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J AOAC Int ; 93(4): 1113-20, 2010.
Article in English | MEDLINE | ID: mdl-20922941

ABSTRACT

A method based on RP-HPLC with indirect UV detection was developed for the determination of phosphates and phosphites as impurities in sodium risedronate. RP separation of the phosphates and phosphites was achieved by adding tetrabutylammonium hydroxide as an ion-pairing agent in the mobile phase. Potassium hydrogen phthalate was added to the mobile phase as an ionic chromophore in order to obtain high background absorption of the mobile phase. Separation was performed on a C18 column using a mixture of pH 8.2 buffer (containing 0.5 mM tetrabutylammonium hydroxide and 1 mM phthalate) and acetonitrile (95 + 5, v/v) as the mobile phase, with indirect UV detection at 248 nm. The validation of the method included determination of specificity/selectivity, linearity, LOD, LOQ, accuracy, precision, and robustness. The LOD was 0.86 microg/mL for phosphates and 0.76 microg/mL for phosphites. The LOQ was 2.60 microg/mL for phosphates and 2.29 microg/mL for phosphites. The developed method is suitable for quantitative determination of phosphates and phosphites as impurities in QC of sodium risedronate.


Subject(s)
Bone Density Conservation Agents/analysis , Chromatography, High Pressure Liquid/methods , Drug Contamination , Etidronic Acid/analogs & derivatives , Phosphates/analysis , Phosphites/analysis , Etidronic Acid/analysis , Limit of Detection , Risedronic Acid , Spectrophotometry, Ultraviolet/methods
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