Yoshiyuki Kobayashi, Masakadzu Yato, R. Ito, Koichi Saito
{"title":"液相色谱/飞行时间质谱法对映体选择性测定保健食品中的辛弗林","authors":"Yoshiyuki Kobayashi, Masakadzu Yato, R. Ito, Koichi Saito","doi":"10.15583/jpchrom.2019.024","DOIUrl":null,"url":null,"abstract":"An enantioselective analytical method for the determination of synephrine, an ingredient in health food, by liquid chromatography/time-of-flight mass spectrometry (LC/TOF-MS) was developed. By derivatizing synephrine with FMOC and using TCI Chiral MB-S as the chiral column, FMOC-synephrine enantiomers were well separated. The electrospray ionization (ESI) negative mode was adopted for TOF-MS measurement. Good linearity ( r > 0.999) was obtained in the concentration range of 0.5 to 50 μg/mL. The limit of detection (LOD, S / N = 3) and the limit of quantification (LOQ, S / N > 10) were 0.25 μg/mL and 0.5 μg/mL, respectively. The intra-day and inter-day accuracy of synephrine enantiomers at the LOQ level (0.5 μg/mL), the intermediate concentration level (10 μg/mL), and the high concentration level (50 μg/mL) ranged from 90.0 to 107.4%. The intra-day and inter-day precisions were ≤ 9.24% and ≤ 10.63%, respectively. As a result of analyzing synephrine-containing health foods using this method, approximately half of the products showed high optical purity with 80–100% enantiomeric excess of the l -isomer. In contrast, nearly 20% of the products contained racemate with 0–50% enantiomeric excess, and variations in optical purity were observed for the products. It was speculated that the l -isomer could be converted into the d -isomer during the manufacturing process.","PeriodicalId":91226,"journal":{"name":"Chromatography (Basel)","volume":" ","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2020-02-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":"{\"title\":\"Enantioselective Determination of Synephrine in Health Food Products by Liquid Chromatography/Time-of-Flight Mass Spectrometry\",\"authors\":\"Yoshiyuki Kobayashi, Masakadzu Yato, R. Ito, Koichi Saito\",\"doi\":\"10.15583/jpchrom.2019.024\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"An enantioselective analytical method for the determination of synephrine, an ingredient in health food, by liquid chromatography/time-of-flight mass spectrometry (LC/TOF-MS) was developed. By derivatizing synephrine with FMOC and using TCI Chiral MB-S as the chiral column, FMOC-synephrine enantiomers were well separated. The electrospray ionization (ESI) negative mode was adopted for TOF-MS measurement. Good linearity ( r > 0.999) was obtained in the concentration range of 0.5 to 50 μg/mL. The limit of detection (LOD, S / N = 3) and the limit of quantification (LOQ, S / N > 10) were 0.25 μg/mL and 0.5 μg/mL, respectively. The intra-day and inter-day accuracy of synephrine enantiomers at the LOQ level (0.5 μg/mL), the intermediate concentration level (10 μg/mL), and the high concentration level (50 μg/mL) ranged from 90.0 to 107.4%. The intra-day and inter-day precisions were ≤ 9.24% and ≤ 10.63%, respectively. As a result of analyzing synephrine-containing health foods using this method, approximately half of the products showed high optical purity with 80–100% enantiomeric excess of the l -isomer. In contrast, nearly 20% of the products contained racemate with 0–50% enantiomeric excess, and variations in optical purity were observed for the products. It was speculated that the l -isomer could be converted into the d -isomer during the manufacturing process.\",\"PeriodicalId\":91226,\"journal\":{\"name\":\"Chromatography (Basel)\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2020-02-20\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Chromatography (Basel)\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.15583/jpchrom.2019.024\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Chromatography (Basel)","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15583/jpchrom.2019.024","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
Enantioselective Determination of Synephrine in Health Food Products by Liquid Chromatography/Time-of-Flight Mass Spectrometry
An enantioselective analytical method for the determination of synephrine, an ingredient in health food, by liquid chromatography/time-of-flight mass spectrometry (LC/TOF-MS) was developed. By derivatizing synephrine with FMOC and using TCI Chiral MB-S as the chiral column, FMOC-synephrine enantiomers were well separated. The electrospray ionization (ESI) negative mode was adopted for TOF-MS measurement. Good linearity ( r > 0.999) was obtained in the concentration range of 0.5 to 50 μg/mL. The limit of detection (LOD, S / N = 3) and the limit of quantification (LOQ, S / N > 10) were 0.25 μg/mL and 0.5 μg/mL, respectively. The intra-day and inter-day accuracy of synephrine enantiomers at the LOQ level (0.5 μg/mL), the intermediate concentration level (10 μg/mL), and the high concentration level (50 μg/mL) ranged from 90.0 to 107.4%. The intra-day and inter-day precisions were ≤ 9.24% and ≤ 10.63%, respectively. As a result of analyzing synephrine-containing health foods using this method, approximately half of the products showed high optical purity with 80–100% enantiomeric excess of the l -isomer. In contrast, nearly 20% of the products contained racemate with 0–50% enantiomeric excess, and variations in optical purity were observed for the products. It was speculated that the l -isomer could be converted into the d -isomer during the manufacturing process.