Figure 1. Chemical structures of paeoniflorin and hyperoside.

Slides:



Advertisements
Similar presentations
HPLC Coupled with Quadrupole Mass Spectrometry and Forensic Analysis of Cocaine.
Advertisements

Copyright © 2015 Wolters Kluwer All Rights Reserved Chapter 1: Pharmacokinetics.
GCMS: gas chromatography and mass spectrometry
Gas chromatography coupled to mass spectrometry Liquid chromatography coupled to mass spectrometry MetMAX – Data alignment COVAIN – Data integration, Statistics.
液相層析質譜分析 LC-MS Method development and Analyte Identification 授課教師:賴滄海教授 授課教師:賴滄海教授
© Copyright 2009 by the American Association for Clinical Chemistry Plasma Renin Activity by Liquid Chromatography– Tandem Mass Spectrometry (LC-MS/MS):
Volume 53, Issue 5, Pages (May 1998)
Figure 1. A typical chromatogram of the target compounds (Table I) by GC–NCI-MS. From: Comparison and Analysis of Organochlorine Pesticides and Hexabromobiphenyls.
Quality analysis of Polygala tenuifolia root by ultrahigh performance liquid chromatography–tandem mass spectrometry and gas chromatography–mass spectrometry 
Results and Discussion
Method Development for the Rapid Separation and Detection of Organic Gunshot Residue by UPLC/MS/MS Jennifer Greaux, BSc*; Danielle Lincoln; Bruce McCord,
Validation of a headspace solid-phase microextraction–GC–MS/MS for the determination of ethyl glucuronide in hair according to forensic guidelines  Ronald.
Figure 1. Typical structure of polysorbate 80.
Invest. Ophthalmol. Vis. Sci ;48(1): doi: /iovs Figure Legend:
Figure 1. Chemical structure of rotenone (CAS No: , mw: 394
Simultaneous determination of mushroom toxins α-amanitin, β-amanitin and muscarine in human urine by solid-phase extraction and ultra-high-performance.
Detection of 3-methylmethcathinone and its metabolites 3-methylephedrine and 3- methylnorephedrine in pubic hair samples by liquid chromatography–high.
Forensic Science International
From: Comparison of High-Resolution Melting Analysis with Denaturing High-Performance Liquid Chromatography for Mutation Scanning in the ABCA4 Gene Invest.
Purple discoloration of the colon found during autopsy: Identification of betanin, its aglycone and metabolites by liquid chromatography–high-resolution.
Yun Sik Nam, Il Keun Kwon, Yeonhee Lee, Kang-Bong Lee 
Figure 1S. Details of the solvent program used for HPLC separation.
Forensic intelligence for medicine anti-counterfeiting
Figure 1. Structures of Tafluprost and four related impurities.
From: Methoxycarbonyl-etomidate:A Novel Rapidly Metabolized and Ultra–short-acting Etomidate Analogue that Does Not Produce Prolonged Adrenocortical Suppression.
Forensic analysis of biodiesel
Journal of Ginseng Research
Volume 71, Issue 1, Pages (January 2007)
Journal of Ginseng Research
Figure 1. (A–C) The chromatograms of FS extract
Journal of Ginseng Research
Footsteps in the snow When will all three heels be in line again?
Bioinformatics Solutions Inc.
Spectra of ESI–MS of 100 μM solution of catechol in H2O at pH 8
Footsteps in the snow When will all three heels be in line again?
Comparison of the pharmacokinetics of Crinone 8% administered vaginally versus Prometrium administered orally in postmenopausal women3  Howard Levine,
Minimum Information Required for A Glycomics Experiment
Comparison of pharmacokinetics of glucosamine and synovial fluid levels following administration of glucosamine sulphate or glucosamine hydrochloride 
Volume 150, Issue 1, Pages e1-e4 (July 2016)
Petter Bjornstad, Amy B. Karger, David M. Maahs 
Jesse C. Seegmiller, John H. Eckfeldt, John C. Lieske 
Rows of coins 1. Take five coins: 1p, 2p, 5p, 10p, 20p.
Results and discussion Technical innovations
Proteomic Approaches to Cancer Biomarkers
Discrimination and Quantification of True Biological Signals in Metabolomics Analysis Based on Liquid Chromatography-Mass Spectrometry  Lixin Duan, István.
Proteomics Moves into the Fast Lane
Year 3 Block 3 Assessment Paper 1 (Answers at the end of the quiz)
Nat. Rev. Nephrol. doi: /nrneph
Rows of coins 1. Take five coins: 1p, 2p, 5p, 10p, 20p.
Year 3 Block 3 Assessment Paper 1 (Answers at the end of the quiz)
Year 3 Block 3 Assessment Paper 1 (Answers after each question)
Copyright © 2004 The McGraw-Hill Companies, Inc. All rights reserved.
EQS 17β-estradiol 17a-ethinyl-estradiol 0.4 ng/L 35 pg/L
Volume 71, Issue 1, Pages (January 2007)
A Sensitive Gas Chromatography-Mass Spectrometry Assay Reveals Increased Levels of Monohydroxyeicosatetraenoic Acid Isomers in Human Plasma After Extracorporeal.
Volume 22, Issue 4, Pages (October 2015)
Straw squares There are 12 straws in this pattern of 5 squares.
Footsteps in the snow When will all three heels be in line again?
Johnson Cheung, Michael E.P. Murphy, David E. Heinrichs 
Volume 17, Issue 4, Pages (April 2010)
Mathematical challenges Year 2 C Handling data and measures
Comparison of two tobramycin nebuliser solutions: Pharmacokinetic, efficacy and safety profiles of T100 and TNS  Dorota Sands, Ewa Sapiejka, Grzegorz.
Tandem mass spectrometry measurements of creatinine in mouse plasma and urine for determining glomerular filtration rate  N. Takahashi, G. Boysen, F.
Mathematical challenges Year 2 C Handling data and measures
Straw squares There are 12 straws in this pattern of 5 squares.
Straw squares There are 12 straws in this pattern of 5 squares.
The kynurenic pathway. The kynurenic pathway. The encircled metabolites were measured and symbols indicate method and biological sample, that is, LC-MS/MS.
Fig. 3 Glycosylation profiling of MIH5 WT and Fc-silent variant using high-resolution native mass spectrometry. Glycosylation profiling of MIH5 WT and.
Mass spectrometry (MS) is an analytical technique that can be used to determine the mass, elemental composition or chemical structure of molecules. Mass.
Presentation transcript:

Figure 1. Chemical structures of paeoniflorin and hyperoside. From: Determination of Paeoniflorin in Rat Plasma by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry and its Application to a Pharmacokinetic Study J Chromatogr Sci. 2017;55(10):1006-1012. doi:10.1093/chromsci/bmx066 J Chromatogr Sci | © Crown copyright 2017.This article contains public sector information licensed under the Open Government Licence v3.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).

Figure 2. Full-scan product ion mass spectra of [M + HCOOH-H]<sup>−</sup> ion and fragmentation pathway for paeoniflorin (A) and [M-H]<sup>−</sup> ion for hyperoside (B). From: Determination of Paeoniflorin in Rat Plasma by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry and its Application to a Pharmacokinetic Study J Chromatogr Sci. 2017;55(10):1006-1012. doi:10.1093/chromsci/bmx066 J Chromatogr Sci | © Crown copyright 2017.This article contains public sector information licensed under the Open Government Licence v3.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).

Figure 3. Chromatograms of paeoniflorin and IS Figure 3. Chromatograms of paeoniflorin and IS. Top, a blank rat plasma sample; middle, a blank plasma spiked with paeoniflorin (1.6 μg/mL) and IS (1.98 μg/mL); bottom, a rat plasma sample after an oral administration of BC (0.675 g/kg) at intervals of 2 h. From: Determination of Paeoniflorin in Rat Plasma by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry and its Application to a Pharmacokinetic Study J Chromatogr Sci. 2017;55(10):1006-1012. doi:10.1093/chromsci/bmx066 J Chromatogr Sci | © Crown copyright 2017.This article contains public sector information licensed under the Open Government Licence v3.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).

Figure 4. Plasma concentration–time profile of paeoniflorin after an oral administration of 0.675 g/kg BC in rats (n = 8). From: Determination of Paeoniflorin in Rat Plasma by Ultra-high Performance Liquid Chromatography-Tandem Mass Spectrometry and its Application to a Pharmacokinetic Study J Chromatogr Sci. 2017;55(10):1006-1012. doi:10.1093/chromsci/bmx066 J Chromatogr Sci | © Crown copyright 2017.This article contains public sector information licensed under the Open Government Licence v3.0 (http://www.nationalarchives.gov.uk/doc/open-government-licence/version/3/).