Lethal and sublethal effects of the emerging contaminant oxytetracycline on the embryo-larval development of Rhinella arenarum.

The antibiotic oxytetracycline (OTC) is commonly used in animal production and can enter aquatic ecosystems, causing adverse effects on non-target species. The aim of this work was to evaluate the lethal and sublethal effects of OTC on the embryonic and larval period of Rhinella arenarum, through standardized bioassays and oxidative stress (catalase-CAT-, superoxide dismutase-SOD-, glutathione S-transferase-GST-, reduced glutathione-GSH- and lipid peroxidation-TBARS-), neurotoxicity (acetylcholinesterase-AChE- and butyrylcholinesterase-BChE-) and genotoxicity (micronuclei test) biomarkers. Mortality was time and stage dependent, being the embryos (504 h-LC50 = 64.04 mg/L) more sensitive than the larvae (504 h-LC50 = 97.74 mg/L). Alterations in the oxidative stress biomarkers were observed mainly in larvae: CAT, SOD and GST decreased and GSH increased significantly. In embryos, only GST decreased significantly. Also, OTC increased the AChE and BChE activities but did not increase the micronuclei frequency. This study shows evidence that the presence of OTC in the environment may have negative effects on amphibians.

Study of the photoinduced degradation of polycyclic musk compounds by solid-phase microextraction and gas chromatography/mass spectrometry.

Polycyclic musks are widely used synthetic fragrances that have been identified during the last few years in biota samples and environmental matrices. Nevertheless, there is a lack of information concerning the photodegradation behavior of these compounds. In this work, the photoinduced degradation of six polycyclic musk compounds (Cashmeran, Celestolide, Phantolide, Galaxolide, Traseolide and Tonalide) was studied using a solid-phase microextraction (SPME) fiber as support. Musk fragrances were extracted from aqueous solutions using SPME fibers that were subsequently exposed to ultraviolet (UV) irradiation for different times. To study the degradation kinetics and to tentatively identify the photoproducts generated, gas chromatography coupled to ion trap mass spectrometry was used. Aqueous photodegradation studies were also performed. The on-fiber photodegradation approach avoids the need for further extraction processes and makes the identification of photoproducts easier, due to their higher concentration on the fibers. All musk compounds were easily photodegraded, suggesting that UV irradiation could work as a decontamination tool for these musks.

Rapid determination of 2,3,7,8-tetrachlorodibenzo-p-dioxin in water samples by using solid-phase microextraction followed by gas chromatography with tandem mass spectrometry.

A rapid and simple method of using solid-phase microextraction was developed for determination of 2,3,7,8-tetrachlorodibenzo-p-dioxin (2,3,7,8-TCDD) in water samples. In this method, the target analyte is extracted from the sample into the polymeric coating of the fused-silica fiber. After exposure, the fiber is thermally desorbed in the heated injection port of the gas chromatograph, and a chromatographic analysis is performed by using low-resolution tandem mass spectrometry. Parameters that may affect the extension of the microextraction process, such as sampling mode, sample volume, temperature, agitation, and sampling time, were studied. Extraction efficiencies for 3 coating fibers were investigated: 100 microm poly(dimethylsiloxane) (PDMS), 65 microm PDMS-divinylbenzene, and 75 microm carboxen-PDMS. Linearity was evaluated (R = 0.999) for a 250-fold concentration range from the fg/mL to the pg/mL level. The 2,3,7,8-TCDD was detected at the fg/mL level when the headspace over the water sample was sampled for 60 min; the limit of detection obtained was better than that of Method 8280B of the U.S. Environmental Protection Agency. The proposed method performed well when applied to the analysis of tap water, lake water, and seawater samples.

On-fiber photodegradation after solid-phase microextraction of p,p'-DDT and two of its major photoproducts, p,p'-DDE and p,p'-DDD.

The potential of performing photochemical studies in solid phase microextraction (SPME) fibers, "photo-SPME", to study the photodegradation of p,p'-DDT and two of its major degradation products, p,p'-DDE and p,p'-DDD, is shown. Analyses were carried out by gas chromatography mass spectroscopy detection. DDT was extracted from aqueous solutions using five different commercial coatings. The fibers were then exposed to UV light emitted by a low-pressure mercury lamp. After 30 min of irradiation, the degradation of DDT only occurred in polydimethylsiloxane fibers. The on-fiber degradation kinetics of p,p'-DDT was studied from 2 to 60 min. A large number of photoproducts were generated and their kinetic behavior was studied. In order to clarify the possible photoreaction pathways for DDT, individual water solutions containing p,p'-DDD or p.p'-DDE were prepared and photo-SPME was performed for each compound at different irradiation times. On the basis of the photoproducts identified, some photodegradation pathways are proposed. Finally, aqueous photodegradation studies followed by SPME were performed and compared to the photo-SPME. This work will show the enormous potential of photo-SPME to perform photodegradation studies.

Optimization of a derivatization-solid-phase microextraction method for the analysis of thirty phenolic pollutants in water samples.

Solid-phase microextraction (SPME) coupled to gas chromatography-mass spectrometry has been applied to the extraction of 30 phenol derivatives from water samples. Analytes were in situ acetylated and headspace solid-phase microextraction was performed. Different parameters affecting extraction efficiency were studied. Optimization of temperature, type of microextraction fiber and volume of sample has been done by means of a mixed-level categorical experimental design, which allows to study main effects and second order interactions. Five different fiber coatings were employed in this study; also, extraction temperature was studied at three levels. Both factors, fiber coating and extraction temperature, were important to achieve high sensitivity. Moreover, these parameters showed a significant interaction, which indicates the different kinetic behavior of the SPME process when different coatings are used. It was found that 75 microm carboxen-polydimethylsiloxane and 100 microm polydimethylsiloxane, yield the highest responses. The first one is specially appropriated for phenol, methylphenols and low chlorinated chlorophenols and the second one for highly chlorinated phenols. The two methods proposed in this study shown good linearity and precision. Practical applicability was demonstrated through the analysis of a real sewage water sample, contaminated with phenols.