WO2000077508A1 - Miniaturisiertes analysensystem mit vorrichtung zum ausschleusen von substanzen - Google Patents
Miniaturisiertes analysensystem mit vorrichtung zum ausschleusen von substanzen Download PDFInfo
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- WO2000077508A1 WO2000077508A1 PCT/EP2000/005205 EP0005205W WO0077508A1 WO 2000077508 A1 WO2000077508 A1 WO 2000077508A1 EP 0005205 W EP0005205 W EP 0005205W WO 0077508 A1 WO0077508 A1 WO 0077508A1
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- 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
- B01L3/502769—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 multiphase flow arrangements
- B01L3/502784—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 multiphase flow arrangements specially adapted for droplet or plug flow, e.g. digital microfluidics
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- 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
- G01N27/44717—Arrangements for investigating the separated zones, e.g. localising zones
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- 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
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- 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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/02—Adapting objects or devices to another
- B01L2200/025—Align devices or objects to ensure defined positions relative to each other
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01L—CHEMICAL OR PHYSICAL LABORATORY APPARATUS FOR GENERAL USE
- B01L2200/00—Solutions for specific problems relating to chemical or physical laboratory apparatus
- B01L2200/06—Fluid handling related problems
- B01L2200/0689—Sealing
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- 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
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- 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
- B01L2300/0816—Cards, e.g. flat sample carriers usually with flow in two horizontal directions
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- 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
- B01L2300/0864—Configuration of multiple channels and/or chambers in a single devices comprising only one inlet and multiple receiving wells, e.g. for separation, splitting
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- 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
- B01L2300/087—Multiple sequential chambers
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- 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
Definitions
- the invention relates to a device for discharging defined fractions of samples after a preparative or analytical
- Liquid phase separation in planar, miniaturized analysis systems from the separation channel into another channel or into another analytical device.
- Planar, miniaturized analysis systems consist of components with integrated channels in which the transport and / or separation of dissolved analytes takes place, for example, by means of capillary electrophoresis or isotachophoresis.
- Such a channel system can have Y-shaped branches and / or X-shaped crossings (see Figure 1). The angles between the channels are freely selectable.
- An X-shaped arrangement of the channels is usually used for introducing sample material, and a Y-branching for discharging.
- the sample components are transported electrokinetically by applying a voltage to the ends of the channels.
- the electrokinetic transport can be redirected if the electrical potentials are switched from one channel to the other branching channel. In this way, a fraction of a sample can be discharged through the branching channel.
- Such discharge processes are controlled either in a time-defined manner or actively controlled in the case of a previous passage analysis. Precise knowledge of the electropherogram and exact reproducibility of the separation process are required for time-controlled discharge.
- the analyte to be isolated can therefore only be obtained from a known sample after its experimental determination Separation time can be removed.
- This method is particularly unsuitable for capillary electrophoresis, since the addition of surface-active substances leads to a change in the zeta potential on the channel walls. This causes a modulation of the electroosmotic force and thus also a modulation of the temporal pattern of the
- Electropherogram For this reason, time-controlled rejection is usually only carried out for checking or confirmation.
- detector systems for ejection devices have so far not been able to be integrated directly into miniaturized, planar analysis systems, so that substances are usually detected and separated after they have left the analysis system.
- the object of the present invention is therefore to provide a device for discharging substances for miniaturized planar analysis systems which is integrated directly into the analysis systems and can be actively controlled.
- the device for discharging should preferably be combinable with detection devices which are based on different principles; thus the removal of analytes would be very versatile.
- detection devices For planar devices for electrophoretic separation processes, an arrangement comprising at least three transport electrodes, a detection device and a switching device has been found, which makes it possible to selectively discharge fractions during the separation process.
- the detection device is designed as an electrical conductivity, impedance or potential measuring device.
- the invention therefore relates to a device for discharging fractions of a sample for planar microstructured analysis systems, which essentially consist of a channel system with at least one Y branch, at least three transport electrodes and at least one detection device in front of said branch point of the channel system and an electrical switching device.
- a preferred embodiment of the invention is a device for discharging, in which the detection device is an electrochemical detector.
- the present invention furthermore relates to the use of a device according to the invention in a planar microstructured analysis system.
- Figure 1 shows an example of an X crossing (X) and a Y branch (Y) of a channel system according to the prior art.
- Figure 2 illustrates the principle of discharge using the device according to the invention.
- Figures 3 and 4 schematically show analysis systems in which an inventive device for discharging substances is integrated.
- Discharge of substances that can be integrated are planar microstructured systems that serve to separate substances.
- the analysis systems can include additional analysis devices or devices for micro-preparative derivatization. Due to the possibility of integrating detectors or a device according to the invention for discharging directly into these systems during the manufacture of analysis systems, substances can be analyzed and separated in the analysis system already during or after the separation. For example in analysis systems in which substances are not only separated and analyzed, but also other e.g. Are subjected to derivatization steps, more than one device for discharging according to the invention can also be integrated.
- the discharge device consists of a detector system which analyzes a channel segment directly in front of the discharge channel, and a branched channel system with corresponding transport electrodes. As soon as the detector indicates that the desired analyte is just before the branch, the transport electrodes are switched at the ends of the channels. The further transport no longer takes place along the separation channel but in the branching discharge channel. This process ends when the detector indicates that the analyte band has passed the ejection point. In this way, defined parts of a sample can be precisely separated from the rest of the sample.
- the process of discharging therefore comprises the following steps:
- the spatially separated sample is transported to a branching point by appropriate electrical voltage.
- a detector which sits close to the branching point, measures the components flowing past or a marker substance, which marks the beginning and the end of an area to be discharged.
- part of the sample is now spatially separated from the rest of the sample.
- the entire process in particular the switching of the potentials between the electrodes, is preferably controlled by means of an electronic switching device.
- Such devices and their use are known to the person skilled in the art.
- the separated substances can then be subjected to further steps, such as separate analyzes, derivatizations, etc., within the analysis system. Furthermore, they can also be removed from the channel system of the analysis system.
- the duct system is provided with additional outputs. These outputs are preferably located in the discharge channels and are closed off by means of a fluid connection, such as a tightly closing pump or pumps and valves.
- a capillary directly follows, via which the separated fraction can be transferred to other containers or devices outside of the analysis system. Accordingly, if there is a separated fraction in a discharge channel, it can 0/77508.
- the removed fraction can be bothersome
- sample components to be analyzed and separated in this way can be ionically dissolved, emulsified, suspended, colloidal or biologically cellular in predominantly aqueous solution.
- the device according to the invention is based on a detector located on the two-dimensional analysis system. Since miniaturized analysis systems can be structured very differently depending on their specific application, the detector must be able to be positioned anywhere in the analysis system. Both detectors can be used for the device according to the invention, the most important parts of which can be integrated, such as
- optical detectors e.g. refractive index, temperature, absorption, fluorescence, Raman, luminescence
- conductivity detectors and optical detectors are preferably used as the detector device.
- optical detectors For example, a recording device for optical fiber optics can be integrated.
- An electrical conductivity measurement is therefore preferably used in the device according to the invention, which measures the electrical current or the electrical voltage drop in the case of directly contacting electrodes or, in the case of galvanically decoupled electrodes, is carried out by measuring the dielectric resistance.
- conductivity electrodes must be integrated at any point in the system, especially shortly before branches along the channel system. This is only possible through a special type of construction of such a system.
- the channel system must be sealed gas and liquid-tight, on the other hand, it must be ensured that chemically inert electrodes can be attached precisely and reproducibly at the desired positions.
- the above-mentioned requirements can only be met by special techniques for the production of two-dimensional analysis systems.
- Microfluids or microstructured analysis systems usually consist of a flow unit, which is at least the channel system and optional Has recesses for the integration of peripheral devices, and peripheral devices, such as detectors, fluid connections, storage vessels, reaction chambers, pumps, control devices etc., which can be integrated into the flow unit or connected to it.
- flow units for microfluidic analysis systems with measuring and control devices for electrical conductivity are systems in which microchannel structures are produced by joining at least two components, such as substrate and cover, which can be closed in a liquid-tight and / or gas-tight manner.
- the systems according to the invention typically consist of at least two components, a cover which is provided with the electrodes and a microstructured substrate. After the components have been produced, they are joined using a special bonding process. In this way, it is possible to integrate the discharge device according to the invention in planar analysis systems.
- the components of the flow unit of the analysis systems preferably consist of commercially available thermoplastics, such as PMMA (polymethyl methacrylate), PC (polycarbonate), polystyrene or PMP (polymethylpentene), cycloolefinic copolymers or thermosetting plastics, such as epoxy resins. All components of a system preferably consist of the same material.
- the components can be produced by methods known to the person skilled in the art.
- Components that contain microstructures can be produced, for example, by established processes such as hot stamping, injection molding or reaction molding.
- Components which can be reproduced using known techniques for mass production are particularly preferably used.
- Microstructured components can have channel structures with cross-sectional areas between 10 and 250,000 ⁇ m 2 .
- the channel system in addition to areas for sample application and a separation channel, the channel system must have at least one X or Y branch originating from a separation channel. In order to integrate several ejection devices, further branches can be introduced at any point in the channel system.
- the electrodes which are required for the discharge device according to the invention are transport electrodes which are located at the ends of the branched channels and enable the potential to be switched between the two channels, and detection electrodes which are preferably between 40 mm and 0.1 ⁇ m before the branch are positioned.
- the electrodes are preferably attached to a component of the system, the cover. To do this, they must have sufficient adhesive strength on the plastic component. This is important for the assembly of the individual components as well as for the later use of the analysis systems. If, for example, If adhesives are used, the adhesive must not detach the electrode from the plastic surface. Furthermore, the electrodes should be made of chemically inert materials such as e.g. Precious metals (platinum, gold) exist.
- Plastic surfaces are typically metallized by electrochemical deposition of metals from metal salt solutions.
- the electrode structures on the plastic components are particularly preferably produced by means of a two-layer technique.
- an adhesion-promoting layer made of chromium oxide is first created.
- chromium oxide shows excellent adhesive properties on plastic surfaces.
- chromium oxide is much more resistant to redox processes.
- the noble metal such as platinum or its alloys or gold, is then applied to the chromium oxide adhesive layer.
- chromium oxide and the noble metal layer to be deposited thereon is preferably carried out on plastic substrates using the lift-off method or by means of the shadow mask technique or the structuring of metallic layers initially applied over the entire surface.
- These process technologies are standard processes in microstructure technology. in the In the following, the work steps required for the two-layer technique for the mentioned processes are briefly described.
- Lift-off process The plastic component to be selectively metallized is coated with a photoresist. This photoresist must not or only slightly dissolve the plastic part to be metallized. For PMMA e.g. a photoresist from Allresist, Berlin (AR 5300/8) has proven to be suitable.
- the metallic layers are applied in a sputtering system.
- the chromium oxide layer is applied during the sputtering process by introducing oxygen into the typically used argon plasma of the sputtering system.
- a conventional chrome target is used as the sputtering target.
- Typical chromium oxide layer thicknesses are 10-50 nm.
- a chromium oxide target can be used directly.
- the sputtering of platinum or its alloys or of gold is carried out immediately afterwards under standard conditions, i.e. in argon plasma.
- the still existing photoresist and with it the metal layer on the lacquer are detached from the plastic component in a developer from Allresist (AR 300-26).
- Shadow mask technique The plastic part to be selectively metallized is covered with a so-called shadow mask. This has cutouts in the areas to be metallized. Through this, the metal layers are tracked down in analogy to the lift-off process!
- a metal layer is first applied to the entire surface of a plastic part that is to be selectively metallized, analogously to the sputtering process already described. This is structured in subsequent process steps, either by selective ablation using, for example, laser ablation (gold and platinum) or, for example, by selective wet-chemical etching.
- a photoresist Hoechst AG, Germany; AZ 5214
- Au gold and platinum
- wet-chemical etching For structuring by means of wet chemical etching, a photoresist (Hoechst AG, Germany; AZ 5214) is first applied, exposed and developed on the metal layer. Gold is then stripped off in cyanide solution in the exposed areas. The electrically non-conductive chromium oxide layer remains. Finally, the remaining photoresist is removed with a developer (eg AR 300-26, Allresist, Berlin).
- the adhesive strength of electrodes produced with chromium as well as with chromium oxide as an adhesive layer using sputter technology was checked with the aid of tear tests.
- the adhesive strength of the chrome oxide layers is significantly greater. Even in the case of ultrasound treatment in alkaline solution, the metal layers which have been produced using chromium oxide as the adhesive layer are significantly more stable compared to metal layers which have been produced using chromium as the adhesive layer.
- a component, the substrate is preferably microstructured and provided with bores or cutouts on the back for filling the channels and / or contacting the electrodes. Furthermore, the use of a so-called sealing lip, i.e. an elevation completely surrounding the channel structures on the substrates with heights between typically 0.5 to 5 ⁇ m, has proven to be very advantageous with regard to the bonding process.
- the other component, the lid is used for covering and is e.g. with electrodes in electrophoretic analysis systems. In this case, the lid is referred to as an electrode lid according to the invention.
- the lid is referred to as an electrode lid according to the invention.
- Analysis systems require a functionalization of the components that deviates from this preferred arrangement.
- all parts of the flow unit of the analysis system that are joined together by means of a bonding method are referred to as components. They can be microstructured, provided with electrodes or have other functionalities. A subdivision of the components into substrates and cover or also electrode cover, if the corresponding component is provided with electrodes, only serves the closer
- the assembly of the components takes place according to the invention with high precision.
- the adhesive must not run into the channels and cover their surface, as this can change the surface properties of the channels. It has been found that this leads, for example, to increased adhesion of analytes, e.g. Proteins, leads to the channel areas that are wetted with adhesive. This in turn affects the separation quality of the analysis systems. Likewise, gluing the electrodes with adhesive affects their functionality.
- the channel for improving the detection sensitivity is preferably narrowed in the vicinity of the detection electrodes. It is important in these areas that no glue gets into the channel.
- the layer thickness is between 0.5 and 10 ⁇ m, preferably between 3 and 8 ⁇ m.
- the application takes place by means of a flat roller application known from printing technology.
- a thin film of adhesive is applied to a second unstructured roller, which is coated with a polymer, by means of a structured metallic anilox roller which holds a defined volume of adhesive.
- This in turn is applied directly to the structured substrate in such a way that there is preferably an adhesive thickness between 3 and 8 ⁇ m on the unstructured surface of the substrate.
- the transfer between the plastic roller and the substrate is influenced by a possible increase in the viscosity of the adhesive (prepolymerization).
- An important advantage of this method is that the substrate does not have to be positioned relative to the roller applying the adhesive, and nevertheless adhesive is only applied in the non-structured areas of the substrate.
- connection method requires a flatness of the components of preferably less than approx. 5 // m / cm component length.
- the adhesive used must not or only very slightly dissolve the surface of the components so that the electrodes are not detached or interrupted by the adhesive during the bonding process.
- the product NOA 72, thiol acrylate from Norland, New Brunswick, NJ, USA is therefore preferably used as the adhesive.
- This adhesive is cured photochemically.
- other types of adhesives such as, for example, thermosetting adhesives, which meet the above-mentioned requirements can also be used for the method.
- the second component with the thin-film electrodes is suitably positioned and pressed onto the substrate, for example on an exposure machine.
- the substrate with the applied adhesive is preferably fixed in the exposure machine in the position otherwise provided for silicon wafers.
- the use of strong glass plates as the pressing surface is preferred since the positioning and the photochemical curing of the adhesive can be carried out directly by irradiation with an Hg lamp (emission wavelength 366 nm).
- the electrode cover is fixed in the position provided for the exposure mask by holding it with a vacuum device milled into a glass plate. Since both the electrode cover and the glass plate used to hold the cover are transparent, the cover can be adjusted with respect to the substrate through this arrangement. If the cover extends beyond the substrate, it can also be held mechanically.
- the positioning of the lid on the substrate can typically take place in addition to an optical mechanical adjustment with the aid of optical adjustment marks, also passively mechanically with the aid of a snap-in device, optically mechanically without special adjustment marks or electrically mechanically with the aid of electrical marks (contacts).
- the corresponding counter structures on the substrate do not require any additional processing, since these are combined with the channel structures in one
- Impression step can be introduced into the substrate.
- at least one component must be made of a transparent one Plastic.
- the two components are positioned with one another and pressed together with an accuracy of at least ⁇ 10 ⁇ m, typically even ⁇ 2 ⁇ m (for example the target position to the actual position of the detector electrode).
- the high positioning accuracy supports the realization of reproducible
- a component is provided with adhesive by means of a process known in printing technology (pad printing).
- the component provided with the electrodes is wetted with the adhesive on the areas which do not lie over a channel when the two components are assembled or which need to be electrically contacted.
- Microstructured components are wetted so that no adhesive gets into the channel structure or other recesses.
- the pad printing is a structured adhesive application.
- Adhesive is stored in a negative form of the substrate. This adhesive is absorbed in a structured manner by a typically silicone cushion and e.g. applied to the cover so that the areas that later form a wall of a fluidic channel are not wetted with adhesive.
- the component with the channel structures is then, as already described, suitably positioned and pressed onto its counterpart. The curing takes place as described above.
- a structured adhesive application using spray techniques e.g. microdrop process
- screen printing technique is also possible, provided that the lateral dissolution of the adhesive application is sufficient.
- pressing the second component or pressing the components together means that the components are suitable be brought into contact with each other.
- the metallized lid and the substrate after they have been adjusted to one another, can first be tacked by means of laser welding.
- the composite is then removed from the adjustment device and the adhesive used is cured in a separate exposure apparatus or an oven. This procedure means process acceleration and simplification, since curing no longer has to take place in the adjustment device.
- thermoplastic materials which are preferably used are largely transparent to laser light in the visible and near-infrared wavelength range, laser welding in this wavelength range requires an absorber layer for absorbing the optical power at the interface between the cover and the substrate.
- the absorber layer is applied simultaneously with the application of the power or detector electrodes.
- the electrode cover can additionally be sputtered with an Edei metal layer as an absorber layer at other points.
- an electrode cover provided with 200 nm thick platinum electrodes which therefore also includes additional platinum surfaces for absorbing the laser power, to a substrate (PMMA base material) is carried out using diode laser radiation (wavelength mixture of 808, 940 and 980 nm) with a power of 40 watts with a focus diameter of 1.6 mm.
- the platinum layer is destroyed during welding.
- the use of a substrate or cover filled with soot particles, for example, is also possible as an absorber. This latter procedure has the disadvantage that at least one channel wall is made of a different material. This also limits the possibilities of coupling optical power into or out of the channel for optical detection purposes.
- transport and detection electrodes can be integrated into the microstructured analysis systems in such a way that one or more discharge devices according to the invention are produced.
- the integration of the discharge devices does not require any additional effort nor is the quality (stability, size, etc.) of the analysis systems influenced.
- the device according to the invention thus represents an important additional functionality for planar microstructured analysis systems. For the first time, it enables the design of multifunctional microstructured analysis systems or flow units for analysis systems.
- the systems are not only able to separate samples, they can also separate, identify and select samples without the sample leaving the analysis system. This also opens up the possibility of only executing certain sample components after being removed from the analysis system, or of subjecting them to further derivatization or analysis steps in the system.
- Electrodes can be positioned anywhere within the channels.
- Structured components can be provided in a liquid-tight and gas-tight manner, for example with electrode covers.
- Analysis systems can be produced inexpensively and in large numbers. Due to the special procedure for joining or bonding, the components are wetted with adhesive in such a way that after joining, no adhesive enters the interior of the duct system, i.e. gets into the channels, the walls or electrodes or other devices protruding into the channel system. This improves the separation quality and analysis sensitivity of the systems. They meet all the requirements that must be placed on a variably usable, precisely working analysis system: • They show high dimensional and volume stability of the channels.
- Plastics • Chemically inert materials can be used for components and electrodes.
- All four channel walls are preferably made of the same material.
- the electrodes can be positioned at any point on the channels with an accuracy of ⁇ 10 ⁇ m.
- the electrodes can be easily connected.
- Figure 2 illustrates the discharge of a substance using the device according to the invention. Three different stages of discharge are shown in pictures A, B and C.
- the schematic discharge device consists of a Y-branched channel system with the transport electrodes 1, 2 and 3 at the ends of the channels.
- Channel section between electrodes 1 and 2 serves as a separation channel, the channel branching off to electrode 3 is the discharge channel. Shortly before the discharge channel branches off, there is a detector electrode 4 in the separation channel.
- substances 5 and 6 to be separated migrate along the separation channel due to a potential between electrodes 1 and 2.
- Image B shows the moment in which the substance 5 being sought passes the detector electrode.
- the detected signal for example the specific relative conductivity, causes the potential to be switched so that there is now a potential between electrodes 1 and 3.
- substance 5 migrates into the discharge channel and is thus separated from substance 6, which is located in the separation channel. After substance 5 has passed the detector area and migrated into the discharge channel, the potential can be switched over again so that no further substances get into the discharge channel.
- FIG. 3 shows schematically an example of a miniaturized planar analysis system with an integrated device according to the invention for ejecting samples.
- the system contains a separation channel T1 with two transport or power electrodes E3 and E5 at the ends and two detection electrodes E1 and E2 just before the branch point V of the channel system.
- a channel branches off, which in turn branches into three.
- a reservoir P At the ends there is a reservoir P, a mixing reactor R and another reservoir with a power electrode E4. If a mixture of substances along the
- Separation channel T1 separated can be determined using the detection electrodes E1 and E2, when the desired sample substance to the Branch point V of the channel system arrives. At this moment the potential is switched so that there is now a potential difference between E5 and E4. As a result, the selected substance migrates into the branch of the canal system. After the detection electrodes E1 and E2 indicate that the substance has passed the junction, the potential can be switched again. The substance secreted into the branch can now be transported mechanically by a liquid stream from the reservoir at E4 into the mixing reactor R.
- other substances for example
- Reactants for derivatization are passed into the mixing reactor, where they mix with the sample substance and, if necessary, react with it.
- Figure 4 schematically shows an example of a miniaturized planar analysis system with an integrated device according to the invention for ejecting samples, a device for feeding defined sample volumes and a separation channel.
- Such an analysis system offers the possibility of giving up a defined large sample volume, for example separating it by means of ITP, by means of the invention
- the Discharge device to separate a certain fraction of the sample and optionally to separate and analyze the separated fraction or the rest of the sample again or to remove it from the system.
- the device for sample application consists of the channel sections K1 and K2, which are delimited by the fluid connections F1 and F2 or F2 and F3. Tightly closing micropumps or micropumps and valves are typically used as fluid connections.
- the volume of the channel section K1 is typically 5 or 10 ⁇ l, that of the channel section K2 0.5 or 1 ⁇ l.
- the given volume of the sample results from the sum of the volumes of the channel sections K1 and K2. If, on the other hand, the volume of the sample is to be smaller, only the channel section K2 is filled by opening the fluid connections F2 and F3.
- the application volume can be varied and adapted to the corresponding requirements of the sample.
- the sample is separated in the subsequent channel system (K3, K4, K5).
- liquid or buffer reservoirs R1, R2 and R3 as well as power electrodes L1, L2 and L3 are located at the ends of the entire channel system, ie subsequently to K1, K4 and K5.
- the buffer reservoirs can be filled via the fluid connections F1, F4 or F5.
- channel section K1 If only channel section K1 is used for sample application, additional channel section K2 can be used to extend the separation distance.
- the separation of the sample can be extended to channel section K3 up to channel section K5.
- the detection is then carried out by means of the detection electrodes D3 and D4 which are attached just before R3. If a fraction of the sample is to be separated from the rest, the device according to the invention is used for the removal. This is formed by the separating channel section K3, the branching point Vz, the two branches
- Channel sections K4 and K5 the detection electrodes D1 and D2 located in front of the branch point Vz, and by a switching device (not shown in the figure) for controlling the power electrodes.
- the potential of the power electrodes L1, L2 and L3 can be modified accordingly. If the transport from L3 to L2 took place first, the fraction can be switched to a potential difference between L3 and L1 at the junction Vz can be discharged into the channel K4. After the fraction Vz has passed, the rest of the sample is transported back to K5 by switching again. The discharged fraction can then be removed from the analysis system via the fluidic connection F4.
- the rest of the sample remaining in K5 can be analyzed again via the detection electrodes D3 and D4.
- the fraction to be discharged can be discharged by switching the power electrodes at Vz in channel section K5, while the rest of the sample is transported in channel section 4.
- the removed fraction at D3 / D4 can be detected again.
- the channel sections K3 and optionally additionally K2 are filled with the first buffer system.
- the channel sections K4 and K5 are filled with the second buffer system. The first separation takes place along K2 / K3.
- a fraction of the sample can then be discharged into channel section K5 or the entire sample can be transferred into this channel section.
- the second separation then takes place.
- the two separations are checked via the detection electrodes D1 and D2 for the first separation and the optional discharge, and with D1 / D2 for checking the second separation.
- an isotachophoretic separation and an electrophoretic separation or two isotachophoretic separations can be combined.
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- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Molecular Biology (AREA)
- General Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Analytical Chemistry (AREA)
- Physics & Mathematics (AREA)
- Dispersion Chemistry (AREA)
- Electrochemistry (AREA)
- Biochemistry (AREA)
- General Physics & Mathematics (AREA)
- Immunology (AREA)
- Pathology (AREA)
- Clinical Laboratory Science (AREA)
- Hematology (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Investigating, Analyzing Materials By Fluorescence Or Luminescence (AREA)
- Investigating Or Analyzing Materials By The Use Of Electric Means (AREA)
Abstract
Description
Claims
Priority Applications (7)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
AU55302/00A AU5530200A (en) | 1999-06-16 | 2000-06-06 | Miniaturized analytical system with a device for withdrawing substances |
EP00940331A EP1188048A1 (de) | 1999-06-16 | 2000-06-06 | Miniaturisiertes analysensystem mit vorrichtung zum ausschleusen von substanzen |
JP2001503516A JP2003502636A (ja) | 1999-06-16 | 2000-06-06 | 物質を排出するための装置を備えた小型化分析システム |
AU54051/00A AU5405100A (en) | 1999-06-16 | 2000-06-15 | Device for preparing samples |
JP2001503518A JP4387624B2 (ja) | 1999-06-16 | 2000-06-15 | 試料作成装置 |
PCT/EP2000/005518 WO2000077511A1 (de) | 1999-06-16 | 2000-06-15 | Vorrichtung zur probenvorbereitung |
EP00938793A EP1194769A1 (de) | 1999-06-16 | 2000-06-15 | Vorrichtung zur probenvorbereitung |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19927535.1 | 1999-06-16 | ||
DE19927535A DE19927535B4 (de) | 1999-06-16 | 1999-06-16 | Miniaturisiertes Analysensystem mit Vorrichtung zum Ausschleusen von Substanzen |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2000077508A1 true WO2000077508A1 (de) | 2000-12-21 |
Family
ID=7911467
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP2000/005205 WO2000077508A1 (de) | 1999-06-16 | 2000-06-06 | Miniaturisiertes analysensystem mit vorrichtung zum ausschleusen von substanzen |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP1188048A1 (de) |
JP (1) | JP2003502636A (de) |
AU (1) | AU5530200A (de) |
DE (1) | DE19927535B4 (de) |
WO (1) | WO2000077508A1 (de) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
KR100852297B1 (ko) | 2003-09-05 | 2008-08-14 | 칼리퍼 라이프 사이언시즈, 인크. | 분석물 주입 시스템 |
JP2010188342A (ja) * | 2002-07-08 | 2010-09-02 | Deltadot Ltd | 物質分離デバイス |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
RU2006126664A (ru) * | 2003-12-23 | 2008-01-27 | Кайлипер Лайф Сайенсиз, Инк. (Us) | Система ввода аналита |
WO2005114167A2 (en) * | 2004-05-13 | 2005-12-01 | Agilent Technologies, Inc. | Controlling sample loading of a specimen |
EP2407777B1 (de) * | 2010-07-06 | 2016-06-22 | molecular control ag | Ausschleusen von durch Isotachophorese getrennten Analyten |
DE102010053749B4 (de) * | 2010-12-08 | 2015-02-19 | Airbus Defence and Space GmbH | Vorrichtung zum Identifizieren biotischer Partikel |
DE102011054659A1 (de) * | 2011-10-20 | 2013-04-25 | AeroMegt GmbH | Verfahren und Vorrichtung zum Messen von Aerosolen in einem großen Volumenstrom |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996004547A1 (en) * | 1994-08-01 | 1996-02-15 | Lockheed Martin Energy Systems, Inc. | Apparatus and method for performing microfluidic manipulations for chemical analysis and synthesis |
WO1996042013A1 (en) * | 1995-06-08 | 1996-12-27 | Visible Genetics Inc. | Microelectrophoresis chip for moving and separating nucleic acids and other charged molecules |
EP0816837A1 (de) * | 1996-07-03 | 1998-01-07 | Caliper Technologies Corporation | Variable Überwachung von elektroosmotischen und/oder elektroforetischen Kräften in einer in einem Fluidum enthaltenen Anordnung durch elektrische Kräfte |
WO1998009161A1 (en) * | 1996-08-26 | 1998-03-05 | The Regents Of The University Of California | Electrochemical detector integrated on microfabricated capillary electrophoresis chips |
WO1998049549A1 (en) * | 1997-04-30 | 1998-11-05 | Orion Research, Inc. | Capillary electrophoretic separation system |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2518126B1 (fr) * | 1981-12-14 | 1986-01-17 | Rhone Poulenc Spec Chim | Procede de metallisation d'articles electriquement isolants en matiere plastique et les articles intermediaires et finis obtenus selon ce procede |
DE3928435A1 (de) * | 1989-08-24 | 1991-02-28 | Schering Ag | Verfahren zur direkten metallisierung eines nicht leitenden substrats |
US5110633A (en) * | 1989-09-01 | 1992-05-05 | Ciba-Geigy Corporation | Process for coating plastics articles |
US5126022A (en) * | 1990-02-28 | 1992-06-30 | Soane Tecnologies, Inc. | Method and device for moving molecules by the application of a plurality of electrical fields |
US5770029A (en) * | 1996-07-30 | 1998-06-23 | Soane Biosciences | Integrated electrophoretic microdevices |
JP3477918B2 (ja) * | 1995-05-29 | 2003-12-10 | 株式会社島津製作所 | キャピラリ電気泳動チップ |
JPH09210960A (ja) * | 1996-01-30 | 1997-08-15 | Shimadzu Corp | キャピラリー電気泳動装置 |
-
1999
- 1999-06-16 DE DE19927535A patent/DE19927535B4/de not_active Expired - Fee Related
-
2000
- 2000-06-06 AU AU55302/00A patent/AU5530200A/en not_active Abandoned
- 2000-06-06 JP JP2001503516A patent/JP2003502636A/ja active Pending
- 2000-06-06 WO PCT/EP2000/005205 patent/WO2000077508A1/de active Application Filing
- 2000-06-06 EP EP00940331A patent/EP1188048A1/de not_active Withdrawn
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO1996004547A1 (en) * | 1994-08-01 | 1996-02-15 | Lockheed Martin Energy Systems, Inc. | Apparatus and method for performing microfluidic manipulations for chemical analysis and synthesis |
WO1996042013A1 (en) * | 1995-06-08 | 1996-12-27 | Visible Genetics Inc. | Microelectrophoresis chip for moving and separating nucleic acids and other charged molecules |
EP0816837A1 (de) * | 1996-07-03 | 1998-01-07 | Caliper Technologies Corporation | Variable Überwachung von elektroosmotischen und/oder elektroforetischen Kräften in einer in einem Fluidum enthaltenen Anordnung durch elektrische Kräfte |
WO1998009161A1 (en) * | 1996-08-26 | 1998-03-05 | The Regents Of The University Of California | Electrochemical detector integrated on microfabricated capillary electrophoresis chips |
WO1998049549A1 (en) * | 1997-04-30 | 1998-11-05 | Orion Research, Inc. | Capillary electrophoretic separation system |
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010188342A (ja) * | 2002-07-08 | 2010-09-02 | Deltadot Ltd | 物質分離デバイス |
KR100852297B1 (ko) | 2003-09-05 | 2008-08-14 | 칼리퍼 라이프 사이언시즈, 인크. | 분석물 주입 시스템 |
KR100971044B1 (ko) * | 2003-09-05 | 2010-07-16 | 칼리퍼 라이프 사이언시즈, 인크. | 분석물 주입 시스템 |
Also Published As
Publication number | Publication date |
---|---|
DE19927535A1 (de) | 2001-01-04 |
DE19927535B4 (de) | 2004-06-17 |
AU5530200A (en) | 2001-01-02 |
EP1188048A1 (de) | 2002-03-20 |
JP2003502636A (ja) | 2003-01-21 |
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