WO1999041015A1 - Miniaturisierter temperaturzonen flussreaktor - Google Patents
Miniaturisierter temperaturzonen flussreaktor Download PDFInfo
- Publication number
- WO1999041015A1 WO1999041015A1 PCT/EP1999/001014 EP9901014W WO9941015A1 WO 1999041015 A1 WO1999041015 A1 WO 1999041015A1 EP 9901014 W EP9901014 W EP 9901014W WO 9941015 A1 WO9941015 A1 WO 9941015A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- substrate
- substrate plate
- flow reactor
- temperature zone
- trenches
- Prior art date
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Classifications
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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
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J19/00—Chemical, physical or physico-chemical processes in general; Their relevant apparatus
- B01J19/0093—Microreactors, e.g. miniaturised or microfabricated reactors
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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
- B01L7/00—Heating or cooling apparatus; Heat insulating devices
- B01L7/52—Heating or cooling apparatus; Heat insulating devices with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples
- B01L7/525—Heating or cooling apparatus; Heat insulating devices with provision for submitting samples to a predetermined sequence of different temperatures, e.g. for treating nucleic acid samples with physical movement of samples between temperature zones
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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
- B01L2300/0874—Three dimensional network
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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
- B01L2300/0883—Serpentine channels
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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
- B01L2300/18—Means for temperature control
- B01L2300/1805—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
- B01L2300/1822—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using Peltier elements
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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
- B01L2300/18—Means for temperature control
- B01L2300/1805—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks
- B01L2300/1827—Conductive heating, heat from thermostatted solids is conducted to receptacles, e.g. heating plates, blocks using resistive heater
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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
- B01L2300/18—Means for temperature control
- B01L2300/1883—Means for temperature control using thermal insulation
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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
- B01L3/502707—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
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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
Definitions
- the invention relates to a miniaturized temperature zone flow reactor, hereinafter referred to as PCR in thermally controlled, biochemical or molecular biological processes, in particular in the process of the so-called polymerase chain reaction, in which certain sequences are multiplied from a mixture of DNA sequences , Applies.
- this sample chamber as a whole also has to be heated and cooled, with which only limited temperature change rates can be achieved.
- the parasitic heat capacity of the sample chamber and possibly a necessary temperature control block with respect to the sample liquid are of increasing importance, so that the high temperature change rates that are conceivable in principle in the case of small liquid volumes cannot be achieved, so that the effectiveness of the method is relative remains low.
- a relatively complex control and regulating effort is required, the heating or cooling output essentially not being consumed in the sample liquid, but rather in the assemblies surrounding it.
- the closest to the present invention is a flow thermal cycler described in WO 96/10456, in which structuring technologies known from so-called microsystem technology are used in order to create a sample receiving chamber which allows dynamic sample treatment even of very small quantities, sometimes very much - 3 -
- the invention is based on the object of specifying a miniaturized temperature zone flow reactor which can carry out thermally controlled, biochemical or molecular biological processes, in particular the process of the polymerase chain reaction, more effectively than according to the prior art.
- the object is achieved by the characterizing features of the first claim.
- Advantageous configurations are covered by the subordinate claims.
- the invention is a cyclic heating and cooling of solutions to different temperature levels in the continuous - 4 -
- Flow in the smallest space in the micrometer range
- three reactions e.g. Denaturation, annealing and extension of DNA
- Different samples can be injected one after the other without mixing with one another, and can then be placed in parallel in sample chambers with the aid of the proposed device.
- the invention provides for three trenched microstructured chips, which consist of a good heat-conductive material, in order to arrange a badly heat-conductive connection chip in such a way that at least one closed flow path is formed through all chips.
- Each of the microchips is subjected to a predeterminable and different temperature.
- the inflow and outflow orifices of the well thermally conductive chips are detected by through openings of the connection chip in such a way that the sample liquid passes from A to B to C and again to A to B to C, the process being repeatable n times, n being the number the trench sections provided in the input (A) and output chip (C).
- the chips kept at the desired temperature are arranged alternately around the connecting chip, so that the different temperature zones are thermally insulated from one another.
- each chip of the same temperature zone its higher thermal conductivity leads to a homogeneous temperature distribution of the liquid passing through it.
- heater and sensor structures in thin-film technology are integrated on the chips.
- External cooling can be limited to the coldest zone.
- a cooling block for example provided with Peltier elements that can be implemented using thin-film technology, is provided on the surface of the coldest chip (B).
- cooling with an air stream is also possible.
- the cooled chip B is provided with return channels which, for example, are so small in cross section that the dwell time - 5 -
- the sample is m i-mated during the return from chip C to chip A in chip B.
- the return channels can also be thermally insulated from chip B.
- an optically transparent material e.g. Pyrex glass
- Pyrex glass for the connecting chip, allows an optical in situ detection of reaction partners in the sample via fluorescence detection of an added dye, which is particularly interesting for analysis purposes.
- the individual samples are injected as drops one after the other into a continuous carrier liquid stream which is pumped through the miniaturized temperature zone flow reactor.
- the serial delivery of the sample liquids can be arranged in a parallel two-dimensional arrangement, e.g. a nanotiter plate or an electrophoresis gel. After filling one chamber with a drop of sample, the reactor is pushed to the next chamber.
- the emergence of a drop can be detected by the refraction of a light beam on the sample drop in the carrier liquid by means of a photometer module. If several, separate flow paths are provided on the proposed temperature zone flow reactor or if several miniaturized temperature zone flow reactors are operated side by side in the manner described above, the serial sample transfer mentioned can be implemented in a parallel arrangement in a very efficient manner.
- Fig. 1 in an exploded view of a possible embodiment of a miniaturized temperature zone flow reactor according to the invention
- Fig. 2 shows a photometer signal at the output of the miniaturized
- a miniaturized temperature zone flow reactor is shown in an exploded view in FIG. For reasons of clarity, only a closed flow path is shown in the example, the path of which is described below.
- a first substrate plate A is provided, which in the example has an external dimension (length, width, thickness) of (8 • 13 • 0.5) mm and into which trenches are made on one side, which are 9 mm long and one width wide of 0.536 mm and a depth of 0.380 mm.
- the length designated here is to be understood to mean the entire individual channel section which is occupied, for example, between an inflow opening az2 and the associated outflow opening aa2, as a result of which this channel section is able to hold a volume of 0.9 ⁇ l in the example.
- a third substrate plate C which in the example has an external dimension (length, width, thickness) of (14 • 13 • 0.5) mm and into which trenches having a length of 22 mm and a width are made on one side of 0.536 mm and a depth of 0.380 mm, so that this single channel section can hold a volume of 2.26 ⁇ l.
- the size to be understood here under length it is to be understood as being the same as stated for the first substrate plate A.
- Both of the above-mentioned substrate platelets A, C consist of a material which has good thermal conductivity, in the example of silicon, and are covered over the entire area on the side opposite the open trench sides by heating means H which can be subjected to a variable, variable temperature.
- these heating means H are formed by meandering and applied directly to the substrate platelets
- Thin film heating elements formed. Furthermore, on these substrates Thin temperature sensor F integrated, which are used to control and regulate the temperature to be set.
- the inflow and outflow orifices azl ... aa4 of the first substrate plate A and the inflow and outflow orifices czl ... ca4 of the third substrate plate C are arranged on one side essentially in a line next to one another on a partial side of the respective substrate plate and spaced apart from one another with the surface , which is opposite the heating medium H, is applied on a first side VI of a poorly thermally conductive and via a connecting chip V provided with through openings Vd, for which a 1.1 mm thick pyrex glass chip is used in the example, and connected to it by anodic bonding, that mentioned inflow and outflow orifices and are covered by the passage openings Vd.
- An and the partial routes Cl ... Cn takes place by means of a second substrate plate B bonded on the second side V2 of the connecting chip V, for which in the example also a silicon chip with the dimensions (12 • 10 • 0 , 5) mm is used, in which longitudinally extending trenches with a length of 9 mm, a width of 0.536 mm and a depth of 0.38 mm are introduced.
- These n channels four in the example: B1 ... B4, each take over the flowing flow from A to C.
- the returning channels are designed in such a way that they are initially formed by trenches, that they have a length of 9 mm, a width of 0.26 mm and a depth of 0.184 mm and are thus able to accommodate a volume of 0.2 ⁇ l, whereas the leading channels B1 ... B4 take up a volume of 0.9 ⁇ l. Furthermore, it is advantageous within the scope of the invention to provide the returning channels BB1 ... BB3 of the substrate plate B with a thermally insulating lining with respect to the wall material of the substrate plate B. This can be carried out in the assembled state of the temperature zone flow reactor by passing it through and attaching a polymer to the wall. In any case, the nick-leading channels should be reduced - 8th -
- Zone A 55 s
- Zone B 55 s in the leading channel
- connection chip (V) is formed from an optically transparent material, for example pyrex glass, and according to the arrangement of the substrate plates A, C, an accessible free space remains between them, the possibility of an optical in situ detection of reaction partners in the sample is via a Fluorescence detection of an added dye is given, which is particularly advantageous for analysis purposes.
- the three temperature zones are designed for carrying out a PCR in such a way that a denaturation of a double-stranded DNA can be carried out in the region of the substrate plate A, that the attachment of primers to single-stranded DNA is possible in the region of the substrate plate B (annealing), and that the primer extension is made possible in the region of the substrate plate C by means of TAQ polymerase.
- the temperatures measured in the exemplary embodiment were: Zone A: 95 ° C; Zone B: 55 ° C; Zone C: 72 ° C.
- the temperature in the zones can be kept constant at 1 ° C by connecting an external proportional controller.
- the carrier liquid passes through each of the zones mentioned four times.
- the first inflow path, formed by the partial path azl to eel in the first substrate plate A and the last outflow path, formed by the partial path cz4 to ca4 in the third substrate plate B are extended to the processes compared to the other n partial trenches provided on the respective substrate plates Allow a longer reaction time for the PCR at the inlet and outlet of the proposed temperature zone flow reactor.
- FIG. 2 shows an example of the signal of such a photometer at the outlet of the miniaturized temperature zone flow reactor, which shows that there is no mixing of individual sample areas during the flow if a liquid, especially an oil, which is immiscible with the sample is used as the carrier medium for the sample transport. is inserted. A colored sample was used for testing.
Abstract
Description
Claims
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
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DE59905737T DE59905737D1 (de) | 1998-02-11 | 1999-02-10 | Miniaturisierter temperaturzonen flussreaktor |
US09/600,694 US6896855B1 (en) | 1998-02-11 | 1999-02-10 | Miniaturized temperature-zone flow reactor |
EP99913166A EP1054735B1 (de) | 1998-02-11 | 1999-02-10 | Miniaturisierter temperaturzonen flussreaktor |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE19805350 | 1998-02-11 | ||
DE19805350.9 | 1998-02-11 |
Publications (1)
Publication Number | Publication Date |
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WO1999041015A1 true WO1999041015A1 (de) | 1999-08-19 |
Family
ID=7857240
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/EP1999/001014 WO1999041015A1 (de) | 1998-02-11 | 1999-02-10 | Miniaturisierter temperaturzonen flussreaktor |
Country Status (4)
Country | Link |
---|---|
US (1) | US6896855B1 (de) |
EP (1) | EP1054735B1 (de) |
DE (1) | DE59905737D1 (de) |
WO (1) | WO1999041015A1 (de) |
Cited By (24)
Publication number | Priority date | Publication date | Assignee | Title |
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WO2001007159A2 (en) * | 1999-07-28 | 2001-02-01 | Genset | Integration of biochemical protocols in a continuous flow microfluidic device |
DE19935433A1 (de) * | 1999-08-01 | 2001-03-01 | Febit Ferrarius Biotech Gmbh | Mikrofluidischer Reaktionsträger |
FR2798604A1 (fr) * | 1999-09-17 | 2001-03-23 | Genset Sa | Dispositif pour la realisation de reactions chimiques ou biochimiques par cyclage thermique |
FR2799139A1 (fr) * | 1999-10-01 | 2001-04-06 | Genset Sa | Dispositif d'analyse biochimique comprenant un substrat microfluidique notamment pour l'amplification ou l'analyse d'acides nucleiques. |
EP1125630A2 (de) * | 2000-02-14 | 2001-08-22 | CPC Cellular Process Chemistry Systems GmbH | Mikroreaktor mit verbessertem Wärmetauscher |
DE10005549A1 (de) * | 2000-02-09 | 2001-09-06 | Cpc Cellular Process Chemistry | Mikroreaktor für Reaktionsmedien in Form einer Suspension |
EP1232785A2 (de) * | 2001-02-15 | 2002-08-21 | Cognis Deutschland GmbH & Co. KG | Chip-Reaktor |
EP1269171A1 (de) * | 2000-03-07 | 2003-01-02 | Northeastern University | Paralleles array unabhängiger thermostaten für säulentrennungen |
WO2003082460A1 (en) * | 2002-03-29 | 2003-10-09 | Casio Computer Co., Ltd. | Chemical reaction apparatus and power supply system |
EP1384022A2 (de) * | 2001-04-06 | 2004-01-28 | California Institute Of Technology | Nukleinsäure-amplifikation verwendende mikrofluidvorrichtungen |
WO2004059309A1 (en) * | 2002-12-20 | 2004-07-15 | Northeastern University | Precision controlled thermostat |
EP1481722A1 (de) * | 2003-05-30 | 2004-12-01 | Sony Corporation | Reaktor und Verfahren zur Herstellung desselben, Reformer und Leistungsversorgungssystem |
WO2005023427A1 (en) * | 2003-09-05 | 2005-03-17 | Stokes Bio Limited | A microfluidic analysis system |
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US6977145B2 (en) | 1999-07-28 | 2005-12-20 | Serono Genetics Institute S.A. | Method for carrying out a biochemical protocol in continuous flow in a microreactor |
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- 1999-02-10 WO PCT/EP1999/001014 patent/WO1999041015A1/de active IP Right Grant
- 1999-02-10 US US09/600,694 patent/US6896855B1/en not_active Expired - Fee Related
- 1999-02-10 DE DE59905737T patent/DE59905737D1/de not_active Expired - Fee Related
- 1999-02-10 EP EP99913166A patent/EP1054735B1/de not_active Expired - Lifetime
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Also Published As
Publication number | Publication date |
---|---|
EP1054735A1 (de) | 2000-11-29 |
DE59905737D1 (de) | 2003-07-03 |
EP1054735B1 (de) | 2003-05-28 |
US6896855B1 (en) | 2005-05-24 |
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