Methods, systems, and devices for real time execution and optimization of concurrent test protocols on a single device

US11249799B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-11249799-B2
Application numberUS-201414181486-A
CountryUS
Kind codeB2
Filing dateFeb 14, 2014
Priority dateSep 26, 2011
Publication dateFeb 15, 2022
Grant dateFeb 15, 2022

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

Provided herein are medical testing devices, systems, and methods that integrate multiplex, multi-technology, multi-configuration, multisample, or multi-threading capabilities. These capabilities are achieved using one or more of a level operations and communications architecture, a protocol execution engine, and a machine vision and processing system, method, or device in order to make testing of biologic or other samples more efficient in terms of cost, time, energy, or by prioritizing at least one other objective.

First claim

Opening claim text (preview).

The invention claimed is: 1. A system for performing biological or chemical assays, comprising: a cartridge for receiving a sample from a single patient; a sample processing device for receiving the cartridge and for containing a plurality of stations, an individual station configured to accept at least a portion of said sample and perform at least one subtask for the biological or chemical assay with said portion of said sample, wherein the sample processing device performs at least an analyte measurement, a blood analysis, and nucleic acid amplification; and a controller that generates a schedule for subtasks performed simultaneously by said plurality of stations based on i) a comparison of the efficiency of said schedule as compared to the efficiency of a schedule in which input processes are scheduled sequentially, wherein a second schedule is determined to be more efficient than a first schedule where said second schedule requires less time, or fewer resources, or both, than said first schedule, and ii) ii) anticipated availability of said plurality of stations, and that provides instructions that effects operations of said plurality of stations to perform said subtasks in accordance with said schedule; wherein reagents are provided to the sample processing device through the cartridge without requiring reagents to be pumped into the device through tubes and/or tanks located outside of the cartridge and wherein the controller is provided with cartridge layout including where each test reagent is located in the cartridge wherein device resources comprises at least one or more pipettes and a centrifuge, wherein each device resource is further characterized by its operating characteristics and capabilities for the controller. 2. The system of claim 1 further comprising a collection station configured to collect information from at least one station, and wherein the controller maintains or modifies said schedule based on the efficiency of said schedule, anticipated availability of said plurality of stations, and said information collected by said collection station. 3. The system of claim 1 wherein said station is selected from the group consisting of: sample preparation station, assay station, detection station, incubation station, and sample handling station. 4. The system of claim 1 wherein at least one station is a centrifuge or a thermal block. 5. The system of claim 1 wherein said schedule is based on a plurality of said subtasks being performed in a predetermined sequence or relative timing of said subtasks. 6. The system of claim 1 wherein said schedule generated by said controller provides reduces the total time required to perform the plurality of subtasks as compared to the total time required by alternative schedules. 7. The system of claim 1 wherein said cartridge receives a sample collection unit configured to accept a sample that has a volume of 250 μL or less. 8. The system of claim 1 , further comprising a detection station, wherein said detection station is configured to collect information regarding the status of an individual biological or chemical assay and utilizing said information effective to maintain or modify the schedule of subtasks. 9. The system of claim 1 , wherein said controller generates a schedule for said plurality of subtasks performed by said plurality of stations using a flexible scheduling algorithm to generate an ordered schedule of subtasks for the plurality of stations of the one or more devices such that when the subtasks are performed by the one or more devices, the input processes are completed in a manner more efficiently than if the input processes were performed sequentially by the plurality of stations. 10. The system of claim 8 , wherein said controller generates a schedule for said plurality of subtasks performed by said plurality of stations using a flexible scheduling algorithm to generate an ordered schedule of subtasks for the plurality of stations of the one or more devices such that when the subtasks are performed by the one or more devices, the input processes are completed in a manner more efficiently than if the input processes were performed sequentially by the plurality of stations. 11. The system of claim 1 , comprising a first station and a second station, wherein said first station is configured to perform a subtask that cannot be performed by said second station. 12. The system of claim 8 , comprising a first station and a second station, wherein said first station is configured to perform a subtask that cannot be performed by said second station. 13. The system of claim 1 , wherein said controller is configured to generate a schedule by using a flexible scheduling algorithm to generate an ordered schedule of subtasks for the plurality of stations of the one or more devices such that when the subtasks are performed by the one or more devices, the input processes are completed in a manner more efficiently than if the input processes were performed sequentially by the plurality of stations. 14. The system of claim 1 , wherein, on average, the set of input processes are performed in less than 80% of the time required if the set of input processes were performed sequentially. 15. The system of claim 1 , wherein the set of input processes are completed with one or more devices consuming less than the total amount of energy required by the one or more devices if the set of input processes were performed sequentially. 16. The system of claim 1 , wherein the set of input processes are completed with a total cost less than that required if the set of input processes were performed sequentially. 17. The system of claim 1 , wherein said plurality of stations are selected from the group containing sample processing stations, detection stations, and supply stations that provide consumable reagents; and further comprising a control unit that is configured to individually control the plurality of stations to perform their associated subtasks according to the generated schedule of subtasks. 18. The system of claim 17 , wherein said sample collection station is configured to accept a sample with a total volume of 250 μL or less. 19. A system for performing biological or chemical assays, comprising: a cartridge for receiving a sample from a single patient; a sample processing device for receiving the cartridge and for containing a plurality of stations, an individual station configured to accept at least a portion of said sample and perform at least one subtask for the biological or chemical assay with said portion of said sample, wherein the sample processing device performs at least an analyte measurement, a blood analysis, and nucleic acid amplification; and a controller that generates a schedule for subtasks performed simultaneously by said plurality of stations based on iii) a comparison of the efficiency of said schedule as compared to the efficiency of a schedule in which input processes are scheduled sequentially, wherein a second schedule is determined to be more efficient than a first schedule where said second schedule requires less time, or fewer resources, or both, than said first schedule, and iv) ii) anticipated availability of said plurality of stations, and that provides instructions that effects operations of said plurality of stations to perform said subtasks in accordance with said schedule; wherein reagents are provided to the sample processing device through the cartridge without requiring reagents to be pumped into the device through tubes and/or tanks located out

Assignees

Inventors

Classifications

  • G06F15/16Primary

    Combinations of two or more digital computers each having at least an arithmetic unit, a program unit and a register, e.g. for a simultaneous processing of several programs {(coordinating program control therefor G06F9/52; in regulating and control system G05B)} · CPC title

  • Scheduling · CPC title

  • in which an application is distributed across nodes in the network (software deployment G06F8/60; multiprogramming arrangements G06F9/46) · CPC title

  • specially adapted for proprietary or special-purpose networking environments, e.g. medical networks, sensor networks, networks in vehicles or remote metering networks · CPC title

  • G06F9/4881Primary

    Scheduling strategies for dispatcher, e.g. round robin, multi-level priority queues · CPC title

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What does patent US11249799B2 cover?
Provided herein are medical testing devices, systems, and methods that integrate multiplex, multi-technology, multi-configuration, multisample, or multi-threading capabilities. These capabilities are achieved using one or more of a level operations and communications architecture, a protocol execution engine, and a machine vision and processing system, method, or device in order to make testing…
Who is the assignee on this patent?
Labrador Diagnostics Llc
What technology area does this patent fall under?
Primary CPC classification G06F15/16. Mapped technology areas include Physics.
When was this patent published?
Publication date Tue Feb 15 2022 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 1 related publication on this page (citations in our corpus or others sharing the same primary CPC).