Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection

A new and sensitive method was developed for the determination of the etimicin (ETM) using precolumn derivatization (PCD) with 9-fluorenylmethyl chloroformate (FMOC-Cl) by a reversed phase separation and subsequent fluorescence detection. The PCD conditions were fully optimized towards the lowest limit of detection. The chromatographic separation was carried out on an Agilent XDB-C8 column at 25 ºC using a constant flow rate of 1.0 mL min-1 and mobile phase of acetonitrile/water (87:13, v/v). The etimicin-FMOC-Cl derivative was monitored by fluorescent detection at λexcitation 265 nm and λemission 315 nm. Neomycin (NMC), a similar base structure compound with ETM, was used as an internal standard. The statistical evaluation of the method was examined and the method was found to be precise and accurate with a linearity range of 0.038-9.69 µg mL-1 (r > 0.9994). The intra- and inter-day precision studies showed good reproducibility with relative standard deviation (R.S.D.) less than 5%, and the relative recovery was 97.80-100.09 % (n = 3). The limit of detection (LOD) and lower limit of quantification (LLOQ) in plasma were 0.01 and 0.02 µg mL-1, respectively. A volume of 50 µL of plasma was sufficient for the determination of etimicin. The established method provides a reliable bioanalytical method to carry out etimicin pharmacokinetics in rat plasma.

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Main Authors: Chang,Xiaojuan, Yu,Zhengping
Format: Digital revista
Language:English
Published: Sociedade Brasileira de Química 2011
Online Access:http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700008
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spelling oai:scielo:S0103-505320110007000082011-07-22Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detectionChang,XiaojuanYu,Zhengping high-performance liquid chromatography 9-fluorenylmethyl chloroformate derivatization etimicin pharmacokinetic A new and sensitive method was developed for the determination of the etimicin (ETM) using precolumn derivatization (PCD) with 9-fluorenylmethyl chloroformate (FMOC-Cl) by a reversed phase separation and subsequent fluorescence detection. The PCD conditions were fully optimized towards the lowest limit of detection. The chromatographic separation was carried out on an Agilent XDB-C8 column at 25 ºC using a constant flow rate of 1.0 mL min-1 and mobile phase of acetonitrile/water (87:13, v/v). The etimicin-FMOC-Cl derivative was monitored by fluorescent detection at λexcitation 265 nm and λemission 315 nm. Neomycin (NMC), a similar base structure compound with ETM, was used as an internal standard. The statistical evaluation of the method was examined and the method was found to be precise and accurate with a linearity range of 0.038-9.69 µg mL-1 (r > 0.9994). The intra- and inter-day precision studies showed good reproducibility with relative standard deviation (R.S.D.) less than 5%, and the relative recovery was 97.80-100.09 % (n = 3). The limit of detection (LOD) and lower limit of quantification (LLOQ) in plasma were 0.01 and 0.02 µg mL-1, respectively. A volume of 50 µL of plasma was sufficient for the determination of etimicin. The established method provides a reliable bioanalytical method to carry out etimicin pharmacokinetics in rat plasma.info:eu-repo/semantics/openAccessSociedade Brasileira de QuímicaJournal of the Brazilian Chemical Society v.22 n.7 20112011-07-01info:eu-repo/semantics/articletext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700008en10.1590/S0103-50532011000700008
institution SCIELO
collection OJS
country Brasil
countrycode BR
component Revista
access En linea
databasecode rev-scielo-br
tag revista
region America del Sur
libraryname SciELO
language English
format Digital
author Chang,Xiaojuan
Yu,Zhengping
spellingShingle Chang,Xiaojuan
Yu,Zhengping
Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection
author_facet Chang,Xiaojuan
Yu,Zhengping
author_sort Chang,Xiaojuan
title Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection
title_short Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection
title_full Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection
title_fullStr Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection
title_full_unstemmed Determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by HPLC with fluorescence detection
title_sort determination of etimicin in rat plasma using 9-fluorenylmethyl chloroformate precolumn derivatization by hplc with fluorescence detection
description A new and sensitive method was developed for the determination of the etimicin (ETM) using precolumn derivatization (PCD) with 9-fluorenylmethyl chloroformate (FMOC-Cl) by a reversed phase separation and subsequent fluorescence detection. The PCD conditions were fully optimized towards the lowest limit of detection. The chromatographic separation was carried out on an Agilent XDB-C8 column at 25 ºC using a constant flow rate of 1.0 mL min-1 and mobile phase of acetonitrile/water (87:13, v/v). The etimicin-FMOC-Cl derivative was monitored by fluorescent detection at λexcitation 265 nm and λemission 315 nm. Neomycin (NMC), a similar base structure compound with ETM, was used as an internal standard. The statistical evaluation of the method was examined and the method was found to be precise and accurate with a linearity range of 0.038-9.69 µg mL-1 (r > 0.9994). The intra- and inter-day precision studies showed good reproducibility with relative standard deviation (R.S.D.) less than 5%, and the relative recovery was 97.80-100.09 % (n = 3). The limit of detection (LOD) and lower limit of quantification (LLOQ) in plasma were 0.01 and 0.02 µg mL-1, respectively. A volume of 50 µL of plasma was sufficient for the determination of etimicin. The established method provides a reliable bioanalytical method to carry out etimicin pharmacokinetics in rat plasma.
publisher Sociedade Brasileira de Química
publishDate 2011
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532011000700008
work_keys_str_mv AT changxiaojuan determinationofetimicininratplasmausing9fluorenylmethylchloroformateprecolumnderivatizationbyhplcwithfluorescencedetection
AT yuzhengping determinationofetimicininratplasmausing9fluorenylmethylchloroformateprecolumnderivatizationbyhplcwithfluorescencedetection
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