1. Field of the Invention
This invention relates to apparatus for performing bioanalytic processing and analysis. In particular, the present invention relates to a bioanalytical reaction device and a cartridge thereof. The cartridge contains at least one sample chamber for storing biological samples, the bioanalytical reaction device can process and analyze.
2. Description of Related Art
One example of a bioanalytical reaction is the DNA polymerase chain reaction. The polymerase chain reaction (PCR) is a technique that permits amplification and detection of nucleic acid sequences. This technique has a wide variety of applications including DNA sequence analysis, detection of genetic mutations, diagnoses of viral infections, to name but a few. With the PCR a specific target sequence or strand of DNA can exponentially amplificated. The polymerase chain reaction comprises repeated cycles of target denaturation by heating the sample, primer annealing at a lower temperature and polymerase-mediated extension at a slight higher temperature. At the last step, the DNA polymerase synthesizes a new DNA strand complementary to the DNA template strand. Under optimal conditions, the amount of DNA target strands is doubled.
Besides to PCR, other bioanalytical reactions are known, for example the ligase chain reaction. More generally, several import bioanalytical methods are dependent upon changing the temperature of samples in a controlled fashion. Therefore, there is a need for the automation of these methods.
Several mechanical and automated bioanalytical reaction devices are known in the art. Certain devices use cartridges for storing biological samples, so that the one or more biological samples in one cartridge can be temporarily stored, while the biological samples in another cartridge can be processed in the bioanalytical reaction device. An operator only needs to remove the one cartridge from the device and insert the other cartridge into the device.
Such cartridges have various interfaces, such as one or more interfaces for heating a sample in the cartridge as well as one or more interfaces for optical reading out the result of the reaction, which is, for example, indicated by a certain color of the sample or by certain illuminating substances.
More specifically, the samples to be processed are stored in one or more chambers in the cartridge. In general, an interface is provided by a wall of one of the chambers through which the sample can be heated or analyzed. If an optical readout has to be performed, the chamber needs a transparent wall as interface.
It may be a problem, that such interfaces can be damaged or become dirty. Especially, when an operator handles such a cartridge, there is the possibility that he touches the cartridge at a location of an interface. An interface in the form of a thin wall can already be damaged by the force applied by a finger. Also, sweat or grease can be deposited on the interface in this way. A damaged or dirty interface can result in leakage from the cartridge or falsification of the optical detection.
It is an object of the invention to provide a safe and simple cartridge.
According to an exemplary embodiment of the invention, a cartridge for a bioanalytical reaction device is provided, the cartridge comprising at least one sample chamber for a sample, the at least one sample chamber having a wall through which the sample can be processed or analyzed by the bioanalytical reaction device, wherein the cartridge comprises a housing and a platform, the platform comprising the at least one sample chamber, wherein the platform is movably connected to the housing, such that the platform is movable between a stowed position, in which the wall is protected by the housing, and an extended position, in which the wall is outside of the housing.
Such a cartridge is protected from becoming damaged or polluted without unnecessarily complicating the structural design of the cartridge and the bioanalytical reaction device.
It is to be understood that herein the term “cartridge” is used for every kind of device capable of being connected with a bioanalytical reaction device. For example, a cartridge may be a holder, magazine, cassette or carrier.
The at least one sample chamber is placed on a platform (or disc or carrier) that can be extended from the cartridge. In the stowed position, the sample chamber is inside the housing of the cartridge. Consequently, the chamber is protected from getting damaged or dirty. For use, the platform is extended from the cartridge, e. g. for enabling it to interface with heaters and optical sensors of a bioanalytical reaction device.
The wall of the at least one sample camber can be a heating interface or, if the wall is translucent (at least for some wavelength), an optical interface for interfacing with components of the bioanalytical reaction device, such as a heater or an optical sensor.
According to a further exemplary embodiment, a cartridge is provided, wherein the at least one sample chamber is connected to a channel for filling the at least one sample chamber, the channel ending in the vicinity of the actuation means.
Vicinity may be understood as relating to a length of one of the following intervals: 0 to 15 millimeters (mm), 0 to 10 mm, and 0 to 5 mm.
The at least one sample chamber is connected to a channel for filling and draining the at least one sample chamber with fluids, such as the solution in which the sample is dissolved. Instead of a channel, every means adapted to conduct a fluid from one point to another, such as a line, a pipe or a hose, can be used. One end of the channel can be connected to a line of the bioanalytical reaction device, which can pump fluids over the line into the sample chamber. The end of the channel is part a fluidal interface of the cartridge.
Placing the end of the channel in the vicinity of the actuation means has the advantage that a mechanical connection for moving the platform and a fluidal connection can be integrated in one component of the cartridge.
According to a further exemplary embodiment, a cartridge is provided, wherein a part of the channel is located within the actuation means. The channel may be located in a shaft for rotating the platform or in a spindle for moving the platform. This is one possibility of integrating the mechanical and the fluidal connection of the cartridge. Further the at least one sample chamber may be filled independent of the position of the platform.
According to a further exemplary embodiment, a cartridge is provided, wherein the wall is arranged at a first side of the platform, wherein the platform has a second side opposite to the first side, and wherein the platform in the extended position is accessible from the first side and the second side by the bioanalytical reaction device for processing or analyzing the sample. The sample within the at least sample chamber may be processed or analyzed simultaneously from two sides of the platform.
According to a further exemplary embodiment, a cartridge is provided, wherein at least one dimension of the cartridge with the platform in the extended position is bigger than this dimension of the cartridge with the platform in the stowed position. Therefore, the cartridge with the platform in the stowed position can easily be stored.
According to a further exemplary embodiment, a cartridge is provided, wherein the platform is rotatably connected to the housing. Preferably, the actuation means is a shaft and the platform is connected to the shaft for rotating the platform about a rotation axis. More preferably, the shaft extends up to an opening in the housing. In this way, the mechanical connection of an actuator of the bioanalytical reaction device to the cartridge for rotating the platform can easily be established. Further, the opening in the housing may provide a guidance for the shaft, and therefore for the platform.
Alternatively, according to a further exemplary embodiment, a cartridge is provided, wherein the platform is slidably connected to the housing. The actuation means may be a spindle for translatorily moving the platform from the stowed position to the extended position.
According to a further exemplary embodiment, a cartridge is provided, wherein the platform has the form of a plate, which, in the stowed position, is arranged between a first wall and a second wall of the housing. A platform in the form of a plate, i. e. a component with one dimension much smaller than the two other dimensions in different directions, can be provided with more than one sample chamber and all of the sample chambers are easily accessible by a bioanalytical reaction device.
According to a further exemplary embodiment, a cartridge is provided, wherein the wall of the at least one sample chamber is thin. For minimizing the thermal barrier, the wall may be thin and can for example be a foil with a high heat conductance. Herein, with a thin wall a wall is meant which has a thickness of about less than 200 micrometers (μm). A thin wall may also optimize the transparence of the optical interface of the at least one sample chamber.
According to a further exemplary embodiment, a cartridge is provided, wherein the at least one sample chamber is formed by an opening in the platform which is covered by a foil or thin layer forming the thin wall.
Another aspect of the invention is a bioanalytical reaction device having a slot or receptacle for receiving the cartridge, comprising an actuator for extending and stowing the platform of the cartridge. The actuator may be a step motor.
According to a further exemplary embodiment, a bioanalytical reaction device is provided, having a reservoir for filling the at least one sample chamber, wherein the reservoir is connectable with the at least one sample chamber over a line ending in a mechanical connection of the actuator with the actuation means for moving the platform. Within the mechanical connection, there also may be the fluidal connection of the bioanalytical reaction device with the cartridge. The fluidal interface or fluidal connection of the bioanalytical reaction device and the mechanical connection are integrated in one component.
According to a further exemplary embodiment, a bioanalytical reaction device is provided having a cartridge presence sensor for detecting the presence and/or the correct insertion of the cartridge in the slot. Only when a cartridge is present in the slot, the bioanalytical reaction device should operate the line for filling the sample chamber. Otherwise, fluids can polute the interior of the bioanalytical reaction device.
According to a further exemplary embodiment, a bioanalytical reaction device is provided, which is adapted to effect the actuator to move the platform in the extended position, when the cartridge presence sensor detects the presence of the cartridge in the slot.
These and other aspects of the invention will be apparent from and elucidated with reference to the embodiment described hereinafter.
Below, an embodiment of the present invention is described in more detail with reference to the attached drawings. It shows:
Further, in
Platform 30 comprises a plate 38 that may be made of plastics. For each sample chamber 34 there is an opening 36 in the plate 38. On one first side of the plate 38, a first or upper foil 40 is applied. For example, the upper foil 40 may be glued to the plate 38. In the shown embodiment, the upper foil 40 has a thickness of about 100 μm. In the region of the opening 36 the upper foil 40 forms a thin wall of the sample chamber, the thin wall being a heating interface 44 of the sample chamber 34. If a heating or cooling source is arranged outside of the sample chamber 34 in the region of the heating interface 44 heat may be transferred to the interior of the sample chamber 34 or may exit it.
On the other second side of the plate 38, opposite to the first side, there is applied a second or lower foil 42 of a translucent material. The lower foil 42 may be glued or in some other way be connected to the plate 38. Also, the lower foil 42 has a thickness of about 100 μm. In the region of the opening 36, the lower foil 42 forms an optical interface 46 of the sample chamber 34. In this region, light can penetrate the translucent lower foil 42. Light coming from the interior of the sample chamber can be detected by an optical sensor arranged near the optical interface 46 of the sample chamber 34.
Further,
It is to be understood, that there are other possibilities to form the sample chamber 34 and the channels 48, 50, 52 within the platform 30. For example, the platform 30 may be manufactured from two parts being mirror symmetric and having openings and grooves which form the sample chambers and the channels, when the two parts are connected with each other. Further, it would be possible, to provide the plate 30 with pits. With a foil or thin layer covering the pits sample chambers can be formed on the plate. In this case, such sample chambers would have only one interface.
From
The shaft 32 with the channels 52 is a fluidal interface 54 of the platform 30.
Since the fluidal interface 54 is in the vicinity of the rotation axis A, it can be accessed over the mechanical connection of the bioanalytical reaction device for rotating the platform 30. Therefore, the mechanical connection and the fluidic connection are combined and the number of connections between the cartridge 10 and a bioanalytical reaction device is reduced.
Over a controller 76 which is connected over control lines 78 with the actuator 64, the pump and reservoir mechanism 68, the heater 72 and the optical sensor 74, the bioanalytical reaction device 60 can control the analysis and processing of the samples in the sample chambers in an automated way. For example, the bioanalytical reaction device 60 can conduct the above mentioned PCR procedure.
Further, it is possible, that the bioanalytical reaction device 60 controls the extension and the stowing of the platform 30 in an automated way. When an operator inserts the cartridge 10 into the slot 62, a mechanical sensor 80 detects the presence of the cartridge 10. Alternatively, the detection can be done with an optical sensor. With this input the controller 76 directs the actuator 64 to rotate the platform 30 in the extended position. After that, several processings, like filling the chambers with different solutions, heating the sample chambers 34 and analyzing the light from the sample chambers 34, can be performed by the controller 76. When the processing and the analysis is done, the controller 76 directs the actuator 64 to rotate the platform 30 back to the stowed position and an operator can remove the cartridge 10 from the bioanalytical reaction device 60.
While the invention has been illustrated and described in detail in the drawings and foregoing description, such illustration and description are to be considered illustrative or exemplary and not restrictive; the invention is not limited to the disclosed embodiment. Other variations to the disclosed embodiment can be understood and effected by those skilled in the art and practising the claimed invention, from a study of the drawings, the disclosure, and the appended claims. In the claims, the word “comprising” does not exclude other elements or steps, and the indefinite article “a” or “an” does not exclude a plurality. A single processor or controller or other unit may fulfill the functions of several items recited in the claims. The mere fact that certain measures are recited in mutually different dependent claims does not indicate that a combination of these measures cannot be used to advantage. Any reference signs in the claims should not be construed as limiting the scope.
Number | Date | Country | Kind |
---|---|---|---|
09157972 | Apr 2009 | EP | regional |
This application is a continuation of International Application Ser. No. PCT/CH2010/000095 filed Apr. 9, 2010, now pending, which claims the benefit under 35 U.S.C. §119(a) of European Patent Application No. EP09157972, filed Apr. 15, 2009, the entire contents of both of which are incorporated herein by reference.
Number | Name | Date | Kind |
---|---|---|---|
3607134 | McIntyre | Sep 1971 | A |
3633877 | Bodine | Jan 1972 | A |
4256697 | Baldwin | Mar 1981 | A |
4371498 | Scordato et al. | Feb 1983 | A |
4571087 | Ranney | Feb 1986 | A |
4849340 | Oberhardt | Jul 1989 | A |
4857274 | Simon | Aug 1989 | A |
4857453 | Ullman et al. | Aug 1989 | A |
4874137 | Chiba | Oct 1989 | A |
4943522 | Eisinger et al. | Jul 1990 | A |
4965047 | Hammond | Oct 1990 | A |
4983523 | Li et al. | Jan 1991 | A |
5004583 | Guruswamy et al. | Apr 1991 | A |
5096669 | Lauks et al. | Mar 1992 | A |
5133937 | Frackleton et al. | Jul 1992 | A |
5147609 | Grenner | Sep 1992 | A |
5219526 | Long | Jun 1993 | A |
5229580 | Chioniere | Jul 1993 | A |
5296374 | Culshaw et al. | Mar 1994 | A |
5397537 | Kanda et al. | Mar 1995 | A |
5500187 | Deoms et al. | Mar 1996 | A |
5504007 | Haynes | Apr 1996 | A |
5504013 | Senior | Apr 1996 | A |
5512159 | Yoshioka et al. | Apr 1996 | A |
5578495 | Wilks | Nov 1996 | A |
5589136 | Northrup et al. | Dec 1996 | A |
5597532 | Connolly | Jan 1997 | A |
5609822 | Carey et al. | Mar 1997 | A |
5609823 | Harttig et al. | Mar 1997 | A |
5622871 | May et al. | Apr 1997 | A |
5627041 | Shartle | May 1997 | A |
5726026 | Wilding et al. | Mar 1998 | A |
5746978 | Bienhaus et al. | May 1998 | A |
5770029 | Nelson et al. | Jun 1998 | A |
5788928 | Carey et al. | Aug 1998 | A |
5843680 | Manian et al. | Dec 1998 | A |
5846487 | Bennett, II | Dec 1998 | A |
5856174 | Lipshutz et al. | Jan 1999 | A |
5882903 | Andrevski et al. | Mar 1999 | A |
5912134 | Shartle | Jun 1999 | A |
5928880 | Wilding et al. | Jul 1999 | A |
5928907 | Woudenberg et al. | Jul 1999 | A |
5945334 | Besemer et al. | Aug 1999 | A |
5994056 | Higuchi | Nov 1999 | A |
6077669 | Little et al. | Jun 2000 | A |
6100084 | Miles et al. | Aug 2000 | A |
6143573 | Rao et al. | Nov 2000 | A |
6210881 | Little et al. | Apr 2001 | B1 |
6329139 | Nova et al. | Dec 2001 | B1 |
6369893 | Christel et al. | Apr 2002 | B1 |
6391541 | Petersen et al. | May 2002 | B1 |
6426225 | Lewis et al. | Jul 2002 | B1 |
6431476 | Taylor et al. | Aug 2002 | B1 |
6440725 | Pourahmadi et al. | Aug 2002 | B1 |
6521181 | Northrup et al. | Feb 2003 | B1 |
6524532 | Northrup | Feb 2003 | B1 |
6551817 | Besemer et al. | Apr 2003 | B2 |
6565815 | Chang et al. | May 2003 | B1 |
6664104 | Pourahmadi et al. | Dec 2003 | B2 |
6699711 | Hahn et al. | Mar 2004 | B1 |
6713297 | McMillan et al. | Mar 2004 | B2 |
6783736 | Taylor et al. | Aug 2004 | B1 |
6818185 | Petersen et al. | Nov 2004 | B1 |
6878540 | Pourahmadi et al. | Apr 2005 | B2 |
6881541 | Petersen et al. | Apr 2005 | B2 |
6887693 | McMillan et al. | May 2005 | B2 |
6893879 | Petersen et al. | May 2005 | B2 |
6987018 | Taylor et al. | Jan 2006 | B2 |
7188001 | Young et al. | Mar 2007 | B2 |
7569346 | Petersen et al. | Aug 2009 | B2 |
20020019060 | Petersen et al. | Feb 2002 | A1 |
20020084329 | Kaye et al. | Jul 2002 | A1 |
20040200909 | McMillan et al. | Oct 2004 | A1 |
20050042137 | Petersen et al. | Feb 2005 | A1 |
20050204373 | Ueno et al. | Sep 2005 | A1 |
20050221281 | Ho | Oct 2005 | A1 |
20060019379 | Taylor et al. | Jan 2006 | A1 |
20060027686 | Taylor et al. | Feb 2006 | A1 |
20060030038 | Taylor et al. | Feb 2006 | A1 |
20080057572 | Petersen et al. | Mar 2008 | A1 |
20100068706 | Pourahmadi et al. | Mar 2010 | A1 |
Number | Date | Country |
---|---|---|
667599 | Oct 1988 | CH |
19820466 | Nov 1999 | DE |
0271448 | Jun 1988 | EP |
0337690 | Oct 1989 | EP |
0512334 | Nov 1992 | EP |
0757830 | Dec 1998 | EP |
0706649 | Jan 2001 | EP |
1383602 | Jun 2006 | EP |
1181098 | Jul 2006 | EP |
0915173 | Jan 2007 | EP |
1179585 | Jul 2008 | EP |
938163 | Oct 1963 | GB |
10-96725 | Apr 1998 | JP |
2005-181143 | Jul 2005 | JP |
2008-145125 | Jun 2008 | JP |
9511454 | Apr 1995 | WO |
9529473 | Nov 1995 | WO |
9838487 | Sep 1998 | WO |
9958637 | Nov 1999 | WO |
2006136990 | Dec 2006 | WO |
WO 2009019448 | Feb 2009 | WO |
2010064160 | Jun 2010 | WO |
Entry |
---|
Machine Translation of JP10096725 A. |
International Search Report dated Jun. 23, 2010 from PCT/CH2010/000095. |
Number | Date | Country | |
---|---|---|---|
20120034687 A1 | Feb 2012 | US |
Number | Date | Country | |
---|---|---|---|
Parent | PCT/CH2010/000095 | Apr 2010 | US |
Child | 13273533 | US |