[article]
Titre : |
Alternative method with amperometric detection for ranitidine determination |
Type de document : |
texte imprimé |
Auteurs : |
Valeria Pfaffen, Auteur ; Patricia Inés Ortiz, Auteur |
Année de publication : |
2010 |
Article en page(s) : |
pp. 4026-4030 |
Note générale : |
Industrial chemistry |
Langues : |
Anglais (eng) |
Mots-clés : |
Amperometric Detection Ranitidine |
Résumé : |
An alternative, simple, and reliable FIA amperometric method for ranitidine quantification was developed. A working glassy carbon electrode and a Ag|AgCl|NaCl (3 M) reference electrode were used. The determination is based on the electrochemical oxidation of ranitidine at 1.2 V in phosphate buffer solution (pH 7.2). The determination of ranitidine in the range of 1 × 10−6 to 2 × 10−5 M was possible with a sampling frequency of 120 h−1. The method was validated and satisfactorily applied to the determination of ranitidine in pharmaceutical formulations with a low limit of detection (6 × 10−7 M) and a quantitative recovery with no interferences from excipients. The results compare favorably with those obtained by the liquid chromatographic method of the U.S. Pharmacopoeia. |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie901895a |
in Industrial & engineering chemistry research > Vol. 49 N° 9 (Mai 2010) . - pp. 4026-4030
[article] Alternative method with amperometric detection for ranitidine determination [texte imprimé] / Valeria Pfaffen, Auteur ; Patricia Inés Ortiz, Auteur . - 2010 . - pp. 4026-4030. Industrial chemistry Langues : Anglais ( eng) in Industrial & engineering chemistry research > Vol. 49 N° 9 (Mai 2010) . - pp. 4026-4030
Mots-clés : |
Amperometric Detection Ranitidine |
Résumé : |
An alternative, simple, and reliable FIA amperometric method for ranitidine quantification was developed. A working glassy carbon electrode and a Ag|AgCl|NaCl (3 M) reference electrode were used. The determination is based on the electrochemical oxidation of ranitidine at 1.2 V in phosphate buffer solution (pH 7.2). The determination of ranitidine in the range of 1 × 10−6 to 2 × 10−5 M was possible with a sampling frequency of 120 h−1. The method was validated and satisfactorily applied to the determination of ranitidine in pharmaceutical formulations with a low limit of detection (6 × 10−7 M) and a quantitative recovery with no interferences from excipients. The results compare favorably with those obtained by the liquid chromatographic method of the U.S. Pharmacopoeia. |
ISSN : |
0888-5885 |
En ligne : |
http://pubs.acs.org/doi/abs/10.1021/ie901895a |
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