Characterization of dermal sensitization potential for industrial or agricultural chemicals with EpiSensA

被引:2
作者
Mizumachi, Hideyuki [1 ]
LeBaron, Matthew J. [2 ]
Settivari, Raja S. [3 ]
Miyazawa, Masaaki [1 ]
Marty, Mary Sue [2 ]
Sakaguchi, Hitoshi [1 ]
机构
[1] Kao Corp, Safety Sci Res, R&D, Ichikai, Tochigi, Japan
[2] Dow Chem Co USA, Toxicol & Environm Res & Consulting, Midland, MI 48674 USA
[3] Haskell R&D Ctr, Corteva Agrisci, Delaware, OH USA
关键词
DPRA; EpiSensA; h‐ CLAT; in vitro; KeratinoSens™ skin sensitization; XENOBIOTIC METABOLISM CAPACITIES; IN-VITRO ALTERNATIVES; SKIN SENSITIZATION; LIPOPHILIC CHEMICALS; CELL-CULTURE; ASSAY; MODEL; POTENCY; HAZARD;
D O I
10.1002/jat.4076
中图分类号
R99 [毒物学(毒理学)];
学科分类号
100405 ;
摘要
The regulatory community is transitioning to the use of nonanimal methods for dermal sensitization assessments; however, some in vitro assays have limitations in their domain of applicability depending on the properties of chemicals being tested. This study explored the utility of epidermal sensitization assay (EpiSensA) to evaluate the sensitization potential of complex and/or "difficult to test" chemicals. Assay performance was evaluated by testing a set of 20 test chemicals including 10 methacrylate esters, 5 silicone-based compounds, 3 crop protection formulations, and 2 surfactant mixtures; each had prior in vivo data plus some in silico and in vitro data. Using the weight of evidence (WoE) assessments by REACH Lead Registrants, 14 of these chemicals were sensitizers and, six were nonsensitizers based on in vivo studies (local lymph node assay [LLNA] and/or guinea pig studies). The EpiSensA correctly predicted 16/20 materials with three test materials as false positive and one silane as false negative. This silane, classified as weak sensitizer via LLNA, also gave a "false negative" result in the KeratinoSens (TM) assay. Overall, consistent with prior evaluations, the EpiSensA demonstrated an accuracy level of 80% relative to available in vivo WoE assessments. In addition, potency classification based on the concentration showing positive marker gene expression of EpiSensA was performed. The EpiSensA correctly predicted the potency for all seven sensitizing methacrylates classified as weak potency via LLNA (EC3 >= 10%). In summary, EpiSensA could identify dermal sensitization potential of these test substances and mixtures, and continues to show promise as an in vitro alternative method for dermal sensitization.
引用
收藏
页码:915 / 927
页数:13
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