Simple and Fast HPLC‐DAD Method for Simultaneous Screening of Four Pharmaceutical Active Compounds in Aqueous Matrices

Abstract A practical, fast, and reproducible method was developed to separate and quantify four pharmaceutically active compounds and one plastic additive considered emerging contaminants in water samples by HPLC‐DAD. The mixture of compounds included metformin (MET), bisphenol A (BPA), estradiol (E2), atorvastatin (ATV), and diclofenac (DCF). The mobile phase used for the chromatography runs was composed of 33:67 (MeCN: 0.05 M phosphate buffer, pH 3 + 0.1% v/v SDS) in gradient mode performed on an Inertsil ODS‐3 column (150 × 4.6 mm, 5 µm) at 23 °C. An efficient separation was achieved in a run time of 10 min, with an LOD and LOQ of 53 µg·L −1 and 160.5 µg·L −1 for MET; 17.6 µg·L −1 and 53.5 µg·L −1 for BPA; 30.1 µg·L −1 and 91.1 µg·L −1 for E2; 13.0 µg·L −1 and 39.4 µg·L −1 for ATV; and 15.8 µg·L −1 and 47.9 µg·L −1 for DCF, respectively. Method suitability parameters were evaluated according to ICH guidelines.

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Publication Details

Journal
ChemistrySelect
Published
2025-04-26
DOI
https://doi.org/10.1002/slct.202500085
Primary Topic
Analytical Chemistry and Chromatography
Type
article
Field-Weighted Citation Impact
0.00

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article

Simple and Fast HPLC‐DAD Method for Simultaneous Screening of Four Pharmaceutical Active Compounds in Aqueous Matrices

Alfonso Benítez‐Mora, Bárbara Rodríguez, Christopher González, Carolina A. León et al.
ChemistrySelect
Analytical Chemistry and Chromatography
article

Simple and Fast HPLC‐DAD Method for Simultaneous Screening of Four Pharmaceutical Active Compounds in Aqueous Matrices

Alfonso Benítez‐Mora, Bárbara Rodríguez, Christopher González, Carolina A. León, Marisol Gómez, Jaime Herrera, Isabel Dı́az
article en

Abstract

Abstract A practical, fast, and reproducible method was developed to separate and quantify four pharmaceutically active compounds and one plastic additive considered emerging contaminants in water samples by HPLC‐DAD. The mixture of compounds included metformin (MET), bisphenol A (BPA), estradiol (E2), atorvastatin (ATV), and diclofenac (DCF). The mobile phase used for the chromatography runs was composed of 33:67 (MeCN: 0.05 M phosphate buffer, pH 3 + 0.1% v/v SDS) in gradient mode performed on an Inertsil ODS‐3 column (150 × 4.6 mm, 5 µm) at 23 °C. An efficient separation was achieved in a run time of 10 min, with an LOD and LOQ of 53 µg·L −1 and 160.5 µg·L −1 for MET; 17.6 µg·L −1 and 53.5 µg·L −1 for BPA; 30.1 µg·L −1 and 91.1 µg·L −1 for E2; 13.0 µg·L −1 and 39.4 µg·L −1 for ATV; and 15.8 µg·L −1 and 47.9 µg·L −1 for DCF, respectively. Method suitability parameters were evaluated according to ICH guidelines.

ChemistrySelectVol. 10(17)
Universidad Bernardo O'Higgins (CL)
Agencia Nacional de Investigación y Desarrollo
Openalex Percentile: Top 92%
Analytical Chemistry and Chromatography
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