Utility of oxidation–reduction reaction for the determination of ranitidine hydrochloride in pure form, in dosage forms and in the presence of its oxidative degradates-Reference-Cited by-同舟云学术

Utility of oxidation–reduction reaction for the determination of ranitidine hydrochloride in pure form, in dosage forms and in the presence of its oxidative degradates

Published:2003-03 Issue:4 Volume:59 Page:695-703
ISSN:1386-1425
Container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy
language:en
Short-container-title:Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy

Author:

Amin A.S,Ahmed I.S,Dessouki H.A,Gouda E.A

Publisher

Elsevier BV

Subject

Spectroscopy,Instrumentation,Atomic and Molecular Physics, and Optics,Analytical Chemistry

Reference33 articles.

1. American Hospital Formulary Service (AHFS), Drug Information, G.K. Mc Evoy (Ed.) Authority of the Broad of Directors of the American Society of Hospital Pharmacists, Bethesda, MD, USA, 1990, pp. 1190–1694.

2. Use of post-column fluorescence derivatization to develop a liquid chromatographic assay for ranitidine and its metabolites in biological fluids

3. Stability indicating spectrodensitometric determination of ranitidine hydrochloride using linear and non-linear regression

4. High-performance thin-layer chromatography for the determination of ranitidine hydrochloride and famotidine in pharmaceuticals

5. Solid-phase extraction and determination of ranitidine in human plasma by a high-performance liquid chromatographic method utilizing midbore chromatography

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