VACCINE FOR SARS-COV-2
    1.
    发明公开

    公开(公告)号:US20240358808A1

    公开(公告)日:2024-10-31

    申请号:US18287771

    申请日:2022-04-22

    Abstract: Personalized cancer vaccines are created by predicting whether a first neoantigen or a second neoantigen of an individual cancer patient has a stronger binding affinity for a human leukocyte antigen (HLA) complex of the patient and creating a particle containing the neoantigen with the stronger predicted binding affinity. Such a predicting step includes artificial intelligence, statistical modeling, or a combination thereof. Such a particle is created by encapsulating the neoantigen with the stronger predicted binding affinity for the HLA complex of the patient in a material. Placing the antigen in a particular sized particle is referred to here as Size Exclusion Antigen Presentation Control, (SEAPAC) used in methods of treating the patient using such a personalized cancer vaccine.

    METHOD AND DEVICES FOR DETECTING VIRUSES AND BACTERIAL PATHOGENS

    公开(公告)号:US20240345066A1

    公开(公告)日:2024-10-17

    申请号:US18754127

    申请日:2024-06-25

    Abstract: The embodiments disclose a sensor for detecting an analyte including at least one substrate, a first conductive layer added to the at least one substrate forming an electrode pattern with at least two working electrodes and one counter electrode, a second conductive layer added to the first conductive layer that forms the electrode pattern with at least two working electrodes and one counter electrode, at least one single-stranded molecule bound to the second conductive layer, wherein the at least one single-stranded molecule binds to the analyte when complementary single-stranded molecules bond together to form a double-stranded molecule, and wherein the binding of the at least one single-stranded molecule bound to the second conductive layer and at least one single-stranded molecule of the analyte generates a profile response indicative of at least a positive or negative or inconclusive test result.

    Production and delivery tracking and sample verification of patient-specific therapeutics

    公开(公告)号:US12112838B2

    公开(公告)日:2024-10-08

    申请号:US18523564

    申请日:2023-11-29

    Applicant: NantCell, Inc.

    Abstract: Systems and methods for tracking biological samples are presented. Intrinsic and extrinsic biological sample data and/or intrinsic and extrinsic patient data may be used to label a biological sample obtained at a point-of-care facility, which may be sent to a processing facility, wherein the labeled biological sample undergoes analysis and/or processing into a labeled therapeutic. The labeled therapeutic is delivered back to the point-of-care facility, wherein the labeled therapeutic is tested for the presence of the additives prior to administration to a patient. Multi-factor validation is performed, including validating the identity of the patient to a container, validating the identity of the labeled biological sample/therapeutic to the container, and thus, validating the identity of the labeled therapeutic to the patient. The entire life cycle of a biological sample used to generate a personalized therapeutic is validated, and ensures that mix-ups or errors in administration are reduced or eliminated.

    System and method for generating a procreant functional program

    公开(公告)号:US12112244B2

    公开(公告)日:2024-10-08

    申请号:US17221384

    申请日:2021-04-02

    Inventor: Kenneth Neumann

    CPC classification number: G06N20/00 A61B5/43 G16H10/40 G16H10/60 G16H20/00

    Abstract: A system for generating a procreant functional program includes a computing device configured to obtain a procreant marker as a function of a procreant system, determine a procreant appraisal as a function of the procreant marker, wherein determining further comprises producing a procreant enumeration as a function of the procreant marker, and determining the procreant appraisal as a function of the procreant enumeration, and a safe range, receive a conduct indicator, identify a functional signature as a function of the conduct indicator, wherein identifying further comprises obtaining a salubrious reference, and identifying the functional signature as a function of the salubrious reference and the conduct indicator using a functional machine-learning model, and generate a functional program as a function of the functional signature and procreant appraisal using a program machine-learning model.

    Method and system for creating reconfigurable bio-processing workflows

    公开(公告)号:US12110481B2

    公开(公告)日:2024-10-08

    申请号:US16607516

    申请日:2018-04-18

    CPC classification number: C12M41/48 C12M23/26 C12M23/28 G16H10/40

    Abstract: A bio-processing system (100) is presented. The bio-processing system (100) includes one or more bio-processing units (110-114), one or more process supporting devices (116, 118), one or more sensors (120-132), and a bio-processing workflow controller (104) wirelessly coupled to at least one of the one or more bio-processing units (110-114), the one or more process supporting devices (116, 118), and the one or more sensors (120-132). The bio-processing workflow controller (104) includes a processor (202) configured to create a reconfigurable bio-processing workflow, and where the reconfigurable bio-processing workflow is representative of an arrangement of one or more of the one or more bio-processing units (110-114), the one or more process supporting devices (116, 118), and the one or more sensors (120-32) to perform at least one bio-processing operation.

    COMPUTER-IMPLEMENTED METHOD AND DEVICE FOR CARRYING OUT A MEDICAL LABORATORY VALUE ANALYSIS

    公开(公告)号:US20240331813A1

    公开(公告)日:2024-10-03

    申请号:US18251058

    申请日:2021-10-25

    CPC classification number: G16H10/40 G16H50/20

    Abstract: A computer-implemented method for providing at least one predicted value for at least one medical laboratory variable, in particular for use in a medical laboratory value analysis. The method includes: providing at least one laboratory value progression which specifies a progression of historical laboratory values of the at least one laboratory variable at at least two historical points in time; ascertaining at least one laboratory variable feature for each of the at least one laboratory variable from the corresponding laboratory value progression; determining the at least one predicted value at a predetermined prediction time on the basis of a trained, data-based prediction model and on the basis of the at least one laboratory variable feature for each of the at least one laboratory value progression.

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