Assay and purity analysis of diatrizoate sodium in drug product by LC
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference8 articles.
1. The United States Pharmacopeial Convention;The United States Pharmacopeia,1995
2. Liquid Chromatographic Assay of Diatrizoic Acid and Its Diiodo Degradation Products in Radio-Opaque Solutions
3. Simple HNMR Spectroscopic Method for Assay of Salts of the Contrast Agent Diatrizoate in Commercial Solutions
4. Liquid chromatographic methods validation for pharmaceutical products
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1. Monitoring of the degradation kinetics of diatrizoate sodium to its cytotoxic degradant using a stability-indicating high-performance liquid chromatographic method;Biomedical Chromatography;2016-08-18
2. A comparative study between three stability indicating spectrophotometric methods for the determination of diatrizoate sodium in presence of its cytotoxic degradation product based on two-wavelength selection;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2015-06
3. Stability indicating spectrophotometric and spectrodensitometric methods for the determination of diatrizoate sodium in presence of its degradation product;Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy;2015-02
4. Diffusion of MRI and CT Contrast Agents in Articular Cartilage under Static Compression;Biophysical Journal;2014-07
5. Development, Validation and Results of Quantitative Stability Testing for Gastrografin®;Current Pharmaceutical Analysis;2014-04
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