Quantification of multi-class antibiotics by UHPLC–MS/MS analysis combined with salt-assisted acetonitrile extraction: comparative evaluation of dairy and poultry manure

ABSTRACT

A comprehensive multiresidue method for the analysis of 33 antibiotics from 7 prevalent classes was comparably investigated for both dairy and poultry manure samples, which can be important pollution sources for the release of antibiotics into the environment. Following salting-out-assisted extraction with acetonitrile, the antibiotics were quantified with ultrahigh-performance liquid chromatography tandem mass spectrometry without a clean-up step. By changing the composition of the mobile phase for chromatography, a pronounced signal enhancement was achieved not only for tetracyclines (TCs) but also for other groups of antibiotics in the manure samples. Although the physicochemical properties of selected antibiotics were quite different, the apparent recovery values from dairy and poultry manure samples by using an extraction solvent comprising McIlvaine buffer and ethylenediaminetetraacetic solution at pH 3 were 86–121% and 89–113%, respectively. Apparent recovery of the antibiotics was not remarkably affected by the extraction solvent over a wide range of pH values, with the exception of the recovery of TC antibiotics from poultry manure, which was in the 53–55% range at pH 8. Furthermore, the poor performance of the analytical method for a few of the antibiotics in poultry manure was correlated with high metal and organic contents of the complicated matrix. The high suppression effects of co-eluted matrix components were compensated by constructing matrix-matched calibration curves and by using internal standards. Simultaneous quantification of seven different antibiotic classes with low limit of detection values varying from 0.38 to 31 μg kg^?1 for dairy manure and from 0.32 to 5.85 μg kg^?1 for poultry manure facilitated their monitoring. The application of the developed analytical method to dairy, broiler and layer-hen manure samples from confined animal feeding operations showed that a wide variety of antibiotics at high concentrations were found in broiler manure.     

Separation and preconcentration of mercury in water samples by ionic liquid supported cloud point extraction and fluorimetric determination

We have developed a cloud point extraction procedure based on room temperature ionic liquid for the preconcentration and determination of mercury in water samples. Mercury ion was quantitatively extracted with tetraethyleneglycol-bis(3- methylimidazolium) diiodide in the form of its complex with 5,10,15,20-tetra-(4-phenoxyphenyl)porphyrin. The complex was back extracted from the room temperature ionic liquid phase into an aqueous media prior to its analysis by spectrofluorimetry. An overall preconcentration factor of 45 was accomplished upon preconcentration of a 20?mL sample. The limit of detection obtained under the optimal conditions is 0.08?μg mL^?1, and the relative standard deviation for 10 replicate assays (at 0.5?g mL^?1 of Hg) was 2.4%. The method was successfully applied to the determination of mercury in tap, river and mineral water samples.

Use of pyrocatechol violet modified sodium dodecyl sulfate coated on alumina for separation and preconcentration of uranium(VI)

A sensitive and selective solid phase extraction procedure for the determination of trace of uranium(VI) has been developed. An alumina-sodium dodecyl sulfate coated on with pyrocatechol violet was used for preconcentration and determination of uranyl ions by spectrophotometry method using Arsenazo III reagent. Sorbed ions were quantitatively eluted using 5 mL of 0.25 mol L⁻¹ HNO₃. The effects of parameters such as pH, amount of alumina, amount of ligand, flow rate, type and concentration of elution agent were examined. The capacity of the sorbent for U(VI) was found to be 0.92 mmol g⁻¹. The relative standard deviation was 1.28% for 10 replicate determinations of U(VI) ion in a solution with a concentration of 1.0 μg mL⁻¹. The practical applicability of the developed sorbent was examined using synthetic and real samples such as standard reference material 2709 (San Joaquin Soil) and 2711 (Montana Soil).     

Acylation of (<Emphasis Type="Italic">R,S</Emphasis>)-1-phenylethanol with ethyl acetate over an immobilized enzyme

Acylation of (R,S)-1-phenylethanol, which is a product of acetophenone hydrogenation, over a Pd-supported catalyst, was studied in ethyl acetate with an immobilized lipase. It was demonstrated that in the presence of hydrogen and Pd/C in the reaction medium the (R,S)-1-phenylethanol acylation rate is not hindered, whereas the selectivity was strongly altered in the latter case, leading to significant amounts of side products.     

Design of meloxicam and lornoxicam transdermal patches: Preparation, physical characterization, ex vivo and in vivo studies

Transdermal patches of meloxicam (MX) and lornoxicam (LX) were aimed to be prepared in order to overcome their side effects by oral application. The strategy was formulation of optimized films to prepare transdermal patches by determination of physical properties and investigation of drug-excipient compatibility. As the next step, in vitro drug release, assesment of anti-inflammatory effect on Wistar Albino rats, ex vivo skin penetration and investigation of factors on drug release from transdermal patches were studied. Hydroxypropyl methylcellulose (HPMC) was concluded to be suitable polymer for formulation of MX and LX transdermal films indicating pharmaceutical quality required. MX and LX transdermal patches gave satisfactory results regarding to the edema inhibition in the assessment of anti-inflammatory effect. MX was found out to be more effective compared to LX on relieving of edema and swelling. These results were supported by data obtained from ex vivo penetration experiments of drug through rat skin. Indicative parameters like log P, molecular weight and solubility constraint on penetration rate of drugs also indicated good skin penetration. Transdermal patches of MX and LX can be suggested to be used especially for the immediate treatment of inflammated area since it displays anti-inflammatory effect, soon.     

Stereo-selectivity in a cyclotriphosphazene derivative bearing an exocyclic P-O moiety

Nucleophilic substitution reactions of N(3)P(3)Cl(4)[O(CH(2))(2)NCH(3)], (1) with the sodium salts of mono- and di-functional alcohols [methanol (2), phenol (3), tetraethyleneglycol (4) and 1,3-propanediol (5)] were carried out in order to investigate a possible directing effect of the spiro O-moiety on the formation of mono-substituted (2a, 3a), non-geminal di-substituted (2c, 3c) and ansa (4a, 5a) derivatives. Compounds isolated from the reactions were characterized by elemental analysis, mass spectrometry, (1)H and (31)P NMR spectroscopy and X-ray crystallographic analysis showed that the substituent OR in compounds (2a, 3a and 2c, 3c) and the ansa-ring in compounds (4a, 5a) formed cis to the P-O moiety of the exocyclic [O(CH(2))(2)NCH(3)] spiro ring. The formation of products (2a-d, 3a-d, 4a, 5a and 5b) was quantified from the (31)P NMR spectra of the reaction mixtures, which showed an overwhelming preference for derivatives (2a, 3a, 2c, 3c, 4a, 5a) with the substituent cis to the P-O moiety of the exocyclic spiro ring (2a, 3a, 2c, 3c, 4a, 5a), except for reaction with 1,3-propanediol where the six-membered ring spiro derivative (5b) was about three times more abundant than the eight-membered ring ansa-derivative (5a). Overwhelming formation of products with the substituent cis to the exocyclic P-O moiety is proof that the cation-assisted mechanism is responsible for the stereo-selectivity in the reactions with alkoxides.     

Laser micro-machined semi-slinky like MEMS structures: Novel interface coolers

Laser micro-machining has recently been considered a precision and reproducible manufacturing technique in MEMS fabrication because of the superior characteristics of a focused laser beam. It is not only a unique tool but also an invisible optical drill. The aim of the present paper is two-fold: to manufacture novel miniaturized titanium 3D MEMS surface structures in order to increase the cooling performance. Second is to find the behaviors of the operational parameters which controlling the laser-material interaction mechanisms and also suggest the best adjustments in order to achieve this novel semi-slinky like spiral MEMS surface structures with using a 20 W ytterbium fiber laser. Pure titanium micro-MEMS product which has novel interface coolers was manufactured using a ytterbium fiber laser (λ=1060 nm) with 40 ns pulse duration. Best adjustments were, respectively, the pulse duration: 40 ns, the pulse energy: 0.4 mJ, the laser scanning speed: 336.1 mm/s, the peak power density: 17.46 ? 10⁸ W/cm².     

Sampling hazelnuts for aflatoxin: uncertainty associated with sampling, sample preparation, and analysis

The variability associated with the aflatoxin test procedure used to estimate aflatoxin levels in bulk shipments of hazelnuts was investigated. Sixteen 10 kg samples of shelled hazelnuts were taken from each of 20 lots that were suspected of aflatoxin contamination. The total variance associated with testing shelled hazelnuts was estimated and partitioned into sampling, sample preparation, and analytical variance components. Each variance component increased as aflatoxin concentration (either B1 or total) increased. With the use of regression analysis, mathematical expressions were developed to model the relationship between aflatoxin concentration and the total, sampling, sample preparation, and analytical variances. The expressions for these relationships were used to estimate the variance for any sample size, subsample size, and number of analyses for a specific aflatoxin concentration. The sampling, sample preparation, and analytical variances associated with estimating aflatoxin in a hazelnut lot at a total aflatoxin level of 10 ng/g and using a 10 kg sample, a 50 g subsample, dry comminution with a Robot Coupe mill, and a high-performance liquid chromatographic analytical method are 174.40, 0.74, and 0.27, respectively. The sampling, sample preparation, and analytical steps of the aflatoxin test procedure accounted for 99.4, 0.4, and 0.2% of the total variability, respectively.