Literature DB >> 1478991

Improved high-performance liquid chromatographic assay method for the enantiomers of ibuprofen.

M R Wright1, S Sattari, D R Brocks, F Jamali.   

Abstract

A rapid, inexpensive and sensitive high-performance liquid chromatographic method for the quantitation of ibuprofen enantiomers from a variety of biological fluids is reported. This method uses a commercially available internal standard and has significantly less interference from endogenous co-extracted solutes than do previously reported methods. The method involves the acid extraction of drug and internal standard [(+/-)-fenoprofen] from the biological fluid with isooctane-isopropanol (95:5) followed by evaporation and derivatization with ethylchloroformate and R-(+)-alpha-phenylethylamine. Excellent linearity was observed between the peak-area ratio and enantiomer concentration (r > 0.99) over a concentration range of 0.25-50 micrograms/ml. This method is suitable for the quantitation of ibuprofen from single-dose pharmacokinetic studies involving either rats or humans.

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Year:  1992        PMID: 1478991     DOI: 10.1016/0378-4347(92)80562-5

Source DB:  PubMed          Journal:  J Chromatogr


  3 in total

1.  Pain-mediated altered absorption and metabolism of ibuprofen: an explanation for decreased serum enantiomer concentration after dental surgery.

Authors:  F Jamali; C M Kunz-Dober
Journal:  Br J Clin Pharmacol       Date:  1999-04       Impact factor: 4.335

2.  Stereoselective disposition of suspensions of conventional and wax-matrix sustained release ibuprofen microspheres in rats.

Authors:  C M Adeyeye; F F Chen
Journal:  Pharm Res       Date:  1997-12       Impact factor: 4.200

Review 3.  Clinical pharmacokinetics of ibuprofen. The first 30 years.

Authors:  N M Davies
Journal:  Clin Pharmacokinet       Date:  1998-02       Impact factor: 6.447

  3 in total

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