Simultaneous determination of moxifloxacin and H2 receptor antagonist in pharmaceutical dosage formulations by RP-HPLC: Application to in vitro drug interactions

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Abstract

Simultaneous determination of moxifloxacin (MOX) and H2- antagonists was first time developed in bulk and formulations. Purospher STAR C18 (250 × 4.6 mm, 5 μm) column was used. The mobile phase (methanol: Water: ACN, 60:45:5 v/v/v, pH 2.7) was delivered at a flow rate of 1.0 mL min-1, eluent was monitored at 236, 270 and 310 nm for cimetidine, famotidine and ranitidine, respectively. The proposed method is specific, accurate (98-103%), precise (intra-day and inter-day variation 0.098-1.970%) and linear (r>0.998). The LOD and LOQ were 0.006-0.018 and 0.019-0.005 μg mL-1, respectively. The statistical parameters were applied to verify the results. The method is applicable to routine analysis of formulations and interaction of MOX with H2-antagonist.

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Sultana, N., Akhtar, M., Shamim, S., Gul, S., & Arayne, M. S. (2011). Simultaneous determination of moxifloxacin and H2 receptor antagonist in pharmaceutical dosage formulations by RP-HPLC: Application to in vitro drug interactions. Quimica Nova, 34(4), 683–688. https://doi.org/10.1590/S0100-40422011000400022

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