AI Article Synopsis

  • - A new extraction method using a natural solvent (L-menthol and lactic acid) was developed to isolate compounds like bisdemethoxycurcumin, demethoxycurcumin, and curcumin from Curcumae Longae Rhizoma and turmeric tea, combined with high-performance liquid chromatography for analysis.
  • - The researchers optimized key parameters (extractant volume, salt concentration, demulsifier consumption, and time) to enhance the efficiency of the extraction process, resulting in precise calibration curves and low detection limits (0.1-0.4 ng/mL) for the compounds.
  • - The method demonstrated excellent performance in analyzing real samples, yielding high recovery rates (85.3-108.9

Article Abstract

A novel solvent terminated microextraction method based on a natural deep eutectic solvent (L-menthol and lactic acid at a molar ratio of 1:2) coupled with high-performance liquid chromatography was proposed, which was utilized for the separation and enrichment of bisdemethoxycurcumin, demethoxycurcumin and curcumin in Curcumae Longae Rhizoma and turmeric tea. The effects of independent parameters on extraction efficiency were optimized by single-factor analysis. Subsequently, four predominated parameters affecting the extraction procedure, including extractant volume, salt concentration, demulsifier consumption, and demulsification time, were further evaluated by a central composite design. Under the optimized conditions, the linear ranges of calibration curves were 0.005-0.5 μg/mL for bisdemethoxycurcumin, 0.004-0.4 μg/mL for demethoxycurcumin, and 0.0045-0.45 μg/mL for curcumin, respectively. In addition, the developed method provided low detection limits (0.1-0.4 ng/mL) and high enrichment factors (279-350). Its intra-day and inter-day precision were carried out by relative standard deviation ranging from 2.2 to 9.2%. Finally, the applicability of this method was assessed by the analysis of Curcumae Longae Rhizoma and turmeric tea samples. The results showed that these samples were detected successfully and the spiked recoveries over the range of 85.3-108.9% with relative standard deviations of 1.6-8.9% were attained, indicating its high relative recoveries with good precision in real sample analysis.

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http://dx.doi.org/10.1002/jssc.202200110DOI Listing

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