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(Reference retrieved automatically from Web of Science through information on FAPESP grant and its corresponding number as mentioned in the publication by the authors.)

Development of analytical method by free solution capillary electrophoresis for furosemide under stress degradation

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Author(s):
de Souza, Aline [1] ; Maria Kedor-Hackmann, Erika Rosa [1] ; Rocha Miritello Santoro, Maria Ines [1] ; Aurora-Prado, Maria Segunda [1]
Total Authors: 4
Affiliation:
[1] Univ Sao Paulo, Fac Pharmaceut Sci, Dept Pharm, Ave Prof Lineu Prestes 580 B-13, BR-05508000 Sao Paulo, SP - Brazil
Total Affiliations: 1
Document type: Journal article
Source: SEPARATION SCIENCE PLUS; v. 2, n. 7, p. 253-261, JUL 2019.
Web of Science Citations: 0
Abstract

A fast, economical, precise and accurate free solution capillary electrophoresis method with photodiode array detector was developed and validated for the determination of furosemide in tablets. The separation was achieved by using a fused silica capillary column with (total length of 30.2 cm x 50.0 mu m id). The optimum separations conditions were: 2.0 mmol L-1 sodium tetraborate buffer solution, pH 9.3 and 10% methanol; hydrodynamic injection 3.45 kPa/5 s; voltage and temperature set at +25 kV and 25 degrees C, respectively, and UV detection at 273 nm. The method allowed the quantitative determination of furosemide and showed good linearity (70.0 to 130.0 mu g mL(-1)) with a correlation coefficient (>0.99). The migration time was 1.8 min. Accuracy repeatability and intermediate precisions were less than 5.0% and the average recovery, 102.1%. Degradation was tested under neutral, acidic and alkaline hydrolysis, as well as under chemical oxidation, thermal and photodegradation. The method was specific and allowed the detection of three potential degradation products with migration times of 1.3, 2.0, and 2.2 min, respectively under oxidation test. Also, one potential degradation product under acidic hydrolysis (2.0 min). The method can be used in quality control laboratories and also as a stability-indicating method for furosemide in tablets. (AU)

FAPESP's process: 12/50595-8 - Application of electrophoretic and cromatographic methods for simultaneous determination of drugs used in the treatment of hypercholesterolemia
Grantee:María Segunda Aurora Prado
Support Opportunities: Regular Research Grants