Kawahara D
Shika Zairyo Kikai. 1989 Jul;8(4):499-516.
Cytotoxicity of zinc oxide-eugenol cement was investigated using collagen gel matrix culture. Diffusibility of the main components into the collagen gel was measured by either atomic absorption or ultraviolet spectroscopy. The agar overlay culture method was also carried out for comparison. Results from solution cultures containing diluted collagen were similar to those with diluted agar. Longer culture with either cement liquid, eugenol, or zinc chloride solution, resulted in more depressed cell growth. The lower the powder/liquid ratio for mixing, the higher the cytotoxicity for all the materials tested in gelled collagen. Also, cytotoxicity levels were always lower in cultures with collagen than in those with agar. Diffusibility of the materials into collagen gel was similar to that into agar, but the of diffused components in collagen gel was less. Thus, the usefulness of collagen gel matrix culture for biological evaluation of dental materials was equivalent to that of agar overlay culture. However, it is suggested that collagen as a tissue matrix might provide a favorable environment for cell culture, and hence allow biocompatibility testing of biomaterials under simulated conditions.
使用胶原凝胶基质培养法研究了氧化锌丁香酚水门汀的细胞毒性。通过原子吸收光谱法或紫外光谱法测量主要成分在胶原凝胶中的扩散性。还采用琼脂覆盖培养法进行比较。含稀释胶原的溶液培养结果与含稀释琼脂的溶液培养结果相似。用水泥液、丁香酚或氯化锌溶液进行更长时间的培养,会导致细胞生长受到更大抑制。混合时的粉液比越低,在胶凝胶原中测试的所有材料的细胞毒性越高。此外,胶原培养中的细胞毒性水平总是低于琼脂培养中的细胞毒性水平。材料在胶原凝胶中的扩散性与在琼脂中的相似,但胶原凝胶中扩散成分的量较少。因此,胶原凝胶基质培养用于牙科材料生物学评价的实用性与琼脂覆盖培养相当。然而,有人认为胶原作为一种组织基质可能为细胞培养提供有利环境,从而能够在模拟条件下对生物材料进行生物相容性测试。