The invention relates to methods for detecting and/or characterising a nanovesicle in a sample or a method of detecting a target that is bound or associated with said nanovesicle, wherein the sample is brought into contact with nanoparticles that are capable of binding on the surface of nanovesicle and form, in situ, a nanoshell that surround said nanovesicle. In a preferred embodiment, the nanovesicle is exosome labelled with fluorescent probes and the nanoparticles are gold nanoparticles (AuNP). The invention also relates to a kit or microfluidic chip for performing such methods, as well as a method of determining the prognosis of a cancer in a subject by performing such methods.

A method for identifying an origin of Chrysanthemi flos is provided, which belongs to the technical field of chemical analysis and detection, and comprises the following steps: mixing Chrysanthemi flos extract with aluminum ion solution, and gold nano-clusters (AuNCs) solution in a solvent, standing for reaction, detecting fluorescence intensity of Chrysanthemi flos, comparing the fluorescence intensity of Chrysanthemi flos to be detected with that of Chrysanthemi flos from a target origin, and determining whether they are from a same origin. According to the application, excited-state intramolecular proton transfer effect between 3-hydroxyflavone derivatives of Chrysanthemi flos and aluminum ions is utilized to enhance the fluorescence of 3-hydroxyflavone derivatives, where AuNCs combines aluminum ions to enhance aggregation-induced fluorescence, and reacts with flavonoids to quench their fluorescence; and visual characterization and traceability of Chrysanthemum morifolium quality are achieved by further comparing obvious rich fluorescence color changes before and after the reaction.

The present disclosure generally relates to a molecular construct for multiphoton fluorescence microscopy imaging. The molecular construct has a first, non-fluorescent configuration (2PAP-C) and a second, fluorescent configuration (2PAP-CL), and comprises a two-photon absorbing probe (2PAP) linked to a photochromic molecule that can be reversibly changed from a first colored isomeric form (C) to a second colorless isomeric form (CL). The first colored form (C) can be isomerized to the second colorless isomeric form (CL) upon absorption of two photons by the two-photon absorbing probe (2PAP). The present disclosure also relates to a method for analyzing a target structure in a multiphoton microscope utilizing the molecular construct. Furthermore, the present disclosure relates to an antibody tagged with the molecular construct, and to the use of the molecular construct for imaging a target structure.

The present invention relates to a method for in situ sensing of water stress in a plant by contacting a plant with a biosensor, where the biosensor comprises a material capable of giving a detectable response to changes in local water potential in the plant and detecting the detectable response thereby sensing water stress in the plant. The invention further relates to a method for determining water potential in a substance, a biosensor, a system for determining water potential in a substance, a method for determining water potential in a substance, a water potential measurement computing device, and a non-transitory computer readable medium having stored thereon instructions for determining water potential in a substance.

The present disclosure discloses an optochemical sensor for determining a measurand correlating with a concentration of an analyte in a measuring fluid, comprising: a housing having an immersion region configured for immersing in the measuring fluid; a removable cap having a sensor spot, the removable cap removably arranged at the immersion region of the housing, wherein the sensor spot is disposed on a circumferential face; a radiation source disposed in the housing for radiating excitation radiation into the removable cap, wherein a deflection module is disposed in the removable cap as to deflect excitation radiation radiated into the removable cap; a radiation receiver disposed in the housing for receiving received radiation emitted by the sensor spot; and a sensor circuit disposed in the housing and configured to control the radiation source, receive signals of the radiation receiver, and generate output signals based on the signals of the radiation receiver.

A photonic gas sensor and a method for producing a photonic gas sensor are disclosed. In an embodiment a photonic gas sensor includes a component housing with at least one cavity, a radiation-emitting semiconductor chip arranged in the cavity and configured to transmit electromagnetic radiation in a first wavelength range, a radiation-detecting semiconductor chip arranged in the cavity and configured to detect electromagnetic radiation in a second wavelength range and an active sensor element having a fluorescent dye configured to emit electromagnetic radiation in the second wavelength range upon being excited by electromagnetic radiation in the first wavelength range, wherein an intensity of the emitted electromagnetic radiation in the second wavelength range changes reversibly in presence of a gas to be detected.

This invention provides methods and systems for measuring the concentration of multiple nucleic acid sequences in a sample. The nucleic acid sequences in the sample are simultaneously amplified, for example, using polymerase chain reaction (PCR) in the presence of an array of nucleic acid probes. The amount of amplicon corresponding to the multiple nucleic acid sequences can be measured in real-time during or after each cycle using a real-time microarray. The measured amount of amplicon produced can be used to determine the original amount of the nucleic acid sequences in the sample. Also provided herein are biosensor arrays, systems and methods for affinity based assays that are able to simultaneously obtain high quality measurements of the binding characteristics of multiple analytes, and that are able to determine the amounts of those analytes in solution. The invention also provides a fully integrated bioarray for detecting real-time characteristics of affinity based assays.

The present disclosure relates to a measuring arrangement for measuring an ozone content in a measured medium, including: a first sensor surface and a second sensor surface; a first cover element adjacent the first sensor surface and including an ozone binder that binds ozone without releasing oxygen or any species further reacting to form oxygen; a second cover element adjacent the second sensor surface and including an ozone converter that reacts with ozone to form oxygen; a measuring sensor configured to generate a first measurement signal dependent on the oxygen concentration at the first sensor surface and a second measurement signal dependent on the oxygen concentration at the second sensor surface; and an electronic evaluation unit configured to determine the ozone content in the measured medium based on the first and the second measurement signals.

A measuring method for measuring dissolved oxygen includes performing a first measurement sequence, including: emitting a first stimulation signal onto a sensor for a first period; detecting a first detection signal; determining a phase shift between the first stimulation signal and the first detection signal; and calculating a first measured value based on the determined phase shift. Performing a second measurement sequence, including a second stimulation signal onto the sensor for a second period, wherein the second stimulation signal is different than the first stimulation signal; detecting a second detection signal; determining a decay time of the second detection signal; calculating a second measured value based on the decay time. The method further includes comparing the first measured value to the second measured value and correcting the first measured value when a difference between the first measured value and the second measured value is greater than a first limit value.

Embodiments described herein generally relate to: sensing and/or authentication using luminescence imaging; diagnostic assays, systems, and related methods; temporal thermal sensing and related methods; and/or to emissive species, such as those excitable by white light, and related systems and methods.