PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION

ABSTRACT A variety of organic compounds and their metabolites used in pharmaceutical and personal care products (PPCP´s) are continuously introduced into the environment by domestic or industrial wastewater. Solid phase extraction (polymeric dinivylbenzene cartridge) and stir bar sorptive extraction...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: SUAZO,FERNANDA, VÁSQUEZ,JOSÉ, RETAMAL,MAURICIO, ASCAR,LORETO, GIORDANO,ADY
Lenguaje:English
Publicado: Sociedad Chilena de Química 2017
Materias:
SPE
Acceso en línea:http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000303597
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:scielo:S0717-97072017000303597
record_format dspace
spelling oai:scielo:S0717-970720170003035972017-09-08PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTIONSUAZO,FERNANDAVÁSQUEZ,JOSÉRETAMAL,MAURICIOASCAR,LORETOGIORDANO,ADY SPE SBSE pharmaceutical and personal care products ABSTRACT A variety of organic compounds and their metabolites used in pharmaceutical and personal care products (PPCP´s) are continuously introduced into the environment by domestic or industrial wastewater. Solid phase extraction (polymeric dinivylbenzene cartridge) and stir bar sorptive extraction (polydimethylsiloxane phase) methodologies were optimized for the determination of some selected PPCP´s in aqueous matrices. Carbamazepine, β estradiol, 3-(4-methylbenzylidene)champhor, benzophenone-1 and ibuprofen were extracted from aqueous samples and methanol was used as conditioning/eluting solvent. The variables involved in the extraction of the analytes in the original sample were studied, pH between 3 and 6 and sample volume between 50 and 500 mL were considered. Three concentration levels were extracted at the optimal conditions of pH 5 and 500 mL of sample volume with a recovery up to 89%. The determination was performed in a GC-MS, and a derivatization step using BSTFA+TMCS (99:1) was needed previous to the injection. Real samples from Maipo River and Villarrica Lake were analyzed with the optimized method, and concentrations below the detection limit were detected.info:eu-repo/semantics/openAccessSociedad Chilena de QuímicaJournal of the Chilean Chemical Society v.62 n.3 20172017-09-01text/htmlhttp://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000303597en10.4067/s0717-97072017000303597
institution Scielo Chile
collection Scielo Chile
language English
topic SPE
SBSE
pharmaceutical and personal care products
spellingShingle SPE
SBSE
pharmaceutical and personal care products
SUAZO,FERNANDA
VÁSQUEZ,JOSÉ
RETAMAL,MAURICIO
ASCAR,LORETO
GIORDANO,ADY
PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION
description ABSTRACT A variety of organic compounds and their metabolites used in pharmaceutical and personal care products (PPCP´s) are continuously introduced into the environment by domestic or industrial wastewater. Solid phase extraction (polymeric dinivylbenzene cartridge) and stir bar sorptive extraction (polydimethylsiloxane phase) methodologies were optimized for the determination of some selected PPCP´s in aqueous matrices. Carbamazepine, β estradiol, 3-(4-methylbenzylidene)champhor, benzophenone-1 and ibuprofen were extracted from aqueous samples and methanol was used as conditioning/eluting solvent. The variables involved in the extraction of the analytes in the original sample were studied, pH between 3 and 6 and sample volume between 50 and 500 mL were considered. Three concentration levels were extracted at the optimal conditions of pH 5 and 500 mL of sample volume with a recovery up to 89%. The determination was performed in a GC-MS, and a derivatization step using BSTFA+TMCS (99:1) was needed previous to the injection. Real samples from Maipo River and Villarrica Lake were analyzed with the optimized method, and concentrations below the detection limit were detected.
author SUAZO,FERNANDA
VÁSQUEZ,JOSÉ
RETAMAL,MAURICIO
ASCAR,LORETO
GIORDANO,ADY
author_facet SUAZO,FERNANDA
VÁSQUEZ,JOSÉ
RETAMAL,MAURICIO
ASCAR,LORETO
GIORDANO,ADY
author_sort SUAZO,FERNANDA
title PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION
title_short PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION
title_full PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION
title_fullStr PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION
title_full_unstemmed PHARMACEUTICAL COMPOUNDS DETERMINATION IN WATER SAMPLES: COMPARISON BETWEEN SOLID PHASE EXTRACTION AND STIR BAR SORPTIVE EXTRACTION
title_sort pharmaceutical compounds determination in water samples: comparison between solid phase extraction and stir bar sorptive extraction
publisher Sociedad Chilena de Química
publishDate 2017
url http://www.scielo.cl/scielo.php?script=sci_arttext&pid=S0717-97072017000303597
work_keys_str_mv AT suazofernanda pharmaceuticalcompoundsdeterminationinwatersamplescomparisonbetweensolidphaseextractionandstirbarsorptiveextraction
AT vasquezjose pharmaceuticalcompoundsdeterminationinwatersamplescomparisonbetweensolidphaseextractionandstirbarsorptiveextraction
AT retamalmauricio pharmaceuticalcompoundsdeterminationinwatersamplescomparisonbetweensolidphaseextractionandstirbarsorptiveextraction
AT ascarloreto pharmaceuticalcompoundsdeterminationinwatersamplescomparisonbetweensolidphaseextractionandstirbarsorptiveextraction
AT giordanoady pharmaceuticalcompoundsdeterminationinwatersamplescomparisonbetweensolidphaseextractionandstirbarsorptiveextraction
_version_ 1714200914734088192