53 results about "Focal volume" patented technology

A method and apparatus are presented for non-invasively monitoring at least one characteristic of a region of interest in a body. The body is illuminated by pulsed light to induce a photoacoustic effect. Acoustic radiation is detected, and measured data indicative thereof is generated. The photoacoustic effect is controlled by carrying out at least one of the following: providing the pulsed light of at least two different wavelength, analyzing the measured data to determine time variations of at least one predetermined parameter of a time dependent acoustic signal for each of wavelength, and determining oxygen saturation level in the region of interest; and operating a plurality of acoustic elements configured for detection of the acoustic radiation, to thereby define a focal volume for acoustic radiation detection to match dimensions of the region of interest.

A system and method for treating skin. The System comprises one or more ultrasound transducers and one or more pairs of RF electrodes. The ultrasound transducers are adapted to focus ultrasound energy at one or more focal volumes in the skin. The RF electrodes are adapted to deliver RF energy to the one or more focal volumes. The method comprises heating the skin to a first temperature at one or more focal volumes in the skin by focusing ultrasound energy at the one or more focal volumes. The focal regions are then heated to a second temperature, the second temperature being higher than the first temperature, by generating an RF current in a region of the skin containing the focal regions.

A shock wave applicator includes a shock wave generator and an asymmetrical reflector portion in a housing. Asymmetry of the reflector portion is combined with one or more wave generators to produce a variety of focal volumes and wave fronts for medical treatment.

A system and method for treating skin. The System comprises one or more ultrasound transducers and one or more pairs of RF electrodes. The ultrasound transducers are adapted to focus ultrasound energy at one or more focal volumes in the skin. The RF electrodes are adapted to deliver RF energy to the one or more focal volumes. The method comprises heating the skin to a first temperature at one or more focal volumes in the skin by focusing ultrasound energy at the one or more focal volumes. The focal regions are then heated to a second temperature, the second temperature being higher than the first temperature, by generating an RF current in a region of the skin containing the focal regions.

The invention provides an apparatus for electromagnetically affecting a particle of interest in a specimen. The apparatus includes (a) a stage capable of supporting the specimen; (b) a detector including at least one camera, wherein the detector is capable of resolving a particle of interest within the specimen; (c) a means for locating the particle of interest in three dimensions; (d) a means for focusing electromagnetic radiation to a focal volume within the specimen; and (e) a means for adjusting the relative positions of the stage and electromagnetic radiation focusing means, thereby positioning the particle of interest within the focal volume.

The method of stimulating a substance is disclosed. The method has the steps of activating an acoustic shock wave generator or source to emit acoustic shock waves; and subjecting the substance to the acoustic shock waves stimulating said substance wherein the substance is positioned within a path of the emitted shock waves and away from a geometric focal volume or point of the emitted shock waves. In one embodiment the emitted shock waves are divergent or near planar. In another embodiment the emitted shock waves are convergent having a geometric focal volume of point at a distance of at least X from the source, the method further comprising positioning the substance at a distance less than the distance X from the source. The substance is a tissue having cells. The tissue can be an organ of a mammal. The mammal may be a human or an animal. The organ may be a heart, a brain, skin, a liver or a kidney or any other organ. The tissue may be muscle, cartilage, tendon, bone, teeth or gums. The tissue may be a part of the vascular system, a part of the nervous system, a part of the urinary or reproductive system, a part of the lymph node or pituitary systems, a part of the ocular system or a part of a skeletal system.

The invention relates to a separation free bioanalytical assay method for measuring an analyte from a biological fluid or suspension comprising of microparticles as a bioaffinity binding solid phase, a biospecific secondary reagent labelled with a two-photon fluorescent dipyrrometheneboron difluoride dye, focusing the laser into the reaction suspension, measuring two-photon excited fluorescence from single microparticles when they randomly float or are guided by the radiation pressure of the excitation laser through the focal volume of the laser beam using a two-photon fluorescent dipyrrometheneboron difluoride dye. The dye has the structure (II): Either at least one of groups R1, R2, R3, R4, R5, R6 and R7 is a substituted or unsubstituted phenyl, thienyl, pyrrolyl, furanyl, oxazolyl, isoxazolyl oxadiazolyl, imidazolyl, benzoxazolyl, benzothiazolyl, benzimidazolyl, benzofuranyl, indolyl, conjugated ethenyl, dienyl or trienyl group, and at least one of the groups R1, R2, R3, R4, R5, R6 or R7 is substituted to yield a chemically reactive group that can be used for selective covalent linkage to other molecules, and at least one of the groups R1, R2, R3, R4, R5, R6 or R7 is substituted to yield a water-solubilizing group, and the remaining groups of R1, R2, R3, R4, R5, R6 and R7 are each independently selected from the group consisting of hydrogen, halogen, alkyl, cyano, carboxy, each of which can optionally be substituted; or groups R1, R2, R3, R5, R6 and R7 are substituted or unsubstituted alkyl groups, R4 is a hydrogen or a substituted or unsubstituted alkyl, and at least one of the groups R1, R2, R3, R4, R5, R6 or R7 is substituted to yield a chemically reactive group that can be used for selective covalent linkage to other molecules; and at least one of the groups R1, R2, R3, R4, R5, R6 or R7 is su

A system and method for providing multi-photon processing treatment to a patient. A localized, multi-photon processing event is initiated within a vicinity of an unwanted pigment in order to remove the pigment. The multi-photon processing event requires a relatively low energy, but very intense, pulse of light. The low amount of energy per pulse allows ablation of the material to be highly localized, with negligible thermal damage to surrounding material. The multi-photon event may be initiated by focusing a suitable electromagnetic pulse, such as a 2 mJ laser pulse having a 100 to 300 femtoseconds pulse duration, into a focal volume small enough that the intensity exceeds 1011 Watts / cm2. A suitably configured Ti:Sapphire solid state laser may provide such pulses at 1-10 kHz. By repeating the multi-photon processing event along the location of a tattoo, the tattoo may be removed with no damage to the surrounding tissue.

A fluorescence focal modulation microscopy system (10) and method (200) is disclosed for high resolution molecular imaging of thick biological tissues (40) with single photon excited fluorescence. Optical sectioning and diffraction limited spatial resolution are retained for imaging inside a multiple-scattering medium by the use of focal modulation, a technique for suppressing the background fluorescence signal excited by the scattered light. The focal modulation microscopy system has a spatial phase modulator (18) inserted in the excitation light path (34), which varies the spatial distribution of coherent excitation light around the focal volume periodically at a preset frequency. A fluorescence focal modulation image (122,142) is formed on a display (114) with the demodulated fluorescence, while a confocal image (120,140) is available simultaneously.

The method of stimulating a plant substance is disclosed. The method has the steps of activating a pressure pulse or an acoustic shock wave generator or source to emit pressure pulse or acoustic shock waves; and subjecting the plant substance to the pressure pulse or acoustic shock waves stimulating said plant substance wherein the substance is positioned within a path of the emitted shock waves. In one embodiment the emitted pressure pulse or shock waves are divergent or near planar. In another embodiment the emitted shock waves are convergent having a geometric focal volume of point at a distance of at least X from the source, the method further comprising positioning the substance at a distance less than the distance X from the source. The substance is a plant tissue having cells. The tissue can be a seed, zygotic embryo or somatic embryogenic culture of somatic embryos of plants. The plant may be a vegetable, tree, shrub or tuber. The tissue may be a part of the root system, a part of the stem system or a part of the leaf system. The method of stimulating includes activating the cells within the treated tissue thereby releasing growth factor proteins or other chemical compositions promoting growth and accelerating germination or plant growth.

A method of attaching or reattaching a ligament, tendon, cartilage or other soft tissue to a bone mass has the steps of: positioning or placing the ligament, tendon, cartilage or other soft tissue adjacent to the bone mass; anchoring or otherwise fastening the ligament, tendon, cartilage or soft tissue to the bone mass; and transmitting shock waves to the ligament, tendon or other soft tissue and the bone mass. Preferably the ligament, tendon, cartilage or other soft tissue is positioned in the path of the emitted shock waves and away from geometric focal volume or point of the emitted shock waves. The shock waves may be transmitted during the surgical procedure or post operatively in one or more treatment dosages or both. In so treating the ligament, tendon, cartilage or other soft tissue should be positioned at a distance away from any geometric focal point to minimize hemorrhaging. The soft tissue may include cartilage or muscle tissue. In the case of cartilage, the tissue can be inserted into a bone mass prepared cavity and optionally anchored there by a covering bone plug.

A diagnostic method and associated system includes the steps of exposing at least one sample location with excitation radiation through a single optical waveguide or a single optical waveguide bundle, wherein the sample emits emission radiation in response to the excitation radiation. The same single optical waveguide or the single optical waveguide bundle receives at least a portion of the emission radiation from the sample, thus providing co-registration of the excitation radiation and the emission radiation. The wavelength of the excitation radiation and emission radiation is synchronously scanned to produce a spectrum upon which an image can be formed. An increased emission signal is generated by the enhanced overlap of the excitation and emission focal volumes provided by co-registration of the excitation and emission signals thus increasing the sensitivity as well as decreasing the exposure time necessary to obtain an image.

Various embodiments include a method of producing chemically pure and stably dispersed metal and metal-alloy nanoparticle colloids with ultrafast pulsed laser ablation. A method comprises irradiating a metal or metal alloy target submerged in a liquid with ultrashort laser pulses at a high repetition rate, cooling a portion of the liquid that includes an irradiated region, and collecting nanoparticles produced with the laser irradiation and liquid cooling. The method may be implemented with a high repetition rate ultrafast pulsed laser source, an optical system for focusing and moving the pulsed laser beams, a metal or metal alloy target submerged in a liquid, and a liquid circulating system to cool the laser focal volume and collect the nanoparticle products. By controlling various laser parameters, and with optional liquid flow movement, the method provides stable colloids of dispersed metal and metal-alloy nanoparticles. In various embodiments additional stabilizing chemical agents are not required.

The method of stimulating a tissue of a subsurface organ is disclosed. The method has the steps of activating an acoustic shock wave generator or source to emit acoustic shock waves; and subjecting the tissue to the acoustic shock waves stimulating said tissue wherein the tissue is positioned within a path of the emitted shock waves and away from a geometric focal volume or point of the emitted shock waves. In one embodiment the emitted shock waves are divergent or near planar. In another embodiment the emitted shock waves are convergent having a geometric focal volume of point at a distance of at least X from the source, the method further comprising positioning the tissue at a distance less than the distance X from the source. The subsurface organ is a tissue having cells. The tissue is a part of the incretin system. The subsurface organ is preferably the pancreas of a diabetic or at risk diabetic patient. The treatment stimulates the pancreatic tissue by an analgesic effect on the nerves and a stimulation of the insulin producing islets.

Disclosed is a method of producing a chemically pure and stably dispersed organic nanoparticle colloidal suspension using an ultrafast pulsed laser ablation process. The method comprises irradiating a target of an organic compound material in contact with a poor solvent with ultrashort laser pulses at a high repetition rate and collecting the nanoparticles of the organic compound produced. The method may be implemented with a high repetition rate ultrafast pulsed laser source, an optical system for focusing and moving the pulsed laser beam, an organic compound target in contact with a poor solvent, and a solvent circulating system to cool the laser focal volume and collect the produced nanoparticle products. By controlling various laser parameters, and with optional poor solvent flow movement, the method provides stable colloids of dispersed organic nanoparticles in the poor solvent in the absence of any stabilizing agents.

A system and method for providing multi-photon processing treatment to a patient. A localized, multi-photon processing event is initiated within a vicinity of an unwanted pigment in order to remove the pigment. The multi-photon processing event requires a relatively low energy, but very intense, pulse of light. The low amount of energy per pulse allows ablation of the material to be highly localized, with negligible thermal damage to surrounding material. The multi-photon event may be initiated by focusing a suitable electromagnetic pulse, such as a 2 mJ laser pulse having a 100 to 300 femtoseconds pulse duration, into a focal volume small enough that the intensity exceeds 1011 Watts / cm2. A suitably configured Ti:Sapphire solid state laser may provide such pulses at 1-10 kHz. By repeating the multi-photon processing event along the location of a tattoo, the tattoo may be removed with no damage to the surrounding tissue.