The invention is directed to a single-use mixer, homogenizer, extractor, fractionater, or slurry producer of substances.
In laboratory operation various devices are known for mixing, homogenizing, extracting, fractionating or slurrying substances mostly to be processed in small amounts, in particular infectious, malodorous, chemically aggressive, or to be kept sterile ones.
Such a device is known from EP-B1 1361917 in which the laboratory test device and the agitating element form a unit and allow that, during processing of the substance, said substance cannot exit and contaminate the environment. The known device allows therefore to process the substance in a closed container and thus by the hermetical seal to avoid any infection, uncontrolled splashing, or spilling due to an accidental tipping of the laboratory test device.
Based on this prior art the object of the present invention is to provide a single-use mixer, homogenizer, extractor, fractionater, or slurry producer in which a complete mixing and homogenization of substances and liquids that can be mixed is allowed, hermetically sealed while maintaining a certain grain size. Another object of the invention comprises that the insertion of liquids and the removal of the mixture or the homogenate can be performed after processing without opening the vessel.
This object is attained according to the invention by a single-use mixture, homogenizer, extractor, fractionater, or slurry producer according to the invention.
Advantageous embodiments of the device are described below.
By the design of the device according to the invention it is possible, after the insertion of the substance to be processed in the vessel, e.g., already on site where the substance is produced, to perform its processing entirely sealed and separated from the environment inside the device and subsequently to remove the product of the processing from the device without opening the device, i.e. without taking the lid off the laboratory test device. The device can be used for different tasks. Depending on the hole size and shape of the sieve serving as a cutter appropriately desired fractions can be achieved. The substance to be processed is separated from the environment during processing by a thin membrane and the membrane maintains this separation even when, after the removal of the substance, the removal tube of the pipette is pulled back out. Using an elastic compression element, the substance to be processed can be carefully pressed against the sieve and is successively guided through the bores in the sieve. Parts of the substance larger than the cross-section of the holes of the sieve are held back by the sieve so that below the sieve only the desired substance fractions to be processed can collect and be directly removed therefrom. The device is preferably made entirely from plastic and per se it can be disposed together with the still remaining, unnecessary or not useful substance portion. The rotary drive for the compression element or, in another embodiment of the invention, the vessel is not contaminated during processing of the substance and thus requires no cleaning.
The single-use mixer according to the invention can be directly filled in a slaughterhouse after tissue samples of animals have been taken from animals, for example and thus the tissue samples can be brought into the laboratory under sterile conditions. Necessary buffer solutions for further processing the tissue samples can subsequently be added in the laboratory through the lid plate and the membrane mounted thereto.
The single-use mixer also allows the content processed therein to be always hermetically sealed, leaving the fraction after fractioning in the mixer, allowing it to incubate (grow) and only later being removed for analysis. This also prevents that the tissue to be examined must be transferred from one vessel to another one between fractionating and the examination.
Using an illustrated exemplary embodiment the invention is explained in greater detail. Shown are:
In
In the center of the ring-shaped plate 15 with the holes 17, a cylinder 19 is arranged that protrudes upwardly, which is closed at the top with a hemi-spherical cap 21. The cap 21 may be embodied with a concave (
The plate 15, as shown in
A hollow-cylindrical casing section 39 is formed at the periphery of the lid plate 31, with a flange 41 protruding inwardly being arranged at its free edge. The diameter D1 of the flange 41, at its free, conically tapering edge, is smaller than the diameter D2 of the encircling brim 5 at the vessel 1. The distance of the free edge of the flange 41 from the bottom 35 of the lid plate 31 is approximately equivalent to the height h of the axial extension of the brim 5 at its root.
At the bottom 35 of the lid plate 31, additional elastic elements 43 are arranged, protruding away from the lid plate 31, which essentially extend beyond the casing section 39. The elastic elements 43 may also comprise striped flaps or helically extending rods. The function of the elastic elements 43 are explained in the following using
The opening 7 of the vessel 1 is closed by the lid plate 31 of the compression element 29. When the compression element 29 is placed onto the opening 7 of the vessel 1, the flange 41 glides beyond the brim 5. The edges of the flange 41 engage below the brim 5 and hold the compression element 29 connected to the vessel 1 in a sealing manner. The elastic elements 43 protrude into the interior of the vessel and press the materials to be processed, inserted into the vessel 1 prior to the placement of the compression element 29, to the surface of the sieve 13 past the cylinder 19 into the circular space between the casing of the cylinder 19 and the casing 11 of the vessel.
The black surfaces 47 in
In the following the operation of the device is explained in greater detail.
The operator fills the substances 45 to be processed into the vessel 1 through the opening 7. Substances 45 to be processed may be infectious, malodorous human or animal tissue. However, it may also comprise other solid matter, which for example has to be dissolved in smaller fractions or intensely mixed with other liquids, which are also added into the vessel 1.
After the insertion of the substance or substances 45 has been filled into the vessel 1, the compression element 29 is pushed onto the opening 7 and the flange 41 snaps below the brim 5. When the compression element 29 is placed on top the content is pressed by the elastic elements 43 via the cap 21 of the cylinder 19 into the circular space and contacts the surface of the sieve 13. In the second exemplary embodiment the content is pressed against the sieve 13 by the friction plate 57. Now the entire device is placed upon a suitable drive 51, which may be embodied cup-shaped and can snap to the cams 9. Either the lid plate 31 is held manually and the drive 51 is engaged, or from the top a holding element (not shown) is lowered to the lid plate 31 in order to hold it. Now, by the drive 51, the vessel 1 is rotated and the substance 47 is pressed by the fixed elastic elements 43 through the holes 17 into the collection chamber 27 or the vessel 1 is rotated and the compression element 29 is held. Therefore, only such fractions of the substance can enter the collection chamber that are either smaller than the diameter of the holes 17 or such that have been separated from the larger fractions by the sharp edges of the holes 17 or by the friction teeth 59. Now, when the small fractions 49 together with the usually added liquids enter the collection chamber 27, said chamber is successively filled and the mixture rises upwards in the cylinder 19 due to the pressure of the elastic elements 49 on the substances 45 located inside the vessel 1. Depending on the embodiment of the slots 37 in the cap 21 some of the fractions 49 or at least the liquid can exit again and is pressed through the sieve 13 for a second time. Chords and other unfragmented parts remain in the upper part of the vessel. Therefore in the lower part, the collection chamber 27, there are only the expected processed products. They may now be removed from the vessel via a pipette 53 without opening it. The tip 55 of the pipette 53 is first deployed through slots 37 into the lid plate 19 and then through the slots 23 into the cap 21 of the cylinder 19 to the collection chamber 27. Now the removal of the processed substances can occur without opening the vessel 1. The remaining unnecessary parts are disposed together with the device. Thus, they never again enter the environment after they have once been inserted into the vessel 1.
Number | Date | Country | Kind |
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92/05 | Jan 2005 | CH | national |
1782/05 | Nov 2005 | CH | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/CH2005/000685 | 11/18/2005 | WO | 00 | 4/24/2007 |
Publishing Document | Publishing Date | Country | Kind |
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WO2006/076820 | 7/27/2006 | WO | A |
Number | Name | Date | Kind |
---|---|---|---|
533141 | Prest | Jan 1895 | A |
605922 | Schule | Jun 1898 | A |
1444346 | Kohr | Feb 1923 | A |
1732618 | Royle | Oct 1929 | A |
1821344 | Kautzman et al. | Sep 1931 | A |
2285721 | Karp | Jun 1942 | A |
3349966 | Schwartzman | Oct 1967 | A |
3581790 | Conte | Jun 1971 | A |
3587982 | Campbell | Jun 1971 | A |
3941317 | Kanor | Mar 1976 | A |
4028190 | McAleer et al. | Jun 1977 | A |
4072275 | Bartels et al. | Feb 1978 | A |
4121775 | Roseberg et al. | Oct 1978 | A |
4212430 | Dale et al. | Jul 1980 | A |
4307846 | Spelsberg | Dec 1981 | A |
4366930 | Trombetti, Jr. | Jan 1983 | A |
4374574 | David | Feb 1983 | A |
4505433 | Selenke | Mar 1985 | A |
4514091 | Kaspar et al. | Apr 1985 | A |
4569612 | Schwartzman et al. | Feb 1986 | A |
4715545 | Hanifl et al. | Dec 1987 | A |
4787562 | Templeton | Nov 1988 | A |
4946286 | Purkapile | Aug 1990 | A |
5067666 | Sussman | Nov 1991 | A |
5261613 | Mullarky | Nov 1993 | A |
5533683 | Fay et al. | Jul 1996 | A |
5580007 | Caviezel et al. | Dec 1996 | A |
5829696 | DeStefano et al. | Nov 1998 | A |
5899624 | Thompson | May 1999 | A |
6405951 | Wu | Jun 2002 | B1 |
6509187 | Brem | Jan 2003 | B2 |
6622949 | Baswick et al. | Sep 2003 | B1 |
7165734 | Bucher | Jan 2007 | B2 |
7225920 | Hoeffkes et al. | Jun 2007 | B2 |
7490976 | Bucher | Feb 2009 | B2 |
7520458 | Schulz | Apr 2009 | B2 |
7699252 | Wu | Apr 2010 | B2 |
7927006 | Bucher | Apr 2011 | B2 |
8092076 | Bucher | Jan 2012 | B2 |
8114360 | Bucher | Feb 2012 | B2 |
8162247 | Faulker | Apr 2012 | B2 |
8597596 | Daf | Dec 2013 | B2 |
20020118596 | Mizutani et al. | Aug 2002 | A1 |
20040000605 | McPherson et al. | Jan 2004 | A1 |
20040035964 | Roggero | Feb 2004 | A1 |
20040196735 | Barker et al. | Oct 2004 | A1 |
20040252582 | Bucher | Dec 2004 | A1 |
20060013064 | Bucher | Jan 2006 | A1 |
20060060686 | Cheng | Mar 2006 | A1 |
20060076442 | Fouse | Apr 2006 | A1 |
20070248499 | Bucher | Oct 2007 | A1 |
20080253223 | Bucher | Oct 2008 | A1 |
20090136384 | Bucher | May 2009 | A1 |
20110171085 | Bucher | Jul 2011 | A1 |
Number | Date | Country |
---|---|---|
0590219 | Oct 1992 | EP |
1361917 | Oct 2001 | EP |
2004035191 | Apr 2004 | WO |
Entry |
---|
English translation of WO 2004/035191 by Bucher (PCT/CH2003/000675), submitted to PTO Mar. 3, 2005 with U.S. Appl. No. 10/526,647. |
Number | Date | Country | |
---|---|---|---|
20080253223 A1 | Oct 2008 | US |