Literature DB >> 1286291

Robotic solid phase extraction and high performance liquid chromatographic analysis of ranitidine in serum or plasma.

T L Lloyd1, T B Perschy, A E Gooding, J J Tomlinson.   

Abstract

A fully automated assay for the analysis of ranitidine in serum and plasma, with and without an internal standard, was validated. It utilizes robotic solid phase extraction with on-line high performance liquid chromatographic (HPLC) analysis. The ruggedness of the assay was demonstrated over a three-year period. A Zymark Py Technology II robotic system was used for serial processing from initial aspiration of samples from original collection containers, to final direct injection onto the on-line HPLC system. Automated serial processing with on-line analysis provided uniform sample history and increased productivity by freeing the chemist to analyse data and perform other tasks. The solid phase extraction efficiency was 94% throughout the assay range of 10-250 ng/mL. The coefficients of variation for within- and between-day quality control samples ranged from 1 to 6% and 1 to 5%, respectively. Mean accuracy for between-day standards and quality control results ranged from 97 to 102% of the respective theoretical concentrations.

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Year:  1992        PMID: 1286291     DOI: 10.1002/bmc.1130060613

Source DB:  PubMed          Journal:  Biomed Chromatogr        ISSN: 0269-3879            Impact factor:   1.902


  1 in total

1.  Effect of sodium acid pyrophosphate on ranitidine bioavailability and gastrointestinal transit time.

Authors:  K M Koch; A F Parr; J J Tomlinson; E P Sandefer; G A Digenis; K H Donn; J R Powell
Journal:  Pharm Res       Date:  1993-07       Impact factor: 4.200

  1 in total

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