Direct screening of tetracyclines in water and bovine milk using room temperature phosphorescence detection

• Published in: Analytica chimica acta Vol. 589; no. 1; pp. 51 - 58
• Main Authors: Traviesa-Alvarez, J.M., Costa-Fernández, J.M., Pereiro, R., Sanz-Medel, A.
• Format: Journal Article
• Language: English
• Published: Amsterdam Elsevier B.V 18.04.2007; Elsevier
• Subjects: Analysis methods; Analytical chemistry; Animals; Applied sciences; Cattle; Chemistry; Exact sciences and technology; General, instrumentation; Luminescent Measurements; Milk - chemistry; Natural water pollution; Optosensing; Pollution; Reproducibility of Results; Room temperature phosphorescence; Screening; Spectrometric and optical methods; Tetracyclines; Tetracyclines - analysis; Water - chemistry; Water treatment and pollution; ASW, Greater Antilles, Puerto Rico, Phosphorescent; Screening; Optosensing; Tetracyclines; Room temperature phosphorescence; Water; Amberlite; Phosphorescence spectrometry; Optical sensor; Chemical sensor; Chemical enrichment; Tetracycline; Hydrochloric acid; Antibiotic; Sample cell; Sodium; Water pollution; Europium complex; Room temperature; Flow injection; Milk; Methanol
• ISSN: 0003-2670; 1873-4324
• DOI: 10.1016/j.aca.2007.02.063

A fast and simple flow-through optosensor was designed and characterized for the direct screening of four tetracycline (TCC) antibiotics (tetracycline, oxytetracycline, chlortetracycline and doxycycline) in water and bovine milk samples. The proposed optosensor provides rapid binary yes/no overall responses, being appropriate for the screening of this family of antibiotics above or below a pre-set concentration threshold. The experimental set-up is based on a flow-injection manifold coupled on-line to a phosphorescence detector. Aliquots of the samples are pretreated with Eu(III) to form room temperature phosphorescent metal chelates and injected in the flow manifold. Those chelates are then on-line retained on a conventional flow-cell (packed with polymeric Amberlite XAD-4 particles) which is placed inside the cell holder of the phosphorimeter. After the emission is registered, the antibiotic–metal complexes are eluted from the packed resin with 1 M HCl (for milk samples a second regeneration step, using methanol, should be performed). A sample throughput of about 20 samples per hour was obtained. Optimum experimental conditions include a pH 9, a Eu(III) concentration of 2 × 10 −4 M and 8 mM sodium sulphite as chemical deoxygenant. The phosphorescence emitted by the europium–TCC complexes was measured at 394 and 617 nm for excitation and emission wavelengths, respectively. The unreliability region, given by the probability of false positives and false negatives, respectively (set at 5% in both cases) was in the range between 0.2 and 11.6 nМ for detection of tetracyclines in water samples (at a cut-off level of 4 nM) and in the range between 165 and 238 nM for detection of tetracyclines in milk (cut-off level fixed at the normative EU level of 200 nM). Finally, the applicability of the proposed screening optosensor was tested for the reliable control of tetracyclines in contaminated and uncontaminated water and milk samples.