Pharmaceutical compounds determination in water samples: Comparison between solid phase extraction and STIR Bar sorptive extraction
Author
dc.contributor.author
Suazo, Fernanda
Author
dc.contributor.author
Sepúlveda Vásquez, José Ignacio
Author
dc.contributor.author
Retamal, Mauricio Antonio
Author
dc.contributor.author
Ascar, Loreto
Author
dc.contributor.author
Giordano, Ady
Admission date
dc.date.accessioned
2018-12-20T15:13:23Z
Available date
dc.date.available
2018-12-20T15:13:23Z
Publication date
dc.date.issued
2017
Cita de ítem
dc.identifier.citation
Journal of the Chilean Chemical Society, Volumen 62, Issue 3, 2018, Pages 3597-3601
Identifier
dc.identifier.issn
07179707
Identifier
dc.identifier.issn
07179324
Identifier
dc.identifier.other
10.4067/s0717-97072017000303597
Identifier
dc.identifier.uri
https://repositorio.uchile.cl/handle/2250/158610
Abstract
dc.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 ne