Yuluan Wu, Ming Liang, Yanping Xian, Rongqiao Chen, Junpeng Hu, Hang Dai, Chenghao Liu and Xiangchang Hou
{"title":"Dispersive liquid–liquid microextraction with a deep eutectic solvent coupled with GC-MS for the determination of chiral carvone in herbaceous plants†","authors":"Yuluan Wu, Ming Liang, Yanping Xian, Rongqiao Chen, Junpeng Hu, Hang Dai, Chenghao Liu and Xiangchang Hou","doi":"10.1039/D4AY02002B","DOIUrl":null,"url":null,"abstract":"<p >Carvone is an important flavoring substance and widely used in the food and chemical industries. Carvone has two optical isomers (<small>L</small>-carvone and <small>D</small>-carvone), which have different aroma characteristics. However, the green extraction of natural carvone and isolation of chiral carvone present challenges, leading to its limited application. In this study, a deep eutectic solvent (DES) was prepared and used as a green extraction solvent for the extraction of carvone from herbaceous plants, and then a chiral chromatography column combined with GC-MS was used for the separation and detection of <small>L</small>-carvone and <small>D</small>-carvone. Response surface methodology was used to optimize the extraction conditions including the volume of DES, extraction time and extraction temperature. The results showed that the extraction recoveries and intra-day precision (<em>n</em> = 6) were 83.5–101.3% and 3.2–6.1% when the volume of DES was 5 mL, and the extraction time and temperature were 25 min and 51 °C, respectively. The MLOD and MLOQ of <small>L</small>-carvone and <small>D</small>-carvone were 8.0 mg kg<small><sup>−1</sup></small> and 25.0 mg kg<small><sup>−1</sup></small>, respectively. The real sample detection results revealed that about 235.8–1600.0 mg kg<small><sup>−1</sup></small> of <small>L</small>-carvone was detected in <em>Mentha spicata</em> L., and 6658.5–9788.6 mg kg<small><sup>−1</sup></small> of <small>D</small>-carvone in <em>Anethum graveolens</em> L. seeds. The established method can be an effective method for the detection of chiral carvone in herbaceous plants.</p>","PeriodicalId":64,"journal":{"name":"Analytical Methods","volume":" 9","pages":" 2171-2180"},"PeriodicalIF":2.7000,"publicationDate":"2025-02-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Analytical Methods","FirstCategoryId":"92","ListUrlMain":"https://pubs.rsc.org/en/content/articlelanding/2025/ay/d4ay02002b","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
Abstract
Carvone is an important flavoring substance and widely used in the food and chemical industries. Carvone has two optical isomers (L-carvone and D-carvone), which have different aroma characteristics. However, the green extraction of natural carvone and isolation of chiral carvone present challenges, leading to its limited application. In this study, a deep eutectic solvent (DES) was prepared and used as a green extraction solvent for the extraction of carvone from herbaceous plants, and then a chiral chromatography column combined with GC-MS was used for the separation and detection of L-carvone and D-carvone. Response surface methodology was used to optimize the extraction conditions including the volume of DES, extraction time and extraction temperature. The results showed that the extraction recoveries and intra-day precision (n = 6) were 83.5–101.3% and 3.2–6.1% when the volume of DES was 5 mL, and the extraction time and temperature were 25 min and 51 °C, respectively. The MLOD and MLOQ of L-carvone and D-carvone were 8.0 mg kg−1 and 25.0 mg kg−1, respectively. The real sample detection results revealed that about 235.8–1600.0 mg kg−1 of L-carvone was detected in Mentha spicata L., and 6658.5–9788.6 mg kg−1 of D-carvone in Anethum graveolens L. seeds. The established method can be an effective method for the detection of chiral carvone in herbaceous plants.