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TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素

Amanita peptide toxins are cyclic polypeptide mushroom toxins that can cause acute liver damage. The fatality rate associated with these toxins is very high. Monitoring the concentration of amanita peptide toxins in human urine can provide valuable information for early clinical diagnosis and treatm...

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Autores principales: FANG, Li, QIU, Fengmei, YU, Xinwei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Editorial board of Chinese Journal of Chromatography 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403809/
https://www.ncbi.nlm.nih.gov/pubmed/34227315
http://dx.doi.org/10.3724/SP.J.1123.2020.06005
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author FANG, Li
QIU, Fengmei
YU, Xinwei
author_facet FANG, Li
QIU, Fengmei
YU, Xinwei
author_sort FANG, Li
collection PubMed
description Amanita peptide toxins are cyclic polypeptide mushroom toxins that can cause acute liver damage. The fatality rate associated with these toxins is very high. Monitoring the concentration of amanita peptide toxins in human urine can provide valuable information for early clinical diagnosis and treatment. Therefore, a TurboFlow online clean-up-liquid chromatography-triple quadrupole mass spectrometry (TF-LC-MS/MS) method was established for the simultaneous quantitative determination of five amanita peptide toxins (α-amanitin, β-amanitin, γ-amanitin, phallacidin, and phalloidin) in human urine. After pre-treatment with high-speed centrifugation, urine samples were analyzed using TF-LC-MS/MS. The main factors influencing purification efficiency, including the TF column, loading solution, eluting solution, transfer flow, and transfer time, were optimized in this study. Under the optimized experimental conditions, the analytes were purified using a TurboFlow(TM) Cyclone column (50 mm×0.5 mm) and separated on a Hypersil GOLD C(18) column (100 mm×2.1 mm) using the mobile phases of methanol and 4 mmol/L aqueous ammonium acetate solution with gradient elution. The analytes were detected in selected reaction monitoring (SRM) mode via positive electrospray ionization. Matrix-matched external standard calibration was used for quantitation. The linear range of the method ranged from 1.0 μg/L to 50.0 μg/L for all five amanita peptide toxins, with correlation coefficients (r(2)) higher than 0.997. The limits of detection were 0.15-0.3 μg/L and the limits of quantification (LOQs) were 0.5-1.0 μg/L for the five amanita peptide toxins in urine. The intra-day and inter-day recoveries of amanita peptide toxins were 87.0%-108.6% and 86.8%-112.7%, respectively, at the spiked levels of 2.0, 5.0, and 10.0 μg/L. The intra-day and inter-day relative standard deviations (RSDs) were less than 14.5%. The method is accurate, rapid, sensitive, easy to operate, and can satisfy the requirements of public health emergency testing or clinical poisoning testing.
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spelling pubmed-94038092022-09-14 TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素 FANG, Li QIU, Fengmei YU, Xinwei Se Pu Technical Notes Amanita peptide toxins are cyclic polypeptide mushroom toxins that can cause acute liver damage. The fatality rate associated with these toxins is very high. Monitoring the concentration of amanita peptide toxins in human urine can provide valuable information for early clinical diagnosis and treatment. Therefore, a TurboFlow online clean-up-liquid chromatography-triple quadrupole mass spectrometry (TF-LC-MS/MS) method was established for the simultaneous quantitative determination of five amanita peptide toxins (α-amanitin, β-amanitin, γ-amanitin, phallacidin, and phalloidin) in human urine. After pre-treatment with high-speed centrifugation, urine samples were analyzed using TF-LC-MS/MS. The main factors influencing purification efficiency, including the TF column, loading solution, eluting solution, transfer flow, and transfer time, were optimized in this study. Under the optimized experimental conditions, the analytes were purified using a TurboFlow(TM) Cyclone column (50 mm×0.5 mm) and separated on a Hypersil GOLD C(18) column (100 mm×2.1 mm) using the mobile phases of methanol and 4 mmol/L aqueous ammonium acetate solution with gradient elution. The analytes were detected in selected reaction monitoring (SRM) mode via positive electrospray ionization. Matrix-matched external standard calibration was used for quantitation. The linear range of the method ranged from 1.0 μg/L to 50.0 μg/L for all five amanita peptide toxins, with correlation coefficients (r(2)) higher than 0.997. The limits of detection were 0.15-0.3 μg/L and the limits of quantification (LOQs) were 0.5-1.0 μg/L for the five amanita peptide toxins in urine. The intra-day and inter-day recoveries of amanita peptide toxins were 87.0%-108.6% and 86.8%-112.7%, respectively, at the spiked levels of 2.0, 5.0, and 10.0 μg/L. The intra-day and inter-day relative standard deviations (RSDs) were less than 14.5%. The method is accurate, rapid, sensitive, easy to operate, and can satisfy the requirements of public health emergency testing or clinical poisoning testing. Editorial board of Chinese Journal of Chromatography 2021-03-08 /pmc/articles/PMC9403809/ /pubmed/34227315 http://dx.doi.org/10.3724/SP.J.1123.2020.06005 Text en https://creativecommons.org/licenses/by/4.0/本文是开放获取文章,遵循CC BY 4.0协议 https://creativecommons.org/licenses/by/4.0/This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Technical Notes
FANG, Li
QIU, Fengmei
YU, Xinwei
TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
title TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
title_full TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
title_fullStr TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
title_full_unstemmed TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
title_short TurboFlow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
title_sort turboflow在线净化-液相色谱-串联质谱法快速检测人尿中鹅膏肽类毒素
topic Technical Notes
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9403809/
https://www.ncbi.nlm.nih.gov/pubmed/34227315
http://dx.doi.org/10.3724/SP.J.1123.2020.06005
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