Quantitative determination of acrivastine and pseudoephedrine hydrochloride in pharmaceutical formulation by high performance liquid chromatography and derivative spectrophotometry
Author:
Publisher
Elsevier BV
Subject
Clinical Biochemistry,Spectroscopy,Drug Discovery,Pharmaceutical Science,Analytical Chemistry
Reference35 articles.
1. Numerical error analysis of derivative spectrometry for the quantitative analysis of mixtures
2. Recent developments in pharmaceutical and clinical analysis
3. Biomedical applications of derivative spectroscopy
4. Determination of chlorpromazine and its sulphoxide in pharmaceutical dosage forms by third-order derivative ultraviolet spectroscopy
Cited by 24 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. Isolation, structure elucidation, and high‐performance liquid chromatography quantification of photolytic degradation impurities in acrivastine;Journal of Separation Science;2022-07-28
2. A Novel Fluorimetric Method for Determination of Pseudoephedrine Hydrochloride in Pharmaceutical Formulations and Blood Serum;TURKISH JOURNAL OF CHEMISTRY;2020-06-01
3. Multicomponent spectrometric analysis of drugs and their preparations;Profiles of Drug Substances, Excipients and Related Methodology;2019
4. Identification, synthesis and structural characterization of process related and degradation impurities of acrivastine and validation of HPLC method;Journal of Pharmaceutical and Biomedical Analysis;2017-01
5. Simultaneous determination of carbinoxamine maleate and pseudoephedrine HCl in their pure form and in their pharmaceutical formulation by HPTLC-densitometric method;European Journal of Chemistry;2016-03-31
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