A nuclear magnetic resonance (NMR) sample analyzer has a plurality of NMR units arrayed in a predetermined relationship to each other. Each of the NMR units includes a sample chamber having a sensitive volume for containing a sample to be analyzed; a radio frequency (RF) transmitting and receiving device proximal the sample chamber; and a magnet surrounding the RF transmitting and receiving device and sample chamber for generating a substantially uniform magnetic field within the sensitive volume and substantially no magnetic field beyond an outside wall of the magnet.

A nuclear magnetic resonance (NMR) apparatus includes at least one magnet configured to induce a static magnetic field in a sample of material to be analyzed, wherein the sample is disposed on one side of the at least one magnet. The at least one magnet is configured such that the static magnetic field induced in the sample of material to be analyzed is substantially planar along lines of equal static magnetic field amplitude. A method includes inducing a static magnetic field in a sample of material to be analyzed. The static magnetic field is substantially planar along surfaces of equal amplitude of the static magnetic field. The inducing originates on one side of the sample. A radio frequency magnetic field is induced in the sample substantially orthogonally to the static magnetic field. NMR phenomena excited in the sample are detected.

A biological detector includes a conduit for receiving a fluid containing one or more magnetic nanoparticle-labeled, biological objects to be detected and one or more permanent magnets or electromagnet for establishing a low magnetic field in which the conduit is disposed. A microcoil is disposed proximate the conduit for energization at a frequency that permits detection by NMR spectroscopy of whether the one or more magnetically-labeled biological objects is/are present in the fluid.

An NMR probe head with an MAS stator (1) supplied with microwave radiation from a microwave guide (9) through an opening in a coil block (2) has a microwave lens (6) and a microwave mirror (8a) on an inner side of the MAS stator. The MAS rotor (3) is surrounded by a solenoid RF coil (5) and the microwave lens is arranged and embodied in the opening of the coil block on the side facing a sample volume (4) such that the cylinder axis of the MAS rotor lies in the focus of the microwave lens. The microwave mirror is arranged on, or in, the inner wall of the MAS stator that lies opposite the microwave guide and has a cylindrical and concave structure, such that the microwave mirror focuses the microwave radiation incident from the sample volume onto the central axis of the MAS rotor.

A rapid cycle dynamic nuclear polarization (DNP) NMR apparatus comprises (i) a cooling unit configured to cool a sample in a capillary, (b) a DNP polarization unit configured to polarize the sample in the capillary, (c) a stripline-based NMR detector comprising a stripline for NMR analysis of the sample in the capillary, (d) a transport unit configured to guide the capillary from the DNP polarization unit to the stripline of stripline-based NMR detector; and (e) a heating unit configured to heat the sample in the capillary before analysis of the sample by the stripline-based NMR detector. Fast (1D-3D) NMR measurements with high resolution may be obtained.

An implantable magnetic relaxation sensor is provided that comprises superparamagnetic nanoparticies functionalized with one or more agents that bond with a biomarker of interest. The sensor is configured for minimally-invasive implantation into a human or animal, and is configured to indicate the implanted sensor's cumulative exposure to the biomarker of interest by analysis using magnetic resonance relaxometry.

A method includes generating, from an integrated oscillator circuit, an oscillating output signal and generating, by an integrated power amplifier (PA) circuit, an amplified oscillating output signal based on the oscillating output signal. The method further includes receiving, by integrated receiver amplifier circuit, an electron spin resonance (ESR) signal from biological samples that include a magnetic species and generating, by the integrated receiver amplifier circuit, an amplified ESR signal based on the received ESR signal. The method further includes receiving, by the integrated receiver amplifier circuit, an electron spin resonance (ESR) signal from magnetic nanoparticles that are loaded with drugs or attached to human cells.

An integrated electron spin resonance (ESR) circuit chip includes a chip substrate, a transmitter circuit, and a receiver circuit. The transmitter circuit and receiver circuit are disposed on the chip substrate. The transmitter circuit includes an oscillator circuit configured to generate an oscillating output signal and a power amplifier (PA) circuit configured to generate an amplified oscillating output signal based on the oscillating output signal. The receiver circuit receives an ESR signal from an ESR probe. The receiver circuit includes a receiver amplifier circuit configured to generate an amplified ESR signal based on the received ESR signal, a mixer circuit configured to receive the amplified ESR signal and to down-convert the amplified ESR signal to a baseband signal, and a baseband amplifier circuit configured to generate an amplified baseband signal based on the baseband signal.

Micro-fluidic chambers for use in a liquid medicament delivery system, include a bottom substrate and a top cover, the top cover being spaced from the bottom substrate so as to define a height of the chamber, wherein, one or more walls or fillings are positioned in the chamber, the walls or fillings defining a fluid channel there between such that the fluid channel extends from an inlet conduit to an inlet of the chamber to an outlet conduit connected to an outlet of the chamber, wherein, each of the walls or fillings has a height less than the height of the chamber so as to define a fluid gap between a top surface of each wall or filling and the top cover; and wherein, the dimensions of the walls or fillings and the chamber are such that the fluid gap will be filled with liquid by capillary forces via the fluid channel when liquid is introduced into the fluid chamber

This invention features systems and methods for the detection of analytes, and their use in the treatment and diagnosis of disease.