Emprego de polimeros de impressão molecular (MIP) na extração e pre-concentração de analitos organicos em amostras biologicas seguido de determinação espectrofotometrica
TL;DRAbstract
The objective of this Thesis was the association between molecularly imprinted polymers and spectrophotometry, with the selectivity obtained through specific binding between analytes and imprinted binding sites of the polymer. In the Chapter 1, a selective MIP for catechol was synthesized, characterized, and employed for the extraction of catechol from guarana (Paullinia cupana) and mate (Ilex paraguariensis) samples, followed by indirect spectophotometric determination of catecol by reduction of Mn(VII) for Mn(II). A limit of quantification, a relative standard deviation (20 mol L -1 , n = 10) and an analytical frequency of 2.7 mol L -1 , <5% and 15h -1 , were obtained, respectively. Accuracy was validated using HPLC. In the Chapter 2, a MIP for nicotine was used for its extraction in urine samples of smokers, followed by its indirect quantification by spectrophotometry (reduction of Mn(VII) to Mn(VI) by nicotine). The limit of quantification and analytic frequency were of 1.1 mmol L
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The objective of this Thesis was the association between molecularly imprinted polymers and spectrophotometry, with the selectivity obtained through specific binding between analytes and imprinted binding sites of the polymer. In the Chapter 1, a selective MIP for catechol was synthesized, characterized, and employed for the extraction of catechol from guarana (Paullinia cupana) and mate (Ilex paraguariensis) samples, followed by indirect spectophotometric determination of catecol by reduction of Mn(VII) for Mn(II). A limit of quantification, a relative standard deviation (20 mol L -1 , n = 10) and an analytical frequency of 2.7 mol L -1 , <5% and 15h -1 , were obtained, respectively. Accuracy was validated using HPLC. In the Chapter 2, a MIP for nicotine was used for its extraction in urine samples of smokers, followed by its indirect quantification by spectrophotometry (reduction of Mn(VII) to Mn(VI) by nicotine). The limit of quantification and analytic frequency were of 1.1 mmol L
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