Determination of fenpyroximate in apples by supercritical fluid extraction and packed capillary liquid chromatography with UV detection

A method using off-line supercritical fluid extraction (SFE) and micro liquid chromatography (μLC) with UV detection at 260 nm, was developed for selective determination of fenpyroximate in apple samples. The packed capillary liquid chromatography method utilises 20 μl injection volumes with on-column focusing. A 350×0.32 mm capillary column packed with Kromasil 100-C₁₈ of 5 μm particle size was used with a mobile phase of acetonitrile–10 mM ammonium acetate (85:15, v/v) at a flow of 5 μl/min. A two-step SFE procedure was used to extract fenpyroximate selectively in 2 g apple samples, with Hydromatrix (HMX) added as a water absorbent at a 1:1 (w:w) ratio. Fenpyroximate was extracted at 200 bar and 90°C for 15 min using carbon dioxide at a flow of 2 ml/min, and solvent trapping collection in 10 ml acetonitrile. The volume of the acetonitrile extract was reduced by evaporation and water was added to a final composition of acetonitrile–water (40:60, v/v). The resulting 2.0 ml solution was filtered using a 0.45 μm poly(vinylidene difluoride) syringe filter before μLC analysis. Validation of the method was accomplished with apple samples spiked with fenpyroximate, covering the range of 0.1 to 1.0 μg/kg. The within-day and between-day repeatabilities were in the range 4–18% relative standard deviation. Accuracy, measured as recovery, was found to be approximately 60%. Apple samples from a field treated with fenpyroximate were analysed. None of the samples contained fenpyroximate above the quantification level.     

1/d corrections for interacting spinless fermions: One-particle properties

One-particle properties of the spinless fermion model with repulsion at half filling are calculated within an approach correct to first order in the inverse of the lattice dimensiond. Continuity of the limitd requires a scaling of the nearest-neighbour hopping proportional to and of the nearest-neighbour interaction proportional to 1/d. Due to this scaling the Hartree approximation becomes exact in infinite dimensions. We show that 1/d corrections comprise the Fock diagram and the local correlation diagram in the self-consistent Dyson equation. This approach is applied to simple-cubic systems in dimensiond=1, 2 and 3. Ground state properties and the charge-density wave phase diagram are calculated. AtT=0 the inclusion of 1/d terms gives only small corrections to the leading Hartree contribution ind=2, 3. ForT>0, however, the 1/d corrections are important. They lead to a non-negligible reduction of the critical temperature. Ind=1 the 1/d corrections are very large, but they do not succeed in removing the spurious phase transition atT>0. The 1/d approach provides a good and tractable approximation ind=3 and probably ind=2, which allows also further systematic improvement.     

Liquid-phase microextraction and capillary electrophoresis of citalopram, an antidepressant drug

A newly developed disposable device for liquid-phase microextraction (LPME) was evaluated for the capillary electrophoresis (CE) of the antidepressant drug citalopram (CIT) and its main metabolite N-desmethylcitalopram (DCIT) in human plasma. CIT and DCIT were extracted from 1 ml plasma samples through hexyl ether immobilised in the pores of a porous polypropylene hollow fibre and into 25 microl of 20 mM phosphate buffer (pH 2.75) present inside the hollow fibre (acceptor phase). Prior to extraction, the samples were made strongly alkaline in order to promote LPME of the basic drugs. Owing to the high ratio between the volumes of sample and acceptor phase, and owing to high partition coefficients, CIT and DCIT were enriched by a factor of 25 to 30. In addition, sample clean-up occurred during LPME since salts, proteins and the majority of endogenic substances were unable to penetrate the hexyl ether layer. Since the extracts were aqueous, they were injected directly into the CE instrument. Limits of quantification (S/N= 10) for CIT and DCIT in plasma were 16.5 ng/ml and 18 ng/ml respectively, while the limits of detection (S/N=3) were 5 ng/ml and 5.5 ng/ml respectively. This enabled CIT (and DCIT) to be analysed within the therapeutic range by LPME-CE and detection limits were comparable with previously reported HPLC methods.     

Smart sampling as the “Spot-on” Method for LC-MS protein analysis from dried blood spots

This perspective explores the feasibility of smart sampling with dried blood spots for the determination of proteins and peptides from human biomatrices using liquid chromatography coupled to mass spectrometry for clinical purposes. The focus is on innovative approaches to transform filter paper from a mere sample carrier to an active element in sample preparation, with the aim of reducing the need for extensive and intensive sample preparation in the conventional sense. Specifically, we discuss the use of modified cellulose to integrate sample preparation at an early stage of sample handling. The use of paper immobilized with either trypsin or monoclonal antibodies for protein digestion and affinity clean-up is discussed as a potential benefit of starting sample preparation instantly at the moment of sampling to optimize time efficiency and enable faster analysis, diagnosis, and follow-up of patients.     

Sports drug testing using immuno-MS: clinical study comprising administration of human chorionic gonadotropin to males

The applicability of a mass spectrometry (MS)-based method for determination of various forms of human chorionic gonadotropin (hCG) in doping analysis was demonstrated. A clinical study involving the hCG-containing pharmaceuticals Pregnyl and Ovitrelle was carried out, comprising a single injection of one pharmaceutical per participant to a total of 24 healthy male voluntaries. Hereafter, serum and urine samples were collected over a period of 14 days. The analysis of the samples using immuno-MS demonstrated elimination profiles of intact hCG for both pharmaceuticals, with last day of detection following administration at day 7 in serum, and at day 10 in urine, at limit of detections as defined by the World Anti-Doping Agency. Furthermore, the method allowed detection and differentiation of the various forms of hCG known to be present in serum and urine as a function of metabolism. For both pharmaceuticals, only the intact hCG was detected in serum, whereas in urine the injection of Pregnyl as hCG source (containing urinary hCG, i.e., most hCG variants) was shown to generate a more complex hCG variant pattern compared to Ovitrelle (contains only intact hCG). By detecting hCG using this MS-based approach in doping analysis, strong analytical evidence is provided minimizing the risk of false-positive and false-negative results.     

A New Tool for Eliminating Indoor Air Quality Complaints

Poor indoor air quality (IAQ) can cause a variety of health problems for building occupants including headaches, respiratory problems, eye irritation and fatigue. Traditional IAQ measurements often fail to identify the root cause of the problems and solutions remain elusive. A new IAQ metric, ultrafine particles, is shown to have a high correlation with complaint areas. Researchers are studying the toxicology of these tiny pollutants on animals and humans. Ultrafine particles are defined as particles smaller than 100nm diameter; nanoparticles, those smaller than 50nm diameter, are a subset of ultrafine particles. A battery-powered, portable condensation particle counter (CPC) can be used to quickly identify the source and transport pathways of ultrafine particle contaminants so they can be eliminated or controlled. The CPC condenses isopropyl alcohol on the particles to grow them to an optically detectable size. The hand-held instrument is fast responding, has a wide concentration range, and can log data to detect trends and short-term excursions. Adding the metric of ultrafine particles may become very important to IAQ investigations in the future.