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1.
J Vet Pharmacol Ther ; 40(2): 200-202, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27292774

ABSTRACT

This study aimed to investigate the pharmacokinetic characteristics of amoxicillin (AMX) in Thai swamp buffaloes, Bubalus bubalis, following single intramuscular administration at two dosages of 10 and 20 mg/kg body weight (b.w.). Blood samples were collected at assigned times up to 48 h. The plasma concentrations of AMX were measured by liquid chromatography-tandem mass spectrometry (LC-MS/MS). The concentrations of AMX in the plasma were determined up to 24 h after i.m. administration at both dosages. The Cmax values of AMX were 3.39 ± 0.18 µg/mL and 6.16 ± 0.18 µg/mL at doses of 10 and 20 mg/kg, respectively. The AUClast values increased in a dose-dependent fashion. The half-life values were 5.56 ± 0.40 h and 4.37 ± 0.23 h at doses of 10 and 20 mg/kg b.w, respectively. Based on the pharmacokinetic data and PK-PD index (T > MIC), i.m. administration of AMX at a dose of 20 mg/kg b.w might be appropriate for the treatment of susceptible Mannheimia haemolytica infection in Thai swamp buffaloes.


Subject(s)
Amoxicillin/pharmacokinetics , Anti-Bacterial Agents/pharmacokinetics , Amoxicillin/administration & dosage , Amoxicillin/blood , Animals , Anti-Bacterial Agents/administration & dosage , Anti-Bacterial Agents/blood , Area Under Curve , Buffaloes/blood , Dose-Response Relationship, Drug , Female , Half-Life , Mannheimia haemolytica/drug effects , Microbial Sensitivity Tests , Pilot Projects
2.
J Vet Pharmacol Ther ; 40(5): 476-485, 2017 Oct.
Article in English | MEDLINE | ID: mdl-27925222

ABSTRACT

The fates of sulfadimethoxine (SDM) for different routes of administration were investigated in muscle tissue of giant freshwater prawns, Macrobrachium rosenbergii, following either intramuscular (i.m.) or gavage administration at a dosage of 50 mg/kg body weight (b.w.). The depletion patterns of SDM were also examined after medicated feed treatment at the feeding concentration of 10 g/kg of feed twice a day at a rate of 1% of total b.w. for five consecutive days. The concentration of SDM in prawn muscle tissue was measured using a high-performance liquid chromatography (HPLC) equipped with ultraviolet detector. Noncompartmental analyses were used to estimate basic pharmacokinetic parameters for the i.m. and gavage data, while a population model was developed to analyze the entire data set including the feed group. Using the Monte Carlo simulations, the withdrawal times (WT) for the orally administered SDM in feed supplement were determined. Maximum concentration of SDM was significantly higher in the i.m. than in the gavage group, and the area under the curve (AUC) value for relative bioavailability following gavage administration was 25.6%. Using Monte Carlo simulation, for a maximum residue limit (MRL) of 0.1 µg/g, the WT for muscle after oral administration of SDM in feed was estimated to be 67 h, while for a MRL of 0.2 µg/g, the WT was estimated to be of 54 h.


Subject(s)
Muscles/metabolism , Palaemonidae/metabolism , Sulfadimethoxine/pharmacokinetics , Administration, Oral , Animals , Chromatography, High Pressure Liquid , Fresh Water , Injections, Intramuscular/veterinary
3.
Mar Pollut Bull ; 201: 116205, 2024 Apr.
Article in English | MEDLINE | ID: mdl-38452629

ABSTRACT

To mitigate marine pollution, we improved the photo-Fenton reaction of modified nanoscale CuO/BiVO4 photocatalysts to resolve the challenge of efficient microplastic degradation in wastewater treatment. Material property analysis and computational results revealed that deposition of CuO onto BiVO4 nanocomposites improved photocatalytic activity by promoting an excess of electrons in CuO and surface charge transfer, resulting in an increased production of e--h+ for ROS generation via H2O2 activation. 1O2 was dominated and identified through quenching experiments, XPS analysis, and EPR. ROS generation increased via H2O2 activation, causing major surface abrasion and increased carbonyl and vinyl indices in microplastics. Treated water had minimal impact on Lycopersicon esculentum Mill. seedling growth but caused considerable mortality in cell lines and Moina macrocopa mortality at greater dosages due to their sensitivity to ions and H2O2 residuals. Overall, this treatment can effectively degrade microplastics, but the dilution of treated water is still needed before being discharged.


Subject(s)
Bismuth , Cladocera , Microplastics , Plastics , Vanadates , Hydrogen Peroxide , Reactive Oxygen Species , Copper , Water , Environment
4.
Mar Pollut Bull ; 205: 116576, 2024 Jun 13.
Article in English | MEDLINE | ID: mdl-38875969

ABSTRACT

The objective of this study was to determine microplastic-antibiotic interaction by examining how heat-activated persulfate decomposed polyamide adsorbed antibiotics and explored the environmental consequences of treated water. Sulfate radicals roughened the microplastic surfaces, significantly enhancing the adsorption capacity of polyamide. The kinetic and isotherm studies provided confirmation that electrostatic interactions were the primary mechanisms, with a minor contribution from H-bonding, highlighting that antibiotic adsorption was prone to occur, especially on the aged surface. Thermodynamic data indicated that the process was spontaneous and exothermic. The results showed significant negative effects of treated water on seed germination, copepod survival, and cell lines at only a higher concentration, due to a decrease in pH and the potential presence of polymer degradates. Our findings revealed the significant impact of decomposed polyamide on the antibiotic adsorption and offered insight into the potential harm that microplastic-treated water might cause to aquatic and marine ecosystems.

5.
J Vet Pharmacol Ther ; 32(3): 229-34, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19646086

ABSTRACT

Fates and residue depletion of enrofloxacin (ER) and its metabolite ciprofloxacin (CP) were examined in giant freshwater prawns, Macrobrachium rosenbergii, following either single oral (p.o.) administration of ER at a dosage of 10 mg/kg body weight (b.w.) or medicated-feed treatment at the feeding concentration of 5 g/kg of feed for five consecutive days. The concentrations of ER and CP in prawn muscle tissues were measured simultaneously using high-performance liquid chromatography (HPLC) equipped with a fluorescence detector. Muscle tissue concentrations of ER and CP were below the detection limit (LOD, 0.015 microg/g for ER; 0.025 microg/g for CP) after 360 and 42 h, following single p.o. administration respectively. Peak muscle concentration (C(max)) of ER was 1.98 +/- 0.22 microg/g whereas CP was measurable at concentrations close to the detection limit of the analytical method after p.o. administration at a single dosage of 10 mg/kg b.w. The concentration of ER in prawn muscle tissue with respect to time was analyzed with a non-compartmental pharmacokinetic model. The elimination half-life and area under the curve of ER were 39.33 +/- 7.27 h and 168.7 +/- 28.7 microg x h/g after p.o. administration at a single dose of 10 mg/kg x b.w. respectively. In medicated-feed treated group, ER was detectable in prawn muscle tissue 11 days postdosing at the dose of 5 g/kg of feed for five consecutive days, which is the value corresponding to the maximum residue limit (MRL) of ER in animal products. The maximum concentrations of ER and CP were 2.77 +/- 0.91 and 0.06 +/- 0.006 microg/g during medicated-feed treatment and postdosing respectively. The values of elimination half-life and absorption half-life of ER after single p.o. administration at a dosage of 10 mg/kg b.w. corresponded well with the values determined from medicated-feed treated group, showing 41.01 +/- 6.62 and 11.36 +/- 3.15 h respectively in M. rosenbergii. Based on data derived from this study, to avoid the ER residue in prawn muscle, it should take at least 11 days postcessation of medicated feed containing ER at the dose concentration of 5 g/kg of feed twice a day at a rate of 1% of total body weight for five consecutive days to wash out the drug from the muscle of M. rosenbergii.


Subject(s)
Anti-Infective Agents/pharmacokinetics , Drug Residues/pharmacokinetics , Fluoroquinolones/pharmacokinetics , Palaemonidae/metabolism , Administration, Oral , Animal Feed , Animals , Anti-Infective Agents/administration & dosage , Chromatography, High Pressure Liquid/veterinary , Ciprofloxacin/administration & dosage , Ciprofloxacin/pharmacokinetics , Enrofloxacin , Fluoroquinolones/administration & dosage , Fresh Water , Muscles/metabolism , Thailand
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