包括有机锡聚氯乙烯(PVC;一种已知的细胞毒性材料)、超高分子量聚乙烯(一种已知的非细胞毒性材料)和可植入组织粘合剂。每种材料都与小鼠3T3成纤维细胞培养物直接接触孵育24小时。使用5分制量表为材料分配视觉评分;评分者对材料身份不知情。使用3-(4,5-二甲基噻唑-2-基)-2,5-二苯基四氮唑溴盐(MTT)比色法进行细胞活力的定量测量;同样,测定操作者对材料身份不知情。调查发现视觉细胞毒性等级与定量细胞活力测量之间存在高度相关性;皮尔逊相关性得出视觉细胞毒性评分与存活细胞百分比之间的相关系数为0.90。推导了一个将视觉细胞毒性评分与存活细胞百分比相关联的方程。本研究结果对于新型生物材料体外细胞毒性研究的设计和解释具有重要意义。