Usually recombinant proteins such as monoclonal antibodies are produced in mammalian cells, since these cells are capable of correctly processing the recombinant proteins. In general batch, fed batch or perfusion cell cultures are used. As higher cell densities can be reached the perfusion process typically employs considerably smaller bioreactors. To achieve high cell densities (>20 million live cells per milliliter) in a continuously operated bioreactor, efficient retention of the cells is necessary. The required degree of retention depends in this case on the growth rate of the cells and on the perfusion rate q/V (media throughput q per bioreactor volume V). The necessary selective retention of viable cells can for example be performed by inclined-channel gravity cell settlers.
Compared with simple settling tanks inclined channel separators on large scales have the advantage of considerably lower volume in relation to the separation area. A publication (Henzler, H.-J., Chemie-Technik, 1, 1992, 3) describes cell retention in inclined channel separators, which can be operated in counterflow, crossflow and in co-current flow. The flow-bearing channel cross section can be provided with plates or tubes. Usually, the inclined channel separators are arranged outside the bioreactor and attached to the bioreactor via an external circuit in order to ensure an easy accessibility of the cell retention system for maintenance and cleaning purposes.
Overall, high cell densities and an associated high productivity in continuous bioreactors may be achieved, if the following requirements are met:
Moreover, to minimize cell damage, in particular owing to inadequate oxygen supply and carbon dioxide removal outside the bioreactor, and also degradation of active ingredients owing to enzymatic activity, cell retention systems with short residence times of the cells in the cell retention system are ideal. One way of minimizing the residence time of cells in the cell retention system is to increase the flow rate in the system. However, this can lead to a wash out of cells at the top of the channels of an inclined channel gravity cell separator (cf.
Thus there is the need for a device and methods for increasing the efficiency of cell settlers.
This objective is solved by a prechamber for an inclined channel gravity cell separator with a multitude of channels for retaining cells from a reactor mixture, wherein said prechamber comprises at least one inlet for flow distribution of an incoming fluid stream and at least one aperture towards the multitude of channels and wherein said prechamber encloses a 3-dimensional space.
This prechamber has the advantage that it leads to a more even and ideally equal distribution of the incoming fluid stream into the channels of the inclined channel gravity cell separator. Thus, the cell load imposed on individual channels is more equally distributed to the channels, resulting in a higher overall efficiency of the inclined channel gravity cell separator. This is the case as cell loss at the top of the channels due to overload of individual channels is minimized.
In addition, the prechamber described herein facilitates minimized resuspension of the already sedimented cells and reintroduction into the channels due to back-mixing with the incoming fluid stream (feed flow).
Moreover possible obstructions to the flow of the reactor mixture are minimized.
As used herein the term “inclined channel gravity cell separator” refers to a device for the retention of cells e.g. from a bioreactor mixture comprising channels which open at the lower and the upper region and are inclined against the direction of gravity i.e. tilted during operation.
Typically, at their lower end the channels lead to at least one receiving chamber comprising a collection region and at their upper end the cell depleted reactor mixture (process fluid, e.g. the harvest) is withdrawn from the inclined channel gravity cell separator.
Thus, cells and cell culture solution are separated in the channels of the inclined channel gravity cell separator. This happens for example, if the cell depleted reactor mixture (process fluid, e.g. the harvest), i.e. the clarified reactor mixture is removed from the upper end of the channels. As a result of this removal reactor mixture comprising the cells to be separated, e.g. cell culture solution from a bioreactor, is sucked into the channels at their lower end. The cells sediment in the channels and counterslide on the underside of the channels against the flow direction to the lower channel ends. Thus cells sediment within the tilted channels and slide in countercurrent flow with respect to the inflowing reactor mixture out of the channels and are collected in the collection region of the at least one receiving chamber.
As used herein the term “prechamber” refers to a device which minimizes back mixing of the separated cells that slide down the channels due to gravity and the inflowing reactor mixture comprising more cells to be separated and which at the same time enables a more even and ideally equal distribution of the flow of the reactor mixture into the channels. The prechamber encloses a three dimensional (3 D) space, i.e. it can hold a predetermined volume of e.g. the incoming fluid stream.
In some embodiments the incoming fluid stream is a reactor mixture.
As used herein the term “reactor mixture” refers to the process fluid comprising the cells to be settled and thereby separated from the fluid they are supplied in.
As used herein the term “aperture” refers to a part of the prechamber through which the incoming fluid stream, i.e. the reactor mixture enters the channels of the inclined channel gravity cell separator. Thus, the aperture facilitates the equal distribution of incoming reactor mixture into the multitude of channels.
In some embodiments the prechamber is formed by an insert and at least one wall of the inclined channel gravity cell separator. In some of these embodiments least one opening is provided opposite to the at least one aperture at the lower end of the prechamber.
As used herein the term “insert” refers to a device that can be introduced into an inclined channel gravity cell separator e.g. into at least one receiving chamber of the inclined channel gravity cell separator.
The at least one opening opposite to the at least one aperture typically leads to a collection region of the at least one receiving chamber of the inclined channel gravity cell separator. It allows the transfer of portions of incoming fluid stream enriched with cells to the receiving chamber and thus prevents the formation of stagnant, non-moved zones with insufficient supply of oxygen to the cells in the prechamber. Stagnant, non-moved zones with insufficient supply of oxygen can cause cell death and finally the release of unwanted impurities, e.g. host cell proteins (HCP's).
In theory when considering flow conditions that prevent cell sedimentation in the prechamber, it is possible to operate the prechamber without the at least one opening opposite to the at least one aperture. However, as the exact composition and the flow conditions of the reactor mixture can vary during operation the prechamber described herein preferably comprises at least one opening opposite to the at least one aperture.
In addition, the at least one opening of the prechamber opposite to the at least one aperture allows larger and smaller cell aggregates to directly enter the receiving chamber.
As mentioned above, in some embodiments the insert is positioned in a receiving chamber of the inclined channel gravity cell separator and hence the prechamber is formed by at least one wall of the receiving chamber and the insert. In some cases of these embodiments, the at least one inlet for flow distribution of an incoming fluid stream is an inlet of the receiving chamber, which was already present before the insert was introduced into the receiving chamber to form the prechamber.
In some embodiments, the insert is spatially fixed via jamming it into the receiving chamber, via guiding it i.e. the as insert is led in grooves, or screwed in. These embodiments enable removal of the insert from the receiving chamber e.g. for cleaning purposes.
In some embodiments the insert is spatially fixed using anti-rotational devices e.g. those depicted in
In case of embodiments schematically depicted in
In some embodiments the antirotational device provides an inclined surface in order to upwardly deflect the inflowing reactor mixture to the at least one aperture (cf.
The minimum area of the at least one aperture of the prechamber is designed in a way that the overpressure in the prechamber does not exceed the hydrostatic pressure difference between sediment in the receiving chamber and the reactor mixture in the prechamber. This prevents the unwanted short cut of reactor mixture into the sediment of the receiving chamber via the at least one opening opposite to the at least one aperture. The width of the indentation is designed in a way that particles are not captured to prevent a slowly blocking of the at least one aperture during the processing of the reactor mixture.
In some embodiments the inclined channel gravity cell separator is autoclavable.
In some embodiments the channels of the inclined channel gravity cell separator have a square cross section. However, other channel geometries such as round, rectangular or eclipse shapes are possible.
In some embodiment the inclined channel gravity cell separator is characterized by:
In some embodiments the insert in characterized by:
Alternatively, the prechamber designed as insert can be welded and/or fixed via adhesive bonding.
Moreover to a person skilled in the art it is apparent that the insert can be spatially fixed within the receiving chamber of an inclined channel gravity cell separator using a combination of the above described means or in case that a receiving chamber comprises more than one insert, the different inserts can be fixed by different means.
In some embodiments the at least one prechamber comprises only one aperture.
In some embodiments the at least one prechamber comprises several apertures. In some of these embodiments, where the at least one prechamber comprises several apertures these apertures are all of the same dimensions. In alternative embodiments where the at least one prechamber comprises several apertures at least two apertures of a given prechamber differ in their dimensions. These differences in dimensions can reflect the difference in flow velocity of the incoming reaction mixtures, e.g. channels where a high flow velocity is expected have smaller apertures to redirect more of the incoming reaction mixture to other channels with larger apertures.
The presence of several apertures leads to a more efficient horizontal distribution. Thus, in addition to a reduction of flow velocity of the incoming fluid stream the one or more inserts as described herein effect an breakdown of the incoming fluid stream into as many partial fluid streams as there are apertures. In other words via employing one or more inserts as described herein the distribution of the slowed down partial fluid stream into the different channels takes place in a focused and predetermined manner resulting a higher overall efficiency of the inclined channel gravity cell separator as the cell load imposed on individual channels is more equally distributed and hence cell loss at the top of the channels due to overload of individual channels as well as back-mixing of the cells in the channels are minimized.
In some embodiments the at least one prechamber comprises as many apertures as there are channels in the inclined channel gravity cell separator.
In some embodiments of the prechamber described above each of said at least one apertures consist of at least one indentation, which is open and at least one elevation, which is closed.
In some embodiments of the prechamber described above for each of said at least one apertures the at least one indentation is a square or a concave cross section to the receiving chamber employing an increased indentation height from the center towards the both walls of the inclined channel where this increase is defined by the pressure or flow profile in the prechamber.
As used herein the term “indentation” refers to the part of the aperture which is open. In other words the reactor mixture enters the channels of the inclined channel gravity cell separator via the at least one indentation of the at least one aperture.
As used herein the term “elevation” refers to the part of the aperture which is closed and thus minimizes back mixing of the separated cells that slide down the channels due to gravity and inflowing reactor mixture comprising more cells to be separated.
Thus, the reactor mixture enters the inclined channel gravity cell separator via the apertures of the prechamber, which equally distribute the reactor mixture, while the combination of indentation and elevations of said apertures minimizes back mixing of the inflowing reactor mixture with the separated cells (cf.
In some embodiments each of the at least one aperture consist of exactly one indentation, which is open and exactly one elevation, which is closed.
In some embodiments of the prechamber described above said prechamber is positioned outside of the inclined channel gravity cell separator and said prechamber either alone or in combination with at least one wall of the inclined channel gravity cell separator forms the at least one aperture.
In some embodiments of the prechamber positioned outside of the inclined channel gravity cell separator, the prechamber further comprises at least one opening wherein the at least one opening connects the prechamber with a receiving chamber of the inclined channel gravity cell separator.
In some embodiments, the insert and/or the prechamber comprise additional means to guide the incoming reactor mixture such as dimples (14) and spoons (15) schematically illustrated in
In some embodiments the prechamber described herein is made of disposable material.
In another aspect what is described herein relates to an inclined channel gravity cell separator with a multitude of channels for retaining cells from a reactor mixture comprising
During an exemplary mode of operation the reactor mixture comprising cells to be separated arrives at a prechamber of an inclined channel gravity cell separator and enters the prechamber via an inlet of the prechamber. In the prechamber the reactor mixture is distributed upwards into the multitude of channels of the inclined channel gravity cell separator via the apertures of the prechamber. The reactor mixture can only pass the apertures at the indentations, which are open. This upward distribution is a result of a removal of the reactor mixture from the inclined channel gravity cell separator at the upper end of the channels. Due to the interaction of factors such as gravity and flow velocity of the reactor mixture as well as cell density etc. of the reactor mixture the cells are separated from the lighter contents of the reactor mixture in the tilted channels. The lighter contents with low particle density and low sedimentation velocity are washed out. The clarified reactor mixture (process fluid e.g. the harvest) leaves the channels at their upper end whereas the cells are caused by gravity to slide down the channels on the channel underside and exit the channels at their lower end towards the collection region of the receiving chamber. Due to the elevation of the apertures of the prechamber and the fact that the cells counterslide on the underside of the channels, the separated cells do not mix with the incoming reactor mixture—i.e. the reactor mixture enters the individual channels at the channel wall opposite the wall at which the cells slide down and the closed elevations minimize any back mixing. Instead the cells that were separated from the reactor mixture in the channels enter the collection region of the receiving chamber. The cells leave the receiving chamber via an outlet e.g. located at the bottom of the receiving chamber for example to be returned to the bioreactor or to be discarded.
In some embodiments of the inclined channel gravity cell separator described herein the inclined channel gravity cell separator comprises one receiving chamber with two prechambers, wherein each prechamber comprises one inlet and wherein said prechambers are formed by an insert and at least one wall of the inclined channel gravity cell separator and wherein at least one opening is present opposite to the at least one aperture of each prechamber.
Preferably, the two inlets for flow distribution of the reactor mixture are located exactly opposite to each other.
Another aspect what is described herein relates to the use of a prechamber as described above or an inclined channel gravity cell separator as described above, for cell separation.
In yet another aspect what is described herein relates to a method of separating cells from a reactor mixture and retaining the cells comprising the following steps:
Furthermore, what is described herein relates to an insert for generating a prechamber according to what is described above, wherein said insert has a body allowing for the formation of at least one aperture towards the multitude of channels as well as for the formation of the at least one opening opposite to the at least one aperture, if the insert is positioned in the inclined channel gravity cell separator.
An example of such an insert for generating a prechamber is a baffle plate.
In this example the inclined channel gravity cell separator is autoclavable and has a settler area of 2.4 m2. Its channels have a square cross section. Moreover, the inclined channel gravity cell separator has a reactor mixture flow (settler feed-flow) of 160 L/h, 25 plates with a length of 1 m and a plate distance of 5 mm. This exemplary inclined channel gravity cell separator has two inserts, each with 26 indentations, each of the indentations is 3 mm wide and 30 mm high.
In other words, in a 3D-view
During an exemplary mode of operation reactor mixture (12) comprising cells to be separated arrives at the prechamber (1) via an inlet (2) for flow distribution. The main part of the reactor mixture (12) is distributed upwards into the multitude of channels (5) of the inclined channel gravity cell separator via the apertures (6) of the prechamber (1), which is formed in this case by the insert (3) and the wall of the receiving chamber (4). The reactor mixture can only pass the apertures (6) at the indentations (7), which are open, but not via an elevation (8). The upward distribution is a result of a removal of the reactor mixture (12) from the inclined channel gravity cell separator (11) at the upper end of the channels (not shown). The prechamber (1) has an opening (10) opposite to the at least one aperture (6), which is here formed between at least one wall of the receiving chamber (4) of the inclined channel gravity cell separator (11) and the insert (3).
Depending on the interaction of factors such as gravity and flow velocity of the reactor mixture (12) as well as cell density etc. of the reactor mixture (12) the cells are separated from the lighter contents of the reactor mixture such as fermentation media, dead cells and cell debris in the tilted channels (5). The clarified reactor mixture leaves the channels at their upper end (not shown) whereas the cells are caused by gravity to slide down the channels (13) and exit the channels (5) at their lower end towards the collection region (9) of the receiving chamber (4). Due to the elevation (8) of the apertures (6) of the insert (3) and the fact that the cells counterslide on the underside of the channels (5), the separated cells should not mix with the incoming reactor mixture—i.e. the reactor mixture (12) enters the individual channels at the channel wall opposite to the wall at which the cells slide down (13) with the closed elevations (8) hindering the entrance to the zones of separated cells (13) and thus minimizing back mixing. Instead the cells that were separated (13) from the reactor mixture (12) in the multitude of channels (5) enter the collection region (9) of the receiving chamber (4). The cells leave the receiving chamber (4) via an outlet e.g. located at the bottom of the receiving chamber for example to be returned to the bioreactor or to be discarded.
a-d illustrates an example of how in embodiments with an insert, said insert is spatially fixed within the at least one receiving chamber (4). In this case each of the two inserts (3) is spatially fixed with one anti-rotation device positioned within each of the two inlets (2). In addition,
a & b illustrate another example of an embodiment with an insert, said insert is spatially fixed within the at least one receiving chamber (4). In this case the anti-rotational device (15) is formed as “spoon” (16). This spoon (16) in combination with additional anti rotational devices (15) spatially fixes the insert (3) in the inlet openings (2) of the receiving chamber (4). In addition, as illustrated in
a & b illustrate another example of an embodiments with an insert, said insert is spatially fixed within the at least one receiving chamber (4). In this example the insert (3) is fixed with the anti-rotational device here an intermediate flange, which is fixed with several screws e.g. screw (17) and sealed by sanitary designed O-ring gaskets vs. the flanges of the inclined channel gravity settler (11). Moreover, the apertures (6) of the insert (3) in this example comprise indentations (7) and elevations (8) and together with the multitude of channels (5) form a comb-like structure, since exactly one aperture is positioned at every channel of the multitude of channels (5). This comb like structure has the effect that the incoming reactor mixture can only pass the apertures (6) at the indentations (7), which are open, but not via an elevation (8). As described above the reactor mixture enters the individual channels at the channel wall opposite the wall at which the cells slide down and the closed elevations (8) minimize any back mixing.
Number | Date | Country | Kind |
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18169131.2 | Apr 2018 | EP | regional |
Filing Document | Filing Date | Country | Kind |
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PCT/EP2019/059935 | 4/17/2019 | WO | 00 |