31 results about "Deep tissue imaging" patented technology

Compounds and methods related to NIR molecular imaging, in-vitro and in-vivo functional imaging, therapy/efficacy monitoring, and cancer and metastatic activity imaging. Compounds and methods demonstrated pertain to the field of peripheral benzodiazepine receptor imaging, metabolic imaging, cellular respiration imaging, cellular proliferation imaging as targeted agents that incorporate signaling agents.

Compounds and methods related to NIR molecular imaging, in-vitro and in-vivo functional imaging, therapy/efficacy monitoring, and cancer and metastatic activity imaging. Compounds and methods demonstrated pertain to the field of peripheral benzodiazepine receptor imaging, metabolic imaging, cellular respiration imaging, cellular proliferation imaging as targeted agents that incorporate signaling agents.

The invention discloses a deep tissue X-ray excitation multispectral tomography system and method. The system comprises an X-ray source, an X-ray flat panel detector, an EMCCD camera, an electric control rotary table, a narrow-band filter, a lead plate, a computer and an animal to be imaged; nano-luminescence materials are excited through an X ray, short-wave infrared light with the specific spectra sections, particularly high penetration depth is emitted, photons penetrate through tissue to reach the surface of an imaged object, the light of different wave length spectra sections is received by an EMCCD camera by being filtered by the narrow-band filter, and an obtained image and a rebuilt result under each spectra section are obtained; multivariate analysis is adopted for carrying out treatment and analysis on multispectral images and rebuilt results, accurate distribution of the nano-luminescence materials in the object is obtained and combined with CT tomography results, and finally a deep tissue multispectral tomography image is obtained. The imaging depth of X-ray excitation multispectral tomography can be effectively improved, and deep tissue imaging of small living animals is achieved.

A method is provided for deep tissue imaging using multi-photon excitation of a fluorescent agent. The fluorescent agent is irradiated with an ultrafast laser to produce an excited singlet state (S_n) which subsequently undergoes non-radiative relaxation to a first singlet state (S₁). The S₁ state undergoes fluorescence to the ground state S₀ to produce an emission wavelength. Both the excitation and emission wavelengths are within the near infrared optical window, thereby permitting deep tissue penetration for both the incoming and outgoing signals.

Exemplary arrangement, apparatus, method and computer accessible can be provided. For example, using the exemplary arrangement, apparatus and method, it is possible to configured to propagate at least one electro-magnetic radiation. Indeed, it is possible to receive, using at least one first arrangement, a first portion of the at least one electro-magnetic radiation directed to a sample and a second portion of the least one electro-magnetic radiation directed to a reference, the first arrangement can be structured to at least partially reflect and at least partially allow to transmit the first and second portions. In addition, it is possible to receive, using a second arrangement, (i) a third portion of the electro-magnetic radiation associated with at least one of the transmitted first portion or the reflected first portion from the sample and (ii) a fourth portion of the electro-magnetic radiation associated with at least one of the second transmitted portion of the least one electro-magnetic radiation or the reflected second portion from the reference. The third and fourth portions can travel at least partially along substantially the same path toward the second arrangement, Further, the second arrangement can be configured to receive the reflected first and second portion(s) which interfere with one another, and generate at least one signal which includes information associated with at least one fluctuation in an uncommon path of the first and second portions prior to a receipt thereof by the at least one first arrangement. In addition or alternatively, the second arrangement can be configured to determine information regarding a spectrally resolved interference associated with the third and fourth portions.

A tissue imaging system includes a laser module for outputting a laser pulse, an optical delay module configured to split a laser pulse received from the laser module into a plurality of time-delayedsub-pulses, a telescope for delivering the sub-pulses from the optical delay module to a target volume and a photodetector configured to collect photons generated within the target volume in responseto excitation of the target volume by the first and second sub-pulses. The system may further include a spatial multiplexing module configured to receive the temporally multiplexed laser pulse from the optical delay module and splitting the temporally multiplexed laser pulse into a plurality of sub-beams including a first sub-beam and a second sub-beam, wherein the first sub-beam and the second sub-beam are spatially separated with respect to a first image plane formed at a first depth within the target volume and with respect to a second image plane formed at a second depth within the targetvolume.

The near-infrared wavelengths (700 nm-900 nm) are a suitable optical window for light penetration and deep tissue imaging. The present invention provides a near-infrared fluorescent blood pool contrast agent. The agent is of use to detect and quantify pathological capillary leak in live animals, e.g., serially imaging of traumatized tissue (muscle) as well as tumors.

The invention discloses a non-reactive mitochondrial tracking fluorescent probe containing a C12 lalkyl chain, and applications of the probe in labeling or displaying of the distribution of mitochondria in cells, and in mitochondrial autophagy observation, wherein the fluorescent probe is a carbazole pyridine salt compound having a structure represented by a formula (I). According to the present invention, the probe can stain mitochondria in normal living cells, and especially can be fixed on mitochondria when the mitochondrial membrane potential is reduced or disappears, such that the resultsshow that the probe can track the dynamic changes of mitochondria; the probe further has good two-photon properties, and can be used for deep tissue imaging; and the probe has low toxicity, can real-timely track the dynamic process of mitochondrial autophagy, and has broad application prospect in the field of fluorescent biomarkers.

The invention discloses an optimized self-adaptive microscopic imaging method and device based on machine learning, and the method comprises the following steps: employing ultra-short pulse laser to collect image data through a point scanning method; constructing a convolutional neural network, and inputting image data to the physical model to obtain a simulation result training network; applyingthe training network obtained through training to an adaptive method to optimize an imaging result and eliminate image distortion and acquiring the optimal phase compensation of system and sample distortion correction through a model fitting method. The method can obtain an imaging result with high optimization performance, high image quality and high imaging speed, has the advantages of high speed, high image quality, good expandability and the like, realizes high-speed wavefront distortion compensation based on machine learning, and has a great application prospect in rapid deep tissue imaging of bioscience.

The invention discloses broadband spectrum fluorescent imaging equipment which is mainly composed of an excitation light source, an imaging camera, a controller, an optical fiber unit, a focusing objective lens, a beam expander, an objective table and the like. The excitation light source, the imaging camera, the optical fiber unit, the focusing objective lens, the beam expander, and the objective table can be controlled by the controller. The fluorescent imaging wavelength coverage of the broadband spectrum fluorescent imaging equipment is 400-1700nm, can perform fluorescent imaging on a to-be-imaged object to obtain a fluorescent imaging picture, and particularly can efficiently and rapidly perform nondestructive deep tissue imaging on a living small animal without damage.

The invention discloses multi-photon ultra-deep tissue imaging equipment based on coherent detection and a detection imaging method thereof. A multi-photon imaging technology is combined with an optical coherence tomography technology to realize ultra-deep and high-molecular specific imaging of a detected sample. The equipment comprises an ultrashort pulse femtosecond laser light source, a light modulation unit and an optical coherence microscopic unit. The light modulation unit modulates input laser to generate continuous spectrum laser. The optical coherence microscopic unit is used for conducting coherent detection on a biological sample. The system can detect OCT and SH-OCT signals of a tissue at the same time and obtain the specific structure of the tissue and the molecular micro-environment information of the surrounding environment of the tissue, and can quantitatively characterize the structure and function of the tissue through an image analysis method. The equipment can reflect the ultra-deep structure and functional information of the tissue, has the advantages of ultra depth, strong molecular specificity recognition capability, high temporal-spatial resolution, rapid imaging and the like, and provides the tissue structure and function information and the molecular specificity information at the same time.

The invention provides a multi-mode optical microscopic imaging device and a microscopic imaging method. The device comprises a coaxial incident optical imaging system and an image processing system, and the coaxial incident optical imaging system comprises a light source output module, an incident illumination module, a miniaturized high numerical aperture objective lens, a light splitting focusing module and a multi-mode imaging module. The method can be applied to an experimental animal in a waking free activity state, and high-resolution and stable blood flow change distribution and nerve activity distribution in the free behavior process of the experimental animal can be obtained at the same time; multiple imaging modes in the same view field area can be fused by adopting a registration fusion technology; based on the implantable miniaturized objective lens, superficial or deep tissue imaging of an experimental animal can be realized.

The invention discloses a three-photon deep tissue imaging method and device, and the method comprises the steps: capturing a low-signal-to-noise-ratio image from a three-photon microscope, and inputting the low-signal-to-noise-ratio image into a high-performance operation unit in a continuous data flow manner; processing the continuous data stream through a pre-trained data enhancement network deployed on the high-performance arithmetic unit to obtain an enhanced data stream with a high signal-to-noise ratio; and synchronously displaying the high signal-to-noise ratio data stream on a display. On the premise that the imaging temporal-spatial resolution is not affected, the three-photon deep tissue imaging signal-to-noise ratio is improved, the algorithm is embedded into a microscopic hardware device, and real-time denoising is achieved.

A magnetic field controlled guidestar for focusing light deep inside scattering media using optical phase conjugation. Compared with the optical and ultrasonic field, the magnetic field has an exceptional penetration depth. The magnetic particle guidestar has a high light-tagging efficiency, good biocompatibility, and a small diameter which enables a sharp and bright focusing deep inside biological tissue. This new method can benefit a wide range of biomedical applications including deep-tissue imaging, neural modulation, and targeted photothermal and photodynamic therapies.

The invention discloses a fluorescence identification dye based on a nile blue matrix and a preparing method and application thereof. The fluorescence identification dye has a structure as shown in the general formula I, wherein R1, R2, R3 and R4 are C1-8 alkyl group, C1-6 alkyl sulfonic acid group and C1-6 alkyl carboxylic acid group respectively, X is halogen, and n is an integer from 1 to 4. The fluorescence identification dye can achieve targeted identification of enzyme KIAA1363 in a specific mode, has excellent tissue permeability, light stability and water solubility, low biotoxicity, excellent near infrared fluorescence property, high sensitivity and low background interference degree, and is suitable for biological sample detection. The fluorescence identification dye conducts identification and distinguishing of cancer cells and tissues and non-cancer cells and tissues by means of KIAA1363 expression difference, and the effect of distinguishing in-vitro cancer cell and tissue samples from non-cancer cell and tissue samples is remarkable especially. The fluorescence identification dye can be applied to deep issue imaging and mouse living imaging, and has high application value in imaging assistance and boundary determination during early diagnosis of cancer and operative treatment of cancer.

The field of view (FOV) of a nonlinear optical microscope (NLOM) is expected to be large enough for employing high-speed raster scanning on a mesoscale volumetric biological sample. Concurrently, three-dimensional (3D) visualization of fine sub-micron biological structures requires high enough lateral and axial resolutions, enforcing a high numerical aperture (NA) objective lens to be employed, thereby limiting the FOV of an NLOM. The invention is directed to a laser scanning NLOM, or to a large-angle optical raster scanning system, for deep biological tissue imaging with a large FOV of more than one square millimeter, up to 1.6×1.6 mm², while simultaneously maintaining a sub-femtoliter effective 3D resolution by means of a high-NA and low magnification objective lens and further maintaining a high acquisition speed with synchronized sampling, limited by the repetition rate of a high repetition rate pulsed laser source, thereby exceeding Nyquist Criterion for resolving micro-optical resolution throughout a horizontal FOV of more than one millimeter.