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Objectives: The purpose of this study was to evaluate the exposure to arsenic in preventive maintenance (PM) engineers in a semiconductor industry by detecting speciated inorganic arsenic metabolites in the urine.
Methods: The exposed group included 8 PM engineers from the clean process area and 13 PM engineers from the ion implantation process area; the non-exposed group consisted of 14 office workers from another company who were not occupationally exposed to arsenic. A spot urine specimen was collected from each participant for the detection and measurement of speciated inorganic arsenic metabolites. Metabolites were separated by high performance liquid chromatography-inductively coupled plasma spectrometry-mass spectrometry.
Results: Urinary arsenic metabolite concentrations were 1.73 g/L, 0.76 g/L, 3.45 g/L, 43.65 g/L, and 51.32 g/L for trivalent arsenic (As3+), pentavalent arsenic (As5+), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), and total inorganic arsenic metabolites (As3+ + As5+ + MMA + DMA), respectively, in clean process PM engineers. In ion implantation process PM engineers, the concentrations were 1.74 g/L, 0.39 g/L, 3.08 g/L, 23.17 g/L, 28.92 g/L for As3+, As5+, MMA, DMA, and total inorganic arsenic metabolites, respectively. Levels of urinary As3+, As5+, MMA, and total inorganic arsenic metabolites in clean process PM engineers were significantly higher than that in the non-exposed group. Urinary As3+ and As5+ levels in ion implantation process PM engineers were significantly higher than that in non-exposed group.
Conclusion: Levels of urinary arsenic metabolites in PM engineers from the clean process and ion implantation process areas were higher than that in office workers. For a complete assessment of arsenic exposure in the semiconductor industry, further studies are needed.
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http://dx.doi.org/10.1186/2052-4374-25-21 | DOI Listing |
PLoS Genet
September 2025
Department of Public Health Sciences, University of Chicago, Chicago, Illinois, United States of America.
Background: In Bangladesh, > 50 million individuals are chronically exposed to inorganic arsenic (iAs) through drinking water, increasing risk for cancer and other iAs-related diseases. Previous studies show that individuals' ability to metabolize and eliminate iAs, and their risk of toxicity, is influenced by genetic variation in the AS3MT and FTCD gene regions.
Methods: To identify additional loci influencing arsenic metabolism, we used data from Bangladeshi individuals to conduct genome-wide association analyses of the relative abundances of arsenic species measured in both urine (n = 6,540) and blood (n = 976).
Ecotoxicol Environ Saf
August 2025
Department of Plant Production and Genetics, Faculty of Agricultural Sciences, University of Guilan, Rasht, Iran; Department of Plant Production and Genetics, Faculty of Agriculture, Urmia University, Urmia, Iran.
Soil and water contamination by heavy metals and nanoplastics poses a critical environmental challenge, threatening agricultural productivity and food safety. This study investigated a novel strategy to mitigate the combined toxicity of arsenic (As) and polymethyl methacrylate nanoplastics (PMMANPs) in wheat using cold plasma (CP) seed priming and a green-synthesized Ag/Zn/Fe nanocomposite (NC). A randomized complete block design (RCBD) with three replications was employed.
View Article and Find Full Text PDFJ Natl Cancer Inst
August 2025
Department of Emergency Medicine, New Taipei Municipal Tucheng Hospital, New Taipei City, Taiwan.
Background: Arsenic from drinking water causes many health hazards including liver diseases, but the long-term effects of arsenic exposure and methylation capability on hepatitis viral infection related liver cancer remain to be elucidated.
Methods: This 19-year community-based follow-up study included 7,837 participants with urinary arsenic metabolites level from an arseniasis area in northeastern Taiwan. They were recruited in 1991-1994 and followed up to December 2021.
Adv Sci (Weinh)
August 2025
Department of Occupational and Environmental Health, School of Public Health, Chongqing Medical University, Chongqing, 400016, People's Republic of China.
As a well-known metalloid, arsenic usually causes human intestinal disorders via contaminated drinking water. However, the mechanisms underlying how arsenic induces intestinal injury remain unresolved, and the effective means of intervention are very limited. By establishing an acute arsenic exposure animal model, this work shows that arsenic disrupts the mechanical, chemical, immunological, and biological barriers of the intestine, and thereby changes the microenvironment in the gut.
View Article and Find Full Text PDFBiol Trace Elem Res
August 2025
Department of Toxicology, School of Public Health, Shanxi Medical University, Taiyuan, 030001, Shanxi, China.
Arsenic is recognized for its harmful effects on neurodevelopment and cognitive function, and neurodegenerative alterations induced by arsenic exposure may eventually lead to Alzheimer's disease (AD). However, the precise changes in the gut microbiome and tryptophan (Trp) metabolism resulting from arsenic exposure, as well as their role in the "microbiome-tryptophan metabolite-brain axis" in AD, remain poorly understood. In this study, the rats were exposed to arsenic in utero, with continued exposure lasting until 185 days after birth, through free drinking water contaminated with varying concentrations of NaAsO (0, 30 mg/L, and100mg/L).
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