Bioreactor using acoustic standing waves

US2016355776A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2016355776-A1
Application numberUS-201615238624-A
CountryUS
Kind codeA1
Filing dateAug 16, 2016
Priority dateMar 15, 2012
Publication dateDec 8, 2016
Grant date

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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.

A perfusion bioreactor includes at least one ultrasonic transducer that can acoustically generate a multi-dimensional standing wave. The standing wave can be used to retain cells in the bioreactor, and can also be utilized to dewater or further harvest product from the waste materials produced in a bioreactor.

First claim

Opening claim text (preview).

1 . A method for obtaining expanded cells, comprising: culturing cells in a system comprising: a bioreactor including a reaction vessel having an internal volume, an agitator, a feed inlet, and an outlet; and a filtering device, comprising: an inlet fluidly connected to the bioreactor outlet; a flow chamber; an ultrasonic transducer and a reflector located opposite the ultrasonic transducer, the ultrasonic transducer being driven to produce a multi-dimensional acoustic standing wave in the flow chamber; and a recycle outlet downstream of the flow chamber connected to a recycle inlet of the reaction vessel; wherein the cells are cultured in a host fluid in the internal volume of the bioreactor to expand the cells; sending a portion of the host fluid containing the cells from the bioreactor to the flow chamber; trapping cells from the host fluid in the multi-dimensional acoustic standing wave; wherein cells that are trapped in the multi-dimensional acoustic standing wave form cell clusters that grow to a critical size and subsequently fall out of the multi-dimensional acoustic standing wave. 2 . The method of claim 1 , further comprising sending the host fluid containing untrapped cells from the flow chamber back to the bioreactor through the recycle outlet of the filtering device. 3 . The method of claim 1 , wherein the multi-dimensional standing wave has an axial force component and a lateral force component which are of the same order of magnitude. 4 . The method of claim 1 , wherein the bioreactor is a perfusion bioreactor. 5 . The method of claim 1 , wherein the flow chamber contains a flexible bag in which the multi-dimensional acoustic standing wave is produced, and wherein the cell clusters that fall out of the multi-dimensional acoustic standing wave fall to a bottom of the bag. 6 . The method of claim 5 , further comprising removing the bag from the flow chamber. 7 . The method of claim 1 , wherein the filtering device is in the form of a flexible bag with the ultrasonic transducer and the reflector attached to opposite surfaces thereof. 8 . The method of claim 1 , wherein the cells are T cells, B cells, or NK cells. 9 . The method of claim 1 , wherein the ultrasonic transducer comprises: a housing having a top end, a bottom end, and an interior volume; and a crystal at the bottom end of the housing having an exposed exterior surface and an interior surface, the crystal being able to vibrate when driven by a voltage signal; and an air gap between the crystal and the top end of the housing. 10 . The system of claim 9 , wherein a backing layer contacts the interior surface of the crystal, the backing layer being made of a substantially acoustically transparent material. 11 . A method for culturing viruses or exosomes, comprising: culturing cells in a system comprising: a bioreactor including a reaction vessel having an internal volume, an agitator, a feed inlet, and an outlet; and a filtering device, comprising: an inlet fluidly connected to the bioreactor outlet; a flow chamber; an ultrasonic transducer and a reflector located opposite the ultrasonic transducer, the ultrasonic transducer being driven to produce a multi-dimensional acoustic standing wave in the flow chamber; a product outlet; and a recycle outlet downstream of the flow chamber connected to a recycle inlet of the reaction vessel; wherein the cells are cultured in a host fluid in the internal volume of the bioreactor to expand the cells, and wherein the cells are engineered to produce the viruses or exosomes; continuously sending a portion of the host fluid from the bioreactor to the flow chamber; trapping the viruses or exosomes in the multi-dimensional acoustic standing wave; wherein the viruses or exosomes that are trapped in the multi-dimensional acoustic standing wave form clusters that grow to a critical size and subsequently fall out of the multi-dimensional acoustic standing wave into the product outlet; and recovering the viruses or exosomes from the product outlet. 12 . The method of claim 11 , further comprising sending the host fluid from the flow chamber back to the bioreactor through the recycle outlet of the filtering device. 13 . The method of claim 11 , wherein the multi-dimensional standing wave has an axial force component and a lateral force component which are of the same order of magnitude. 14 . The method of claim 11 , wherein the bioreactor is a perfusion bioreactor. 15 . The method of claim 11 , wherein the flow chamber contains a flexible bag in which the multi-dimensional acoustic standing wave is produced, and wherein the cell clusters that fall out of the multi-dimensional acoustic standing wave fall to a bottom of the bag. 16 . The method of claim 15 , further comprising removing the bag from the flow chamber. 17 . The method of claim 11 , wherein the filtering device is in the form of a flexible bag with the ultrasonic transducer and the reflector attached to opposite surfaces thereof. 18 . The method of claim 11 , wherein the cells are Chinese hamster ovary (CHO) cells, NSO hybridoma cells, baby hamster kidney (BHK) cells, or human cells. 19 . The method of claim 11 , wherein the ultrasonic transducer comprises: a housing having a top end, a bottom end, and an interior volume; and a crystal at the bottom end of the housing having an exposed exterior surface and an interior surface, the crystal being able to vibrate when driven by a voltage signal; and an air gap between the crystal and the top end of the housing. 20 . The system of claim 19 , wherein a backing layer contacts the interior surface of the crystal, the backing layer being made of a substantially acoustically transparent material.

Assignees

Inventors

Classifications

  • C12M47/10Primary

    Separation or concentration of fermentation products (bioreactors combined with means for distillation or extraction of liquid fuel C12M43/02) · CPC title

  • Means for mixing, agitating or circulating fluids in the vessel (by introduction of gas C12M29/06, C12M29/14, mixing in general or mixers per se B01F; mixing in apparatus for chemical or physical processes B01J) · CPC title

  • Separating microorganisms from the culture medium; Concentration of biomass (separating microorganisms from their culture media C12N1/02) · CPC title

  • Bags · CPC title

  • C12M35/04Primary

    Mechanical means, e.g. sonic waves, stretching forces, pressure or shear stimuli · CPC title

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What does patent US2016355776A1 cover?
A perfusion bioreactor includes at least one ultrasonic transducer that can acoustically generate a multi-dimensional standing wave. The standing wave can be used to retain cells in the bioreactor, and can also be utilized to dewater or further harvest product from the waste materials produced in a bioreactor.
Who is the assignee on this patent?
Flodesign Sonics Inc
What technology area does this patent fall under?
Primary CPC classification C12M47/10. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Dec 08 2016 00:00:00 GMT+0000 (Coordinated Universal Time) (A1). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).