Prenatal paraben exposure and atopic dermatitis-related outcomes among children.

BACKGROUND: Parabens, widely used as preservatives in cosmetics, foods, and other consumer products, are suspected of contributing to allergy susceptibility. The detection of parabens in the placenta or amniotic fluid raised concerns about potential health consequences for the child. Recently, an increased asthma risk following prenatal exposure has been reported. Here, we investigated whether prenatal paraben exposure can influence the risk for atopic dermatitis (AD). METHODS: 261 mother-child pairs of the German mother-child study LINA were included in this analysis. Eight paraben species were quantified in maternal urine obtained at gestational week 34. According to the parental report of physician-diagnosed AD from age 1 to 8 years, disease onset, and persistence, childhood AD was classified into four different phenotypes. RESULTS: 4.6% (n = 12) and 12.3% (n = 32) of the children were classified as having very early-onset AD (until age two) either with or without remission, 11.9% (n = 31) as early-onset (after age two), and 3.1% (n = 8) as childhood-onset AD (after age six). Exposure to ethylparaben and n-butylparaben was associated with an increased risk to develop very early-onset AD without remission (EtP: adj.OR/95% CI:1.44/1.04-2.00,nBuP:adj.OR/95% CI:1.95/1.22-3.12). The effects of both parabens were predominant in children without a history of maternal AD and independent of children's sex. CONCLUSION: Prenatal EtP or nBuP exposure may increase children's susceptibility for persistent AD with disease onset at very early age. This association was particularly pronounced in children without a history of maternal AD, indicating that children without a genetic predisposition are more susceptible to paraben exposure.

A false positive finding in liquid chromatography/triple quadrupole mass spectrometry analysis by a non-isobaric matrix component: the case of benzotriazole in urine for human biomonitoring.

RATIONALE: Multi-residual methods employing liquid chromatography coupled to triple quadrupole mass spectrometry (LC/MS/MS) with selected reaction monitoring (SRM) are attractive also for human biomonitoring (HBM). A new process is determined that can lead to false positive findings by matrix components that are not isobaric to the analyte of interest. METHODS: Benzotriazole (1H-BT) was false positively detected in 87 human urine samples analyzed by ultra-high-performance-(UHP)-LC/MS/MS. The quantifier/qualifier ratio (Q/q ratio) did not match. This was further confirmed by negative results with an optimized gradient. Investigations were performed by UHPLC/high-resolution (HR)MS and model compounds to reveal the identity of the disturbing matrix compound and the way that it interfered with 1H-BT detection. RESULTS: A formula of C7 H5 NO (m/z 120.0444) was found at the retention time of 1H-BT (m/z 120.0556) belonging to an in-source product ion of a heavier co-eluting compound. Product ion spectra and Q/q ratios of model compounds indicated a benzene sub-structure with a carbonyl and amine functional group in the ortho- or para-position. Finally, folic acid was confirmed as the disturbing urine component, exhibiting an in-source fragment with the nominal mass of 1H-BT and the same product ions as used in the SRM mode for UHPLC/MS/MS monitoring. CONCLUSIONS: Interferences in SRM detection need not be due to co-eluting isobaric matrix compounds, but can originate from in-source fragmentation of heavier ions. Rigid quality control measures are recommended for LC/MS/MS analysis, especially for small molecules in complex sample matrices to overcome the selectivity limits of SRM. Copyright © 2016 John Wiley & Sons, Ltd.

Ultrasound-assisted hydrolysis of conjugated parabens in human urine and their determination by UPLC-MS/MS and UPLC-HRMS.

Parabens are preservatives widely used in personal care products, pharmaceutical formulations as well as in food, and they are considered endocrine disruptors. For application in biomonitoring studies we developed a method for the determination of eight parabens from human urine. Sample preparation was enhanced and simplified by the combination of ultrasound-assisted enzymatic hydrolysis of conjugates (glucuronide and sulfate) followed by an extraction-free cleanup step. Quantification, using deuterated parabens as internal standards, was performed by ultrahigh-performance liquid chromatography coupled to either triple-quadrupole (UPLC-QqQ) or time-of-flight (UPLC-QqTOF) mass spectrometry. Full chromatographic separation of three butyl paraben isomers was achieved. Limits of quantification for both mass analyzers ranged from 0.1 to 0.5 µg/L for methyl, ethyl, n-/isopropyl, n-/isobutyl, and benzyl paraben in 200 µL of urine sample. The method was tested for applicability and showed high precision (intra- and interday 0.9-14.5%) as well as high accuracy (relative recovery 95-132%). A total of 39 urine samples were analyzed by both mass analyzers. The results agreed well, with a trend to higher deviation at low concentrations (less than 10 µg/L). Methyl, ethyl, and n-propyl paraben were detected most frequently (in more than 87% of the samples) with median concentrations ranging from 0.8 to 16.6 µg/L. Female urine showed higher median concentrations for all parabens, which may indicate higher exposure due to lifestyle. This method permits accurate and high-throughput analysis of parabens for epidemiological studies. Further, the UPLC-QqTOF approach provides additional information on human exposure to other compounds by post-acquisition analysis.

Maternal paraben exposure triggers childhood overweight development.

Parabens are preservatives widely used in consumer products including cosmetics and food. Whether low-dose paraben exposure may cause adverse health effects has been discussed controversially in recent years. Here we investigate the effect of prenatal paraben exposure on childhood overweight by combining epidemiological data from a mother-child cohort with experimental approaches. Mothers reporting the use of paraben-containing cosmetic products have elevated urinary paraben concentrations. For butyl paraben (BuP) a positive association is observed to overweight within the first eight years of life with a stronger trend in girls. Consistently, maternal BuP exposure of mice induces a higher food intake and weight gain in female offspring. The effect is accompanied by an epigenetic modification in the neuronal Pro-opiomelanocortin (POMC) enhancer 1 leading to a reduced hypothalamic POMC expression. Here we report that maternal paraben exposure may contribute to childhood overweight development by altered POMC-mediated neuronal appetite regulation.

Matrix effects in human urine analysis using multi-targeted liquid chromatography-tandem mass spectrometry.

Different sample preparation methods were tested for human urine for the subsequent analysis with a LC-MS/MS multimethod to quantify 65 micropollutants (pesticides, pharmaceuticals, personal care products, industrial chemicals and metabolites) within the general population. Direct injection of diluted urine revealed highly variable and often severe signal suppression for nearly all analytes at relevant concentration levels during electrospray ionization. Urine samples were highly variable in their total organic carbon (500-10,000mgL(-1)) and creatinine (0.35-13mM) content as well as in electrical conductivity (3-19mScm(-1)) but these differences did not correlate clearly with the strength of matrix effects. Therefore, matrix removal by solid phase extraction was intended and different mixed-mode sorbents were tested. Results showed poor apparent recoveries likely due to insufficient separation of target analytes and matrix compounds for all tested sorbents. The wide variability and high concentration levels of urine constituents strongly affect electrospray ionization as well as recovery during extraction at the sub-microgram per liter level. Especially, the hydrophobic interaction at the hydrophilic-lipophilic-balanced sorbent was affected. It is concluded that the urine matrix is too strong, too diverse and too variable to allow one sample preparation method for the very diverse analytes of a LC-MS/MS multimethod. Instead dedicated methods appear more promising.