Development and validation of a stability-indicating analytical method for the quantitation of oxytocin in pharmaceutical dosage forms
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference18 articles.
1. Oxytocin
2. The Complete Drug Reference;Martindale,2002
3. The separation of nonapeptides by reversed-phase high-performance liquid chromatography
4. Quantitative analysis of nonapeptides in pharmaceutical dosage forms by high-performance liquid chromatography
5. Introduction to Modern Liquid Chromatography;Snyder,1979
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2. Factors to consider in developing individual pharmaceutical product quality risk profiles useful to government procurement agencies;Acta Pharmaceutica Sinica B;2016-01
3. Capillary electrophoresis separation of the desamino degradation products of oxytocin;ELECTROPHORESIS;2013-12-02
4. A New Extraction Method for the Determination of Oxytocin in Milk by Enzyme Immune Assay or High-Performance Liquid Chromatography: Validation by Liquid Chromatography–Mass Spectrometry;Food Analytical Methods;2012-12-06
5. Photodegradation of Oxytocin and Thermal Stability of Photoproducts;Journal of Pharmaceutical Sciences;2012-09
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