Bundesrepublik Deutschland, Vertreten Durch Den Bundesminister Für Wirtschaft Und Energie

Bundesrepublik Deutschland, Vertreten Durch Den Bundesrepublik Für Wirtschaft Und Energie

Bam Bundesanstalt Fuer Materialforschung Und-pruefung

Institut Dr. Foerster Gmbh & Co. Kg

Phase Holographic Imaging Phi Ab

Bundesrepublik Deutschland, Vertreten Durch Die Bundesministerin Für Wirtschaft Und Energie

Sigma-aldrich Gmbh

Bundesrepublik Deutschland, Vertreten Durch Die Bundesministerin Für Wirtschaft Und Energie, Diese Vertreten Durch Den Präsidenten Der Bundesanstalt Für Materialforgchung Und- Prüfung (Bam)

Bundesrepublik Deutschland, Vertreten Durch Diebundesministerin Für Energie Wirtschaft Und Energie

Fluka Gmbh

Bam Bundesanstalf Fur Materialforschung Und - Prufung

Bam Bundesanstalt Fur Materialforschung Und-pruefung

Bam Bundesanstalt Fur Materialforschung Und-prufung

Bundesanstalt Fur Materialforschung Und -prufung (bam)

Bundesrepublik Deutschland, Vertreten Durch Den Bundesminister Für Wirtschaft Und Energie, Dieser Vertreten Durch Den Präsidenten Der

Knut Rurack

Katrin Hoffmann

Ute Resch-Genger

Pierre Nording

Dietmar Pfeifer

Jérémy Bell

Monika Spieles

Bernhard Schönenberger

Angelika Hoffmann

Christian Monte

Wei Wan

Mustafa Biyikal

Raúl Gotor

Börje Sellergren

Tobias Fischer

Sudhirkumar Shinde

Thomas Behnke

Kornelia Gawlitza

Estela Climent

Anette Gjörloff-Wingren

Yuecheng Zhang

Zahra El-Schich

Martha Wamaitha Kimani

Shan Jiang

Dominik Sarma

Anette Gjörloff Wingren

Ana B Descalzo

Jerie Zbynek

Benedikt Heller

Martha Kimani

Anette GJÖRLOFF Wingren

A test strip comprising a porous matrix, the test strip includes a sample application zone for applying a liquid sample including an analyte; a reporter release zone, having a sensing material, the sensing material being adapted to selectively interact with the analyte by releasing an optical reporter, the reporter release zone being arranged downstream of the sample application zone; and a detection zone, having a capture material, the capture material being adapted to selectively bind the optical reporter and being arranged downstream of the reporter release zone.

Label-free optical detection in capture zones immobilized on strips for lateral flow assays

A double fluorescent particle comprises: a core with a first fluorescence; and a molecularly imprinted polymer (MIP) shell with a second fluorescence; wherein the MIP is an organic polymer comprising elements selected from the group consisting of: C, H, O, N, P, and S; wherein the MIP is adapted to selectively bind to a cell surface structure; wherein the first fluorescence is generated by an entity selected from the group consisting of: a carbon nanodot, an alkaline earth metal fluoride, a dye-doped polymer, a dye-doped stabilized micelle, a P-dot—i.e. a π-conjugated polymer, a quantum dot doped polymer, a rare earth metal ion doped polymer, a dye-doped silica, a rare-earth ion doped silica, and a rare earth ion doped alkaline earth metal fluoride nanoparticle; wherein the second fluorescence is generated by an entity selected from the group consisting of: a dye, a molecular probe, an indicator, a probe monomer, an indicator monomer, and a cross-linker, and wherein the first and second fluorescence differ at least by an emission wavelength and/or by an excitation wavelength.

Fluorescent particles with molecularly imprinted fluorescent polymer shells for cell staining applications in cytometry and microscopy

A detection reagent is disclosed in the form of a dye having the basic structure of a 4-(phenylethynyl)-phenyl-amine, a 4-(phenylethenyl)-phenyl-amine and/or a biphenylamine derivative. The dye can be used as detection reagent for nitroaromatics, nitroalkanes, nitroamines, nitrates, nitric acid, nitrous acid, nitrogen oxides, and additionally for sulphur dioxide (which is produced with the degradation of black powder). The dye can be an asymmetric triphenylamine derivative, which can lead to a fluorescence quenching, which can be used analytically in the case of electron abstraction.

Fluorescent dye films for detecting NOx-based explosives in the air, in solutions, and from wipe samples

A method for the detection of hydrocarbon contamination in a sample is disclosed. The method includes contacting a sample with a molecular probe. The molecular probe has a photoluminescence which is environmentally sensitive. The photoluminescence from the molecular probe is collected. The method includes determining whether the photoluminescence is indicative of a hydrocarbon contaminated sample. A test strip for the detection of hydrocarbon contamination in a sample is also disclosed. The test strip includes a molecular probe embedded in a substrate and/or immobilized to the substrate, the molecular probe having a photoluminescence which is environmentally sensitive to hydrocarbon contaminated sample.

Detection of hydrocarbon contamination in soil and water

A method for the detection of adulterated gasoline in a sample is disclosed. The method includes contacting a sample with an immobilized molecular probe, the immobilized molecular probe having a photoluminescence which is environmentally sensitive; collecting the photoluminescence from the immobilized molecular probe; and determining whether the photoluminescence is indicative of adulterated gasoline. A test strip for the detection of adulterated gasoline in a sample is also disclosed, including an immobilized molecular probe embedded in a substrate and/or immobilized to the substrate, the immobilized molecular probe having photoluminescence which is environmentally sensitive to adulterated gasoline. The method and test strips are designed to be robust, portable, and within the capabilities of untrained personnel.

Detection of adulterated gasoline using an environmentally sensitive photoluminescent molecular probe

A method for detecting an analyte comprising 2,4,6-trinitrotoluene in a sample comprising: providing an indicator solution, comprising a cation and an anion; bringing in contact and/or interacting the indicator solution and the sample comprising the analyte; photocatalytically induced forming of an anionic TNT sigma complex, comprising the analyte and the anion, by means of exposure of the indicator solution and the sample brought in contact with one another; fluorescence optically detecting the formed anionic TNT sigma complex.

Highly selective and sensitive detection of 2,4,6-trinitrotoluene by means of fluorescence enhancement using UV-induced photoreaction with anions

Hybrid microparticle having a polymer core and a shell which surrounds the polymer core at least in sections and which has a silicon dioxide layer; characterized by an RF value, the RF value being defined as the ratio of an external surface area amenable to the adsorption of nitrogen to a surface area which is computable from an arithmetic mean diameter of the hybrid microparticle considered as an ideal sphere, where the shell has a structure selected from:

Process for synthesizing hybrid core-shell microparticles comprising a polymer core and a silicon dioxide shell with controlled structure and surface

The present invention relates to a molecularly imprinted polymer for binding glycans, wherein the molecularly imprinted polymer is obtainable by providing a saccharide template such as a glycan; providing at least two functional monomers capable of cooperatively; interacting with the template; providing a crosslinking monomer; polymerizing the monomers optionally dissolved in a solvent, in presence of the saccharide template; and removing the template from the formed polymer. The invention is also related to a method for their production and use of the molecularly imprinted polymer.

Molecularly imprinted polymers

The invention relates to difluoroboradiazaindacene dyes of the formula (1) where

Difluoroboradiazaindacene dyes

The invention is directed to a method and a kit for calibrating a photoluminescence measurement system, in particular a fluorescence measurement system. The kit includes a number of fluorescence standards i and their corrected and certified fluorescence spectra I(&#x3bb;), whereby the fluorescence standards i are selected, so that their spectrally corrected fluorescence spectra I(&#x3bb;) cover a broad spectral range with high intensity. The standards are characterized by large half-widths FWHMof their bands of at least 1400 cm. According to the method of the invention, partial correction functions F(&#x3bb;) are generated by forming the quotient of the measured fluorescence spectra J(&#x3bb;) and the corresponding corrected fluorescence spectra I(&#x3bb;), which are then combined to form a total correction function F(&#x3bb;) for a broad spectral range. The combination factors &#x3b1;are hereby computed by statistical averaging of consecutive partial correction functions F(&#x3bb;) over only a predefined, limited overlap region &#x3bb;&#xb1;&#x394;&#x3bb;about the mutual crossover wavelength &#x3bb;.

Method and kit for calibrating a photoluminescence measurement system

Method and kit for calibrating a photoluminescence measurement

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Berlin, Germany

Knut Rurack