THE CHANGING ECONOMIC SPATIAL STRUCTURE OF EUROPE

Many theoretical and practical works aim at describing the spatial structure of Europe, where spatial relations have undergone continuous change. This article gives an overview of models describing the spatial structure of Europe. Their diversity is highlighted by listing of these models, without any claim to completeness. Our study aims at describing the economic spatial structure of Europe with bi-dimensional regression analysis based on the gravitational model. With the help of the gravity model, we get a spatial image of the spatial structure of Europe. With these images, we can justify the appropriateness of the models based on different methodological backgrounds by comparing them with our results. Our goal is not to create and show a new model that overwrites the existing ones, but rather to contribute to understanding the European spatial structure through a new methodological approach

Recurrent Scedosporium apiospermum mycetoma successfully treated by surgical excision and terbinafine treatment: a case report and review of the literature

Background: Scedosporium apiospermum is an emerging opportunistic filamentous fungus, which is notorious for its high levels of antifungal ‑resistance. It is able to cause localized cutaneous or subcutaneous infections in both immu‑ nocompromised and immunocompetent persons, pulmonary infections in patients with predisposing pulmonary diseases and invasive mycoses in immunocompromised patients. Subcutaneous infections caused by this fungus frequently show chronic mycetomatous manifestation. Case report: We report the case of a 70 ‑year ‑old immunocompromised man, who developed a fungal mycetoma‑ tous infection on his right leg. There was no history of trauma; the aetiological agent was identified by microscopic examination and ITS sequencing. This is the second reported case of S. apiospermum subcutaneous infections in Hungary, which was successfully treated by surgical excision and terbinafine treatment. After 7 months, the patient remained asymptomatic. Considering the antifungal susceptibility and increasing incidence of the fungus, Sce - dosporium related subcutaneous infections reported in the past quarter of century in European countries were also reviewed. Conclusions: Corticosteroid treatment represents a serious risk factor of S. apiospermum infections, especially if the patient get in touch with manure ‑enriched or polluted soil or water. Such infections have emerged several times in European countries in the past decades. The presented data suggest that besides the commonly applied voricona‑ zole, terbinafine may be an alternative for the therapy of mycetomatous Scedosporium infections

Development and study of an amperometric biosensor for the in vitro measurement of low concentration of putrescine in blood

An amperometric biosensor was developed for the in vitro determination of putrescine in blood samples because elevated level of putrescine in blood can be a diagnostic indicator of certain kinds of cancer. The electrochemical transducer consisted of a flat form, three electrode amperometric micro-cell fabricated with thin film photolithography on flexible Kapton® substrate. An immobilized putrescine oxidase (PUO) layer provided the biocatalytic oxidation of the putrescine, while the generated hydrogen peroxide was detected on the platinum-working electrode. An electropolymerized poly(m-phenylenediamine) (pPDA) size-exclusion layer was used to protect the working electrode from fouling and to prevent signal generation by common electroactive interferents present in blood. The preparation of the biocatalytic enzyme- and outer protective layers was optimized for improved sensitivity and response time. A detection limit of 50 nM was achieved in pH-adjusted whole blood samples, which is below pathological levels. © 2002 Elsevier Science B.V. All rights reserved

Screen-printed amperometric microcell for proline iminopeptidase enzyme activity assay

A microfabricated amperometric microcell was designed and used for the determination of proline iminopeptidase (PIP) enzyme activity in 2-10-μl samples. The measurements were made in the range of 10.3-841.5 mU/ml enzyme activities. The sensitivity of the determinations was between -0.0195 and -0.0203 μA ml/mU per min. The coefficient of variation of the determined values ranged between 2.8 (at 561.2 mU/ml) and 24.1% (at 10.3 mU/ml). The microcell was manufactured on an alumina substrate using screen-printed graphite working and Ag/AgCl reference electrodes. Elevated PIP activity in the vaginal fluid is a biochemical indicator of bacterial vaginosis. The method is appropriate to differentiate between normal (66±145 mU/ml) and elevated, diseased (704±145 mU/ml), values. Copyright (C) 2000 Elsevier Science S.A

Amperometric microcells for alkaline phosphatase assay

To develop simple electrochemical immunoassays, a screen printed amperometric microcell with graphite working and Ag/AgCl reference electrodes was tested for the determination of alkaline phosphatase enzyme (ALP) and anti-humanIgG conjugated ALP (α-hIgG-ALP) activity in 5-10 μl samples. To ensure reproducible, steady state conditions, the working electrode surface was coated with mass-transport controlling hydrogel layer. The kinetic response curves of the hydrogel coated electrodes were linear. In addition, the hydrogel layer reduced the nonspecific adsorption of the α-hIgG-ALP conjugate on the working electrode surface. The measurements were made in the range of 2 ÷ 4000 mU ml-1enzyme activities using ascorbic acid 2-phosphate (AAP) as the enzyme substrate. AAP is commercially available, non-toxic and has excellent stability. The sensitivity of the determinations was about 71% of the sensitivity which could be achieved using p-aminophenylphosphate (PAPP), a not easily accessible and unstable enzyme substrate. The experimentally determined kinetic parameters of the ALP enzyme catalyzed reactions were the same with the bare and hydrogel layer coated electrodes

Wet and dry chemistry kits for total creatine kinase activity using a microfabricated, planar, small-volume, amperometric cell

A novel microfabricated amperometric microcell is used for total creatine kinase (CK) activity determination. The microcell employs a photolithograpically prepared flat form electrode pair for detection. The enzyme-catalyzed reaction takes place in a thin liquid film, supported by a replaceable porous, hydrophillic membrane, resting on the working electrode surface. Simple, two electrode, amperometry was used, to avoid overvoltage shocks caused by \u27open\u27 circuits. An electrochemically prepared size-exclusion membrane was utilized on the working electrode to provide selectivity for the amperometric detection of hydrogen peroxide. Two different analytical reaction sequences following the CK catalyzed creatine phosphate hydrolysis were investigated. Both result in hydrogen peroxide production. The rate of hydrogen peroxide production is proportional to the total CK activity, and it is followed after the dispensation of sample into the microcell. The slope of the amperometric current-time curve is evaluated as the analytical signal. Copyright (C) 1998 Elsevier Science B.V