Anastasia Zotou

Determination of biogenic amines as dansyl derivatives in alcoholic beverages by high-performance liquid chromatography with fluorimetric detection and characterization of the dansylated amines by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry.

A sensitive high-performance liquid chromatographic method for the simultaneous determination of 11 biogenic amines has been developed. The method involves addition of an internal standard (1,7-diaminoheptane), pre-column dansylation of the amines and subsequent solid-phase extraction of the derivatives through C18 cartridges. The dansylamides were separated on an Inertsil ODS-3 column (250 x 4 mm I.D., 5 microm) using a 35-min gradient elution with a binary system of acetonitrile-water, a flow-rate of 1 ml min(-1) and fluorescence detection at excitation and emission wavelengths of 320 and 523 nm, respectively. The identity of the dansyl derivatives was confirmed by liquid chromatography-atmospheric pressure chemical ionization mass spectrometry. Linearity of derivatization was obtained for concentrations ranging from 0.008 to 40.0 mg l(-1). The within- and between-day relative standard deviations ranged from 0.2 to 7.6% and 0.3 to 8.6%, respectively. The overall process was successfully applied to identify and quantify biogenic amines in white-, red- and Retsina Greek wines and Greek beers, after treatment with polyvinylpyrrolidone.

Sensitive LC determination of ciprofloxacin in pharmaceutical preparations and biological fluids with fluorescence detection

A simple and highly sensitive isocratic reversed-phase high-performance liquid chromatographic method (RP-HPLC) has been developed for the determination of ciprofloxacin. Separation of ciprofloxacin and anthranilic acid (internal standard) was achieved on a Kromasil 100, C(18), 5 microm (250 x 4.6 mm i.d.) reversed-phase column, using fluorescence detection with lambda(exc)=300 nm and lambda(emi)=458 nm. The mobile phase consisted of acetonitrile-methanol-acetate buffer (pH 3.60; 0.05 M) (10:30:60 v/v/v) containing 1% v/v acetic acid. The analysis was performed in less than 9 min, with a flow rate of 0.8 ml min(-1). A rectilinear relationship was observed for concentrations between 0.005 and 1.0 microg ml(-1) of ciprofloxacin in aqueous standard solutions and serum and the detection limit was 20 pg injected on-column. The intra- and inter-day relative standard deviation (n=8) ranged from 1.6 to 2.6% and from 1.9 to 4.8%, respectively, calculated at three concentration levels of standard solutions. Direct measurements of ciprofloxacin in pharmaceutical preparations and in serum, after precipitation of proteins, were performed with high precision and accuracy. The application of the method to urine samples involved a solid-phase extraction treatment of the samples using C(18) cartridges. The linear working range in urine extended from 0.05 to 2.0 microg ml(-1) and the detection limit was 0.2 ng injected on-column.

LC-determination of five paraben preservatives in saliva and toothpaste samples using UV detection and a short monolithic column

The present study reports the development and application of an HPLC-UV method for the simultaneous separation and determination of five paraben preservatives (methyl-, ethyl-, propyl-, n-butyl- and iso-butyl-paraben) in real samples. All analytes were separated efficiently in less than 20 min using a simple H(2)O:ACN linear gradient and a short monolithic column (50 mm x 4.6mm i.d.) at a flow rate of 3.0mL min(-1). Phenoxyethanol was used as chromatographic internal standard. The method was validated for linearity, limits of detection and quantification, accuracy and precision. Human saliva and toothpaste samples were analyzed after SPE pretreatment on Licrolut RP-18 cartridges. The detection limits varied between 0.1 and 0.3 mg L(-1) in all cases and the percent recoveries between 86 and 113%.

Determination of biogenic amines in wines and beers by high performance liquid chromatography with pre-column dansylation and ultraviolet detection

SummaryA sensitive high performance liquid chromatographic method for the simultaneous determination of eleven biogenic amines, using 1,7-diaminoheptane as internal standard, has been developed. The method involves pre-column derivatization of the amines with dansyl chloride and subsequent solid phase extraction of the derivatives through C18 cartridges. The derivatization and solid phase extraction procedures were optimized. The separation of dansylamides was achieved on an Inertsil ODS-3 column (250×4 mm I.D. 5 μm) using a 35-min gradient elution method with a binary system of acetonitrile-water, a flow rate of 1 mL.min1 with UV detection at 254 nm. Linearity of derivatization was obtained for concentrations ranging from 0.025 to 3.0 mg.L1. The within- and between-day relative standard deviations ranged from 0.4 to 5.7% and 0.6 to 7.3% respectively. The overall process was successfully applied to identify and quantify biogenic amines in white, red and Retsina Greek wines and Greek beers, after their treatment with polyvinylpyrrolidone.

An overview of recent advances in HPLC instrumentation

This review highlights the fundamentals and the most prominent advances in the field of HPLC instrumentation over the last decades. Fundamental aspects and practical considerations of column switching, conventional (heart-cut) and comprehensive two-dimensional LC are presented. Different aspects of microcolumn- and nanoliquid-chromatography are reviewed. Recent progress in column technology and the demands and developments in instrumentation and accessories for miniaturized LC are also discussed. In the field of miniaturization, particularly in chip-based nano-LC systems, some aspects on micro-fluidic chip fabrication, using particle-packed HPLC microchips or polymer-based monoliths, are addressed. An introduction to ultra performance LC (UPLC) is also presented.

Simultaneous Reversed-Phase Gradient-HPLC Analysis of Anthranilic Acid Derivatives in Anti-Inflammatory Drugs and Samples of Biological Interest

Abstract A simple, rapid and sensitive reversed-phase gradient High-Performance Liquid Chromatographic (HPLC) method is proposed for the determination of anthranilic acid derivatives in anti-inflammatory drugs and biological fluids. HPLC analyses are performed with a Lichrosorb-RP 18, 10 μm, 250×4 mm I. D., column employing gradient elution for the development of the chromatogram. The gradient system is formed with the following solutions: A = 0.065M ammonium acetate and B = methanol. The flow rate is 0.8 ml/min and the detection is achieved at 282 nm. The retention time is 4.63 min for flufenamic, 4.99 min for mefenamic and 5.46 min for tolfenamic acid. The absolute detection limits are 0.5 ng for flufenamic acid, 0.7 ng for mefenamic acid and 1.0 ng for tolfenamic acid. The linearity is observed up to 70 ng for the flufenamic acid, 70 ng for the mefenamic acid and 80 ng for the tolfenamic acid injected. The method involves the use of solid phase extraction for sample clean-up and subsequent separation o...

Ethyl propiolate as a post-column derivatization reagent for thiols: development of a green liquid chromatographic method for the determination of glutathione in vegetables.

The present study reports the development, validation and application of a new green liquid chromatographic method for the determination of glutathione (GSH) in vegetable samples. In this work we introduce-for the first time-ethyl propiolate (EP) as an advantageous post-column derivatization reagent for thiolic compounds. GSH (t(R)=6.60 min) and N-acetylcysteine (NAC, internal standard) (t(R)=11.80 min) were separated efficiently from matrix endogenous compounds by using a 100% aqueous mobile phase (0.1%, v/v CH(3)COOH in 1 mmol L(-1) EDTA, Q(V)=0.5 mL min(-1)) and a Prevail(®) reversed phase column that offers the advantage of stable packing material in aqueous mobile phases. The parameters of the post-column reaction (pH, amount concentration of the reagent, flow rates, length of the reaction coil and temperature) were studied. The linear determination range for GSH was 1-200 μmol L(-1) and the LOD was 0.1 μmol L(-1) (S/N=3). Total endogenous GSH was determined in broccoli, potato, asparagus and Brussels sprouts using the standards addition approach. The accuracy was evaluated by both recovery experiments (R=91-110%) and comparison to an o-phthalaldehyde/glycine corroborative post-column derivatization fluorimetric method.

LC of sulfonamide residues in poultry muscle and eggs extracts using fluorescence pre-column derivatization and monolithic silica column

A new, rapid, sensitive and selective HPLC method with fluorescence detection is described for the simultaneous determination of 12 sulfonamides, in the presence of putrescine as internal standard, after pre-column derivatization with fluorescamine. The drugs were separated on a Chromolith Performance RP-18 column (100x4.6 mm), using a gradient elution with a binary mobile phase of methanol/0.05 M acetate buffer (pH 3.4). Linearity of derivatization was obtained for concentrations from 3.0 to 300 microg/L in standard solutions. The whole procedure was evaluated and fully validated, according to the European Union Decision 2002/657/EC, for the determination of sulfonamides in turkey muscle and hen eggs following SPE. The LODs varied from 2 to 17 microg/kg in turkey and 2 to 15 microg/kg in egg samples. The average recoveries ranged between 96.9-108.6% in turkey muscle and 96.0-108.4% in egg samples, respectively.

Optimization and validation of a dissolution test for selegiline hydrochloride tablets by a novel rapid HPLC assay using a monolithic stationary phase.

The present study reports the optimization and validation of a dissolution test for selegiline.HCl tablets using a new high-performance liquid chromatographic (HPLC) method. Rapid separation of the analyte from sample matrix was achieved in less than 60s using a Cromolith RP-18e monolithic column using UV detection at 220 nm. Thorough validation of the assay based on pre-defined criteria included linearity, LOD/LOQ, accuracy, precision, selectivity and ruggedness. The dissolution test was optimized in terms of dissolution medium, basket (type I)/paddle (type II) agitation and rotation speed. Its ruggedness was also validated. The presented analytical and dissolution procedures are currently being applied in the quality and stability control of Cosmopril tablets (5mg/tablet selegiline.HCl, Cosmopharm Ltd., Korinthos, Greece).

Determination of anatoxin-a and homoanatoxin in blue—green algal extracts by high-performance liquid chromatography and gas chromatography—mass spectrometry

The production of cyanobacterial toxins as anatoxin-a in the UK by blue—green algae such as Oscillatoria and Anabaena flos-aquae is a potential health hazard, especially to animals, birds and fish. A sensitive reversed-phase ion-pair high-performance liquid chromatographic (RP-HPLC) method is described for the measurement of the neurotoxins anatoxin-a (AnTx) and homoanatoxin (HomoAnTx) in the presence of lyophilized algal extract. A base-deactivated C18 column material was used with acetonitrile—phosphate buffer (pH 3) and sodium dodecyl sulfate as ion-pair reagent with ultraviolet detection at 227 nm. Linear calibrations were obtained between 2 and 93 ng on-column for AnTx·HCI and 2–112 ng on-column for HomoAnTx·HCI with limits of detection of 1 and 2 ng on-column, respectively. A sample of Oscillatoria bloom material collected from Loch Insh, Scotland, in 1991 was found by this method to contain approximately 0.8 mg of AnTx·HCl per gram of lyophilized extract. Homoanatoxin was not present. The identity of AnTx was confirmed by the isolation of the AnTx peak by RP-HPLC, its derivatization to N-butylAnTx and its analysis by RP-HPLC and gas chromatography—mass spectrometry.