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dc.contributor.authorChalermporn Thongpoonen_US
dc.contributor.authorBoonsom Liawruangrathen_US
dc.contributor.authorSaisunee Liawruangrathen_US
dc.contributor.authorR. Alan Wheatleyen_US
dc.contributor.authorAlan Townshenden_US
dc.date.accessioned2018-09-11T08:55:21Z-
dc.date.available2018-09-11T08:55:21Z-
dc.date.issued2006-09-18en_US
dc.identifier.issn07317085en_US
dc.identifier.other2-s2.0-33747773384en_US
dc.identifier.other10.1016/j.jpba.2006.03.001en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=33747773384&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/61573-
dc.description.abstractA simple, rapid and precise flow injection chemiluminescence (FI-CL) method is proposed for the determination of cefadroxil and is suitable for application to other antibiotics containing phenolic hydroxyl groups. A possible mechanism for this selectivity is suggested. The method is based on the CL-emitting reaction between cefadroxil and potassium permanganate in sulfuric acid medium, enhanced by formaldehyde (HCHO). Under the optimum conditions, calibration graphs over the ranges of 0.05-0.8 and 1.0-10.0 μg ml-1were obtained. The proposed method was successfully applied to the determination of cefadroxil in pharmaceutical formulations with no evidence of interference from common excipients. The detection limit (3σ) of this method is 25 ng ml-1(6.9 × 10-8mol l-1). The relative standard deviation was less than 2% for 0.4 and 4.0 μg ml-1cefadroxil (n = 20). The sample throughput was found to be 120 h-1. © 2006.en_US
dc.subjectChemistryen_US
dc.subjectPharmacology, Toxicology and Pharmaceuticsen_US
dc.titleFlow injection chemiluminescence determination of cefadroxil using potassium permanganate and formaldehyde systemen_US
dc.typeJournalen_US
article.title.sourcetitleJournal of Pharmaceutical and Biomedical Analysisen_US
article.volume42en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsUniversity of Hullen_US
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