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January 20, 2026Open Chemistry0 citationsOpen Access

Use of a choline chloride-urea based deep eutectic solvent for the improvement of HPLC resolution in complex botanical extracts

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APAída Parra-NaranjoCDCecilia Delgado-MontemayorNWNoemí Waksman‐Minsky

Key Points

  • The aim is to develop a validated chromatographic method for analyzing hepatodamianol in T. diffusa extracts using a specific deep eutectic solvent.
  • Developed a chromatographic method with a Hypersil GOLD RP C 18 column.
  • Used methanol-0.1% formic acid as the mobile phase.
  • Applied the method to standardized extracts of T. diffusa.
  • Assessed linearity, precision, and accuracy in measuring hepatodamianol.
  • Resolution improved from 0.76 to 2.59 with DES.
  • Method displayed linearity from 5 to 100 μg mL−1.
  • Intra-day precision had an RSD below 2%, inter-day below 8%.
  • Recoveries ranged between 97.46% and 105.65%.
  • Detection and quantification limits were 0.87 μg mL−1 and 4.45 μg mL−1 respectively.

Abstract

Abstract Turnera diffusa is a plant with hepatoprotective activity. Hepatodamianol – a biomarker of this plant – is identified as the main compound responsible for this activity. There are no chromatographic methods with adequate peak resolution for quantifying this analyte in T. diffusa extracts. Deep Eutectic Solvents (DESs) have emerged as an option to improve the performance of chromatographic systems. Therefore, the present study aimed to develop and validate a chromatographic method for hepatodamianol analysis in the presence of a Choline chloride-Urea (ChCl-Ur) based DES and its application in standardized extracts of T. diffusa . The developed method used a Hypersil GOLD RP C 18 column with methanol-0.1 % formic acid aqueous solution as the mobile phase. The use of DES for sample dissolution increased the resolution from 0.76 to 2.59. The method was linear (5–100 μg mL −1 ); it exhibited high precision and accuracy with relative standard deviations below 2 and 8 % for intra- and inter-day precision, respectively, and recoveries between 97.46 and 105.65 %. The detection and quantification limits were 0.87 μg ml −1 and 4.45 μg ml −1 , respectively. The proposed method efficiently analyzed the standardized extracts of T. diffusa , thus representing a quality control tool for herbal products based on this species.

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Cite This Study

Parra-Naranjo et al. (2026) studied this question.

synapsesocial.com/papers/696f1a849e64f732b51eebc6https://doi.org/10.1515/chem-2025-0219
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