PHARMACEUTICAL EQUIVALENCE OF METRONIDAZOLE TABLETS USING THE FLOW-THROUGH CELL (USP APPARATUS 4) AND MEDIA OF PHYSIOLOGICAL pH RANGE

YADIRA JIMENEZ-FLORES; MARCELA HURTADO; JOSE RAUL MEDINA-LOPEZ

doi:10.22159/ijap.2022v14i4.44759

Authors

YADIRA JIMENEZ-FLORES Departamento Sistemas Biológicos, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico https://orcid.org/0000-0002-4159-8403
MARCELA HURTADO Departamento Sistemas Biológicos, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico https://orcid.org/0000-0003-3546-5986
JOSE RAUL MEDINA-LOPEZ Departamento Sistemas Biológicos, Universidad Autónoma Metropolitana-Xochimilco, Mexico City, Mexico https://orcid.org/0000-0002-4159-8403

DOI:

https://doi.org/10.22159/ijap.2022v14i4.44759

Keywords:

Flow-through cell, Generic drug products, Metronidazole tablets, USP Apparatus 4

Abstract

Objective: The aim of this work was to evaluate the pharmaceutical equivalence of metronidazole tablets through the study of hydrodynamics of the flow-through cell (USP Apparatus 4) on the dissolution performance of four commercial formulations (500 mg). The results were compared with those found using the USP basket apparatus.

Methods: Experiments were performed with 0.1 N hydrochloric acid (pH 1.2), acetate buffer pH 4.5 and phosphate buffer pH 6.8. A USP Apparatus 4 was used with laminar flow at 16 ml/min and 22.6-mm cells. USP basket apparatus was used with 900 ml of each dissolution medium. The dissolution profiles were compared in terms of the mean dissolution time and dissolution efficiency.

Results: Significant differences in MDT and DE values of generic formulations vs. reference with both USP apparatuses were found (*P<0.05) hence, dissolution profiles of metronidazole generic formulations cannot be considered similar to the dissolution profile of the reference. After using some equations to explain the release performance of metronidazole, dissolution data were well adjusted to Peppas-Sahlin and logistic models when the flow-through cell was used.

Conclusion: The main problem found with the studied formulations was that generic drug products showed different dissolution performances than the reference, and they did not meet the biowaiver criteria for either class I or class III drugs; therefore, they cannot be considered therapeutic equivalents.

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