Sterile connector for the sterile transfer of a liquid medium
AssigneeSartorius Stedim Biotech GmbH
InventorMario DEUSE
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AssigneeSartorius Stedim Biotech GmbH
InventorMario DEUSE
Estimating the term…
The invention relates to a sterile connector for the sterile transfer of a liquid medium, in particular a biological medium, from a liquid container (2) into a fluid chamber (3, 3), wherein the sterile connector (1) has a first coupling device (5) and a second coupling device (6). It is proposed that the first coupling device (5) has a fluid inlet (7) and a fluid outlet (8) and also a first cannula (9), the latter having an end which is directed away from the fluid inlet (7) and forms the fluid outlet (8), that the second coupling device (6) has a fluid passage (10) which, in an initial state of the sterile connector (1), is covered axially by a first septum (11), that the fluid outlet (8), in the initial state of the sterile connector (1), is arranged in a hermetically sealed region of the first coupling device (5) and the surface (11a) of the first septum (11) facing axially away from the fluid passage (10) is arranged in a hermetically sealed region of the second coupling device (6), and that, in a fluidic connection process starting from the initial state of the sterile connector (1), a fluidic connection between the fluid inlet (7) and the fluid passage (10) can be produced by the fact that the end of the first cannula (9) forming the fluid outlet (8) pierces the first septum (11) of the second coupling device (6).
A sterile connector for the sterile transfer of a liquid, in particular a biological medium, from a liquid container (2) into a fluid chamber (3, 3′), for example of a bioprocess-technical system (4), in particular of a bioreactor, wherein the sterile connector (1) has a first and a second coupling device (5, 6),
The sterile connector as claimed in any of the preceding claims, characterized in that the region of the second coupling device (6), which in the initial state is hermetically sealed, is delimited at least partially, preferably completely, by the first septum (11) and a second septum (12);
The sterile connector as claimed in any of the preceding claims, characterized in that the first coupling device (5) has a second cannula (17) which is arranged coaxially to the first cannula (9) and through which the first cannula (9) can be moved;
The sterile connector as claimed in any of the preceding claims, characterized in that the region of the first coupling device (5), which is hermetically sealed in the initial state of the sterile connector (1), is delimited towards the environment at least partially by at least one sealing envelope (18, 23) of the first coupling device (5).
The sterile connector as claimed in any of the preceding claims, characterized in that the first coupling device (5) comprises a first sealing envelope (18), in particular in the form of a bellows, which in the initial state radially surrounds the axial cannula portion of the second cannula (17) which pierces the second septum (12) during the coupling process;
The sterile connector as claimed in any of the preceding claims, characterized in that the coupling process causes an axial cannula portion of the second cannula (17) to pierce the first sealing envelope (18);
The sterile connector as claimed in any of the preceding claims, characterized in that the second cannula (17) is fixed to a cannula holder (19) which is mounted so as to be axially movable in the first coupling device (5);
The sterile connector as claimed in any of the preceding claims, characterized in that a guide device (20) is provided which, during the coupling process, causes an axial guiding of the first coupling device (5) relative to the second coupling device (6);
The sterile connector as claimed in any of the preceding claims, characterized in that the first coupling device (5) comprises a second sealing envelope (23), in particular in the form of a hose which is closed at one end, which in the initial state radially surrounds an axial cannula portion of the first cannula (9) having the fluid outlet (8) which during the activation process pierces the first septum (11);
The sterile connector as claimed in any of the preceding claims, characterized in that the activation process causes an axial cannula portion of the first cannula (9) to pierce the second sealing envelope (23).
The sterile connector as claimed in any of the preceding claims, characterized in that an actuation element (24) is provided on the cannula holder (19) for manual actuation of the cannula holder (19), by means of which the cannula holder (19) together with the second cannula (17) and the second coupling device (6) can be moved generally linearly, in particular also rotationally, relative to the first coupling device (5) during the activation process;
The sterile connector as claimed in any of the preceding claims, characterized in that the actuation element (24) is axially, in particular also rotationally, movable in the guide opening (25) during the activation process;
The sterile connector as claimed in any of the preceding claims, characterized in that the fluid passage (10) of the second coupling device (6) opens into a fluid chamber (3′) of the second coupling device (6) which has a fluid outlet (15) fluidically connected to the fluid passage (10) or which is otherwise closed.
Dependencies are inferred from the claim text.