Determination of the (+)- and (-)-enantiomers of Pirprofen in Human Plasma by High-performance Liquid Chromatography
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A high-performance liquid chromatographic (HPLC) method was developed to determine the (+)- and (-)-enantiomers of pirprofen, an anti-inflammatory drug. After addition of an internal standard, the plasma sample was brought onto a glass column pre-packed with silica and eluted with dichloromethane. The extracts were derivatized with 1,1'-carbonyldiimidazole and R (+)-1-methylbenzylamine to form the two diastereomeric amides. The diastereoisomers were separated on a chiral column by HPLC with ultraviolet detection at 272 nm using n-hexane-dichloromethane (64:36, v/v) as the mobile phase. The limit of quantitation was 0.992 mumol/l (0.25 microgram/ml) for each enantiomer.
Protein binding and stereoselectivity of nonsteroidal anti-inflammatory drugs.
Lapicque F, Muller N, Payan E, Dubois N, Netter P Clin Pharmacokinet. 1993; 25(2):115-23.
PMID: 8403735 DOI: 10.2165/00003088-199325020-00004.
Etodolac clinical pharmacokinetics.
Brocks D, Jamali F Clin Pharmacokinet. 1994; 26(4):259-74.
PMID: 8013160 DOI: 10.2165/00003088-199426040-00003.
Pharmacokinetics of enantiomers of chiral non-steroidal anti-inflammatory drugs.
Jamali F Eur J Drug Metab Pharmacokinet. 1988; 13(1):1-9.
PMID: 3294019 DOI: 10.1007/BF03189920.
Stereoselectivity in clinical pharmacokinetics and drug development.
Campbell D Eur J Drug Metab Pharmacokinet. 1990; 15(2):109-25.
PMID: 2200681 DOI: 10.1007/BF03190194.
Evans A Eur J Clin Pharmacol. 1992; 42(3):237-56.
PMID: 1577041 DOI: 10.1007/BF00266343.