Re-evaluation of Developmental and Reproductive Toxicity of Ortho- Phenylphenol (OPP) and Sodium Ortho-Phenylphenate (SOPP)
|Eric S.C. Kwok* and Marilyn Silva|
|Medical Toxicology Branch, Department of Pesticide Regulation (DPR), California Environmental Protection Agency (CalEPA), Sacramento, California, USA|
|*Corresponding Author :||Eric SC Kwok
Medical Toxicology Branch, Department of Pesticide Regulation (DPR)
California Environmental Protection Agency (CalEPA)
Sacramento, California, USA
E-mail: [email protected]
|Received August 27, 2013; Accepted October 01, 2013; Published October 03, 2013|
|Citation: Kwok ESC, Silva M (2013) Re-evaluation of Developmental and Reproductive Toxicity of Ortho-Phenylphenol (OPP) and Sodium Ortho-Phenylphenate (SOPP). Cell Dev Biol 2: 123 doi:10.4172/2168-9296.1000123|
|Copyright: © 2013 Kwok ESC, et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.|
Background: Due to widespread usage, the general public including pregnant women is routinely exposed to the fungicides, Ortho-Phenylphenol (OPP) and Sodium OrthoâÂ€Â‘Phenylphenate (SOPP), from many sources. Previous data reviews concluded no effects on development or reproduction in animal studies but upon re-analysis we realize that alternative interpretation may exist.
Methods: Developmental and reproductive effects were assessed from studies performed in rats, mice, and rabbits. We identified the most sensitive endpoint(s) for OPP or SOPP as they related to fetal developmental or reproductive toxicity. For quantifying the potential health risk associated with the exposure to OPP or SOPP, we used the lowest dose that caused no developmental or reproductive toxicity or benchmark dose analysis.
Results: Developmental effects in OPP-treated rats and mice were decreased fetal body weight, increased incidences in delayed skeletal ossification and postâÂ€Â‘implantation loss. In addition, fetal mice exposed to SOPP exhibited malformation. Similar to rats and mice, postâÂ€Â‘implantation loss was the developmental effect noted in OPPtreated rabbits. Except for the rats, maternal toxicity appeared to be minimal (mice) or not observed (rabbits) at the lowest dose where developmental effects occurred (mice: cleft plate; rabbits: resorptions). We did not find evidence of OPP affecting reproductive functions but significant deviations from FIFRA Guidelines in these studies may prevent adequate assessment of the reproductive toxicity especially the effects on fertility and mating.
Conclusions: The revised data analysis suggests that OPP and SOPP induce fetal toxicity in the absence of maternal effects. Our re-evaluation would be useful in the formulation of a current or updated regulatory strategy for the developmental toxicity of OPP and SOPP.