2017
DOI: 10.1002/rcm.7881
|View full text |Cite
|
Sign up to set email alerts
|

Determination of artemisitene in rat plasma by ultra‐performance liquid chromatography/tandem mass spectrometry and its application in pharmacokinetics

Abstract: The UPLC/MS/MS assay was validated for linearity, accuracy, stability, extraction recovery, matrix effects, and intra-day and inter-day precision. The method, for the first time, achieved some pharmacokinetic parameters and was successfully applied to a pharmacokinetic study Copyright © 2017 John Wiley & Sons, Ltd.

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

0
7
0

Year Published

2018
2018
2023
2023

Publication Types

Select...
6

Relationship

0
6

Authors

Journals

citations
Cited by 6 publications
(7 citation statements)
references
References 15 publications
0
7
0
Order By: Relevance
“…e same pattern was with peak 60 weighed 723.2134 (C 33 H 40 O 18 ) and therefore it was suspected to be Jasmigeniposide A [22]. Peaks us, artemisitene was detected at peak of 51, and peak 48 was identified as artemisitene [38].…”
Section: Identification Of 67 Components In Rdn Injection Using Uhplcmentioning
confidence: 60%
“…e same pattern was with peak 60 weighed 723.2134 (C 33 H 40 O 18 ) and therefore it was suspected to be Jasmigeniposide A [22]. Peaks us, artemisitene was detected at peak of 51, and peak 48 was identified as artemisitene [38].…”
Section: Identification Of 67 Components In Rdn Injection Using Uhplcmentioning
confidence: 60%
“…The established methods were validated according to standard guidelines used for method validation in many published studies for confirming the specificity, linearity, accuracy and precision, recovery, and matrix effect in bioanalytical methods 18–22 …”
Section: Methodsmentioning
confidence: 99%
“…The established methods were validated according to standard guidelines used for method validation in many published studies for confirming the specificity, linearity, accuracy and precision, recovery, and matrix effect in bioanalytical methods. [18][19][20][21][22] The intra-day precision (n = 5 for each QC sample, each individually prepared and analyzed) was evaluated for rat plasma on the same day, and the inter-day precision was evaluated on three consecutive days.…”
Section: Methods Validationmentioning
confidence: 99%
“…Establishing a high‐throughout, high‐specificity and high‐sensitivity analytical method is necessary . Among the available analytical techniques, ultrahigh‐performance liquid chromatography coupled to Fourier transform ion cyclotron resonance mass spectrometry (UHPLC/FT‐ICR‐MS) is a powerful and reliable analytical approach for detecting and identifying drug metabolites in vivo .…”
Section: Introductionmentioning
confidence: 99%
“…[13][14][15] Establishing a high-throughout, high-specificity and high-sensitivity analytical method is necessary. 16,17 Among the available analytical techniques, ultrahigh-performance liquid chromatography coupled to Fourier transform ion cyclotron resonance mass spectrometry (UHPLC/FT-ICR-MS) is a powerful and reliable analytical approach for detecting and identifying drug metabolites in vivo. [18][19][20] It can provide not only high mass accuracy/resolution and elemental composition, but also fragmentation information, which can facilitate the structural elucidation of metabolites.…”
Section: Introductionmentioning
confidence: 99%