LC–MS/MS Determination of Ginsenoside Compound K and its Metabolite 20( S )-Protopanaxadiol in Human Plasma and Urine: Applications in a Clinical Study
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)-protopanaxadi...
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Published in | Bioanalysis Vol. 11; no. 5; pp. 365 - 380 |
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Main Authors | , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
England
Newlands Press
01.03.2019
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Subjects | |
Online Access | Get full text |
ISSN | 1757-6180 1757-6199 |
DOI | 10.4155/bio-2018-0185 |
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Abstract | 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.
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.
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.
ChiCTR-TRC-14004824. |
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AbstractList | 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. 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. 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. 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. ChiCTR-TRC-14004824. |
Author | Huang, Wei-Hua Tan, Zhi-Rong Xie, Xiao-Nv Ouyang, Dong-Sheng Yang, Li Peng, Jing-Bo Wang, Chun-Yang Chen, Yao Wang, Yi-Cheng |
Author_xml | – sequence: 1 givenname: Li surname: Yang fullname: Yang, Li organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 2 givenname: Chun-Yang surname: Wang fullname: Wang, Chun-Yang organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 3 givenname: Xiao-Nv surname: Xie fullname: Xie, Xiao-Nv organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 4 givenname: Yi-Cheng surname: Wang fullname: Wang, Yi-Cheng organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 5 givenname: Jing-Bo surname: Peng fullname: Peng, Jing-Bo organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 6 givenname: Wei-Hua surname: Huang fullname: Huang, Wei-Hua organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 7 givenname: Yao surname: Chen fullname: Chen, Yao organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 8 givenname: Dong-Sheng surname: Ouyang fullname: Ouyang, Dong-Sheng organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Institute of Clinical Pharmacology, Central South University, Hunan Key Laboratory of Pharmacogenetics, Changsha410078, PR China – sequence: 9 givenname: Zhi-Rong surname: Tan fullname: Tan, Zhi-Rong organization: Department of Clinical Pharmacology, Xiangya Hospital, Central South University, 87 Xiangya Road, Changsha410008, PR China, Engineering Research Center of Applied Technology of Pharmacogenomics, Ministry of Education, 110 Xiangya Road, Changsha41007, PR China, National Clinical Research Center for Geriatric Disorders, 87 Xiangya Road, Changsha410008, Hunan, PR China |
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Snippet | Ginsenoside compound K (CK) is considered to be a potential therapeutic drug for rheumatoid arthritis because of its good anti-inflammatory activity. The... Aim: Ginsenoside compound K (CK) is considered to be a potential therapeutic drug for rheumatoid arthritis because of its good anti-inflammatory activity. The... |
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SubjectTerms | Acids Anti-inflammatory agents Arthritis, Rheumatoid Biological products Chromatography Chromatography, Liquid - methods Female Ginsenosides Ginsenosides - pharmacology Ginsenosides - therapeutic use Humans Inflammation Ions Male Mass spectrometry Mass spectroscopy Metabolites Microorganisms Panax - chemistry Pharmaceuticals Plasma Rheumatoid arthritis Sapogenins - pharmacology Sapogenins - therapeutic use Scientific imaging Studies Tandem Mass Spectrometry - methods Urine |
Title | LC–MS/MS Determination of Ginsenoside Compound K and its Metabolite 20( S )-Protopanaxadiol in Human Plasma and Urine: Applications in a Clinical Study |
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