Citas bibligráficas
Berrocal, J., Medina, J. (2008). Validación de método analítico de valoración de naproxeno sódico 550 mg. tableta por cromatografía líquida de alta performance [Tesis, Universidad Nacional Mayor de San Marcos]. https://hdl.handle.net/20.500.12672/865
Berrocal, J., Medina, J. Validación de método analítico de valoración de naproxeno sódico 550 mg. tableta por cromatografía líquida de alta performance [Tesis]. PE: Universidad Nacional Mayor de San Marcos; 2008. https://hdl.handle.net/20.500.12672/865
@misc{renati/476584,
title = "Validación de método analítico de valoración de naproxeno sódico 550 mg. tableta por cromatografía líquida de alta performance",
author = "Medina Julca, Jessica",
publisher = "Universidad Nacional Mayor de San Marcos",
year = "2008"
}
-- The Validation of analytic methods is an all-round part of the Quality Control System, because it confers reliability to analytical results obtained in the laboratory to ensure that a specific medicine meets stablished quality requirements. This work presents the Validation of an Analytical Method to perform a quantitative analysis to the active component from 550 mg Sodium Naproxeno tablets using High Performance Liquid Chromatography (HPLC) according to the USP 26.The validation is based on enough dates from laboratory which supports validity of analytical methods. Some important statistical parameters are: Linearity, exactitude, precision, selectivity and specificity. Linearity measures the capacity of the analytic method for producing results which are directly proportional to concentration of an active substance within a specific range, called the work range. The exactitude measures how near the results obtained by the chosen method and the real value are. This is often expressed as recovery percentage.
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