WO2003006163A1 - Analysevorrichtung - Google Patents
Analysevorrichtung Download PDFInfo
- Publication number
- WO2003006163A1 WO2003006163A1 PCT/EP2002/007629 EP0207629W WO03006163A1 WO 2003006163 A1 WO2003006163 A1 WO 2003006163A1 EP 0207629 W EP0207629 W EP 0207629W WO 03006163 A1 WO03006163 A1 WO 03006163A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- analysis device
- reservoirs
- base plate
- analysis
- cover plate
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/50273—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the means or forces applied to move the fluids
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502715—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by interfacing components, e.g. fluidic, electrical, optical or mechanical interfaces
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44704—Details; Accessories
- G01N27/44743—Introducing samples
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44756—Apparatus specially adapted therefor
- G01N27/44782—Apparatus specially adapted therefor of a plurality of samples
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N27/00—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means
- G01N27/26—Investigating or analysing materials by the use of electric, electrochemical, or magnetic means by investigating electrochemical variables; by using electrolysis or electrophoresis
- G01N27/416—Systems
- G01N27/447—Systems using electrophoresis
- G01N27/44756—Apparatus specially adapted therefor
- G01N27/44791—Microapparatus
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/06—Auxiliary integrated devices, integrated components
- B01L2300/0627—Sensor or part of a sensor is integrated
- B01L2300/0645—Electrodes
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0809—Geometry, shape and general structure rectangular shaped
- B01L2300/0829—Multi-well plates; Microtitration plates
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0861—Configuration of multiple channels and/or chambers in a single devices
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2300/00—Additional constructional details
- B01L2300/08—Geometry, shape and general structure
- B01L2300/0887—Laminated structure
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2400/00—Moving or stopping fluids
- B01L2400/04—Moving fluids with specific forces or mechanical means
- B01L2400/0403—Moving fluids with specific forces or mechanical means specific forces
- B01L2400/0415—Moving fluids with specific forces or mechanical means specific forces electrical forces, e.g. electrokinetic
- B01L2400/0421—Moving fluids with specific forces or mechanical means specific forces electrical forces, e.g. electrokinetic electrophoretic flow
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L3/00—Containers or dishes for laboratory use, e.g. laboratory glassware; Droppers
- B01L3/50—Containers for the purpose of retaining a material to be analysed, e.g. test tubes
- B01L3/502—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures
- B01L3/5027—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip
- B01L3/502707—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures by integrated microfluidic structures, i.e. dimensions of channels and chambers are such that surface tension forces are important, e.g. lab-on-a-chip characterised by the manufacture of the container or its components
-
- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N35/00—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor
- G01N35/00029—Automatic analysis not limited to methods or materials provided for in any single one of groups G01N1/00 - G01N33/00; Handling materials therefor provided with flat sample substrates, e.g. slides
- G01N2035/00099—Characterised by type of test elements
- G01N2035/00148—Test cards, e.g. Biomerieux or McDonnel multiwell test cards
-
- H—ELECTRICITY
- H05—ELECTRIC TECHNIQUES NOT OTHERWISE PROVIDED FOR
- H05K—PRINTED CIRCUITS; CASINGS OR CONSTRUCTIONAL DETAILS OF ELECTRIC APPARATUS; MANUFACTURE OF ASSEMBLAGES OF ELECTRICAL COMPONENTS
- H05K1/00—Printed circuits
- H05K1/02—Details
- H05K1/0272—Adaptations for fluid transport, e.g. channels, holes
Definitions
- the invention relates to an analysis device comprising a base body with a surface, wherein at least one analysis device is arranged in the base body and consists of at least two reservoirs that are flow-connected to at least one channel.
- microchannels Systems formed from microchannels are used in microsystem technology as so-called microfluidic systems for miniaturized chemical or biochemical analysis systems. Areas of application of such microchannel systems are e.g. drug discovery, chemical diagnostics, genome analysis, environmental analysis and combinatorial chemistry. The special feature is that only very small quantities of honey are transported or manipulated. Areas of application include micro-reactors in which chemical reactions take place, or microtiter plates.
- the sample is separated and analyzed in its various components in a thin capillary, the width of which is on the order of a few 10 ⁇ m, under the influence of an electric field.
- microchannel structures are formed by a base plate and a cover plate, the microchannels being formed in a flat surface of the base plate and closed by placing a flat surface on the cover plate. At the ends of the microchannels, openings are formed in the cover plate through which the samples can be fed.
- Electrodes are to be inserted and made correspondingly small. However, this requires an increased degree of precision for the mechanical control for feeding the electrodes. This can lead to malfunctions in the contacting and thus to impaired functional reliability. It is therefore the object of the invention to provide an analysis device for electrochemical or electrokinetic examinations, by means of which its handling is simplified.
- an analysis device comprising a base body with a surface, at least one analysis device being arranged in the base body and consisting of at least two reservoirs which are flow-connected to at least one channel, characterized in that in the base body or two electrical conductors are arranged on the surface, a first end region of which is connected to one of the at least two reservoirs and a second end region of the conductor is connected to a contact point on the surface of the base body or forms this contact point.
- the functional reliability is increased by the electrical conductors or contact points attached to the base body of the analysis device, and in particular by the contact points attached at a distance from the reservoirs of the analysis devices, the liquids or samples that are located in the reservoirs or channels of the analysis device , not by importing or
- Removing electrodes in or out of the reservoirs can be disrupted.
- Another advantage is the design of the analysis device, according to which the grand body is formed from a base plate and a cover plate, the base plate and the cover plate being connected to one another at surfaces, since this forms the analysis device
- Channels or reservoir parts can be produced by forming depressions in one of the surfaces of the base and / or the cover plate.
- the channels can be closed in a simple manner in such a way that they are only accessible from the outside through the reservoirs at their end regions.
- connection method being selected from a group comprising the methods of gluing, vapor deposition, insertion into depressions and moldings, has the advantage that the analysis devices are in one compact form can be formed and in particular the risk of damage to the conductor is minimized.
- the development of the analysis device has the advantage that for the current transfer between the Conductor and the liquidity in the reservoir, a sufficiently large wettable surface of the conductor is available and thus the contact resistance can be kept low. Having a sufficiently large conductor surface area for the current transfer is advantageous given the small dimensions of the reservoirs, as are used for microchannel structures.
- the design of the analysis device is particularly advantageous, according to which the first end region of the conductor is formed by an electrode which extends between the reservoir bottom and an underside of the base plate, since analysis devices which are structured in a particularly simple manner can thereby be produced.
- Electrodes reaching the underside of the base plate it is in fact possible to arrange all conductors and their contact points exclusively on the underside of the base plate. If the base plate is produced as a plastic injection molded part, there is thus the possibility of producing electrodes, conductors and their contact points as one-piece parts, inserting these parts into an injection mold and thus producing the base plate provided with electrical conductors in a single step.
- the contact points are formed with a contact area with an inner circle diameter and the reservoirs with an opening with an inner circle diameter and the inner circle diameter of the contact area is larger than the inner circle diameter of the openings of the reservoirs.
- a further development of the analysis device is also advantageous, the contact points being arranged only on a common end region of the base body, since appropriate adapters can thereby be used for contacting the contact points, which adapters only have to be fed to the analysis device from one side.
- the analysis device according to which the conductors are made of a material, the material being selected from a group comprising the materials metal, electrically conductive plastic, conductivity paste and electrically conductive lacquer, has the advantage that analysis devices can be produced as a result whose electrical cables are suitable for performing capillary electrophoresis tests have sufficient electrical conductivity.
- the base body is designed according to a standard size of a microtiter plate or several analysis devices are arranged according to a standard grid of a microtiter plate or a predeterminable number of analysis devices is arranged, the number being selected from a group comprising the numbers formed by the mathematical formula 3 x 2 N , where N is a natural number, or 96 analysis devices, since this uses automated systems, as are customary for microtiter plates, to carry out corresponding analyzes can be.
- the reservoirs can be treated with the samples using standardized pipetting devices.
- the channel is designed as a microchannel or the analysis device is designed with four reservoirs and two reservoirs are each connected to a channel and the two channels are each connected by a common crossing area
- the advantage is achieved that that on the one hand there are very homogeneous flow conditions in the microchannels due to the capillary action and on the other hand a very small volume of a few 100 pl can be separated from the crossover area of the two channels for carrying out capillary electrophoresis studies.
- the advantage is achieved that the reservoirs on the analysis device are distributed equally, i.e. with a maximum distance between two immediately adjacent reservoirs.
- the base plate and the cover plate are made of plastic, the plastics being selected from a group comprising the materials polymethyl methacrylate, polycarbonate, polystyrene, polysulfone and cycloolefin copolymer, since this makes transparent base bodies of analysis - Direction can be produced that a detection of the reactions in the channels of the Allow analysis facilities.
- a further development of the analysis device offers the advantage that it is possible to avoid disturbing scattered light when detecting fluorescent sample components.
- the at least one channel being formed by depressions in at least one of the surfaces of the base plate and the cover plate and at least those parts of the surfaces of the base plate and the cover plate which directly surround the reservoirs and the channels, are connected to one another in a liquid-tight manner using a connection method, the connection method being selected from a group which comprises the methods of gluing, application of polymerizable binders, adhesion promotion by temporary treatment with a solvent, thermal sealing, ultrasound welding and laser welding, since this undisturbed homogeneous flow conditions in the channels can be achieved.
- FIG. 1 shows an analysis device consisting of a base plate and a cover plate
- FIG. 2 shows a view of the analysis device according to FIG. 1;
- FIG. 4 shows a section of an analysis device according to FIG. 1;
- FIG. 6 shows a section of an analysis device with a contact point according to FIG. 1;
- Fig. 8 shows a section of an analysis device with a contact point and conductors on the
- FIG. 9 shows an exemplary embodiment of an analysis device with reservoirs in a square grid
- FIG. 10 shows a section of an analysis device according to FIG. 9;
- FIG. 11 shows an underside of an analysis device according to FIG. 9;
- FIG. 12 shows a basic illustration of an analysis device according to FIG. 9;
- FIG. 14 shows a section of an analysis device according to FIG. 13.
- the base body 1 and 2 show an analysis device according to the invention consisting of a plate-shaped base body 1.
- the base body 1 is formed by a base plate 2 and a cover plate 3, which are connected to one another on a surface 4 of the base plate 2 and a
- a total of 96 analysis devices 6 (partially shown in broken lines) are formed in the base body 1 formed by the base plate 2 and the cover plate 3.
- the analysis devices 6 are used to carry out electrochemical investigations or reaction NEN.
- a plurality of contact points 9 are formed on the surface 4 of the base plate 2.
- the analysis devices 6 also each have four reservoirs 10 through which the samples and buffer solutions can be supplied.
- the reservoirs 10 are designed as cylindrical passages in the cover plate 3.
- the outer dimensions of the base body 1 of the analysis device are designed according to a standard size of a microtiter plate. Accordingly, the analysis devices 6 are also designed in a rectangular grid according to a standard grid of a microtiter plate with 96 units.
- a row width 11, i.e. the lateral distance between the analysis devices 6 is 9 mm in each case in the direction of the longitudinal extent of the base body 1 and also perpendicular to it.
- the arrangement of the reservoirs 10 is based on a rectangular grid with a row width 12 of 2.25 mm, i.e. the row width 12 corresponds to a quarter of the row width 11 of the analysis devices 6 and thus a standard grid of a microtiter plate with 1536 units.
- the base body 1 or the base plate 2 or the cover plate 3 can be integrally connected to a frame at its or its edge regions.
- a frame is advantageously designed in a form known from standardized microtiter plates.
- the base plate 2 and the cover plate 3 are advantageously made of polymethyl methacrylate.
- plastics such as polycarbonate, polystyrene, polysulfone and cycloolefin copolymer are also possible.
- at least one of the two plates is made of a transparent plastic, since this enables the reactions in the analysis devices 6 to be detected from the outside.
- the surfaces 4, 5 of the base plate 2 and the cover plate 3 are thermal, for example by methods such as gluing, the application of polymerizable binders Sealing, ultrasonic welding or laser welding connected.
- This connection of the base plate 2 and the cover plate 3 is advantageously carried out by brief treatment with a solvent, so that the surfaces 4, 5 dissolve slightly and, after the base plate 2 and the cover plate 3 have been joined, firmly connect them to one another.
- FIG. 3 shows a basic illustration of an analysis device 6, as is embodied several times in the base body 1 (FIG. 1) of the analysis device.
- the analysis device 6 consists of four reservoirs 10, two reservoirs 10 being connected to one another in terms of flow through a channel 13 and two further reservoirs 10 through a channel 14.
- the channel 13 and the channel 14 cross each other in a common crossing area 15.
- the two channels 13 and 14 are designed as so-called microchannels and have a width 16 of 200 ⁇ m and a depth 17 (FIG. 4) of 100 ⁇ m.
- Cross sections of the channels 13, 14 with a width 16 in an area smaller than 200 ⁇ m and a depth 17 in an area smaller than 100 ⁇ m are advantageous.
- the meandering part of the channel 14 between the reservoir 10 located at its one end region and the crossing region 15 has a length of approximately 40 mm.
- Such an analysis device 6 is suitable for carrying out examinations using the capillary electrophoresis method. For this, first in a first
- the sample is then filled and, by applying a voltage to the two reservoirs 10 connected by the channel 13, the sample is passed through the channel 13 in the direction of the Crossing area 15 moves.
- an electrical voltage is now applied in a second step between the two reservoirs 10, which are connected to one another by the channel 14, so that the Sample volume located at the intersection, which corresponds to approximately 500 pl, is caused to move in
- FIG. 4 shows a section of an analysis device according to FIG. 1.
- Analysis device consists of the base plate 2 and the cover plate 3, the base plate 2 having a thickness 20 of approximately 2 mm and the cover plate 3 having a thickness 21 of approximately 2 mm also being formed. Thicknesses 20, 21 in an area smaller than 2 mm, preferably in an area smaller than 1 mm, are advantageous.
- a reservoir 10 which is designed as a cylindrical passage.
- the channels 13 and 14 are formed in the surface 4 of the base plate 2 with a depth 17 of 50 ⁇ m. At the end regions of the channels 13 and 14 are connected reservoir bottoms 22, which are also formed with the depth 17. The reservoirs 10 are thus fluidly connected to the channels 13, 14.
- the channels 13 and 14 and the reservoir bottoms 22 in the surface 4 are produced by stamping with a suitably designed stamp at elevated temperature. Alternatively, their production can also be carried out by other methods, such as Injection molding or removal of the material can be carried out using a laser.
- the bottom plate 2 and the top plate 3 are firmly connected on their surfaces 4 and 5, wherein at least parts of the surfaces 4 and 5 of the bottom plate and the top plate, which the
- channels 13 and 14 can of course also in the surface 5 of the cover plate 3, but also partially in the surface 4 of the base plate 2 and partially in the Surface 5 of the cover plate 3 take place.
- the fact that analysis devices 6 are arranged in the base body 1 is not restricted to the fact that the channels 13 and 14 must be formed exclusively in the interior of the base body 1.
- the channels 13 and 14 it is also possible for the channels 13 and 14 to be formed as depressions in a surface located on the outer body 1.
- FIG. 5 shows the base plate 2.
- a plurality of units of channels 13 and 14 and reservoir bases 22 belonging to analysis devices 6 are formed in a right-angled pattern, as explained in the descriptions for FIGS. 3 and 4 .
- 4 electrical conductors 23 and electrical conductors 24 are attached to the surface.
- a first end region 30 of the conductor 23 is connected to one of the contact points 9 at its second end region on the surface 4 of the base plate 2.
- the conductor 24 is connected to a further contact point 9 with a first end region 31 on the reservoir bottom 22 of the second end of the channel 14.
- the conductors 23 and 24, respectively are formed by the conductors 23 and 24, respectively.
- each the reservoir bottoms 22 in the end region of the shorter part of the channel 14 of analysis devices 6 of a row each electrically connected to a common contact point 9.
- the conductors 23 and 24 and the contact points 9 are preferably applied to the surface 4 of the base plate 2 by vapor deposition with gold using appropriate shadow masks. A first end region of the conductors 23 and 24 is thus connected to a reservoir 10 and a second end region of the conductors 23 and 24 forms a contact point 9.
- Suitable materials for the conductors are primarily metals such as gold or platinum, but also other electrically conductive materials such as electrically conductive plastics, conductors.
- Electrically conductive materials such as electrically conductive plastics, conductors.
- FIG. 6 shows a section of an analysis device with a contact point 9 according to FIG. 1.
- the reservoir 10 with the contact point 9 stands on the surface 4 of the base plate 2, i.e. a contact point 9 on a surface of the base body 1 in an electrically conductive connection.
- An inner circle diameter 32 of the contact surface of the contact point 9 is substantially larger than an inner circle diameter 33 of an opening 34 of the reservoir 10. This considerably facilitates the application of the electrical voltage to the reservoir 10. Compared to the insertion of electrodes through the openings 34 into the reservoirs 10, the attachment of electrodes at the contact points 9 therefore requires a lower degree of mechanical accuracy.
- the inner circle diameter 32, 33 of the contact surface is the determining variable for the susceptibility to errors of the contacting process.
- the attachment of electrical conductors to the base body 1 thus simplifies the handling of the analysis devices and thus also increases their functional reliability, since contacting the contact points 9 requires less mechanical precision.
- Fig. 7 shows the cover plate 3, with an upper side 35, i.e. the side of the cover plate 3 facing away from the surface 5 is shown. Only the openings 34 of the reservoirs 10 are visible on the upper side 35 of the analysis devices.
- Conductors 36 and conductors 37 are attached to the upper side 35 of the cover plate 3, each of which is in electrically conductive connection with contact points 9. These conductors 36 and 37 serve to make electrical contact with the reservoirs 10, which are connected to one another by the channel 13 (not shown).
- FIG. 8 shows a section of an analysis device with a contact point 9 and conductors 36 on the upper side 35 of the cover plate 3 according to FIG. 1.
- the reservoir 10 is connected to the contact point 9 by the electrical conductor 36.
- the electrical conductor 36 extends from the top 35 of the cover plate 3 through the opening 34 of the reservoir 10 on the walls thereof. In this way, at least part of the reservoir wall is formed by a conductor 36.
- the fact that part of the reservoir wall is formed by a conductor or that part of the reservoir bottom is formed by the conductor also means that the reservoir wall or the reservoir bottom is coated with a conductor.
- FIG. 9 shows a further exemplary embodiment of an analysis device with reservoirs 10 arranged in a square grid.
- the reservoirs 10 belonging to a total of 96 analysis devices 6 are arranged in a square grid.
- a row width 12 of the reservoirs 10 is equal to half a value of a row width 11 of the analysis devices 6.
- the analysis devices 6 and the reservoirs 10 are each arranged according to a standard grid of a microtiter plate.
- the row width 11 has a value of 9 mm in the direction of the longitudinal extent of the base body 1 and also perpendicular to it.
- the row width 12 of the reservoirs 10 has a value of 4.5 mm.
- An advantage of the arrangement of the reservoirs 10 described is that the distance of a reservoir 10 from the nearest reservoirs 10 has the maximum possible value. When the reservoirs 10 are filled with the sample liquid, the risk of the sample liquid overflowing to an adjacent reservoir 10 is thus largely reduced.
- FIG. 10 shows a section of an analysis device according to FIG. 9.
- the first end region, to which the conductor 23 is connected in an electrically conductive manner to the reservoir 10 or the reservoir bottom 22, is formed by an electrode 43.
- the electrode 43 extends between the reservoir bottom 22 and an underside 44 of the base plate 2. Due to the formation of the end regions of the conductors 23 and also the conductors 24, 36, 37 (not shown) by electrodes 43 which are located between the reservoir bases 22 and extend the underside 44 of the base plate 2, the conductors 23, 24; 36, 37 can be advantageously arranged on the underside 44 of the base plate 2.
- the contact points 9 and the electrodes 43 in each case preferably structures formed in one piece, can advantageously be formed in or on the base plate 2 by an injection molding process.
- FIG. 11 shows an underside of the analysis device according to FIG. 9.
- the conductors 23, 24 and 36, 37 of several analysis devices 6 lead to the same Chen contact point 9.
- the contact points 9 are advantageously arranged on a common end region of the base body 1. However, it is of course also possible to arrange the contact points 9 at different end regions of the base body 1.
- arrangements of the conductors as described in FIGS. 5 and 8 can also be combined with the arrangement as described in FIGS. 10 and 11. That some of the conductors can be arranged on the surface 4 of the base plate 2 (FIG. 5) or on the upper side 35 of the cover plate 3 (FIGS. 7 and 8), while another part of the conductors runs on the underside 44 of the base plate 2 ,
- FIG. 12 shows a basic illustration of an analysis device according to FIG. 9.
- the arrangement of the reservoirs 10 is arranged with the row width 12, which corresponds to half the value of the row values 11 of 9 mm.
- the cross section of the channels 13 and 14 is designed in the same way as in the exemplary embodiment according to FIGS. 3 and 4, i.e. the width 16 is 100 ⁇ m and the depth 17 (FIG. 10) is 50 ⁇ m.
- An analysis device 6, as shown in FIG. 12, is also suitable for carrying out investigations using the capillary electrophoresis method.
- the base body 1 consisting of the base plate 2 and the cover plate 3 is designed according to a standard size of a microtiter plate.
- 96 analysis devices 6 are arranged according to a standard grid of a microtiter plate with a row width 11 of 9 mm in the direction of the longitudinal extent of the main body 1 as well as normally.
- the design of the analysis devices 6 (shown partly in broken lines) corresponds to that as described in FIG. 3.
- the arrangement of the reservoirs 10 is aligned with a standard grid of a microtiter plate with 1536 units.
- FIGS. 1, 2, 3, 4, 5, 6, 7, 8; 9, 10, 11, 12; 13, 14 shown form the subject of independent, inventive solutions.
- the related tasks and solutions according to the invention can be found in the detailed descriptions of these figures.
- Base body Base body, base plate, cover plate, surface, surface, analysis device, contact point, reservoir, row width, row width, channel, channel, crossover area, width, depth, and thickness, reservoir bottom
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- Analytical Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- General Physics & Mathematics (AREA)
- Biochemistry (AREA)
- Physics & Mathematics (AREA)
- Electrochemistry (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Dispersion Chemistry (AREA)
- Hematology (AREA)
- Clinical Laboratory Science (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Other Investigation Or Analysis Of Materials By Electrical Means (AREA)
- Polarising Elements (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Abstract
Description
Claims
Priority Applications (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP02764657A EP1404447B1 (de) | 2001-07-09 | 2002-07-09 | Analysevorrichtung |
DE50212792T DE50212792D1 (de) | 2001-07-09 | 2002-07-09 | Analysevorrichtung |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US09/901,467 US6835293B2 (en) | 2001-07-09 | 2001-07-09 | Analysis system |
US09/901,467 | 2001-07-09 | ||
AT10662001A AT500433B1 (de) | 2001-07-09 | 2001-07-09 | Analysevorrichtung |
ATA1066/2001 | 2001-07-09 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2003006163A1 true WO2003006163A1 (de) | 2003-01-23 |
Family
ID=25608486
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2002/007629 WO2003006163A1 (de) | 2001-07-09 | 2002-07-09 | Analysevorrichtung |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP1404447B1 (de) |
AT (1) | ATE408454T1 (de) |
DE (1) | DE50212792D1 (de) |
WO (1) | WO2003006163A1 (de) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004062923A1 (de) * | 2004-12-28 | 2006-07-06 | Hirschmann Laborgeräte GmbH & Co. KG | Vorrichtung zur Förderung von Fluiden, Verfahren zur Herstellung derselben und Pipette mit einer solchen Vorrichtung |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0581413A2 (de) * | 1992-07-17 | 1994-02-02 | Beckman Instruments, Inc. | System für Mehrkanalkapillarelektrophorese |
US5876675A (en) * | 1997-08-05 | 1999-03-02 | Caliper Technologies Corp. | Microfluidic devices and systems |
US6103199A (en) * | 1998-09-15 | 2000-08-15 | Aclara Biosciences, Inc. | Capillary electroflow apparatus and method |
-
2002
- 2002-07-09 EP EP02764657A patent/EP1404447B1/de not_active Expired - Lifetime
- 2002-07-09 AT AT02764657T patent/ATE408454T1/de active
- 2002-07-09 WO PCT/EP2002/007629 patent/WO2003006163A1/de active IP Right Grant
- 2002-07-09 DE DE50212792T patent/DE50212792D1/de not_active Expired - Lifetime
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0581413A2 (de) * | 1992-07-17 | 1994-02-02 | Beckman Instruments, Inc. | System für Mehrkanalkapillarelektrophorese |
US5876675A (en) * | 1997-08-05 | 1999-03-02 | Caliper Technologies Corp. | Microfluidic devices and systems |
US6103199A (en) * | 1998-09-15 | 2000-08-15 | Aclara Biosciences, Inc. | Capillary electroflow apparatus and method |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE102004062923A1 (de) * | 2004-12-28 | 2006-07-06 | Hirschmann Laborgeräte GmbH & Co. KG | Vorrichtung zur Förderung von Fluiden, Verfahren zur Herstellung derselben und Pipette mit einer solchen Vorrichtung |
Also Published As
Publication number | Publication date |
---|---|
EP1404447B1 (de) | 2008-09-17 |
DE50212792D1 (de) | 2008-10-30 |
ATE408454T1 (de) | 2008-10-15 |
EP1404447A1 (de) | 2004-04-07 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
DE19947496C2 (de) | Mikrofluidischer Mikrochip | |
DE60312220T2 (de) | Vorrichtung zum abgeben einer probe in elektrospray-massenspektrometern | |
DE60303107T2 (de) | Vorrichtung zum Einspritzen und Mischen von flüssigen Mikrotröpfchen | |
EP1019718B2 (de) | Zur zelluntersuchung mittels der patch clamp-methode bestimmte vorrichtung und verfahren | |
DE60035111T2 (de) | Mikrofluidische systeme mit indizierungskomponenten | |
DE102009023430A1 (de) | Vorrichtung und Verfahren zum Steuern von Fluidströmen in Lab-on-a-Chip-Systemen sowie Verfahren zum Herstellen der Vorrichtung | |
US6835293B2 (en) | Analysis system | |
EP1843833B1 (de) | Verfahren und vorrichtung zur dosierung und durchmischung kleiner flüssigkeitsmengen, apparat und verwendung | |
EP1086371B1 (de) | Vorrichtung und verfahren zur miniaturisierten, hochparallelen elektrophoretischen trennung | |
DE102010041833B4 (de) | Mikrofluidikchip mit mehreren Zylinder-Kolben-Anordnungen | |
EP1404447B1 (de) | Analysevorrichtung | |
DE10154601B4 (de) | Ein Mikrobauelement mit einem integrierten hervorstehenden Elektrospray-Emitter und ein Verfahren zum Herstellen des Mikrobauelements | |
EP1833598B1 (de) | Verfahren und vorrichtung zur dosierung und durchmischung kleiner flüssigkeitsmengen | |
AT500433B1 (de) | Analysevorrichtung | |
EP2739965B1 (de) | Elektrochemischer sensor | |
EP1322947A1 (de) | Verfahren zum herstellen einer 3-d-mikrodurchflusszelle und 3-d-mikrodurchflusszelle | |
DE29923907U1 (de) | Miniaturisierter Objektträger zur Durchführung einer Vielzahl von Testreihen im Submikroliterbereich | |
EP3199240A1 (de) | Mikrofluidische flusszelle mit integrierter elektrode und verfahren zu ihrer herstellung | |
DE102017123249A1 (de) | Vorrichtung zur Bestimmung des Volumens einer Flüssigkeit | |
DE19949538C2 (de) | Mikrokapillare und Verfahren zu deren Herstellung | |
WO2000058721A1 (de) | Elektrophoresechip sowie gerät zum betreiben eines elektrophoresechips | |
DE10141148B4 (de) | Mikrodispenser | |
WO2002087760A1 (de) | Verfahren und anordnung zur speicherung und dosierung von kleinen flüssigkeitsmengen | |
DE60109292T2 (de) | Kombinierte Vorrichtung zur Behandlung biologischer Mikromatrizen | |
DE102005000834B4 (de) | Verfahren und Vorrichtung zur Dosierung und Durchmischung kleiner Flüssigkeitsmengen |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
AK | Designated states |
Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ DE DK DM DZ EC EE ES FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW Kind code of ref document: A1 Designated state(s): AE AG AL AM AT AT AU AZ BA BB BG BR BY BZ CA CH CN CO CR CU CZ CZ DE DE DK DK DM DZ EC EE EE ES FI FI GB GD GE GH GM HR HU ID IL IN IS JP KE KG KP KR KZ LC LK LR LS LT LU LV MA MD MG MK MN MW MX MZ NO NZ OM PH PL PT RO RU SD SE SG SI SK SK SL TJ TM TN TR TT TZ UA UG US UZ VN YU ZA ZM ZW |
|
AL | Designated countries for regional patents |
Kind code of ref document: A1 Designated state(s): GH GM KE LS MW MZ SD SL SZ TZ UG ZM ZW AM AZ BY KG KZ MD RU TJ TM AT BE BG CH CY CZ DE DK EE ES FI FR GB GR IE IT LU MC NL PT SE SK TR BF BJ CF CG CI CM GA GN GQ GW ML MR NE SN TD TG |
|
121 | Ep: the epo has been informed by wipo that ep was designated in this application | ||
DFPE | Request for preliminary examination filed prior to expiration of 19th month from priority date (pct application filed before 20040101) | ||
WWE | Wipo information: entry into national phase |
Ref document number: 2002764657 Country of ref document: EP |
|
WWP | Wipo information: published in national office |
Ref document number: 2002764657 Country of ref document: EP |
|
NENP | Non-entry into the national phase |
Ref country code: JP |
|
WWW | Wipo information: withdrawn in national office |
Country of ref document: JP |
|
WWG | Wipo information: grant in national office |
Ref document number: 2002764657 Country of ref document: EP |