EP1313562B1 - Multiwell filtration plate and method for producing the same - Google Patents
Multiwell filtration plate and method for producing the same Download PDFInfo
- Publication number
- EP1313562B1 EP1313562B1 EP01964906A EP01964906A EP1313562B1 EP 1313562 B1 EP1313562 B1 EP 1313562B1 EP 01964906 A EP01964906 A EP 01964906A EP 01964906 A EP01964906 A EP 01964906A EP 1313562 B1 EP1313562 B1 EP 1313562B1
- Authority
- EP
- European Patent Office
- Prior art keywords
- outlet
- filtration plate
- well
- multiwell filtration
- connecting piece
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Expired - Lifetime
Links
Images
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
- B01L3/5025—Containers for the purpose of retaining a material to be analysed, e.g. test tubes with fluid transport, e.g. in multi-compartment structures for parallel transport of multiple samples
- B01L3/50255—Multi-well filtration
Definitions
- the invention relates to a new multi-well filtration plate, preferably in 96-well or in 384-well format, consisting of two separate parts, which are firmly and tightly interconnected.
- the first part represents a sample receiving part with filter plates, and the second part acts as a discharge part after filtration.
- This plate according to the invention is particularly suitable for high-throughput applications in nucleic acid technology and for protein purification and analysis.
- the new multi-well filtration plate consists of two tightly connected individual parts.
- the upper part of the plate is defined as a sample receiving part 1, the lower part of the plate as a discharge part 2 with filter 3.
- This outlet part 2 comprises for each well according to the invention shaped outlets 4, via which the filtrate in a collecting vessel, such as. a deep-well plate, for further determination runs.
- the outlet part is thus vzw by the correspondingly shaped outlet spout 4, depending on the plate. 96 or 384.
- outlet nozzles have an inner angle of inclination of 15-25 °, preferably 20 ° and have at the junction with the upper part each about 1.0-1.5mm, preferably 1.0mm thick support paragraph (seal paragraph) 5 for stabilizing the filter cartridge 3 , Their length is about 5-15mm.
- 96-well plates have spouts with a length of 10-15 mm, vzw. they have a length of 12 mm.
- 384-well plates have spout with a length of about 5-8 mm, vzw. they have a length of 5 to 6 mm. Possibly. the filtration plate is coupled to the outlet vessel.
- outlet nozzles are usually round, in a further embodiment, they may be formed at the outlet end or starry with at least 8 openings.
- the internal tilt angle of 15-25 °, preferably 20 °, and the special outlet design allow easy and complete leakage of the filtered sample into the collecting vessel, eg the deep-well plate (minimizing the dead volume, almost 0).
- the length of the outlet with vzw. about 12 mm for 96-well plates and with vzw. 5 to 6 mm for 384 well plates can avoid the highly problematic cross-contamination
- Multi-well filtration plate according to the invention can also be used for applications in PCR-based infection diagnostics.
- the extension of the outlet connection furthermore has the consequence that, in contrast to previously known filtration plates, the filtration plate according to the invention has an increased capacity of uptake volume with a chamber volume of more than 1 ml for 96 well plates and approx. 300 ⁇ l for 384 well plates, ie Overall, larger sample volumes can be processed than previously customary. This also leads to more reproducible results. This applies in particular to the application of the 384-well plates, which is very much desired by the person skilled in the art, and whose throughput could thus be increased by 4-6 times.
- the invention also provides the process for producing the new multi-well filtration plate.
- Both parts of the multi-well filtration plate are firmly connected to each other in a special production process via a hydraulic compression.
- the compression takes place in each case at the recesses with the outlet connection (96 or 384).
- Toollike, the inner Verpressungskanten are sharpened so that during the compression, in which the filter element 3, such. B. a filter mat is placed between upper 1 and lower part 2, the wells corresponding filters are punched clean.
- These punched filter cartridges are pressed with the upper part in the lower part and lie down on the support shoulder 5 in the lower part.
- By hydraulic pressure plate upper part, filter plate and plate bottom are firmly and tightly pressed together.
- the production of the multi-well filtration plate is preferably carried out by injection molding with carefully adjusted injection molding parameters.
- the filtration panels of the invention are made of known materials, e.g. Polystyrene or polypropylene.
- the injection molding material used is preferably a high-quality polystyrene. Since only precisely fitting injection-molded parts are used, the compression takes place without sealing lips, etc.
- the invention ideally solves all existing problems.
- the plate is produced by means of a new technological process, which makes it possible to transport a filter material into the multi-well filtration plate in a highly efficient and cost-effective manner.
- the novel multi-well filtration plate is constructed in its constructive dimensioning that can be eliminated on the shape of the spout previously known cross contamination.
- External dimensions (width and length) of the plate and the arrangement of the wells correspond to a normal microtitration plate, with a further advantage in increasing the volume of the reaction cavities to about 1 ml (96 well) or to about 300 ⁇ l (384 well).
- the plate is also easy to use in protein purification and analysis.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- General Health & Medical Sciences (AREA)
- Hematology (AREA)
- Clinical Laboratory Science (AREA)
- Analytical Chemistry (AREA)
- Apparatus Associated With Microorganisms And Enzymes (AREA)
- Filtering Materials (AREA)
- Sampling And Sample Adjustment (AREA)
- Automatic Analysis And Handling Materials Therefor (AREA)
- Devices For Use In Laboratory Experiments (AREA)
- Preparation Of Compounds By Using Micro-Organisms (AREA)
- Separation Using Semi-Permeable Membranes (AREA)
Abstract
Description
Die Erfindung betrifft eine neue Multiwell-Filtrationsplatte, vorzugsweise im 96-Well-oder im 384-Well-Format, bestehend aus zwei Einzelteilen, die fest und dicht miteinander verbunden sind. Der erste Teil stellt einen Probeaufnahmeteil mit Filterplättchen dar, und der zweite Teil fungiert als Auslaufteil nach erfolgter Filtration. Diese erfindungsgemäße Platte ist insbesondere für Hochdurchsatzapplikationen in der Nukleinsäuretechnik sowie für die Proteinaufreinigung und -analytik geeignet.The invention relates to a new multi-well filtration plate, preferably in 96-well or in 384-well format, consisting of two separate parts, which are firmly and tightly interconnected. The first part represents a sample receiving part with filter plates, and the second part acts as a discharge part after filtration. This plate according to the invention is particularly suitable for high-throughput applications in nucleic acid technology and for protein purification and analysis.
In den letzten Jahren zeichnete sich ein zunehmender Trend zur Automatisierung bei der Isolierung und Aufreinigung von Nukleinsäuren ab. Die Ursachen liegen darin begründet, dass sich in allen Forschungsfeldern der modernen Biotechnologie molekularbiologische Verfahren immer stärker etablieren. Nicht zuletzt durch die DNA-Sequenzierung innerhalb weltweiter Genomprojekte (z.B. Humanes Genomprojekt) ist eine Automatisierung der Isolierung und Aufreinigung von Plasmid-DNA eine zwingende Voraussetzung geworden. Die Notwendigkeit der Entwicklung von Automatisierungsvarianten beschränkt sich dabei nicht nur auf den Bereich der Plasmid-DNA-Isolierung. Mehr und mehr gewinnt auch die automatisierte Isolierung genomischer DNA aus unterschiedlichsten Ausgangsmaterialien und Mengen sowie die Isolierung von RNA an Bedeutung. Dies umfasst alle Bereiche der molekularen Basisforschung und zunehmend auch den Diagnostikbereich. Verfahren der automatisierten Isolierung von Nukleinsäuren werden z.Z. über Mikrotestplatten mit eingebauten Filtermaterialien realisiert. Dabei sind z.Z. Verwendung findende Formate sog. 96-Well bzw. 384-Well-Mikrotestplatten.In recent years, there has been an increasing trend toward automation in the isolation and purification of nucleic acids. The reasons lie in the fact that in all research fields of modern biotechnology molecular biological procedures are becoming increasingly established. Not least through DNA sequencing within global genome projects (e.g., human genome project), automation of isolation and purification of plasmid DNA has become a mandatory requirement. The need for the development of automation variants is not limited to the field of plasmid DNA isolation. Increasingly, the automated isolation of genomic DNA from a wide variety of starting materials and quantities as well as the isolation of RNA are gaining in importance. This encompasses all areas of basic molecular research and increasingly also the diagnostics sector. Methods of automated isolation of nucleic acids are currently being used. implemented using microplates with built-in filter materials. There are z.Z. Forms used are so-called 96-well or 384-well microplates.
Die z.Z. verfügbaren 96-Well-Mikrotestplatten mit Filtermaterial sind allerdings für Hochdurchsatzapplikationen extrem teuer. Dies resultiert aus den relativ komplizierten Herstellungsverfahren zur Einbringung des Filtermaterials in die Mikrotestplatte (US-A 4,948,442). Darüber hinaus realisiert bisher keine der bekannten Mikrotestplatten mit Filtereinsatz einen ausreichend hohen Schutz vor Kreuzkontaminationen von Proben bei Anwendung zur Isolierung und Aufreinigung von Nukleinsäuren. Die Ursache liegt in den viel zu kurzen Auslaufstutzen am Boden der Multiwell-Filtrationsplatten. Ein weiteres Problem sind die geringen Volumina der Reaktionskavitäten, z.B. beschrieben im EP-A1 0,098,534. Auch die bekannten 384-Well-Platten des Standes der Technik gestatten nur den Durchsatz geringer Volumina im jeweiligen Analyseverfahren, diese Volumina liegen bei ca. 50-80 µl. Für die Durchführung von Analysen, insbesondere zur automatischen Analyse, und für den Einsatz in Kombination mit Laborrobotem sind in den meisten Fällen jedoch Testplatten, die einen Durchsatz mit großen Volumina erlauben, erforderlich.However, the 96-well microtiter plates with filter material currently available are extremely expensive for high-throughput applications. This results from the relatively complicated manufacturing process for introducing the filter material into the microplate (US-A 4,948,442). Moreover, so far none of the known microtest plates with filter insert realized a sufficiently high protection against cross-contamination of samples when used for the isolation and purification of nucleic acids. The reason lies in the much too short discharge spigot at the bottom of the multiwell filtration plates. Another problem is the low volumes of the reaction cavities, for example described in EP-A1 0,098,534. Even the known 384-well plates of the prior art allow only the throughput of small volumes in the respective analysis method, these volumes are about 50-80 ul. For carrying out analyzes, in particular for automatic Analysis, and for use in combination with laboratory robots, however, test plates that allow high volume throughput are required in most cases.
Der Erfindung lag deshalb die Aufgabe zugrunde, eine Multiwell-Filtrationsplatte bereitzustellen, die Schutz vor Kreuzkontaminationen der Proben gewährt, die kostengünstig herstellbar und vielschichtig einsetzbar ist, wie z.B. für Hochdurchsatzapplikationen in der Nukleinsäuretechnik und in der Proteintechnik.It is an object of the present invention to provide a multi-well filtration plate which provides protection against cross-contamination of the samples, which is inexpensive to produce and versatile in use, e.g. for high-throughput applications in nucleic acid technology and in protein technology.
Die neue Multiwell-Filtrationsplatte besteht aus zwei dicht verbundenen Einzelteilen. Der obere Teil der Platte wird als Probenaufnahmeteil 1 definiert, der untere Teil der Platte als Auslaufteil 2 mit Filter 3. Dieser Auslaufteil 2 umfaßt für jedes Well erfindungsgemäß geformte Auslaufstutzen 4, über die das Filtrat in ein Auffanggefäß, wie z.B. eine Deep-Well-Platte, zur weiteren Bestimmung läuft. Im wesentlichen ist der Auslaufteil also durch die entsprechend besonders geformten Auslaufstutzen 4, je nach Platte vzw. 96 oder 384, gekennzeichnet.The new multi-well filtration plate consists of two tightly connected individual parts. The upper part of the plate is defined as a
Diese Auslaufstutzen besitzen einen inneren Neigungswinkel von 15-25°, vorzugsweise 20° und weisen an der Anschlußstelle zum Oberteil jeweils einen ca. 1,0-1,5mm, vorzugsweise 1,0mm starken Auflageabsatz (Dichtungsabsatz) 5 zur Stabilisierung des Filtereinsatzes 3 auf. Ihre Länge beträgt ca. 5-15mm. 96-Well-Platten weisen Auslaufstutzen mit einer Länge von 10-15 mm auf, vzw. besitzen sie eine Länge von 12 mm. 384-Well-Platten weisen Auslaufstutzen mit einer Länge von ca. 5-8 mm auf, vzw. besitzen sie eine Länge von 5 bis 6 mm. Ggf. ist die Filtrationsplatte an das Auslaufgefäß gekoppelt.These outlet nozzles have an inner angle of inclination of 15-25 °, preferably 20 ° and have at the junction with the upper part each about 1.0-1.5mm, preferably 1.0mm thick support paragraph (seal paragraph) 5 for stabilizing the
Desweiteren sind die Auslaufstutzen in der Regel rund, in einer weiteren Ausführungsvariante können sie am Auslaufende oder ganz sternenförmig mit mindestens 8 Öffnungen ausgebildet sein.Furthermore, the outlet nozzles are usually round, in a further embodiment, they may be formed at the outlet end or starry with at least 8 openings.
Der innere Neigungswinkel von 15-25°, vorzugsweise 20°, und das besondere Auslaufdesign ermöglichen ein problemloses und vollständiges Auslaufen der gefilterten Probe in das Auffanggefäß, z.B. die Deep-Well Platte (Minimierung des Todvolumens, nahezu 0). Durch die Länge der Auslaufstutzen mit vzw. ca. 12 mm für 96-Well-Platten und mit vzw. 5 bis 6 mm für 384 Well-Platten (bekannte Mikrotiterplatten besitzen Ausläufe mit einer maximalen Länge von 9 mm (96 Well) und < 5 mm (384 Well) können die hochproblematischen Kreuzkontaminationen vermieden werden. Damit ist die erfindungsgemäße Multiwell-Filtrationsplatte auch für Anwendungen in der PCRbasierenden Infektionsdiagnostik nutzbar.The internal tilt angle of 15-25 °, preferably 20 °, and the special outlet design allow easy and complete leakage of the filtered sample into the collecting vessel, eg the deep-well plate (minimizing the dead volume, almost 0). By the length of the outlet with vzw. about 12 mm for 96-well plates and with vzw. 5 to 6 mm for 384 well plates (known microtiter plates have spouts with a maximum length of 9 mm (96 wells) and <5 mm (384 wells) can avoid the highly problematic cross-contamination Multi-well filtration plate according to the invention can also be used for applications in PCR-based infection diagnostics.
Die Verlängerung der Auslaufstutzen hat desweiteren zur Folge, dass im Gegensatz zu bislang bekannten Filtrationsplatten die erfindungsgemäße Filtrationsplatte eine vergrößerte Aufnahmevolumen-Kapazität mit einem Kammervolumen von über 1 ml für 96 Well Platten und ca. 300 µl für 384 Well-Platten besitzt, d.h., es können insgesamt größere Probenvolumina als bislang üblich verarbeitet werden. Das führt somit auch zu reproduzierbareren Ergebnissen. Besonders gilt dies für die vom Fachmann sehr gewünschte Anwendung der 384-Well-Platten, deren Durchsatz damit um das 4―6 fache gesteigert werden konnte.The extension of the outlet connection furthermore has the consequence that, in contrast to previously known filtration plates, the filtration plate according to the invention has an increased capacity of uptake volume with a chamber volume of more than 1 ml for 96 well plates and approx. 300 μl for 384 well plates, ie Overall, larger sample volumes can be processed than previously customary. This also leads to more reproducible results. This applies in particular to the application of the 384-well plates, which is very much desired by the person skilled in the art, and whose throughput could thus be increased by 4-6 times.
Gegenstand der Erfindung ist auch das Verfahren zur Herstellung der neuen Multiwell-Filtrationsplatte. Beide Teile der Multiwell-Filtrationsplatte werden in einem besonderen Produktionsablauf fest miteinander über eine hydraulische Verpressung verbunden. Die Verpressung erfolgt jeweils an den Vertiefungen mit den Auslaufstutzen (96 bzw. 384). Werkzeugmäßig sind die inneren Verpressungskanten so geschärft, dass bei der Verpressung, bei der der Filtereinsatz 3 , wie z. B. eine Filtermatte, zwischen Ober- 1 und Unterteil 2 gelegt wird, den Vertiefungen entsprechende Filter sauber gestanzt werden. Diese ausgestanzten Filtereinsätze werden mit dem Oberteil in das Unterteil gepresst und legen sich auf den Auflageabsatz 5 im Unterteil auf. Durch hydraulischen Druck werden Plattenoberteil, Filterplättchen und Plattenunterteil fest und dicht miteinander verpresst.The invention also provides the process for producing the new multi-well filtration plate. Both parts of the multi-well filtration plate are firmly connected to each other in a special production process via a hydraulic compression. The compression takes place in each case at the recesses with the outlet connection (96 or 384). Toollike, the inner Verpressungskanten are sharpened so that during the compression, in which the
Eine solche Verpressung wird erfindungsgemäß möglich, da Unterteil und Oberteil der neuen Multiwell-Filtrationsplatten in zwei absoluten Präzisionswerkzeugen (Heißkanaltechnik), die exakt aufeinander abgestimmt sind, mit einer maximalen Toleranz von 1/1000 mm, gefertigt werden. Scharfe Schneidkanten an den Verpressungsteilen der beiden Plattenteile ermöglichen das Ausstanzen von Einzelfiltern aus einer Filterplatte in einem Arbeitsgang mit dem eigentlichen Verpressen. Das Verpressen erfolgt direkt, d.h. es sind gemäß der Erfindung weder Nut noch Feder (wie aus dem allgemeinen Stand der Technik bekannt) erforderlich, was einen erheblichen technologischen Vorteil bedeutet.Such compression is possible according to the invention, since lower part and upper part of the new multi-well filtration plates in two absolute precision tools (hot runner technology), which are precisely matched, with a maximum tolerance of 1/1000 mm, are made. Sharp cutting edges on the pressing parts of the two plate parts allow the punching of individual filters from a filter plate in one operation with the actual pressing. The pressing is done directly, ie there are according to the invention, neither groove nor spring (as known from the general state of the art) required, which means a significant technological advantage.
Die Herstellung der Multiwell-Filtrationsplatte erfolgt bevorzugt im Spritzgußverfahren mit sorgfältig eingestellten Spritzgußparametern. Die erfindungsgemäßen Filtrationsplatten bestehen aus an sich bekannten Materialien, wie z.B. Polystyrol oder Polypropylen. Das eingesetzte Spritzgußmaterial ist bevorzugt ein hochwertiges Polystyrol. Da nur passgenaue Spritzgussteile verwendet werden, erfolgt die Verpressung ohne Dichtungslippen u.ä..The production of the multi-well filtration plate is preferably carried out by injection molding with carefully adjusted injection molding parameters. The filtration panels of the invention are made of known materials, e.g. Polystyrene or polypropylene. The injection molding material used is preferably a high-quality polystyrene. Since only precisely fitting injection-molded parts are used, the compression takes place without sealing lips, etc.
Die Erfindung löst in idealster Weise alle bestehenden Probleme. Die Herstellung der Platte erfolgt mittels eines neuen technologischen Verfahrens, welches hocheffizient und preiswert die Verbringung eines Filtermaterials in die Multiwell-Filtrationsplatte ermöglicht. Weiterhin ist die neuartige Multiwell-Filtrationsplatte in ihrer konstruktiven Dimensionierung so aufgebaut, dass über die Form der Auslaufstutzen bisher bekannte Kreuzkontaminationen beseitigt werden können. Außenmaße (Breite und Länge) der Platte und die Anordnung der Vertiefungen (vorzugsweise 8 x 12 Matrix) entsprechen einer normalen Mikrotitrationsplatte, wobei ein weiterer Vorteil in der Erhöhung der Volumina der Reaktionskavitäten auf ca. 1 ml (96 Well) bzw. auf ca. 300 µl (384 Well) besteht. Damit können prinzipiell alle Standardapplikationen der automatisierten Isolierung und Aufreinigung von Nukleinsäuren problemlos mit einer Platte realisiert werden. Des weiteren ist die Platte ebenfalls in der Proteinaufreinigung und - analytik problemlos einsetzbar.The invention ideally solves all existing problems. The plate is produced by means of a new technological process, which makes it possible to transport a filter material into the multi-well filtration plate in a highly efficient and cost-effective manner. Furthermore, the novel multi-well filtration plate is constructed in its constructive dimensioning that can be eliminated on the shape of the spout previously known cross contamination. External dimensions (width and length) of the plate and the arrangement of the wells (preferably 8 x 12 matrix) correspond to a normal microtitration plate, with a further advantage in increasing the volume of the reaction cavities to about 1 ml (96 well) or to about 300 μl (384 well). Thus, in principle, all standard applications of automated isolation and purification of nucleic acids can be easily realized with a plate. Furthermore, the plate is also easy to use in protein purification and analysis.
Anschließend wird die Erfindung an den folgenden Beispielen näher erläutert..
- Fig. 1
- Gesamtansicht einer 96-Well-Vorrichtung
- Fig. 2a
- Längsschnitt der einzelnen Vorrichtungsteile
- Fig. 2b
- Längsschnitt mit Filtermembran
- Fig. 3
- Auslaufstutzen als Querschnitt
- Fig. 1
- Overall view of a 96-well device
- Fig. 2a
- Longitudinal section of the individual device parts
- Fig. 2b
- Longitudinal section with filter membrane
- Fig. 3
- Outlet as a cross section
- 11
- Probeaufnahmeteil (Oberteil)Sample receiving part (upper part)
- 22
- Auslaufteil (Unterteil)Outlet part (lower part)
- 33
- Filtereinsatzfilter cartridge
- 44
- Auslaufstutzenoutlet connection
- 55
- Auflageabsatzsupporting shoulder
- 66
- Auslaufende (rund oder sternenförmig)Expiring (round or star shaped)
Claims (8)
- Method for producing a multiwell filtration plate, characterized by producing the sample holder part (1) and the outlet part (2) comprising the outlet connecting piece (4) via hot channel technology, directly aligned with each other, with a maximum tolerance of 1/1000mm, and by connecting them at the depressions of the outlet connecting pieces via hydraulic compression so that a firm and tight connection is formed, further characterized by forming sharp, inner compression edges by using suitable tools, so that when a filter insert (3) is placed between sample holder part (1) and outlet part (2) during compression, filters are punched out into the corresponding depressions, which are pressed against the outlet piece (2) by the sample holder part (1) and are fixed on the supporting shoulder (5).
- Multiwell filtration plate produced by a method according to claim 1.
- Multiwell filtration plate according to claim 2, further characterized by a sample holder part (1) that is firmly and tightly connected to the outlet part (2), that comprises an outlet connecting piece (4) for each well and that has a length of 10-15mm in the case of a 96 well plate, wherein a supporting shoulder (5) carrying a filter insert (3) is present at the connection of sample holder part and outlet part.
- Multiwell filtration plate according to claims 2-3, characterized by an outlet connecting piece (4) that is round or by an outlet connecting piece bottom portion (6) that is star-shaped.
- Multiwell filtration plate according to claim 4, characterized by a star-shaped outlet connecting piece bottom portion (6) that has eight openings.
- Multiwell filtration plate according to claims 2-5, characterized by being a 96 well plate, wherein the outlet connecting piece (4) has a length of 10-15mm, preferably 12mm.
- Multiwell filtration plate according to claims 2, 4 or 5, characterized by being a 384 well plate.
- Use of a multiwell filtration plate according to claims 2-7 for high-throughput applications related to nucleic acids.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE10041825 | 2000-08-02 | ||
DE10041825A DE10041825A1 (en) | 2000-08-25 | 2000-08-25 | Multiwell filtration plate and process for its manufacture |
PCT/DE2001/003137 WO2002016035A1 (en) | 2000-08-25 | 2001-08-22 | Multiwell filtration plate and method for producing the same |
Publications (2)
Publication Number | Publication Date |
---|---|
EP1313562A1 EP1313562A1 (en) | 2003-05-28 |
EP1313562B1 true EP1313562B1 (en) | 2006-10-25 |
Family
ID=7653785
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP01964906A Expired - Lifetime EP1313562B1 (en) | 2000-08-25 | 2001-08-22 | Multiwell filtration plate and method for producing the same |
Country Status (10)
Country | Link |
---|---|
US (1) | US6830732B1 (en) |
EP (1) | EP1313562B1 (en) |
JP (1) | JP2004506918A (en) |
CN (1) | CN1471432A (en) |
AT (1) | ATE343426T1 (en) |
AU (1) | AU2001285706A1 (en) |
DE (2) | DE10041825A1 (en) |
DK (1) | DK1313562T3 (en) |
ES (1) | ES2275719T3 (en) |
WO (1) | WO2002016035A1 (en) |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2372464B (en) * | 2001-02-22 | 2003-05-14 | Vivascience Ltd | Method of isolating a charged compound |
JP4245354B2 (en) * | 2001-05-31 | 2009-03-25 | ポール・コーポレーション | Well for fluid processing |
US7375807B2 (en) * | 2002-07-15 | 2008-05-20 | Avantium International B.V. | System for the preparation of multiple solid state samples, in particular for spectroscopic and microscopic analysis |
AU2003284031A1 (en) * | 2002-10-10 | 2004-05-04 | Irm, Llc | Capacity altering device, holder and methods of sample processing |
DE10310025A1 (en) * | 2003-03-06 | 2004-09-16 | Rheinisch-Westfälisch- Technische Hochschule Aachen | Holder to take a number of disposable pipettes/protective caps in a matrix layout, for screening chemical or biological or medical samples, has springs under the holder openings for trouble-free automatic manipulation |
US7063216B2 (en) | 2003-09-04 | 2006-06-20 | Millipore Corporation | Underdrain useful in the construction of a filtration device |
US8968679B2 (en) * | 2005-05-19 | 2015-03-03 | Emd Millipore Corporation | Receiver plate with multiple cross-sections |
WO2008157278A1 (en) * | 2007-06-15 | 2008-12-24 | Smithkline Beecham Corporation | Antibody formulations |
US20100089938A1 (en) * | 2008-04-11 | 2010-04-15 | Arta Motadel | Pipette tip handling devices and methods |
EP2276572B1 (en) | 2008-04-11 | 2018-12-19 | Biotix, Inc. | Pipette tip handling devices and methods |
US8590736B2 (en) | 2009-04-11 | 2013-11-26 | Biotix, Inc. | Automated pipette tip loading devices and methods |
USD697227S1 (en) | 2009-04-11 | 2014-01-07 | Biotix, Inc. | Pipette tip handling device set |
DE102009057223B4 (en) * | 2009-12-05 | 2016-03-24 | Chemagen Biopolymer-Technologie Aktiengesellschaft | Sample vessel matrix and its production process |
WO2014018751A1 (en) * | 2012-07-27 | 2014-01-30 | Emory University | Cell filtration device |
Family Cites Families (28)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3295686A (en) * | 1965-05-20 | 1967-01-03 | Rockridge Lab | Filter unit |
DE3214287A1 (en) * | 1981-04-23 | 1982-12-02 | Günther Prof. Dipl.-Ing. Dr. 8047 Graz Knapp | Tube for carrying out a radioimmunoassay |
US4948442A (en) | 1985-06-18 | 1990-08-14 | Polyfiltronics, Inc. | Method of making a multiwell test plate |
US4948564A (en) | 1986-10-28 | 1990-08-14 | Costar Corporation | Multi-well filter strip and composite assemblies |
US4902481A (en) | 1987-12-11 | 1990-02-20 | Millipore Corporation | Multi-well filtration test apparatus |
DE3843610A1 (en) * | 1988-01-13 | 1989-07-27 | Stephan Dr Diekmann | DISCONNECTING OR REACTION PILLAR UNIT |
DE3804429A1 (en) * | 1988-02-12 | 1989-08-24 | Schleicher & Schuell Gmbh | DISPOSABLE FILTER |
US5108704A (en) | 1988-09-16 | 1992-04-28 | W. R. Grace & Co.-Conn. | Microfiltration apparatus with radially spaced nozzles |
JPH02151769A (en) * | 1988-12-02 | 1990-06-11 | Jeol Ltd | Reaction container |
SE9000650L (en) * | 1989-02-28 | 1990-08-29 | Asahi Optical Co Ltd | Separation of cells or viruses |
US5141719A (en) | 1990-07-18 | 1992-08-25 | Bio-Rad Laboratories, Inc. | Multi-sample filtration plate assembly |
US5264184A (en) * | 1991-03-19 | 1993-11-23 | Minnesota Mining And Manufacturing Company | Device and a method for separating liquid samples |
US5205989A (en) * | 1991-09-18 | 1993-04-27 | Minnesota Mining And Manufacturing Company | Multi-well filtration apparatus |
US5368729A (en) * | 1993-07-23 | 1994-11-29 | Whatman, Inc. | Solid phase extraction device |
US5620662A (en) | 1993-08-23 | 1997-04-15 | Brandeis University | Temporary liquid storage cavities in a centrifuge tube lid |
US5595653A (en) * | 1994-07-15 | 1997-01-21 | Cera, Inc. | Microcolumn for extraction of analytes from liquids |
US5846493A (en) * | 1995-02-14 | 1998-12-08 | Promega Corporation | System for analyzing a substance from a solution following filtering of the substance from the solution |
DE29505652U1 (en) * | 1995-04-01 | 1996-04-25 | Boehringer Mannheim Gmbh, 68305 Mannheim | Vessel for the reduced contamination treatment of liquids |
US5874004A (en) * | 1996-06-19 | 1999-02-23 | Sheila H. Dewitt | Phase separation filter device |
US5792430A (en) * | 1996-08-12 | 1998-08-11 | Monsanto Company | Solid phase organic synthesis device with pressure-regulated manifold |
US6027694A (en) | 1996-10-17 | 2000-02-22 | Texperts, Inc. | Spillproof microplate assembly |
US6054100A (en) * | 1996-11-18 | 2000-04-25 | Robbins Scientific Corporation | Apparatus for multi-well microscale synthesis |
US5888831A (en) * | 1997-03-05 | 1999-03-30 | Gautsch; James W. | Liquid-sample-separation laboratory device and method particularly permitting ready extraction by syringe of the separated liquid sample |
US6391241B1 (en) | 1997-06-06 | 2002-05-21 | Corning Incorporated | Method of manufacture for a multiwell plate and/or filter plate |
US5906796A (en) * | 1997-08-04 | 1999-05-25 | Ansys, Inc. | Solid phase extraction plate |
WO1999019067A1 (en) * | 1997-10-10 | 1999-04-22 | Biosepra, Inc. | Aligned multiwell multiplate stack and method for processing biological/chemical samples using the same |
US6159368A (en) * | 1998-10-29 | 2000-12-12 | The Perkin-Elmer Corporation | Multi-well microfiltration apparatus |
US20010001643A1 (en) * | 1998-12-08 | 2001-05-24 | Nigel Simpson | Modular solid phase extraction plate assembly |
-
2000
- 2000-08-25 DE DE10041825A patent/DE10041825A1/en not_active Ceased
- 2000-10-30 US US09/702,099 patent/US6830732B1/en not_active Expired - Lifetime
-
2001
- 2001-08-22 JP JP2002520949A patent/JP2004506918A/en active Pending
- 2001-08-22 DE DE50111329T patent/DE50111329D1/en not_active Expired - Lifetime
- 2001-08-22 DK DK01964906T patent/DK1313562T3/en active
- 2001-08-22 AU AU2001285706A patent/AU2001285706A1/en not_active Abandoned
- 2001-08-22 EP EP01964906A patent/EP1313562B1/en not_active Expired - Lifetime
- 2001-08-22 CN CNA018179266A patent/CN1471432A/en active Pending
- 2001-08-22 WO PCT/DE2001/003137 patent/WO2002016035A1/en active IP Right Grant
- 2001-08-22 ES ES01964906T patent/ES2275719T3/en not_active Expired - Lifetime
- 2001-08-22 AT AT01964906T patent/ATE343426T1/en active
Also Published As
Publication number | Publication date |
---|---|
DE50111329D1 (en) | 2006-12-07 |
ES2275719T3 (en) | 2007-06-16 |
CN1471432A (en) | 2004-01-28 |
ATE343426T1 (en) | 2006-11-15 |
DK1313562T3 (en) | 2007-02-26 |
EP1313562A1 (en) | 2003-05-28 |
AU2001285706A1 (en) | 2002-03-04 |
DE10041825A1 (en) | 2002-03-07 |
JP2004506918A (en) | 2004-03-04 |
US6830732B1 (en) | 2004-12-14 |
WO2002016035A1 (en) | 2002-02-28 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP1313562B1 (en) | Multiwell filtration plate and method for producing the same | |
DE102008042581B4 (en) | Microfluidic extraction and reaction device | |
EP1194240B1 (en) | Device for handling liquid samples, production method for said device and system for handling liquid samples | |
DE4143639C2 (en) | Process for the isolation and purification of nucleic acids | |
DE10117275B4 (en) | Device for archiving and analyzing materials | |
DE19823719B4 (en) | Method for concentrating substances | |
DE102010041579A1 (en) | Microfluidic unit with separation columns | |
DE19941905A1 (en) | Sample chamber for the liquid treatment of biological samples | |
EP2174715A1 (en) | Pipette tip with separating material | |
WO2006116964A2 (en) | Method for depositing samples in modules and an adapter | |
DE10209897A1 (en) | Micro Components Connection System | |
DE10213272A1 (en) | Device and method for coupling lines to fluidic microsystems | |
DE2257575B2 (en) | System for dead volume-free coupling for chromatography | |
WO2013072110A1 (en) | Microfluidic filter element for separating sample components from a biological sample fluid | |
DE10106199A1 (en) | Method for isolating nucleic acids from a nucleic acid-containing liquid sample | |
DE4014602C2 (en) | ||
EP1262759A1 (en) | Device for processing samples | |
DE19962577A1 (en) | Chromatography material and method using the same | |
DE112020004213T5 (en) | Controlled chemical synthesis using polymeric substrates and nanofluidic separation systems | |
EP2100134B1 (en) | Device for field flow fractionation | |
EP1547671B1 (en) | Ceramic membrane filter for filtering liquids | |
WO2001059424A1 (en) | Method and device fo collecting fractions after material separation | |
EP1622715A1 (en) | Component used in microprocess control | |
EP2739967A1 (en) | Laterally perfused chromatography element | |
DE212014000128U1 (en) | Device for separating components of a solution |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
17P | Request for examination filed |
Effective date: 20030313 |
|
AK | Designated contracting states |
Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
AX | Request for extension of the european patent |
Extension state: AL LT LV MK RO SI |
|
RAP1 | Party data changed (applicant data changed or rights of an application transferred) |
Owner name: INVITEK GESELLSCHAFT FUER BIOTECHNIK & BIODESIG Owner name: AHN BIOTECHNOLOGY GMBH |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: HILLEBRAND, TIMO Inventor name: BENDZKO, PETER Inventor name: HOFFMANN, HANS-JUERGEN |
|
17Q | First examination report despatched |
Effective date: 20030909 |
|
GRAP | Despatch of communication of intention to grant a patent |
Free format text: ORIGINAL CODE: EPIDOSNIGR1 |
|
GRAS | Grant fee paid |
Free format text: ORIGINAL CODE: EPIDOSNIGR3 |
|
GRAA | (expected) grant |
Free format text: ORIGINAL CODE: 0009210 |
|
AK | Designated contracting states |
Kind code of ref document: B1 Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: IE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20061025 |
|
REG | Reference to a national code |
Ref country code: GB Ref legal event code: FG4D Free format text: NOT ENGLISH |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: EP |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FG4D Free format text: LANGUAGE OF EP DOCUMENT: GERMAN |
|
REF | Corresponds to: |
Ref document number: 50111329 Country of ref document: DE Date of ref document: 20061207 Kind code of ref document: P |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: SE Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20070125 |
|
GBT | Gb: translation of ep patent filed (gb section 77(6)(a)/1977) |
Effective date: 20070110 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: T3 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: PT Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20070326 |
|
ET | Fr: translation filed | ||
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FG2A Ref document number: 2275719 Country of ref document: ES Kind code of ref document: T3 |
|
REG | Reference to a national code |
Ref country code: IE Ref legal event code: FD4D |
|
PLBE | No opposition filed within time limit |
Free format text: ORIGINAL CODE: 0009261 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: NO OPPOSITION FILED WITHIN TIME LIMIT |
|
26N | No opposition filed |
Effective date: 20070726 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: MC Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20070831 Ref country code: GR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20070126 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: CY Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20061025 Ref country code: LU Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20070822 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: TR Free format text: LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT Effective date: 20061025 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: ES Payment date: 20100830 Year of fee payment: 10 Ref country code: NL Payment date: 20100823 Year of fee payment: 10 Ref country code: CH Payment date: 20100825 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: FR Payment date: 20100901 Year of fee payment: 10 Ref country code: IT Payment date: 20100826 Year of fee payment: 10 Ref country code: FI Payment date: 20100820 Year of fee payment: 10 Ref country code: AT Payment date: 20100820 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: GB Payment date: 20100823 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DK Payment date: 20100825 Year of fee payment: 10 |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: BE Payment date: 20100823 Year of fee payment: 10 |
|
BERE | Be: lapsed |
Owner name: INVITEK G.- FUR BIOTECHNIK & BIODESIGN MBH. Effective date: 20110831 Owner name: AHN BIOTECHNOLOGY G.M.B.H. Effective date: 20110831 |
|
REG | Reference to a national code |
Ref country code: NL Ref legal event code: V1 Effective date: 20120301 |
|
REG | Reference to a national code |
Ref country code: CH Ref legal event code: PL |
|
GBPC | Gb: european patent ceased through non-payment of renewal fee |
Effective date: 20110822 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: LI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110831 Ref country code: CH Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110831 |
|
REG | Reference to a national code |
Ref country code: DK Ref legal event code: EBP |
|
REG | Reference to a national code |
Ref country code: FR Ref legal event code: ST Effective date: 20120430 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: FI Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110822 Ref country code: IT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110822 Ref country code: BE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110831 Ref country code: NL Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20120301 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DK Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110831 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: GB Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110822 Ref country code: FR Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110831 |
|
REG | Reference to a national code |
Ref country code: AT Ref legal event code: MM01 Ref document number: 343426 Country of ref document: AT Kind code of ref document: T Effective date: 20110822 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: AT Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110822 |
|
REG | Reference to a national code |
Ref country code: ES Ref legal event code: FD2A Effective date: 20130606 |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: ES Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20110823 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 50111329 Country of ref document: DE Representative=s name: 24IP LAW GROUP SONNENBERG FORTMANN, DE |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R081 Ref document number: 50111329 Country of ref document: DE Owner name: INVITEK MOLECULAR GMBH, DE Free format text: FORMER OWNERS: INVITEK GESELLSCHAFT FUER BIOTECHNIK & BIODESIGN MBH, 13125 BERLIN, DE; AHN BIOTECHNOLOGIE GMBH, 99734 NORDHAUSEN, DE Ref country code: DE Ref legal event code: R082 Ref document number: 50111329 Country of ref document: DE Representative=s name: 24IP LAW GROUP SONNENBERG FORTMANN, DE Ref country code: DE Ref legal event code: R081 Ref document number: 50111329 Country of ref document: DE Owner name: STRATEC BIOMEDICAL AG, DE Free format text: FORMER OWNERS: INVITEK GESELLSCHAFT FUER BIOTECHNIK & BIODESIGN MBH, 13125 BERLIN, DE; AHN BIOTECHNOLOGIE GMBH, 99734 NORDHAUSEN, DE Ref country code: DE Ref legal event code: R081 Ref document number: 50111329 Country of ref document: DE Owner name: AHN BIOTECHNOLOGIE GMBH, DE Free format text: FORMER OWNERS: INVITEK GESELLSCHAFT FUER BIOTECHNIK & BIODESIGN MBH, 13125 BERLIN, DE; AHN BIOTECHNOLOGIE GMBH, 99734 NORDHAUSEN, DE |
|
PGFP | Annual fee paid to national office [announced via postgrant information from national office to epo] |
Ref country code: DE Payment date: 20181022 Year of fee payment: 18 |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R082 Ref document number: 50111329 Country of ref document: DE Representative=s name: 24IP LAW GROUP SONNENBERG FORTMANN, DE Ref country code: DE Ref legal event code: R081 Ref document number: 50111329 Country of ref document: DE Owner name: AHN BIOTECHNOLOGIE GMBH, DE Free format text: FORMER OWNERS: AHN BIOTECHNOLOGIE GMBH, 99734 NORDHAUSEN, DE; STRATEC BIOMEDICAL AG, 75217 BIRKENFELD, DE Ref country code: DE Ref legal event code: R081 Ref document number: 50111329 Country of ref document: DE Owner name: INVITEK MOLECULAR GMBH, DE Free format text: FORMER OWNERS: AHN BIOTECHNOLOGIE GMBH, 99734 NORDHAUSEN, DE; STRATEC BIOMEDICAL AG, 75217 BIRKENFELD, DE |
|
REG | Reference to a national code |
Ref country code: DE Ref legal event code: R119 Ref document number: 50111329 Country of ref document: DE |
|
PG25 | Lapsed in a contracting state [announced via postgrant information from national office to epo] |
Ref country code: DE Free format text: LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES Effective date: 20200303 |