Utilize este identificador para referenciar este registo: http://hdl.handle.net/10400.22/6761
Título: Sulfadiazine-selective determination in aquaculture environment: Selective potentiometric transduction by neutral or charged ionophores
Autor: Almeida, Sofia A. A.
Heitor, A.M.
Montenegro, M.C.B.S.M.
Sales, M. Goreti F.
Palavras-chave: Sulphadiazine
Cyclodextrin-based ionophore
Porphyrin-based ionophore
Data: 2011
Editora: Elsevier
Resumo: Solid-contact sensors for the selective screening of sulfadiazine (SDZ) in aquaculture waters are reported. Sensor surfaces were made from PVC membranes doped with tetraphenylporphyrin-manganese(III) chloride, α-cyclodextrin, β-cyclodextrin, or γ-cyclodextrin ionophores that were dispersed in plasticizer. Some membranes also presented a positive or a negatively charged additive. Phorphyrin-based sensors relied on a charged carrier mechanism. They exhibited a near-Nernstian response with slopes of 52 mV decade−1 and detection limits of 3.91 × 10−5 mol L−1. The addition of cationic lipophilic compounds to the membrane originated Nernstian behaviours, with slopes ranging 59.7–62.0 mV decade−1 and wider linear ranges. Cyclodextrin-based sensors acted as neutral carriers. In general, sensors with positively charged additives showed an improved potentiometric performance when compared to those without additive. Some SDZ selective membranes displayed higher slopes and extended linear concentration ranges with an increasing amount of additive (always <100% ionophore). The sensors were independent from the pH of test solutions within 2–7. The sensors displayed fast response, always <15 s. In general, a good discriminating ability was found in real sample environment. The sensors were successfully applied to the fast screening of SDZ in real waters samples from aquaculture fish farms. The method offered the advantages of simplicity, accuracy, and automation feasibility. The sensing membrane may contribute to the development of small devices allowing in locus measurements of sulfadiazine or parent-drugs.
URI: http://hdl.handle.net/10400.22/6761
DOI: 10.1016/j.talanta.2011.06.022
Versão do Editor: http://www.sciencedirect.com/science/article/pii/S0039914011005078
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