Jones P A, King A V
Safety and Environmental Assurance Centre, Unilever Colworth, Sharnbrook, Bedfordshire MK44 1LQ, UK.
Toxicol In Vitro. 2003 Oct-Dec;17(5-6):703-8. doi: 10.1016/s0887-2333(03)00101-2.
Testing for phototoxic hazard is usually carried out for product ingredients intended for use on skin, which may be exposed to sunlight. Unilever currently uses the validated in vitro 3T3 Neutral Red Uptake phototoxicity test (NRU PT). This protocol involves 2-3 experiments, each taking 3 days to perform. One person can test up to seven test materials plus positive control at any one time, requiring approximately 0.5 g test material. Higher throughput is required where libraries of potential actives are being generated and screening for potential phototoxicants is required. A proposed HTS protocol would use the NRU PT, but only one concentration (10 microg/ml) in a single experiment. The validity of the HTS protocol was investigated by a retrospective examination of data from 86 materials previously tested. Phototoxic hazard predictions made using the conventional NRU PT were compared with those obtained if only data at 10 microg/ml were considered. A majority of 73 materials (84.9%) gave agreement in predictions between the two protocols; for 13 materials (15.1%) the assessments did not agree. There were no false positives; however, there were some false negatives, i.e., predicted as phototoxic from the conventional assay, but non-phototoxic at 10 microg/ml. As this protocol is intended for screening purposes only it is considered that this would be acceptable at this stage in material selection. One person could screen 128 test materials in 3 days, requiring <1 mg test material, giving a substantial increase in productivity. Any material selected for further development and inclusion in a formulation may require further confirmatory testing, e.g. using a human skin model assay for phototoxicity.
通常会对用于皮肤且可能暴露于阳光下的产品成分进行光毒性危害测试。联合利华目前使用经过验证的体外3T3中性红摄取光毒性试验(NRU PT)。该方案涉及2至3个实验,每个实验需要3天时间完成。一个人在任何时候最多可以测试七种测试材料以及阳性对照,大约需要0.5克测试材料。在生成潜在活性成分库并需要筛选潜在光毒性物质时,需要更高的通量。一种提议的高通量筛选方案将使用NRU PT,但在单个实验中仅使用一种浓度(10微克/毫升)。通过回顾性检查之前测试的86种材料的数据,研究了高通量筛选方案的有效性。将使用传统NRU PT做出的光毒性危害预测与仅考虑10微克/毫升数据时获得的预测进行了比较。73种材料中的大多数(84.9%)在两种方案的预测中结果一致;13种材料(15.1%)的评估结果不一致。没有假阳性结果;然而,有一些假阴性结果,即从传统试验预测为光毒性,但在10微克/毫升时无光毒性。由于该方案仅用于筛选目的,因此在材料选择的现阶段,认为这是可以接受的。一个人可以在3天内筛选128种测试材料,所需测试材料不到1毫克,生产率大幅提高。任何被选中用于进一步开发并纳入配方的材料可能都需要进一步的验证测试,例如使用人体皮肤模型进行光毒性试验。