IP Library Granted Patent US 12,448,659
Granted Patent B2
US 12,448,659 · App. 17/253,067 · Granted Oct 21, 2025

Method in bioprocess purification system

Inventors: Key Hyckenberg (Uppsala, SE); Helena Skoglar (Uppsala, SE); Gunnar Malmquist (Uppsala, SE); Mikael Carlsten (Uppsala, SE); Roger Lundqvist (Uppsala, SE); Dan Andersson (Uppsala, SE); Linda Mathiasson (Uppsala, SE); Lars Mattsson (Uppsala, SE); Sara Sendabo (Uppsala, SE); Mikael Berg (Uppsala, SE)
Assignee: Cytiva Sweden AB
C12Q3/00C12M29/10C12M41/12C12M41/42C12M41/48C12M47/12
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Quick Facts
Patent No.
US 12,448,659
App. No.
17/253,067
Granted
Oct 21, 2025
Kind
B2
Abstract

The present invention relates to a method for optimizing a bioprocess purification system comprising a bioreactor configured to provide a harvest comprising a target composition, and a purification process arranged downstream the bioreactor and being configured for purification of the harvest to produce a target product having a desired characteristics. The method comprising: a) detecting ( 32 ) at least one quality attribute indicative of characteristics of the target product in a downstream process, b) identifying ( 33 ) correlations between the at least one quality attribute measured in the downstream process and parameters to control a cell culture process in the bioreactor, and c) controlling ( 34 ) the cell culture process to meet the desired characteristics based on the identified correlations, whereby the target characteristics is within a p re-determined range.

Claims (16)

1. A method for controlling a bioprocess purification system comprising a continuous cell culture process in a bioreactor comprising cells capable of expressing a target product and a downstream purification process arranged downstream the continuous cell culture process and being configured for purification of harvest fluid from the continuous cell culture process to purify the target product from said harvest fluid, the method comprising:

a) withdrawing harvest fluid from the continuous cell culture process;

b) at least partly purifying the target product from the harvest fluid in the downstream purification process;

c) detecting at least one quality attribute indicative of characteristics of the at least partly purified target product;

d) identifying correlations between the at least one quality attribute measured in the downstream purification process and parameters to control the continuous cell culture process in the bioreactor; and

e) controlling the continuous cell culture process to meet desired characteristics based on the identified correlations; whereby the target characteristics are within a pre-determined range; and wherein the downstream purification process comprises:

i) a hold step comprising collecting a pre-determined volume or a pre-determined mass of the target product from the harvest fluid, whereby step ii) below starts when the pre-determined volume value is reached, or when the pre-determined mass is reached;

ii) a capture step comprising a continuous chromatography process or a semi-continuous chromatography process;

iii) a viral inactivation step comprising performing batch mode chromatography to filter the target product based on volume, time, temperature, and pH;

iv) a polishing step comprising a straight through processing (STP) with a connected batch step or continuous chromatography with a continuous load step, or a combination thereof; and

v) a delivery step comprising for subjecting the target product to an ultra-filtration step, prior to continuous or batch delivery of the target product, to further filter the target product based on pH, conductivity, absorbance, volume, and pressure.

2. The method according to claim 1 , wherein step e) further comprises controlling a concentration of the target product in the harvest fluid being fed into the downstream purification process.

3. The method according to claim 1 , wherein step e) further comprises controlling the cell culture process to adjust a composition of the harvest fluid being fed into the downstream purification process.

4. The method according to claim 1 , wherein the continuous cell culture process is a perfusion type process and step e) further comprises controlling temperature and/or aeration and/or agitation.

5. The method according to claim 1 , wherein step c) further comprises analyzing readings from at least one sensor arranged downstream the continuous cell culture process to obtain readings related to the quality attributes.

6. The method according to claim 5 , wherein the step of analyzing readings from at least one sensor comprises using at least one analytic method selected from the group consisting of: Mass Spectroscopy, (MS), Light Scattering, Size Exclusion Chromatography, (SEC), and Rahman.

Assignments (2)
CHANGE OF NAME Recorded Dec 18, 2020
From: GE HEALTHCARE BIO-SCIENCES AB
To: CYTIVA SWEDEN AB
Reel/Frame 054806/0819 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Dec 17, 2020
From: HYCKENBERG, KEY; SKOGLAR, HELENA; MALMQUIST, GUNNAR; CARLSTEN, MIKAEL; LUNDQVIST, ROGER; ANDERSSON, DAN; MATHIASSON, LINDA; MATTSON, LARS; SENDABO, SARA; BERG, MIKAEL
To: GE HEALTHCARE BIO-SCIENCES AB
Reel/Frame 054675/0523 →
Priority Claims (1)
GB 1810772 · Jun 29, 2018 · national
Continuity (1)
Related Publication 20210269888A1 · Sep 2, 2021
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