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中国临床药理学与治疗学 ›› 2007, Vol. 12 ›› Issue (7): 748-755.

• 基础研究 • 上一篇    下一篇

应用液相色谱-质谱联用技术检测血浆样品中丹参酚酸类成分的浓度

陈平1, 路通1, 吴伯英2, 杜飞飞1, 高秀梅3, 张伯礼3, 李川1   

  1. 1中国科学院上海药物研究所上海药物代谢研究中心, 上海 201203;
    2四川省凉山食品药品检验所, 西昌 615000, 四川;
    3天津中医药大学, 天津 300193
  • 收稿日期:2007-05-17 修回日期:2007-06-15 出版日期:2007-07-26 发布日期:2020-10-27
  • 通讯作者: 李川, 男, 博士, 研究员, 博士生导师, 研究方向:药代动力学及中药学。Tel/Fax:021-50803106 E-mail:chli@mail.shcnc.ac.cn
  • 作者简介:陈平,女,博士研究生,研究方向:药代动力学。
  • 基金资助:
    国家“973” 计划基金项目资助(2004CB518902;2005CB523403);国家自然科学基金资助(90209044);上海市基金资助项目(04DZ19215)。

LC-MS/MS-based measurement of danshen phenolic acids in plasma

CHEN Ping1, LU Tong1,WU Bo-ying2, DU Fei-fei1, GAO Xiu-mei3, ZHANG Bo-li3, LI Chuan1   

  1. 1Center for DMPK Research, Shanghai Institute of Materia Medica, SIBS, Chinese Academy of Sciences, Shanghai 201203, China;
    2Liangshan Institute for Food and Drug Control, Xichang 615000, Sichuan, China;
    3TianjinUniversity of Traditional Chinese Medicine, Tianjin 300193, China
  • Received:2007-05-17 Revised:2007-06-15 Online:2007-07-26 Published:2020-10-27

摘要: 目的: 研究丹参酚酸中丹参素(tanshinol,TSN)、原儿茶醛(protocatechualdehyde, PCA)、丹酚酸A(salvianolic acid A, SAA)、丹酚酸B(salvianolic acid B, SAB)及丹酚酸D(salvianolic acid D, SAD)的电喷雾串联质谱(ESI-MS/MS)检测特性, 为开展复方丹参滴丸药代研究, 建立灵敏可靠的定量分析血浆样品中丹参酚酸浓度的方法。方法: 研究丹参酚酸的电离模式及效率、二级质谱的碎片离子及打碎效率;建立有效可靠的从血浆样品中提取被测丹参酚酸物质的前处理方法;优化色谱条件、减少分析干扰、促进质谱检测;围绕准确性、精密度和提取回收率等进行方法学验证。结果: 电喷雾(ESI)负离子模式能有效实现丹参酚酸被测化合物的电离。以下离子对m/z197→135、137→108、493→295、717→519、417→197分别为被测化合物TSN、PCA、SAA、SAB、SAD 提供最佳的选择离子对监测(SRM)检测条件。为取得可靠的分析结果, 建立了两个分析方法: 其一用于测定血浆样品中的TSN;其二用于测定血浆样品中的PCA、SAA、SAB 和SAD 。两个分析方法均以HCl 酸化血样后用乙酸乙酯提取的方法处理血浆样品, 其中, TSN的提取回收率在57.7%~61.6%之间;PCA、SAA、SAB 和SAD 的提取回收率在38.0%~58.9%之间。TSN 的线性范围为2.7~2000.0 ng/mL, 相关系数r为0.999, 最低检测限(LLOQ)为2.7 ng/mL;PCA、SAA、SAB 及SAD 的线性范围为1.4~1000.0 ng/mL或4.1~1000.0 ng/mL, 相关系数r>0.99, LLOQ 分别为1.4 ng/mL (PCA)和4.1 ng/mL(SAA、SAB 和SAD)。两个分析方法的日内准确性和精密度分别为90%~112%和2.5%~14.5%;日间准确性和精密度分别为91%~110%和0.7%~9.8%。结论: 成功建立了能够灵敏可靠地测定血浆样品中5 种丹参酚酸化合物浓度的分析方法, 此方法可用于复方丹参滴丸的药代动力学研究。

关键词: 丹参素, 原儿茶醛, 丹参酚酸, 液相色谱-质谱联用技术, 血药浓度

Abstract: AIM: To develop sensetive and specific LC-MS/MS-based methods for measurement of plasma tanshinol (TSN), protocatechualdehyde (PCA), and salvianolic acid A, B, and D (SAA, SAB, and SAD)in supporting the pharmacokinetic evaluation of Cardiotonic pills, a standardized danshen-containing cardiovascular phytomedicine. METHODS: Electrospray ionization (ESI)patterns and efficiency of the analytes, along with their fragmentation, were investigated to achieve sensitive ESI-MS/MS detection.Sample preparation was also studied to effectively recover the analytes from plasma.Meanwhile, chromatographic conditions were optimized to avoid matrix component interference on analyte ESI-detection. The newly developed analytical methods were evaluated with respect to accuracy, precison, selectivity, sensitivity, and stability. RESULTS: The negative ion ESI gave a high ionization efficiency for the analytes.The precursor-to-product ion pairs m z 197→135, 136→108, 493→295, 717→519, and 417→197 were used for sensitive and specific SRM of TSN, PCA, SAA, SAB, and SAD, repectively.For the best measurement of the analytes, two methods were developed, i.e., one for determination of plasma TSN and the other one for simultanious determination of plasma PCA, SAA, SAB, and SAD.The sample preparation for the two quantification methoids involved acidifying the plasma sample with HCl before EtOAc-based liquid-liquid extraction;the extraction efficiency was 57.7%-61.6% for TSN from plasma or 38.0%-58.9% for PCA、SAA、SAB, and SAD in parallel from plasma.Matrix-matched standard curves of the peak area of a given analytes versus the nominal plasma concentration were linear for concentrations of TSN between 2.7 ng/mL and 2 000.0 ng/mL, with a correlation coefficient 0.999 and a lower limit of quantification 2.7 ng/mL, while linear dynamic ranges for PCA, SAA, SAB, and SAD were 1.37 or 4.1-1000.0 ng/mL, with correlation coefficients>0.99 and lower limits of quantification 1.4 ng/mL for PCA and 4.1 ng/mL for SAA, SAB, and SAD.Both the quantification methods demonstrated a within-run assay accuracy and presion 90%-112% and 2.5%-15%, respectively and a between-run data 91%-110% and 0.7%-9.4%, respectively.Further, the applicability of the newly developed analytical methods was demonstrated in a pilot plasma pharmacokinetic study in a beagle dog receiving an intravenous dose of injectable extract from Cardiotonic pills. CONCLUSION: Sensetive and specific LC-MS/MS-based methods for measurement of plasma TSN and for measurement of plasma PCA, SAA, SAB, and SAD in parallel are developed and validated, which are applicable to pharmacokinetic evaluation of Cardiotonic pills.

Key words: tanshinol, protocatechualdehyde, salvianolic acids, LC-MS/MS, plasma concentration

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