Avl Ag

Avl Medical Instruments Ag

F. Hoffmann-la Roche Ag

Avl Medical Instruments

Active Motif Chromeon Gmbh

Bayer Aktiengesellschaft

Ciba-geigy Corporation

National Institute of Advanced Industrial Science and Technology

Merck Patent Gesellschaft MIT Beschrankter Haftung

Chromeon Gmbh

Otto S Wolfbeis

Marco J Leiner

Tobias Werner

Herbert Kroneis

Hermann J Marsoner

Helmut List

Christian Huber

Helmut Offenbacher

Hellfried Karpf

Ingo Klimant

Douglas E Bell

Alfred Leitner

Andrei Boila-Gockel

Jorg Daub

Thomas Gareis

Ute Kosch

Stefan Heinl

Susannah Young

Matthias Kollmannsberger

Horst Harnisch

Erich Kleinhappl

Masanori Ando

Edmund Urbano

Werner E Ziegler

Karl Harnoncourt

Gerald Kirchmayer

Wolfgang Trettnak

Nikolai N Romanov

Vladimir M Mirsky

Meng Wu

Erich Ziegler

Zhihong Lin

Axel Durkop

Petra Braun Geb Hochmuth

Leonie Weiss

A bioanalytical method for determining catalases and peroxidases using europium ions.

Bioanalytical measuring method for determining catalases and peroxidases, as well as conjugates, substrates, activators and inhibitors thereof

The present invention concerns biological methods of determination using enzymes from the group of oxidases and using optical indicators from the group of lanthanoid-ligand complexes.

Bioanalytical measuring method using oxidases and lanthanoid-ligand complexes

New reactive dyes are described which can be used to fluorescently label bioorganic molecules such as amino acids, proteins, antibodies, nucleotides and also polymer particles. The color of the new dyes and conjugates thereof can be varied over a wide range. In contrast to known symmetric cyanine dyes, the dyes of the invention contain only one reactive group. Hence the labelling takes place without the interfering cross-linking that occurs with bireactive dyes. Their fluorescence quantum yields are very high (especially in the conjugated form). Conjugates thereof with proteins, oligonucleotides or particles can be used in fluorescence-based analytical methods of determination e.g. in immunoassays, in hybridization assays, in cytometry or for pharmaceutical screening.

Fluorochromes for labelling biomolecules and polymer particles and bioanalytical and screening methods based thereon

The present invention provides an ozone detecting material comprising a polymer prepared by polymerization of at least one monomer selected from the group consisting of 2-, 3-, 4-halogen substituted anilines or aniline substituted with C-alkyl in N-position, and diphenylamine, formed into a thin film coated on a transparent substrate, waveguide, or optical fiber, or additionally comprising a component selected from electro-conductive fine carbon powder, a semiconductive metal oxide, or a semiconductive polymer material, and a method for detecting ozone comprising the steps of contacting this ozone detecting material with an ozone-containing gas and determining the light absorption rate and/or electrical conductivity of the ozone detecting material at that time.

Ozone detecting material and method for detecting ozone

An optical-chemical sensor which is suitable for the continuous and discontinuous determination by luminescence optics of the concentration of chloride in an aqueous sample and which comprises a luminescence indicator (I) and a polymer (H) carrying the luminescence indicator (I) is characterized in that the luminescence indicator (I) is a non-lipophile acridine or bisacridine compound and the polymer (H) is a linear-chain hydrophile polymer soluble in an organic solvent, whereby it is possible to excite the sensor by commercially available LEDs, to manufacture very large numbers thereof at a moderate cost and in a reproducible way and, preferably, to use it for the determination of physiological chloride concentrations and the sensor furthermore has a wide dynamic measuring range for the determination of chloride; a high sensitivity, stability and reproducibility; a high selectivity for chloride; and a low pH cross-sensitivity.

Optical-chemical sensor

The sensor membrane of an optical sensor for detection of O.sub.2, H.sub.2 O.sub.2, SO.sub.2 or halogenated hydrocarbons in a sample contains an indicator substance that is homogeneously immobilized in the polymer matrix of the sensor membrane and is, at least indirectly, in contact with the sample, changing at least one of its optical properties upon a change of the parameter to be measured. The indicator substance contains an inorganic salt of a transition metal complex with .alpha.-diimine ligands. The indicator substance is homogeneously distributed in the polymer matrix, which essentially consists of at least one substance belonging to the group of cellulose derivatives, polystyrenes, polytetrahydrofuranes, or their respective derivatives.

Sensor membrane of an optical sensor

In a sensor layer for quantitative determination of at least one chemical component in a gaseous or liquid sample medium containing a chromophore which is directly or indirectly responsive to the component being determined by changing its absorption spectrum, and a luminophore which is not responsive to the component being determined, where there is an at least partial overlap between the emission spectrum of the luminophore and the absorption spectrum of the chromophore, and where the energy transfer between luminophore and chromophore produces a measurable change in at least one luminescence characteristic of the luminophore, the luminophore L and the chromophore .GAMMA. are ionic substances with differing electrical charges, which are incorporated in a matrix material that is permeable to the chemical component being determined.

Luminescence-optical method and sensor layer for quantitative

The invention relates to a compound having the general Formula I in which one of the groups R.sub.1,R.sub.2,R.sub.3,R.sub.4,R.sub.5,R.sub.6 and R.sub.7 represents an ionophoric moiety and the remaining groups each independently are hydrogen, a lipophilic or hydrophilic group or a reactive group for coupling to a polymer or a biomolecule, or R.sub.2 forms an aromatic ring system together with R.sub.3 and R.sub.5 forms an aromatic ring system together with R.sub.6. the compound of the invention is useful as a luminescence indicator for cations.

Luminescence indicator including ionophoric moiety

The invention relates to a compound having the general Formula I ##STR1## in which one of the groups R.sub.1, R.sub.2, R.sub.3, R.sub.4, R.sub.5, R.sub.6 and R.sub.7 represents an ionophoric moiety and the remaining groups each independently are hydrogen, a lipophilic or hydrophilic group or a reactive group for coupling to a polymer or a biomolecule, or R.sub.2 forms an aromatic ring system together with R.sub.3 and R.sub.5 forms an aromatic ring system together with R.sub.6. The compound of the invention is useful as a luminescence indicator for alkali ions.

Luminescence indicator

For the purpose of reversible optical indication of the pH of a sample, a hydrophilic accommodating layer is disposed on a hydrophobic mechanically stable support element, which layer contains the indicator dye proper in an immobilized form. This provides a sensor membrane which can be fabricated in a simple manner and is cost-effective, which has a rapid response time and can also be fabricated as a mass product to be used only once.

Sensor membrane for indicating the PH of a sample, the fabrication and

For quality control of packaged organic substances, preferably packaged foods and drugs, the materials to be examined are brought into contact with a planar optical sensor element which is applied on the inside of the wrapping and responds to a change in the gas composition in the gas space above the sample by a change in color or fluorescence. The change of one of the optical properties of the sensor element is detected visually or opto-electronically.

Method for quality control of packaged organic substances and packaging

A method for the continuous and reversible determination of the concentration of an enzyme substrate such as glucose in an specimen, wherein the specimen is brought into contact with a corresponding enzyme selected from oxidases and oxygenases and to which a flavin coenzyme (FMN, FAD) is bonded, the flavin coenzyme changing to a reduced form by the enzyme substrate and to an oxidized form by molecular oxygen dissolved in the specimen, and the change in the fluorescence spectrum, produced by means of the reduction of the flavin coenzyme, is measured.

Method for the determination of the concentration of an enzyme substrate

For optical determination of the catalytic enzyme activity of a sample by means of enzyme reactants which are split under the influence of the enzyme to be measured, the enzyme reactant is placed at the end of an optical fiber and brought into contact with the sample to be determined. The measurements are carried out by observing the rate of change in spectral characteristics of the enzyme reactant, or its reaction products, resulting from the enzyme reaction. The method permits measurements of undiluted blood and in-vivo determinations of enzyme activities.

Method for optical determination of the catalytic enzyme activity and

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Graz, Austria

Otto S Wolfbeis