Methods for controlling the growth of prokaryotic and eukaryotic cells

US2020172846A1 · US · A1

Patent metadata
FieldValue
Publication numberUS-2020172846-A1
Application numberUS-202016780640-A
CountryUS
Kind codeA1
Filing dateFeb 3, 2020
Priority dateMar 29, 2018
Publication dateJun 4, 2020
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.

The present disclosure relates to methods for control of cell growth rates where cell growth is measured in situ. The methods are applicable to bacterial cells, mammalian cells, non-mammalian eukaryotic cells, plant cells, yeast cells, fungi, and archea.

First claim

Opening claim text (preview).

We claim: 1 . An automated cell processing system comprising a cell growth device comprising: a housing; a motor; a thermal control device; a spectrophotometer; a processor; an electrical connection configured to be electrically coupled to the thermal control device; and a rotating growth vial wherein the rotating growth vial comprises a vial; a drive engagement mechanism configured to engage with the motor to spin the vial; and a light path through the vial for a light beam generated by the spectrophotometer, wherein the spectrophotometer is configured to measure and deliver to the processor an optical density of cells in the vial; a cell concentration module; and a transformation module; wherein the processor accepts input from a user, receives from the spectrophotometer the optical density of the cells in the vial, through the electrical connection directs the thermal control device to adjust the temperature of the vial. 2 . The automated cell processing system of claim 1 , wherein optical density is measured at a pre-programmed wavelength. 3 . The automated cell processing system of claim 1 , wherein optical density is measured at a wavelength selected by a user. 4 . The automated cell processing system of claim 1 , wherein the optical density is measured continuously. 5 . The automated cell processing system of claim 1 , wherein the optical density is measured at intervals specified by the user or programmed into the processor. 6 . The automated cell processing system of claim 1 , wherein the processor notifies a user when a desired optical density is reached. 7 . The automated cell processing system of claim 1 , wherein the vial volume is 2-100 ml. 8 . The automated cell processing system of claim 1 , wherein the cells are grown to a target optical density value at a target time. 9 . The automated cell processing system of claim 1 , wherein the vial is fabricated from polycarbonate or polypropylene. 10 . The automated cell processing system of claim 1 , wherein the transformation module comprises a flow-through electroporation device. 11 . An automated cell processing system comprising: a cell growth device comprising a housing; a motor; a thermal control device; a spectrophotometer; a processor; an electrical connection configured to be electrically coupled to the thermal control device; and a disposable rotating cell growth vial wherein the disposable rotating growth vial comprises a vial; a drive engagement mechanism connected to the motor and configured to spin the vial; and a first light path through the vial to measure an optical density of cells in the vial via the spectrophotometer; a transformation module; and an editing module; wherein the processor accepts input from a user, receives from the spectrophotometer the optical density of the cells, and through the electrical connection directs the thermal device to adjust the temperature of the vial to grow the cells. 12 . The automated cell processing system of claim 11 , wherein the optical density is measured at a pre-programmed wavelength. 13 . The automated cell processing system of claim 11 , wherein the optical density is measured at a wavelength selected by a user. 14 . The automated cell processing system of claim 11 , wherein the optical density is measured continuously. 15 . The automated cell processing system of claim 11 , wherein the optical density is measured at intervals specified by the user or programmed into the processor. 16 . The automated cell processing system of claim 11 , wherein the processor notifies a user when a desired optical density is reached. 17 . The automated cell processing system of claim 11 , wherein the cells are grown to a target optical density value at a target time. 18 . The automated cell processing system of claim 11 , wherein the transformation module comprises a flow-through electroporation device. 19 . The automated cell processing system of claim 11 , further comprising a liquid handling system controlled by the processor. 20 . The automated cell processing system of claim 11 , wherein the vial further comprises a second light path.

Assignees

Inventors

Classifications

  • Stirrer or mobile mixing elements · CPC title

  • C12M35/04Primary

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

  • Flask, bottle or test tube · CPC title

  • Electrical or electromagnetic means, e.g. for electroporation or for cell fusion · CPC title

  • Multiple separable units; Modules · CPC title

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Frequently asked questions

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What does patent US2020172846A1 cover?
The present disclosure relates to methods for control of cell growth rates where cell growth is measured in situ. The methods are applicable to bacterial cells, mammalian cells, non-mammalian eukaryotic cells, plant cells, yeast cells, fungi, and archea.
Who is the assignee on this patent?
Inscripta Inc
What technology area does this patent fall under?
Primary CPC classification C12M35/04. Mapped technology areas include Chemistry & Metallurgy.
When was this patent published?
Publication date Thu Jun 04 2020 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).