Literature DB >> 7251755

Simultaneous determination of trimethoprim, sulphamethoxazole and N4-acetylsulphamethoxazole in serum and urine by high-performance liquid chromatography.

R Gochin, I Kanfer, J M Haigh.   

Abstract

The simultaneous determination of trimethoprim, sulphamethoxazole and N4-acetyl-sulphamethoxazole in serum and urine by high-performance liquid chromatography using sulphafurazole as internal standard is described. The separation was achieved on a reversed-phase column employing acetic acid-methanol as the mobile phase with spectrophotometric detection at 230 nm. Precise simultaneous quantitative analysis of the relative components has been achieved at levels of 0.1 microgram/ml for trimethoprim and 1.0 microgram/ml for both sulphamethoxazole and its N4-acetyl metabolite using 1 ml of serum of urine.

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Year:  1981        PMID: 7251755     DOI: 10.1016/s0378-4347(00)80076-6

Source DB:  PubMed          Journal:  J Chromatogr


  5 in total

1.  Penetration of brodimoprim into human neutrophils and intracellular activity.

Authors:  P C Braga; M Dal Sasso; S Maci; G Bondiolotti; E Fonti; S Reggio
Journal:  Antimicrob Agents Chemother       Date:  1996-10       Impact factor: 5.191

Review 2.  Clinical pharmacokinetics of enzyme inhibitors in antimicrobial chemotherapy.

Authors:  I D Watson; M J Stewart; D J Platt
Journal:  Clin Pharmacokinet       Date:  1988-09       Impact factor: 6.447

3.  N1-glucosides as urinary metabolites of sulphadimidine, sulphamerazine and sulphamethoxazole.

Authors:  B Ahmad; J W Powell
Journal:  Eur J Drug Metab Pharmacokinet       Date:  1988 Jul-Sep       Impact factor: 2.441

4.  Liquid chromatographic determination of efficacy of incorporation of trimethoprim and sulfamethoxazole in brine shrimp (Artemia spp.) used for prophylactic chemotherapy of fish.

Authors:  H J Nelis; F Léger; P Sorgeloos; A P De leenheer
Journal:  Antimicrob Agents Chemother       Date:  1991-12       Impact factor: 5.191

5.  A Physiologically-Based Pharmacokinetic Model of Trimethoprim for MATE1, OCT1, OCT2, and CYP2C8 Drug-Drug-Gene Interaction Predictions.

Authors:  Denise Türk; Nina Hanke; Thorsten Lehr
Journal:  Pharmaceutics       Date:  2020-11-10       Impact factor: 6.321

  5 in total

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