LC-MS/MS determination of ginsenoside compound K and its metabolite 20 (S)-protopanaxadiol in human plasma and urine : applications in a clinical study
AIM: Ginsenoside compound K (CK) is considered to be a potential therapeutic drug for rheumatoid arthritis because of its good anti-inflammatory activity. The purpose of this work was to establish a rapid, sensitive and specific method for determination of CK and its active metabolite 20(S)-protopanaxadiol (20(S)-PPD). Materials & methods: The analytes and internal standards were extracted by liquid-liquid extraction. Then, were separated by high performance liquid phase and determined by triple quadrupole mass spectrometry.
RESULTS: A LC-MS/MS using liquid-liquid extraction was developed for determining CK over the concentration range 1.00-1002.00 ng/ml and 0.15-54.30 ng/ml for 20(S)-PPD. The lower limits of quantification for CK and 20(S)-PPD were 1.00 and 0.15 ng/ml, respectively.
CONCLUSION: This method was successfully validated for detecting both CK and 20(S)-PPD in the human plasma and urine, and was proved to be suitable for the pharmacokinetic study of CK in healthy Chinese volunteers.
CLINICAL TRIAL REGISTRATION NUMBER: ChiCTR-TRC-14004824.
Medienart: |
E-Artikel |
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Erscheinungsjahr: |
2019 |
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Erschienen: |
2019 |
Enthalten in: |
Zur Gesamtaufnahme - volume:11 |
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Enthalten in: |
Bioanalysis - 11(2019), 5 vom: 26. März, Seite 365-380 |
Sprache: |
Englisch |
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Beteiligte Personen: |
Yang, Li [VerfasserIn] |
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Links: |
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Themen: |
20()-protopanaxadiol |
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Anmerkungen: |
Date Completed 26.07.2019 Date Revised 26.07.2019 published: Print-Electronic Citation Status MEDLINE |
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doi: |
10.4155/bio-2018-0185 |
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funding: |
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Förderinstitution / Projekttitel: |
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PPN (Katalog-ID): |
NLM294969217 |
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520 | |a AIM: Ginsenoside compound K (CK) is considered to be a potential therapeutic drug for rheumatoid arthritis because of its good anti-inflammatory activity. The purpose of this work was to establish a rapid, sensitive and specific method for determination of CK and its active metabolite 20(S)-protopanaxadiol (20(S)-PPD). Materials & methods: The analytes and internal standards were extracted by liquid-liquid extraction. Then, were separated by high performance liquid phase and determined by triple quadrupole mass spectrometry | ||
520 | |a RESULTS: A LC-MS/MS using liquid-liquid extraction was developed for determining CK over the concentration range 1.00-1002.00 ng/ml and 0.15-54.30 ng/ml for 20(S)-PPD. The lower limits of quantification for CK and 20(S)-PPD were 1.00 and 0.15 ng/ml, respectively | ||
520 | |a CONCLUSION: This method was successfully validated for detecting both CK and 20(S)-PPD in the human plasma and urine, and was proved to be suitable for the pharmacokinetic study of CK in healthy Chinese volunteers | ||
520 | |a CLINICAL TRIAL REGISTRATION NUMBER: ChiCTR-TRC-14004824 | ||
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700 | 1 | |a Huang, Wei-Hua |e verfasserin |4 aut | |
700 | 1 | |a Chen, Yao |e verfasserin |4 aut | |
700 | 1 | |a Ouyang, Dong-Sheng |e verfasserin |4 aut | |
700 | 1 | |a Tan, Zhi-Rong |e verfasserin |4 aut | |
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