CN101998825A - 局部杀体外寄生虫剂组合物 - Google Patents
局部杀体外寄生虫剂组合物 Download PDFInfo
- Publication number
- CN101998825A CN101998825A CN2009801128866A CN200980112886A CN101998825A CN 101998825 A CN101998825 A CN 101998825A CN 2009801128866 A CN2009801128866 A CN 2009801128866A CN 200980112886 A CN200980112886 A CN 200980112886A CN 101998825 A CN101998825 A CN 101998825A
- Authority
- CN
- China
- Prior art keywords
- composition
- described composition
- igr
- animal
- growth regulator
- 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.)
- Granted
Links
- 239000000203 mixture Substances 0.000 title claims abstract description 124
- 230000000699 topical effect Effects 0.000 title abstract description 11
- RFEJUZJILGIRHQ-XRIOVQLTSA-N 2,3-dihydroxybutanedioic acid;3-[(2s)-1-methylpyrrolidin-2-yl]pyridine Chemical compound OC(=O)C(O)C(O)C(O)=O.OC(=O)C(O)C(O)C(O)=O.CN1CCC[C@H]1C1=CC=CN=C1 RFEJUZJILGIRHQ-XRIOVQLTSA-N 0.000 title abstract 2
- 239000013057 ectoparasiticide Substances 0.000 title abstract 2
- 241000238631 Hexapoda Species 0.000 claims abstract description 29
- 239000003630 growth substance Substances 0.000 claims abstract description 26
- UFTFJSFQGQCHQW-UHFFFAOYSA-N triformin Chemical compound O=COCC(OC=O)COC=O UFTFJSFQGQCHQW-UHFFFAOYSA-N 0.000 claims abstract description 15
- 241001465754 Metazoa Species 0.000 claims description 44
- 239000003112 inhibitor Substances 0.000 claims description 22
- 239000000041 non-steroidal anti-inflammatory agent Substances 0.000 claims description 18
- 229940021182 non-steroidal anti-inflammatory drug Drugs 0.000 claims description 18
- -1 caproic acid triglycerides Chemical class 0.000 claims description 14
- 230000035800 maturation Effects 0.000 claims description 11
- 229930002897 methoprene Natural products 0.000 claims description 11
- 229950003442 methoprene Drugs 0.000 claims description 11
- 239000003963 antioxidant agent Substances 0.000 claims description 10
- 230000003078 antioxidant effect Effects 0.000 claims description 9
- 239000003795 chemical substances by application Substances 0.000 claims description 9
- 239000003814 drug Substances 0.000 claims description 9
- 150000003626 triacylglycerols Chemical class 0.000 claims description 9
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical compound C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 claims description 8
- 239000002671 adjuvant Substances 0.000 claims description 8
- 229920002101 Chitin Polymers 0.000 claims description 7
- 244000078703 ectoparasite Species 0.000 claims description 7
- 238000007639 printing Methods 0.000 claims description 7
- 230000003110 anti-inflammatory effect Effects 0.000 claims description 6
- CKVMAPHTVCTEMM-ALPQRHTBSA-N milbemycin oxime Chemical compound O1[C@H](C)[C@@H](C)CC[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\2)O)C[C@H]4C1.C1C[C@H](C)[C@@H](CC)O[C@@]21O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)C(=N/O)/[C@H]3OC\1)O)C[C@H]4C2 CKVMAPHTVCTEMM-ALPQRHTBSA-N 0.000 claims description 6
- 238000003672 processing method Methods 0.000 claims description 6
- 230000003637 steroidlike Effects 0.000 claims description 6
- 239000012622 synthetic inhibitor Substances 0.000 claims description 6
- OEDUIFSDODUDRK-UHFFFAOYSA-N 5-phenyl-1h-pyrazole Chemical compound N1N=CC=C1C1=CC=CC=C1 OEDUIFSDODUDRK-UHFFFAOYSA-N 0.000 claims description 5
- 239000003120 macrolide antibiotic agent Substances 0.000 claims description 5
- 238000000034 method Methods 0.000 claims description 5
- FZRBKIRIBLNOAM-UHFFFAOYSA-N (E,E)-2-propynyl 3,7,11-trimethyl-2,4-dodecadienoate Chemical compound CC(C)CCCC(C)CC=CC(C)=CC(=O)OCC#C FZRBKIRIBLNOAM-UHFFFAOYSA-N 0.000 claims description 4
- 239000005898 Fenoxycarb Substances 0.000 claims description 4
- QQQYTWIFVNKMRW-UHFFFAOYSA-N diflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C=C1 QQQYTWIFVNKMRW-UHFFFAOYSA-N 0.000 claims description 4
- POLCUAVZOMRGSN-UHFFFAOYSA-N dipropyl ether Chemical compound CCCOCCC POLCUAVZOMRGSN-UHFFFAOYSA-N 0.000 claims description 4
- HJUFTIJOISQSKQ-UHFFFAOYSA-N fenoxycarb Chemical compound C1=CC(OCCNC(=O)OCC)=CC=C1OC1=CC=CC=C1 HJUFTIJOISQSKQ-UHFFFAOYSA-N 0.000 claims description 4
- 229930001540 kinoprene Natural products 0.000 claims description 4
- 125000003403 methoprene group Chemical group 0.000 claims description 4
- 239000007921 spray Substances 0.000 claims description 4
- 239000005891 Cyromazine Substances 0.000 claims description 3
- LVQDKIWDGQRHTE-UHFFFAOYSA-N cyromazine Chemical compound NC1=NC(N)=NC(NC2CC2)=N1 LVQDKIWDGQRHTE-UHFFFAOYSA-N 0.000 claims description 3
- 229950000775 cyromazine Drugs 0.000 claims description 3
- FYQGBXGJFWXIPP-UHFFFAOYSA-N hydroprene Chemical compound CCOC(=O)C=C(C)C=CCC(C)CCCC(C)C FYQGBXGJFWXIPP-UHFFFAOYSA-N 0.000 claims description 3
- 229930000073 hydroprene Natural products 0.000 claims description 3
- 238000004519 manufacturing process Methods 0.000 claims description 2
- NJPPVKZQTLUDBO-UHFFFAOYSA-N novaluron Chemical compound C1=C(Cl)C(OC(F)(F)C(OC(F)(F)F)F)=CC=C1NC(=O)NC(=O)C1=C(F)C=CC=C1F NJPPVKZQTLUDBO-UHFFFAOYSA-N 0.000 claims description 2
- FUZZWVXGSFPDMH-UHFFFAOYSA-N n-hexanoic acid Natural products CCCCCC(O)=O FUZZWVXGSFPDMH-UHFFFAOYSA-N 0.000 claims 1
- 238000002425 crystallisation Methods 0.000 description 18
- 230000008025 crystallization Effects 0.000 description 18
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 8
- 235000006708 antioxidants Nutrition 0.000 description 8
- NFGXHKASABOEEW-UHFFFAOYSA-N 1-methylethyl 11-methoxy-3,7,11-trimethyl-2,4-dodecadienoate Chemical compound COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C NFGXHKASABOEEW-UHFFFAOYSA-N 0.000 description 7
- 239000013078 crystal Substances 0.000 description 7
- 239000002904 solvent Substances 0.000 description 7
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 5
- 238000002360 preparation method Methods 0.000 description 5
- 230000005764 inhibitory process Effects 0.000 description 4
- 239000000463 material Substances 0.000 description 4
- 239000003921 oil Substances 0.000 description 4
- 235000019198 oils Nutrition 0.000 description 4
- 229920000036 polyvinylpyrrolidone Polymers 0.000 description 4
- 235000013855 polyvinylpyrrolidone Nutrition 0.000 description 4
- 230000000638 stimulation Effects 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
- 241000282326 Felis catus Species 0.000 description 3
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 3
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 229920003171 Poly (ethylene oxide) Polymers 0.000 description 3
- 239000002202 Polyethylene glycol Substances 0.000 description 3
- 239000003093 cationic surfactant Substances 0.000 description 3
- 230000002349 favourable effect Effects 0.000 description 3
- 210000004209 hair Anatomy 0.000 description 3
- 239000002917 insecticide Substances 0.000 description 3
- 229920001223 polyethylene glycol Polymers 0.000 description 3
- GVJHHUAWPYXKBD-IEOSBIPESA-N (R)-alpha-Tocopherol Natural products OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 description 2
- IIZPXYDJLKNOIY-JXPKJXOSSA-N 1-palmitoyl-2-arachidonoyl-sn-glycero-3-phosphocholine Chemical compound CCCCCCCCCCCCCCCC(=O)OC[C@H](COP([O-])(=O)OCC[N+](C)(C)C)OC(=O)CCC\C=C/C\C=C/C\C=C/C\C=C/CCCCC IIZPXYDJLKNOIY-JXPKJXOSSA-N 0.000 description 2
- ZNQVEEAIQZEUHB-UHFFFAOYSA-N 2-ethoxyethanol Chemical compound CCOCCO ZNQVEEAIQZEUHB-UHFFFAOYSA-N 0.000 description 2
- 239000005660 Abamectin Substances 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 2
- 239000004322 Butylated hydroxytoluene Substances 0.000 description 2
- LCGLNKUTAGEVQW-UHFFFAOYSA-N Dimethyl ether Chemical compound COC LCGLNKUTAGEVQW-UHFFFAOYSA-N 0.000 description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 2
- 239000004372 Polyvinyl alcohol Substances 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- ZTHYODDOHIVTJV-UHFFFAOYSA-N Propyl gallate Chemical compound CCCOC(=O)C1=CC(O)=C(O)C(O)=C1 ZTHYODDOHIVTJV-UHFFFAOYSA-N 0.000 description 2
- 241000718000 Pulex irritans Species 0.000 description 2
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 239000013543 active substance Substances 0.000 description 2
- 125000000217 alkyl group Chemical group 0.000 description 2
- WGVKWNUPNGFDFJ-DQCZWYHMSA-N beta-Tocopherol Natural products OC1=CC(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C WGVKWNUPNGFDFJ-DQCZWYHMSA-N 0.000 description 2
- 235000019282 butylated hydroxyanisole Nutrition 0.000 description 2
- 235000010354 butylated hydroxytoluene Nutrition 0.000 description 2
- 239000004202 carbamide Substances 0.000 description 2
- 239000003153 chemical reaction reagent Substances 0.000 description 2
- OROGSEYTTFOCAN-DNJOTXNNSA-N codeine Chemical compound C([C@H]1[C@H](N(CC[C@@]112)C)C3)=C[C@H](O)[C@@H]1OC1=C2C3=CC=C1OC OROGSEYTTFOCAN-DNJOTXNNSA-N 0.000 description 2
- 229920001577 copolymer Polymers 0.000 description 2
- FLKPEMZONWLCSK-UHFFFAOYSA-N diethyl phthalate Chemical compound CCOC(=O)C1=CC=CC=C1C(=O)OCC FLKPEMZONWLCSK-UHFFFAOYSA-N 0.000 description 2
- XXJWXESWEXIICW-UHFFFAOYSA-N diethylene glycol monoethyl ether Chemical compound CCOCCOCCO XXJWXESWEXIICW-UHFFFAOYSA-N 0.000 description 2
- 229940075557 diethylene glycol monoethyl ether Drugs 0.000 description 2
- 238000009792 diffusion process Methods 0.000 description 2
- 239000000839 emulsion Substances 0.000 description 2
- 229950006719 fluazuron Drugs 0.000 description 2
- JYGXADMDTFJGBT-VWUMJDOOSA-N hydrocortisone Chemical compound O=C1CC[C@]2(C)[C@H]3[C@@H](O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 JYGXADMDTFJGBT-VWUMJDOOSA-N 0.000 description 2
- 239000000787 lecithin Substances 0.000 description 2
- 235000010445 lecithin Nutrition 0.000 description 2
- 229940067606 lecithin Drugs 0.000 description 2
- 239000004530 micro-emulsion Substances 0.000 description 2
- 244000045947 parasite Species 0.000 description 2
- 239000000546 pharmaceutical excipient Substances 0.000 description 2
- 229920002451 polyvinyl alcohol Polymers 0.000 description 2
- 239000001267 polyvinylpyrrolidone Substances 0.000 description 2
- 150000003254 radicals Chemical class 0.000 description 2
- GEHJYWRUCIMESM-UHFFFAOYSA-L sodium sulfite Chemical compound [Na+].[Na+].[O-]S([O-])=O GEHJYWRUCIMESM-UHFFFAOYSA-L 0.000 description 2
- 239000004094 surface-active agent Substances 0.000 description 2
- 239000000725 suspension Substances 0.000 description 2
- FUFLCEKSBBHCMO-UHFFFAOYSA-N 11-dehydrocorticosterone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)C(=O)CO)C4C3CCC2=C1 FUFLCEKSBBHCMO-UHFFFAOYSA-N 0.000 description 1
- OAYXUHPQHDHDDZ-UHFFFAOYSA-N 2-(2-butoxyethoxy)ethanol Chemical compound CCCCOCCOCCO OAYXUHPQHDHDDZ-UHFFFAOYSA-N 0.000 description 1
- WMDZKDKPYCNCDZ-UHFFFAOYSA-N 2-(2-butoxypropoxy)propan-1-ol Chemical compound CCCCOC(C)COC(C)CO WMDZKDKPYCNCDZ-UHFFFAOYSA-N 0.000 description 1
- RFVNOJDQRGSOEL-UHFFFAOYSA-N 2-hydroxyethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCO RFVNOJDQRGSOEL-UHFFFAOYSA-N 0.000 description 1
- AZSNMRSAGSSBNP-UHFFFAOYSA-N 22,23-dihydroavermectin B1a Natural products C1CC(C)C(C(C)CC)OC21OC(CC=C(C)C(OC1OC(C)C(OC3OC(C)C(O)C(OC)C3)C(OC)C1)C(C)C=CC=C1C3(C(C(=O)O4)C=C(C)C(O)C3OC1)O)CC4C2 AZSNMRSAGSSBNP-UHFFFAOYSA-N 0.000 description 1
- QCAHUFWKIQLBNB-UHFFFAOYSA-N 3-(3-methoxypropoxy)propan-1-ol Chemical compound COCCCOCCCO QCAHUFWKIQLBNB-UHFFFAOYSA-N 0.000 description 1
- IBSREHMXUMOFBB-JFUDTMANSA-N 5u8924t11h Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C(C)C)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 IBSREHMXUMOFBB-JFUDTMANSA-N 0.000 description 1
- SPBDXSGPUHCETR-JFUDTMANSA-N 8883yp2r6d Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O[C@@H]([C@@H](C)CC4)C(C)C)O3)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C.C1C[C@H](C)[C@@H]([C@@H](C)CC)O[C@@]21O[C@H](C\C=C(C)\[C@@H](O[C@@H]1O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C1)[C@@H](C)\C=C\C=C/1[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\1)O)C[C@H]4C2 SPBDXSGPUHCETR-JFUDTMANSA-N 0.000 description 1
- 241000934067 Acarus Species 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N Acetaminophen Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- KWIUHFFTVRNATP-UHFFFAOYSA-N Betaine Natural products C[N+](C)(C)CC([O-])=O KWIUHFFTVRNATP-UHFFFAOYSA-N 0.000 description 1
- NLZUEZXRPGMBCV-UHFFFAOYSA-N Butylhydroxytoluene Chemical compound CC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 NLZUEZXRPGMBCV-UHFFFAOYSA-N 0.000 description 1
- JFLRKDZMHNBDQS-UCQUSYKYSA-N CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C Chemical compound CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C(=C[C@H]3[C@@H]2CC(=O)O1)C)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C.CC[C@H]1CCC[C@@H]([C@H](C(=O)C2=C[C@H]3[C@@H]4C[C@@H](C[C@H]4C=C[C@H]3C2CC(=O)O1)O[C@H]5[C@@H]([C@@H]([C@H]([C@@H](O5)C)OC)OC)OC)C)O[C@H]6CC[C@@H]([C@H](O6)C)N(C)C JFLRKDZMHNBDQS-UCQUSYKYSA-N 0.000 description 1
- MFYSYFVPBJMHGN-ZPOLXVRWSA-N Cortisone Chemical compound O=C1CC[C@]2(C)[C@H]3C(=O)C[C@](C)([C@@](CC4)(O)C(=O)CO)[C@@H]4[C@@H]3CCC2=C1 MFYSYFVPBJMHGN-ZPOLXVRWSA-N 0.000 description 1
- MFYSYFVPBJMHGN-UHFFFAOYSA-N Cortisone Natural products O=C1CCC2(C)C3C(=O)CC(C)(C(CC4)(O)C(=O)CO)C4C3CCC2=C1 MFYSYFVPBJMHGN-UHFFFAOYSA-N 0.000 description 1
- 241000490513 Ctenocephalides canis Species 0.000 description 1
- 241000258924 Ctenocephalides felis Species 0.000 description 1
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 description 1
- 239000001836 Dioctyl sodium sulphosuccinate Substances 0.000 description 1
- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
- 102000002322 Egg Proteins Human genes 0.000 description 1
- 108010000912 Egg Proteins Proteins 0.000 description 1
- IAYPIBMASNFSPL-UHFFFAOYSA-N Ethylene oxide Chemical compound C1CO1 IAYPIBMASNFSPL-UHFFFAOYSA-N 0.000 description 1
- HEFNNWSXXWATRW-UHFFFAOYSA-N Ibuprofen Chemical compound CC(C)CC1=CC=C(C(C)C(O)=O)C=C1 HEFNNWSXXWATRW-UHFFFAOYSA-N 0.000 description 1
- 241000270322 Lepidosauria Species 0.000 description 1
- 241001397515 Leptopsylla segnis Species 0.000 description 1
- 229930195725 Mannitol Natural products 0.000 description 1
- ZRVUJXDFFKFLMG-UHFFFAOYSA-N Meloxicam Chemical compound OC=1C2=CC=CC=C2S(=O)(=O)N(C)C=1C(=O)NC1=NC=C(C)S1 ZRVUJXDFFKFLMG-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- LRHPLDYGYMQRHN-UHFFFAOYSA-N N-Butanol Chemical class CCCCO LRHPLDYGYMQRHN-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- WHNWPMSKXPGLAX-UHFFFAOYSA-N N-Vinyl-2-pyrrolidone Chemical group C=CN1CCCC1=O WHNWPMSKXPGLAX-UHFFFAOYSA-N 0.000 description 1
- OHLUUHNLEMFGTQ-UHFFFAOYSA-N N-methylacetamide Chemical compound CNC(C)=O OHLUUHNLEMFGTQ-UHFFFAOYSA-N 0.000 description 1
- RCEAADKTGXTDOA-UHFFFAOYSA-N OS(O)(=O)=O.CCCCCCCCCCCC[Na] Chemical compound OS(O)(=O)=O.CCCCCCCCCCCC[Na] RCEAADKTGXTDOA-UHFFFAOYSA-N 0.000 description 1
- GOOHAUXETOMSMM-UHFFFAOYSA-N Propylene oxide Chemical compound CC1CO1 GOOHAUXETOMSMM-UHFFFAOYSA-N 0.000 description 1
- 241000238680 Rhipicephalus microplus Species 0.000 description 1
- 241001481696 Rhipicephalus sanguineus Species 0.000 description 1
- 241000258242 Siphonaptera Species 0.000 description 1
- 239000005930 Spinosad Substances 0.000 description 1
- QAOWNCQODCNURD-UHFFFAOYSA-L Sulfate Chemical compound [O-]S([O-])(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-L 0.000 description 1
- 235000004240 Triticum spelta Nutrition 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- ZGYHHEBYTCCRSA-UHFFFAOYSA-N [F].COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C Chemical compound [F].COC(C)(C)CCCC(C)CC=CC(C)=CC(=O)OC(C)C ZGYHHEBYTCCRSA-UHFFFAOYSA-N 0.000 description 1
- 229950008167 abamectin Drugs 0.000 description 1
- DPXJVFZANSGRMM-UHFFFAOYSA-N acetic acid;2,3,4,5,6-pentahydroxyhexanal;sodium Chemical compound [Na].CC(O)=O.OCC(O)C(O)C(O)C(O)C=O DPXJVFZANSGRMM-UHFFFAOYSA-N 0.000 description 1
- 150000001252 acrylic acid derivatives Chemical class 0.000 description 1
- 230000009471 action Effects 0.000 description 1
- 150000005215 alkyl ethers Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 150000008051 alkyl sulfates Chemical class 0.000 description 1
- 150000003863 ammonium salts Chemical class 0.000 description 1
- 239000002280 amphoteric surfactant Substances 0.000 description 1
- 239000003945 anionic surfactant Substances 0.000 description 1
- 150000001450 anions Chemical class 0.000 description 1
- 239000008365 aqueous carrier Substances 0.000 description 1
- 235000010323 ascorbic acid Nutrition 0.000 description 1
- 239000011668 ascorbic acid Substances 0.000 description 1
- 229960005070 ascorbic acid Drugs 0.000 description 1
- RRZXIRBKKLTSOM-XPNPUAGNSA-N avermectin B1a Chemical compound C1=C[C@H](C)[C@@H]([C@@H](C)CC)O[C@]11O[C@H](C\C=C(C)\[C@@H](O[C@@H]2O[C@@H](C)[C@H](O[C@@H]3O[C@@H](C)[C@H](O)[C@@H](OC)C3)[C@@H](OC)C2)[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 RRZXIRBKKLTSOM-XPNPUAGNSA-N 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 229960003237 betaine Drugs 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 239000001768 carboxy methyl cellulose Substances 0.000 description 1
- IVUMCTKHWDRRMH-UHFFFAOYSA-N carprofen Chemical compound C1=CC(Cl)=C[C]2C3=CC=C(C(C(O)=O)C)C=C3N=C21 IVUMCTKHWDRRMH-UHFFFAOYSA-N 0.000 description 1
- 229960003184 carprofen Drugs 0.000 description 1
- 239000004359 castor oil Substances 0.000 description 1
- 235000019438 castor oil Nutrition 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 235000019868 cocoa butter Nutrition 0.000 description 1
- 229940110456 cocoa butter Drugs 0.000 description 1
- 229960004126 codeine Drugs 0.000 description 1
- 239000012141 concentrate Substances 0.000 description 1
- 229960004544 cortisone Drugs 0.000 description 1
- 239000002385 cottonseed oil Substances 0.000 description 1
- 235000012343 cottonseed oil Nutrition 0.000 description 1
- 239000006071 cream Substances 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- 235000019329 dioctyl sodium sulphosuccinate Nutrition 0.000 description 1
- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- QLFZZSKTJWDQOS-YDBLARSUSA-N doramectin Chemical compound O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1[C@@H](OC)C[C@H](O[C@@H]2C(=C/C[C@@H]3C[C@@H](C[C@@]4(O3)C=C[C@H](C)[C@@H](C3CCCCC3)O4)OC(=O)[C@@H]3C=C(C)[C@@H](O)[C@H]4OC\C([C@@]34O)=C/C=C/[C@@H]2C)/C)O[C@H]1C QLFZZSKTJWDQOS-YDBLARSUSA-N 0.000 description 1
- 229960003997 doramectin Drugs 0.000 description 1
- 239000002552 dosage form Substances 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000008030 elimination Effects 0.000 description 1
- 238000003379 elimination reaction Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- YOWNVPAUWYHLQX-UHFFFAOYSA-N fluazuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC=C(Cl)C(OC=2C(=CC(=CN=2)C(F)(F)F)Cl)=C1 YOWNVPAUWYHLQX-UHFFFAOYSA-N 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000009472 formulation Methods 0.000 description 1
- 235000010382 gamma-tocopherol Nutrition 0.000 description 1
- WIGCFUFOHFEKBI-UHFFFAOYSA-N gamma-tocopherol Natural products CC(C)CCCC(C)CCCC(C)CCCC1CCC2C(C)C(O)C(C)C(C)C2O1 WIGCFUFOHFEKBI-UHFFFAOYSA-N 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 235000011187 glycerol Nutrition 0.000 description 1
- ZEMPKEQAKRGZGQ-XOQCFJPHSA-N glycerol triricinoleate Natural products CCCCCC[C@@H](O)CC=CCCCCCCCC(=O)OC[C@@H](COC(=O)CCCCCCCC=CC[C@@H](O)CCCCCC)OC(=O)CCCCCCCC=CC[C@H](O)CCCCCC ZEMPKEQAKRGZGQ-XOQCFJPHSA-N 0.000 description 1
- 229940100242 glycol stearate Drugs 0.000 description 1
- 239000003966 growth inhibitor Substances 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 230000036541 health Effects 0.000 description 1
- OROGSEYTTFOCAN-UHFFFAOYSA-N hydrocodone Natural products C1C(N(CCC234)C)C2C=CC(O)C3OC2=C4C1=CC=C2OC OROGSEYTTFOCAN-UHFFFAOYSA-N 0.000 description 1
- 229960000890 hydrocortisone Drugs 0.000 description 1
- RNYJXPUAFDFIQJ-UHFFFAOYSA-N hydron;octadecan-1-amine;chloride Chemical compound [Cl-].CCCCCCCCCCCCCCCCCC[NH3+] RNYJXPUAFDFIQJ-UHFFFAOYSA-N 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 208000015181 infectious disease Diseases 0.000 description 1
- 239000004615 ingredient Substances 0.000 description 1
- 230000000749 insecticidal effect Effects 0.000 description 1
- WFKAJVHLWXSISD-UHFFFAOYSA-N isobutyramide Chemical compound CC(C)C(N)=O WFKAJVHLWXSISD-UHFFFAOYSA-N 0.000 description 1
- 229960002418 ivermectin Drugs 0.000 description 1
- 239000007788 liquid Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 239000000594 mannitol Substances 0.000 description 1
- 235000010355 mannitol Nutrition 0.000 description 1
- 229960001929 meloxicam Drugs 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- YZBLFMPOMVTDJY-CBYMMZEQSA-N moxidectin Chemical compound O1[C@H](C(\C)=C\C(C)C)[C@@H](C)C(=N/OC)\C[C@@]11O[C@H](C\C=C(C)\C[C@@H](C)\C=C\C=C/2[C@]3([C@H](C(=O)O4)C=C(C)[C@@H](O)[C@H]3OC\2)O)C[C@H]4C1 YZBLFMPOMVTDJY-CBYMMZEQSA-N 0.000 description 1
- 229960004816 moxidectin Drugs 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- 150000002825 nitriles Chemical class 0.000 description 1
- 210000004681 ovum Anatomy 0.000 description 1
- 150000002923 oximes Chemical class 0.000 description 1
- 235000019865 palm kernel oil Nutrition 0.000 description 1
- 239000003346 palm kernel oil Substances 0.000 description 1
- 229960005489 paracetamol Drugs 0.000 description 1
- 239000002798 polar solvent Substances 0.000 description 1
- 229920000223 polyglycerol Polymers 0.000 description 1
- 239000000244 polyoxyethylene sorbitan monooleate Substances 0.000 description 1
- 235000010482 polyoxyethylene sorbitan monooleate Nutrition 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 229920000053 polysorbate 80 Polymers 0.000 description 1
- 229940068968 polysorbate 80 Drugs 0.000 description 1
- 239000004540 pour-on Substances 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- ULWHHBHJGPPBCO-UHFFFAOYSA-N propane-1,1-diol Chemical class CCC(O)O ULWHHBHJGPPBCO-UHFFFAOYSA-N 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- HNJBEVLQSNELDL-UHFFFAOYSA-N pyrrolidin-2-one Chemical compound O=C1CCCN1 HNJBEVLQSNELDL-UHFFFAOYSA-N 0.000 description 1
- 125000001453 quaternary ammonium group Chemical group 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 210000001732 sebaceous gland Anatomy 0.000 description 1
- 210000002374 sebum Anatomy 0.000 description 1
- 235000019812 sodium carboxymethyl cellulose Nutrition 0.000 description 1
- 229920001027 sodium carboxymethylcellulose Polymers 0.000 description 1
- APSBXTVYXVQYAB-UHFFFAOYSA-M sodium docusate Chemical compound [Na+].CCCCC(CC)COC(=O)CC(S([O-])(=O)=O)C(=O)OCC(CC)CCCC APSBXTVYXVQYAB-UHFFFAOYSA-M 0.000 description 1
- 235000010265 sodium sulphite Nutrition 0.000 description 1
- AKHNMLFCWUSKQB-UHFFFAOYSA-L sodium thiosulfate Chemical compound [Na+].[Na+].[O-]S([O-])(=O)=S AKHNMLFCWUSKQB-UHFFFAOYSA-L 0.000 description 1
- 235000019345 sodium thiosulphate Nutrition 0.000 description 1
- GGHPAKFFUZUEKL-UHFFFAOYSA-M sodium;hexadecyl sulfate Chemical compound [Na+].CCCCCCCCCCCCCCCCOS([O-])(=O)=O GGHPAKFFUZUEKL-UHFFFAOYSA-M 0.000 description 1
- 229940014213 spinosad Drugs 0.000 description 1
- 239000004544 spot-on Substances 0.000 description 1
- 238000005507 spraying Methods 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 239000000375 suspending agent Substances 0.000 description 1
- 238000013268 sustained release Methods 0.000 description 1
- 239000012730 sustained-release form Substances 0.000 description 1
- 238000002560 therapeutic procedure Methods 0.000 description 1
- 239000002076 α-tocopherol Substances 0.000 description 1
- 235000004835 α-tocopherol Nutrition 0.000 description 1
- 235000007680 β-tocopherol Nutrition 0.000 description 1
- 239000011590 β-tocopherol Substances 0.000 description 1
- 239000002478 γ-tocopherol Substances 0.000 description 1
- QUEDXNHFTDJVIY-DQCZWYHMSA-N γ-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1 QUEDXNHFTDJVIY-DQCZWYHMSA-N 0.000 description 1
Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
- A01N25/00—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
- A01N25/02—Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing liquids as carriers, diluents or solvents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/08—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
- A61K47/14—Esters of carboxylic acids, e.g. fatty acid monoglycerides, medium-chain triglycerides, parabens or PEG fatty acid esters
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
- A61K31/22—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin
- A61K31/23—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms
- A61K31/231—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids of acyclic acids, e.g. pravastatin of acids having a carboxyl group bound to a chain of seven or more carbon atoms having one or two double bonds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K45/00—Medicinal preparations containing active ingredients not provided for in groups A61K31/00 - A61K41/00
- A61K45/06—Mixtures of active ingredients without chemical characterisation, e.g. antiphlogistics and cardiaca
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0014—Skin, i.e. galenical aspects of topical compositions
- A61K9/0017—Non-human animal skin, e.g. pour-on, spot-on
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
- A61P33/14—Ectoparasiticides, e.g. scabicides
Landscapes
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Animal Behavior & Ethology (AREA)
- Public Health (AREA)
- Epidemiology (AREA)
- Zoology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Engineering & Computer Science (AREA)
- Emergency Medicine (AREA)
- Organic Chemistry (AREA)
- Dentistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Environmental Sciences (AREA)
- Tropical Medicine & Parasitology (AREA)
- Agronomy & Crop Science (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Toxicology (AREA)
- Wood Science & Technology (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Dermatology (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
Abstract
一种局部杀体外寄生虫剂组合物,所述组合物包含昆虫生长调节剂和至少一种C6-C12中链甘油三酯,其中,所述组合物包含相对于全部组合物至少为60%(w/v)的甘油三酯。
Description
技术领域
本发明涉及一种包含昆虫生长调节剂的局部施药用杀体外寄生虫剂组合物,及其在减少或抑制体外寄生虫成熟的处理方法中的用途。具体而言,所述局部组合物可以用在减少或抑制寄生于动物身上的蚤类和蜱类成熟的处理方法中。
背景技术
诸如烯虫酯、烯虫乙酯、烯虫炔酯、苯氧威、吡丙醚、环丙氨嗪、氟脲杀(dimilin)和双苯氟脲等昆虫生长调节剂(IGR)是一类抑制壳质合成或抑制寄生虫由不成熟阶段(如卵和幼虫)发展为成虫的杀虫剂。
可使用昆虫生长调节剂处理的常见体外寄生虫包括蚤类和蜱类,例如,蚤目和猫栉头蚤和犬栉头蚤、如致痒蚤等人蚤、如印鼠客蚤等鼠蚤和如牛和狗的那些蜱类(前者例如为微小牛蜱,后者例如为血红扇头蜱)。
已知的局部杀体外寄生虫剂组合物可以为点涂(spot-on)产品的形式。通常,仅将几毫升此类含有杀体外寄生虫剂的点涂产品施用在动物背部的局部区域上。施药24小时后,动物的整个皮肤表面都受到所述杀体外寄生虫剂的保护。据信,该杀虫剂在施用后即刻吸附在皮肤表面上并溶解在皮肤皮脂中,并从该处通过扩散而沿表面传播。据信,杀虫剂的蓄积处形成在皮脂腺中,由此提供长期的药物供应,例如提供6周~8周的保护。
含对蜱类有效的烯虫酯的制剂的实例包括美国专利第5,194,264号,其中描述了水性/极性溶剂烯虫酯组合物。美国专利第6,492,419号公开了一种昆虫生长调节剂(IGR)处于赋形剂中的组合物,所述赋形剂包含悬浮剂、阴离子表面活性剂、非离子表面活性剂或其混合物,和水性载体。
现存的一种烯虫酯-氟虫腈组合点涂产品(FrontlineTM Plus)将这两种产品溶解在乙醇和多种辅料中,所述辅料包括为了获得稳定性且抑制特别是在动物皮肤表面上的活性物的结晶所需的聚维酮、二乙二醇单乙醚和抗氧化剂。
已知的制剂通常需要溶剂的混合物和/或存在一种或多种结晶抑制剂,以提供防止其中活性物(IGR)从经处理的动物的皮肤表面析出晶体的稳定的组合物。
发明内容
本发明的一个目的在于提供一种包含昆虫生长调节剂(特别是烯虫酯)的用于对人类或动物施用的稳定的局部组合物,所述组合物优选不需在溶剂体系中存在佐剂和/或结晶抑制剂,并且在已处理数周的人类或动物的表面上还提供有效水平的杀虫活性。
本发明的第一方面提供了一种包含昆虫生长调节剂和至少一种C6-C12中链甘油三酯的局部杀体外寄生虫剂组合物,其中,所述组合物包含相对于总组合物至少为60%(重量/体积,w/v)的甘油三酯。
本发明的第二方面提供了一种在以治疗法处理人体或动物体的方法中使用的如本文所述的组合物。
本发明的第三方面提供了在减少或抑制动物皮肤上的体外寄生虫幼虫成熟的处理方法中使用的如本文所述的组合物,其中,将所述组合物在局部施用在动物的皮肤上。
本发明的第四方面提供了本文所述的组合物用于减少或抑制动物皮肤上或动物环境中的外寄生虫幼虫成熟中的应用。
本发明的第五方面提供了一种试剂盒,所述试剂盒在同一包装体中分别包含至少一个含有本文所述的组合物的容器和至少一个含有选自抗氧化剂和其它活性物中的至少一种佐剂的容器。
本发明人意外地发现,通过使用包含至少为60%(w/v)的至少一种C6-C12中链甘油三酯的溶剂,可以生产稳定的局部组合物,而无需包含额外的佐剂或其它结晶抑制剂。形成不含结晶抑制剂的稳定的局部组合物是有利的,因为该产品可以更容易、更迅速和更低廉地进行生产,同时仍能提供用于减少或清除体外寄生虫的高效且有效的局部组合物。意外地发现,即使没有额外的结晶抑制剂存在,所述组合物在施用后也不会在动物的皮肤上结晶。还发现,这些组合物具有良好的可贮藏能力。此外,这些组合物不对施用部位的皮肤产生刺激,或者只对施用部位的皮肤产生较低的刺激。
具体实施方式
本文限定的每一方面可以与任何一个或多个其它方面相结合,除非明确指出了相反的情况。特别是,指明为优选或有利的任何特征可以与一个或多个任何其它指明为优选或有利的特征相结合。
优选的是,昆虫生长调节剂选自烯虫酯、烯虫乙酯、烯虫炔酯、苯氧威、吡丙醚、环丙氨嗪、氟脲杀和双苯氟脲及其两种以上的混合物。最优选的是,昆虫生长调节剂为烯虫酯。
昆虫生长调节剂可以0.1%~100%(重量/体积,w/v)存在,优选为以1%~40%(w/v)存在,更优选为5%~20%(w/v),最优选为8%~15%(w/v),进而更优选为以12%(w/v)存在。
本文所用的术语“C6-C12中链甘油三酯”包括所有药学或兽医可接受的饱和或不饱和脂肪族甘油三酯,所述甘油三酯的链中具有6~12个碳原子。
C6-C12中链甘油三酯可以是单一的甘油三酯,也可以是两种以上的混合物。实例为C6、C8、C10和/或C12链甘油三酯。适合的甘油三酯为neobee油、椰子油和棕榈仁油。
优选的是,中链甘油三酯衍生自棉籽油。
优选的是,组合物包含至少80%(w/v)、更优选至少90%(w/v)的至少一种中链甘油三酯。组合物可以包含相对于全部组合物至少80%(w/v)、更优选至少90%(w/v)的特定中链甘油三酯,例如C6、C8、C10或C12链甘油三酯。组合物可以包含相对于全部组合物至少80%(w/v)、更优选至少90%(w/v)的至少两种或更多种中链甘油三酸酯。
优选的是,本发明的组合物为非水性组合物。优选组合物包含相对于全部组合物为小于1%(w/v)、更优选小于0.5%(w/v)的水。最优选的是,组合物不含任何水。
局部组合物中可以存在其它适用溶剂。适用的其它溶剂包括但不限于丙酮、乙腈、苯甲醇、丁基二甘醇、二甲基乙酰胺、二甲基甲酰胺、二丙二醇正丁醚、乙醇、异丙醇、甲醇、乙二醇单乙醚、乙二醇单甲醚、单甲基乙酰胺、二丙二醇单甲醚、液态聚氧乙二醇、丙二醇、2-吡咯烷酮,特别是N-甲基吡咯烷酮、二乙二醇单乙醚、乙二醇、邻苯二甲酸二乙酯及其两种以上的混合物。优选的附加溶剂为乙醇、异丙醇、苯甲醇或丁醇。
优选的是,本发明的组合物不含结晶抑制剂。这具有下述优点:组合物可以更低廉且更高效地进行制备,同时仍然保持有效。
有利的是,本发明的组合物包含相对于全部组合物为小于25%(w/v),更优选为小于10%(w/v),更优选为小于1%(w/v)的结晶抑制剂。
本文所用的术语“结晶抑制剂”可以用来指代抑制昆虫生长抑制剂在组合物中形成晶体的试剂或物质。结晶抑制剂优选符合以下测试:其中,20℃下将10ml包含10%(w/v)抑制剂的组合物放置在玻璃载玻片上,保持24小时。然后以肉眼观察该载玻片。可接受的抑制剂是它的加入使得生成了很少晶体或者未生成晶体的那些抑制剂,所述情况具体是少于10个晶体、优选少于5个晶体、更优选为0个晶体。本文所用的术语“结晶抑制剂”不包括脂肪酸或C4-C24脂肪族酸。
在一个替代性实施方式中,本发明的组合物可以包含至少一种结晶抑制剂。合适的结晶抑制剂是本领域中已知的,包括但不限于聚乙烯吡咯烷酮、聚乙烯醇、乙酸乙烯酯和乙烯基吡咯烷酮的共聚物、聚乙二醇、苯甲醇、甘露醇、甘油、山梨醇、聚氧乙烯化山梨聚糖酯;卵磷脂、羧甲基纤维素钠、如甲基丙烯酸酯等丙烯酸衍生物、烷基硫酸盐,特别是十二烷基硫酸钠和十六烷基硫酸钠;十二烷基苯磺酸钠、二辛基磺基琥珀酸钠;阳离子表面活性剂,如式N+R’R”R”’R””Y-的水溶性季铵盐,其中基团R为烃基(可选的是经羟基化的),并且Y-为诸如卤化物、硫酸盐和磺酸盐阴离子等强酸的阴离子;十六烷基三甲基溴化铵为可使用的阳离子表面活性剂,基团R可选为经羟基化的烃基时的式NR’R”R”’的铵盐;十八胺盐酸盐为可使用的阳离子表面活性剂,非离子表面活性剂如可选进行聚氧乙烯化的山梨聚糖酯(特别是聚山梨酸酯80)、聚氧乙烯化烷基醚;聚乙二醇硬脂酸酯、蓖麻油的聚氧乙烯化衍生物、聚甘油酯、聚氧乙烯化脂肪醇、氧化乙烯和氧化丙烯的共聚物,两性表面活性剂如十二烷基取代的甜菜碱化合物,或者优选这些结晶抑制剂中的至少两种物质的混合物。优选的是,结晶抑制剂为聚乙烯基吡咯烷酮、聚乙烯醇、聚乙二醇、苯甲醇和/或卵磷脂。
组合物可以包含选自抗氧化剂和其它活性物中的至少一种佐剂。
合适的抗氧化剂包括但不限于丁基羟基茴香醚(BHA)、丁基化羟基甲苯、抗坏血酸、α-、β-或γ-生育酚、偏二亚硫酸钠、没食子酸丙酯、硫代硫酸钠及其两种以上的混合物。优选的抗氧化剂为丁基羟基茴香醚(BHA)和丁基化羟基甲苯。抗氧化剂的加入可有利于延长组合物的储藏寿命。
优选的是,相对于全部组合物,组合物中抗氧化剂存在的浓度为0.005%~1%(w/v),更优选为0.01%~0.05%(w/v)。
其它活性物可以选自其它苯基吡唑、多杀菌素(spinosad)、非甾体抗炎药(NSAID)、甾体抗炎药、大环内酯、米尔倍霉素肟(milbemycine oxime)、昆虫生长调节剂、壳质合成抑制剂和RNA抑制剂中的一种或多种。
合适的非甾体抗炎药(NSAID)包括但不限于布洛芬、卡洛芬、美洛昔康和对乙酰氨基酚。
合适的甾体抗炎药包括但不限于可待因、可的松和氢化可的松。
米尔倍霉素肟的实例包括但不限于阿维菌素、伊维菌素、赛拉菌素、莫西菌素、阿巴克丁和多拉克汀。
合适的昆虫生长调节剂包括但不限于烯虫酯、吡丙醚、烯虫炔酯和苯氧威。
壳质合成抑制剂的实例包括但不限于杀铃脲、虱螨脲、氯代氟佐隆(chlorofluazuron)和氟佐隆。
其它活性物的适用量取决于采用的活性物。相对于全部组合物,其它活性物存在的浓度通常为0.1%~30%(w/v),优选为5%~20%(w/v)。
其它活性物包括可与本发明的组合物一起喷淋、喷射或涂抹在皮肤上的试剂。这些活性物包括例如喷雾器所需的常用推进气体,如丙烷、丁烷、二甲醚、CO2或卤代低级烷基气体(例如,卤代C1-C4烷基)及其两种以上的混合物。
在本发明的一个实施方式中,组合物由昆虫生长调节剂和包含至少一种C6-C12中链甘油三酯的溶剂构成。
本发明的组合物通常通过简单混合上述组分制备。有利的是,首先将昆虫生长调节剂混合至主溶剂中,然后加入其它成分或佐剂。
本发明的组合物通常用于宠物、特别是猫和狗,并且一般通过附着在皮肤上施用(“点涂”或“浇淋”(pour on)施用)。这通常是针对表面积小于10cm2(一般为5cm2~10cm2)的区域进行的局部施用。组合物可以例如在一个点或两个以上的点处施用,并优选定位在动物双肩之间。组合物在附着后扩散,特别是扩散至动物整个身体各处,然后干燥,且不会发生结晶或改变皮毛的外观(特别是不存在任何淡白色淤积物或任何积尘外观)或手感。本发明的组合物可以是点涂制剂或喷雾制剂。
本发明的组合物可以是对动物点涂施用的浓缩的乳液、微乳液、悬浮液或溶液的形式。在次优选的实施方式中,组合物可以是浇淋类型的喷雾、乳液、微乳液、悬浮液或溶液,或者是用于局部施用的油、霜、膏或任何其它流体制剂的形式。
本发明的组合物因其功效、作用速度和动物的毛发在施用及干燥后宜人的外观而特别有利。
优选的是,对小型动物如猫和狗每4周施用本发明的组合物,更优选每8周或12周施用本发明的组合物。
对于狗的施用量通常为0.25ml~3ml,对于猫的施用量通常为0.25ml~1ml。
本发明的组合物可用于治疗人类、大型和小型动物、鸟和爬行动物的昆虫感染。优选的是,所治疗的动物为人类、牛、马、鸟或小型动物。最优选的是其为猫或狗。治疗的动物体型越大,施用组合物的剂量越大。本发明的组合物特别适用于施用给狗和猫。
本发明的组合物的施用优选为对每kg动物体重提供1mg/kg~30mg/kg剂量的昆虫生长调节剂,更优选为5mg/kg~25mg/kg,还更优选为10mg/kg~20mg/kg。
本发明的组合物可用于通过消除或减少受感染动物中成熟的体外寄生虫,并通过消除或减少对受感染动物的相应的刺激(无论程度轻重),而改善动物皮毛的外观和质地。本发明的一个目的是通过减少或消除存在于动物皮毛中的成熟寄生虫而提供清洁动物皮毛的非治疗性方法。经处理的动物具有更好看和触感更好的毛发。
另外,本发明的组合物可以作预防性使用,以抑制或减少如蚤类乃至蜱类等体外寄生虫幼虫的成熟。可使用组合物使得将经处理的动物作为载体使用,从而根除或减少动物环境(例如卧垫、地毯、地板和墙壁)中的昆虫(例如蜱类)。
在一个实施方式中,本发明提供了一种治疗处理方法,可将组合物用在所述处理方法中,以抑制动物皮肤上的体外寄生虫幼虫的成熟,其中所述组合物局部地施用于动物的皮肤上。此处所述的方法可用于控制体外寄生虫、特别是蜱类。
本发明的一个方面提供了本文所述的组合物在制造用于抑制或减少动物皮肤上的体外寄生虫幼虫成熟的药物中的应用。
本发明的另一实施方式提供了用于抑制和减少动物皮肤上的体外寄生虫幼虫成熟的方法,所述方法包括将本文限定的局部组合物施用在动物皮肤上。优选的是,所述局部组合物为点涂组合物的形式。优选的是,所述组合物施用在动物的双肩之间。优选的是,所述动物是狗或猫。优选的是,所述组合物包含烯虫酯。优选的是,将组合物以单位剂型施用。
本发明的一个方面提供了一种试剂盒,所述试剂盒在同一包装体中分别包含至少一个含有如本文所述的组合物的容器和至少一个含有选自抗氧化剂和其它活性物中的至少一种佐剂的容器。所述其它活性物选自苯基吡唑、多杀菌素、非甾体抗炎药(NSAID)、甾体抗炎药、大环内酯、米尔倍霉素肟、其它昆虫生长调节剂、壳质合成抑制剂和RNA抑制剂中的一种或多种。优选的是,其它活性物为昆虫生长调节剂。
可选的是,在施用本发明的局部组合物的同时、之前或之后,可以向动物皮肤施用另一活性试剂。所述另一活性试剂施用在动物身上的位置可以与本发明的组合物所施用的位置相同或不同。优选的是,所述另一活性物为昆虫生长调节剂。其它活性物可选自苯基吡唑、多杀菌素、非甾体抗炎药(NSAID)、甾体抗炎药、大环内酯、米尔倍霉素肟、其它昆虫生长调节剂、壳质合成抑制剂和RNA抑制剂中的一种或多种。所述另一活性物可以同时施用,也可以交替施用。例如,可以使用双头涂药器施用所述活性物,所述双头涂药器中分别盛放含有两种活性物的组合物,而可以同时或交替地控制释放一种或两种活性物。
参考以下非限制性实施例,本发明可以得到进一步地说明。
制备含有以下浓度(W/V)的本发明的组合物:
实施例1
烯虫酯12%(w/v)
Neobee油q.s.(足量)100%
皮肤耐受性测试:
对猫和狗进行皮肤耐受性测试。
未观察到刺激
未观察到结晶
Claims (17)
1.一种局部杀体外寄生虫剂组合物,所述组合物包含昆虫生长调节剂和至少一种C6-C12中链甘油三酯,其中,所述组合物包含相对于全部组合物至少为60%(w/v)的甘油三酯。
2.如权利要求1所述的组合物,所述组合物包含相对于全部组合物至少为80%(w/v)的甘油三酯。
3.如权利要求2所述的组合物,所述组合物包含相对于全部组合物至少为90%(w/v)的甘油三酯。
4.如前述权利要求中任一项所述的组合物,其中,所述组合物由昆虫生长调节剂和甘油三酯组成。
5.如前述权利要求中任一项所述的组合物,其中,所述甘油三酯包含己酸甘油三酯、辛酸甘油三酯、癸酸甘油三酯或十二酸甘油三酯或其两种以上的混合物。
6.如前述权利要求中任一项所述的组合物,其中,所述昆虫生长调节剂选自烯虫酯、烯虫乙酯、烯虫炔酯、苯氧威、吡丙醚、环丙氨嗪、氟脲杀和双苯氟脲及其两种以上的混合物。
7.如权利要求6所述的组合物,其中,所述昆虫生长调节剂为烯虫酯。
8.如权利要求1~3或5~7中任一项所述的组合物,所述组合物包含选自抗氧化剂和其它活性物中的至少一种佐剂。
9.如权利要求8所述的组合物,其中,所述其它活性物选自苯基吡唑、多杀菌素、非甾体抗炎药(NSAID)、甾体抗炎药、大环内酯、米尔倍霉素肟、其它昆虫生长调节剂、壳质合成抑制剂和RNA抑制剂中的一种或多种。
10.如前述权利要求中任一项所述的组合物,其中,所述昆虫生长调节剂以相对于全部组合物为0.1%~40%(w/v)的浓度存在。
11.如前述权利要求中任一项所述的组合物,所述组合物为动物用点涂或喷雾制剂的形式。
12.如前述权利要求中任一项所述的组合物,所述组合物用于以治疗法处理人体或动物体的方法中。
13.如权利要求1~11中任一项所述的组合物,所述组合物用在减少或抑制动物皮肤上的体外寄生虫幼虫成熟的处理方法中,其中,将所述组合物局部地施用在所述动物的皮肤上。
14.权利要求1~11中任一项所述的组合物在制造用于减少或抑制动物皮肤上的体外寄生虫幼虫成熟的药物中的应用。
15.权利要求1~11中任一项所述的组合物用于减少或抑制动物皮肤上或动物环境中的体外寄生虫幼虫成熟中的应用。
16.一种试剂盒,所述试剂盒在同一包装体中分别包含至少一个含有如权利要求1~11中任一项所述的组合物的容器和至少一个含有选自抗氧化剂和其它活性物中的至少一种佐剂的容器。
17.如权利要求16所述的试剂盒,其中,所述其它活性物选自苯基吡唑、多杀菌素、非甾体抗炎药(NSAID)、甾体抗炎药、大环内酯、米尔倍霉素肟、其它昆虫生长调节剂、壳质合成抑制剂和RNA抑制剂中的一种或多种。
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0804619.5 | 2008-03-12 | ||
GBGB0804619.5A GB0804619D0 (en) | 2008-03-12 | 2008-03-12 | A topical ectoparasiticide composition |
PCT/GB2009/000669 WO2009112837A2 (en) | 2008-03-12 | 2009-03-11 | A topical ectoparasiticide composition |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101998825A true CN101998825A (zh) | 2011-03-30 |
CN101998825B CN101998825B (zh) | 2014-03-19 |
Family
ID=39328008
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN200980112886.6A Expired - Fee Related CN101998825B (zh) | 2008-03-12 | 2009-03-11 | 局部杀体外寄生虫剂组合物 |
Country Status (20)
Country | Link |
---|---|
US (2) | US20110288039A1 (zh) |
EP (1) | EP2271211A2 (zh) |
JP (1) | JP5425109B2 (zh) |
KR (1) | KR20110009092A (zh) |
CN (1) | CN101998825B (zh) |
AP (1) | AP2978A (zh) |
AU (1) | AU2009224009B2 (zh) |
BR (1) | BRPI0909356A2 (zh) |
CA (1) | CA2718364C (zh) |
CO (1) | CO6300896A2 (zh) |
CR (1) | CR11697A (zh) |
EA (1) | EA020336B1 (zh) |
GB (1) | GB0804619D0 (zh) |
IL (1) | IL208087A0 (zh) |
MX (1) | MX2010009957A (zh) |
MY (1) | MY177352A (zh) |
NZ (1) | NZ587927A (zh) |
UA (1) | UA103190C2 (zh) |
WO (1) | WO2009112837A2 (zh) |
ZA (1) | ZA201006644B (zh) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116173017A (zh) * | 2022-12-01 | 2023-05-30 | 浙江科瑞特生物科技有限公司 | 一种安全高效非泼罗尼犬猫通用型外用驱虫剂及制备方法 |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2010215542A (ja) * | 2009-03-13 | 2010-09-30 | Aasu Biochem Kk | 非ヒト動物から外部寄生虫を駆除する、または非ヒト動物への外部寄生虫の接触を防ぐための組成物、および当該組成物の利用 |
UA108641C2 (uk) | 2010-04-02 | 2015-05-25 | Паразитицидна композиція, яка містить чотири активних агенти, та спосіб її застосування | |
JP6589697B2 (ja) * | 2016-03-04 | 2019-10-16 | 住友化学株式会社 | 液状農薬 |
WO2023076666A1 (en) * | 2021-10-31 | 2023-05-04 | One-Derings LLC | Insect-repellent personal-care composition |
Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0249409A2 (en) * | 1986-06-07 | 1987-12-16 | Coopers Animal Health Limited | Liquid Formulations |
CN1122565A (zh) * | 1993-05-10 | 1996-05-15 | 麦克公司 | 含聚合物材料、二元醇类和甘油酯类的涂施制剂 |
US5942525A (en) * | 1995-05-11 | 1999-08-24 | Ecto Development Corporation | Spot treatment of animals with pyriproxyfen and an insecticide |
CN1283990A (zh) * | 1997-12-03 | 2001-02-14 | 麦克公司 | 含有氢化蓖麻油的长效注射制剂 |
WO2005053746A1 (en) * | 2003-12-04 | 2005-06-16 | Jurox Pty Ltd | Improved parasiticide composition |
US20050169966A1 (en) * | 2000-06-08 | 2005-08-04 | Ivy Animal Health, Inc. | Growth promoting pharmaceutical implant |
WO2006007630A1 (en) * | 2004-07-22 | 2006-01-26 | Jurox Pty Ltd | Aqueous insecticidal/parasiticide formulation |
US20060046988A1 (en) * | 2004-08-30 | 2006-03-02 | Albert Boeckh | Methoprene formulations for the control of tick infestations |
Family Cites Families (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3029426A1 (de) * | 1980-08-02 | 1982-03-11 | Bayer Ag, 5090 Leverkusen | Gegen zwecken wirksame pour-on-formulierungen |
GB8304927D0 (en) * | 1983-02-22 | 1983-03-23 | Wellcome Found | Pesticidal formulations |
US5602107A (en) * | 1993-05-10 | 1997-02-11 | Merck & Co., Inc. | Pour-on formulations consisting of gylcols, glycerides and avermectin compounds |
US6413536B1 (en) * | 1995-06-07 | 2002-07-02 | Southern Biosystems, Inc. | High viscosity liquid controlled delivery system and medical or surgical device |
JP4038835B2 (ja) * | 1997-06-16 | 2008-01-30 | 住友化学株式会社 | 動物用有害生物防除剤 |
US6174540B1 (en) * | 1998-09-14 | 2001-01-16 | Merck & Co., Inc. | Long acting injectable formulations containing hydrogenated caster oil |
-
2008
- 2008-03-12 GB GBGB0804619.5A patent/GB0804619D0/en not_active Ceased
-
2009
- 2009-03-11 NZ NZ587927A patent/NZ587927A/en not_active IP Right Cessation
- 2009-03-11 BR BRPI0909356-7A patent/BRPI0909356A2/pt not_active Application Discontinuation
- 2009-03-11 US US12/922,221 patent/US20110288039A1/en not_active Abandoned
- 2009-03-11 MX MX2010009957A patent/MX2010009957A/es not_active Application Discontinuation
- 2009-03-11 AU AU2009224009A patent/AU2009224009B2/en not_active Ceased
- 2009-03-11 EP EP09719073A patent/EP2271211A2/en not_active Withdrawn
- 2009-03-11 KR KR1020107021382A patent/KR20110009092A/ko not_active Application Discontinuation
- 2009-03-11 CA CA2718364A patent/CA2718364C/en not_active Expired - Fee Related
- 2009-03-11 CN CN200980112886.6A patent/CN101998825B/zh not_active Expired - Fee Related
- 2009-03-11 EA EA201071062A patent/EA020336B1/ru not_active IP Right Cessation
- 2009-03-11 UA UAA201012052A patent/UA103190C2/uk unknown
- 2009-03-11 MY MYPI2010004277A patent/MY177352A/en unknown
- 2009-03-11 AP AP2010005418A patent/AP2978A/xx active
- 2009-03-11 JP JP2010550259A patent/JP5425109B2/ja not_active Expired - Fee Related
- 2009-03-11 WO PCT/GB2009/000669 patent/WO2009112837A2/en active Application Filing
-
2010
- 2010-09-12 IL IL208087A patent/IL208087A0/en unknown
- 2010-09-16 ZA ZA2010/06644A patent/ZA201006644B/en unknown
- 2010-09-27 CR CR11697A patent/CR11697A/es unknown
- 2010-10-12 CO CO10126561A patent/CO6300896A2/es not_active Application Discontinuation
-
2015
- 2015-03-11 US US14/644,871 patent/US20150224195A1/en not_active Abandoned
Patent Citations (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0249409A2 (en) * | 1986-06-07 | 1987-12-16 | Coopers Animal Health Limited | Liquid Formulations |
CN1122565A (zh) * | 1993-05-10 | 1996-05-15 | 麦克公司 | 含聚合物材料、二元醇类和甘油酯类的涂施制剂 |
US5942525A (en) * | 1995-05-11 | 1999-08-24 | Ecto Development Corporation | Spot treatment of animals with pyriproxyfen and an insecticide |
CN1283990A (zh) * | 1997-12-03 | 2001-02-14 | 麦克公司 | 含有氢化蓖麻油的长效注射制剂 |
US20050169966A1 (en) * | 2000-06-08 | 2005-08-04 | Ivy Animal Health, Inc. | Growth promoting pharmaceutical implant |
WO2005053746A1 (en) * | 2003-12-04 | 2005-06-16 | Jurox Pty Ltd | Improved parasiticide composition |
WO2006007630A1 (en) * | 2004-07-22 | 2006-01-26 | Jurox Pty Ltd | Aqueous insecticidal/parasiticide formulation |
US20060046988A1 (en) * | 2004-08-30 | 2006-03-02 | Albert Boeckh | Methoprene formulations for the control of tick infestations |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN116173017A (zh) * | 2022-12-01 | 2023-05-30 | 浙江科瑞特生物科技有限公司 | 一种安全高效非泼罗尼犬猫通用型外用驱虫剂及制备方法 |
Also Published As
Publication number | Publication date |
---|---|
WO2009112837A2 (en) | 2009-09-17 |
CO6300896A2 (es) | 2011-07-21 |
UA103190C2 (uk) | 2013-09-25 |
CR11697A (es) | 2011-01-10 |
US20150224195A1 (en) | 2015-08-13 |
US20110288039A1 (en) | 2011-11-24 |
AU2009224009A1 (en) | 2009-09-17 |
AP2010005418A0 (en) | 2010-10-31 |
GB0804619D0 (en) | 2008-04-16 |
CA2718364A1 (en) | 2009-09-17 |
MY177352A (en) | 2020-09-14 |
CA2718364C (en) | 2016-01-26 |
JP2011515347A (ja) | 2011-05-19 |
IL208087A0 (en) | 2010-12-30 |
AP2978A (en) | 2014-09-30 |
MX2010009957A (es) | 2010-11-25 |
JP5425109B2 (ja) | 2014-02-26 |
WO2009112837A3 (en) | 2010-02-18 |
EP2271211A2 (en) | 2011-01-12 |
AU2009224009B2 (en) | 2013-08-29 |
EA020336B1 (ru) | 2014-10-30 |
ZA201006644B (en) | 2011-05-25 |
KR20110009092A (ko) | 2011-01-27 |
NZ587927A (en) | 2012-06-29 |
CN101998825B (zh) | 2014-03-19 |
EA201071062A1 (ru) | 2011-04-29 |
BRPI0909356A2 (pt) | 2015-08-04 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2010227340B2 (en) | A topical parasiticide composition | |
EP1887866B1 (en) | Spot-on formulations for combating parasites | |
JP5057667B2 (ja) | ペット寄生虫の治療・予防用組成物 | |
US6998131B2 (en) | Spot-on formulations for combating parasites | |
JP2005132844A (ja) | 哺乳動物、特に犬猫のノミを防除するための殺虫剤の組合せ | |
CN101998825B (zh) | 局部杀体外寄生虫剂组合物 | |
GB2464449A (en) | A topical ectoparasiticide composition | |
JP2001520669A (ja) | 小型哺乳動物の寝床のノミを根絶する方法および手段 | |
AU2010212672B2 (en) | Topical composition | |
GB2457734A (en) | Topical phenyl pyrazole insecticide composition | |
JP2019502665A (ja) | 獣医薬製剤 | |
JP2016521271A (ja) | 改善された殺外部寄生生物性製剤 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
GR01 | Patent grant | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20140319 Termination date: 20170311 |
|
CF01 | Termination of patent right due to non-payment of annual fee |