Leslie M. Bragg

Tissue-Specific In Vivo Bioconcentration of Pharmaceuticals in Rainbow Trout (Oncorhynchus mykiss) Using Space-Resolved Solid-Phase Microextraction

The space-resolved solid-phase microextraction (SR-SPME) technique was employed to study the tissue-specific bioconcentration of pharmaceuticals in live fish. The segmented design of the SPME fibers allowed for the simultaneous determination of pharmaceutical residues in fish dorsal-epaxial muscle and adipose tissue with a single SPME fiber. The miniaturized fiber endowed the technique with high spatial resolution allowing for quantification of analytes within adjacent, relatively small tissues of immature rainbow trout. The pre-equilibrium sampling and kinetic calibration approach yielded efficient and accurate quantitation of pharmaceuticals in fish tissue. The ability of the SPME method to repeatedly sample the same fish circumvents problems arising from interanimal variation, thus improving the precision of generated bioconcentration kinetic profiles. In vivo monitoring with SR-SPME was validated with in vitro liquid extraction of tissue samples using methanol. Of the nine compounds evaluated, five (atrazine, gemfibrozil, carbamazepine, ibuprofen, and fluoxetine) bioconcentrated in adipose and muscle tissue over the eight exposure days. Although the accumulation of analytes in both tissues was positively correlated, each compound partitioned with differing affinities as modified by their hydrophobicity and unique molecular structure. Water samples analyzed using the SPME technique yielded results similar to those determined by solid-phase extraction (SPE); however, SPME was more rapid and operationally much simpler. This study illustrates the application conditions for in situ SR-SPME while demonstrating the potential of these miniaturized SPME fibers for simultaneous in vivo repeated sampling of multiple tissues.

Comparison of thin-film microextraction and stir bar sorptive extraction for the analysis of polycyclic aromatic hydrocarbons in aqueous samples with controlled agitation conditions

The characterization of a poly(dimethylsiloxane) (PDMS) thin film for active extraction of some polycyclic aromatic hydrocarbons was investigated in both a 1-L aqueous solution and a flow-through system. The thin film was attached to an electric bench-drill at a constant rotation speed for constant agitation and fast extraction. The performance of a PDMS-coated stir bar at a constant stirring speed was also investigated. The comparison showed that the extraction rate was much higher when using the thin film than the stir bar, and that the equilibration time was greatly shortened due to the larger surface area/volume ratio of the thin film. The extraction rate was roughly proportional to surface area of the extraction phase during the initial stage of the extraction process; the amount of analyte extracted was proportional to the ratio of the extraction phase between the thin film and the stir bar. Different agitation and stirring rates of the thin film and stir bar were applied for extraction, revealing that extraction efficiency can be improved by increasing rotation rate. The application of rotated thin film in the field proved it is a valid and easily operated method for the determination of polycyclic aromatic hydrocarbons (PAHs) in a campus river. However, the stir bar is not as convenient as a thin film in field sampling.

Sampling-rate calibration for rapid and nonlethal monitoring of organic contaminants in fish muscle by solid-phase microextraction.

Solid-phase microextraction (SPME) is a promising technique for determining organic contaminants within biotic systems. Existing in vivo SPME-kinetic calibration (SPME-KC) approaches are unwieldy due to the necessity of predetermining a distribution coefficient for the analyte of interest in the tissue and the preloading of a calibrating compound to the fiber. In this study, a rapid and convenient SPME alternative calibration method for in vivo analysis, termed SPME-sampling rate (SPME-SR) calibration, was developed and validated under both laboratory and field conditions to eliminate such presampling requirements. Briefly, the SPME probe is inserted into tissue, in this study fish dorsal-epaxial muscle, for 20 min allowing the concentrations of target analytes in the fish muscle to be determined by the extracted amount of analyte and the predetermined sampling rates. Atrazine, carbamazepine, and fluoxetine were detected nonlethally in the low ppb levels within fish muscle, with both laboratory and field-derived results obtained by in vivo SPME-KC comparable (within a factor of 1.27) to those obtained by lethal sampling followed by tissue liquid extraction. The technique described in this study represents an important advance which broadens the application of SPME in vivo sampling technology.

Fast analysis of volatile organic compounds and disinfection by-products in drinking water using solid-phase microextraction-gas chromatography/time-of-flight mass spectrometry

A fast method was developed for the extraction and analysis of volatile organic compounds, including disinfection by-products (DBPs), with headspace solid-phase microextraction (HS-SPME) and gas chromatography/mass spectrometry (GC/MS) techniques. A GC/time-of-flight (TOF)-MS instrument, which had fast acquisition rates and powerful deconvolution software, was used. Under optimum conditions total runtime was 45s. Volatile organic compounds (VOCs), including purgeable A and B compounds (listed in US Environmental Protection Agency method 624), were identified in standard water samples. Extraction times were 1min for more volatile compounds and 2min for less volatile compounds. The method was applied to the analysis of water samples treated under different disinfection processes and the results were compared with those from a liquid-liquid extraction method.

Validation and use of in vivo solid phase micro-extraction (SPME) for the detection of emerging contaminants in fish.

A variety of emerging chemicals of concern are released continuously to surface water through the municipal wastewater effluent discharges. The ability to rapidly determine bioaccumulation of these contaminants in exposed fish without sacrificing the animal (i.e. in vivo) would be of significant advantage to facilitate research, assessment and monitoring of their risk to the environment. In this study, an in vivo solid phase micro-extraction (SPME) approach was developed and applied to the measurement of a variety of emerging contaminants (carbamazepine, naproxen, diclofenac, gemfibrozil, bisphenol A, fluoxetine, ibuprofen and atrazine) in fish. Our results indicated in vivo SPME was a potential alternative extraction technique for quantitative determination of contaminants in lab exposures and as well after exposure to two municipal wastewater effluents (MWWE), with a major advantage over conventional techniques due to its ability to non-lethally sample tissues of living organisms.

Solid-phase microextraction under controlled agitation conditions for rapid on-site sampling of organic pollutants in water

An electric drill coupled with a solid-phase microextraction (SPME) polydimethylsiloxane (PDMS) fiber or a PDMS thin film was used for rapid sampling of polycyclic aromatic hydrocarbons (PAHs) in aqueous samples. Laboratory experiments demonstrated that the sampling rates of SPME fiber and thin film can be predicted theoretically. Compared with the SPME fiber, the PDMS thin film active sampler exhibited a higher sampling rate and much better sensitivity due to its higher surface-to-volume ratio and its larger extraction phase volume. The amount of the analytes extracted by the thin film was around 100 times higher than those obtained by fiber, for both 5 min rapid sampling and equilibrium extraction. A new thin film active sampler was then developed for rapid on-site water sampling. The sampling kit included a portable electric drill, a copper mesh pocket, a piece of thin film, and a liner. Laboratory experiments indicated that the sampling remained in the linear uptake phase with this sampler to 8 min for the PAHs. Field test illustrated that this novel sampler was excellent for rapid on-site water sampling due to its short sampling period, high sampling efficiency and durability The thin film sampling kit facilitates on-site sampling, sample preparation, storage and transport. This new sampler is more user-friendly and easier to commercialize than previous samplers.

Occurrence and degree of intersex (testis–ova) in darters (Etheostoma SPP.) across an urban gradient in the Grand River, Ontario, Canada

The variability and extent of the intersex condition (oocytes in testes, or testis-ova) was documented in fish along an urban gradient in the Grand River, Ontario, Canada, that included major wastewater treatment plant outfalls. A method for rapid enumeration of testis-ova was developed and applied that increased the capacity to quantify intersex prevalence and severity. Male rainbow darters (Etheostoma caeruleum) sampled downstream of the first major wastewater outfall (Waterloo) had a significant increase, relative to 4 upstream reference sites, in the mean proportion of fish with at least 1 testis-oocyte per lobe of testes (9-20% proportion with ≤ 1 testis-oocyte/lobe vs 32-53% and >1.4 testis-oocyte/lobe). A much higher mean incidence of intersex proportion and degree was observed immediately downstream of the second wastewater outfall (Kitchener; 73-100% and 8-70 testis-oocyte/lobe); but only 6.3 km downstream of the Kitchener outfall, the occurrence of intersex dropped to those of the reference sites. In contrast, downstream of a tertiary treated wastewater outfall on a small tributary, intersex was similar to reference sites. Estrogenicity, measured using a yeast estrogen screen, followed a similar pattern, increasing from 0.81 ± 0.02 ng/L 17b-estradiol equivalents (EEq) (Guelph), to 4.32 ± 0.07 ng/L (Waterloo), and 16.99 ± 0.40 ng/L (Kitchener). Female rainbow darter downstream of the Kitchener outfall showed significant decreases in gonadosomatic index and liver somatic index, and increases in condition factor (k) relative to corresponding reference sites. The prevalence of intersex and alterations in somatic indices suggest that exposure to municipal wastewater effluent discharges can impact endocrine function, energy use, and energy storage in wild fish.

Advanced Oxidation Treatment of Drinking Water: Part I. Occurrence and Removal of Pharmaceuticals and Endocrine-Disrupting Compounds from Lake Huron Water

The current study focuses on the occurrence of selected endocrine disrupting compounds, pharmaceuticals and personal care products in Lake Huron Water and their removal using ozone/hydrogen peroxide based pre-coagulation, advanced oxidation process (AOP). Raw Lake Huron water spiked with nine target compounds was treated in a dual train pilot scale treatment plant. None of the target chemicals showed any significant removals following conventional treatment processes (coagulation, sedimentation and filtration). Five of the nine target pollutants plummeted to concentrations below the method detection limits following AOP. For all the target compounds AOP treatment provided higher removal compared to conventional treatment.

Photocatalytic decomposition of organic micropollutants using immobilized TiO2 having different isoelectric points

Organic micropollutants found in the environment are a diverse group of compounds that includes pharmaceuticals, personal care products, and endocrine disruptors. Their presence in the aquatic environment continues to be a concern as the risk they pose towards both the environment and human health is still inconclusive. Removal of these compounds from water and wastewater is difficult to achieve and often incomplete, but UV-TiO2 is a promising treatment approach. In this study, the efficiency of titanium dioxide (TiO2) immobilized on porous supports were tested for treatment of target pharmaceuticals and their metabolites under UV-LED exposure, a potential low energy and cost effective alternative to conventional UV lamps. Immobilization was completed using two different methods: (1) dip coating of TiO2 onto quartz fiber filters (QFT) or (2) thermal-chemical oxidation of porous titanium sheets (PTT). Comparison against experimental controls (dark QFT, dark PTT, and photolysis using UV-LED only) showed that UV-LED/PTT and UV-LED/QFT treatments have the potential to reduce the concentrations of the target compounds. However, the treatments were found to be selective, such that individual pharmaceuticals were removed well using QFT and PTT but not both. The complementary treatment behavior is likely driven by electrostatic interactions of charged compounds with the membranes. QFT membranes are negatively charged at the experimental pH (4.5-5) while PTT membranes are positively charged. As a result, cationic compounds interact more with QFT while anionic compounds with PTT. Neutral compounds, however, were found to be recalcitrant under any treatment conditions suggesting that ionic interactions were important for reactions to occur. This behavior can be advantageous if specificity is required. The behavior of pharmaceutical metabolites is similar to the parent compounds. However, isomeric metabolites of atorvastatin with functional groups in para and ortho configurations behave differently, suggesting that the positioning of functional groups can have an impact in their interaction with the immobilized TiO2. It was also apparent that PTT can be reused after cleaning by heat treatment. Overall, these newly synthesized membrane materials have potential applications for treatment of trace organic contaminants in water.

Simulation of the fate of selected pharmaceuticals and personal care products in a highly impacted reach of a Canadian watershed.

Municipal wastewater treatment plants (WWTPs) dispose of numerous trace organic contaminants in the receiving waters that can impact biological function in aquatic organisms. However, the complex nature of WWTP effluent mixtures and a wide variety of potential mechanisms that can alter physiological and reproductive development of aquatic organisms make it difficult to assess the linkages and severity of the effects associated with trace organic contaminants. This paper describes a surface water quality modeling exercise that was performed to understand the relevant contaminant fate and transport processes necessary to accurately predict the concentrations of trace organic compounds present in the aquatic environment. The target compounds modeled include a known antiandrogenic personal care product (triclosan) and selected pharmaceuticals (venlafaxine, naproxen, and carbamazepine). The WASP 7.5 model was adapted and calibrated to reflect approximately ten kilometers of reach of the Grand River watershed that is highly influenced by a major urban WWTP. Simulation of the fate and transport of the target compounds revealed that flow-driven transport processes (advection and dispersion) greatly influenced the behavior of the target contaminants in the aquatic environment. However, fate mechanisms such as photolysis and biodegradation can play an important role in the attenuation of some compounds. The exception was carbamazepine where it was shown to act as a conservative tracer compound for wastewater specific contaminants in the water phase. The calibrated water quality model can now be employed in a number of future applications. Prediction of fate and transport of other trace organic contaminants across the watershed and assessment of the performance of WWTP infrastructure upgrades in the removal of these compounds are just a few examples.