Quality of Vancomycin for Injection Formulations in Brazil

Author:

Secco Gabriela1,Sachetti Cristiane1,Rossato-Grando Luciana Grazziotin1,Regina Hahn Siomara1,Pagnussat Lidiane Riva2,da Cruz Fresco Paula Maria Façanha3,Dallazem Bertol Charise1

Affiliation:

1. Curso de Farmacia, Instituto de Ciencias Biologicas, Universidade de Passo Fundo, Passo Fundo, RS, Brazil

2. Servico de Controle de Infeccao Hospitalar, Hospital Sao Vicente de Paulo, Passo Fundo, RS, Brazil

3. Departamento de Ciencias do Medicamento, Laboratorio de Farmacologia, Faculdade de Farmacia, Universidade do Porto, Porto, Portugal

Abstract

Background: The presence of impurities in vancomycin compromised the safety and contributed to decrease of its use for years. In Brazil, vancomycin generic drug represents an option to reduce hospital costs. However, the controversy over the quality of these formulations and their relationship to effectiveness and safety raised concerns. Objective and Methods: To assess in vitro quality of vancomycin injections through uniformity of weight, pH, clarity of solution, microbiological assay and impurities determination by High Performance Liquid Chromatography (HPLC). Results: The samples were approved in the tests. Conclusion: The injectable formulations of vancomycin proved to be safe for use in hospital environment. This work contributes to increase health professionals’ confidence on generic vancomycin.

Publisher

Bentham Science Publishers Ltd.

Subject

Pharmaceutical Science,Molecular Medicine,Biochemistry,Biophysics

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