Journal
CHEMOSPHERE
Volume 286, Issue -, Pages -Publisher
PERGAMON-ELSEVIER SCIENCE LTD
DOI: 10.1016/j.chemosphere.2021.131636
Keywords
Polyhexamethylene guanidine phosphate (PHMG-P); Developmental toxicity; Reproductive toxicity; Extended one-generation reproductive toxicity study (EOGRTS); Hazard identification
Categories
Funding
- Ministry of Environment, Republic of Korea [2016001360006]
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Polyhexamethylene guanidine phosphate (PHMG-P), a primary biocide in humidifier disinfectants, can cause fatal pulmonary disease in Korea. Inhalation of PHMG-P during pregnancy adversely affects maternal health and embryo-fetal development. Prenatal exposure to PHMG-P results in increased perinatal death rates, decreased viability index, lower birth weight, and systemic toxicities in offspring. These findings suggest that prenatal PHMG-P exposure has long-term effects on offspring health and could impact human risk assessment.
Inhalation exposure to polyhexamethylene guanidine phosphate (PHMG-P), one of the primary biocides used in humidifier disinfectants, caused a fatal pulmonary disease in Korea. Pregnant women were also exposed to PHMG-P, and subsequent studies showed that PHMG-P inhalation during pregnancy adversely affects their health and embryo-fetal development. However, the postnatal developmental effects after birth on prenatally PHMG-P-exposed offspring have not yet been investigated. Therefore, in this study, we aimed to examine the postnatal development of prenatally PHMG-P-exposed offspring. Pregnant rats (22 or 24 females per group) were exposed to PHMG-P during pregnancy in a whole-body inhalation chamber at the target concentrations of 0, 0.14, 1.60, and 3.20 mg/m(3). After parturition, the prenatally exposed offspring were transferred to non-exposed surrogate mothers to minimize the secondary effects of severe maternal toxicities. Postnatal development of offspring was then examined with a modified extended one-generation reproductive toxicity study design. At 3.20 mg/m(3) PHMG-P, increased perinatal death rates and decreased viability index (postnatal survival of offspring between birth and postnatal day 4) were observed. In addition, F1 offspring had lower body weight at birth that persisted throughout the study. PHMG-P-exposed pregnant rats also had severe systemic toxicities and increased gestation period. At 1.60 mg/m(3) PHMG-P, a decreased viability index was also observed with systemic toxicities of PHMG-P-exposed pregnant rats. These results indicate that prenatal PHMG-P exposure adversely affects the offspring's future health and could be used for human risk assessment.
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