2004
DOI: 10.1093/jaoac/87.5.1033
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Determination of Maduramicin in Feedingstuffs and Premixtures by Liquid Chromatography: Development, Validation, and Interlaboratory Study

Abstract: A reversed-phase liquid chromatography method for determination of maduramicin in feedingstuffs and premixtures was developed, validated, and interlaboratory studied. The extraction solvent was methanol. Maduramicin was detected at 520 nm after postcolumn derivatization with vanillin.

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Cited by 19 publications
(13 citation statements)
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“…A complete necropsy was performed, and samples were taken for routine histology and bacteriology. Pellets were examined for the presence of organochlorine and organophosphate pesticides, pyrethroids, mycotoxins and ionophores (maduramicin, narasin, lasalocid, monensin and salinomycin) as described by Hamilton et al, 1981 andDe Jong et al, 2004. Chromatographic analysis for ionophores was carried out on a LC-10AVP Shimadzu High Performance Liquid Chromatograph.…”
Section: Methodsmentioning
confidence: 99%
“…A complete necropsy was performed, and samples were taken for routine histology and bacteriology. Pellets were examined for the presence of organochlorine and organophosphate pesticides, pyrethroids, mycotoxins and ionophores (maduramicin, narasin, lasalocid, monensin and salinomycin) as described by Hamilton et al, 1981 andDe Jong et al, 2004. Chromatographic analysis for ionophores was carried out on a LC-10AVP Shimadzu High Performance Liquid Chromatograph.…”
Section: Methodsmentioning
confidence: 99%
“…Both methods have the advantages of high analytic sensitiveness and accurate detection results. However, MD has no fluorophore or UV absorption, so it requires derivatization before detection in the high-performance liquid chromatography assays (Jong et al, 2004). The process of sample preparation is also complicated, and requires purification with solid-phase extraction (SPE).…”
Section: Introductionmentioning
confidence: 99%
“…Kostadinović, Univerzitet u Novom Sadu, Institut za prehrambene tehnologije, Bulevar cara Lazara 1, 21000 Novi Sad, Novi Sad, Srbija. E-pošta: ljiljana.kostadinovic@fins.uns.ac.rs Rad primljen: 13. maj, 2013 Rad prihvaćen: 5. septembar, 2013 njuje tečna hromatografija sa fluorescentnom [3,4] ili UV detekcijom [5][6][7][8][9]. Ove metode uključuju predkolonsku ili postkolonsku derivatizaciju ili ekstrakciju kolonskom hromatografijom, a obezbeđuju donju granicu detekcije od oko 1mg/kg, osim u slučaju lasalocida i narasina (0,5 mg/kg).…”
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