32 research outputs found

    University of Twente at GeoCLEF 2006: geofiltered document retrieval

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    In this report we describe the approach of the University of Twente to the 2006 Geo-CLEF task. It is based on retrieval by content and the subsequent filtering by geographical relevance utilizing a gazetteer. The results do not show an improvement inretrieval performance when taking geographical information into account

    Komplexe des Magnesium, Zink und Rhodium mit N,N-Chelatliganden, die Diimin-, Diamin-Gruppen enthalten: Synthesen, Strukturen und Katalysen

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    In dieser Arbeit wurden eine Reihe von Oxalamidinen und Chinoxalinen mit variablen elektronischen und sterischen Eigenschaften als Chelatliganden fĂŒr Magnesium, Zink und Rhodium eingesetzt. Mit den Magnesiumkomplexen wurden Untersuchungen zur CO2-Aufnahme und -ĂŒbertragung durchgefĂŒhrt. Die Zinkkomplexe wurden als Katalysatoren fĂŒr die Copolymerisation von Cyclohexenoxid mit CO2 eingesetzt. Die Rhodiumkomplexe dienten als Katalysatoren fĂŒr die Hydrierung von Hydroformylierung ungesĂ€ttigter Substrate

    Electrospun poly(d/l-lactide-co-l-lactide) hybrid matrix: a novel scaffold material for soft tissue engineering

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    Electrospinning is a long-known polymer processing technique that has received more interest and attention in recent years due to its versatility and potential use in the field of biomedical research. The fabrication of three-dimensional (3D) electrospun matrices for drug delivery and tissue engineering is of particular interest. In the present study, we identified optimal conditions to generate novel electrospun polymeric scaffolds composed of poly-d/l-lactide and poly-l-lactide in the ratio 50:50. Scanning electron microscopic analyses revealed that the generated poly(d/l-lactide-co-l-lactide) electrospun hybrid microfibers possessed a unique porous high surface area mimicking native extracellular matrix (ECM). To assess cytocompatibility, we isolated dermal fibroblasts from human skin biopsies. After 5 days of in vitro culture, the fibroblasts adhered, migrated and proliferated on the newly created 3D scaffolds. Our data demonstrate the applicability of electrospun poly(d/l-lactide-co-l-lactide) scaffolds to serve as substrates for regenerative medicine applications with special focus on skin tissue engineering

    Clinical Performance of the Automated LIAISONÂź Meridian H. pylori SA Stool Antigen Test

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    Background. Antigens derived from Helicobacter pylori can be used as stool biomarkers to assist in the diagnosis of H. pylori infection. Since current assays have variable performance, we assessed the clinical performance of the automated LIAISONÂź Meridian H. pylori SA chemiluminescent immunoassay against more invasive biopsy tests that are considered to be the “gold standard” (Composite Reference Method). Methods. This prospective multisite study enrolled patients undergoing an esophagogastroduodenoscopy with collection of biopsy and stool specimens. Adult patients (≄22 years) participated in the study from February 2017 to August 2018. Specimens of the stomach were tested by three methods, known as the Composite Reference Method: (1) histological evaluation, (2) culture of the organism, and (3) rapid urease detection test. H. pylori in stool was detected using the automated LIAISONÂź Meridian H. pylori SA assay, a chemiluminescent immunoassay. Statistical analyses were performed using MedCalc 18.11.6. Results. 277 patients (63% female) were included in the study. The prevalence of infected subjects was 24.2% in this study cohort. Clinical performance assessed against the Composite Reference Method showed very good agreement (Cohen’s kappa=0.922), with good sensitivity (95.5%) and specificity (97.6%). Reproducibility study results showed total imprecision ranging from 3.1% to 13.9% CV. Conclusion. The automated LIAISONÂź Meridian H. pylori SA assay brings reliable noninvasive testing for H. pylori to the laboratory that is in very good agreement with the current, more invasive biopsy-based methods such as histology, culture, or rapid urease test. The clinical trial identifiers are NCT03060746 (pretherapy) and NCT03060733 (posttherapy)
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