NZ523353A - Starch-based, meatless extruded shaped articles for easy administration to animals - Google Patents
Starch-based, meatless extruded shaped articles for easy administration to animalsInfo
- Publication number
- NZ523353A NZ523353A NZ523353A NZ52335301A NZ523353A NZ 523353 A NZ523353 A NZ 523353A NZ 523353 A NZ523353 A NZ 523353A NZ 52335301 A NZ52335301 A NZ 52335301A NZ 523353 A NZ523353 A NZ 523353A
- Authority
- NZ
- New Zealand
- Prior art keywords
- spp
- starch
- active compound
- alkyl
- extruded shaped
- Prior art date
Links
- 229920002472 Starch Polymers 0.000 title claims abstract description 39
- 235000019698 starch Nutrition 0.000 title claims abstract description 38
- 239000008107 starch Substances 0.000 title claims abstract description 36
- 241001465754 Metazoa Species 0.000 title claims abstract description 29
- 150000001875 compounds Chemical class 0.000 claims abstract description 55
- 239000003814 drug Substances 0.000 claims abstract description 9
- 238000004519 manufacturing process Methods 0.000 claims abstract description 4
- 108010002156 Depsipeptides Proteins 0.000 claims description 24
- 238000000034 method Methods 0.000 claims description 12
- 244000079386 endoparasite Species 0.000 claims description 11
- 239000000463 material Substances 0.000 claims description 11
- 230000001717 pathogenic effect Effects 0.000 claims description 11
- OHRURASPPZQGQM-GCCNXGTGSA-N romidepsin Chemical compound O1C(=O)[C@H](C(C)C)NC(=O)C(=C/C)/NC(=O)[C@H]2CSSCC\C=C\[C@@H]1CC(=O)N[C@H](C(C)C)C(=O)N2 OHRURASPPZQGQM-GCCNXGTGSA-N 0.000 claims description 10
- 235000013372 meat Nutrition 0.000 claims description 9
- 210000004185 liver Anatomy 0.000 claims description 7
- 150000001413 amino acids Chemical class 0.000 claims description 6
- BVKZGUZCCUSVTD-UHFFFAOYSA-N carbonic acid Chemical group OC(O)=O BVKZGUZCCUSVTD-UHFFFAOYSA-N 0.000 claims description 6
- 229920002301 cellulose acetate Polymers 0.000 claims description 5
- 244000144977 poultry Species 0.000 claims description 5
- 238000002360 preparation method Methods 0.000 claims description 5
- 239000003995 emulsifying agent Substances 0.000 claims description 4
- 239000003906 humectant Substances 0.000 claims description 4
- 239000003755 preservative agent Substances 0.000 claims description 4
- 238000007493 shaping process Methods 0.000 claims description 4
- 235000019629 palatability Nutrition 0.000 claims description 3
- 239000004014 plasticizer Substances 0.000 claims description 3
- 239000007858 starting material Substances 0.000 claims description 3
- 235000000346 sugar Nutrition 0.000 claims description 3
- 230000002335 preservative effect Effects 0.000 claims description 2
- 241000282472 Canis lupus familiaris Species 0.000 abstract description 11
- 235000019568 aromas Nutrition 0.000 abstract description 6
- 241000282326 Felis catus Species 0.000 abstract description 5
- 241000283086 Equidae Species 0.000 abstract description 3
- 239000003795 chemical substances by application Substances 0.000 abstract description 2
- -1 benzyloxycarbonyl radicals Chemical class 0.000 description 98
- 239000000203 mixture Substances 0.000 description 16
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 14
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 11
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 11
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 10
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 9
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 description 9
- 229910052736 halogen Inorganic materials 0.000 description 9
- 150000002367 halogens Chemical class 0.000 description 9
- 125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 9
- 229910052739 hydrogen Inorganic materials 0.000 description 7
- 239000001257 hydrogen Substances 0.000 description 7
- 125000002887 hydroxy group Chemical group [H]O* 0.000 description 7
- 150000003254 radicals Chemical group 0.000 description 7
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 7
- 125000003229 2-methylhexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 6
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 6
- 125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 125000004210 cyclohexylmethyl group Chemical group [H]C([H])(*)C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C1([H])[H] 0.000 description 6
- 125000003187 heptyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000004435 hydrogen atom Chemical group [H]* 0.000 description 6
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 6
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 6
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 6
- 125000002347 octyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 6
- 125000001147 pentyl group Chemical group C(CCCC)* 0.000 description 6
- 125000003548 sec-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 6
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 6
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 6
- 229920002554 vinyl polymer Polymers 0.000 description 6
- 125000003710 aryl alkyl group Chemical group 0.000 description 5
- 230000037396 body weight Effects 0.000 description 5
- 125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 5
- 230000003287 optical effect Effects 0.000 description 5
- 125000000217 alkyl group Chemical group 0.000 description 4
- 238000010171 animal model Methods 0.000 description 4
- 125000003118 aryl group Chemical group 0.000 description 4
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
- 125000006622 cycloheptylmethyl group Chemical group 0.000 description 4
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
- 125000004851 cyclopentylmethyl group Chemical group C1(CCCC1)C* 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 125000004029 hydroxymethyl group Chemical group [H]OC([H])([H])* 0.000 description 4
- 235000013594 poultry meat Nutrition 0.000 description 4
- 125000006413 ring segment Chemical group 0.000 description 4
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 4
- 125000004066 1-hydroxyethyl group Chemical group [H]OC([H])([*])C([H])([H])[H] 0.000 description 3
- JQCSUVJDBHJKNG-UHFFFAOYSA-N 1-methoxy-ethyl Chemical group C[CH]OC JQCSUVJDBHJKNG-UHFFFAOYSA-N 0.000 description 3
- CIWBSHSKHKDKBQ-JLAZNSOCSA-N Ascorbic acid Chemical compound OC[C@H](O)[C@H]1OC(=O)C(O)=C1O CIWBSHSKHKDKBQ-JLAZNSOCSA-N 0.000 description 3
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 3
- 241000282887 Suidae Species 0.000 description 3
- 241000209140 Triticum Species 0.000 description 3
- 235000021307 Triticum Nutrition 0.000 description 3
- 235000015278 beef Nutrition 0.000 description 3
- 238000009395 breeding Methods 0.000 description 3
- 230000001488 breeding effect Effects 0.000 description 3
- 125000004369 butenyl group Chemical group C(=CCC)* 0.000 description 3
- 125000002057 carboxymethyl group Chemical group [H]OC(=O)C([H])([H])[*] 0.000 description 3
- 239000000969 carrier Substances 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 3
- 125000001041 indolyl group Chemical group 0.000 description 3
- 244000144972 livestock Species 0.000 description 3
- 125000004184 methoxymethyl group Chemical group [H]C([H])([H])OC([H])([H])* 0.000 description 3
- 235000019426 modified starch Nutrition 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- QTBSBXVTEAMEQO-UHFFFAOYSA-M Acetate Chemical compound CC([O-])=O QTBSBXVTEAMEQO-UHFFFAOYSA-M 0.000 description 2
- 229910002012 Aerosil® Inorganic materials 0.000 description 2
- 241000272517 Anseriformes Species 0.000 description 2
- 241000204727 Ascaridia Species 0.000 description 2
- 241000283690 Bos taurus Species 0.000 description 2
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 2
- PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 description 2
- 229930091371 Fructose Natural products 0.000 description 2
- 239000005715 Fructose Substances 0.000 description 2
- RFSUNEUAIZKAJO-ARQDHWQXSA-N Fructose Chemical compound OC[C@H]1O[C@](O)(CO)[C@@H](O)[C@@H]1O RFSUNEUAIZKAJO-ARQDHWQXSA-N 0.000 description 2
- 241000282412 Homo Species 0.000 description 2
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- 240000003183 Manihot esculenta Species 0.000 description 2
- 235000016735 Manihot esculenta subsp esculenta Nutrition 0.000 description 2
- 229920000881 Modified starch Polymers 0.000 description 2
- 229910019142 PO4 Inorganic materials 0.000 description 2
- 241001494479 Pecora Species 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
- VYPSYNLAJGMNEJ-UHFFFAOYSA-N Silicium dioxide Chemical compound O=[Si]=O VYPSYNLAJGMNEJ-UHFFFAOYSA-N 0.000 description 2
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- 235000002595 Solanum tuberosum Nutrition 0.000 description 2
- CZMRCDWAGMRECN-UGDNZRGBSA-N Sucrose Chemical compound O[C@H]1[C@H](O)[C@@H](CO)O[C@@]1(CO)O[C@@H]1[C@H](O)[C@@H](O)[C@H](O)[C@@H](CO)O1 CZMRCDWAGMRECN-UGDNZRGBSA-N 0.000 description 2
- 229930006000 Sucrose Natural products 0.000 description 2
- GWEVSGVZZGPLCZ-UHFFFAOYSA-N Titan oxide Chemical compound O=[Ti]=O GWEVSGVZZGPLCZ-UHFFFAOYSA-N 0.000 description 2
- 240000008042 Zea mays Species 0.000 description 2
- 235000016383 Zea mays subsp huehuetenangensis Nutrition 0.000 description 2
- 235000002017 Zea mays subsp mays Nutrition 0.000 description 2
- 125000005041 acyloxyalkyl group Chemical group 0.000 description 2
- 125000003342 alkenyl group Chemical group 0.000 description 2
- 125000004183 alkoxy alkyl group Chemical group 0.000 description 2
- 125000005078 alkoxycarbonylalkyl group Chemical group 0.000 description 2
- 125000000278 alkyl amino alkyl group Chemical group 0.000 description 2
- 125000006350 alkyl thio alkyl group Chemical group 0.000 description 2
- 125000004103 aminoalkyl group Chemical group 0.000 description 2
- 125000005160 aryl oxy alkyl group Chemical group 0.000 description 2
- 125000004429 atom Chemical group 0.000 description 2
- WPYMKLBDIGXBTP-UHFFFAOYSA-N benzoic acid group Chemical group C(C1=CC=CC=C1)(=O)O WPYMKLBDIGXBTP-UHFFFAOYSA-N 0.000 description 2
- 125000005242 carbamoyl alkyl group Chemical group 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 125000004181 carboxyalkyl group Chemical group 0.000 description 2
- 229910052801 chlorine Inorganic materials 0.000 description 2
- 239000000460 chlorine Substances 0.000 description 2
- 125000001316 cycloalkyl alkyl group Chemical group 0.000 description 2
- 125000000753 cycloalkyl group Chemical group 0.000 description 2
- 125000004985 dialkyl amino alkyl group Chemical group 0.000 description 2
- 125000001301 ethoxy group Chemical group [H]C([H])([H])C([H])([H])O* 0.000 description 2
- 229910052731 fluorine Inorganic materials 0.000 description 2
- 239000011737 fluorine Substances 0.000 description 2
- 235000013305 food Nutrition 0.000 description 2
- 125000002795 guanidino group Chemical group C(N)(=N)N* 0.000 description 2
- 239000001341 hydroxy propyl starch Substances 0.000 description 2
- 125000002768 hydroxyalkyl group Chemical group 0.000 description 2
- DNZMDASEFMLYBU-RNBXVSKKSA-N hydroxyethyl starch Chemical compound OC[C@H]1O[C@H](O)[C@H](O)[C@@H](O)[C@@H]1O.OCCOC[C@H]1O[C@H](OCCO)[C@H](OCCO)[C@@H](OCCO)[C@@H]1OCCO DNZMDASEFMLYBU-RNBXVSKKSA-N 0.000 description 2
- 229940050526 hydroxyethylstarch Drugs 0.000 description 2
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- 235000009973 maize Nutrition 0.000 description 2
- 125000005358 mercaptoalkyl group Chemical group 0.000 description 2
- 125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 description 2
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- 125000000286 phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 2
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- 239000000902 placebo Substances 0.000 description 2
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- 125000005913 (C3-C6) cycloalkyl group Chemical group 0.000 description 1
- 125000006272 (C3-C7) cycloalkyl group Chemical group 0.000 description 1
- 125000003088 (fluoren-9-ylmethoxy)carbonyl group Chemical group 0.000 description 1
- ZORQXIQZAOLNGE-UHFFFAOYSA-N 1,1-difluorocyclohexane Polymers FC1(F)CCCCC1 ZORQXIQZAOLNGE-UHFFFAOYSA-N 0.000 description 1
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- 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 1
- WEYSQARHSRZNTC-UHFFFAOYSA-N 1h-benzimidazol-2-ylcarbamic acid Chemical class C1=CC=C2NC(NC(=O)O)=NC2=C1 WEYSQARHSRZNTC-UHFFFAOYSA-N 0.000 description 1
- FSVJFNAIGNNGKK-UHFFFAOYSA-N 2-[cyclohexyl(oxo)methyl]-3,6,7,11b-tetrahydro-1H-pyrazino[2,1-a]isoquinolin-4-one Chemical compound C1C(C2=CC=CC=C2CC2)N2C(=O)CN1C(=O)C1CCCCC1 FSVJFNAIGNNGKK-UHFFFAOYSA-N 0.000 description 1
- 125000000094 2-phenylethyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])* 0.000 description 1
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Classifications
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- 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
- A61K9/20—Pills, tablets, discs, rods
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- 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
- A61K9/0053—Mouth and digestive tract, i.e. intraoral and peroral administration
- A61K9/0056—Mouth soluble or dispersible forms; Suckable, eatable, chewable coherent forms; Forms rapidly disintegrating in the mouth; Lozenges; Lollipops; Bite capsules; Baked products; Baits or other oral forms for animals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P33/00—Antiparasitic agents
Landscapes
- Health & Medical Sciences (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Public Health (AREA)
- Animal Behavior & Ethology (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Zoology (AREA)
- Nutrition Science (AREA)
- Physiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Tropical Medicine & Parasitology (AREA)
- Organic Chemistry (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
- Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)
- Fodder In General (AREA)
- Feed For Specific Animals (AREA)
- Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10031044A DE10031044A1 (de) | 2000-06-26 | 2000-06-26 | Endoparasitizide Mittel zur freiwilligen oralen Aufnahme durch Tiere |
| PCT/EP2001/006836 WO2002000202A1 (de) | 2000-06-26 | 2001-06-18 | Endoparasitizide mittel zur freiwilligen oralen aufnahme durch tiere |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| NZ523353A true NZ523353A (en) | 2006-09-29 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| NZ523353A NZ523353A (en) | 2000-06-26 | 2001-06-18 | Starch-based, meatless extruded shaped articles for easy administration to animals |
Country Status (22)
Families Citing this family (24)
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|---|---|---|---|---|
| DE10104362A1 (de) * | 2001-02-01 | 2002-08-08 | Bayer Ag | Kristallmodifikation eines cyclischen Depsipeptids mit besserer Wirksamkeit |
| WO2003030653A2 (en) * | 2001-10-05 | 2003-04-17 | Rubicon Scientific Llc | Animal feeds including actives and methods of using same |
| ATE419373T1 (de) * | 2002-11-12 | 2009-01-15 | Kitasato Inst | Anthelmintische substanz fki-1033 und verfahren zur herstellung davon |
| DE10328666A1 (de) * | 2003-06-26 | 2005-01-13 | Bayer Healthcare Ag | Tabletten enthaltend Geschmacks-und/oder Aromastoffe |
| TWI366442B (en) * | 2003-07-30 | 2012-06-21 | Novartis Ag | Palatable ductile chewable veterinary composition |
| US7396819B2 (en) * | 2003-08-08 | 2008-07-08 | Virbac Corporation | Anthelmintic formulations |
| DE10351448A1 (de) * | 2003-11-04 | 2005-06-09 | Bayer Healthcare Ag | Geschmackstoffhaltige Arzneimittelformulierungen mit verbesserten pharmazeutischen Eigenschaften |
| WO2005094210A2 (en) * | 2004-03-12 | 2005-10-13 | The Hartz Mountain Corporation | Multi-action anthelmintic formulations |
| DE102008022520A1 (de) * | 2008-05-07 | 2009-11-12 | Bayer Animal Health Gmbh | Feste Arzneimittelformulierung mit verzögerter Freisetzung |
| DE102009012423A1 (de) * | 2009-03-10 | 2010-09-16 | Bayer Animal Health Gmbh | Zubereitung auf Ölbasis |
| US8697174B2 (en) | 2010-01-27 | 2014-04-15 | Ainsworth Pet Nutrition | Treats and methods for producing same |
| ES2806256T3 (es) | 2010-10-12 | 2021-02-17 | Bayer Ip Gmbh | Productos masticables blandos no basados en almidón |
| WO2013037650A1 (fr) | 2011-09-15 | 2013-03-21 | Friulchem Spa | Compositions pour administration orale aux animaux, leurs procedes d'obtention et leurs utilisations |
| WO2014033230A1 (fr) | 2012-08-31 | 2014-03-06 | Friulchem Spa | Compositions pour administration orale aux animaux, leurs procedes d'obtention et leurs utilisations |
| CA2859787C (en) | 2011-12-21 | 2020-09-08 | Bayer Intellectual Property Gmbh | Preparations containing amorphous emodepside |
| TR201909461T4 (tr) | 2012-02-06 | 2019-07-22 | Boehringer Ingelheim Animal Health Usa Inc | Si̇stemi̇k olarak etki̇ eden akti̇f maddeleri̇ i̇çeren parazi̇ti̇si̇dal oral veteri̇nerli̇ğe ai̇t bi̇leşi̇mler, bunlarin yöntemleri̇ ve kullanimlari |
| ES2633611T5 (es) | 2012-04-04 | 2023-09-26 | Intervet Int Bv | Composiciones farmacéuticas orales sólidas de compuestos de isoxazolina |
| ES2916216T3 (es) | 2015-05-20 | 2022-06-29 | Boehringer Ingelheim Animal Health Usa Inc | Compuestos de depsipéptidos antihelmínticos |
| US9808010B2 (en) | 2015-07-06 | 2017-11-07 | Virbac Corporation | Chewable composition |
| AU2016380868B2 (en) | 2015-12-28 | 2019-11-28 | Boehringer Ingelheim Animal Health USA Inc. | Anthelmintic depsipeptide compounds |
| WO2017194415A1 (de) * | 2016-05-12 | 2017-11-16 | Bayer Animal Health Gmbh | Verfahren zur herstellung von formkörpern zur verabreichung an tiere |
| AU2017361099A1 (en) | 2016-11-16 | 2019-06-06 | Boehringer Ingelheim Animal Health USA Inc. | Anthelmintic depsipeptide compounds |
| EP3878436A1 (en) | 2020-03-09 | 2021-09-15 | Bayer Animal Health GmbH | Soft chewable formed body for the administration to animals |
| CN113558008A (zh) * | 2021-07-20 | 2021-10-29 | 中国科学院动物研究所 | 基于小型哺乳动物觅食的媒介传播疾病控制方法 |
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-
2000
- 2000-06-26 DE DE10031044A patent/DE10031044A1/de not_active Withdrawn
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2001
- 2001-06-13 AR ARP010102815A patent/AR030231A1/es unknown
- 2001-06-18 MX MXPA02012597A patent/MXPA02012597A/es active IP Right Grant
- 2001-06-18 US US10/311,419 patent/US7914816B2/en not_active Expired - Fee Related
- 2001-06-18 DE DE50114129T patent/DE50114129D1/de not_active Expired - Lifetime
- 2001-06-18 ES ES01957856T patent/ES2310185T3/es not_active Expired - Lifetime
- 2001-06-18 HU HU0301252A patent/HUP0301252A3/hu unknown
- 2001-06-18 KR KR1020027017197A patent/KR20030023874A/ko not_active Withdrawn
- 2001-06-18 WO PCT/EP2001/006836 patent/WO2002000202A1/de not_active Ceased
- 2001-06-18 EP EP01957856A patent/EP1296655B1/de not_active Revoked
- 2001-06-18 AT AT01957856T patent/ATE401059T1/de not_active IP Right Cessation
- 2001-06-18 JP JP2002504984A patent/JP5356637B2/ja not_active Expired - Fee Related
- 2001-06-18 CN CN01811848A patent/CN1438879A/zh active Pending
- 2001-06-18 BR BRPI0111914A patent/BRPI0111914B1/pt not_active IP Right Cessation
- 2001-06-18 NZ NZ523353A patent/NZ523353A/en not_active IP Right Cessation
- 2001-06-18 RU RU2003102367/15A patent/RU2003102367A/ru not_active Application Discontinuation
- 2001-06-18 CA CA2413698A patent/CA2413698C/en not_active Expired - Fee Related
- 2001-06-18 IL IL15335701A patent/IL153357A0/xx unknown
- 2001-06-18 AU AU2001279664A patent/AU2001279664C1/en not_active Ceased
- 2001-06-18 CZ CZ20024141A patent/CZ20024141A3/cs unknown
- 2001-06-18 PL PL01369267A patent/PL369267A1/xx not_active Application Discontinuation
- 2001-06-18 AU AU7966401A patent/AU7966401A/xx active Pending
-
2002
- 2002-12-20 ZA ZA200210351A patent/ZA200210351B/en unknown
- 2002-12-23 NO NO20026209A patent/NO20026209L/no not_active Application Discontinuation
-
2006
- 2006-06-02 AU AU2006202367A patent/AU2006202367A1/en not_active Abandoned
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2010
- 2010-07-12 AU AU2010202939A patent/AU2010202939A1/en not_active Abandoned
Also Published As
| Publication number | Publication date |
|---|---|
| CA2413698C (en) | 2011-11-08 |
| AU2010202939A1 (en) | 2010-07-29 |
| BRPI0111914B1 (pt) | 2016-06-14 |
| JP5356637B2 (ja) | 2013-12-04 |
| BR0111914A (pt) | 2003-05-13 |
| AU2006202367A1 (en) | 2006-06-22 |
| HUP0301252A3 (en) | 2004-09-28 |
| EP1296655A1 (de) | 2003-04-02 |
| US7914816B2 (en) | 2011-03-29 |
| CA2413698A1 (en) | 2002-12-23 |
| IL153357A0 (en) | 2003-07-06 |
| JP2004504277A (ja) | 2004-02-12 |
| EP1296655B1 (de) | 2008-07-16 |
| AU2001279664B2 (en) | 2006-03-02 |
| AU2001279664C1 (en) | 2010-06-10 |
| DE50114129D1 (de) | 2008-08-28 |
| AU7966401A (en) | 2002-01-08 |
| HUP0301252A2 (hu) | 2003-08-28 |
| KR20030023874A (ko) | 2003-03-20 |
| RU2003102367A (ru) | 2004-07-27 |
| MXPA02012597A (es) | 2003-05-14 |
| ATE401059T1 (de) | 2008-08-15 |
| US20040043925A1 (en) | 2004-03-04 |
| AR030231A1 (es) | 2003-08-13 |
| CN1438879A (zh) | 2003-08-27 |
| ZA200210351B (en) | 2004-02-04 |
| CZ20024141A3 (cs) | 2003-03-12 |
| ES2310185T3 (es) | 2009-01-01 |
| PL369267A1 (en) | 2005-04-18 |
| NO20026209L (no) | 2003-01-23 |
| NO20026209D0 (no) | 2002-12-23 |
| WO2002000202A1 (de) | 2002-01-03 |
| DE10031044A1 (de) | 2002-01-03 |
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