SYSTEMS, METHODS, AND DEVICES FOR THREE-DIMENSIONAL IMAGING, MEASUREMENT, AND DISPLAY OF WOUNDS AND TISSUE SPECIMENS

    公开(公告)号:US20250069224A1

    公开(公告)日:2025-02-27

    申请号:US18943247

    申请日:2024-11-11

    Abstract: The present disclosure provides methods, systems, and devices for coregistering imaging data to form three-dimensional superimposed images of a biological target such as a wound, a tumor, or a surgical bed. A three-dimensional map can be generated by projecting infrared radiation at a target area, receiving reflected infrared radiation, and measuring depth of the target area. A three-dimensional white light image can be created from a captured two-dimensional white light image and the three-dimensional map. A three-dimensional fluorescence image can be created from a captured two-dimensional fluorescence image and the three-dimensional map. The three-dimensional white light image and the three-dimensional fluorescence image can be aligned using one or more fiducial markers to form a three-dimensional superimposed image. The superimposed image can be used to track wound healing and to excise cancerous tissues, for example, breast tumors. Images can be in the form of videos.

    Systems, methods, and devices for three-dimensional imaging, measurement, and display of wounds and tissue specimens

    公开(公告)号:US12141964B2

    公开(公告)日:2024-11-12

    申请号:US17423449

    申请日:2020-01-17

    Abstract: The present disclosure provides methods, systems, and devices for coregistering imaging data to form three-dimensional superimposed images of a biological target such as a wound, a tumor, or a surgical bed. A three-dimensional map can be generated by projecting infrared radiation at a target area, receiving reflected infrared radiation, and measuring depth of the target area. A three-dimensional white light image can be created from a captured two-dimensional white light image and the three-dimensional map. A three-dimensional fluorescence image can be created from a captured two-dimensional fluorescence image and the three-dimensional map. The three-dimensional white light image and the three-dimensional fluorescence image can be aligned using one or more fiducial markers to form a three-dimensional superimposed image. The superimposed image can be used to track wound healing and to excise cancerous tissues, for example, breast tumors. Images can be in the form of videos.

    COMPOSITIONS AND METHODS FOR LUNG PRESERVATION

    公开(公告)号:US20240251783A1

    公开(公告)日:2024-08-01

    申请号:US18565387

    申请日:2022-03-08

    CPC classification number: A01N1/0226 A01N1/0284

    Abstract: Provided is a lung preservation composition comprising a non-carbonic buffered nutrient media, preferably a phosphate buffered nutrient media, and a dextran, optionally Dextran 40 and and optionally prostaglandin E1 (PGE1), and optionally at least one of alpha 1 antitrypsin (A1AT), an impermeant, optionally raffinose, an antioxidant, optionally glutathione, and necrostatin-1. Also described is a method of preserving a lung prior to and/or during transplant using said lung preservation composition, and kits comprising one or more components of the lung preservation composition.

    DIAGNOSTIC ASSAYS FOR MOVEMENT DISORDERS
    7.
    发明公开

    公开(公告)号:US20240241136A1

    公开(公告)日:2024-07-18

    申请号:US18537455

    申请日:2023-12-12

    CPC classification number: G01N33/6896 G01N2333/4728 G01N2800/2835

    Abstract: In an aspect, there is provided a method for differentiating movement disorders in a subject, comprising performing a seeding amplification assay for alpha-synuclein in a subject sample utilizing a specific buffer conditions, measuring the alpha-synuclein aggregation of the sample in the assay based on at least one of the following kinetic parameters: lag time, growth phase, T50, ThT max and AUC; and differentiating between Parkinson's Disease (PD) and Multiple System Atrophy (MSA) based on said sample kinetic parameters compared to control kinetic parameters, wherein control kinetic parameters for MSA show at least a two-fold difference from the control kinetic parameters for PD.

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