Schendel K U, Erdinger L, Komposch G, Sonntag H G
Poliklinik für Kieferorthopädie, Universität Heidelberg.
Fortschr Kieferorthop. 1995 Jan;56(1):41-8. doi: 10.1007/BF02265838.
Public concern and issues of liability have made product safety a major concern throughout the medical field including orthodontics. The purpose of this study was to test the biocompatibility of the new neon colored plastic materials to be used for removable orthodontic appliances before they reach the market and are used in patient treatment. In addition, eight modifications of this synthetic material, which has been used in appliances for many years, were examined without neon color. The procedures established tested for: 1. mutagenicity, 2. toxicity, and 3. irritation of the mucous membrane. As alternatives to using animals the Ames Test, the Agar Overlay Assay, and the HET-CAM Test were employed to test for these properties. The tests revealed that, when the manufacturer's instructions are followed, neither the polymerized materials as used in patient appliances nor the shavings resulting from the orthodontist or the technician grinding the appliance exhibit mutagenic, toxic, or irritating properties.
公众的关注以及责任问题使得产品安全成为包括正畸学在内的整个医学领域的主要关注点。本研究的目的是在新型霓虹色塑料材料进入市场并用于患者治疗之前,测试其用于可摘正畸矫治器的生物相容性。此外,还对这种已在矫治器中使用多年的合成材料的八种未添加霓虹色的变体进行了研究。所建立的程序针对以下方面进行测试:1. 致突变性,2. 毒性,3. 对黏膜的刺激性。作为使用动物的替代方法,采用了艾姆斯试验、琼脂覆盖试验和鸡胚绒毛尿囊膜试验来测试这些特性。测试表明,按照制造商的说明使用时,患者矫治器中使用的聚合材料以及正畸医生或技术人员打磨矫治器产生的碎屑均不具有致突变性、毒性或刺激性。