{"title":"高效液相色谱-质谱联用法测定海茱萸四种化合物在大鼠血浆和组织中的药动学和组织分布。","authors":"Yuhuang Wu, Liyan Li, Guxu Ming, Xinyue Ma, Changfu Liang, Yonghui Li, Xiaoning He","doi":"10.1155/2022/5297603","DOIUrl":null,"url":null,"abstract":"<p><p>A rapid, sensitive, selective, and accurate HPLC-MS/MS method was developed and validated for the simultaneous determination of chlorogenic acid, naucleactonin C, khaephuoside A 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside in rat plasma and tissues after oral administration of <i>Nauclea officinalis</i> extracts. Chloramphenicol was used as an internal standard (IS). The plasma and tissue samples were extracted by protein precipitation with methanol-ethyl acetate (1 : 1, v/v) including 0.1% (v/v) formic acid. The chromatographic separation was achieved by using an C18 column with gradient elution using mobile phase, which consisted of 0.1% formic acid water (A) and acetonitrile (B) and the flow rate of 0.8 mL/min. Mass spectrometric detection was performed in multiple reaction monitoring (MRM) mode utilizing electrospray ionization (ESI) in negative mode. The developed method exhibited good linearity (determination coefficients, <i>R</i> <sup>2</sup> ≥ 0.9849), and the lower limits of quantification were 2, 5, 5, and 25 ng/mL for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside. The intraday and interday precisions (relative standard deviation, RSD) were less than 12.65%, while the accuracy was ranged from 86.31 to 114.17%. The recovery rate were 51.85-97.06%, 75.99-106.68%, 77.46-105.35%, and 68.36-103.75% for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside the matrix effects were 50.17-116.62%, 86.75-115.99%, 45.79-87.44%, and 51.60-92.34% for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside in different matrix. The developed method was successfully applied to a pharmacokinetic study and tissue distribution of four compounds in rats after oral administration of <i>Nauclea officinalis</i> extracts.</p>","PeriodicalId":14974,"journal":{"name":"Journal of Analytical Methods in Chemistry","volume":"2022 ","pages":"5297603"},"PeriodicalIF":2.3000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797307/pdf/","citationCount":"0","resultStr":"{\"title\":\"Measurement of Pharmacokinetics and Tissue Distribution of Four Compounds from <i>Nauclea officinalis</i> in Rat Plasma and Tissues through HPLC-MS/MS.\",\"authors\":\"Yuhuang Wu, Liyan Li, Guxu Ming, Xinyue Ma, Changfu Liang, Yonghui Li, Xiaoning He\",\"doi\":\"10.1155/2022/5297603\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>A rapid, sensitive, selective, and accurate HPLC-MS/MS method was developed and validated for the simultaneous determination of chlorogenic acid, naucleactonin C, khaephuoside A 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside in rat plasma and tissues after oral administration of <i>Nauclea officinalis</i> extracts. Chloramphenicol was used as an internal standard (IS). The plasma and tissue samples were extracted by protein precipitation with methanol-ethyl acetate (1 : 1, v/v) including 0.1% (v/v) formic acid. The chromatographic separation was achieved by using an C18 column with gradient elution using mobile phase, which consisted of 0.1% formic acid water (A) and acetonitrile (B) and the flow rate of 0.8 mL/min. Mass spectrometric detection was performed in multiple reaction monitoring (MRM) mode utilizing electrospray ionization (ESI) in negative mode. The developed method exhibited good linearity (determination coefficients, <i>R</i> <sup>2</sup> ≥ 0.9849), and the lower limits of quantification were 2, 5, 5, and 25 ng/mL for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside. The intraday and interday precisions (relative standard deviation, RSD) were less than 12.65%, while the accuracy was ranged from 86.31 to 114.17%. The recovery rate were 51.85-97.06%, 75.99-106.68%, 77.46-105.35%, and 68.36-103.75% for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside the matrix effects were 50.17-116.62%, 86.75-115.99%, 45.79-87.44%, and 51.60-92.34% for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-<i>β</i>-apiofuroseyl(1 ⟶ 2)-<i>β</i>-D-glucopyranoside in different matrix. The developed method was successfully applied to a pharmacokinetic study and tissue distribution of four compounds in rats after oral administration of <i>Nauclea officinalis</i> extracts.</p>\",\"PeriodicalId\":14974,\"journal\":{\"name\":\"Journal of Analytical Methods in Chemistry\",\"volume\":\"2022 \",\"pages\":\"5297603\"},\"PeriodicalIF\":2.3000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9797307/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of Analytical Methods in Chemistry\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1155/2022/5297603\",\"RegionNum\":3,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"CHEMISTRY, ANALYTICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of Analytical Methods in Chemistry","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1155/2022/5297603","RegionNum":3,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"CHEMISTRY, ANALYTICAL","Score":null,"Total":0}
引用次数: 0
摘要
建立了一种快速、灵敏、选择性、准确的高效液相色谱-质谱联用方法,用于同时测定大鼠口服核桃仁提取物后血浆和组织中绿原酸、核内聚素C、海马甲苷A 3,4-二甲氧基苯基-1- o -β-apiofuroseyl(1 × 2)-β- d -葡萄糖吡喃苷的含量。以氯霉素为内标。血浆和组织样品采用甲醇-乙酸乙酯(1:1,v/v)(含0.1% (v/v)甲酸)的蛋白质沉淀法提取。色谱分离采用C18柱,流动相为0.1%甲酸水(A) -乙腈(B),流速为0.8 mL/min,梯度洗脱。质谱检测采用多反应监测(MRM)模式,电喷雾电离(ESI)在负模式下进行。绿原酸、核内素C、海马甲苷A和3,4-二甲氧基-1- o -β-apiofuroseyl -β- d - glucopyrano苷的定量下限分别为2、5、5和25 ng/mL,线性关系良好(r2≥0.9849)。日内、日间精密度(相对标准偏差,RSD)均小于12.65%,准确度为86.31 ~ 114.17%。绿原酸、核内聚素C、khapho苷A和3,4-二甲氧基-1- o -β-apiofuroseyl(1 ~ 2)-β- d - glucopyrano苷的回收率分别为51.85 ~ 97.06%、75.99 ~ 106.68%、77.46 ~ 105.35%和68.36 ~ 103.75%,基质效应分别为50.17 ~ 116.62%、86.75 ~ 115.99%、45.79 ~ 87.44%和3,4-二甲氧基-1- o -β-apiofuroseyl(1 ~ 2)-β- d - glucopyrano苷。该方法成功地应用于口服核桃树提取物后4种化合物在大鼠体内的药动学研究和组织分布。
Measurement of Pharmacokinetics and Tissue Distribution of Four Compounds from Nauclea officinalis in Rat Plasma and Tissues through HPLC-MS/MS.
A rapid, sensitive, selective, and accurate HPLC-MS/MS method was developed and validated for the simultaneous determination of chlorogenic acid, naucleactonin C, khaephuoside A 3,4-dimethoxyphenyl-1-O-β-apiofuroseyl(1 ⟶ 2)-β-D-glucopyranoside in rat plasma and tissues after oral administration of Nauclea officinalis extracts. Chloramphenicol was used as an internal standard (IS). The plasma and tissue samples were extracted by protein precipitation with methanol-ethyl acetate (1 : 1, v/v) including 0.1% (v/v) formic acid. The chromatographic separation was achieved by using an C18 column with gradient elution using mobile phase, which consisted of 0.1% formic acid water (A) and acetonitrile (B) and the flow rate of 0.8 mL/min. Mass spectrometric detection was performed in multiple reaction monitoring (MRM) mode utilizing electrospray ionization (ESI) in negative mode. The developed method exhibited good linearity (determination coefficients, R2 ≥ 0.9849), and the lower limits of quantification were 2, 5, 5, and 25 ng/mL for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-β-apiofuroseyl(1 ⟶ 2)-β-D-glucopyranoside. The intraday and interday precisions (relative standard deviation, RSD) were less than 12.65%, while the accuracy was ranged from 86.31 to 114.17%. The recovery rate were 51.85-97.06%, 75.99-106.68%, 77.46-105.35%, and 68.36-103.75% for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-β-apiofuroseyl(1 ⟶ 2)-β-D-glucopyranoside the matrix effects were 50.17-116.62%, 86.75-115.99%, 45.79-87.44%, and 51.60-92.34% for chlorogenic acid, naucleactonin C, khaephuoside A, and 3,4-dimethoxyphenyl-1-O-β-apiofuroseyl(1 ⟶ 2)-β-D-glucopyranoside in different matrix. The developed method was successfully applied to a pharmacokinetic study and tissue distribution of four compounds in rats after oral administration of Nauclea officinalis extracts.
期刊介绍:
Journal of Analytical Methods in Chemistry publishes papers reporting methods and instrumentation for chemical analysis, and their application to real-world problems. Articles may be either practical or theoretical.
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