Determination and Risk Assessment of Six Hepatotoxic Pyrrolizidine Alkaloids in Verbenae Herba

Ke ZAN; Cui-ling CHEN; Ying ZHOU; Tian-tian ZUO; Hong-yu JIN; Ying WANG; Shuang-cheng MA

doi:10.13422/j.cnki.syfjx.20211953

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Determination and Risk Assessment of Six Hepatotoxic Pyrrolizidine Alkaloids in Verbenae Herba

更新时间：2021-11-12

- Determination and Risk Assessment of Six Hepatotoxic Pyrrolizidine Alkaloids in Verbenae Herba
- Chinese Journal of Experimental Traditional Medical Formulae Vol. 27, Issue 24, Pages: 157-162(2021)
- 作者机构：
  
  1.中国食品药品检定研究院，北京 102629
  2.梧州市食品药品检验所，广西梧州 543000
  3.浙江省食品药品检验研究院，国家药品监督管理局中成药质量评价重点实验室，杭州 310052
- 作者简介：
- 基金信息：
- DOI：10.13422/j.cnki.syfjx.20211953
  CLC： R22;R28;R931;O657
- Published：20 December 2021，
  
  Published Online：11 October 2021，
  
  Received：14 July 2021，
- 稿件说明：
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昝珂,陈翠玲,周颖等.马鞭草中6个肝毒性吡咯里西啶生物碱的含量测定及风险评估[J].中国实验方剂学杂志,2021,27(24):157-162.

ZAN Ke,CHEN Cui-ling,ZHOU Ying,et al.Determination and Risk Assessment of Six Hepatotoxic Pyrrolizidine Alkaloids in Verbenae Herba[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(24):157-162.
昝珂,陈翠玲,周颖等.马鞭草中6个肝毒性吡咯里西啶生物碱的含量测定及风险评估[J].中国实验方剂学杂志,2021,27(24):157-162. DOI： 10.13422/j.cnki.syfjx.20211953.

ZAN Ke,CHEN Cui-ling,ZHOU Ying,et al.Determination and Risk Assessment of Six Hepatotoxic Pyrrolizidine Alkaloids in Verbenae Herba[J].Chinese Journal of Experimental Traditional Medical Formulae,2021,27(24):157-162. DOI： 10.13422/j.cnki.syfjx.20211953.

摘要

目的

建立超高效液相色谱-串联质谱法（UPLC-MS/MS）对马鞭草中6个肝毒性吡咯里西啶生物碱的含量进行测定，并根据测定结果进行初步的风险评估。

方法

选择Waters ACQUITY UPLC HSS T3色谱柱（2.1 mm×100 mm，1.8 μm），以含0.05%甲酸和2.5 mmol·L

-1

甲酸铵的水溶液（A）及含0.05%甲酸和2.5 mmol·L

-1

甲酸铵的乙腈溶液（B）为流动相进行梯度洗脱（0~12 min，3%~8%B；12~25 min，8%~15%B；25~26 min，15%~3%B；26~30 min，3%B），流速0.3 mL·min

-1

，柱温40 ℃，进样量1 μL；电喷雾离子源（ESI），正离子模式下多反应监测模式，通过优化三重四极杆的MS参数及6个分析物的MS参数进行定性、定量分析。根据含量测定结果，采用暴露限值（MOE）结合热水提取转移率进行风险评估。

结果

通过仪器精密度、线性范围、重复性、稳定性和加样回收试验等方法学验证，其结果均符合定量分析的要求。印美定、石松胺、印美定氮氧化物、石松胺氮氧化物、蓝蓟定氮氧化物和蓝蓟定的线性范围分别为0.984~49.20，0.994~49.70，1.012~50.60，1.032~51.60，1.004~50.20，1.016~50.80 µg·L

-1

，这6个成分在线性范围内峰面积与质量浓度均具有良好线性关系（

≥0.999 0）；平均加样回收率在87.2%~94.2%，RSD均

4.0%；MOE均

1万。

结论

建立的UPLC-MS/MS稳定可行，可为马鞭草中肝毒性吡咯里西啶生物碱的质量控制和安全性评价提供科学依据。

Abstract

Objective

To establish ultra-performance liquid chromatography-tandem mass spectrometry （UPLC-MS/MS） for simultaneous determination of six hepatotoxic pyrrolizidine alkaloids in Verbenae Herba， and to carry out preliminary risk assessment according to the research results.

Method

An ACQUITY UPLC HSS T3 column （2.1 mm×100 mm， 1.8 μm） was used for analysis with 0.05% formic acid and 2.5 mmol·L

-1

ammonium formate in water （A）-0.05% formic acid and 2.5 mmol·L

-1

ammonium formate in acetonitrile （B） as mobile phase for gradient elution （0-12 min， 3%-8%B； 12-25 min， 8%-15%B； 25-26 min， 15%-3%B； 26-30 min， 3%B）， the flow rate was 0.3 mL·min

-1

， the column temperature was 40 ℃， and the injection volume was 1 μL. MS system was operated by electrospray ionization （ESI） in the positive ion mode with multiple reaction monitoring mode. MS parameters of triple quadrupole and six analytes were optimized for qualitative and quantitative analysis. According to the determination results， the risk assessment was carried out by using margin of exposure （MOE） combined with transfer rate of hot water extraction.

Result

Based on the instrument precision， linear range， repeatability， stability， recovery and other methodological validations， the results were in conformity with relevant standards of quantitative analysis. The linear ranges of intermedine， lycopsamine， intermedine

-oxide， lycopsamine

-oxide， echimidine

-oxide and echimidine were good （

≥0.999 0） between peak area and mass concentration in the ranges of 0.984-49.20， 0.994-49.70， 1.012-50.60， 1.032-51.60， 1.004-50.20， 1.016-50.80 µg·L

-1

， respectively. The average recoveries of these six analytes were 87.2%-94.2% with relative standard deviation （RSD）

4.0%. Their MOE values were

10 000.

Conclusion

The UPLC-MS/MS established in this study is stable and feasible， which can provide scientific basis for the quality control and safety evaluation of hepatotoxic pyrrolizidine alkaloids in Verbenae Herba.

关键词

马鞭草肝毒性成分吡咯里西啶生物碱（PAs）超高效液相色谱-串联质谱法（UPLC-MS/MS）含量测定风险评估暴露限值（MOE）

Keywords

Verbenae Herbahepatotoxic componentspyrrolizidine alkaloids （PAs）ultra-performance liquid chromatography-tandem mass spectrometry （UPLC-MS/MS）determinationrisk assessmentmargin of exposure （MOE）

references

国家药典委员会.中华人民共和国药典：一部［M］.北京：中国医药科技出版社，2020：53-54.

中国科学院《中国植物志》编辑委员会.中国植物志：第65卷［M］.北京：科学出版社，1982：15-16.

刘雅琳，苗晋鑫，田硕，等.马鞭草化学成分及其药理作用研究进展［J］.河南中医，2021，41（2）：294-299.

何俊，樊瑜琪，杨丰文，等.马鞭草化学成分及药理活性研究进展［J］.天津中医药，2020，37（11）：1205-1212.

马金华，杨勇勋.马鞭草的化学成分研究［J］.西南民族大学学报：自然科学版，2019，45（6）：579-582.

高江国，王长虹，李岩，等.吡咯里西啶生物碱的药理作用，毒性及药（毒）物代谢动力学研究进展［J］.中国中药杂志，2009，34（5）：506-511.

郭严，张世荣，文良志，等.我国吡咯烷生物碱致肝窦阻塞综合征的临床特征分析［J］.临床肝胆病杂志，2018，34（6）：1277-1281.

孙潇翔，向娥，邱帅凯，等.吡咯里西啶生物碱毒性作用研究进展［J］.中国药物警戒，2019，16（2）：76-80.

LETSYO E，JERZ G，WINTERHALTER P，et al.Incidence of pyrrolizidine alkaloids in herbal medicines from German retail markets risk assessment［J］.Phytother Res，2017，31（12）：1903-1909.

WANG J C，ZHANG M，CHEN L H，et al.Determination of toxic pyrrolizidine alkaloids in traditional Chinese herbal medicines by UPLC-MS/MS and accompanying risk assessment for human health［J］.Molecules，2021，26（6）：1648.

王涛，宋海波.吡咯里西啶类生物碱肝毒性研究进展及风险分析［J］.医药导报，2018，37（9）：1033-1037.

BOLECHOVÁ M，CÁSLAVSKÝ J，POSPICHALOVÁ M，et al.UPLC-MS/MS method for determination of selected pyrrolizidine alkaloids in feed［J］.Food Chem，2015，170：265-270.

DZUMAN Z，ZACHARIASOVA M，VEPRIKOVA Z，et al.Multi-analyte high performance liquid chromatography coupled to high resolution tandem mass spectrometry method for control of pesticide residues，mycotoxins，and pyrrolizidine alkaloids［J］.Anal Chim Acta，2015，863：29-40.

MARTINELLO M，BORIN A，STELLA R，et al.Development and validation of a QuEChERS method coupled to liquid chromatography and high resolution mass spectrometry to determine pyrrolizidine and tropane alkaloids in honey［J］.Food Chem，2017，234：295-302.

CHEN L，MULDER P P J，PEIJNENBURG A，et al.Risk assessment of intake of pyrrolizidine alkaloids from herbal teas and medicines following realistic exposure scenarios［J］.Food Chem Toxicol，2019，136：142-153.

PICRON J F，HERMAN M，HOECK E V，et al.Analytical strategies for the determination of pyrrolizidine alkaloids in plant based food and examination of the transfer rate during the infusion process［J］.Food Chem，2018，266：514-523.

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