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Phytoremediation of pharmaceuticals
Forróvá, Barbora ; Bělonožníková, Kateřina (advisor) ; Kubíčková, Božena (referee)
Anxiolytics, sedatives, hypnotics and antidepressants are some of the most prescribed pharmaceuticals today. As their consumption increases, there is a growing risk of them leaking into surface water and soil, where they can be accumulated, interfere with key biological processes in animal cells or contaminate the food chain. With this is related an increasing need to find ways to ensure the removal of these substances from contaminated sites. There is a wide range of methods for decontamination, however not all of them are affordable and sufficiently environmentally friendly. Phytoremediation is one of the most environmentally and economically friendly ways used for removing pharmaceuticals and other xenobiotics from the environment. In this work, the effects of the drugs diazepam, rohypnol and trazodone on the antioxidant system of maize (Zea mays, L., cultivar DKC 3969) plants grown under sterile conditions hydroponically in vitro were studied. The effects these drugs had on the plants were monitored through the activity of important antioxidant enzymes, peroxidases and glutathione-S-transferases, as well as through non-enzymatic markers of antioxidant capacity and the content of substances indicative of oxidative stress, malondialdehyde and H2O2. A significant increase in phenolic content was...
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Phytoextraction of benzodiazepines
Rychlovská, Kristýna ; Smrček, Stanislav (advisor) ; Soudek, Petr (referee)
The aim of this study was to carry out experiments with maize (Zea mays) for the purpose of finding out the efficiency of phytoextraction of chosen pharmaceuticals from the nutrient solution. The plants were cultivated for three weeks in a sterile environment. Then was added a nutrient solution enriched with chosen benzodiazepines - diazepam, flunitrazepam, nitrazepam and bromazepam - in concentration 5-10 mg/L. The samples from each plant were taken every day (24 hours) and then were analyzed with HPLC/UV. The efficiency of phytoextraction was evaluated in two ways. The first one as an percentage of a decrease of the concentration of the pharmaceuticals in the solution with time, the second one as an amount of phytoextracted pharmaceutical in milligrames per gram of the plant matter. From the standpoint of the decrease of the concentration was as the most efficient measured the phytoextraction of nitrazepam (74,7 %), less efficient diazepam and bromazepam (55,2 %, respectively 53,9 %) and the least efficient flunitrazepam (38,0 %). When converted to the mass of the plant matter the most efficient was found the phytoextraction of bromazepam (0,08 mg of drug to 1 gram of plant matter), lower efficiency by bromazepam and diazepam (both 0,02 mg) and the lowest again by flunitrazepam (0,01 mg). key...
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Voltammetric determination of diazepam and nordiazepam on meniscus modified silver solid amalgam electrode
Samiec, Petr ; Fischer, Jan (advisor) ; Vyskočil, Vlastimil (referee)
Voltammetric methods for the determination of diazepam (DZ) and nordiazepam (NDZ) were developed. Techniques differential pulse voltammetry (DPV) and DC voltammetry were used for determination of DZ and NDZ at meniscus modified silver solid amalgam electrode (m-AgSAE). The effect of pHa on the intensity of signal was observed in the mixture of Britton-Robinson buffer and methanol (9:1), and in the mixture of 0.1 mol.l−1 NaOH and methanol (9:1). The stability of the signal during repeated measurements in the mixture of 0.1 mol.l−1 NaOH and methanol (9:1), and in the mixture of BR buffer and methanol (9:1) was monitored. Optimal pHa 13.2 of medium of 0.1 mol.l−1 NaOH and methanol (9:1) was used for determination of DZ with DPV and DCV techniques. Optimal pHa 10.1 of medium of BR buffer and methanol (9:1) was used for determination of NDZ with DPV and DCV techniques. Under these conditions linear dependencies calibration were measured. Concentration range of DZ was measured with DCV in range of 10x10−5 - 6x10−6 mol.l−1 and with DPV technique in range of 10x10−5 - 2x10−6 mol.l−1 . Concentration range of NDZ was measured with DCV technique in range of 10x10−5 - 4x10−6 mol.l−1 and with DPV technique in range of 10x10−5 - 2x10−6 mol.l−1 . The limit of detection for DZ was calculated 6.6x10−6 mol.l−1 with DCV and...
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Phytoextraction of benzodiazepines
Rychlovská, Kristýna ; Smrček, Stanislav (advisor) ; Soudek, Petr (referee)
The aim of this study was to carry out experiments with maize (Zea mays) for the purpose of finding out the efficiency of phytoextraction of chosen pharmaceuticals from the nutrient solution. The plants were cultivated for three weeks in a sterile environment. Then was added a nutrient solution enriched with chosen benzodiazepines - diazepam, flunitrazepam, nitrazepam and bromazepam - in concentration 5-10 mg/L. The samples from each plant were taken every day (24 hours) and then were analyzed with HPLC/UV. The efficiency of phytoextraction was evaluated in two ways. The first one as an percentage of a decrease of the concentration of the pharmaceuticals in the solution with time, the second one as an amount of phytoextracted pharmaceutical in milligrames per gram of the plant matter. From the standpoint of the decrease of the concentration was as the most efficient measured the phytoextraction of nitrazepam (74,7 %), less efficient diazepam and bromazepam (55,2 %, respectively 53,9 %) and the least efficient flunitrazepam (38,0 %). When converted to the mass of the plant matter the most efficient was found the phytoextraction of bromazepam (0,08 mg of drug to 1 gram of plant matter), lower efficiency by bromazepam and diazepam (both 0,02 mg) and the lowest again by flunitrazepam (0,01 mg). key...
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Voltammetric determination of diazepam and nordiazepam on meniscus modified silver solid amalgam electrode
Samiec, Petr ; Fischer, Jan (advisor) ; Vyskočil, Vlastimil (referee)
Voltammetric methods for the determination of diazepam (DZ) and nordiazepam (NDZ) were developed. Techniques differential pulse voltammetry (DPV) and DC voltammetry were used for determination of DZ and NDZ at meniscus modified silver solid amalgam electrode (m-AgSAE). The effect of pHa on the intensity of signal was observed in the mixture of Britton-Robinson buffer and methanol (9:1), and in the mixture of 0.1 mol.l−1 NaOH and methanol (9:1). The stability of the signal during repeated measurements in the mixture of 0.1 mol.l−1 NaOH and methanol (9:1), and in the mixture of BR buffer and methanol (9:1) was monitored. Optimal pHa 13.2 of medium of 0.1 mol.l−1 NaOH and methanol (9:1) was used for determination of DZ with DPV and DCV techniques. Optimal pHa 10.1 of medium of BR buffer and methanol (9:1) was used for determination of NDZ with DPV and DCV techniques. Under these conditions linear dependencies calibration were measured. Concentration range of DZ was measured with DCV in range of 10x10−5 - 6x10−6 mol.l−1 and with DPV technique in range of 10x10−5 - 2x10−6 mol.l−1 . Concentration range of NDZ was measured with DCV technique in range of 10x10−5 - 4x10−6 mol.l−1 and with DPV technique in range of 10x10−5 - 2x10−6 mol.l−1 . The limit of detection for DZ was calculated 6.6x10−6 mol.l−1 with DCV and...
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Voltammetric determination of diazepam and nordiazepam on meniscus modified silver solid amalgam electrode
Samiec, Petr ; Fischer, Jan (advisor) ; Vyskočil, Vlastimil (referee)
Voltammetric methods for the determination of diazepam (DZ) and nordiazepam (NDZ) were developed. Techniques differential pulse voltammetry (DPV) and DC voltammetry for determination of both substances at meniscus modified silver solid amalgam electrode (m-AgSAE) were used. Effect of pHa in media of mixture of Britton-Robinson buffer and methanol (9:1) and 0,1 mol.l-1 NaOH was studied. Stability of the signal with repeated measurements in 0,1 mol.l-1 and methanol (9:1) was monitored. Optimal pHa 13,2 of 0,1 mol.l-1 NaOH was used for determination of DZ by DPV and DCV techniques. Optimal pHa 10,2 in media of mixture of Britton-Robinson buffer and methanol (9:1) was used for determination of NDZ by DPV and DCV techniques. Under these conditions were measured linear dependences in the calibration. Concentration range of DZ was measured with DCV in range of 1.10-4 - 6.10-6 mol.l-1 and DPV with DCV technique in range of 1.10-4 - 2.10-6 mol.l-1. Concentration range of NDZ was measured with DCV technique in range of 1.10-4 - 4.10-6 mol.l-1 and DPV technique in range of 1.10-4 - 2.10-6 mol.l-1. The limit of detection was calculated for DZ 6,6 .10-6 mol.l-1 with DCV and 1.10-6 mol.l-1 with DPV. The limit of detection was calculated for NDZ 5,5.10-6 mol.l-1 with DCV and 1,7.10-6 mol.l-1 with DPV. Developed method...
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