A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia

Detalhes bibliográficos
Autor(a) principal: Al-Qaim,Fouad F.
Data de Publicação: 2014
Outros Autores: Abdullah,Md P., Othman,Mohamed R., Latip,Jalifah, Afiq,Wan
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Journal of the Brazilian Chemical Society (Online)
Texto Completo: http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000200010
Resumo: Pharmaceuticals are synthetic or natural chemicals that can be found in prescription medicines, over-the-counter therapeutic drugs and veterinary drugs. The occurrence of pharmaceuticals in the environment and the water cycle at trace levels (in the range of nanograms to low micrograms per litre) has been widely discussed and published in literature in the past decade. The increase in detection is largely attributable to the advances in analytical techniques and instrumentation. This paper describes development, optimisation and validation of a method for the simultaneous analysis of 7 multi-class pharmaceuticals (caffeine (CAF), Prazosin (PRZ), enalapril maleate (ENL), carbamazepine (CBZ), nifedipine (NFD), levonorgestrel (LNG), simvastatin (SMV)) using solid phase extraction (SPE cartridges Oasis HLB) followed by liquid chromatography-time-of-flight/mass spectrometry (LC-ESI-TOF/MS). Its linearity, 0.5-250 µg L-1, provided determination coefficients (R²) above 0.99 for all compounds. The Instrumental Quantification Limits (IQLs) for all pharmaceuticals ranged from 0.5-5 µg L-1 in the solvent as a standard mixture (i.e., direct injection). The extraction efficiency (EE%) was more than 40% and 60% in river and deionised water for most of compounds, respectively. Limit of quantification (LOQ) for all pharmaceutic als ranged from 13-800 ng L-1 in spiked river water. The inter and intra day precision of the method, calculated as the relative standard deviation (RSD%), 2.33-22.3% and 0.6-9.9%, respectively, except for caffeine, which has a RSD% of 20.1% at 50 µg L-1. Matrix effect was investigated and ranged from 10-41%. Out of seven pharmaceuticals, six pharmaceutical compounds were detected in the river water sample.
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spelling A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysiabasic pharmaceuticalsLC-ESI-TOF/MSsolid phase extractionextraction efficiencyTangkas riverPharmaceuticals are synthetic or natural chemicals that can be found in prescription medicines, over-the-counter therapeutic drugs and veterinary drugs. The occurrence of pharmaceuticals in the environment and the water cycle at trace levels (in the range of nanograms to low micrograms per litre) has been widely discussed and published in literature in the past decade. The increase in detection is largely attributable to the advances in analytical techniques and instrumentation. This paper describes development, optimisation and validation of a method for the simultaneous analysis of 7 multi-class pharmaceuticals (caffeine (CAF), Prazosin (PRZ), enalapril maleate (ENL), carbamazepine (CBZ), nifedipine (NFD), levonorgestrel (LNG), simvastatin (SMV)) using solid phase extraction (SPE cartridges Oasis HLB) followed by liquid chromatography-time-of-flight/mass spectrometry (LC-ESI-TOF/MS). Its linearity, 0.5-250 µg L-1, provided determination coefficients (R²) above 0.99 for all compounds. The Instrumental Quantification Limits (IQLs) for all pharmaceuticals ranged from 0.5-5 µg L-1 in the solvent as a standard mixture (i.e., direct injection). The extraction efficiency (EE%) was more than 40% and 60% in river and deionised water for most of compounds, respectively. Limit of quantification (LOQ) for all pharmaceutic als ranged from 13-800 ng L-1 in spiked river water. The inter and intra day precision of the method, calculated as the relative standard deviation (RSD%), 2.33-22.3% and 0.6-9.9%, respectively, except for caffeine, which has a RSD% of 20.1% at 50 µg L-1. Matrix effect was investigated and ranged from 10-41%. Out of seven pharmaceuticals, six pharmaceutical compounds were detected in the river water sample.Sociedade Brasileira de Química2014-02-01info:eu-repo/semantics/articleinfo:eu-repo/semantics/publishedVersiontext/htmlhttp://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000200010Journal of the Brazilian Chemical Society v.25 n.2 2014reponame:Journal of the Brazilian Chemical Society (Online)instname:Sociedade Brasileira de Química (SBQ)instacron:SBQ10.5935/0103-5053.20130294info:eu-repo/semantics/openAccessAl-Qaim,Fouad F.Abdullah,Md P.Othman,Mohamed R.Latip,JalifahAfiq,Waneng2014-02-14T00:00:00Zoai:scielo:S0103-50532014000200010Revistahttp://jbcs.sbq.org.brONGhttps://old.scielo.br/oai/scielo-oai.php||office@jbcs.sbq.org.br1678-47900103-5053opendoar:2014-02-14T00:00Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)false
dc.title.none.fl_str_mv A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
title A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
spellingShingle A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
Al-Qaim,Fouad F.
basic pharmaceuticals
LC-ESI-TOF/MS
solid phase extraction
extraction efficiency
Tangkas river
title_short A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
title_full A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
title_fullStr A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
title_full_unstemmed A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
title_sort A validation method development for simultaneous LC-ESI-TOF/MS analysis of some pharmaceuticals in Tangkas river-Malaysia
author Al-Qaim,Fouad F.
author_facet Al-Qaim,Fouad F.
Abdullah,Md P.
Othman,Mohamed R.
Latip,Jalifah
Afiq,Wan
author_role author
author2 Abdullah,Md P.
Othman,Mohamed R.
Latip,Jalifah
Afiq,Wan
author2_role author
author
author
author
dc.contributor.author.fl_str_mv Al-Qaim,Fouad F.
Abdullah,Md P.
Othman,Mohamed R.
Latip,Jalifah
Afiq,Wan
dc.subject.por.fl_str_mv basic pharmaceuticals
LC-ESI-TOF/MS
solid phase extraction
extraction efficiency
Tangkas river
topic basic pharmaceuticals
LC-ESI-TOF/MS
solid phase extraction
extraction efficiency
Tangkas river
description Pharmaceuticals are synthetic or natural chemicals that can be found in prescription medicines, over-the-counter therapeutic drugs and veterinary drugs. The occurrence of pharmaceuticals in the environment and the water cycle at trace levels (in the range of nanograms to low micrograms per litre) has been widely discussed and published in literature in the past decade. The increase in detection is largely attributable to the advances in analytical techniques and instrumentation. This paper describes development, optimisation and validation of a method for the simultaneous analysis of 7 multi-class pharmaceuticals (caffeine (CAF), Prazosin (PRZ), enalapril maleate (ENL), carbamazepine (CBZ), nifedipine (NFD), levonorgestrel (LNG), simvastatin (SMV)) using solid phase extraction (SPE cartridges Oasis HLB) followed by liquid chromatography-time-of-flight/mass spectrometry (LC-ESI-TOF/MS). Its linearity, 0.5-250 µg L-1, provided determination coefficients (R²) above 0.99 for all compounds. The Instrumental Quantification Limits (IQLs) for all pharmaceuticals ranged from 0.5-5 µg L-1 in the solvent as a standard mixture (i.e., direct injection). The extraction efficiency (EE%) was more than 40% and 60% in river and deionised water for most of compounds, respectively. Limit of quantification (LOQ) for all pharmaceutic als ranged from 13-800 ng L-1 in spiked river water. The inter and intra day precision of the method, calculated as the relative standard deviation (RSD%), 2.33-22.3% and 0.6-9.9%, respectively, except for caffeine, which has a RSD% of 20.1% at 50 µg L-1. Matrix effect was investigated and ranged from 10-41%. Out of seven pharmaceuticals, six pharmaceutical compounds were detected in the river water sample.
publishDate 2014
dc.date.none.fl_str_mv 2014-02-01
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000200010
url http://old.scielo.br/scielo.php?script=sci_arttext&pid=S0103-50532014000200010
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv 10.5935/0103-5053.20130294
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv text/html
dc.publisher.none.fl_str_mv Sociedade Brasileira de Química
publisher.none.fl_str_mv Sociedade Brasileira de Química
dc.source.none.fl_str_mv Journal of the Brazilian Chemical Society v.25 n.2 2014
reponame:Journal of the Brazilian Chemical Society (Online)
instname:Sociedade Brasileira de Química (SBQ)
instacron:SBQ
instname_str Sociedade Brasileira de Química (SBQ)
instacron_str SBQ
institution SBQ
reponame_str Journal of the Brazilian Chemical Society (Online)
collection Journal of the Brazilian Chemical Society (Online)
repository.name.fl_str_mv Journal of the Brazilian Chemical Society (Online) - Sociedade Brasileira de Química (SBQ)
repository.mail.fl_str_mv ||office@jbcs.sbq.org.br
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