TWI494061B - 含有因得克(indoxacarb)之區域局部投藥調配物 - Google Patents
含有因得克(indoxacarb)之區域局部投藥調配物 Download PDFInfo
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- TWI494061B TWI494061B TW103114936A TW103114936A TWI494061B TW I494061 B TWI494061 B TW I494061B TW 103114936 A TW103114936 A TW 103114936A TW 103114936 A TW103114936 A TW 103114936A TW I494061 B TWI494061 B TW I494061B
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- ectoparasites
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- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- VMGAPWLDMVPYIA-HIDZBRGKSA-N n'-amino-n-iminomethanimidamide Chemical compound N\N=C\N=N VMGAPWLDMVPYIA-HIDZBRGKSA-N 0.000 description 1
- UQKAOOAFEFCDGT-UHFFFAOYSA-N n,n-dimethyloctan-1-amine Chemical compound CCCCCCCCN(C)C UQKAOOAFEFCDGT-UHFFFAOYSA-N 0.000 description 1
- DVEKCXOJTLDBFE-UHFFFAOYSA-N n-dodecyl-n,n-dimethylglycinate Chemical class CCCCCCCCCCCC[N+](C)(C)CC([O-])=O DVEKCXOJTLDBFE-UHFFFAOYSA-N 0.000 description 1
- LKHFSBPQVCSCHJ-UHFFFAOYSA-N n-phenyl-2h-oxadiazine-4-carboxamide Chemical class N=1NOC=CC=1C(=O)NC1=CC=CC=C1 LKHFSBPQVCSCHJ-UHFFFAOYSA-N 0.000 description 1
- QNSIFYWAPWSAIJ-UHFFFAOYSA-N naftalofos Chemical compound C1=CC(C(N(OP(=O)(OCC)OCC)C2=O)=O)=C3C2=CC=CC3=C1 QNSIFYWAPWSAIJ-UHFFFAOYSA-N 0.000 description 1
- 229920005615 natural polymer Polymers 0.000 description 1
- 239000013642 negative control Substances 0.000 description 1
- 229960002715 nicotine Drugs 0.000 description 1
- SNICXCGAKADSCV-UHFFFAOYSA-N nicotine Natural products CN1CCCC1C1=CC=CN=C1 SNICXCGAKADSCV-UHFFFAOYSA-N 0.000 description 1
- FBUKVWPVBMHYJY-UHFFFAOYSA-N nonanoic acid Chemical compound CCCCCCCCC(O)=O FBUKVWPVBMHYJY-UHFFFAOYSA-N 0.000 description 1
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- 230000003000 nontoxic effect Effects 0.000 description 1
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- 229950003126 oxyclozanide Drugs 0.000 description 1
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- 239000002245 particle Substances 0.000 description 1
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- 239000008389 polyethoxylated castor oil Substances 0.000 description 1
- 229910052700 potassium Inorganic materials 0.000 description 1
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- 239000002244 precipitate Substances 0.000 description 1
- 239000003755 preservative agent Substances 0.000 description 1
- 230000008569 process Effects 0.000 description 1
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- ZPWFUIUNWDIYCJ-UHFFFAOYSA-N propan-2-yl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC(C)C ZPWFUIUNWDIYCJ-UHFFFAOYSA-N 0.000 description 1
- 235000010388 propyl gallate Nutrition 0.000 description 1
- 239000000473 propyl gallate Substances 0.000 description 1
- 229940075579 propyl gallate Drugs 0.000 description 1
- RUOJZAUFBMNUDX-UHFFFAOYSA-N propylene carbonate Chemical compound CC1COC(=O)O1 RUOJZAUFBMNUDX-UHFFFAOYSA-N 0.000 description 1
- QHGVXILFMXYDRS-UHFFFAOYSA-N pyraclofos Chemical compound C1=C(OP(=O)(OCC)SCCC)C=NN1C1=CC=C(Cl)C=C1 QHGVXILFMXYDRS-UHFFFAOYSA-N 0.000 description 1
- OIMWEHOYHJJPJD-UHFFFAOYSA-N pyridine;pyrimidine Chemical compound C1=CC=NC=C1.C1=CN=CN=C1 OIMWEHOYHJJPJD-UHFFFAOYSA-N 0.000 description 1
- NHDHVHZZCFYRSB-UHFFFAOYSA-N pyriproxyfen Chemical compound C=1C=CC=NC=1OC(C)COC(C=C1)=CC=C1OC1=CC=CC=C1 NHDHVHZZCFYRSB-UHFFFAOYSA-N 0.000 description 1
- 206010037844 rash Diseases 0.000 description 1
- BOLDJAUMGUJJKM-LSDHHAIUSA-N renifolin D Natural products CC(=C)[C@@H]1Cc2c(O)c(O)ccc2[C@H]1CC(=O)c3ccc(O)cc3O BOLDJAUMGUJJKM-LSDHHAIUSA-N 0.000 description 1
- 229940108410 resmethrin Drugs 0.000 description 1
- VEMKTZHHVJILDY-FIWHBWSRSA-N resmethrin Chemical compound CC1(C)[C@H](C=C(C)C)C1C(=O)OCC1=COC(CC=2C=CC=CC=2)=C1 VEMKTZHHVJILDY-FIWHBWSRSA-N 0.000 description 1
- 238000012552 review Methods 0.000 description 1
- WKEDVNSFRWHDNR-UHFFFAOYSA-N salicylanilide Chemical compound OC1=CC=CC=C1C(=O)NC1=CC=CC=C1 WKEDVNSFRWHDNR-UHFFFAOYSA-N 0.000 description 1
- 229950000975 salicylanilide Drugs 0.000 description 1
- 208000026451 salivation Diseases 0.000 description 1
- 150000004671 saturated fatty acids Chemical class 0.000 description 1
- 239000000932 sedative agent Substances 0.000 description 1
- 230000001624 sedative effect Effects 0.000 description 1
- AFJYYKSVHJGXSN-KAJWKRCWSA-N selamectin Chemical group O1[C@@H](C)[C@H](O)[C@@H](OC)C[C@@H]1O[C@@H]1C(/C)=C/C[C@@H](O[C@]2(O[C@@H]([C@@H](C)CC2)C2CCCCC2)C2)C[C@@H]2OC(=O)[C@@H]([C@]23O)C=C(C)C(=N\O)/[C@H]3OC\C2=C/C=C/[C@@H]1C AFJYYKSVHJGXSN-KAJWKRCWSA-N 0.000 description 1
- 229960002245 selamectin Drugs 0.000 description 1
- 239000002453 shampoo Substances 0.000 description 1
- 239000000344 soap Substances 0.000 description 1
- HRZFUMHJMZEROT-UHFFFAOYSA-L sodium disulfite Chemical compound [Na+].[Na+].[O-]S(=O)S([O-])(=O)=O HRZFUMHJMZEROT-UHFFFAOYSA-L 0.000 description 1
- 229940001584 sodium metabisulfite Drugs 0.000 description 1
- 235000010262 sodium metabisulphite Nutrition 0.000 description 1
- 229910052938 sodium sulfate Inorganic materials 0.000 description 1
- 235000011152 sodium sulphate 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
- 239000002689 soil Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 229940035044 sorbitan monolaurate Drugs 0.000 description 1
- 239000001587 sorbitan monostearate Substances 0.000 description 1
- 235000011076 sorbitan monostearate Nutrition 0.000 description 1
- 229940035048 sorbitan monostearate Drugs 0.000 description 1
- 239000000600 sorbitol Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 238000010561 standard procedure Methods 0.000 description 1
- 229940114926 stearate Drugs 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 150000003467 sulfuric acid derivatives Chemical class 0.000 description 1
- 229910021653 sulphate ion Inorganic materials 0.000 description 1
- 238000003786 synthesis reaction Methods 0.000 description 1
- 230000009897 systematic effect Effects 0.000 description 1
- 230000008685 targeting Effects 0.000 description 1
- QYPNKSZPJQQLRK-UHFFFAOYSA-N tebufenozide Chemical compound C1=CC(CC)=CC=C1C(=O)NN(C(C)(C)C)C(=O)C1=CC(C)=CC(C)=C1 QYPNKSZPJQQLRK-UHFFFAOYSA-N 0.000 description 1
- CJDWRQLODFKPEL-UHFFFAOYSA-N teflubenzuron Chemical compound FC1=CC=CC(F)=C1C(=O)NC(=O)NC1=CC(Cl)=C(F)C(Cl)=C1F CJDWRQLODFKPEL-UHFFFAOYSA-N 0.000 description 1
- RWRDLPDLKQPQOW-UHFFFAOYSA-N tetrahydropyrrole Substances C1CCNC1 RWRDLPDLKQPQOW-UHFFFAOYSA-N 0.000 description 1
- OULAJFUGPPVRBK-UHFFFAOYSA-N tetratriacontan-1-ol Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCO OULAJFUGPPVRBK-UHFFFAOYSA-N 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- DHCDFWKWKRSZHF-UHFFFAOYSA-L thiosulfate(2-) Chemical compound [O-]S([S-])(=O)=O DHCDFWKWKRSZHF-UHFFFAOYSA-L 0.000 description 1
- 210000001519 tissue Anatomy 0.000 description 1
- 235000010384 tocopherol Nutrition 0.000 description 1
- 229960001295 tocopherol Drugs 0.000 description 1
- 229930003799 tocopherol Natural products 0.000 description 1
- 239000011732 tocopherol Substances 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 239000012976 trial formulation Substances 0.000 description 1
- NFACJZMKEDPNKN-UHFFFAOYSA-N trichlorfon Chemical compound COP(=O)(OC)C(O)C(Cl)(Cl)Cl NFACJZMKEDPNKN-UHFFFAOYSA-N 0.000 description 1
- 229960000323 triclabendazole Drugs 0.000 description 1
- XAIPTRIXGHTTNT-UHFFFAOYSA-N triflumuron Chemical compound C1=CC(OC(F)(F)F)=CC=C1NC(=O)NC(=O)C1=CC=CC=C1Cl XAIPTRIXGHTTNT-UHFFFAOYSA-N 0.000 description 1
- 229960004418 trolamine Drugs 0.000 description 1
- 231100000397 ulcer Toxicity 0.000 description 1
- 150000004670 unsaturated fatty acids Chemical class 0.000 description 1
- 235000021122 unsaturated fatty acids Nutrition 0.000 description 1
- 239000008158 vegetable oil Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 230000002087 whitening effect Effects 0.000 description 1
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound 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 1
Classifications
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- A61K31/535—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines
- A61K31/5395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with at least one nitrogen and one oxygen as the ring hetero atoms, e.g. 1,2-oxazines having two or more nitrogen atoms in the same ring, e.g. oxadiazines
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- 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
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- A—HUMAN NECESSITIES
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- A01N43/00—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
- A01N43/72—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms
- A01N43/88—Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with nitrogen atoms and oxygen or sulfur atoms as ring hetero atoms six-membered rings with three ring hetero atoms
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- 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
- A01N47/00—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid
- A01N47/08—Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom not being member of a ring and having no bond to a carbon or hydrogen atom, e.g. derivatives of carbonic acid the carbon atom having one or more single bonds to nitrogen atoms
- A01N47/28—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
- A01N47/38—Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the group >N—CO—N< where at least one nitrogen atom is part of a heterocyclic ring; Thio analogues thereof
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- 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
- A01N53/00—Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K31/21—Esters, e.g. nitroglycerine, selenocyanates
- A61K31/215—Esters, e.g. nitroglycerine, selenocyanates of carboxylic acids
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- A—HUMAN NECESSITIES
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- 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
- A61K47/10—Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers
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- 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
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
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- A61K9/0012—Galenical forms characterised by the site of application
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- Oil, Petroleum & Natural Gas (AREA)
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- Dermatology (AREA)
- Organic Chemistry (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Catching Or Destruction (AREA)
Description
本發明關於一種區域局部投藥調配物,尤指一種含有因得克之區域局部投藥調配物。
動物通常易滋生體外寄生蟲(例如蠅及虱)並且感染體內寄生蟲(例如絲蟲及腸內蛔蟲)。家畜(例如貓及犬)通常滋生有一或多種以下體外寄生蟲:貓蚤及犬蚤(貓櫛頭蚤(Ctenocephalides felis)、犬櫛頭蚤(Ctenocephalides canis)及諸如此類)、蜱(扇頭蜱(Rhipicephalus spp.)、硬蜱(Ixodes spp.)、革蜱(Dermacentor spp.)、鈍眼蜱(Amblyoma spp.)及諸如此類)及蟎(蠕行蟎(Demodex spp.)、疥蟎(Sarcoptes scabei.)、耳癢蟎(Otodectes cynotis.)及諸如此類)。
蚤係一特殊問題,因其不僅對動物或人類的健康產生不利影響,且亦引起相當大的心理壓力。此外,蚤亦係動物(包括人類)中病原體(例如犬絛蟲(犬複孔絛蟲(Dipylidium caninum)))之傳病媒介。
類似地,蜱亦有害於動物或人類的身體及心理健康。然而,與蜱有關之最嚴重問題係其係病原體之傳病媒介,該等病原體可在人類及動物二者中引起疾病。由蜱引起之主要疾病包括疏
螺旋體病(borreliose)(由伯格多弗疏螺旋體(Borrelia burgdorferi)引起之萊姆(Lyme)病)、巴貝蟲病(babesiose)(或梨漿蟲病(piroplasmoses),由巴貝蟲(Babesia sp.)引起)及立克次體病(rickettsiose)(亦稱作洛基山(Rocky Mountain)斑疹熱)。蜱亦在寄主中釋放引起炎症或麻痹之毒素。有時,此等毒素對寄主係致命的。此外,蟎尤其難以防治,因為對該等寄生蟲起作用之有效物質極少且其需要頻繁處理。
同樣,農場動物亦易滋生寄生蟲。例如,牛會受大量寄生蟲侵襲。在農場動物中非常普遍之寄生蟲係蜱屬牛蜱(Boophilus),尤其微小牛蜱(B.microplus或cattle tick)、褪色牛蜱(B.decoloratus)及具環牛蜱(B.annulatus)。蜱(例如微小牛蜱(Boophilus microplus))尤其難以控制,因為其生存在農場動物以之為食之牧草中。其他重要的牛寄生蟲包括引起蠅蛆病之蠅,例如人膚蠅(Dermatobia hominis)(在巴西稱為皮蠅(Berne))及幼蟲滋生於寄主動物組織中之螺旋蠅(Cochlyomia hominivorax或screwworm)。此外,絲光綠蠅(Lucilia sericata或greenbottle)、銅綠蠅(Lucilia cuprina)(由此蠅引起之損害在Australia、New Zealand及South Africa普遍稱為麗蠅侵襲)種類係羊蠅蛆病之重要起因。其成蟲期構成寄生蟲之昆蟲包括:騷擾血蠅(Haematobia irritans或horn fly);虱,例如牛顎虱(Linognathus vituli)等;及蟎,例如疥蟎(Sarcoptes scabiei)及羊痂恙蟲(Psoroptes ovis)。以上列示並非詳盡無遺,此項技術中熟知之其他體外寄生蟲亦對動物及人類有害。此等包括(例如)遷移雙翅類幼蟲,例如皮蠅(Hypoderma spp.)及羊狂蠅(Oestrus ovis)。
已嘗試使用含有各種殺蟲劑之蚤項圈控制家畜上的體外寄生蟲。然而,體外寄生蟲仍存在於動物之附近,例如在寵物主人之屋內。除非動物環境永久處於殺蟲劑物質中(在此情況下
難以解決毒性及再滋生問題),否則難以達成該環境內體外寄生蟲之滅絕。因此,此項技術中需要持久且有效之試劑來滅絕家畜上之體外寄生蟲,以降低抗體外寄生蟲試劑之使用頻率及成本,其中該等試劑須便於貯存及施用且對家畜及其環境呈現極小毒性風險。
美國專利第5,462,938號揭示與噁二嗪甲醯苯胺化合物有關之新穎殺蟲劑組合物及方法,該等噁二嗪甲醯苯胺化合物具有對抗棲息於家庭住所、葉面及土壤中之農業及非農業害蟲之功效。其中揭示之化合物(S)-7-氯-2,5-二氫-2-[[(甲氧基羰基)-[4-(三氟甲氧基)苯基]胺基]羰基]茚并[1,2-e][1,3,4]噁二嗪-4a(3H)-甲酸甲酯,常用名:因得克,或DPX-KN128已由美國環境保護署(EPA)註冊為"低風險"殺蟲劑,化學代碼為067710,CAS編號為173584-44-6,U.S.EPA PC 067710(S-異構體)。英國的Journal of Pharmacology(2001)132,587-595;doi:10.1038/sj.bjp.0703853以"Indoxacarb,an Oxadinzine Insecticide,Blocks Insect Neuronal Sodium Channels"為標題,揭示了調查因得克在美洲大蠊(Periplaneta Americana)中作為神經元鈉通道抑制劑之作用方式的研究。Research Disclosure,1997年5月,第39786期以"Mixtures of Arthropodicides and Fungicides"為標題揭示了因得克與其他殺蟲劑在陸地或空中施用之殺蟲劑調配物中組合使用以保護植物免受節肢動物害蟲侵害之用途。美國專利第6,395,765號B1係關於利用局部施藥於家畜身體之局部區域治療及防止家畜上寄生害蟲之組合物。
在一態樣中,本發明提供一種控制家畜上體外寄生蟲之組
合物及方法,該控制家畜上體外寄生蟲包括滅絕家畜上體外寄生蟲;減少家畜上體外寄生蟲之數量;及/或預防家畜上滋生體外寄生蟲。該方法包括將體外寄生學上有效量之包含因得克及獸醫學上可接受之載劑的局部調配物局部施用於累計表面積小於或等於家畜總表面積之10%之局部區域。本發明組合物亦可視情況包含另外的殺蟲劑。
在一較佳態樣中,本發明提供一種控制家畜滋生體外寄生蟲之組合物及方法,包括將體外寄生學上有效量之包含存於獸醫學上可接受之溶劑中之因得克及視情況另外包含晶化抑制劑的區域局部調配物局部施用於表面積小於或等於家畜總表面積之10%之局部區域。
本發明揭示較佳之溶劑、晶化抑制劑、施藥方式及此等調配物之劑量。
本專利申請者特意將所有引用文獻的全部內容併入本發明揭示內容中。此外,當以一範圍、較佳範圍或一較佳上限值及較佳下限值列表給出一量、濃度或其他值或參數時,須將其理解為係特定揭示由任何一對任何上限範圍限值或較佳值與任何下限範圍限值或較佳值形成的所有範圍,無論是否單獨揭示該等範圍。當在本文中列舉一數值範圍時,除非另有說明,否則該範圍意欲包括其端點及在該範圍內的所有整數及分數。本發明之範圍並非意欲限於當界定一範圍時所列舉之特定
值。
本專利申請者已發現,可使用特定類型因得克調配物有效控制家畜之體外寄生蟲滋生:將局部調配物施用於表面積小於或等於家畜總表面積之10%之局部區域。該等調配物及方法尤其有利於口服或經注射治療所有動物較為困難或耗時之情形下的動物。因此,本發明提供用於控制體外寄生蟲之局部調配物,該調配物包含因得克及獸醫學上可接受之溶劑。本專利申請者已發現某些因得克區域局部調配物令人驚奇地有效且持久。
定義
本發明提供以下與本專利申請者揭示內容有關之定義。
本文所用術語"控制家畜上體外寄生蟲"包括滅絕家畜上體外寄生蟲;減少家畜上體外寄生蟲之數量;及/或預防家畜上滋生體外寄生蟲。
本文所用術語"家畜"包括由人類作為伴侶動物、寵物、耕畜或為了食物、毛皮、皮革、羊毛或其他動物產品而作為牲畜飼養之任何動物;或發現其與人類相關,使得控制此動物上體外寄生蟲係期望的之動物。本發明尤其適用之一般家畜包括母牛、馬、驢、豬、駱駝、鳥、犬、貓、鹿、綿羊或山羊。
本文所用術語"體外寄生蟲"包括存活在動物體外於任何生命階段(包括卵、幼蟲或成蟲形式)之寄生蟲。在家畜上難以解決之一般體外寄生蟲包括(例如)蚤、虱、蜱及蟎。
通常特別關注哺乳動物及鳥之節肢動物體外寄生蟲。實例性節肢動物包括彼等在表A中概述者,如下。
因此,昆蟲害蟲包括(例如)咬蟲,例如蠅及蚊、蟎、蜱、
虱、蚤、蝽、寄生蛆及諸如此類。
咬蟲包括(例如)遷移雙翅類幼蟲,例如牛之皮蠅屬、馬之胃蠅(Gastrophilus)及齧齒動物之黃蠅(Cuterebra sp.)以及所有類型的叮咬蠅及蚊。舉例而言,吸血成蠅包括(例如)騷擾血蠅(horn fly或Haematobia irritans)、馬蠅(horse fly或Tabanus spp.)、螫蠅(stable fly或Stomoxys calcitrans)、黑蠅(black fly或Simulium spp.)、斑虻(deer fly或Chrysops spp.)、虱蠅(louse fly或Melophagus ovinus)、舌蠅(tsetse fly或lossina spp)。寄生蠅蛆包括(例如)膚蠅(羊狂蠅及黃蠅(Cuterebra spp.))、麗蠅(blow fly或Phaenicia spp.)、螺旋蠅(screwworm或Cochlyomia hominivorax)、牛皮蠅(cattle grub或Hypoderma spp.)及羊毛蠕蟲。蚊包括(例如)庫蚊(Culex spp.)、瘧蚊(Anopheles spp.)及伊蚊(Aedes spp.)。
蟎包括中氣門目(Mesostigmata spp.),例如mesostigmatids(例如雞蟎、雞皮刺蟎(Dermanyssus gallinae));疥蟎(itch或scab mite),例如疥蟎科(Sarcoptidae spp.)(例如疥蟎);畜疥蟎,例如癢蟎科(Psoroptidae spp.),包括牛足蟎(Chorioptes bovis)及羊痂恙蟲;恙蟎,例如恙蟎科(Trombiculidae spp.)(例如北美恙蟎(North American chigger或Trombicula alfreddugesi)。
蜱包括(例如)軟體蜱,其包括隱喙蜱科(Argasidae spp.),例如銳緣蜱(Argas spp.)及鈍緣蜱(Ornithodoros spp.);硬體蜱,包括硬蜱科(Ixodidae spp.),例如血紅扇頭蜱(Rhipicephalus sanguineus)及牛蜱(Boophilus spp.)。
虱包括(例如)吸血虱,例如禽虱(Menopon spp.)及牛羽虱(Bovicola spp.);咬虱,例如血虱(Haematopinus spp.)、長顎虱
(Linognathus spp.)及盲虱(Solenopotes spp.)。
蚤包括(例如)櫛頭蚤(Ctenocephalides spp.),例如犬蚤(犬櫛頭蚤(Ctenocephalides canis))及貓蚤(貓櫛頭蚤(Ctenocephalides felis));客蚤(Xenopsylla spp.),例如印鼠客蚤(oriental rat flea或Xenopsylla cheopis);及人蚤(Pulex spp.),例如人蚤(human flea或Pulex irritans)。
蝽包括(例如)臭蟲科(Cimicidae)或(例如)普通臭蟲(溫帶臭蟲(Cimex lectularius));錐蝽亞科(Triatominae spp.),包括錐鼻蟲(亦稱作接吻蟲);(例如)長紅獵蝽(Rhodnius prolixus)及錐蝽(Triatoma spp.)。
通常,蠅、蚤、虱、蚊、蚋、蟎、蜱及腸蟲引起牲畜及伴侶動物部分極大損失。節肢動物寄生蟲亦對人類有害且可在人類及動物中傳播引起疾病之有機體。
許多其他節肢動物害蟲及體外寄生蟲在業內已知且亦意欲由本發明化合物處理。此等在以下中詳細列舉:D.S.Kettle之MEDICAL AND VETERINARY ENTOMOLOGY(Publ.John Wiley & Sons,New York及Toronto);R.O.Drummand,J.E.George及S.E.Kunz之CONTROL OF ARTHROPOD PESTS OF LIVESTOCK:A REVIEW OF TECHNOLOGY(Publ.CRC Press,Boca Raton,Florida),二者之內容皆以其整體引用的方式併入本文中。
本文所用"體外寄生學上有效量"係有效滅絕家畜上體外寄生蟲;減少家畜上體外寄生蟲之數量;及/或預防此動物上滋生體外寄生蟲之量。
本文所用術語"因得克"或DPX-KN128或名稱KN128皆係指式I之S異構體,
其中*代表光學活性中心。
因得克之系統化學名稱係(S)-7-氯-2,5-二氫-2-[[(甲氧基羰基)[4-(三氟甲氧基)苯基]胺基]羰基]茚并[1,2-e][1,3,4]噁二嗪-4a(3H)-甲酸甲酯。式I之R異構體或(R)-7-氯-2,5-二氫-2-[[(甲氧基羰基)[4-(三氟甲氧基)苯基]胺基]羰基]茚并[1,2-e][1,3,4]噁二嗪-4a(3H)-甲酸甲酯並不顯示殺蟲活性。WO/9963825闡述了活性S異構體與非活性R異構體以及基本上純淨之S異構體之各種混合物的用途。DuPont已將S異構體命名為DPX-KN128及R異構體命名為DPX-KN127且為方便起見在本說明書中將使用彼命名法。因得克或DPX-KN128已註冊為CAS編號173584-44-6。
式I化合物可藉由在WO 92/11249、WO 95/29171及WO 98/05656中揭示之一或多種方法製備,如反應圖1所示。
本文所用"區域局部調配物"係外表上施用於小於或等於10%動物總表面積之流體調配物。本文"區域局部調配物"可係指"本發明調配物"。區域局部調配物可係流體(包括水性懸浮液),例如澆塗調配物及點塗調配物、噴塗調配物、乳液、油、乳膏及軟膏。本文所用"區域局部投藥調配物"係流體調配物,其包括當施藥於小於或等於10%家畜總表面積時,可有效滅絕家畜上體外寄生蟲;減少家畜上體外寄生蟲之數量;及/或預防家畜上滋生體外寄生蟲之量的因得克及獸醫學上可接受之載劑。本文"區域局部調配物"可係指"本發明調配物"。在某些較佳實施例中,該區域局部調配物可包含晶化抑制劑。"流體調配物"包括(例如)液體調配物,例如澆塗調配物、點塗調配物及噴塗調配物,其可呈溶液、乳液(水包油或油包水)、懸乳液、微乳液、懸浮液(水性或非水性)、油、乳膏及軟膏形式。"流體調配物"亦可包括粉末、可分散於水之顆粒劑、可濕性粉劑及氣溶膠。"流體調配物"可隨時可用或使用前需要製備(例如用水稀釋)。
本文所用術語"持久功效"意指本發明調配物在一特定時間段內或條件下(例如在給定數量之水性沖洗內或在給定數量日、週或月內)保持控制體外寄生蟲(即滅絕家畜上體外寄生蟲;減少家畜上體外寄生蟲之數量;及/或預防家畜上滋生體外寄生蟲)之能力。在某些實施例中,功效足夠持久,使得單次處理後看到功效至多降低20%、10%或5%。在上下文中,術語"功效"係指調配物控制體外寄生蟲滋生之能力。
本文所用術語"點塗"及"澆塗"係指施藥於動物上局部區域之調配物,其中該局部區域具有小於或等於10%動物總表面積之累計表面積,且亦係指將組合物施藥於動物之局部表面積之方法,其中該(等)局部面積累計包括小於或等於10%動物總表
面積。
本文所用術語"獸醫學上可接受之"係指不會在家畜體內或身上引起明顯的不良反應並且另外在該動物之周圍環境中在人類可能暴露於此環境中之情況下不會造成人類毒性危險或其他不良反應之治療成份、治療組合物或治療方法。
本文所用術語"獸醫學上可接受之載劑"係指在本發明組合物中除因得克外的所有成份,或在組合物包含因得克加上一或多種附加殺蟲活性成份之情形下,在此組合物中除因得克及其他殺蟲活性成份外的成份。可包括在獸醫學上可接受之載劑內之成份或化合物的實例包括溶劑、晶化抑制劑、抗氧化劑、佐劑、共溶劑、著色劑、表面活性劑、油、光穩定劑、增黏劑、懸浮劑、推進劑、增積劑及增香劑或掩蔽劑。
本文所用詞語"包括(comprises或comprising)"欲作為無限制過渡短語,其意指涵蓋指定成份,但不一定排除其他未指定成份。
本文所用短語"實質上由組成(consists essentially of及consisting essentially of)"意欲指不包括對本發明調配物之基本特性具有重要影響之附加組份及/或試劑。具體而言,抑制因得克及/或殺蟲劑晶化之附加組份及/或試劑在調配物中會對該調配物產生重要影響。因此,當使用術語"實質上由組成(consists essentially of及consisting essentially of)"時,將不包含該晶化抑制劑,除非在彼調配物中明確包含彼晶化抑制劑。
短語"由組成(consisting of及consists of)"意作為過渡,意指除僅微量痕跡雜質外僅包括所列舉成份。
在一態樣中,本發明提供一種控制家畜上滋生體外寄生蟲
(例如消滅及/或預防體外寄生蟲(例如成蚤或蜱)滋生)之方法。該方法包括將體外寄生學上有效量之包含因得克及獸醫學上可接受之載劑的區域局部調配物局部施用於動物皮膚之局部區域,該局部區域具有小於或等於10%家畜總表面積之表面積。
本發明調配物包括所謂的"澆塗"及"點塗"調配物。除將本發明調配物施用於家畜皮膚之健康或正常區域之表面上外,此等局部區域亦可包括表皮層之傷口(例如切口或潰瘍)或可全部由其組成。因此,在某些實施例中,本發明亦用於治療傷口處之體外寄生蟲感染。
在某些實施例中,將該調配物施用於單一局部區域,該單一局部區域係等於或小於10%、5%或2%之動物總表面積,或施用於家畜皮膚之兩或多處局部區域或面積的組合,該兩或多處局部區域或面積共同組成小於10%、5%或2%之動物總表面積。未受限於任何特定作用機制,吾人相信在區域局部施藥後活性成份(因得克)會擴散至局部區域之外以對整個家畜身體或其大部分提供體外寄生控制。在較佳實施例中,將本發明調配物係利用"點塗"或"澆塗"施用至動物皮膚而施用於皮膚之單一點或區域。在尤其適用於貓及犬之某些實施例中,此施用係局部限於一等於或小於10公分2,具體而言介於5與10公分2之間之表面積。在某些尤佳之實施例中,將該調配物施用於沿動物背線之一或多點。例如,對於低劑量體積,肩部間之單個點係適宜的;然而,對於高劑量體積,推薦沿背部之多個位置施藥。
在某些較佳實施例中,該等調配物由於其功效、持久性及施藥及乾燥後動物毛皮之舒適外表而尤佳,該等較佳調配物已設計成即使在存在高濃度活性物質之情況下亦可最小化或消
除毛髮上之晶化並保持皮毛之妝容外表而無黏性或黏性外表。因此,在另一態樣中,本發明提供用於滅絕、減少及/或預防家畜滋生體外寄生蟲之區域局部調配物,其包含有效量之因得克及包括晶化抑制劑之獸醫學上可接受之載劑。本文所用之晶化抑制劑係將其施用於動物後,可使可見的因得克晶體或因得克及/或調配物之任何其他殺蟲劑的沉澱形成最小化之物質。用作晶化抑制劑之候選化合物可使用此項技術中通常習知之分析法進行試驗。例如,可在玻璃片上將候選晶化化合物添加至因得克及獸醫學上可接受之溶劑中(在20℃下,達24小時),其後用肉眼觀察該組合物以確定是否形成晶體。或者,可將包含候選化合物之區域局部調配物於室溫下施用於家畜,其後用肉眼觀察該動物以確定是否形成晶體。
其他晶化抑制劑之實例包括:三醋精、聚乙烯基吡咯啶酮、聚乙烯醇、乙酸乙烯酯與乙烯基吡咯啶酮之共聚物、聚乙二醇、聚乙氧基化山梨醇酐酯;卵磷脂、丙烯酸系衍生物(例如甲基丙烯酸酯及其他)、陰離子表面活性劑(例如鹼金屬硬脂酸鹽,尤其係硬脂酸鈉、硬脂酸鉀或硬脂酸銨);硬脂酸鈣;三乙醇胺硬脂酸酯;松香酸鈉;烷基硫酸鹽,尤其係月桂基硫酸鈉及十六烷基硫酸鈉;十二烷基苯磺酸鈉、二辛基磺基琥珀酸鈉;脂肪酸(尤其係彼等衍生自椰子油者);陽離子表面活性劑,例如式N+
R'R"R'"R"",Y-
之水溶性四級銨鹽,其中R基團係視情況羥基化之烴基團,且Y-
係強酸之陰離子,例如鹵化物、硫酸根及磺酸根陰離子;十六烷基三甲基溴化銨係可使用的陽離子表面活性劑之一;式N+
R'R"R'"之胺鹽,其中該等R基團係視情況羥基化之烴基團;十八胺氫氯酸鹽係可使用的陽離子表面活性劑之一;非離子型表面活性劑,例如(視情況)聚乙氧基化山梨醇酐酯(具體而言Polysorbate 80)、聚乙氧基化烷基醚;聚乙二
醇硬脂酸鹽、聚乙氧基化蓖麻油衍生物、聚甘油酯、聚乙氧基化脂肪醇、聚乙氧基化脂肪酸、環氧乙烷與環氧丙烷之共聚物;兩性表面活性劑(例如經取代之月桂基甜菜鹼化合物),或較佳係該等化合物中至少兩種的混合物。
晶化抑制劑可以任何適當比例及濃度存在以使得有效抑制選定調配物中特定劑量的因得克晶化。亦可使用晶化抑制劑之組合。在某些實施例中,晶化抑制劑之比例係1至60%(W/V)、5至50%(W/V)或10至40%(W/V)。因此,在最佳實施例中,一旦塗敷,則調配物於動物身體上擴散並然後乾燥而不晶化或改變外表(尤其係不出現任何發白沉澱或多塵外表)或改變動物之毛皮或皮膚之觸感。
較佳之調配物在功效方面應足夠持久,以降低與將調配物投與家畜有關之使用頻率及成本。在某些情形下,施用調配物至多兩次/週、至多一次/週、至多一次/月或至多一次/三個月。因此,本發明之某些調配物保持至少48小時、1週、1個月、2個月或(在某些情形下)長達3個月之持久功效。該等調配物亦可足夠持久以經受住用水溶液(例如肥皂及水)對家畜之沖洗。因此,該調配物可在至少一次或甚至五次水溶液沖洗後保持持久功效。
使用本發明調配物可處理多種體外寄生蟲。在某些實施例中,體外寄生蟲係蚤、蠅或虱,包括蚤卵、蚤幼蟲、蠅卵或蠅幼蟲。當本發明調配物設計成以蚤卵、蚤幼蟲、蠅卵或蠅幼蟲為處理目標時,會破壞蚤及/或蠅之生命週期進而減小環境族群壓力。就本發明之目的而言,術語蚤應理解為蚤目(Siphonaptera)寄生蚤之所有一般或偶然物種,且尤其係櫛頭蚤,尤其係貓櫛頭蚤(cat flea或C.felis)及犬櫛頭蚤(dog flea或C.canis)、印鼠客蚤(rat flea或Xenopsylla cheopis)及人蚤(human flea或Pulex
irritans)。
當需要控制該動物上或該動物附近體外寄生蟲之情況下,可用本發明調配物治療任何適當家畜。在某些較佳實施例中,家畜係哺乳動物,例如母牛、馬、驢、豬、鳥、駱駝、犬、貓、鹿、綿羊或山羊。
該區域局部調配物可藉由簡單混合如上所述之組份製備或在載劑係乳液、懸浮液或懸乳液之情形下,會需要劇烈攪拌或均質化且在因得克(DPX-KN128)係以固體形式(懸浮液、懸乳液、粉末、粉劑或顆粒)存在之情形下,需要碾磨以減小因得克(DPX-KN128)之粒徑。由於在所主張之調配物中因得克及較佳成份的化學上定義之性質,製備本發明調配物之方法對熟習此項技術者係顯而易見的。例如,活性物質可在獸醫學上可接受之溶劑中混合並然後添加獸醫學上可接受之載劑的其他組份,或獸醫學上可接受之載劑可指定為包括除因得克外調配物之所有成份,並然後將因得克(及視情況其他殺蟲活性成份)添加至獸醫學上可接受之載劑組合物。
在某些實施例中,載劑內之附加組份會係抗氧化劑。有用之抗氧化劑包括(例如)丁羥基茴香醚、丁羥基甲苯、抗壞血酸、亞硫酸鹽、偏亞硫酸氫鹽或硫代硫酸鹽(例如硫代硫酸鈉、偏亞硫酸氫鈉、偏亞硫酸氫鉀等)、沒食子酸丙酯及/或生育酚或不多於兩種該等試劑之混合物。
本發明調配物中可包含一或多種另外的殺蟲劑。有用之殺蟲劑包括昆蟲生長調節劑、有機磷酸酯殺蟲劑、胺基甲酸酯殺蟲劑、有機氯殺蟲劑、除蟲菊素殺蟲劑、擬除蟲菊酯殺蟲劑、煙鹼殺蟲劑、新煙鹼類殺蟲劑、含銅殺蟲劑、驅腸蟲劑、苯并咪唑殺蟲劑、水楊醯替苯胺殺蟲劑、經取代之苯酚殺蟲劑、嘧
啶殺蟲劑及咪唑并噻唑殺蟲劑。尤佳係甲脒殺蟲劑(例如三亞蟎)、縮胺基脲殺蟲劑(例如metaflumazone)及苯基吡唑(例如費普尼)。已在美國專利第5,232,940號、第6,096,329號、第6,395,765號及第6,716,442號中對費普尼予以闡述,其內容以引用方式併入本文中。在一此實施例中,該調配物包含有效量之費普尼及因得克。
在某些實施例中,咪唑并噻唑殺蟲劑係左旋咪唑。嘧啶殺蟲劑可係噻嘧啶。經取代之苯酚殺蟲劑可係硝碘酚腈。水楊醯替苯胺殺蟲劑可係氯生太爾(closantel)或羥氯紮胺(oxyclozanide)。苯并咪唑殺蟲劑可係阿苯達唑(albendazole)或三氯苯達唑(triclabendazole)。驅腸蟲劑可係大環內酯,例如阿弗菌素(avermectin)(例如伊維菌素(ivermectin))或米爾倍黴素(milbemycin)(例如莫昔克丁(moxidectin))。有機磷酸酯殺蟲劑可係雙特松(dicrotophos)、託福松(terbufos)、大滅松(dimethoate)、大利松(diazinon)、二硫松(disulfoton)、三氯松(trichlorfon)、穀速松(azinphos-methyl)、陶斯松(chlorpyrifos)、馬拉松(malathion)、滅多松(oxydemeton-methyl)、達馬杉(methamidophos)、歐殺松(acephate)、乙基巴拉松(ethyl parathion)、甲基巴拉松(methyl parathion)、美文松(mevinphos)、福瑞松(phorate)、三硫磷(carbofenthion)、裕必松(phosalone)、萘酞磷(naphthalophos)或白克松(pyraclofos)。胺基甲酸酯殺蟲劑可係加保利(carbaryl)、加保扶(carbofuran)、得滅克(aldicarb)或加保扶(carbofuran)。擬除蟲菊酯殺蟲劑可係亞烈寧(allethrin)、苄呋菊酯(resmethrin)、百滅寧(permethrin)、德它美寧(deltamethrin)或泰滅寧(tralomethrin)。含銅殺蟲劑可係氫氧化銅(II)或氧氯化銅硫酸鹽(即(Cu2Cl(OH)3)與(Cu4(OH)6(SO4)混合)。新煙鹼類殺蟲劑可係益達胺(imidacloprid)、烯啶蟲胺(nitenpyram)或達特南
(dinotefuran)。
另外,在某些實施例中,殺蟲劑係除蟲菊素殺蟲劑、蘇雲金芽孢桿菌(Bacillus thuringensis)毒素、乙酯殺蟎醇(chlorobenzilate)、賽扶寧(cyfluthrin)、賽滅寧(cypermethrin)、殺蟎醇(dicofol)、安殺番(endosulfan)、伊芬化利(esfenvalerate)、芬化利(fenvalerate)、賽洛寧(lambda-cyhalothrin)、甲氧氯、硫磺、環戊二烯類、蘭尼汀(ryania)、KT-199(一種驅腸蟲抗生素)或吡喹酮(praziquantel)。
昆蟲生長調節劑可係甲殼質合成抑制劑或幼態生長激素模擬劑。在某些實施例中,昆蟲生長調節劑係印苦楝子素、戴芬蘭(diofenolan)、芬諾西克(fenoxycarb)、烯蟲乙酯(hydroprene)、烯蟲炔酯(kinoprene)、甲氧普烯(methoprene)、比普西芬(pyriproxyfen)、四氫苄腈、克福隆(chlorfluazuron)、西洛美秦(cyromazine)、二福隆(diflubenzuron)、氟佐隆(fluazuron)、福環脲(flucycloxuron)、氟芬隆(flufenoxuron)、六伏隆(hexaflumuron)、祿芬隆(lufenuron)、諾華隆(novaluron)、得布芬載(tebufenozide)、得福隆(teflubenzuron)及殺蟲隆(triflumuron)。
該等附加殺蟲劑可以使該調配物之功效及持久性最佳化的量存在。具體而言,該等附加殺蟲劑可在約0.05%至約80%之範圍內存在。在一較佳實施例中,該調配物中之附加殺蟲劑係百滅寧,其以約30%至約75%的量存在。在另一較佳實施例中,附加殺蟲劑係費普尼,其以約5%至約25%的量存在。
在另一較佳實施例中,附加殺蟲劑係伊維菌素,其以約0.05%至約10%的量存在。在另一較佳實施例中,附加殺蟲劑係阿巴美丁(abamectin),其以約0.05%至約10%的量存在。在另一較佳實施例中,附加殺蟲劑係莫昔克丁,其以約0.05%至
約10%的量存在。在另一較佳實施例中,附加殺蟲劑係多拉克汀(doramectin),其以約0.05%至約10%的量存在。在另一較佳實施例中,附加殺蟲劑係依立諾克丁(eprinomectin),其以約0.05%至約10%的量存在。在另一較佳實施例中,附加殺蟲劑係司拉克丁(selamectin),其以約0.05%至約10%的量存在。在另一較佳實施例中,附加殺蟲劑係甲氧普烯,其以約1%至約20%的量存在。在另一較佳實施例中,附加殺蟲劑係S-甲氧普烯,其以約1%至約20%的量存在。
雖然在有效、持久及在妝容上理想的調配物製備中為因得克選擇適當溶劑係一重要方面,但多種獸醫學上可接受之溶劑可用於本發明。本文所用"獸醫學上可接受之溶劑"係當局部施用於家畜時係無毒的且能夠充分溶解因得克形成溶液之溶劑。例如,本發明獸醫學上可接受之溶劑不會引起家畜上表皮層之疹或炎症。獸醫學上可接受之溶劑一般不易點燃,或若點燃,則不會迅速燃盡。獸醫學上可接受之溶劑亦可在施用於該家畜後顯得無油污。
在某些實施例中,獸醫學上可接受之溶劑具有介於0與40之間、介於0與20之間或介於0與10之間之介電常數。
可用於本發明之獸醫學上可接受之溶劑的實例包括二乙二醇單丁基醚、甘油三醋酸酯、二乙二醇單甲基醚、二乙二醇單乙基醚、苯甲酸苄基酯、乙二醇單丁基醚、乳酸乙酯、二丙二醇單甲基醚、乙二醇單丁基醚乙酸酯、異丙醇、苄醇、乙醯乙酸乙酯、2-吡咯啶酮、二甲基異山梨醇、二丙酮醇、四氫呋喃醇、丙二醇單甲基醚、乙醇、碳酸丙二酯、鄰苯二甲酸二乙酯、三乙酸甘油酯、乙酸庚酯、辛酸甲酯/癸酸甲酯、N,N-二甲基辛醯胺、乙酸戊酯、乙酸己酯、乙酸環己酯、乙二醇二乙酸酯、乙酸甲氧基丙基酯、呋喃醇、鄰苯二甲酸二丁酯、N-甲基
吡咯啶酮、甘油縮甲醛、2,6-二甲基-4-庚酮、甲基乙基酮、甲基異丁基酮及環己酮。
在某些較佳實施例中,對於因得克獸醫學上可接受之溶劑係二醇醚或乙酸烷酯,例如乙醯乙酸乙酯。在某些尤佳實施例中,獸醫學上可接受之溶劑係乙醯乙酸乙酯或二丙二醇單甲基醚。
某些本發明調配物亦可包含附加試劑,例如佐劑、共溶劑、著色劑、表面活性劑、展膜油劑、抗氧化劑、光穩定劑、懸浮劑、推進劑、增積劑及/或增黏劑。著色劑係批准用於動物且可溶解或懸浮之所有著色劑。在此項技術中已熟知選擇並使用該等附加試劑以達成局部調配物中某些期望特徵。
光穩定劑實例係自二苯甲酮類或novantisolic acid之物質。
增黏劑之實例係纖維素衍生物、澱粉衍生物、聚丙烯酸酯、聚乙烯基吡咯啶酮及天然聚合物(例如藻酸鹽及明膠)。
佐劑可包括展膜油劑,例如肉豆蔻酸異丙酯、二丙二醇壬酸酯、聚矽氧油、脂肪酸酯、三酸甘油酯及脂肪醇。例如,澆塗及點塗調配物可較佳包含有助於迅速分佈於寄主動物皮膚表面及毛皮中之載劑且通常稱為展膜油劑。許多展膜油劑/溶劑組合物係適宜的,例如油性溶液;醇溶液及異丙醇溶液,例如2-辛基十二烷醇或油醇溶液;單羧酸酯之溶液,例如肉豆蔻酸異丙酯、棕櫚酸異丙酯、月桂酸草酸酯、油酸甾酯、油酸癸酯、月桂酸己酯、油酸油醇酯、油酸癸酯、鏈長C12
-C18
之飽和脂肪醇之己酸酯;二羧酸之酯溶液,例如鄰苯二甲酸二丁酯、間苯二甲酸二異丙酯、己二酸二異丙酯、己二酸二正丁基酯或脂肪酸之酯溶液,例如二醇。較有利的是亦有醫藥或化妝品工業習
知之分散劑存在。實例係吡咯啶-2-酮、N-烷基吡咯啶-2-酮、丙酮、聚乙二醇及其醚及酯、丙二醇或合成三酸甘油酯。
本發明調配物可進一步包含去水山梨醇單月桂酸酯、二丙二醇單甲基醚、三乙醇胺、苄醇、異丙醇及/或乙醯乙酸乙酯。
有用之陰離子表面活性劑包括鹼性硬脂酸鹽,尤其係硬脂酸鈉、硬脂酸鉀或硬脂酸銨;硬脂酸鈣;三乙醇胺硬脂酸酯;松香酸鈉;烷基硫酸鹽,尤其係月桂基硫酸鈉及十六烷基硫酸鈉;十二烷基苯磺酸鈉、二辛基磺基琥珀酸鈉;脂肪酸,尤其係彼等衍生自椰子油者。
有用之陽離子表面活性劑包括式N+
R'R"R'"R"",Y-
之水溶性四級銨鹽,其中R基團係視情況羥基化之烴基團,且Y-
係強酸之陰離子,例如鹵化物、硫酸根及磺酸根陰離子;十六烷基三甲基溴化銨係可使用的陽離子表面活性劑之一。
有用之陽離子表面活性劑包括式N+
R'R"R'"之胺鹽,其中該等R基團係H或視情況羥基化之烴基團;十八胺氫氯酸鹽係可使用的陽離子表面活性劑之一。
有用之非離子型表面活性劑包括聚氧乙烯化山梨醇酐酯(具體而言Polysorbate 80)、聚氧乙烯化烷基醚;聚乙二醇硬脂酸鹽、聚氧乙烯化蓖麻油衍生物、聚甘油酯、聚氧乙烯化脂肪醇、聚氧乙烯化脂肪酸、環氧乙烷與環氧丙烷之共聚物。有用之兩性表面活性劑包括經取代之月桂基甜菜鹼化合物。
選擇可使該等調配物之功效及持久性最佳化的本發明調配物中因得克之劑量及濃度。在某些實施例中,調配物中因得克之濃度係至少100克/公升、150克/公升或200克/公升;或1至50%(w/v)、5至35%(w/v)或10至20%(w/v)。在某些較佳實施例中,濃度係約200克/公升或20%(w/v)。在某些應用中(例
如當家畜係寵物時),亦選擇可使施用調配物後任何不期望之動物外表(例如,因得克之白色晶體)最小化之濃度。投與給家畜之因得克的總量一般係1至50毫克/公斤體重、2至25毫克/公斤體重或5至15毫克/公斤體重。
在某些實施例中,將該調配物施用於動物背部及背部之若干點處或沿背部線施用,且以低體積施用,例如5至20毫升/100公斤或10毫升/100公斤。在某些實施例中,總體積係10至150毫升/動物,有時限於50毫升。例如,根據動物體重施用於動物之體積可約0.3至1毫升(對於貓)且約0.5至5毫升(對於犬)。
在某些實施例中,獸醫學上可接受之載劑可以乳液或溶液形式施用於動物皮膚之局部區域(例如兩個肩部之間,如在點塗類應用中)。調配物可包括溶液(噴塗、澆塗、散塗或點塗至動物)、油、乳膏、軟膏或任何其他適於局部投藥之流體調配物。澆塗及點塗調配物可澆、點或噴至皮膚之限定區域。澆塗及點塗調配物可藉由在皮膚耐受之適宜溶劑或溶劑混合物中溶解、懸浮或乳化活性化合物製備。該調配物可能呈室溫下穩定、隨時可用之溶液形式,區域局部施用於動物上。
獸醫學上可接受之乳液係油包水類型或水包油類型。其藉由將因得克溶解於疏水或親水相中並用其他相之溶劑,藉助適宜乳化劑及(若合適)其他佐劑(例如著色劑、吸收促進劑、防腐劑、抗氧化劑、光穩定劑及/或增黏物質)均質化該相製備。
疏水相(油)之實例包括石蠟油、聚矽氧油、天然植物油(例如芝麻種油、杏仁油、蓖麻油)、合成三酸甘油酯,例如辛酸/癸酸二甘油酯、自鏈長C8-12
之植物脂肪酸或與其他特定選擇之天然脂肪酸形成之三酸甘油酯混合物、飽和或不飽和脂肪酸(亦可含有羥基)之部分甘油酯混合物及C8
/C10
-脂肪酸之單-及二甘
油酯。脂肪酸酯例如硬脂酸乙酯、己二酸二正丁酯、月桂酸己酯、二丙二醇壬酸酯、一般鏈長之具支鏈脂肪酸與鏈長C16
-C18
之飽和脂肪醇之酯、肉豆蔻酸異丙酯、棕櫚酸異丙酯、鏈長C12
-C18
之飽和脂肪醇辛酸酯/癸酸酯、硬脂酸異丙酯、油酸油醇酯、癸基油酸酯、油酸乙酯、乳酸乙酯、蠟脂肪酸酯,例如鄰苯二甲酸二丁酯、己二酸二異丙酯、與後者有關之酯混合物、及脂肪醇,例如異十三烷醇、2-辛基十二烷醇、十六烷基硬脂醇及油醇。
親水相溶劑包括水、乙醇、丙二醇、甘油、山梨醇及其混合物。乳化劑包括非離子型表面活性劑,例如聚氧乙基化蓖麻油、聚氧乙基化去水山梨醇單油酸酯、去水山梨醇單硬脂酸酯、甘油單硬脂酸酯、聚氧乙基硬脂酸酯、烷基苯酚聚乙二醇醚;兩性表面活性劑,例如N-月桂基-β-亞胺基二丙酸二鈉或卵磷脂;陰離子表面活性劑,例如月桂基硫酸鈉、脂肪醇醚硫酸鹽、單/二烷基聚乙二醇醚正磷酸酯之單乙醇胺鹽;陽離子表面活性劑,例如十六烷基三甲基氯化銨。
有用之增黏物質及穩定乳液之物質包括羧基甲基纖維素、甲基纖維素及其他纖維素及澱粉衍生物、聚丙烯酸酯、藻酸鹽、明膠、阿拉伯樹膠、聚乙烯基吡咯啶酮、聚乙烯醇、甲基乙烯基醚與馬來酸酐之共聚物、聚乙二醇、蠟、膠質二氧化矽或上述物質之混合物。
本發明之材料及方法藉由以下實例進一步闡釋。該等實例用以闡釋而非限制本發明。
用完全隨機化設計(基於繁殖及治療前蚤數分級並劃分成組)實施知情預期縱向人為滋生寄生蟲功效禽畜研究。有5個治療組(每組有6只犬)及一個非治療對照組。
在第-7天徵募三十三(33)只成犬(拉布拉多尋回犬(Labrador Retriever)及傑克羅素梗犬(Jack Russell Terrier)),進行臨床檢查,稱重,加以標記並分配用以實施禽畜研究。在第-5天並再次在第-2天使每只犬人為滋生100只蚤(貓櫛頭蚤)。在第-1天在所有犬上進行蚤拇指計數並選用30只犬。基於繁殖及蚤計數將該等犬隨機分成5個相似的含有6只動物的組且該等組分配用於進行禽畜研究。在第0天,用區域局部投藥調配物治療組B、C、D及E,該調配物含有溶解於二甲基異山梨醇(DMI)與丙二醇單甲基醚之混合物(以體積計,90%二甲基異山梨醇(DMI)及10%丙二醇單甲基醚)之因得克(DPX-K128)以形成因得克(DPX-K128)總濃度為75、100、125或150克/公升。製備該調配物之原料係DPX-K128與DPX-KN127(式1之R-異構體)之混合物且含有70.43%因得克(DPX-K128)。因此每需要1克因得克(DPX-K128),即使用1.42克該混合物。將該調配物以0.1毫升/1公斤之比率經由點塗施用(即以液體形式施用於小於或等於10%動物之表面積)於背側中線投藥。組A仍不實施治療用作對照。組B以7.5毫克/公斤之比率投藥;組C以10.0毫克/公斤之比率投藥;組D以12.5毫克/公斤之比率投藥;及組E以15.0毫克/公斤之比率投藥。
蚤拇指計數在24小時時實施。蚤梳計數在治療後48小時實施且然後所有犬用Capstar®口服錠劑(Nitenpyram,Novartis Animal Health)治療以在下次滋生前除去所有蚤。動物在治療後第7、14、21及28天重新滋生100只成蚤。每次滋生後24小
時時,實施蚤梳計數,隨後藉由Capstar治療。
在治療後第一48小時中,組D(12.5毫克/公斤)及組E(15.0毫克/公斤)分別顯示99.0%及100%之蚤滋生減少(在24小時)及100%及99.4%之蚤滋生減少(在48小時)。組B(7.5毫克/公斤)及C(10.0毫克/公斤)亦顯示較佳之減少功效,二者均達到97.9%減少(在24小時)及分別達到99.4%及100%減少(在48小時)。
自48小時計數直至治療後第29天四個組皆顯示100%或接近100%(所有皆99%)減少之較佳持久功效。
在完成上文實驗1中闡述之研究時,再使用組E中之6只犬實施為期兩週之沖洗研究。
在兩週時間段內,組E中六隻犬中之四隻每週在無殺蟲劑之水浴中沖洗兩次,而組E中其他兩隻犬不沖洗並用作對照。在治療後第43天,使該6只犬滋生100只蚤並然後在第44天藉助蚤梳計數評價其保留蚤滋生之能力。結果顯示於下表1中。
該等結果表明所有犬皆具有低蚤計數並仍對保持蚤滋生有抗力,其在第44天即使在4次徹底之洗髮水水浴沖洗後仍顯示高持久性。
該研究係知情、預期縱向隨機化臨床功效禽畜研究,其用含有3只犬之組,每只犬接受5次治療;4次試驗調配物治療及一次陰性對照(無治療)之一。將動物基於繁殖及治療前蚤計數分級,然後隨機自批分成組。將動物人為滋生並按照標準方法實施寄生蟲計數。
二十(20)只成犬(拉布拉多尋回犬及傑克羅素梗)在第-6天入選該研究並在第-4天每只皆人為滋生100只蚤(貓櫛頭蚤)。在第-1天,進行蚤計數並挑選引入18只犬。基於繁殖及蚤計數將該等犬隨機分成6個相似的含有3只動物的組且該等組隨機分撥進行禽畜研究。每只犬再次滋生100只蚤。在第-1天,再次在所有犬上進行蚤計數。在第0天,用4種不同的15.0毫克/公斤因得克(DPX-KN128)區域局部投藥調配物之一治療組B、C、D及E,如下表2所示。氧化矽上DPX-KN128:DPX-KN127之3:1混合物係該等調配物之原料。該材料含有56.2%因得克(DPX-KN128)。因此每需要1毫克因得克(DPX-KN128),即使用1.78克該混合物。該等調配物以點塗劑量自頸基部至肩部施藥。對於組B、C及D,媒劑係二甲基異山梨醇(DMI)且對於組E,媒劑含有40克/公升聚乙烯基吡咯啶酮、47克/公升乙氧基化蓖麻油、33克/公升乙醇並用1-甲基-2-吡咯啶酮稀釋定容。
仍不對組A實施治療。
在治療後24及48小時實施蚤計數。在治療後第7、14、21、28、35及42天重新進行蚤滋生並且在每次滋生後24及48小時進行蚤計數。
除組B外,用所有調配物之治療在治療後44天內皆達成較佳(100%或接近100%減少)之蚤控制。組B在治療後37天內觀察到較佳控制。該等結果呈現於表3中。
下表4提供某些製備之局部投藥調配物的列表。
實施一系列研究以評價在施用於成年比格(beagle)犬後各種因得克局部溶液安全性、外表及流淌潛力。對於表5中列舉之所有實驗,隨機分配重量介於10與20公斤之間之雄犬及雌犬至每個調配物組。每只犬施用1.5毫升劑量體積,此釋放15毫克因得克/公斤體重之最小劑量。在施藥時,將治療點處之毛髮左右分梳並且將該等調配物直接施用於肩胛之間一處位置的皮膚。然後仔細觀察施藥點及毛髮毛皮之溶液鋪展、殘留物及淹濕跡象並確定是否有任何溶液在治療後流出動物(在5、15、30、60及180分鐘及24小時)。在治療後24小時檢查接近治療點之皮膚及毛髮有無任何不利反應。
表5提供在16個單獨實驗中試驗之調配物的成份列表。除研究編號X07-055-12(6只犬/調配物)及研究X07-055-13及X07-055-14(36只犬/調配物)外,在每一研究中每一調配物皆施藥於四隻犬。
所有該等調配物皆係安全的且對所治療犬之皮膚或毛髮
無不利作用。調配物V、Z、AB、AC、AE、AF、AG及AH確定為具有較佳商用點塗治療特徵。該等較佳特徵包括:施用時無滴落或流掉、乾燥時出現殘留物或晶體最少及施藥點之相對較快乾燥。具有最不期望特徵(即出現滴落/流掉、殘留物及淹濕)之調配物係調配物C、E、G、J、Q及S。剩餘調配物之特徵在二者之間。
Claims (8)
- 一種用於控制家畜滋生體外寄生蟲之區域局部點塗調配物,該調配物以重量計包含:1-50%因得克(Indoxacarb);0.05-80%百滅寧(permethrin);及足量乙醯乙酸乙酯。
- 如請求項第1項所述之調配物,其中前述調配物進一步包含:5-25%因得克(Indoxacarb);30-75%百滅寧(permethrin);及足量乙醯乙酸乙酯。
- 一種用於控制家畜滋生體外寄生蟲之區域局部點塗調配物,該調配物以重量計包含:1-50%因得克(Indoxacarb);0.05-80%百滅寧(permethrin);及足量丙二醇單甲基醚。
- 如請求項第3項所述之調配物,其中前述調配物進一步包含:5-25%因得克(Indoxacarb);30-75%百滅寧(permethrin);及足量丙二醇單甲基醚。
- 一種用於控制家畜滋生體外寄生蟲之區域局部調配物,該調配物以重量計包含:5-25%因得克(Indoxacarb);5-25%費普尼(fipronil);及足量乙醯乙酸乙酯。
- 一種用於控制家畜滋生體外寄生蟲之區域局部調配物,該調配物以重量 計包含:5-25%因得克(Indoxacarb);5-25%費普尼(fipronil);及足量丙二醇單甲基醚。
- 一種區域局部點塗調配物,其實質上由因得克(Indoxacarb)、百滅寧(permethrin)及獸醫學上可接受之溶劑組成,其中該溶劑組成係選自由乙醯乙酸乙酯或丙二醇單甲基醚所組成之群。
- 一種區域局部點塗調配物,其實質上由因得克(Indoxacarb)、費普尼(fipronil)及獸醫學上可接受之溶劑組成,其中該溶劑組成係選自由乙醯乙酸乙酯或二丙二醇單甲基醚所組成之群。
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| UA (1) | UA95967C2 (zh) |
| WO (1) | WO2008030385A2 (zh) |
| ZA (1) | ZA200901429B (zh) |
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| UA108641C2 (uk) | 2010-04-02 | 2015-05-25 | Паразитицидна композиція, яка містить чотири активних агенти, та спосіб її застосування | |
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| BR112016029854B1 (pt) | 2014-06-19 | 2022-01-11 | The Regents Of The University Of Minnesota | Composição para atrair percevejos de cama, método para tratar um artigo, método para tratar uma área infestada com percevejos de cama, armadilha para capturar insetos e método para tratar uma área que está em risco de contaminação com percevejos de cama |
| SI3157534T1 (sl) | 2014-06-19 | 2022-08-31 | Attillaps Holdings | Inhibitorji acetilholinesteraze za zdravljenje dermatoloških obolenj |
| CN104255769A (zh) * | 2014-09-25 | 2015-01-07 | 北京燕化永乐生物科技股份有限公司 | 农药组合物 |
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