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dc.contributor.authorThe Therapeutic Guidelines Group of the World Small Animal Veterinary Association
dc.contributor.authorPelligand, L.
dc.contributor.authorBaker, D.
dc.contributor.authorSivagurunathan, A.
dc.contributor.authorKovačević, Z.
dc.contributor.authorSuemanotham, N.
dc.contributor.authorStair, J. L.
dc.contributor.authorScott, M.
dc.contributor.authorLiu, F.
dc.contributor.authorPage, S. W.
dc.contributor.authorGuardabassi, L.
dc.contributor.authorSteagall, P. V.
dc.date.accessioned2023-07-04T15:15:01Z
dc.date.available2023-07-04T15:15:01Z
dc.date.issued2023-06-21
dc.identifier.citationThe Therapeutic Guidelines Group of the World Small Animal Veterinary Association , Pelligand , L , Baker , D , Sivagurunathan , A , Kovačević , Z , Suemanotham , N , Stair , J L , Scott , M , Liu , F , Page , S W , Guardabassi , L & Steagall , P V 2023 , ' Quality of amoxicillin/clavulanic acid oral formulations for intended veterinary use in the UK, Malaysia, Serbia and Thailand ' , Journal of Small Animal Practice (JSAP) , pp. 1-9 . https://doi.org/10.1111/jsap.13648
dc.identifier.issn0022-4510
dc.identifier.otherJisc: 1158514
dc.identifier.otherpublisher-id: jsap13648
dc.identifier.othersociety-id: jsap-2022-0309.r1
dc.identifier.otherORCID: /0000-0002-1756-4561/work/138281085
dc.identifier.otherORCID: /0000-0003-0650-6590/work/138281119
dc.identifier.urihttp://hdl.handle.net/2299/26474
dc.descriptionPublisher Copyright: © 2023 The Authors. Journal of Small Animal Practice published by John Wiley & Sons Ltd on behalf of British Small Animal Veterinary Association.
dc.description.abstractObjectives: Amoxicillin/clavulanate is the most commonly used oral antimicrobial drug in companion animals. The objective of the study was to detect types and frequency of deficits in the quality of veterinary oral formulations of amoxicillin/clavulanate in various countries. Materials and Methods: In a prospective study with purposive sampling, amoxicillin/clavulanate tablet formulations for canine use were collected in four countries (wholesalers or veterinary practice) and shipped to a central bioanalytical laboratory. Twenty‐four samples were collected from the UK (nine), Malaysia (nine), Serbia (four) and Thailand (two), yielding 18 different formulations (10 veterinary). Packaging inspection, tablet disintegration and content assay were conducted (validated high‐performance liquid chromatography with ultra‐violet detection); content was acceptable when within the 90% to 120% pre‐specified range (US Pharmacopeia). Results: Secondary packaging was present for 13 of 24 samples and primary packaging integrity was verified for all but one sample. Amoxicillin trihydrate/potassium clavulanate label ratio was 4:1, except for three formulations (2:1). Tablet dose strength ranged from 250 to 625 mg. All formulations contained both analytes. For amoxicillin, two of 24 samples were out of specification with 72.8% (Malaysia) and 82.3% (Thailand) of labelled content. For clavulanate, four of 24 samples were out of specification with 46.9% (Serbia), 79.0% (UK), 84.3% (Serbia) and 86.5% (Thailand) of labelled content. One formulation (Thailand) failed for both analytes. Clinical Significance: Antimicrobial formulations of substandard quality have negative consequences for efficacy in patients and potentially promote antimicrobial resistance. There was evidence of substandard formulations in all countries, not only for amoxicillin but especially for clavulanate; this could compromise equitable access to acceptable quality essential veterinary medicines worldwide.en
dc.format.extent9
dc.format.extent3814268
dc.language.isoeng
dc.relation.ispartofJournal of Small Animal Practice (JSAP)
dc.titleQuality of amoxicillin/clavulanic acid oral formulations for intended veterinary use in the UK, Malaysia, Serbia and Thailanden
dc.contributor.institutionSchool of Physics, Astronomy and Mathematics
dc.contributor.institutionScience & Technology Research Institute
dc.contributor.institutionDepartment of Engineering and Technology
dc.contributor.institutionDepartment of Clinical, Pharmaceutical and Biological Science
dc.contributor.institutionCentre for Health Services and Clinical Research
dc.contributor.institutionPsychopharmacology, Drug Misuse and Novel Psychoactive Substances Unit
dc.contributor.institutionCentre for Hazard Detection and Protection Research
dc.contributor.institutionSchool of Life and Medical Sciences
dc.contributor.institutionNanopharmaceutics
dc.contributor.institutionBioadhesive Drug Delivery Group
dc.contributor.institutionPharmaceutics
dc.contributor.institutionPharmaceutical Analysis and Product Characterisation
dc.contributor.institutionCentre for Research into Topical Drug Delivery and Toxicology
dc.contributor.institutionCentre for Research in Mechanisms of Disease and Drug Discovery
dc.description.statusPeer reviewed
dc.identifier.urlhttp://www.scopus.com/inward/record.url?scp=85163199836&partnerID=8YFLogxK
rioxxterms.versionofrecord10.1111/jsap.13648
rioxxterms.typeJournal Article/Review
herts.preservation.rarelyaccessedtrue


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