Rapid separation of desloratadine and related compounds in solid pharmaceutical formulation using gradient ion-pair chromatography
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference24 articles.
1. Determination of desloratadine in drug substance and pharmaceutical preparations by liquid chromatography
2. LC determination of loratadine and related impurities
3. Impurity profile study of loratadine
4. Study of overload for basic compounds in reversed-phase high performance liquid chromatography as a function of mobile phase pH
5. Simultaneous determination of vinclozolin and detection of its degradation products in mouse plasma, serum and urine, and from rabbit bile, by high-performance liquid chromatography
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1. A methodology employing retention modeling for achieving control space in liquid chromatography method development using quality by design approach;Journal of Chromatography A;2021-01
2. Ionisable substances chromatography: A new approach for the determination of Ketoprofen, Etoricoxib, and Diclofenac sodium in pharmaceuticals using ion – pair HPLC;Heliyon;2020-08
3. Development and Validation of a Stability-Indicating Ion-Pair RP-HPLC Method for Determination of Bethanechol with UV Detection: Application to Pharmaceutical Analysis;Pharmaceutical Chemistry Journal;2019-07-15
4. “Inverse” cloud point extraction coupled with large volume injection ion-pair chromatography: A green route integrating extraction, challenging sample cleanup and on-column concentration into fast simple operation;Talanta;2018-12
5. Desloratadine-Eudragit® RS100 Nanoparticles: Formulation and Characterization;Turkish Journal of Pharmaceutical Sciences;2017-08-01
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