The present invention relates to the art of fluid handling system systems, and in particular to an automated fluid handling system that is highly flexible and configurable. The fluid handling system may e.g. be a liquid chromatography system, a filtration system, a chemical synthesis system or the like.
There is a large range of fluid handling systems e.g. in laboratories. Such systems comprise a number of fluid handling units, e.g. one or more pumps, valves, mixers, sensor units etc of different types. Said fluid handling units are interconnected by fluid conduits in the form of, rigid or flexible tubes or the like. Even though some systems may be designed for a specific type of application with a specific flow path, there often exists a need for flexibility and ability to alter or optimize the fluid flow path of the system. Moreover, upgrading is often restricted to specific kits provided by the manufacturer, and upgrade kits often is supplied as external add-on equipment to be arranged besides the original system, thus enlarging the foot print of the system and that need to be connected to the system both fluidically and electrically (i.e. to a system control bus or the like). Moreover, replacement of defect fluid handling units is a time consuming and delicate task.
One type of liquid handling system is liquid chromatography systems which is a standard method in laboratories, and there are a broad range of liquid chromatography systems available on the market. Common to most of the present systems is the lack of flexibility in adapting the instrument to a variety of different applications.
The object of the invention is to provide a new fluid handling system, which system overcomes one or more drawbacks of the prior art. This is achieved by the fluid handling system as defined in the independent claims.
One advantage with such a fluid handling systems is that the system may easily be upgraded without need for add-on equipment, and that the flow path may be easily optimized for new experimental setups.
Embodiments of the invention are defined in the dependent claims.
The invention will be described in detail below with reference to the drawings, in which
According to one embodiment, there is provided an automated fluid handling system comprising a housing and two or more fluid handling units arranged as interchangeable modular components with an external fluidics section and an internal non fluidics section, and wherein the housing comprises a liquid handling panel with two or more of component positions for receiving said interchangeable modular components such that the external fluidics section is separated from the non fluidics section by the liquid handling panel.
According to another embodiment, there is provided a fluid handling system in the form of a liquid chromatography system comprising a housing, two or more high pressure pumps, at least one sensor unit and a plurality of fluid control valves of at least two different configurations, wherein at least the fluid control valves are arranged as interchangeable modular components and the housing comprises a liquid handling panel with a plurality of component positions for receiving said modular components.
The disclosed embodiment is supplied with three high precision pumps 7, 10, 12. There are two System pumps 7, 10, System pump A 10 and System pump B 7, and one Sample pump 12. The System pumps 7, 10 may be used individually, or in combination to generate isocratic or gradient elution in purification methods. The Sample pump 12 is dedicated for direct loading of sample onto a column, or for filling of sample loops.
Function of the Pumps:
Each pump module consists of two pump heads (not shown). The individual heads are identical but actuated in opposite phase to each other by individual stepper motors, controlled by a microprocessor. The two pistons and pump heads work alternately to give a continuous, low pulsation, liquid delivery. The flow rate of the two System pumps may be varied between about 0.001 ml/min and 25.000 ml/min and the maximum operating pressure is about 20 MPa. The flow rate of the Sample pump may e.g. be varied between 0.01 and 25 ml/min and according to one embodiment the maximum operating pressure is 10 MPa.
According to one embodiment, the plurality of fluid control valves of at least two different configurations are valves of rotary type. Such a motorized rotary valve may consist of a Valve head with a number of defined bores with channels to the inlet and outlet ports of the valve. The Rotary disc, mounted on the motor, has a number of defined channels. The pattern of channels of the Rotary disc together with the pattern and location of the ports of the Valve head, define the flow path and function of each type of valve. When the Rotary disc turns, the flow path in the valve changes.
One embodiment of fluid control valves are Inlet valves A and B (9, 6 respectively) that are used to select which buffers or samples to use in a run, and Sample inlet valve 15 that is located before Sample pump 12. Inlet valve A 91 is located before System pump A 10, Inlet valve B 6 is located before System pump B 10, and Sample inlet valve 15 is located before Sample pump 12. Inlet valve A and Inlet valve B are connected to another embodiment of a fluid control valve in the form of a Quaternary valve 5. The Quaternary valve is used for automatic buffer preparation, and for formation of quaternary gradients. The number of inlets can be increased by installing component modules with extra inlet valves. Inlet valve A and Inlet valve B enable automatic changing between different buffers and wash solutions, and can be used to generate gradients by mixing buffer A and buffer B. The air sensors integrated in Inlet valve A and Inlet valve B can be used to prevent introduction of air into the pumps and columns.
The Quaternary valve is used for automatic mixing of four different solutions. The Quaternary valve opens one inlet port at a time, and the different solutions are mixed in a Mixer 14 to form the desired buffer. The opening time in the switching valve is controlled by the system. The volume for each inlet port opening increases stepwise when the flow increases. To obtain a homogeneous buffer composition, one has to make sure to use a mixer chamber volume suitable for the flow rate of the method.
The Quaternary valve can be used to create a gradient using four different solutions simultaneously in any combination. The percentage of each solution is controlled by instructions in the method. It is possible to form gradients that changes the percentage of two, three or four solutions linearly over time. This is useful when advanced methods are developed.
The Sample inlet valve 15 enables automatic loading of different samples when using the Sample pump 12 to inject sample directly onto the column or to fill a sample loop. The Sample inlet valve has an inlet dedicated for buffer. This Buffer inlet is used in methods to fill the Sample pump with solution before sample is introduced. The Buffer inlet is also used to wash the Sample pump with buffer between runs. The air sensor integrated in the Sample inlet valve is e.g. used when sample is applied from a vessel onto a column by selecting Inject all sample using air sensor in the Sample application phase of a method. This function uses the Buffer inlet is used to finalize sample injection and to remove air from the Sample pump.
Still another embodiment of fluid control valve may be an Injection valve 1, which is used to direct sample onto the column. The valve enables usage of a number of different sample application techniques. A sample loop can be connected to the Injection valve and filled either automatically using the Sample pump or manually using a syringe. The sample can also be injected directly onto the column using the Sample pump.
Still another embodiment of fluid control valve may be a Column valve 2 that is used for connection of columns to the system, and to direct the flow onto the column. Up to five columns can be connected to the disclosed embodiment of said valve simultaneously. The valve also has a built-in bypass capillary that enables bypassing of connected columns.
The number of column positions can be increased by installing an extra Column valve. Both top and bottom of each column shall be connected to the Column valve. The top of the column shall be connected to one of the A ports (e.g., 1A), and the bottom of the column shall be connected to the corresponding B port (e.g., 1B). The flow direction can be set either from the top of the column to the bottom of the column, Down flow, or from the bottom of the column to the top of the column, Up flow. In the default flow path of the Column valve the columns are bypassed. Pressure monitors that measures the actual pressure over the column are integrated into the inlet and outlet ports of the Column valve.
Still another embodiment of fluid control valve may be a pH valve 17 that has an integrated flow cell where a pH electrode can be installed. This enables in-line monitoring of pH during the run. A flow restrictor is connected to the pH valve and can be included in the flow path to generate a backpressure high enough to prevent formation of air bubbles in the UV flow cell. The pH valve is used to direct the flow to the pH electrode and to the flow restrictor, or to bypass one or both.
Still another embodiment of fluid control valve may be an Outlet valve 18 that is used to direct the flow to a Fraction collector (not shown), to any of e.g. 10 outlet ports, or to waste. The number of outlets can be increased by installing an extra Outlet valve.
A Mixer 14 may e.g. be located after System pump A and System pump B and before the Injection valve. The purpose of the Mixer is to make sure that the buffers from the System pumps are mixed to give a homogenous buffer composition. The Mixer has a built-in filter that prevents impurities from entering the flow path.
To fulfill a desired purpose, with the disclosed liquid chromatography system it is possible to adapt and extend the flow path in a simple and a flexible way. Up to three extra fluid control valves or the like can be installed using the free valve positions. Dummy modules are installed in these positions at delivery. To obtain an optional flow path, it is also possible to move the standard fluid control valves to other positions. There are also two types of extra air sensors available which can be installed before Sample inlet valve or after Injection valve.
In the configuration disclosed in
In the configuration disclosed in
In the configuration disclosed in
Optional modules are easy to install in the disclosed modular liquid chromatography system. The dummy module is removed with a hexagon wrench and a bus cable is disconnected. The bus cable is connected to the optional fluid control valve or the like which is assembled in the instrument. The module is then added to the System properties in the control software. The available optional modules may e.g. be pre-configured to give the desired function. However, the function of a valve may e.g. be changed by changing the Node ID.
As is disclosed in
The liquid handling panel 22 of the fluid handling system may e.g. be designed in any suitable manner to allow the modular components to be arranged in an efficient manner.
In
According to one embodiment, different component modules are automatically identified by the master control unit, whereby they may be moved essentially freely between different positions. Moreover, the master control unit may be arranged to provide said information to Chromatography control software whereby experimental setup and planning may be performed. In one embodiment, the control system may be arranged to provide an optimized layout of the component modules with respect to the present layout of the liquid handling panel and available component modules for a specific experimental setup.
According to one embodiment, the interchangeable panel sections 34 of
Number | Date | Country | Kind |
---|---|---|---|
0950431-7 | Jun 2009 | SE | national |
Number | Name | Date | Kind |
---|---|---|---|
4044593 | Haruki et al. | Aug 1977 | A |
4125464 | Burger et al. | Nov 1978 | A |
5065614 | Hartman et al. | Nov 1991 | A |
5730867 | Drew et al. | Mar 1998 | A |
5766460 | Bergstrom et al. | Jun 1998 | A |
5896273 | Varghese et al. | Apr 1999 | A |
5959841 | Allen et al. | Sep 1999 | A |
6190617 | Clark et al. | Feb 2001 | B1 |
6355164 | Wendell et al. | Mar 2002 | B1 |
6434018 | Waltz | Aug 2002 | B1 |
6599484 | Zigler et al. | Jul 2003 | B1 |
6741463 | Akhtar et al. | May 2004 | B1 |
6832622 | Hassel et al. | Dec 2004 | B2 |
6968958 | Auchner et al. | Nov 2005 | B2 |
7374674 | Miyauchi et al. | May 2008 | B2 |
7641242 | Pelt | Jan 2010 | B2 |
7910067 | Knight et al. | Mar 2011 | B2 |
7932090 | Carter et al. | Apr 2011 | B2 |
8821718 | Blomberg et al. | Sep 2014 | B2 |
9404902 | Blomberg et al. | Aug 2016 | B2 |
9671420 | Blomberg et al. | Jun 2017 | B2 |
9709589 | Blomberg et al. | Jul 2017 | B2 |
9709590 | Blomberg et al. | Jul 2017 | B2 |
9709591 | Blomberg et al. | Jul 2017 | B2 |
20020185442 | Maiefski et al. | Dec 2002 | A1 |
20040089057 | Hobbs et al. | May 2004 | A1 |
20040264145 | Miller et al. | Dec 2004 | A1 |
20050051468 | Miyauchi et al. | Mar 2005 | A1 |
20060047466 | White | Mar 2006 | A1 |
20060274082 | Cochran et al. | Dec 2006 | A1 |
20070025413 | Hays et al. | Feb 2007 | A1 |
20070081308 | Ishida | Apr 2007 | A1 |
20070095126 | Bailey et al. | May 2007 | A1 |
20070097636 | Johnson et al. | May 2007 | A1 |
20070247826 | Grady et al. | Oct 2007 | A1 |
20080023653 | Lee et al. | Jan 2008 | A1 |
20080035542 | Mourtada et al. | Feb 2008 | A1 |
20080233653 | Hess et al. | Sep 2008 | A1 |
20170284985 | Blomberg et al. | Oct 2017 | A1 |
Number | Date | Country |
---|---|---|
2567575 | Aug 2003 | CN |
101358952 | Feb 2009 | CN |
1984739 | May 1968 | DE |
1418503 | Dec 1975 | DE |
19847439 | Apr 2000 | DE |
0309596 | Apr 1989 | EP |
2002333438 | Nov 2002 | JP |
2005106813 | Apr 2005 | JP |
0022429 | Apr 2000 | WO |
2000022429 | Apr 2000 | WO |
2001089681 | Nov 2001 | WO |
2005042146 | May 2005 | WO |
2006134035 | Dec 2006 | WO |
2007036712 | Apr 2007 | WO |
Entry |
---|
“Manual ADI 2040 Process Analyzer” 1999-2007, Applikon Analytical B.V., pp. 1-134 (part 1). |
“Manual ADI 2040 Process Analyzer” 1999-2007, Applikon Analytical B.V., pp. 346-619 (part 2). |
ADE 2040 Process Analyzer Manual—Basic Operation, Applikon Analytical, Version 1.4, pp. 1-30, Jul. 2006. |
ADI 2040 Process Analyzer Manual—Analysis Methods, Applikon Analytical, Sep. 2002, pp. 1-44, Version 1.4. |
ADI 2040 Process Analyzer Manual—Basic Maintenance & Spare parts, Applikon Analytical, Mar. 2008, Version 1.53, pp. 1-48. |
ADI 2040 Process Analyzer Manual—Configuration, Applikon Analytical, Version 1.4, pp. 1-44, Jul. 2006. |
ADI 2040 Process Analyzer Manual—Hardware & Installation, Applikon Analytical, Version 1.53, p. 144, May 2008. |
ADI 2040 Process Analyzer Manual—Serial Communication, Applikon Analytical, Version 1.4, pp. 134, Apr. 2006. |
ADI 2040 Process Analyzer Manual, Applikon Analytical, pp. 1-10, Apr. 1999. |
ADI 2040 Process Analyzer, Manual, Applikon Analytical, 1999-2007, Bio-Rad Labs, Inc. v. GE Healthcare Biosciences AB, IPR2015-01826, Bio-Rad Ex. 1002, pp. 1-619. |
ADI 2045 VA Instrument Manual, Applikon Analytical, 2007, pp. 1-80, Version 1.2. |
ADI Process Analyzer Manual—Advanced Operation, Applikon Analytical, Version 1.53, pp. 1-78, Oct. 2007. |
Andreas Schmid, “The Energy Issue in Whole Cell Oxyfunctionalization,” GreenChem Symposium, Nov. 9, 2006, pp. 5349-5386. |
APC, “Rack Enclosures and Open Frame Racks for Server and Networking Applications in IT Environments,” Rack Systems, 2006, pp. 4619-4638. |
Applikon Analytical Confidential, “Analyzers 1999-2008,” Bio-Rad Ex. 1004, Jul. 8, 2015, pp. 1323-1326. |
Applikon Analytical, “Box Wet Part Module 3X,” Bio-Rad Ex. 1003, 1 page, Feb. 11, 2008. |
Applikon Analytical, “Multi-purpose wet chemical analysis,” Process Analyzer ADI 2040, Sep. 2008, pp. 1547-1554. |
Applikon Analytical, “Trace Metal and Plating Bath Analysis,” ADI2045VA Process Analyzer, Sep. 2007, pp. 1555-1562. |
350 Professional IC Manual, Metrohm, AnCat-MCS-2.850.3030, May 2009, Bio-Rad Labs, Inc. v. GE Healthcare Biosciences AB, IPR2015-01826, Bio-Rad Ex. 1017, pp. 1-143, BIO-RAD001337-BIO-RAD001479. |
Bilsker, Petition for Inter Parties Review, Bio-Rad Laboratories, Inc, v. GE Healthcare Bio-Science AB Sep. 2015, pp. 1-71. |
Bio-Rad Laboratories, Inc., “Biologic Duoflow Chromatography System,” Instruction Manual, 2003,pp. 5810-6048. |
Brinkmann, “875 ProcessLab Components,” ProcessLab, pp. 1-26, Mar. 2001. |
Brinkmann, “875 ProcessLab Hardware,” ProcessLab, pp. 1-15, Mar. 2007. |
Brinkmann, “Is ProcessLab Explosion-Proof?” ProcessLab, pp. 1-12, Mar. 2001. |
Carvo ILP 6000 60mm Stroke OEM Syringe Pump, Tecan Group, Ltd., Internet Archive, 1 page, pp. 5700. |
Decision to Institute, Inter Partes Review 2015-01826, Feb. 29, 2016. |
Dionex, “ICS-3000 Ion Chromatography System Operator's Manual,” Thermo Scientific, Jan. 2008, pp. 4779-5170. |
Eda Tezcanli, “An Analytical Survey on Customization at Modular Systems in the Context of Industrial Design,” A Thesis Submitted to the Graduate School of Engineering and Sciences of Izmir Institute of Technology in Partial Fulfillment of the Requirements for the Degree of Master of Science in Industrial Design, Jan. 2006,pp. 501-5809. |
EP Office Action dated Feb. 26, 2014 Issued on Corresponding EP Application No. 10786454.8. |
European Search Report and Form 1507 issued in European U.S. Appl. No. 16/205,536 dated Mar. 17, 2017 (8 pages). |
Final Written Decision, Inter Partes Review 2015-01826, Feb. 6, 2017. |
General Electric, “Operating Instructions Original Instructions,” KTA pure, Apr. 2014, pp. 3785-3928. |
General Electric, “User Manual,” AKTA pure, Dec. 2014, pp. 3929-4445. |
Gilson, Inc., “2007-2008 Product Guide,” Bio-Rad Ex. 1010 pp. 1-37. |
Gilson, Inc., “402 Syringe Pump User's Guide,” Bio-Rad Ex. 1011, Jun. 2001, pp. 1-86. |
Gilson, Inc., “402 Syringe Pump User's Guide,” Jul. 2003, pp. 5208-5293. |
Gilson, Inc., “Brochure,” 2003, 1 Page, pp. 5345. |
Gilson, Inc., “Gilson Product Guide,” 2004, pp. 5294-5343. |
Gilson, Inc., “Product Guide,” The Element of Purification, Jul. 2008, pp. 5171-5207. |
Gilson, Inc., “Spec Sheet,” 2003, 1 Page, pp. 5344. |
Gilson, Inc., “User's Guide,” 2003, 1 Page, pp. 5346. |
H. Schafer, “Compact View of a Modular Design or a new Philosophy in Metrohm IC,” Processional IC, pp. 1-90, Sep. 2007. |
J. Van Burg, “EU Declaration of Conformity,” Manual ADI 2045VA, 2007, pp. 620-1322. |
John Loffink, “Dell PowerEdge M1000e Modular Enclosure Architecture,” Dell Enterprise White Paper, Jan. 2008, pp. 4577-4618. |
JP Office Action, dated Dec. 17, 2013, Issued on Corresponding JP Application No. 2012-514920. |
Labomatic Instruments AG, “Customer-specific preparative HPLC Systems,” 5387-5389, date unknown. |
Labomatic, “Labomatic HPLC valve and column system panel,” pp. 5347-5348, date unknown. |
Larry Tucker et al., “Videotaped Deposition of METROHM 30 (B) (6),” GE Healthcare vs. Bio-Rad, Aug. 10, 2015, pp. 1-292. |
Metrohm 811 Online IC/ 821 Compact Online IC Brochure, pp. 1-11. |
Metrohm-850 Processional IC Manual, http://products.matrohm.com, pp. 1-146, date unknown. |
Metrohm 850 Professional IC teardown system, (2.850.2220 ProfIC Anion MCS HP Gradient), Aug. 2016, pp. 1-9. |
Metrohm AG, “850 Professional IC,” Bio-Rad Ex, 1017, pp. 1337-1479, Feb. 2007. |
Metrohm—Intelligent Ion Chromatography, www.professional-ic.com, 2012, pp. 1-28. |
Metrohm Ion analysis, “IC Pump-2.872.0010,” 872 Extension Module, pp. 1-67, May 2009. |
Metrohm-Peak, Inc., “Determination of Anions+ Oxyhalides in Various Waters by Suppressed Conductivity (US EPA method 300 A&B),” IC Application Work AW US6-0125-052007, 2007, pp. 001327-001336. |
Office Action issued in Chinese Patent Application No. 201510602257.9 dated Jul. 13, 2016. |
Tecan Group Ltd, “Cavro OEM Pumps and Valves,” 2008, 1 Page, pp. 5699. |
Tecan Systems, “Cavro XLP 6000 Modular Syringe Pump,” Operating Manual, Part I, Oct. 2005, pp. 5542-5698. |
Thomas Koshy, “Declaration of Thomas Koshy,” in the United States District Court for the Southern District of New York, Civil Action No. 1:14-cv-07080-L TS, pp. 1-3, Oct. 30, 2014. |
United States Patent and Trademark Office, “Bio-Rad Laboratores, Inc. v. GE Healthcare Bio-Sciences AB,” Case: IPR2015-01826, U.S. Pat. No. 8,821,718 B2, Paper No. 11, Entered: Feb. 29, 2016, pp. 1-47. |
United States Patent and Trademark Office, “Bio-Rad Laboratories, Inc. v. GE Healthcare Bio-Sciences AB,” Declaration of Dr. Bruce Gale in Support of Bio-Rad Laboratories' Petition for Institution of an IPR on U.S. Pat. No. 8,821,718, pp. 1-84, Sep. 2015. |
Waters Corporation, “Waters 2767 Sample Manager, Injector, and Collector,” Installation and Maintenance Guide, 2006, pp. 5390-5541. |
Number | Date | Country | |
---|---|---|---|
20230243861 A1 | Aug 2023 | US |
Number | Date | Country | |
---|---|---|---|
Parent | 16788836 | Feb 2020 | US |
Child | 18131043 | US | |
Parent | 15624547 | Jun 2017 | US |
Child | 16788836 | US | |
Parent | 15205956 | Jul 2016 | US |
Child | 15624547 | US | |
Parent | 15165876 | May 2016 | US |
Child | 15205956 | US | |
Parent | 14463039 | Aug 2014 | US |
Child | 15165876 | US | |
Parent | 13376929 | US | |
Child | 14463039 | US |