Hydrogen peroxide oxidation for in situ remediation of trichloroethylene – from the laboratory to the field

In this paper we present the remediation possibilities of a trichloroethylene contaminated site of a former metalworking plant in Hungary, where high TCE concentration (150 μg/L to 35.000 μg/L) was detected in the groundwater. Lab-scale experiments were performed to compare the potential bioremediation technology-alternatives eg.: enhanced biodegradation; pump & treat by UV irradiation (photodegradation); in situ chemical oxidation (ISCO) applying different oxidants (KMnO4, Na2S2O8 and H2O2). The lab-scale experiments showed in all cases reduction of the TCE-concentration of the water. Comparing the removal efficacy and concerning the time requirement ISCO was the most effective in laboratory studies

Assessing Toxicity of Organic Aquatic Micropollutants Based on the Total Chlorophyll Content of Lemna minor as a Sensitive Endpoint

The present study examined the chlorophyll content in a 7-day contact time experiment series. Lemna minor was exposed to caffeine, benzophenone, bisphenol A, 3,4-dichlorophenol, metamizole-Na, Na-diclofenac, acetochlor, atrazine, diuron, metazachlor and metolachlor to find a convenient sensitive response to the tested chemicals including some emerging micropollutants. The results demonstrated the differences in sensitivity to the tested micropollutants. As anticipated the industrial chemicals and the pesticides were the most toxic. The lowest observed effect concentration (LOEC) values determined for 3,4-dichlorophenol, acetochlor, diuron, metazachlor and metolachlor were 2.5 µg/L, 0.05 µg/L, 0.5 µg/L, 5 µg/L and 0.5 µg/L, respectively. These values were comparable with the environmental concentrations reported in literature. Our study provides valuable information on the feasibility of Lemna minor total chlorophyll method as a sensitive and reliable bioassay for testing toxicity at µg/L range and it may support risk assessment of organic micropollutants in freshwater ecosystems

How Does Experimental Design Modify the Result of Daphnia magna Heartbeat Rate Test? ─ Analyses of Factors Affecting the Sensitivity of the Test System

Development of an unconventional test method involves usually the comparison of biological responses under a variety of test conditions. The quality of these biological methods relies on an appropriate experimental design. The Daphnia magna heartbeat rate as a physiological endpoint for assessing aquatic pollution has been of minor interest so far; nonetheless, this could be an early and sensitive indicator of the harmful effect of micropollutants. Our aim was to set up the optimal experimental design of the heartbeat rate test. The studied factors were the composition of the test medium, the age of the test organism, and the exposure time, at triclosan concentrations between 0.2–2000 μg/L. According to the evaluation of test results the optimal test condition for the heartbeat rate test assumes tap water as test medium, 10-day-old test organisms and 48 h exposure time

In vivo imaging of Aminopeptidase N (CD13) receptors in experimental renal tumors using the novel radiotracer 68Ga-NOTA-c(NGR)

Purpose: Aminopeptidase N (APN/CD13) plays an important role in tumor neoangiogenic process and the development of metastases. Furthermore, it may serve as a potential target for cancer diagnosis and therapy. Previous studies have already shown that asparagine–glycine–arginine (NGR) peptides specifically bind to APN/CD13. The aim of the study was to synthesize and investigate the APN/CD13 specificity of a novel 68Ga-labeled NOTA-c(NGR) molecule in vivo using miniPET. Methods: c[KNGRE]-NH2 peptide was conjugated with p-SCN-Bn-NOTA and was labeled with Ga-68 (68Ga-NOTA-c(NGR)). Orthotopic and heterotopic transplanted mesoblastic nephroma (NeDe) bearing Fischer-344 rats were prepared, on which biodistribution studies and miniPET scans were performed for both 68Ga-NOTA-c(NGR) and amb3 integrin selective 68Ga-NODAGA-[c(RGD)]2 tracers. APN/CD13 receptor expression of NeDe tumors and metastases was analyzed by western blot. Results: 68Ga-NOTA-c(NGR) was produced with high specific activity (5.13–5.92 GBq/lmol) and with excellent radiochemical purity (95%<), at all cases. Biodistribution studies in normal rats showed that uptake of the 68Ga-NOTA-c(NGR) was significantly (p 6 0.05) lower in abdominal organs in comparison with 68Ga-NODAGA-[c(RGD)]2. Both radiotracers were mainly excreted from the kidney. In NeDe tumor bearing rats higher 68Ga-NOTA-c(NGR) accumulation was found in the tumors than that of the 68Ga-NODAGA-[ c(RGD)]2. Using orthotopic transplantation, metastases were developed which showed specific 68Ga-NOTA-c(NGR) uptake. Western blot analysis confirmed the presence of APN/CD13 expression in NeDe tumors and metastases