Optimization of Forced Degradation Using Experimental Design and Development of a Stability-Indicating Liquid Chromatographic Assay Method for Rebamipide in Bulk and Tablet Dosage Form-Reference-Cited by-同舟云学术

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Optimization of Forced Degradation Using Experimental Design and Development of a Stability-Indicating Liquid Chromatographic Assay Method for Rebamipide in Bulk and Tablet Dosage Form

Published:2011 Issue:1 Volume:79 Page:85-96
ISSN:0036-8709
Container-title:Scientia Pharmaceutica
language:
Short-container-title:Sci. Pharm.

Author:

SONAWANE Sandeep

Publisher

MDPI AG

Subject

Pharmaceutical Science

Cited by 12 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Quantitative Detection of Rebamipide by Zero order UV-Spectrophotometry using Dimethyl Formamide Solvent System;Research Journal of Pharmacy and Technology;2024-07-24

2. Determination of rebamipide in human plasma by a validated liquid chromatography-tandem mass spectrometry: Application in pharmacokinetics research;PAK J PHARM SCI;2023

3. HPLC–PDA identification and resolution of rufinamide forced degradation impurities: A congregated chemometric expedite optimization coupled with factorials and desirability;Biomedical Chromatography;2022-02-06

4. Optimization of a forced degradation study of atorvastatin employing an experimental design approach;Macedonian Journal of Chemistry and Chemical Engineering;2018-11-15

5. Review on Implementation of Multivariate Approach for Forced Degradation Study and Impurity Profiling with Regulatory Considerations;Chromatographia;2017-09-07

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