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A Simple Method for Automated Solid Phase Extraction of Water Samples for Immunological Analysis of Small Pollutants
Published on: January 1, 2016
Quantitative analysis of unconjugated and total bisphenol A in human urine using solid-phase extraction and
Brigitte Buscher1, Dick van de Lagemaat1, Wolfgang Gries2
1TNO Triskelion BV, Utrechtseweg 48, Zeist, The Netherlands.
Accurate bisphenol A (BPA) analysis in human urine requires strict contamination control. This study details challenges and precautions for reliable BPA biomonitoring using UPLC-MS/MS.
Area of Science:
- Environmental Chemistry
- Analytical Chemistry
- Toxicology
Background:
- Bisphenol A (BPA) is ubiquitous, posing contamination risks in biomonitoring.
- Accurate analysis of BPA at sub-parts-per-billion levels is challenging due to pervasive environmental contamination.
- Previous HPLC-MS/MS methods for unconjugated and total BPA in urine were adapted.
Purpose of the Study:
- To document challenges in implementing and qualifying a BPA analysis method.
- To develop and discuss precautions against BPA contamination during sample handling and analysis.
- To ensure reliable bisphenol A biomonitoring in human urine.
Main Methods:
- Combined and transferred previously developed HPLC-MS/MS methods for unconjugated and total BPA.
- Developed and evaluated methods in independent laboratories.
- Applied UPLC-MS/MS calibrated from 0.05 to 25 ng/mL.
Main Results:
- Quantification limits were 0.1 ng/mL for unconjugated BPA and 0.2 ng/mL for total BPA.
- The method was successfully applied to urine samples from 20 volunteers.
- Acceptable recovery and repeatability were achieved with stringent contamination control.
Conclusions:
- Bisphenol A can be reliably analyzed in human urine.
- Minimizing contamination from sample collection to analysis is critical for accurate biomonitoring.
- The study provides a validated UPLC-MS/MS method with essential contamination control strategies.
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