Literature DB >> 660463

Stability of furosemide in aqueous systems.

A G Ghanekar, V Das Gupta, C W Gibbs.   

Abstract

A stability-indicating assay for furosemide based on high-pressure liquid chromatography was developed. The method is sensitive, accurate, and precise. The standard deviation based on six injections of the standard solution was +/- 1.37%. This method was used to study furosemide stability in various aqueous solutions and dosage forms. Stability tests were conducted at room temperature as well as at higher temperatures (45, 65, and 85 degrees) at various pH values and with different vehicles. Some decomposition products were identified.

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Year:  1978        PMID: 660463     DOI: 10.1002/jps.2600670621

Source DB:  PubMed          Journal:  J Pharm Sci        ISSN: 0022-3549            Impact factor:   3.534


  4 in total

1.  Effect of cryogrinding on chemical stability of the sparingly water-soluble drug furosemide.

Authors:  Karolina Adrjanowicz; Kamil Kaminski; Katarzyna Grzybowska; Lukasz Hawelek; Marian Paluch; Irena Gruszka; Daniel Zakowiecki; Wieslaw Sawicki; Przemyslaw Lepek; Wojciech Kamysz; Lukasz Guzik
Journal:  Pharm Res       Date:  2011-06-25       Impact factor: 4.200

2.  Furosemide ethanol-free oral solutions for paediatric use: formulation, HPLC method and stability study.

Authors:  Lukáš Zahálka; Sylva Klovrzová; Ludmila Matysová; Zdenka Šklubalová; Petr Solich
Journal:  Eur J Hosp Pharm       Date:  2017-08-02

3.  RP-HPLC Method for Simultaneous Estimation of Frusemide and Amiloride Hydrochloride in Tablet Formulation.

Authors:  B P Nagori; Renu Solanki
Journal:  Indian J Pharm Sci       Date:  2010-05       Impact factor: 0.975

4.  Hospital preparations of ethanol-free furosemide oral solutions: Formulation and stability study.

Authors:  Charles Bavouma Sombié; J E Kéré Guetambaba; Hermine Zimé Diawara; Josias Yaméogo; Salfo Ouédraogo; Jonathan Goole; Rasmané Semdé
Journal:  J Adv Pharm Technol Res       Date:  2022-04-07
  4 in total

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