Optimization of a liquid–liquid extraction method for HPLC–DAD determination of penicillin-V in human plasma

2002 ◽  
Vol 72 (1) ◽  
pp. 85-92 ◽  
Author(s):  
Andrei Medvedovici ◽  
Mihaela Ionescu ◽  
Constantin Mircioiu ◽  
Victor David
2014 ◽  
Vol 97 (4) ◽  
pp. 1061-1066 ◽  
Author(s):  
Bilal Yilmaz ◽  
Huseyin Sahin ◽  
Vedat Akba ◽  
Ali Fuat Erdem

Abstract This paper describes a GC/MS method for the determination of flurbiprofen in human plasma. Flurbiprofen and internal standard ibuprofen were extracted from plasma by using a liquid–liquid extraction method. Derivatization was carried out using N-Methyl-N-(trimethylsilyl)trifluoroacetamide. The calibration curve was linear between the concentration range of 0.10 and 5.0 μg/mL. Intraday and interday precision values for flurbiprofen in plasma were less than 5.49%, and accuracy (relative error) was better than 5.33%. The extraction recoveries of flurbiprofen from human plasma were between 93.6 and 98.6%. The LOD and LOQ of flurbiprofen were 0.03 and 0.10 μg/mL, respectively. This assay was applied to determine the pharmacokinetic parameters of flurbiprofen in healthy Turkish volunteers who had been given 100 mg of flurbiprofen.


2005 ◽  
Vol 28 (9) ◽  
pp. 1299-1309 ◽  
Author(s):  
Min Kyo Jeoung ◽  
Kyoung Soon Kim ◽  
Chang Soo Kim ◽  
Nam Hee Kim ◽  
Youn‐Bok Chung ◽  
...  

2019 ◽  
Vol 55 (13) ◽  
pp. 2303-2312 ◽  
Author(s):  
Janiele Mayara Ferreira De Almeida ◽  
Elania Maria Fernandes Silva ◽  
Lourena Mafra Veríssimo ◽  
Nedja Suely Fernandes

2012 ◽  
Vol 2012 ◽  
pp. 1-4 ◽  
Author(s):  
Shravan Bankey ◽  
Ganesh Tapadiya ◽  
Jasvant Lamale ◽  
Deepti Jain ◽  
Shweta Saboo ◽  
...  

A simple, accurate, and precise HPLC method was developed and validated for determination of rimonabant in human plasma. Following liquid-liquid extraction, chromatographic separation was accomplished using C18 column with mobile phase consisting of acetonitrile : water (90 : 10, v/v), drug was detected at 260 nm using UVdetector. The LOD and LOQ were 3.0 and 10.0 μg/L, respectively. The method is linear in the interval 50.0–1000.0 μg/L. The average extraction recovery of drug from plasma was found to be 92.2%. The percent CV of the method was found to be less than 10.8%, and accuracy was found between 94.5 and 106.7%. The assay may be applied to a pharmacokinetic and bioequivalence study of rimonabant.


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