Determination of boscalid, pyraclostrobin and trifloxystrobin in dried grape and apricot by HPLC/UV method

dc.contributor.authorDost, K
dc.contributor.authorÖksüz, M
dc.contributor.authorCittan, M
dc.contributor.authorMutlu, B
dc.contributor.authorTural, B
dc.date.accessioned2025-04-10T10:27:00Z
dc.date.available2025-04-10T10:27:00Z
dc.description.abstractThis paper describes the development of extraction and high-performance liquid chromatography with ultraviolet detection methods for the determination of boscalid, pyraclostrobin, and trifloxystrobin. The extraction method includes classical solid-liquid and liquid-liquid extraction methods. The fungicides and the internal standard were separated in less than 6.5 min on an ODS column with acetonitrile/water mobile phase at 1.5 mL min- 1 flow rate and detected at 265 nm. The limit of detection and quantification were 0.0084 and 0.0280 mg kg-1 for boscalid; 0.0032 and 0.0106 mg kg- 1 for pyraclostrobin; 0.0113 and 0.0377 mg kg- 1 for trifloxystrobin. The reproducibility of the method was lower than 0.6 % and 0.7 % relative standard deviation in terms of retention time for within day and between days, respectively, lower than 1.4 % in terms of the ratio of peak areas for both within day and between days. The accuracy of the analysis method in terms of relative error was lower than 11 % at low, 8 % at medium and 1 % at high concentrations. The recoveries were between 99-106 % for boscalid, 70-82 % for pyraclostrobin and 52-64 % for trifloxystrobin. These developed methods were then applied for the determination of selected fungicides in dried grape and apricot samples.
dc.identifier.e-issn1096-0481
dc.identifier.issn0889-1575
dc.identifier.urihttp://hdl.handle.net/20.500.14701/34598
dc.language.isoEnglish
dc.titleDetermination of boscalid, pyraclostrobin and trifloxystrobin in dried grape and apricot by HPLC/UV method
dc.typeArticle

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