scholarly journals A Novel QbD Based SPE-HPLC Bio-analytical Method for Edaravone in Rat Plasma, A Pharmacokinetic Study

2016 ◽  
Vol 50 (4) ◽  
pp. 563-573
Author(s):  
Suraj Fanse ◽  
Madhuri Baghel ◽  
Prachi Bhamre ◽  
Sadhana Rajput
Keyword(s):  
Pharmacokinetic Study ◽  
Analytical Method ◽  
Rat Plasma

Determination and pharmacokinetic study of kaempferide in rat plasma by UPLC

2015 ◽  
Vol 7 (24) ◽  
pp. 10238-10242
Author(s):  
Song-Feng Lv ◽  
Xiang-Hong Wang ◽  
Bo Wang ◽  
Hong-Wei Li ◽  
Xiao-Lei Zhang ◽  
...  
Keyword(s):  
Liquid Chromatography ◽  
Pharmacokinetic Study ◽  
Analytical Method ◽  
Internal Standard ◽  
Ultra Performance Liquid Chromatography ◽  
Rat Plasma

In this study, a simple, sensitive, and robust analytical method based on ultra-performance liquid chromatography (UPLC) has been developed for the determination of kaempferide in rat plasma using diazepam as the internal standard (IS).

Quantification of annonacin in Rat plasma: Application to pharmacokinetic study

Planta Medica ◽  
2014 ◽  
Vol 80 (16) ◽  
Author(s):  
N Bonneau ◽  
I Schmitz Afonso ◽  
D Touboul ◽  
A Brunelle ◽  
P Champy
Keyword(s):  
Pharmacokinetic Study ◽  
Rat Plasma

LC–MS/MS Determination of Apigenin in Rat Plasma and Application to Pharmacokinetic Study

2020 ◽  
Vol 21 ◽  
Author(s):  
Shixing Zhu ◽  
Jiayuan Zhang ◽  
Zhihua Lv ◽  
Mingming Yu
Keyword(s):  
Formic Acid ◽  
Pharmacokinetic Study ◽  
Ammonium Acetate ◽  
Rat Plasma ◽  
Biological Properties ◽  
Plasma Samples ◽  
Supply Rate ◽  
Natural Plant ◽  
Ammonium Acetate Buffer

Background: Apigenin, a natural plant flavone, has been shown to possess a variety of biological properties. Objective: In this report, a highly selective and sensitive LC-MS/MS method was developed and validated for the determination of apigenin in rat plasma. Methods: Analysts were separated on the HSS T3 column (1.8 μm 2.1×100 mm) using acetonitrile and 0.1% formic acid in 2 mM ammonium acetate buffer at a supply rate of 0.200 mL/min as eluent in gradient model. Results: Plasma samples were treated by protein precipitation using acetonitrile for the recovery ranging from 86.5% to 90.1% for apigenin. The calibration curves followed linearity in the concentration range of 0.50-500 ng/mL. The inter-day and intra-day precisions at different QC levels within 13.1% and the accuracies ranged from -10.6% to 8.6%. Conclusion: The assay has been successfully applied to the pharmacokinetic study of apigenin in rats.

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