Flumequine Research Articles

Activation of ferrate(VI) by ammonia in oxidation of flumequine: Kinetics, transformation products, and antibacterial activity assessment

This paper presents ammonia-enhanced oxidation of flumequine (FLU), a representative fluoroquinolone antibiotic, by ferrate(VI) (FeVIO42−, Fe(VI)). The second-order rate constants (k) without ammonia were 9.34±1.04 and 1.16±0.04M−1s−1 at pH 8.0 and 9.0, respectively. These values of k increased linearly with the concentrations of ammonia ([NH4+]+[NH3]) and were 50.00±6.20 and 14.42±1.44M−1s−1 for 0.01M ammonia at pH 8.0 and 9.0, respectively. Oxidized products (OPs) of FLU in the presence of ammonia were identified using liquid chromatography-high resolution mass spectrometry. When ammonia was present in the solution, the distribution of OPs changed from the profile of OPs obtained in the absence of ammonia. The quantitative microbiological assays of Fe(VI)-treated FLU solutions using Escherichia coli and Bacillus subtilis indicated that Fe(VI) oxidation could effectively eliminate the residual antibacterial activity of FLU. Removal experiments demonstrate that the presence of ammonia could also enhance the removal of FLU from water containing humic acid, river water, and wastewater.

TiO2/ZnO Supported on Sepiolite: Preparation, Structural Characterization, and Photocatalytic Degradation of Flumequine Antibiotic in Aqueous Solution

In this study, TiO2, ZnO, TiO2/ZnO (Ti/Zn), and TiO2/ZnO/Sep (Ti/Zn/Sep) catalysts have been synthesized using sol–gel and chemical precipitation method. Their photocatalytic performances have been compared using Flumequine (FLQ) antibiotic. X-ray diffraction (XRD), Fourier transform infrared spectra (FTIR), scanning electron microscopy (SEM), N2-adsorption, and the determination of a zero point charge has been used to characterize the synthesized catalysts. The degradation studies showed that the catalytic efficiency of Ti/Zn/Sep is higher than that for other catalysts. The operational parameters such as pH, initial FLQ concentration, and catalyst dosage were evaluated. UV–vis and high-resolution mass spectroscopy (HRMS) analyses were used to determine the degradation efficiency and products. ZnO played a major role in the FLQ degradation process, and sepiolite contributed to adsorption of FLQ on the catalyst surface enormously. The catalysts exhibited 11%, 23%, 63%, and 85% degradation efficiency for ZnO, TiO2, Ti/Zn, and Ti/Zn/Sep in the decomposition of FLQ, respectively.

Synergistic effect of aqueous removal of fluoroquinolones by a combined use of peroxymonosulfate and ferrate(VI)

This paper examines for the first time the combined use of ferrate(VI) (FeVIO42−, Fe(VI)) with peroxymonosulfate (PMS) to oxidize four fluoroquinolones (FQs) (flumequine (FLU), enrofloxacin (ENR), marbofloxacin (MAR), and ofloxacin (OFL)) at pH 7.0 and 25.0 °C. The results demonstrate that a combination of PMS and Fe(VI) synergistically enhance removal of FQs compared to the removal seen with either PMS or Fe(VI) alone. The oxidized products (OPs) of the reaction of FLU with the PMS-Fe(VI) system, identified by liquid chromatography high-resolution mass spectrometry (LC-HRMS) techniques, showed transformation products resulted from hydroxylation, ring cleavage, and de-fluorination processes. Thus, the combination of PMS and Fe(VI) can be developed as an innovative oxidative technology to remove contaminants from water.

Antimicrobial Susceptibilities of Flavobacterium psychrophilum Isolates from the Great Lakes Basin, Michigan.

Flavobacterium psychrophilum is a serious pathogen of salmonids worldwide, a matter that is compounded by the lack of effective vaccine preparations. As a result, biosecurity measures and antimicrobial agents remain the only available methods to control diseases caused by F. psychrophilum. It is feared that antimicrobial use may have led to the development of F. psychrophilum strains with reduced susceptibility. Therefore, the primary objective of this study was to determine the antimicrobial susceptibility profiles of 50 F. psychrophilum isolates from Michigan in response to 10 antimicrobial compounds. As recommended by the Clinical and Laboratory Standard Institute and the World Organization of Animal Health, a standardized microdilution broth assay was employed to determine the minimum inhibitory concentrations (MICs) for ampicillin (AMP), gentamicin (GEN), enrofloxacin (ENRO), oxolinic acid (OXO), flumequine (FLUQ), trimethoprim-sulphamethoxazole (SXT), ormetoprim-sulphadimethoxine (PRI), erythromycin (ERY), florfenicol (FFN), and oxytetracycline (OXY). Epidemiological cutoff values were calculated using the normalized resistance interpretation (CONRI) and the ECOFFinder analysis methods (COECOFF). The MIC distributions in response to OXY exhibited bimodality, indicating the presence of isolates with reduced susceptibility in addition to the wild-type isolates. The OXY epidemiological cutoff values (COECOFF <0.06 μg/ml; CONRI <0.12 μg/ml) demonstrated that 24% of Michigan isolates exhibited reduced susceptibility to this commonly used drug. No other antimicrobial exhibited a bimodal distribution of MICs. This study represents the first antimicrobial susceptibility assessment of F. psychrophilum strains recovered from Michigan and contributes valuable data to the worldwide validation efforts to determine universal epidemiological cutoff values of this deadly fish pathogen.

Trace-Level Determination of Oxolinic Acid and Flumequine in Soil, River Bed Sediment, and River Water Using Microwave-Assisted Extraction and High-Performance Liquid Chromatography with Fluorimetric Detection

ABSTRACTThis work presents the optimization of analytical procedures for the determination of two antibiotics, oxolinic acid (OA) and flumequine (FL), in bed sediment, river water, and soil samples. Three extraction methods (microwave-assisted extraction (MAE), ultrasonication, and reflux) were tested, and the highest recoveries were obtained with MAE (94 ± 3% and 95 ± 3% for OA and FL, respectively). A solid-phase extraction (SPE) clean-up step was optimized by comparing two polymeric sorbents: Oasis HLB and Oasis MAX. The final extracts were analyzed by liquid chromatography with fluorimetric detection. Limits of detection (LOD) obtained for OA and FL in soil and sediment ranged from 0.3 to 0.5 µg kg−1. Meanwhile, a novel SPE procedure was also implemented for OA and FL determination in river water samples. It also relied on the use of Oasis MAX, and recovery rates were in the range 90–94%; LODs were 2 ng L−1 for both OA and FL. These methods were applied for the analysis of samples taken in the Seine River basin (France). The obtained results demonstrated the widespread occurrence of OA and FL, at ng L−1 and µg kg−1 levels in water and sediment/soil, respectively, and their persistence in the environment.

Sulfate radical-based oxidation of fluoroquinolone antibiotics: Kinetics, mechanisms and effects of natural water matrices

Widespread occurrence of fluoroquinolone antibiotics (FQs) in surface water, groundwater, soil and sediment has been reported and their remediation is essentially needed. Sulfate radical (SO4−) based advanced oxidation processes (SR-AOPs) are promising technologies for soil and groundwater remediation. In this study, the degradation kinetics, mechanisms, and effects of natural water matrices on heat-activated persulfate (PS) oxidation of FQs were systematically investigated. Experimental results clearly demonstrated that 92% of CIP was removed within 180 min (pH = 7, 60 °C). Higher temperature and lower pH facilitated the degradation of ciprofloxacin (CIP). The piperazine moiety of CIP was identified as the reactive site for SO4− attack by comparison with substructural analogs, flumequine (FLU) and 1-(2-fluorophenyl) piperazine (FPP). A comparison of the degradation of CIP, norfloxacin (NOR), enrofloxacin (ENR) and ofloxacin (OFL) confirmed that the presence of cyclopropane ring also influence the degradation of FQs. Water matrix significantly influenced the degradation of CIP and ENR, and the degradation rate followed the order of Milli-Q water (pH = 7) > groundwater > artificial seawater > artificial surface water > lake water. Degradation products of CIP in different water matrix were enriched by solid phase extraction (SPE) and then analyzed by liquid chromatography-electrospray ionization-triple quadrupole mass spectrometry (LC-ESI-MS/MS). Detailed transformation pathways of CIP were proposed and were compared with respect to different water matrices. Four transformation pathways including stepwise piperazine ring oxidation, OH/F substitution, hydroxylation, and cyclopropane ring cleavage were proposed for CIP degradation. Results clearly show that the water matrix influenced the degradation of FQs appreciably, a phenomenon that should be taken into consideration when applying SR-AOPs for remediation of soil and groundwater contaminated by FQs.

Validation of a Chiral Liquid Chromatographic Method for the Degradation Behavior of Flumequine Enantiomers in Mariculture Pond Water.

In this work, flumequine (FLU) enantiomers were separated using a Chiralpak OD-H column, with n-hexane-ethanol (20:80, v/v) as the mobile phase at a flow rate of 0.6 mL/min. Solid phase extraction (SPE) was used for cleanup and enrichment. The limit of detection, limit of quantitation, linearity, precision, and intra/interday variation of the chiral high-performance liquid chromatography (HPLC) method were determined. The developed method was then applied to investigate the degradation behavior of FLU enantiomers in mariculture pond water samples. The results showed that the degradation of FLU enantiomers under natural, sterile, or dark conditions was not enantioselective. Chirality 28:649-655, 2016. © 2016 Wiley Periodicals, Inc.

Degradation of fluoroquinolone antibiotics by ferrate(VI): Effects of water constituents and oxidized products

The degradation of five fluoroquinolone (FQ) antibiotics (flumequine (FLU), enrofloxacin (ENR), norfloxacin (NOR), ofloxacin (OFL) and marbofloxacin (MAR)) by ferrate(VI) (FeVIO42−, Fe(VI)) was examined to demonstrate the potential of this iron-based chemical oxidant to treat antibiotics in water. Experiments were conducted at different molar ratios of Fe(VI) to FQs at pH 7.0. All FQs, except FLU, were degraded within 2 min at [Fe(VI)]:[FQ] ≤ 20.0. Multiple additions of Fe(VI) improved the degradation efficiency, and provided greater degradation than a single addition of Fe(VI). The effects of anions, cations, and humic acid (HA), usually present in source waters and wastewaters, on the removal of FLU were investigated. Anions (Cl−, SO42−, NO3−, and HCO3−) and monovalent cations (Na+ and K+) had no influence on the removal of FLU. However, multivalent cations (Ca2+, Mg2+, Cu2+, and Fe3+) in water decreased the efficiency of FLU removal by Fe(VI). An increase in the ionic strength of the solution, and the presence of HA in the water, also decreased the percentage of FLU removed by Fe(VI). Experiments on the removal of selected FQs, present as co-existing antibiotics in pure water, river water, synthetic water and wastewater, were also conducted to demonstrate the practical application of Fe(VI) to remove the antibiotics during water treatment. The seventeen oxidized products (OPs) of FLU were identified using solid phase extraction-liquid chromatography-high-resolution mass spectrometry. The reaction pathways are proposed, and are theoretically confirmed by molecular orbital calculations.

Effect of various storage conditions on the stability of quinolones in raw milk

ABSTRACTResearch on the storage stability of antibiotic residues in milk is important for method development or validation, milk quality control and risk assessment during screening, confirmation, qualitative or quantitative analysis. This study was conducted using UPLC-MS/MS to determine the stability of six quinolones – ciprofloxacin (CIP), danofloxacin (DAN), enrofloxacin (ENR), sarafloxacin (SAR), difloxacin (DIF) and flumequine (FLU) – in raw milk stored under various conditions to investigate if quinolones degrade during storage of milk, and finally to determine optimal storage conditions for analysis and scientific risk assessment of quinolone residues in raw milk. The storage conditions included different temperatures and durations (4°C for 4, 8, 24 and 48 h; –20°C for 1, 7 and 30 days; –80°C for 1, 7 and 30 days), thawing temperatures (25, 40 and 60°C), freeze–thaw cycles (1–5), and the addition of different preservatives (sodium thiocyanate, sodium azide, potassium dichromate, bronopol and methanal). Most quinolones exhibited high stability at 4°C for up to 24 h, but began to degrade after 48 h. In addition, no degradation of quinolones was seen when milk samples were stored at –20°C for up to 7 days; however, 30 days of storage at –20°C resulted in a small amount of degradation (about 30%). Similar results were seen when samples were stored at –80°C. Moreover, no losses were observed when frozen milk samples were thawed at 25, 40 or 60°C. All the quinolones of interest, except sarafloxacin, were stable when milk samples were thawed at 40°C once and three times, but unstable after five freeze–thaw cycles. Preservatives affected the stability of quinolones, but the effects differed depending on the preservative and quinolone. The results of this study indicate optimum storage protocols for milk samples, so that residue levels reflect those at the time of initial sample analysis, and should improve surveillance programmes for quinolones in raw milk.

Fast removal of the antibiotic flumequine from aqueous solution by ozonation: Influencing factors, reaction pathways, and toxicity evaluation

As one of the first generation of fluoroquinolone antibiotics, flumequine (FLU) has been detected ubiquitously in surface waters and municipal wastewaters. In light of FLU's possible adverse effects on aquatic species, the removal of this antibiotic has received worldwide attention. In this study, the kinetics, transformation products, mechanisms and toxicity variations of the ozonation process for FLU were systematically determined. The possible effects of solution pH, addition of inorganic ions, dissolved organic matter, and tert-butyl-alcohol (a radical scavenger), as well as the type of water matrices on FLU removal by ozonation, were studied from the perspective of the degradation kinetics. The data obtained suggested that ozone can be used as an effective oxidant for the fast removal of FLU from natural waters. Using liquid chromatography-mass spectrometry, a total of thirteen transformation products of FLU during ozonation were identified, and their specific reaction mechanisms were also proposed. The degradation pathways involving the hydroxylation, decarboxylation and defluorination were tentatively proposed. Meanwhile, the generation of three low-molecular-weight carboxylic acids was also observed. In addition, the potential toxicity of the transformation mixtures of FLU by ozone was evaluated. Overall, this paper can be a unique contribution to the systematic elucidation of the ozonation process of this antibiotic in water.

Cross-Contamination of Residual Emerging Contaminants and Antibiotic Resistant Bacteria in Lettuce Crops and Soil Irrigated with Wastewater Treated by Sunlight/H2O2.

The sunlight/H2O2 process has recently been considered as a sustainable alternative option compared to other solar driven advanced oxidation processes (AOPs) in advanced treatment of municipal wastewater (WW) to be reused for crop irrigation. Accordingly, in this study sunlight/H2O2 was used as disinfection/oxidation treatment for urban WW treatment plant effluent in a compound parabolic collector photoreactor to assess subsequent cross-contamination of lettuce and soil by contaminants of emerging concern (CECs) (determined by QuEChERS extraction and LC-QqLIT-MS/MS analysis) and antibiotic resistant (AR) bacteria after irrigation with treated WW. Three CECs (carbamazepine (CBZ), flumequine (FLU), and thiabendazole (TBZ) at 100 μg L(-1)) and two AR bacterial strains (E. coli and E. faecalis, at 10(5) CFU mL(-1)) were spiked in real WW. A detection limit (DL) of 2 CFU mL(-1) was reached after 120 min of solar exposure for AR E. coli, while AR E. faecalis was more resistant to the disinfection process (240 min to reach DL). CBZ and TBZ were poorly removed after 90 min (12% and 50%, respectively) compared to FLU (94%). Lettuce was irrigated with treated WW for 5 weeks. CBZ and TBZ were accumulated in soil up to 472 ng g(-1) and 256 ng g(-1) and up-taken by lettuce up to 109 and 18 ng g(-1), respectively, when 90 min treated WW was used for irrigation; whereas no bacteria contamination was observed when the bacterial density in treated WW was below the DL. A proper treatment time (>90 min) should be guaranteed in order to avoid the transfer of pathogens from disinfected WW to irrigated crops and soil.

Degradation of flumequine in aqueous solution by persulfate activated with common methods and polyhydroquinone-coated magnetite/multi-walled carbon nanotubes catalysts

In recent years, flumequine (FLU) has been ubiquitously detected in surface waters and municipal wastewaters. In light of its potential negative impacts to aquatic species, growing concern has been arisen for the removal of this antibiotic from natural waters. In this study, the kinetics, degradation mechanisms and pathways of aqueous FLU by persulfate (PS) oxidation were systematically determined. Three common activation methods, including heat, Fe2+ and Cu2+, and a novel heterogeneous catalyst, namely, polyhydroquinone-coated magnetite/multi-walled carbon nanotubes (Fe3O4/MWCNTs/PHQ), were investigated to activate PS for FLU removal. It was found that these three common activators enhanced FLU degradation obviously, while several influencing factors, such as solution pH, inorganic ions (especially HCO3− at 5 mmol/L) and dissolved organic matter extracts, exerted their different effects on FLU removal. The catalysts were characterized, and an efficient catalytic degradation performance, high stability and excellent reusability were observed. The measured total organic carbon levels suggested that FLU can be effectively mineralized by using the catalysts. Radical mechanism was studied by combination of the quenching tests and electron paramagnetic resonance analysis. It was assumed that sulfate radicals predominated in the activation of PS with Fe3O4/MWCNTs/PHQ for FLU removal, while hydroxyl radicals also contributed to the catalytic oxidation process. In addition, a total of fifteen reaction intermediates of FLU were identified, from which two possible pathways were proposed involving hydroxylation, decarbonylation and ring opening. Overall, this study represented a systematical evaluation regarding the transformation process of FLU by PS, and showed that the heterogeneous catalysts can efficiently activate PS for FLU removal from the water environment.

Optimization of the enzymatic elimination of flumequine by laccase-mediated system using response surface methodology

Response surface methodology (RSM) was applied to optimize the removal of flumequine (FLU) from aqueous solution by laccase from Trametes versicolor. Box–Behnken design (BBD) with four variables namely pH, temperature, FLU initial concentration, and 2,2-azinobis(3-ethylbenzthiazoline-6-sulfonic acid) (ABTS) concentration was used to optimize these factors. The results showed that the predicted values for FLU removal were close to the experimental values, and the R2 (0.9967) indicated that the regression was able to give a good prediction of response for the FLU removal process in the studied range. Optimization of the factors levels was carried out in two approaches. At first, all factors were set in the studied range. The selected optimal conditions for the maximum removal of FLU (98.27%) were predicted as: temperature of 39.64°C, pH of 4.06, FLU initial concentration of 90.74 mg L−1, and ABTS concentration of 1.35 mM. Then, the optimization was carried out by minimizing the amount of ABTS, maximizing the FLU initial concentration, and maximizing the removal efficiency. The recommended optimum conditions are: temperature of 39.19°C, pH value of 4.32, FLU initial concentration of 125 mg L−1, and ABTS concentration of 0.28mM with the percentage FLU removal of 77.76%.

Screening method for the determination of tetracyclines and fluoroquinolones in animal drinking water by liquid chromatography with diode array detector.

A liquid chromatography - diode array detector (HPLC-DAD) procedure has been developed for the determination of oxytetracycline (OTC), tetracycline (TC), chlorotetracycline (CTC), doxycycline (DC), enrofloxacin (ENR), ciprofloxacin (CIP), sarafloxacin (SAR) and flumequine (FLU) residues in animal drinking water. This method was applied to animal drinking water. Solid-phase extraction (SPE) clean-up on an Oasis HLB cartridge allowed an extract suitable for liquid chromatographic analysis to be obtained. Chromatographic separation was carried out on a C18 analytical column, using gradient elution with 0.1% trifluoroacetic acid - acetonitrile - methanol at 30°C. The flow-rate was 0.7 mL/min and the eluate was analysed at 330 nm. The whole procedure was evaluated according to the requirements of the Commission Decision 2002/657/EC, determining specificity, decision limit (CCα), detection capacity (CCβ), limit of detection (LOD), limit of quantification (LOQ), precision and accuracy during validation of the method. The recoveries of TCs and FQs from spiked samples at the levels of 10, 100 and 1000 μg/L were higher than 82%. The developed method based on HPLC-DAD has been applied for the determination of four tetracyclines and four fluoroquinolones in animal drinking water samples.

Surface Acoustic Wave Sensor for Selective Detection of Flumequine

A surface acoustic wave (SAW) sensor functionalized with a thin layer of polypyrrole (PPy) molecularly imprinted polymer (MIP) was designed for the selective detection of flumequine (FLU), a fluoroquinolone antibiotic usually used in intensive aquaculture. Contrarily to previous studies, in which immunosensors were developed to detect low levels of fluoroquinolone, here, the recognition layer does not require any special treatment for stability over a long period of time. The detection limit was of order of 10-6 M and the sensitivity was estimated at 9.4 ± 0.4°/mM. Selectivity tests, made with levofloxacin, show that the developed sensor displayed an excellent recognition capacity toward flumequine. Quantum chemical calculations, based on the density functional theory (DFT), have permitted to highlight the nature of interactions between the investigated molecular systems and polypyrrole matrix.

Design of a polypyrrole MIP-SAW sensor for selective detection of flumequine in aqueous media. Correlation between experimental results and DFT calculations

A shear horizontal surface acoustic wave sensor (SH-SAW) operating at 104 MHz was functionalized with a polypyrrole (PPy) molecularly imprinted polymer (MIP) for selective detection of flumequine (FLU) in aqueous media.

Determination of fluoroquinolone antibiotics by microchip capillary electrophoresis along with time-resolved sensitized luminescence of their terbium(III) complexes

We report on the time-resolved detection of the three fluoroquinolone (FQs) antibiotics ciprofloxacin (CIP), enrofloxacin (ENR) and flumequine (FLU). On addition of terbium(III) ions, the terbium(III)-FQs chelates are formed in-situ in an on-capillary derivatization reaction of a microfluidic system. The laser-induced terbium(III)-sensitized luminescence of the chelates is measured at excitation/emission wavelengths of 337/545 nm. The analytes can be separated and quantified within less than 4 min. A solid phase extraction step for analyte preconcentration can be included prior to chelation and microchip capillary electrophoresis. The analytical ranges of the calibration graphs for CIP, ENR and FLU are from 10.6 to 60.0, 10.3 to 51.0, and 11.5 to 58.8 ng mL−1, respectively, and the detection limits are 3.2, 3.1 and 3.6 ng mL−1, respectively. The precision was established at two concentration levels of each analyte and revealed relative standard deviations in the range from 3.0 to 10.2 %. The method was applied to the analysis of FQ-spiked water samples.

Simultaneous Determination of Flumequine and Oxolinic Acid Residues in Aquatic Products Using Pressurized Capillary Electrochromatography

A rapid method for detection of flumequine (FQ) and oxolinic acid (OA) residues from fish tissues was established using pressurized capillary electrochromatography (pCEC). Residual FQ and OA were extracted from fish tissue samples with acidified acetonitrile and purified on an Oasis HLB C18 solid-phase extraction column. The extract was then analyzed by pCEC with the mobile phase (pH = 3) consisting of acetonitrile and 15 mM ammonium acetate (45: 55, v/v, respectively) at the flow rate of 0.07 mL/min, detection wavelength of 324 nm, and applied voltage of −10 kV. Baseline separation of FQ and OA was achieved in 10 min; both drugs showed good linearity in the range of 0.2–5 μg/mL. The recoveries of FQ and OA were between 82 and 92 % (relative standard deviation = 3.63–5.96). The limits of detection for FQ and OA were 0.1 and 0.08 mg/kg, respectively.

Pharmacokinetic/pharmacodynamic evaluation of the efficacy of flumequine in treating colibacillosis in turkeys

Flumequine (FLU) is used in the treatment of systemic bacterial infections in poultry, including colibacillosis, which is a common disease in turkeys. The pharmacokinetic (PK) behavior of FLU administered to 32 healthy turkeys as an oral bolus via gavage or as 10-h pulsed administration in drinking water were compared, using the authorized dose of 15 mg/kg and the double dose of 30 mg/kg. The minimum inhibitory concentrations (MIC) of 235 Escherichia coli field strains isolated from poultry were determined for pharmacodynamics (PD) to develop a PK/PD model. Blood samples were collected at established times over 24 h, and the obtained plasma was analyzed using a liquid chromatography tandem mass spectrometry method that was validated in-house. A monocompartmental model and a noncompartmental model were applied to the data to obtain the PK results. For both types of administration and both dosages, the ratios of the maximum concentration (Cmax)/MIC50 and the area under the plasma concentration-time curve (AUC)/MIC50 achieved were considerably lower than the fluoroquinolone breakpoints usually adopted for efficacy. The Cmax/MIC50 and AUC0–24/MIC50 ratios were, respectively, 0.67 ± 0.09 and 4.76 ± 0.48 and 1.18 ± 0.35 and 7.05 ± 2.40 for the 15 and 30 mg/kg bolus doses, respectively. After 10-h pulsed administration of 15 mg/kg, values of Cmax/MIC50, 0.19 ± 0.02 on d 1 and 0.30 ± 0.08 on d 5 of therapy were obtained, the AUC/MIC50 ratios were 2.09 ± 0.29 and 3.22 ± 0.93 on d 1 and 5, respectively. Higher values were obtained with the doubled dose of 30 mg/kg: the Cmax/MIC50 ratios were 0.49 ± 0.11 on d 1 and 0.69 ± 0.18 on d 5; the AUC/MIC50 ratios were 5.15 ± 1.15 and 6.57 ± 1.92 on d 1 and 5, respectively. Based on these results, FLU administration should be adopted when specific diagnostic findings indicate its efficacy, and revising the dosage scheme to comply with the prudent and responsible use of antimicrobials in veterinary medicine is advisable.

Simultaneous Determination of Danofloxacin and Flumequine in Milk Based on Fluorescence Spectroscopy and Chemometrics Tools

The aim of this paper was to develop a rapid screening method to determine danofloxacin (DANO) and flumequine (FLU) in milk by fluorescence spectroscopy combined with three different chemometric tools. In this study, 2-D fluorescence data and multivariate calibration based on a partial least squares discriminant analysis (PLS-DA) regression were combined to simultaneously qualify and quantify DANO and FLU concentrations in commercial ultra-high-temperature (UHT) sterilized and pasteurized milk. Calibration sets based on the UHT whole milk from brand A were built and performed using a partial least squares (PLS) regression after deproteinization. Prediction sets based on 13 types of milk were analyzed using principal component analysis (PCA), principal PLS-DA, and PLS regression models. The multivariate calibration models were better able to determine the DANO and FLU concentrations than the univariate models, and these models could be applied to other types of milk. In contrast to the PLS-DA, which had good sensitivity and specificity, the PCA yielded less satisfactory results. In the quantitative analysis, the recoveries of the two analytes were reasonable and the root mean square error of prediction was within the acceptable range. The relative standard deviations of the predicted DANO and FLU concentrations on the various testing days were 9.2 and 6.2 %, respectively, demonstrating that the analytical method had a good reproducibility.