A method for irradiating a medium includes irradiating the medium with an electromagnetic wave which is scattered in the medium and modulated in frequency at a position in the medium; obtaining information corresponding to an interference pattern generated by interference between the modulated electromagnetic wave and a reference wave; and generating a phase conjugate wave, based on the obtained information, which irradiates the medium.

The present disclosure provides a complex having satisfactory dispersibility and stable luminescence characteristics. A complex of the present disclosure includes: a first substance having a property of specifically binding to a target substance; a quantum dot that contains silicon as a main component and that is negatively charged on a surface; and a linker substance that contains a compound represented by general formula (1) below and that covers the surface of the quantum dot, where the first substance has been immobilized on the surface of the quantum dot through the linker substance:
XLSi(R.sub.1)(R.sub.2)(OR.sub.3)(1)
where X is a basic functional group; R.sub.1, R.sub.2, and R.sub.3 are each independently an alkyl group; and L is an alkylene group.

A method, apparatus, and article of manufacture for irradiating one or more targets within a sample with electromagnetic (EM) radiation. One or more targets within the sample are controllably defined with an acoustic field. The sample is irradiated with input EM radiation having an input wavefront. An amount of frequency shifted EM radiation is detected, wherein at least some of the input EM radiation that passes through the acoustic field at the targets is shifted in frequency to form the frequency shifted EM radiation. The input wavefront is modified, using feedback comprising the amount of the frequency shifted EM radiation that is detected, into a modified wavefront. The sample is irradiated using the input EM radiation comprising the modified wavefront, and the process is repeated as desired.

A magneto-optical bio-detection device including: a sample cell, a coil, a magnetic core, a light source and a light detection unit. The sample cell is filled with a solution containing a detection object and a magnetic biosensor capable of combining with the detection object to form a magnetic cluster. The coil is used for producing an oscillating magnetic field. The magnetic core has a guide portion, and an upper magnetic pole and a lower magnetic pole located at both ends of the guide portion; on a cross section orthogonal to the oscillating magnetic field, a cross-sectional area of the upper magnetic pole is less than a cross-sectional area of the guide portion. The light source is used for emitting light rays to penetrate the sample cell. The light detection unit is used for receiving the light rays that penetrated the sample cell to produce a detection signal.

A magneto-optical defect center magnetometer, such as a diamond nitrogen vacancy (DNV) magnetometer, can include an excitation source, a magneto-optical defect center element, a collection device, a top plate, a bottom plate, and a printed circuit board. The excitation source, the magneto-optical defect center element, and the collection device are each mounted to the printed circuit board.

The invention relates to a method and a sensor device (100) for the detection of clusters (C) of magnetic particles (MP) in a sample volume (111), particularly of clusters (C) consisting of two magnetic particles (MP) with different binding sites that are bound to a target molecule in a sandwich configuration. Output light (L2) originating from an interaction of input light (L1) with clusters (C) of magnetic particles (MP) is detected. Moreover, the magnetic particles (MP, C) are actuated by a magnetic actuation field (B), wherein said actuation is at least once interrupted by a pause. In this way a high output signal can be achieved that properly reflects the amount of specifically bound clusters (C).

An optical system uses a sample medium disposed within an optical cavity, receives an input beam that may be non-coherent or coherent, and produces an optical energy from the input beam, by creating birefringent-induced beam components each cavity traversal, forming a mixed quantum state beam for the input beam. The mixed quantum state beam exits the cavity, and the energy distribution of the exiting beam is analyzed over a range of tuned input beam frequencies to uniquely identify circularly birefringent the materials within the sample medium, e.g., amino acids, proteins, or other circular birefringent molecules, biological or otherwise.

The present disclosure is directed towards characterizing liquids through the use of magnetic discs that rotate in response to dynamic magnetic fields. In some embodiments, a light beam is transmitted into the liquid while the magnetic discs rotate, and one or more parameters a light beam signal associated with the transmitted light beam are identified. Various characteristics of the liquid may be detected based on the one or more parameters of the light beam signal.

Imaging systems and methods using fluorescent nanodiamonds are disclosed. The imaging systems and methods including applying a time-varying magnetic field to a specimen containing fluorescent nanodiamonds and comparing the fluorescence obtained with different magnetic fields to provide an image of the specimen.

A point-of-care diagnostic system that includes a cartridge and a reader. The cartridge can contain a patient sample, such as a blood sample. The cartridge is inserted into the reader and the patient sample is analyzed. The reader contains various analysis systems, such as a magneto-optical system that measures a light transmission differential through the patient sample in varying magnetic fields. The reader can process data from the various patient sample analysis to provide interpretative results indicative of a disease, infection and/or condition of the patient.