Laboratory sample distribution system and laboratory automation system

Information

  • Patent Grant
  • 10996233
  • Patent Number
    10,996,233
  • Date Filed
    Monday, November 19, 2018
    5 years ago
  • Date Issued
    Tuesday, May 4, 2021
    3 years ago
  • Inventors
    • Hermann; Pius
    • Baer; Jonathan
  • Original Assignees
  • Examiners
    • Wright; Kathryn
    Agents
    • Roche Diagnostics Operations, Inc.
Abstract
A laboratory sample distribution system comprising a transport plane in which the transport plane is covered by an electrically conductive material is presented. A laboratory automation system comprising such a laboratory sample distribution system is also presented.
Description
BACKGROUND

The present disclosure generally relates to a laboratory sample distribution system comprising a transport plane, a number of sample container carriers, a driver configured to move the sample container carriers on the transport plane, and a control device configured to control the movement of the sample container carriers on top of the transport plane by driving the driver such that the sample container carriers move along corresponding transport paths. The present disclosure also relates to a laboratory automation system comprising a number of laboratory stations and a laboratory sample distribution system.


Known laboratory sample distribution systems are typically used in laboratory automation systems in order to transport samples contained in sample containers between different laboratory stations.


However, there is a need for to optimize a laboratory sample distribution system and a laboratory automation system comprising a laboratory sample distribution system.


SUMMARY

According to the present disclosure, a laboratory sample distribution system is presented. The laboratory sample distribution system can comprise a transport plane. The transport plane can be covered by a first electrically conductive material. The laboratory sample distribution system can also comprise a number of sample container carriers, a driver configured to move the sample container carriers on the transport plane, and a control device configured to control the movement of the sample container carriers on top of the transport plane by driving the driver such that the sample container carriers move along corresponding transport paths.


Accordingly, it is a feature of the embodiments of the present disclosure to to further optimize a laboratory sample distribution system and a laboratory automation system comprising a laboratory sample distribution system. Other features of the embodiments of the present disclosure will be apparent in light of the description of the disclosure embodied herein.





BRIEF DESCRIPTION OF THE SEVERAL VIEWS OF THE DRAWINGS

The following detailed description of specific embodiments of the present disclosure can be best understood when read in conjunction with the following drawings, where like structure is indicated with like reference numerals and in which:



FIG. 1 illustrates a laboratory automation system comprising a laboratory sample distribution system according to an embodiment of the present disclosure.



FIG. 2 illustrates a sample container carrier in a perspective bottom side view according to an embodiment of the present disclosure.





DETAILED DESCRIPTION

In the following detailed description of the embodiments, reference is made to the accompanying drawings that form a part hereof, and in which are shown by way of illustration, and not by way of limitation, specific embodiments in which the disclosure may be practiced. It is to be understood that other embodiments may be utilized and that logical, mechanical and electrical changes may be made without departing from the spirit and scope of the present disclosure.


The laboratory sample distribution system can comprise a transport plane. The laboratory sample distribution system can further comprise a number of sample container carriers and a driver configured to move the sample container carriers on (over) the transport plane. The laboratory sample distribution system can further comprise a control device, e.g., in the form of a microprocessor or a personal computer, configured to control the movement of the sample container carriers on top of the transport plane by driving the driver such that the sample container carriers move along corresponding transport paths. The transport plane can be covered by (coated with) or can be made of a (first) electrically conductive material.


By use of the electrically conductive material covering the transport plane, electric charges arising during movement of the sample container carriers can be distributed over the transport plane and can, if appropriate grounding is present, be conducted to ground in order to eliminate the electric charges from the transport plane. This can reduce electric charges on the transport plane that can disturb operation of the laboratory sample distribution system.


According to an embodiment, the first electrically conductive material can be or can comprise a copolyester material.


According to an embodiment, the first electrically conductive material can be or can comprise a polyethylene terephthalate material.


According to an embodiment, the first electrically conductive material can be an optically bright material. This has been proven suitable for optically surveilling operation of the laboratory sample distribution system.


According to an embodiment, the first electrically conductive material can lack a carbon-based electrically conducting additive. In other words, the first electrically conductive material can be free of a carbon-based electrically conducting additive. This has been proven suitable in order to get an optically bright material being electrically conducting.


According to an embodiment, the transport plane can have a grained surface. This can further reduce friction between the transport plane and the sample container carriers.


According to an embodiment, each sample container carrier can comprise a flat bottom surface for moving on the transport plane. The bottom surface can be covered by or can be made of a (second) electrically conductive material. This can allow for an easy transport of electric charges present on the bottom surface of the transport plane, where the electric charges can be distributed or discharged.


According to an embodiment, the second electrically conductive material can be or can comprise an ultra-high molecular polyethylene.


According to an embodiment, the first electrically conductive material and/or the second electrically conductive material can be or can comprise an electrically conductive polymer.


According to an embodiment, the first electrically conductive material and/or the second electrically conductive material can comprise an electrically conducting additive. The electrically conducting additive can be used to achieve an electrically conductive material without using dark carbon-based materials.


According to an embodiment, the electrically conducting additive can be a polyaniline material or another electrically conductive polymer.


According to an embodiment, the first electrically conductive material and/or the second electrically conductive material can be low friction and/or low wear materials. This can further reduce friction or wear between the transport plane and the sample container carriers when the sample container carriers move on the transport plane.


According to an embodiment, the first electrically conductive material and/or the second electrically conductive material can be configured to at least approximately equate gliding friction and static friction. This has been proven suitable for longtime reliable operation. Especially, spilling can be prevented by this measure. The first electrically conductive material and/or the second electrically conductive material can be configured to exactly equate gliding friction and static friction.


According to an embodiment, the driver can be formed as electromagnetic actuators located as a grid having rows and columns below the transport plane and controllable by the control device. The sample container carriers can each comprise a magnetically active device, e.g., in the form of a permanent magnet, for interaction with a magnetic field generated by the electromagnetic actuators such that a magnetic drive force can be applied to the sample container carriers. Such an embodiment can allow for reliable operation using magnetic drive forces in order to drive the sample container carriers on the transport plane.


A laboratory automation system comprising a number of laboratory stations such as, for example, pre-analytical, analytical and/or post-analytical stations, and an above laboratory sample distribution system is also presented. With regard to the laboratory sample distribution system, all embodiments and variations discussed herein can be applied.


The stations may be arranged adjacent to the laboratory sample distribution system.


Pre-analytical stations may be configured to perform any kind of pre-processing of samples, sample containers and/or sample container carriers.


Analytical stations may be configured to use a sample, or part of the sample, and a reagent to generate a measuring signal. The measuring signal can indicate if and in what concentration, if any, an analyte exists.


Post-analytical stations may be configured to perform any kind of post-processing of samples, sample containers and/or sample container carriers.


The pre-analytical, analytical and/or post-analytical stations may comprise at least one of a decapping station, a recapping station, an aliquot station, a centrifugation station, an archiving station, a pipetting station, a sorting station, a tube type identification station, a sample quality determining station, an add-on buffer station, a liquid level detection station, and a sealing/desealing station.


It can be noted that for the first electrically conductive material, a material called PET Eastar 6763 (including 12 percent by weight PETG Funaden perm AS (14-05189))/Funaden el. Cond. (eroding structure K29 VDI 3400), Ra 2.8, has been proven as a suitable material. For the second electrically conductive material, the material PE-UHMW-S-Bright-ESD of Murtfeldt, Ra 3.2, has been proven suitable. The Ra-terms determine the roughness of the respective material.


Referring initially to FIG. 1, FIG. 1 shows a laboratory automation system 10 comprising a laboratory sample distribution system 100 and a number of pre-analytical, analytical and/or post-analytical stations 20 arranged adjacent to the laboratory sample distribution system 100. Self-evidently, more than the two stations 20 depicted in FIG. 1 may be comprised in the laboratory automation system 10.


The laboratory sample distribution system 100 can comprise a transport plane 110 below which a plurality of electromagnetic actuators in the form of electromagnets 120 can be positioned in rows and columns. The electromagnets 120 can be implemented as solenoids having solid ferromagnetic cores 125.


Sample container carriers 140 can be positioned on the transport plane 110 and can be moved by the electromagnets 120, because each sample container carrier 140 can comprise a magnetically active device 141 in the form of a permanent magnet.


While it can be understood that a plurality of sample container carriers 140 can be positioned on the transport plane 110, due to simplicity only a single sample container carrier 140 is depicted in FIG. 1. The sample container carrier 140 can hold and carry a sample container 145, in which a sample to be analyzed can be contained.


The laboratory sample distribution system 100 can be configured to transport the sample container carriers 140 and/or the sample containers 145 between the laboratory stations 20. The laboratory stations 20 can be positioned adjacent to the transport plane 110 such that a sample container carrier 140 can be used to transport a sample contained in the sample container 145 to a respective laboratory station 20.


A plurality of Hall-sensors 130 can be arranged such that positions of respective sample container carriers 140 on the transport plane 110 can be detected.


The laboratory sample distribution system 100 can further comprise a control device 150. The control device 150 can be configured to control movement of the sample container carriers 140 on the transport plane by driving the electromagnets 120 such that the sample container carriers 140 independently and simultaneously move along corresponding transport paths.


The transport plane 110 can be covered or coated with a first electrically conductive material 111.


In the present case, the first electrically conductive material 111 can comprise a copolyester material and a polyethylene terephthalate material. The first electrically conductive material 111 can be optically bright and can comprise an electrically conductive additive being a polymer such that no carbon-based electrically conductive additives have to be used. Furthermore, the first electrically conductive material 111 can be connected to a grounding 112 such that electric charges can be discharged to ground.



FIG. 2 shows the sample container carrier 140 with its sample container 145 in a perspective view, such that a bottom surface 142 of the sample container carrier 140 is visible.


The bottom surface 142 can be covered or coated by a second electrically conductive material 143, which can be comprised of an ultra-high molecular polyethylene comprising an electrically conductive polymer.


The sample container carriers 140 can each comprise a magnetically active device 141 in the form of a permanent magnet for interaction with a magnetic field generated by the electromagnetic actuators 120 such that a magnetic drive force can be applied to the sample container carriers 140.


The electric charges, generated when operating the sample distribution system 100 by moving the sample container carriers 140 over the transport plane 110, can be safely discharged, thus avoiding malfunctions.


It is noted that terms like “preferably,” “commonly,” and “typically” are not utilized herein to limit the scope of the claimed embodiments or to imply that certain features are critical, essential, or even important to the structure or function of the claimed embodiments. Rather, these terms are merely intended to highlight alternative or additional features that may or may not be utilized in a particular embodiment of the present disclosure.


Having described the present disclosure in detail and by reference to specific embodiments thereof, it will be apparent that modifications and variations are possible without departing from the scope of the disclosure defined in the appended claims. More specifically, although some aspects of the present disclosure are identified herein as preferred or particularly advantageous, it is contemplated that the present disclosure is not necessarily limited to these preferred aspects of the disclosure.

Claims
  • 1. A laboratory sample distribution system, the laboratory sample distribution system comprising: a transport plane, wherein the transport plane is covered by a first electrically conductive material, the first electrically conductive material includes a copolyester material or polyethylene terephthalate material;a number of sample container carriers, and each of the number of sample container carrier comprises a flat bottom surface for moving on the transport plane, the bottom surface being covered with a second electrically conductive material;a driver configured to move the sample container carriers on the transport plane, wherein the driver; anda control device configured to control the movement of the sample container carriers on top of the transport plane by driving the driver such that the sample container carriers move along corresponding transport paths,wherein the driver is configured as electromagnetic actuators located below the transport plane and is controllable by the control device; andwherein each of the number of the sample container carriers each further comprise a magnetically active device for interaction with a magnetic field generated by the electromagnetic actuators such that a magnetic drive force is applied to each of the number of the sample container carriers.
  • 2. The laboratory sample distribution system according to claim 1, wherein the first electrically conductive material is an optically bright material.
  • 3. The laboratory sample distribution system according to claim 1, wherein the first electrically conductive material lacks a carbon-based electrically conducting additive.
  • 4. The laboratory sample distribution system according to claim 1, wherein the transport plane has a grained surface.
  • 5. The laboratory sample distribution system according to claim 1, wherein the second electrically conductive material comprises an ultrahigh molecular polyethylene.
  • 6. The laboratory sample distribution system according to claim 1, wherein the first electrically conductive material and/or the second electrically conductive material is an electrically conductive polymer.
  • 7. The laboratory sample distribution system according to claim 1, wherein the first electrically conductive material and/or the second electrically conductive material comprises an electrically conducting additive.
  • 8. The laboratory sample distribution system according to claim 7, wherein the electrically conducting additive is an electrically conducting polymer.
  • 9. The laboratory sample distribution system according to claim 1, wherein the first electrically conductive material and/or the second electrically conductive material is a low friction and/or low wear material.
  • 10. The laboratory sample distribution system according to claim 1, wherein the first electrically conductive material and/or the second electrically conductive material is configured to at least approximately equate gliding friction and static friction.
  • 11. A laboratory automation system, the laboratory automation system comprising: a number of laboratory stations; and a laboratory sample distribution system according to claim 1.
Priority Claims (1)
Number Date Country Kind
16172825 Jun 2016 EP regional
CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of PCT/EP2017/063201, filed May 31, 2017, which is based on and claims priority to EP 16172825.8, filed Jun. 3, 2016, which is hereby incorporated by reference.

US Referenced Citations (189)
Number Name Date Kind
3273727 Rogers et al. Sep 1966 A
3653485 Donlon Apr 1972 A
3901656 Durkos et al. Aug 1975 A
4150666 Brush Apr 1979 A
4395164 Beltrop et al. Jul 1983 A
4544068 Cohen Oct 1985 A
4771237 Daley Sep 1988 A
5120506 Saito et al. Jun 1992 A
5295570 Grecksch et al. Mar 1994 A
5309049 Kawada et al. May 1994 A
5457368 Jacobsen et al. Oct 1995 A
5523131 Isaacs et al. Jun 1996 A
5530345 Murari et al. Jun 1996 A
5636548 Dunn et al. Jun 1997 A
5641054 Mod et al. Jun 1997 A
5651941 Stark et al. Jul 1997 A
5720377 Lapeus et al. Feb 1998 A
5735387 Polaniec et al. Apr 1998 A
5788929 Nesti Aug 1998 A
6045319 Uchida et al. Apr 2000 A
6062398 Thalmayr May 2000 A
6141602 Igarashi et al. Oct 2000 A
6151535 Ehlers Nov 2000 A
6184596 Ohzeki Feb 2001 B1
6191507 Peltier et al. Feb 2001 B1
6206176 Blonigan et al. Mar 2001 B1
6255614 Yamakawa et al. Jul 2001 B1
6260360 Wheeler Jul 2001 B1
6279728 Jung et al. Aug 2001 B1
6293750 Cohen et al. Sep 2001 B1
6429016 McNeil Aug 2002 B1
6444171 Sakazume et al. Sep 2002 B1
6571934 Thompson et al. Jun 2003 B1
7028831 Veiner Apr 2006 B2
7078082 Adams Jul 2006 B2
7122158 Itoh Oct 2006 B2
7278532 Martin Oct 2007 B2
7326565 Yokoi et al. Feb 2008 B2
7425305 Itoh Sep 2008 B2
7428957 Schaefer Sep 2008 B2
7578383 Itoh Aug 2009 B2
7597187 Bausenwein et al. Oct 2009 B2
7850914 Veiner et al. Dec 2010 B2
7858033 Itoh Dec 2010 B2
7875254 Garton et al. Jan 2011 B2
7939484 Loeffler et al. May 2011 B1
8240460 Bleau et al. Aug 2012 B1
8281888 Bergmann Oct 2012 B2
8502422 Lykkegaard Aug 2013 B2
8796186 Shirazi Aug 2014 B2
8833544 Stoeckle et al. Sep 2014 B2
8973736 Johns et al. Mar 2015 B2
9056720 Van De Loecht et al. Jun 2015 B2
9097691 Onizawa et al. Aug 2015 B2
9187268 Denninger et al. Nov 2015 B2
9211543 Ohga et al. Dec 2015 B2
9239335 Heise et al. Jan 2016 B2
9423410 Buehr Aug 2016 B2
9423411 Riether Aug 2016 B2
9567167 Sinz Feb 2017 B2
9575086 Heise et al. Feb 2017 B2
9593970 Sinz Mar 2017 B2
9598243 Denninger et al. Mar 2017 B2
9618525 Malinowski et al. Apr 2017 B2
9658241 Riether et al. May 2017 B2
9664703 Heise et al. May 2017 B2
9772342 Riether Sep 2017 B2
9791468 Riether et al. Oct 2017 B2
9810706 Riether et al. Nov 2017 B2
9902572 Mahmudimanesh et al. Feb 2018 B2
9939455 Schneider et al. Apr 2018 B2
9952242 Riether Apr 2018 B2
9969570 Heise et al. May 2018 B2
9989547 Pedain Jun 2018 B2
10094843 Malinowski et al. Oct 2018 B2
10119982 Baer Nov 2018 B2
10288634 Kaeppeli May 2019 B2
20020009391 Marquiss et al. Jan 2002 A1
20030092185 Qureshi et al. May 2003 A1
20040050836 Nesbitt et al. Mar 2004 A1
20040084531 Itoh May 2004 A1
20050061622 Martin Mar 2005 A1
20050109580 Thompson May 2005 A1
20050194333 Veiner et al. Sep 2005 A1
20050196320 Veiner et al. Sep 2005 A1
20050226770 Allen et al. Oct 2005 A1
20050242963 Oldham et al. Nov 2005 A1
20050247790 Itoh Nov 2005 A1
20050260101 Nauck et al. Nov 2005 A1
20050271555 Itoh Dec 2005 A1
20060000296 Salter Jan 2006 A1
20060047303 Ortiz et al. Mar 2006 A1
20060219524 Kelly et al. Oct 2006 A1
20070116611 DeMarco May 2007 A1
20070210090 Sixt et al. Sep 2007 A1
20070248496 Bondioli et al. Oct 2007 A1
20070276558 Kim Nov 2007 A1
20080012511 Ono Jan 2008 A1
20080029368 Komori Feb 2008 A1
20080056328 Rund et al. Mar 2008 A1
20080131961 Crees et al. Jun 2008 A1
20090004732 LaBarre et al. Jan 2009 A1
20090022625 Lee et al. Jan 2009 A1
20090081771 Breidford et al. Mar 2009 A1
20090128139 Drenth et al. May 2009 A1
20090142844 Le Comte Jun 2009 A1
20090180931 Silbert et al. Jul 2009 A1
20090322486 Gerstel Dec 2009 A1
20100000250 Sixt Jan 2010 A1
20100152895 Dai Jun 2010 A1
20100175943 Bergmann Jul 2010 A1
20100186618 King Jul 2010 A1
20100255529 Cocola et al. Oct 2010 A1
20100300831 Pedrazzini Dec 2010 A1
20100312379 Pedrazzini Dec 2010 A1
20110050213 Furukawa Mar 2011 A1
20110124038 Bishop et al. May 2011 A1
20110172128 Davies et al. Jul 2011 A1
20110186406 Kraus et al. Aug 2011 A1
20110287447 Norderhaug et al. Nov 2011 A1
20120037696 Lavi Feb 2012 A1
20120129673 Fukugaki et al. May 2012 A1
20120178170 Van Praet Jul 2012 A1
20120211645 Tullo et al. Aug 2012 A1
20120275885 Furrer et al. Nov 2012 A1
20120282683 Mototsu Nov 2012 A1
20120295358 Ariff et al. Nov 2012 A1
20120310401 Shah Dec 2012 A1
20130034410 Heise Feb 2013 A1
20130153677 Leen et al. Jun 2013 A1
20130180824 Kleinikkink et al. Jul 2013 A1
20130263622 Mullen et al. Oct 2013 A1
20130322992 Pedrazzini Dec 2013 A1
20140170023 Saito et al. Jun 2014 A1
20140202829 Eberhardt et al. Jul 2014 A1
20140234949 Wasson et al. Aug 2014 A1
20150014125 Hecht Jan 2015 A1
20150101911 Friedman Apr 2015 A1
20150140668 Mellars et al. May 2015 A1
20150166265 Pollack et al. Jun 2015 A1
20150241457 Miller Aug 2015 A1
20150273468 Croquette et al. Oct 2015 A1
20150273691 Pollack Oct 2015 A1
20150276775 Mellars et al. Oct 2015 A1
20150276782 Riether Oct 2015 A1
20150337400 Wilson et al. Nov 2015 A1
20160003859 Wenczel et al. Jan 2016 A1
20160025756 Pollack et al. Jan 2016 A1
20160054341 Edelmann Feb 2016 A1
20160229565 Margner Aug 2016 A1
20160297626 Jochim Oct 2016 A1
20160341750 Sinz et al. Nov 2016 A1
20160341751 Huber et al. Nov 2016 A1
20170059599 Riether Mar 2017 A1
20170097372 Heise et al. Apr 2017 A1
20170101277 Malinowski Apr 2017 A1
20170108522 Baer Apr 2017 A1
20170131307 Pedain May 2017 A1
20170131310 Volz et al. May 2017 A1
20170138971 Heise et al. May 2017 A1
20170168079 Sinz Jun 2017 A1
20170174448 Sinz Jun 2017 A1
20170184622 Sinz et al. Jun 2017 A1
20170248623 Kaeppeli et al. Aug 2017 A1
20170248624 Kaeppeli et al. Aug 2017 A1
20170363608 Sinz Dec 2017 A1
20180067141 Mahmudimanesh et al. Mar 2018 A1
20180074087 Heise et al. Mar 2018 A1
20180106821 Vollenweider et al. Apr 2018 A1
20180128848 Schneider et al. May 2018 A1
20180156835 Hassan Jun 2018 A1
20180188280 Malinowski Jul 2018 A1
20180210000 van Mierlo Jul 2018 A1
20180210001 Reza Jul 2018 A1
20180217174 Malinowski Aug 2018 A1
20180217176 Sinz et al. Aug 2018 A1
20180224476 Birrer et al. Aug 2018 A1
20180340951 Kaeppell Nov 2018 A1
20180340952 Kaeppeli et al. Nov 2018 A1
20180348244 Ren Dec 2018 A1
20180348245 Schneider et al. Dec 2018 A1
20190018027 Hoehnel Jan 2019 A1
20190076845 Huber et al. Mar 2019 A1
20190076846 Durco et al. Mar 2019 A1
20190094251 Malinowski Mar 2019 A1
20190094252 Waser et al. Mar 2019 A1
20190101468 Haldar Apr 2019 A1
20190285660 Kopp et al. Sep 2019 A1
20200200783 Durco Jun 2020 A1
Foreign Referenced Citations (97)
Number Date Country
201045617 Apr 2008 CN
102109530 Jun 2011 CN
3909786 Sep 1990 DE
102012000665 Aug 2012 DE
102011090044 Jul 2013 DE
0601213 Oct 1992 EP
0775650 May 1997 EP
0916406 May 1997 EP
1122194 Aug 2001 EP
1524525 Apr 2005 EP
2119643 Nov 2009 EP
2148117 Jan 2010 EP
2327646 Jun 2011 EP
2447701 May 2012 EP
2500871 Sep 2012 EP
2502675 Feb 2014 EP
2887071 Jun 2015 EP
3073270 Sep 2016 EP
3121603 Jan 2017 EP
2165515 Apr 1986 GB
S56-147209 Nov 1981 JP
60-223481 Nov 1985 JP
61-081323 Apr 1986 JP
S61-069604 Apr 1986 JP
S61-094925 May 1986 JP
S61-174031 Aug 1986 JP
S61-217434 Sep 1986 JP
S62-100161 May 1987 JP
S63-31918 Feb 1988 JP
S63-48169 Feb 1988 JP
S63-82433 May 1988 JP
S63-113853 May 1988 JP
S63-290101 Nov 1988 JP
S64-023907 Jan 1989 JP
1148966 Jun 1989 JP
H01-266860 Oct 1989 JP
H02-87903 Mar 1990 JP
H02-175802 Jul 1990 JP
03-112393 May 1991 JP
03-192013 Aug 1991 JP
H03-38704 Aug 1991 JP
H04-127063 Apr 1992 JP
H05-69350 Mar 1993 JP
H05-142232 Jun 1993 JP
H05-180847 Jul 1993 JP
06-26808 Feb 1994 JP
H06-148198 May 1994 JP
06-156730 Jun 1994 JP
06-211306 Aug 1994 JP
07-228345 Aug 1995 JP
07-236838 Sep 1995 JP
H07-301637 Nov 1995 JP
H09-17848 Jan 1997 JP
H11-083865 Mar 1999 JP
H11-264828 Sep 1999 JP
H11-304812 Nov 1999 JP
H11-326336 Nov 1999 JP
2000-105243 Apr 2000 JP
2000-105246 Apr 2000 JP
2001-124786 May 2001 JP
2001-240245 Sep 2001 JP
2005-001055 Jan 2005 JP
2005-249740 Sep 2005 JP
2006-106008 Apr 2006 JP
2006-221024 Aug 2006 JP
2007-309675 Nov 2007 JP
2007-314262 Dec 2007 JP
2007-322289 Dec 2007 JP
2009-036643 Feb 2009 JP
2009-062188 Mar 2009 JP
2009-145188 Jul 2009 JP
2009-300402 Dec 2009 JP
2010-243310 Oct 2010 JP
2010-271204 Dec 2010 JP
2011-121688 Jun 2011 JP
2013-172009 Feb 2013 JP
2013-190400 Sep 2013 JP
685591 Sep 1979 SU
1996036437 Nov 1996 WO
2003042048 May 2003 WO
2007024540 Mar 2007 WO
2008133708 Nov 2008 WO
2009002358 Dec 2008 WO
2010042722 Apr 2010 WO
2012170636 Jul 2010 WO
2010087303 Aug 2010 WO
2010129715 Nov 2010 WO
2012158520 Nov 2012 WO
2012158541 Nov 2012 WO
2013064656 May 2013 WO
2013152089 Oct 2013 WO
2013169778 Nov 2013 WO
2013177087 Nov 2013 WO
2013177163 Nov 2013 WO
2014059134 Apr 2014 WO
2014071214 May 2014 WO
2015104263 Jul 2015 WO
Non-Patent Literature Citations (1)
Entry
International Search Report dated Sep. 4, 2017, in Application No. PCT/EP2017/063201, 4 pages.
Related Publications (1)
Number Date Country
20190086433 A1 Mar 2019 US
Continuations (1)
Number Date Country
Parent PCT/EP2017/063201 May 2017 US
Child 16195216 US