This application relates to a lighting fixture having the ability to sterilize pathogens such as bacteria, fungi, and viruses.
Lighting fixtures are common in commercial buildings and homes. For example, fluorescent bulb fixtures have been used in commercial buildings and homes for years. Over the last decade or so, Light Emitting Diode (LED) based lighting fixtures have been developed which generally have the same size, shape, and mounting hardware as do traditional fluorescent bulb fixtures (typically 2×2 feet or 2×4 feet). This allows older fluorescent bulb fixtures to be easily replaced by LED based fixtures, which is beneficial because LED fixtures are more energy efficient, more reliable, and easier to maintain when compared with fluorescent fixtures. Another benefit of LED fixtures is that they can provide radiation suitable to provide disinfection as well as providing visual white light. For example, U.S. Patent Application Publication 2018/0147417 discloses a LED chip useable in a lighting fixture. The LED chip includes a first LED that emits light at 405 nm in the near ultraviolet (UV) range. (The wavelength of light in the visible spectrum ranges from 380 nm at the UV end of the spectrum to 740 nm at the infrared (IR) end of the spectrum). The LED chip also includes a second LED that emits at 450 nm in the blue range of visible light. The LEDs in the chip are coated by a phosphor material, and for the most part the 405 nm radiation passes through the phosphor without absorption. The 450 nm radiation by contrast interacts with the phosphor where it is converted to higher wavelengths, which results in a broader white light emission spectrum. In sum, the LED chip produces an overall spectrum with a peak at 405 nm, as well as a broader-wavelength white spectrum. The inclusion of a significant amount of 405 nm light in the overall spectrum is beneficial, because radiation at that wavelength is known to disrupt certain microbial biological processes. For example, the '417 Publication explains that 405 nm radiation causes reactive oxygen species generation in cells, which in turn prevent cell metabolism and effectively suppresses bacterial growth. 405 nm radiation has also been reported as providing disinfection against fungi. See R. M. Tomb et al., “New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination,” Food & Environmental Virology, Vol. 9(2), pp. 159-67 (2017).
While LED fixture having disinfection properties such as those just described are beneficial, the inventor sees room for improvement. For one, other wavelengths—such as 470 nm—have also been shown to have antibacterial as well as antifungal properties. See, e.g., A. J. DeLucca et al., “Blue Light (470 nm) Effectively Inhibits Bacterial and Fungal Growth,” Letters in Applied Biology, Vol 55, pp. 460-66 (2012). But wavelengths such as 405 nm and 470 nm may not be effective against viruses. The article by R. M. Tomb, cited above, investigates the use of 405 nm radiation to inactivate viruses, and while promising results were shown, it appears that much higher doses of 405 nm radiation may be necessary to provide viral disinfection. As 405 nm radiation may be irritating to human eyes, see '417 Publication, it may not be useful to increase the intensity of 405 nm radiation in an otherwise white-light LED fixture in the hopes that it will also kill viruses.
Furthermore, the flux or energy density of pathogen-inactivating radiation, such as at 405 and 470 nm, provided by a light fixture may not be sufficient to inactivate air borne pathogens. In short, the volume of the room in which a light fixture is placed may be too large to effectively inactivate air borne pathogens.
The inventor discloses a comprehensive solution in the form of a white light LED fixture with effective disinfection properties against bacteria, fungi, and viruses. As discussed further below, the white light LED fixture includes a fan to continuously draw air into the light fixture. The air drawn in is irradiated with UV radiation within the fixture, such as is provided from UV LED chips. The relatively small volume of the light fixture allows the flux or energy density of the UV radiation to be made more intense. After the air is sterilized, it can be put back into the room or building in which the fixture is placed. The white light provided by white light LEDs in the fixture provides illumination, and can further provide significant emission peaks at 405 nm and 470 nm which is also useful to pathogen inactivation.
An example of a disinfecting light fixture 10 is shown in
The light box 12 includes white LED chips 28 which provide for illumination and whose spectrum additionally and preferably includes significant radiation at 405 nm and 470 nm, as explained further below. The light box 12 includes a fan 20 protected by a grate 22. The fan 20 is used to draw air into the UV sterilization box 14 where the air is disinfected with UV radiation provided by UV LED chips 82 (
Notice then that the disinfecting light fixture 10 includes different means of providing sterilization of pathogens. The white LED chips 28, as well as providing white light for illumination, include significant radiation at 405 and 470 nm, which are useful in inactivating at least bacteria and fungi in the air and on surfaces in the room being illuminated, as discussed above. Other air borne pathogens—in particular viruses—are drawn into the fixture by the fan 20 and subjected to high intensity UV radiation provided by the UV LED chips 82 in the UV sterilization box 14. Such UV radiation should inactivate such air borne viruses, see C. D. Lytle et al., “Predicted Inactivation of Viruses of Relevance to Biodefense by Solar Radiation,” J. Virology (Vol. 79 (22), pp. 14244-52 (2005), and would be expected to provide further sterilization of other air borne pathogens (bacteria and fungi) as well. The air as sterilized by the fixture 10 can then be put back into the room where the fixture 10 is located, or otherwise may be input into the air handling system of the building, as explained further below. Notice that the fixture 10's sterilization properties makes it particularly well suited for use in locations where pathogens can be problematic, such as hospitals, nursing homes, etc. Fixture 10 is also useful when incorporated into grow light systems use to grow plants, such as in the system described in U.S. Pat. No. 10,440,900, which is incorporated herein by reference in its entirety. Sterilization is important in this context as well, because growing plants are susceptible to pathogens such as viruses, bacteria, and fungi.
The top view shows that the UV sterilization box 14 can include a section 15 for necessary system electronics, as described later. The bottom view shows the underside of the fixture 10 that which would provide illumination into the room. The fixture 10's diffuser 40 (
As shown in the emission spectrum of the white LED chip 28 in
Further sterilization—in particular, of viruses—is provided by the UV sterilization box 14, although before discussing such details, the construction of the light fixture 10 is described, starting with
The diffuser 40 is positioned between the white LED chips 28 and the room to be illuminated, and is shown in further detail in
As noted, the circuit board 24 can be formed in segments, and
To summarize, when the fan 20 is operating, air is drawn through fan grate 22, through the hole 25 in the circuit board(s) 24, and through holes 56 in the back plane 50 and into the UV sterilization box 14, whose construction is discussed next. As best shown in
Components of the fixture 10 may be coated with antimicrobial or reflective materials. For example, the interior surfaces of the UV sterilization box 14 may be coated with Titanium Dioxide. As well as having antimicrobial properties, Titanium Dioxide is highly reflective, thus encouraging reflection of the UV radiation within the UV sterilization box 14. This is preferred to absorption of the UV radiation, because absorption removes useful energy that could otherwise be used for disinfection of pathogens. In one example, the coating can comprise Paint Shield®, manufactured by Sherwin Williams. Such a coating can be applied to the vertical surfaces of the baffles 70, and could also be applied to the underside of the top cover 62, and the top side of the bottom surface 60.
The top cover 62 is preferably affixed to the side surfaces 64 using screws 18. This allows the top cover 62 to be removed to perform maintenance on the fixture 10, such as to clean or remove the baffles 70 or to repair or replace system electronics, as explained subsequently. The top cover 62 can be affixed to the UV sterilization box 14 using other methods which allow it to be opened and reclosed for maintenance purposes. Although not shown, the hose connectors 16a and 16b may also connect to one or more holes provided in the top cover 62.
The UV sterilization box 14 preferably includes a safety switch 103 designed to cut power to the UV LED chips 82 when the top cover 26 is removed. This is to prevent accidental UV exposure to persons who may be assembling or maintaining the light fixture 10. This switch 103 can be provided in the UV sterilization box 14 in different ways, but as shown the switch is mounted to the top flange of the side surface 64. As one skilled will understand, switch 103 includes a contact surface that will be depressed by the top cover 62 when it is connected to the UV sterilization box 14, thus closing the switch 103 and enabling the UV LED chips 82 to receive power. When the top cover 62 is removed, the contact surface is not depressed and switch 103 is thus opened to prevent activation of the UV LED chips 82. Operation of the safety switch 103 is discussed further below with reference to
The UV sterilization box 14 is preferably fully constructed and then affixed to the light box 12. In the example shown, this occurs using screws 52 which affix the bottom surface 60 of the UV sterilization box 14 to the back plane 50 of the light box 12. However, the UV sterilization box 14 and light box 12 can be affixed using different means. Furthermore, the UV sterilization box 14 and light box 12 need not be separately constructed and then attached to each other. Instead, the fixture 10 may be constructed in a manner that integrates the functionality of the UV sterilization box 14 and the light box 12. Having said this, it can be preferable to manufacture each separately, as this makes it easier to retrofit otherwise standard light boxes 12 with a UV sterilization box 14.
As best seen in
To more completely sterilize the air in the air flow paths, the non-linear air flow path includes UV LED chips 82, which may be formed on LED strips 80. The UV LED chips 82 and strips 80 are shown to the left in
Preferably, as much of the non-linear air flow paths are exposed to UV radiation as possible, and so in
Assuming that the height of the UV sterilization box 14 is about 4.5 inches (H2,
In one example, each of the UV LED chips 82 on UV LED strips 80 produces UV radiation with a peak wavelength in the range of 200 to 280 nm, which generally corresponds to the range of UV-C wavelengths. More preferably, the UV radiation has a peak wavelength in the range of 240 to 260 nm, or in the range of 260 to 280 nm. UV radiation in this range has been shown to be particularly useful to inactivate viruses by targeting their nucleic acids. See K. Bergmann, “UV-C Irradiation: A New Viral Inactivation Method for Biopharmaceuticals,” America Pharmaceutical Review, Vol 17(6) (November 2014).
While
As shown in
Electronics section 15 may also include one or more ports 84 to allow signaling to be output from driver circuitry 92b to the UV LED chips 82 in the UV sterilization box 14 and to the safety switch 103. One skilled will understand that such signaling will connect to each of the UV LED strips 80. In this regard, it can be useful to connect the various UV LED strips 80 within the UV sterilization box in a manner to reduce the amount of signaling and connections required. Although not shown, the bottom surface 60 can include a circuit board to assist in routing signaling to the UV LED strips 80. Preferably, port(s) 84 are optically blocked after the signaling has passed through to prevent UV light from entering electronics section 15. It is preferable to include the system electronics within section 15 so it can be easily accessed. For example, top cover 62 of the UV sterilization box 14 can be removed (using screws 18,
System electronics are shown in
It may be desired to separately control one or more aspects of the fixture 10. For example, it may be desired at a given time to drive only the white LED chips 28 to provide illumination to a room the fixture 10 is placed in, but to not drive the UV LED chips 82 to provide UV disinfection. Conversely, it may be desired at a given time (e.g., at night) to drive only the UV LED chips 82 to provide UV disinfection, but to not drive the white LED chips 28 to provide illumination. In this regard, the fixture 10 can include or be controlled by one or more switches 100, 102, or 104. For example, switch 100 comprises a master switch used to control all operations of the fixture, i.e., to control driving the white and UV LED chips 28 and 82, and the fan 20. Switch 102 can be used to independently control the white LED chips 28. Switch 104 can be used to independently control the UV LED chips 82 and the fan 20. Switch 104 is useful because it would normally be expected that the fan 20 and UV LED chips 82 would be enabled together, with the fan 20 drawing air flow into the UV sterilization box 14 that includes the chips 82. That being said, the UV LED chips 82 and fan 20 could also be independently controlled by their own switches. Any of the switches shown could comprise wall-mounted switches to which the fixture 10 is connected. Alternatively, the switches can appear in the light fixture (section 15) as part of the system electronics. In this respect, the switches may be controlled by a remote control, with system electronics including a wireless receiver (e.g., a Bluetooth receiver) for receiving input from the remote control.
System electronics can further include a safety switch 103. As described earlier, this switch 103 is designed to open to cut power to the UV LED chips 82 (e.g., via driver circuitry 92b) when the top cover 62 is removed from the UV sterilization box 14. As shown, safety switch 103 is in series with switch 104, and so would also disable power to the fan 20. However, switch 103 could also be located in the circuitry to cut power to only the LED driver circuitry 92b.
As discussed above, the UV sterilization box 14 includes one or more hose connectors 16a and 16b which output sterilized air, and such sterilized air is preferably distributed back into the room or building in which the fixture 10 appears.
Many modifications to the disclosed fixture 10 can be made, and the fixture 10 can be used in different environments to useful ends. For example, the white LED chips 28 may not include significant peaks at either or both of 405 nm or 470 nm, although the inclusion of these wavelengths is preferred to further aid sterilization that the fixture 10 provides. In fact, the white LED chips 28 may not be used, and instead other white light sources (e.g., bulbs) could be used in the fixture 10, with disinfection occurring strictly through use of the fan 20 and the UV sterilization box 14. The UV sterilization box 14 could include UV radiation sources other than UV LED chips. For example, various UV emitting bulbs could be used inside the UV sterilization box 14.
The fixture 10 can be used in environments where pathogens may be present, and in particular air borne pathogens. This can include hospitals, nursing homes, operating rooms, restrooms, kitchens, etc. Fixture 10 can also be used in a grow farm setting, in which light fixtures 10 are used to grow plants. For example, the disclosed fixture can be used in the context of the above-incorporated '900 patent, and can include the various improvements to a light fixture that are disclosed in that document.
Although particular embodiments of the present invention have been shown and described, it should be understood that the above discussion is not intended to limit the present invention to these embodiments. It will be obvious to those skilled in the art that various changes and modifications may be made without departing from the spirit and scope of the present invention. Thus, the present invention is intended to cover alternatives, modifications, and equivalents that may fall within the spirit and scope of the present invention as defined by the claims.
Number | Name | Date | Kind |
---|---|---|---|
3670193 | Thorington et al. | Jun 1972 | A |
3992646 | Corth | Nov 1976 | A |
5012609 | Ignatius et al. | May 1991 | A |
5278432 | Ignatius et al. | Jan 1994 | A |
6242752 | Soma et al. | Jun 2001 | B1 |
6791259 | Stokes et al. | Sep 2004 | B1 |
7658891 | Barnes | Feb 2010 | B1 |
8074397 | Yoneda | Dec 2011 | B2 |
8297782 | Bafetti | Oct 2012 | B2 |
8302346 | Hunt et al. | Nov 2012 | B2 |
8398264 | Anderson | Mar 2013 | B2 |
8453376 | Chen | Jun 2013 | B2 |
8476844 | Hancock et al. | Jul 2013 | B2 |
8508204 | Deurenbeg et al. | Aug 2013 | B2 |
9039966 | Anderson et al. | May 2015 | B2 |
9046227 | Aurelien | Jun 2015 | B2 |
9145590 | Evans et al. | Sep 2015 | B2 |
9162077 | Nigola et al. | Oct 2015 | B2 |
9333274 | Peterson | May 2016 | B2 |
9368695 | Aurelien | Jun 2016 | B2 |
9439989 | Lalicki | Sep 2016 | B2 |
9581310 | Wu et al. | Feb 2017 | B2 |
9681515 | Rantala | Jun 2017 | B2 |
9750105 | Rantala | Aug 2017 | B2 |
10104740 | Rantala | Oct 2018 | B2 |
10398000 | Rantala | Aug 2019 | B2 |
10440900 | Higgins | Oct 2019 | B1 |
20030124023 | Burgess et al. | Jul 2003 | A1 |
20040008523 | Butler | Jan 2004 | A1 |
20050055070 | Jones et al. | Mar 2005 | A1 |
20050207159 | Maxik | Sep 2005 | A1 |
20060022582 | Radkov | Feb 2006 | A1 |
20060071589 | Radkov | Apr 2006 | A1 |
20060186377 | Takahashi et al. | Aug 2006 | A1 |
20060261742 | Ng et al. | Nov 2006 | A1 |
20060262545 | Piepgras et al. | Nov 2006 | A1 |
20060284199 | Matheson | Dec 2006 | A1 |
20080008620 | Alexiadis | Jan 2008 | A1 |
20080245788 | Choong et al. | Oct 2008 | A1 |
20080278927 | Li et al. | Nov 2008 | A1 |
20080305004 | Anderson et al. | Dec 2008 | A1 |
20080315217 | Van Der Wel | Dec 2008 | A1 |
20090018621 | Vogler et al. | Jan 2009 | A1 |
20090034236 | Reuben | Feb 2009 | A1 |
20090231832 | Zukauskas et al. | Sep 2009 | A1 |
20090267484 | Kasakura et al. | Oct 2009 | A1 |
20100001648 | De Clercq et al. | Jan 2010 | A1 |
20100121420 | Fiset et al. | May 2010 | A1 |
20100232135 | Munehiro et al. | Sep 2010 | A1 |
20100244724 | Jacobs et al. | Sep 2010 | A1 |
20100246169 | Anderson et al. | Sep 2010 | A1 |
20110315956 | Tischler | Dec 2011 | A1 |
20120068615 | Duong et al. | Mar 2012 | A1 |
20120099303 | Li et al. | Apr 2012 | A1 |
20120281408 | Owen et al. | Nov 2012 | A1 |
20120286304 | LeToquin et al. | Nov 2012 | A1 |
20120320607 | Kinomoto et al. | Dec 2012 | A1 |
20130077299 | Hussell et al. | Mar 2013 | A1 |
20130139437 | Maxik | Jun 2013 | A1 |
20130194795 | Onaka | Aug 2013 | A1 |
20130313516 | David et al. | Nov 2013 | A1 |
20130313546 | Yu | Nov 2013 | A1 |
20130318869 | Aikala | Dec 2013 | A1 |
20130320299 | Li | Dec 2013 | A1 |
20140034991 | McKenzie et al. | Feb 2014 | A1 |
20140152194 | Beyer | Jun 2014 | A1 |
20140254131 | Osinski et al. | Sep 2014 | A1 |
20140328046 | Aanegola et al. | Nov 2014 | A1 |
20150014715 | Hsing Chen et al. | Jan 2015 | A1 |
20150049459 | Peeters et al. | Feb 2015 | A1 |
20150083221 | Boonekamp et al. | Mar 2015 | A1 |
20150129781 | Kretschmann | May 2015 | A1 |
20150182646 | Anderson et al. | Jul 2015 | A1 |
20150196002 | Friesth | Jul 2015 | A1 |
20150342125 | Krijn et al. | Dec 2015 | A1 |
20160015840 | Gordon | Jan 2016 | A1 |
20160030610 | Peterson | Feb 2016 | A1 |
20160088802 | Nicole et al. | Mar 2016 | A1 |
20160249810 | Darty et al. | Sep 2016 | A1 |
20160271281 | Clynne et al. | Sep 2016 | A1 |
20160273717 | Krames et al. | Sep 2016 | A1 |
20160276550 | David et al. | Sep 2016 | A1 |
20160375161 | Hawkins et al. | Dec 2016 | A1 |
20160375162 | Marry et al. | Dec 2016 | A1 |
20160375163 | Hawkins et al. | Dec 2016 | A1 |
20170014538 | Rantala | Jan 2017 | A1 |
20180147417 | Rantala | May 2018 | A1 |
20180224093 | Dutta et al. | Aug 2018 | A1 |
20190113219 | Niemiec | Apr 2019 | A1 |
20190292315 | Niemiec | Sep 2019 | A1 |
20200009286 | Zarcone | Jan 2020 | A1 |
20200288646 | Howe | Sep 2020 | A1 |
Number | Date | Country |
---|---|---|
2856725 | Jun 2013 | CA |
201797809 | Apr 2011 | CN |
103947469 | Jul 2014 | CN |
103947470 | Jul 2014 | CN |
104056289 | Sep 2014 | CN |
2554583 | Feb 2013 | EP |
S6420034 | Jan 1989 | JP |
2003339845 | Dec 2003 | JP |
1020130125436 | Nov 2013 | KR |
1020170114678 | Oct 2017 | KR |
102042655 | Nov 2019 | KR |
2001014012 | Mar 2001 | WO |
2002067660 | Sep 2002 | WO |
2003063902 | Aug 2003 | WO |
2004033028 | Apr 2004 | WO |
2006100303 | Sep 2006 | WO |
2006126482 | Nov 2006 | WO |
2007012875 | Feb 2007 | WO |
2007049180 | May 2007 | WO |
2009045107 | Apr 2009 | WO |
2009056838 | May 2009 | WO |
2013141824 | Sep 2013 | WO |
2014188303 | Nov 2014 | WO |
2015066099 | May 2015 | WO |
2016019029 | Feb 2016 | WO |
WO-2018221505 | Dec 2018 | WO |
Entry |
---|
Argyroudi-Akoyunoglou et al., “Photoinduced Changes in the Chlorophyll a to Chlorophyll b Ratio in Young Bean Plants,” Plant Physiology, Aug. 1970, 46(2), pp. 247-249. |
Beelmann et al., “Post-harvest Vitamin D Enrichment of Fresh Mushrooms,” HAL Project # MU07018, Apr. 30, 2009, Penn State University. |
Carvalho et al., “Sequential Light Programs Shape Kale (Brassica napus) Sprout Appearance and Alter Metabolic and Nutrient Content,” Horticulture Research 1, Article No. 8, 2014. |
Eytan et al., “Changes in Photosystem I Activity and Membrane Organization During Degreening and Greening of a Chlamydomon as Reinhardi Mutant, y-1,” The Journal of Biological Chemistry, vol. 249, No. 3, Issue of Feb. 10, , p. 738-744, 1974. |
Kleuter et al., “Photosynthesis in Cucumbers with Pulsed or Continuous Light,” Transactions of the ASABE, 23(2): 0437-0442, 1980. |
Lefsrud et al., “Irradiance from Distinct Wavelength Light-Emitting Diodes Affect Secondary Metabolites in Kale,” HortScience, vol. 43, No. 7, pp. 2243-2244, 2008. |
Nicklisch, Andreas, “Growth and Light Absorption of Some Planktonic Cyanobacteria, Diatoms and Chlorophyceae Under Stimulated Natural Light Fluctuations,” Journal of Plankton Research, vol. 20, Issue 1, pp. 105-119, 1998. |
Olle et al., “The Effects of Light-Emitting Diode Lighting on Greenhouse Plant Growth and Quality,” Agricultural and Food Science, vol. 22, No. 2, pp. 223-234, 2013. |
Sforza et al., “Adjusted Light and Dark Cycles Can Optimize Photosynthetic Efficiency in Algae Growing in Photobioreactors,” PLos ONE, 7(6): e38975, 2012. |
Tennessen et al. “Efficiency of Photosynthesis in Continuous and Pulsed Light Emitting Diode Irradiation,” Photosynthesis Research, 44(3), pp. 261-269, 1995. |
Vánninen et al. “Prospecting the Use of Artificial Lighting for Integrated Pest Management,” ISHS Acta Horticulturae, 956, pp. 593-608, 2010. |
Yeh et al., “High-Brightness LEDs—Energy Efficient Lighting Sources and their Potential in Indoor Plant Cultivation,” Renewable and Sustainable Energy Reviews, vol. 13, Issue 8, pp. 2175-2180, 2009. |
R.M. Tomb et al., “New Proof-of-Concept in Viral Inactivation: Virucidal Efficacy of 405 nm Light Against Feline Calicivirus as a Model for Norovirus Decontamination,” Food & Environmental Virology, vol. 9(2), 23 pages (2017). |
A.J. DeLucca et al., “Blue Light (470 nm) Effectively Inhibits Bacterial and Fungal Growth,” Letters in Applied Biology, vol. 55., pp. 460-466 (2012). |
C.D. Ltyle et al., “Predicted Inactivation of Viruses of Relevance to Biodefense by Solar Radiation,” J. Virology (vol. 79 (22), pp. 14244-14252 (2005). |
K. Bergmann, “UV-C Irradiation: A New Viral Inactivation Method for Biopharmaceuticals,” America Pharmaceutical Review, vol. 17(6) (Nov. 2014). |
Pinter, Matt, et al., “IEC/EN 62471 (Eye Safety) for LED Lighting Products—Standards for Eye and Skin Safety,” Smart Vision Lights, 2009, 4 pages. |
Neumark, et al., “Wide Bandgap Light Emitting Materials and Devices,” John Wiley & Sons, 2008, 50 pages. |
Dai, Tianhong, et al., “Blue Light for Infectious Diseases: Propionibacterimn Acnes, Helicobacter Pylori, and Beyond?” National Institutes of Health—Drug Resist Update, Aug. 2012, 15(4), pp. 223-236. |
Daicho, Hisayoshi, et al., “A Novel Phosphor for Glareless White Light-Emitting Diodes,” Nature Communications, 3:1132, Oct. 16, 2012, 8 pages. |
Setlur, Anant A., “Phosphors for LED-based Solid-State Lighting,” The Electrochemical Society Interface, Winter 2009, 5 pages. |
TRI-R Project Brochure, Toshiba Materials Co., LTD., retrieved on Aug. 18, 2017, 16 pages. |
Extended European Search Report regarding corresponding EP Application No. 20201893.3, dated Mar. 30, 2021. |
Communication Pursuant to Article 94(3) EPC regarding corresponding European Patent Application No. 20201893.3, dated Jan. 27, 2022. |
Number | Date | Country | |
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20210317981 A1 | Oct 2021 | US |