Negative Paper Spray Ionization Mass Spectrometry for the Determination of Endocrine-Disrupting Chemicals with Application to Paraben Analysis in Cosmeticsopen access
- Authors
- Cho, Seonyoung; Amatya, Sarmila Shrestha; Bahng, Hyerin; Lee, Eungyeong; Ko, Yunsang; Cha, Sangwon
- Issue Date
- Nov-2025
- Publisher
- MDPI
- Keywords
- paraben; endocrine-disrupting chemicals; cosmetics; paper spray ionization; tandem mass spectrometry
- Citation
- Molecules, v.30, no.22, pp 1 - 14
- Pages
- 14
- Indexed
- SCIE
SCOPUS
- Journal Title
- Molecules
- Volume
- 30
- Number
- 22
- Start Page
- 1
- End Page
- 14
- URI
- https://scholarworks.dongguk.edu/handle/sw.dongguk/62274
- DOI
- 10.3390/molecules30224356
- ISSN
- 1420-3049
1420-3049
- Abstract
- Paper spray ionization mass spectrometry (PSI-MS) enables rapid analysis with minimal sample preparation, yet negative-ion mode performance has been limited by poor sensitivity and unstable signals, similar to conventional electrospray ionization. In this study, we optimized negative PSI tandem MS (MS/MS) for twelve endocrine-disrupting chemicals (EDCs) and related biomarkers-including bisphenols, phthalates, parabens, and substituted phenols-used as model analytes. A systematic solvent and additive screen identified 1 mM ammonium fluoride in methanol and 0.1% ammonium hydroxide in 9:1 MeOH/carbon tetrachloride as optimal conditions, providing enhanced deprotonated-ion intensities and improved stability. Calibration curves generated under these conditions showed excellent linearity, with limits of quantitation (LOQs) in the low-ppb range. Application to cosmetic formulations demonstrated reliable paraben quantitation. In fortified hand cream, LOQs below 1 mg/kg were achieved, with recoveries of 93-110% and intra- and inter-day precision below 10% RSD. Notably, PSI-MS/MS performance was comparable to LC-MS/MS, without a separation step. These results demonstrate the feasibility of optimized negative PSI-MS as a sensitive and robust tool for paraben determination in cosmetics and highlight its potential as a versatile platform for broader EDC quantification.
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Collections - College of Natural Science > Department of Chemistry > 1. Journal Articles

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