AI Article Synopsis

  • * The study developed a β-cyclodextrin crosslinked with citric acid device (BCD-CA μ-SPE) that effectively preconcentrates selected EDCs before analysis via high-performance liquid chromatography.
  • * The BCD-CA μ-SPE method showed excellent sensitivity, with detection limits as low as 0.27 μg/L and high recovery rates (80.2%-99.9%) when tested on various water types, proving to be an efficient solution for EDC quantification.

Article Abstract

Endocrine disruptor compounds (EDCs) such as plasticisers, surfactants, pharmaceutical products, personal care products and pesticides are frequently released into the environmental waters. Therefore, a sensitive and environmentally friendly method is entailed to quantify these compounds at their trace level concentrations. This study encapsulated the β-cyclodextrin crosslinked with citric acid in a polypropylene membrane protected-μ-solid phase extraction (BCD-CA μ-SPE) device for preconcentrating the EDCs (triclosan, triclocarban, 2-phenylphenol, 4-tert-octylphenols and bisphenol A) in real water samples before the analysis by high-performance liquid chromatography. FT-IR and TGA results indicated that BCD-CA was successfully synthesised with the formation of ester linkage (1078.33 cm) and O-H stretching from carboxylic acid (3434.70 cm) with higher thermal stability as compared with native CD with the remaining weight above 72.1% at 500 °C. Several critical parameters such as the sorbent loading, type and amount of salts, extraction time, sample volume, sample pH, type and volume of desorption solvents and desorption time were sequentially optimised and statistically validated. Under the optimum condition, the use of BCD-CA μ-SPE device had manifested good linearity (0.5-500 μg L) with the determination of the coefficient range of 0.9807-0.9979. The p-values for the F-test and t-test (6.60 × 10 - 1.77 × 10) were lesser than 0.05 and low detection limits ranging from 0.27 to 0.84 μg L for all studied EDCs. The developed technique was also successfully applied for EDC analyses in four distinct real water samples, namely, wastewater, river water, tap water and mineral water, with good EDCs recoveries (80.2%-99.9%), low relative standard deviations (0.1%-3.8%, n = 3) with enrichment factor ranging from 9 to 82 folds. These results signified the potential of the BCD-CA μ-SPE device as an efficient, sensitive, and environmentally friendly approach for analyzing EDCs.

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http://dx.doi.org/10.1016/j.chemosphere.2022.135075DOI Listing

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Endocrine disrupting compounds (EDCs) are extensively found in the environment and severely impacting human health. In addressing this issue, the beta-cyclodextrin crosslinked citric acid (BCD-CA) had been previously employed in membrane-protected micro-solid phase extraction for sequestering EDCs from water medium; and the findings revealed that BCD-CA possessed a selectivity property. On that account, the potential of BCD-CA towards competitive adsorption of selected EDCs was investigated in terms of adsorption mechanism and selectivity property.

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Article Synopsis
  • * The study developed a β-cyclodextrin crosslinked with citric acid device (BCD-CA μ-SPE) that effectively preconcentrates selected EDCs before analysis via high-performance liquid chromatography.
  • * The BCD-CA μ-SPE method showed excellent sensitivity, with detection limits as low as 0.27 μg/L and high recovery rates (80.2%-99.9%) when tested on various water types, proving to be an efficient solution for EDC quantification.
View Article and Find Full Text PDF

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