TREA

Applicator

Follow

Information

  • Patent Grant
  • D900312
  • Patent Number
    D900,312
  • Date Filed
    Thursday, June 15, 2017
    7 years ago
  • Date Issued
    Tuesday, October 27, 2020
    4 years ago
  • US Classifications
    Field of Search
    • US
    • D24 108
    • D24 112
    • D24 113
    • D24 114
    • D24 115
    • D24 127-131
    • D24 133
    • D24 186
    • D24 216
    • D24 224
    • D24 111
    • D24 119
    • D24 137
    • D24 138
    • D24 141
    • D24 147
    • D24 177
    • D24 214
    • D24 222
    • D09 418
    • D09 434
    • D09 435
    • D09 447
    • D09 448
    • D09 449
    • D09 452
    • D09 453
    • D09 454
    • D09 724
    • D28 7
    • D23 233-250
    • D23 207
    • D23 209
    • D23 365
    • CPC
    • A61M25/00
    • A61M39/00
    • A61M27/00
    • A61M25/0043
    • A61M25/0067
    • A61M25/0097
    • A61F2/958
    • B01D35/143
    • B01D2201/304
    • B01D27/10
    • B01D27/106
    • A61K31/12
    • A61K31/365
    • A61K36/29
    • A61K31/7048
    • A61K31/60
  • International Classifications
    • 2402
    • Term of Grant
      15Years
Information
Abstract
Description


FIG. 1 is a perspective view of an applicator;



FIG. 2 is a right side view thereof, the left side view being a mirror image to the right side view;



FIG. 3 is a top view thereof; and,



FIG. 4 is a bottom view thereof.


The surface shading shown in FIGS. 1-2 indicates that the claimed applicator is opaque. Material, texture, color, surface finish and surface ornamentation form no part of the claimed design.


The dot-dash-dot lines represent the bounds of the claimed design that form no part of the claimed design. The remaining broken lines illustrate portions of the applicator that form no part of the claimed design.


Claims
  • The ornamental design for an applicator, as shown and described.
US Referenced Citations (44)
Number Name Date Kind
4148874 Smith Apr 1979 A
5445462 Johnson et al. Aug 1995 A
5590780 O'Meara Jan 1997 A
5702694 Chamness Dec 1997 A
6066124 Caillouette May 2000 A
D436661 Berry Jan 2001 S
6547467 Quintero Apr 2003 B2
6673031 Mark Jan 2004 B2
6811342 Pauchet Nov 2004 B2
8518076 Stenton Aug 2013 B2
8871801 Levitt Oct 2014 B2
D771250 Zhang Nov 2016 S
D772407 Zhang Nov 2016 S
D801830 Zhang Nov 2017 S
10195635 Sporrer Feb 2019 B2
D868160 Lam Nov 2019 S
20030068331 Battaglia et al. Apr 2003 A1
20040242770 Feldstein et al. Dec 2004 A1
20040254561 Stenton Dec 2004 A1
20050019418 Crutchfield et al. Jan 2005 A1
20050111900 Fazzolari et al. May 2005 A1
20050169696 Albisetti Aug 2005 A1
20060110415 Gupta May 2006 A1
20060180613 Manesis Aug 2006 A1
20070000566 Gueret Jan 2007 A1
20070111954 Crutchfield et al. May 2007 A1
20070187437 Lord Aug 2007 A1
20080146674 Rosenberg et al. Jun 2008 A1
20080195040 Clark et al. Aug 2008 A1
20090311028 Odermatt et al. Dec 2009 A1
20110208136 Sollingen et al. Aug 2011 A1
20110212033 Tamarkin et al. Sep 2011 A1
20120016320 Lin Jan 2012 A1
20120148520 Strobel et al. Jun 2012 A1
20120190658 Studin Jul 2012 A1
20120312709 Kaufman Dec 2012 A1
20130004230 Kirk et al. Jan 2013 A1
20130197075 Levitt Aug 2013 A1
20140275248 Johnson Sep 2014 A1
20150118164 Tamarkin et al. Apr 2015 A1
20160193177 Davidson Jul 2016 A1
20170305925 Piotrowski et al. Oct 2017 A1
20190002474 Davidson et al. Jan 2019 A1
20190031674 Davidson et al. Jan 2019 A1
Foreign Referenced Citations (25)
Number Date Country
101012230 Aug 2007 CN
101108854 Jan 2008 CN
101798309 Aug 2010 CN
102146086 Aug 2011 CN
102268006 Dec 2011 CN
102336765 Feb 2012 CN
102526146 Jul 2012 CN
202730045 Feb 2013 CN
202920809 May 2013 CN
0841059 May 1998 EP
14837297.2 Mar 2017 EP
05-058914 Mar 1993 JP
10-114626 May 1998 JP
11-319064 Nov 1999 JP
11-335303 Dec 1999 JP
2005-187330 Jul 2005 JP
2007-269693 Oct 2007 JP
2010-235471 Oct 2010 JP
47-39621 Aug 2011 JP
2013-507367 Mar 2013 JP
WO 2012131238 Oct 2012 WO
PCTUS2014052184 Nov 2014 WO
WO 2015027111 Feb 2015 WO
WO 2016100732 Jun 2016 WO
WO 2018226894 Dec 2018 WO
Non-Patent Literature Citations (36)
Entry
Verrica Develops a Solution for Common Warts https://www.dermatologytimes.com/view/verrica-develops-solution-common-warts Nov. 13, 2018 (Year: 2018).
Extended European Search Report, dated Mar. 10, 2017, in connection with EP 14837297.2.
International Search Report and Written Opinion, dated Nov. 20, 2014, in connection with PCT/US2014/052184.
Extended European Search Report, dated Oct. 26, 2018, in connection with EP 15871116.8.
Supplementary European Search Report, dated Aug. 8, 2018, in connection with EP 16740681.8.
Extended European Search Report, dated Dec. 4, 2018, in connection with EP 16740681.8.
Invitation to Pay Additional Fees, mailed Aug. 27, 2018, in connection with PCT/U52018/03653.
International Search Report and Written Opinion, dated Oct. 22, 2018, in connection with PCT/US2018/036353.
Invitation to Pay Additional Fees, mailed Sep. 20, 2018, in connection with PCT/US2018/037808.
International Search Report and Written Opinion, dated Nov. 13, 2018, in connection with PCT/US2018/037808.
International Preliminary Report on Patentability dated Dec. 26, 2019 in connection with International Application No. PCT/US2018/037808.
Invitation to Pay Additional Fees, mailed Dec. 10, 2018, in connection with PCT/US2018/054373.
International Search Report and Written Opinion, dated Apr. 3, 2019 in connection with PCT/US2018/054373.
International Preliminary Report on Patentability dated Apr. 16, 2020, in connection with International Application No. PCT/US2018/054373.
[No Author Listed] CAS RN 27607-77-8. Entered STN: Nov. 16, 1984 28 pages.
[No Author Listed] CAS RN 76262-87-8. Entered STN: Nov. 16, 1984 19 pages.
[No Author Listed] CAS RN 89672-77-5. Entered STN: Nov. 16, 1984 29 pages.
Aitken et al., Fragmentation patterns in the gas-phase pyrolysis of some bi- and tri-cyclic sulfolanes related to the 8-thiabicyclo[4.3.0]non-3-ene 8,8-dioxide ring system. J Chem Soc. Perkin Transactions 1. 1994;16:2301-2308.
Anderson et al., Practical Process Research and Development. 1st Edition. Academic Press. Mar. 20, 2000 81-111.
Augé et al., Catalysis by Lithium Cation: Lithium Trifluoromethanesulfonate as a Substitute for Lithium Perchlorate in Cycloadditions. Synlett 2000;6:877-9.
Bouacha et al., A theoretical study of the mechanism, stereoselectivity and Lewis acid catalyst on the Diels-Alder cycloaddition between furan and activated alkenes. Tetrahedron Letters. 2013;54:4030-4033.
Braddock et al., Stereochemistry of the Catalysed Diels-Alder Reaction between Cyclopentadiene and Dimethyl Monothionofumarate; Soft versus Hard Lewis Acids. J. Chem. Soc. Chem. Commun. Jan. 1, 1993;16:1244-6. doi: https://doi.org/10.1039/C39930001244.
Brion et al., On the lewis acid catalyzed diels-alder reaction of furan. regio- and stereospecific synthesis of substituted cyclohexenols and cyclohexadienols.Tetrahedron Letters. 1982;23(50):5299-302. https://doi.org/10.1016/S0040-4039(00)85823-2.
Hollis et al., Homogeneous catalysis. Titanium complex [Ti(Cp)2(CF3SO3)2] and zirconium complex [Zr(Cp)2(CF3SO3)2THF], efficient catalysts for the Diels-Alder reaction. Organometallics. Aug. 1, 1992;11(8):2745-8. https://doi.org/10.1021/om00044a004.
Hollis et al., Homogenous Catalysis: Transition Metal Based Lewis Acid Catalysts. Tetrahedron. 1993;49(25):5415-30. doi: https://doi.org/10.1016/S0040-4020(01)87259-8.
Houk et al, On Lewis Acid catalysis of diels-alder reactions. J Am Chem Soc. Jun. 13, 1973;95(12):4094-4096.
Huang, Catalysts for Hetero Diels-Alder Reaction of Imines. Chinese Journal of Organic Chemistry. Oct. 2003;23(10):1064-75.
Hubbard et al., Lewis Acid Catalyzed Diels—Alder Reactions of Highly Hindered Dienophiles. J. Org. Chem. 1998;63(12):4143-4146.
Hunt et al., Why do catalytic quantities of lewis acid generally yield more product than 1.1 equiv in the intramolecular diels-adler reaction with a furan diene? Competitive complexation NMR studies provide an answer. J Am Chem Soc. 1995;117:1049-1056.
Kharitonov et al., Synthetic transformations of higher terpenoids: VIII. [4+2]-Cycloaddition reactions of lambertianic acid. Russian J Organic Chem. 2003;39(1):57-74.
Lange et al., Synthesis of 4-carboxy-2-thiabicyclo [3.2.0] Heptan-6-ones via 3-carboxy-2,3-dihydrothiophenes: potential β-lactamase inhibitors. Tetrahedron Lett. 1985;26(15):1791-1794.
Pagni et al., A chemical, spectroscopic, and theoretical assessment of the lewis acidity of LiClO4 in Diethyl Ether. J. Org Chem. 1993;58:3130-3133.
Prabhakar Reddy et al., Synthesis, cytotoxic activity and structure-activity relationships of hedychenone analogues. Bioorg Med Chem Lett. Apr. 15, 2010;20(8):2525-8. doi: 10.1016/j.bmcl.2010.02.101. Epub Mar. 3, 2010.
Song et al., Ionic liquids as powerful media in scandium triflate catalysed Diels—Alder reactions: significant rate acceleration, selectivity improvement and easy recycling of catalyst. Chem Commun. 2001;12:1122-3.
Sperry et al., Studies on the Diels—Alder reaction of annulated furans: application to the synthesis of substituted phenanthrenes. Tetrahedron Letters. Apr. 18, 2005;46(16):2789-93. Doi: 10.1016/j.tetlet.2005.02.148.
Tseng et al., Synthesis and Evaluation of Cantharidinimides on Human Cancer Cells. J Exp Clin Med. Oct. 2012;4(5):280-283.