2003
DOI: 10.1016/j.chroma.2003.08.066
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Evaluation of multiple solid-phase microextraction as a technique to remove the matrix effect in packaging analysis for determination of volatile organic compounds

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Cited by 36 publications
(18 citation statements)
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“…The DVB-CAR-PDMS fibre was better than the CAR-PDMS fibre for MHS-SPME, since it provided a better exponential decay with the number of cycles and increased peak areas. Since MHS-SPME provides a total area value corresponding to an exhaustive extraction, independent of the type of matrix, 30 calibration can be carried out using aqueous solutions under extraction conditions different from those used to process the solid samples. Verbenone, borneol and camphor were the most abundant compounds in the rosemary extract analysed.…”
Section: Features Of the Methodsmentioning
confidence: 99%
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“…The DVB-CAR-PDMS fibre was better than the CAR-PDMS fibre for MHS-SPME, since it provided a better exponential decay with the number of cycles and increased peak areas. Since MHS-SPME provides a total area value corresponding to an exhaustive extraction, independent of the type of matrix, 30 calibration can be carried out using aqueous solutions under extraction conditions different from those used to process the solid samples. Verbenone, borneol and camphor were the most abundant compounds in the rosemary extract analysed.…”
Section: Features Of the Methodsmentioning
confidence: 99%
“…Multiple headspace-SPME (MHS-SPME) 29 is a recent method developed to quantify solid samples, since it removes the influence of the matrix effect. 30 The technique is based on extrapolation to an exhaustive extraction of the compounds through three or four cycles of consecutive extractions from the same sample. In this way the total area can be calculated according to equation (1):…”
Section: Introductionmentioning
confidence: 99%
“…As an equilibrium method, SPME depends on analyte partitioning between the sample and the fused silica fiber coated with a solid sorbent. María Teresa Tena and others (Ezquerro and others ) had proved that multiple SPME was useful to the direct quantification of solid samples removing any matrix effect, with water as reliable solvent to prepare the calibration solutions. Using the water as dilutors of samples for HS‐SPME‐GC‐MS analysis was also validated by Mesías and others ().…”
Section: Methodsmentioning
confidence: 99%
“…Acoplamentos entre técnicas para confirmar a identidade de compostos químicos têm sido relatados na literatura, tais como a cromatografia em fase gasosa acoplada à espectrometria de massas (CG-EM) [5][6][7]27,31,41,48,[50][51][52][53][54] e a cromatografia em fase gasosa acoplada à espectroscopia no infravermelho (CG-IV). 55,56 Feigenbaum et al 51 citam o emprego de CG-FTIR-EM com colunas longas e a injeção direta de extratos no cromatógrafo.…”
Section: Identificação E Quantificação De Compostos Voláteisunclassified
“…46,48 Uma variação desta técnica é a extração em múltiplos estágios, com o objetivo de eliminar a influência da matriz sólida (amostra) na análise quantitativa de componentes voláteis, uma vez que, teoricamente, sucessivas extrações ocasionam um declínio exponencial de extração, promovendo uma melhor recuperação dos analitos de interesse. 46 …”
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