Que Mai Nguyen Thi, Hoa Do Thi, Thu Phuong Ngo Thi, Cam Pham Nguyet
{"title":"高效液相色谱法测定功能性食品样品中的紫杉醇","authors":"Que Mai Nguyen Thi, Hoa Do Thi, Thu Phuong Ngo Thi, Cam Pham Nguyet","doi":"10.47866/2615-9252/vjfc.3967","DOIUrl":null,"url":null,"abstract":"A method using high performance liquid chromatography with UV - Vis detector was developed for quantification of taxifolin in supplements. In this study, the supplements were homogenized, extracted by ultrasonication with methanol. Taxifolin in test solution was separated on C18 column (250 × 4.6 mm, 5 µm) with mobile phase containing methanol and 0.3 % acetic acid solution (40 : 60) using isocratic elution at a flow rate of 1.0 mL/min, with UV detection at 290 nm. The analytical method was validated for specificity, linearity, precision and accuracy according to AOAC. The detector response for taxifolin was linear over the selected concentration range from 1.04 to 78.23 µg/mL with a correlation coefficient 0.9996. The repeatability (RSD, n = 7) were from 1.1 to 1.4 % respectively. The recovery was between 98.1 and 105.9 %. The method was successfully applied for analysis of taxifolin in 7 supplements at solid, liquid and oil form.","PeriodicalId":12896,"journal":{"name":"Heavy metals and arsenic concentrations in water, agricultural soil, and rice in Ngan Son district, Bac Kan province, Vietnam","volume":"40 4 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Determination of taxifolin in functional food samples by high - performance liquid chromatography (HPLC - UV Vis)\",\"authors\":\"Que Mai Nguyen Thi, Hoa Do Thi, Thu Phuong Ngo Thi, Cam Pham Nguyet\",\"doi\":\"10.47866/2615-9252/vjfc.3967\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"A method using high performance liquid chromatography with UV - Vis detector was developed for quantification of taxifolin in supplements. In this study, the supplements were homogenized, extracted by ultrasonication with methanol. Taxifolin in test solution was separated on C18 column (250 × 4.6 mm, 5 µm) with mobile phase containing methanol and 0.3 % acetic acid solution (40 : 60) using isocratic elution at a flow rate of 1.0 mL/min, with UV detection at 290 nm. The analytical method was validated for specificity, linearity, precision and accuracy according to AOAC. The detector response for taxifolin was linear over the selected concentration range from 1.04 to 78.23 µg/mL with a correlation coefficient 0.9996. The repeatability (RSD, n = 7) were from 1.1 to 1.4 % respectively. The recovery was between 98.1 and 105.9 %. The method was successfully applied for analysis of taxifolin in 7 supplements at solid, liquid and oil form.\",\"PeriodicalId\":12896,\"journal\":{\"name\":\"Heavy metals and arsenic concentrations in water, agricultural soil, and rice in Ngan Son district, Bac Kan province, Vietnam\",\"volume\":\"40 4 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-09-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Heavy metals and arsenic concentrations in water, agricultural soil, and rice in Ngan Son district, Bac Kan province, Vietnam\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.47866/2615-9252/vjfc.3967\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Heavy metals and arsenic concentrations in water, agricultural soil, and rice in Ngan Son district, Bac Kan province, Vietnam","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.47866/2615-9252/vjfc.3967","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
建立了一种高效液相色谱-紫外-可见检测器定量食品添加剂中紫杉醇的方法。在本研究中,补品均质,超声提取与甲醇。采用C18色谱柱(250 × 4.6 mm, 5µm),流动相为甲醇和0.3%醋酸溶液(40∶60),流速为1.0 mL/min,紫外检测波长为290 nm,等密度洗脱。根据AOAC对分析方法的特异性、线性度、精密度和准确度进行了验证。在1.04 ~ 78.23µg/mL范围内,检测器对紫杉醇的响应呈线性关系,相关系数为0.9996。重复性(RSD, n = 7)分别为1.1% ~ 1.4%。回收率在98.1% ~ 105.9%之间。该方法成功地应用于7种补充物中杉木素的固体、液体和油态分析。
Determination of taxifolin in functional food samples by high - performance liquid chromatography (HPLC - UV Vis)
A method using high performance liquid chromatography with UV - Vis detector was developed for quantification of taxifolin in supplements. In this study, the supplements were homogenized, extracted by ultrasonication with methanol. Taxifolin in test solution was separated on C18 column (250 × 4.6 mm, 5 µm) with mobile phase containing methanol and 0.3 % acetic acid solution (40 : 60) using isocratic elution at a flow rate of 1.0 mL/min, with UV detection at 290 nm. The analytical method was validated for specificity, linearity, precision and accuracy according to AOAC. The detector response for taxifolin was linear over the selected concentration range from 1.04 to 78.23 µg/mL with a correlation coefficient 0.9996. The repeatability (RSD, n = 7) were from 1.1 to 1.4 % respectively. The recovery was between 98.1 and 105.9 %. The method was successfully applied for analysis of taxifolin in 7 supplements at solid, liquid and oil form.