The present invention relates to aseptic connectors, and more particularly to aseptic connectors with sensors useful in the cultivation of cells. The invention also relates to a method of forming an aseptic connection.
In the production of biopharmaceuticals there is a trend towards single-use systems, not least for the cell cultivation operations. Typical single-use systems for cell cultivation involve bioreactors where the cell culture is contained in a flexible bag, either an inflatable self-supporting bag where agitation is provided by rocking (see e.g. U.S. Pat. No. 6,190,913), or a bag supported by a stainless steel support structure where agitation is usually provided by an impeller (see e.g. U.S. Pat. No. 7,629,167) or pneumatically (see e.g. WO 2007/068945A1).
In both types of system there is a need for applying sensors in contact with the cell culture, in order to monitor important variables such as cell density, pH, oxygen concentration and concentrations of various metabolites and/or nutrients. Such sensors are typically integrated with the bag via welded ports as in EP2503320. However, many sensors cannot be sterilised by the same methods that are preferred to use for sterilisation of the bag.
Accordingly there is a need for a convenient technology to connect separately packaged sensors aseptically to a single-use bioreactor bag.
One aspect of the invention is to provide a connection unit for aseptic connection of sensors to a bioreactor bag. This is achieved with a first connection unit as defined herein.
One advantage is that the connection unit can be packaged separately and be sterilized by a different method than the bioreactor bag. Further advantages are that the sensors can be stored under refrigeration and that the risk of damage to the sensors by folding of the bag can be eliminated. Yet further advantages are that the number of ports on the bag can be minimized and that several different sensor combinations can conveniently be provided for one single bag type.
A second aspect of the invention is to provide a connection unit to be mounted on a bag and capable of connecting aseptically to a connection unit with sensors. This is achieved with a second connection unit as defined in the claims.
A third aspect of the invention is to provide an aseptic connection of sensors to a bioreactor bag. This is achieved with a connection as defined in the claims.
A fourth aspect of the invention is to provide a method of aseptically connecting sensors to a bioreactor bag. This is achieved with a method as defined in the claims.
Further suitable embodiments of the invention are described in the dependent claims.
In one aspect, illustrated by
In certain embodiments, the first connector unit comprises at least two, such as at least three or at least four sensor surfaces. It is advantageous to have several sensor surfaces in the same connector unit, in that only one port is needed. Cultivation of cells typically requires the monitoring of several variables and it is desirable to have a minimum number of ports, as each port adds cost and may carry a risk of breaching the sterility. One or more of these sensor surfaces, such as at least two, three or four sensor surfaces, may be enzymatic sensor surfaces, i.e. sensors surfaces comprising an immobilized enzyme, although one or more of the sensor surfaces may additionally or alternatively be electrochemical sensor surfaces or sensor surfaces based on optical dyes. Enzymatic sensors are commonly used for e.g. sensing of glucose (using immobilized glucose oxidase) and glutamine (typically using immobilized glutaminase) and may also be used for sensing of other nutrients/metabolites in cell cultivation. Enzymatic sensors need to be refrigerated during storage and may not be compatible with radiation sterilization methods commonly used for bioreactor bags. Hence, there is a particular need for separately packaged enzymatic sensors to be aseptically connected with the bag immediately before use. A first connector unit with enzymatic sensors may e.g. be sterilized using ethylene oxide, hydrogen peroxide or other chemical sterilants. By selecting suitable sensors from the group above and combining them with heat resistant polymers the sensor patch can also be sterilized by autoclaving or electron beam processing. The stability of enzymatic and dye based sensors during sterilization and storage can be enhanced if they are packaged in protective atmosphere (e.g. N2 or Ar) to prevent oxidation. Such a protective atmosphere is easier to achieve for a separate sensor patch than for the whole bag.
In some embodiments, a ratio between a depth 16 and a width 17 of the recess 4 is less than 1, such as less than 0.5 or less than 0.25. It is advantageous to have a low depth-to-width ratio, as this diminishes the risk of clogging the recess with cells during cultivation. The risk for cell clogging can be further reduced by having the sensor surfaces mounted on a movable member, as illustrated in
In a second aspect, illustrated by
In some embodiments, a ratio between a depth 26 and a width 27 of the second opening 15 is less than 1, such as less than 0.5 or less than 0.25. It is advantageous to have a low depth-to-width ratio, as this diminishes the risk of clogging the recess with cells during cultivation. Alternatively, or additionally, the second opening can have beveled edges 31 as illustrated in
In a third aspect the present invention discloses an aseptic connection formed by the mating of the first connection unit 1 of any one of the embodiments disclosed above with the second connection unit 2 of any one of the embodiments disclosed above. The connection may further comprise a clamp 23, holding the first and second units together. As discussed above, this can e.g. be a Tri-Clamp or Tri-Clover clamp. The clamp may engage the flanges 21,22 of the first and second units. The aseptic connection may have a total height, h, of less than 3 cm, such as less than 2 cm. This enables use of the connection on the bottom side of a rocking bioreactor bag, as in
In a fourth aspect, the invention discloses a method of forming an aseptic connection, comprising the steps of:
In some embodiments, the method further comprises a step d) of applying a clamp over the mated first and second connection units to secure the connection.
In certain embodiments, the second connection unit 2 is arranged on a flexible bioreactor bag 30, with the second opening 15 forming a port in a wall 20 of the flexible bioreactor bag and the method further comprises a step e) of adding cell culture media and cells to the bag.
In some embodiments, the method further comprises a step f) of cultivating cells in the bag and monitoring at least two parameters with the sensor surfaces.
This written description uses examples to disclose the invention, including the best mode, and also to enable any person skilled in the art to practice the invention, including making and using any devices or systems and performing any incorporated methods. The patentable scope of the invention is defined by the claims, and may include other examples that occur to those skilled in the art. Such other examples are intended to be within the scope of the claims if they have structural elements that do not differ from the literal language of the claims, or if they include equivalent structural elements with insubstantial differences from the literal languages of the claims. Any patents or patent applications mentioned in the text are hereby incorporated by reference in their entireties, as if they were individually incorporated.
| Number | Date | Country | Kind |
|---|---|---|---|
| 1550111-7 | Feb 2015 | SE | national |
This application is a continuation of U.S. application Ser. No. 15/545,378 filed on Jul. 21, 2017, which claims the priority benefit of PCT/EP2016/051954 filed on Jan. 29, 2016 which claims priority benefit of Swedish Application No. 1550111-7 filed Feb. 4, 2015. The entire contents of which are hereby incorporated by reference herein.
| Number | Name | Date | Kind |
|---|---|---|---|
| 7832296 | Klees | Nov 2010 | B2 |
| 20050163667 | Krause | Jul 2005 | A1 |
| 20050239197 | Katerkamp et al. | Oct 2005 | A1 |
| 20070185472 | Baumfalk et al. | Aug 2007 | A1 |
| 20080132876 | Felt | Jun 2008 | A1 |
| 20090230633 | Willemstyn et al. | Sep 2009 | A1 |
| 20110124035 | Broadley et al. | May 2011 | A1 |
| 20110236962 | Loebbert et al. | Sep 2011 | A1 |
| 20130137950 | Harttig et al. | May 2013 | A1 |
| 20130289517 | Williams et al. | Oct 2013 | A1 |
| 20140170671 | McGarr et al. | Jun 2014 | A1 |
| 20140260712 | Damren et al. | Sep 2014 | A1 |
| 20150344161 | Selker et al. | Dec 2015 | A1 |
| Number | Date | Country |
|---|---|---|
| 102004015703 | Nov 2005 | DE |
| 2010017519 | Feb 2010 | WO |
| 2011075036 | Jun 2011 | WO |
| 2012128703 | Sep 2012 | WO |
| 2013063550 | May 2013 | WO |
| 2013147688 | Oct 2013 | WO |
| 2015184189 | Dec 2015 | WO |
| Entry |
|---|
| Chinese Office Action for CN Application No. 201680008689.X mailed May 12, 2021 (18 pages with English translation). |
| Japanese Office Action for JP Application No. 2017-539615 mailed Feb. 10, 2020 (9 pages with English translation). |
| PCT International Search Report and Written Opinion for PCT Application No. PCT/EP2016/051954 mailed Apr. 11, 2016 (11 pages). |
| PCT International-Type Search Report for ITS/SE15/00016 mailed Feb. 4, 2015 (6 pages). |
| Weichert et al., “Integrated Optical Single-Use Sensors: Moving Toward a True Single-Use Factory for Biologics and Vaccine Production,” BioProcess International, 2014, 12(5), http://www.bioprocessintl.com/upstream-processing/upstream-single-use-technologies/integrated-optical-single-use-sensors-moving-toward-true-single-use-factory-biologics-vaccine-production/. |
| Database WPI, XP-002755786 (1 page). |
| Number | Date | Country | |
|---|---|---|---|
| 20210253993 A1 | Aug 2021 | US |
| Number | Date | Country | |
|---|---|---|---|
| Parent | 15545378 | US | |
| Child | 17235195 | US |