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PHARMACEUTICAL ANALYSIS

Validation of a Quantitative Method Determination of Estradiol in Pharmaceutical Products using UV-Vis Molecular Absorption Spectrometry

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Pages 3272-3296 | Received 27 Aug 2008, Accepted 10 Sep 2008, Published online: 04 Dec 2008
 

Abstract

This article describes the development and validation of a quantitative analytical method for determination of estradiol in several pharmaceutical products (powder, tablets, cream, solutions for injection) using UV-vis molecular absorption spectrometry. The proposed method is accurate, precise, sensitive, and selective and can be used in quality control laboratories.

Notes

Notes. Sample 1: 0.5 mL estradiol stock solution + 5 ml EtOH + NaOH 0.1 N to 50 mL volumetric flask. Sample 2: 3.0 mL estradiol stock solution + 5 ml EtOH + NaOH 0.1 N to 50 mL volumetric flask. Sample 3: 7.0 mL estradiol stock solution + 5 ml EtOH + NaOH 0.1 N to 50 mL volumetric flask.

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