WO1997042816A1 - Lutte contre les ectoparasites - Google Patents
Lutte contre les ectoparasites Download PDFInfo
- Publication number
- WO1997042816A1 WO1997042816A1 PCT/IE1997/000038 IE9700038W WO9742816A1 WO 1997042816 A1 WO1997042816 A1 WO 1997042816A1 IE 9700038 W IE9700038 W IE 9700038W WO 9742816 A1 WO9742816 A1 WO 9742816A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- concentrate
- wetting solution
- amount
- present
- animal
- 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.)
- Ceased
Links
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
Definitions
- the invention relates to the control of ectoparasites in animals and in particular to the prevention and control of blowfly strike and/or for the treatment and control of lice, keds and ticks and/or for the treatment and control of scab in animals, especially sheep.
- insecticides for controlling ectoparasites in animals are formulated as emulsifiable concentrates.
- emulsifiable concentrates On dispersion of such concentrates in water generally particles in the micron size range are produced. This particle size range adversely effects the spread of the insecticide on the animal.
- known emulsifiable concentrates are generally formulated using hydrocarbon solvents which in some cases are not environmentally friendly.
- This invention is therefore directed towards providing an improved method for preventing and controlling ectoparasites in animals and to an animal wetting solution used in the method which will overcome at least some of these difficulties.
- the invention provides a method for preventing and controlling ectoparasites in animals by (a) diluting an aqueous emulsion concentrate containing 25 to 250 g/litre of a substantially water insoluble insecticide in a concentrate delivery system containing a surfactant system, and an co-solvent mixture of a N-Ci to C 4 alkyl pyrrolidone and a N-C 6 to C 14 alkyl pyrrolidone to form a homogenous, aqueous animal wetting solution containing from 25 to 500 mg/litre of the insecticide; and (b) wetting the animal with an effective insecticidal amount of said solution.
- the emulsion concentrate is a macroemulsion, hydrogel concentrate or, most preferably an aqueous microemulsion concentrate.
- the ectoparasites may be blowfly, lice, keds, ticks and/or scab.
- the animals are sheep.
- the animals are hooved animals such as cattle, goats, deer, horses or camels.
- the animals may also be domesticated pets such as dogs and cats.
- domesticated pets the concentrate may be formulated as in a standard pet shampoo formulation.
- the animals may be feathered animals, especially poultry.
- the insecticide is a pyrethroid insecticide, especially cypermethrin.
- the concentrate contains from 50 to 150, especially approximately 100 g/1 of the insecticide.
- the wetting solution contains from 80 to 120, especially approximately 100 mg/litre of insecticide. This concentration is particularly advantageous for preventing and controlling blowfly strike and/or for the treatment and control of lice, keds and ticks especially in sheep.
- the wetting solution may contain from 180 to 220, especially approximately 200 mg/litre of insecticide. This concentration is particularly advantageous for the treatment and/or control of scab, especially in sheep.
- the animals are wetted by plunge dipping animals in the wetting solution.
- the method preferably includes the step after dipping a number of animals, of topping up the dipping solution with a solution formed by diluting the concentrate at a dilution ratio of from 1:250 to 1:1000, preferably 1:500.
- the invention provides a method for preventing and controlling blowfly strike and/or for the treatment and control of lice, keds and ticks in sheep by diluting an aqueous microemulsion concentrate containing approximately 100 g/litre of cypermethrin to form a homogenous aqueous sheep dipping solution containing approximately 100 mg/litre of cypermethrin, and plunge dipping sheep in the dipping solution.
- the invention provides a method for the treatment and/or control of scab in sheep by diluting an aqueous microemulsion concentrate containing approximately 100 g/litre of cypermethrin to form a homogenous aqueous sheep dipping solution containing approximately 200 mg/litre of cypermethrin, and plunge dipping sheep in the dipping solution.
- the invention provides an animal wetting solution containing from 0.25 ppm to 50 ppm insecticide per kg body weight, derived from an ectoparasiticidal concentrate containing:
- the ectoparasiticidal concentrate is a microemulsion concentrate.
- the N-C; to Ct, alkyl pyrrolidone is preferably present in the concentrate in an amount of from 3 to 30, preferably 18 to 22 and ideally approximately 20 wt%.
- the N-C ! to C 4 alkyl pyrrolidone is N-methyl-2-pyrrolidone.
- one of the N- C 6 to C 14 alkyl pyrrolidone is present in the concentrate in an amount of from 2 to 15, preferably 8 to 10 and ideally approximately 9 wt% .
- the N-C 6 to C 14 alkyl pyrrolidone is N-octyl-2-pyrrolidone.
- the surfactant system is a mixture of surfactants.
- the surfactant system includes an alkoxylated alkyl phenol which is preferably present in the concentrate in an amount of from 50 to 54, ideally approximately 52 wt%.
- the alkoxylated alkyl phenol is ethoxylated nonyl phenol .
- the surfactant system includes a non-ionic surfactant which is preferably present in the concentrate in an amount of from 5 to 80, preferably 8 to 10 and ideally approximately 9 wt%.
- the non ionic surfactant is a difunctional block copolymer terminating in primary hydroxyl groups .
- the concentrate includes a buffer.
- the buffer is selected from one or more of a phosphated alkoxylated alkylphenol, a hydrophobic acid, or a hydrophobic base.
- the buffer is present in the concentrate in an amount of from 0.025 to 2 wt%, preferably 0.5 to 1.5 wt%, and ideally approximately 1 wt% .
- the buffer is preferably present in an amount to achieve a pH of from 3 to 6.5, preferably 3.5 to 5.5, and ideally approximately 4.
- the buffer may be a phosphated ethoxylated nonylphenol .
- the buffer is preferably present in an amount to achieve a pH of from 8 to 9.
- the animal wetting solution may be in the form of an animal dipping solution, an animal pour-on solution, or in the form of a standard pet shampoo formulation.
- the invention also provides an ectoparasiticidal concentrate for use in forming an animal wetting solution of the invention.
- compositions of the present invention have numerous advantages including at least one of:-
- N-Cj to C 4 pyrrolidones have coating and insecticide complexing properties.
- N-C 6 to C 18 alkyl pyrrolidones have lanolin wetting and spreading properties and are capable of forming micelles when used in the present emulsion concentrates with the ethoxylated nonylphenol detergent and the ethylene oxide-propylene oxide-ethylene oxide block copolymer.
- the formulation given in the Example includes the following branded chemicals:
- Pluronic L31 (Trade Mark of BASF) is a difunctional block copolymer terminating in primary hydroxyl groups . It is a non-ionic surfactant.
- IGEPAL CO-630 (Trade mark of Rhone Poulenc) is an ethoxylated nonylphenol detergent and acts as an emulsifier.
- Rhodofac RE-610 (Trade Mark of Rhone Poulenc) is a phosphated ethoxylated nonylphenol buffer/emulsifier.
- N-methyl-2-pyrrolidone used was AGSOL Exl available from ISP Europe.
- N-octyl-2-pyrrolidone used was AGSOL Ex8 available from ISP Europe.
- a microemulsion concentrate was prepared as follows.
- the N-methyl 2-pyrrolidone is placed in a batch mixing vessel having a volume of 1200 litres and fitted with a propeller mixer.
- the N-octyl-2-pyrrolidone is then added to the batch vessel and the contents are mixed.
- the Igepal CO-630TM is then added to the vessel and mixing is continued.
- Pluronic-LSlTM is added to the vessel with continuing mixing.
- Rhodafac RE 610TM is then added and mixing is continued for 30 minutes.
- Cypermethrin is prepared by liquifying at a temperature of from 37°C to 40°C. The liquified cypermethrin is added to the vessel and mixing is continued for 60 minutes.
- the pale yellow liquid thus formed is poured into multi- layered plastics containers having an internal polyamide layer.
- the containers are of 1 litre, 2 litre and 5 litre capacity.
- N-methyl-2-pyrrolidone and N-octyl-2- pyrrolidone facilitate dissolution.
- the two surfactants, Igepal 00-630TM and Pluronic-L31TM form micelles when the microemulsion concentrate is added to water. These micelles provide a means of incorporating the active into an aqueous vehicle at a concentration greater than the solubility of the active.
- Rhodafac RE 610TM acts as a buffer.
- Cypermethrin normally has a solubility of from 0.01 to 0.2 mg/1 at 20°C.
- microemulsion concentrate of the invention Using the microemulsion concentrate of the invention, however, a solubility of greater than 100 mg/1 can be achieved.
- the microemulsion concentrate has the following analysis:
- Rhodafac RE 610TM 1.0% w/w
- the microemulsion concentrate is used as follows. A dip bath was filled with the required quantity (typically 1000 litres) of clean water. A measured volume of the microemulsion concentrate is poured into the water at a rate of 10 ml of microemulsion concentrate per 10 litres of water to achieve the desired strength of 100 mg/1. After thorough stirring, sheep are immersed in the bath until the fleece is completely saturated with the dip wash. The sheep's head is plunged under at least twice.
- the volume of dip in the bath may be replenished at a rate of 10 ml per 5 litres of added water.
- the overall percentage strike rate was as follows:
- the trial showed that the product is effective for 4-7 weeks in preventing the development of Blowfly myiasis of sheep.
- untreated controls maintained moderate/high burdens of lice and keds for the trial duration.
- the buffer may be selected from a hydrophobic acid or base alternatives such as nonylphenol phosphoric acid, tristearyl phenyl ethoxylated phosphonic acid and dodecylbenzene sulfonic acid.
- the insecticide matrix may require buffering to a pH of 3 to 6.5, preferably 3.5 to 5.5 or as close to pH 4 as convenient for acid stable insecticides and as close to pH 8 to 9 for base stable insecticides.
Landscapes
- Life Sciences & Earth Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Health & Medical Sciences (AREA)
- Toxicology (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Agronomy & Crop Science (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Priority Applications (4)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU31869/97A AU718950B2 (en) | 1996-05-15 | 1997-05-14 | Control of ectoparasites |
| EP97927341A EP0901321A1 (fr) | 1996-05-15 | 1997-05-14 | Lutte contre les ectoparasites |
| NZ332213A NZ332213A (en) | 1996-05-15 | 1997-05-14 | Control of ectoparasites with an aqueous solution of a pyrethroid (cypermethrin) an alkyl pyrrolidone and a surfactant used as an animal wetting solution to control blowfly ticks and scab |
| GB9821315A GB2326341B (en) | 1996-05-15 | 1997-05-14 | Control of ectoparasites |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IE960347A IE960347A1 (en) | 1996-05-15 | 1996-05-15 | Control of ectoparasites |
| IE960347 | 1996-05-15 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| WO1997042816A1 true WO1997042816A1 (fr) | 1997-11-20 |
Family
ID=11041162
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/IE1997/000038 Ceased WO1997042816A1 (fr) | 1996-05-15 | 1997-05-14 | Lutte contre les ectoparasites |
Country Status (8)
| Country | Link |
|---|---|
| EP (1) | EP0901321A1 (fr) |
| AR (1) | AR007143A1 (fr) |
| AU (1) | AU718950B2 (fr) |
| GB (1) | GB2326341B (fr) |
| IE (1) | IE960347A1 (fr) |
| NZ (1) | NZ332213A (fr) |
| WO (1) | WO1997042816A1 (fr) |
| ZA (1) | ZA974164B (fr) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2007143298A3 (fr) * | 2006-04-28 | 2009-04-30 | Summit Vetpharm Llc | Insecticides topiques à concentration élevée contenant des pyréthroïdes |
| EP1432315A4 (fr) * | 2001-09-06 | 2009-07-15 | Isp Investments Inc | Preparation medicamenteuse stable pour le soin des animaux |
| US8178116B2 (en) | 2002-04-29 | 2012-05-15 | Piedmont Pharmaceuticals, Llc | Methods and compositions for treating ectoparasite infestation |
| AU2012203409B2 (en) * | 2006-04-28 | 2012-09-06 | Ceva Animal Health, Llc | High concentration topical insecticides containing pyrethroids |
Families Citing this family (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US8752734B2 (en) | 2009-02-11 | 2014-06-17 | Ds Smith Plastics Limited | Disposable assembly for a reusable urn or vessel |
| US10112820B1 (en) | 2016-01-19 | 2018-10-30 | Dss Rapak, Inc. | Beverage dispensing system with disposable liner and faucet |
Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0388122A1 (fr) * | 1989-03-13 | 1990-09-19 | Scientific Chemicals (Proprietary) Limited | Formulation pesticide |
| WO1991008665A1 (fr) * | 1989-12-11 | 1991-06-27 | Isp Investments Inc. | Systeme de distribution pour produits chimiques destines a l'agriculture |
| WO1992013454A1 (fr) * | 1991-02-12 | 1992-08-20 | Isp Investments Inc. | Stabilisation de microemulsions en utilisant des tampons d'acide hydrophobe |
| WO1993000809A1 (fr) * | 1991-07-05 | 1993-01-21 | Isp Investments Inc. | Systeme de distribution de produits chimiques pour l'agriculture |
-
1996
- 1996-05-15 IE IE960347A patent/IE960347A1/en not_active IP Right Cessation
-
1997
- 1997-05-14 WO PCT/IE1997/000038 patent/WO1997042816A1/fr not_active Ceased
- 1997-05-14 NZ NZ332213A patent/NZ332213A/xx not_active IP Right Cessation
- 1997-05-14 ZA ZA9704164A patent/ZA974164B/xx unknown
- 1997-05-14 AU AU31869/97A patent/AU718950B2/en not_active Ceased
- 1997-05-14 GB GB9821315A patent/GB2326341B/en not_active Expired - Fee Related
- 1997-05-14 EP EP97927341A patent/EP0901321A1/fr not_active Withdrawn
- 1997-05-15 AR ARP970102035A patent/AR007143A1/es not_active Application Discontinuation
Patent Citations (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP0388122A1 (fr) * | 1989-03-13 | 1990-09-19 | Scientific Chemicals (Proprietary) Limited | Formulation pesticide |
| WO1991008665A1 (fr) * | 1989-12-11 | 1991-06-27 | Isp Investments Inc. | Systeme de distribution pour produits chimiques destines a l'agriculture |
| WO1992013454A1 (fr) * | 1991-02-12 | 1992-08-20 | Isp Investments Inc. | Stabilisation de microemulsions en utilisant des tampons d'acide hydrophobe |
| WO1993000809A1 (fr) * | 1991-07-05 | 1993-01-21 | Isp Investments Inc. | Systeme de distribution de produits chimiques pour l'agriculture |
Cited By (7)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| EP1432315A4 (fr) * | 2001-09-06 | 2009-07-15 | Isp Investments Inc | Preparation medicamenteuse stable pour le soin des animaux |
| US8178116B2 (en) | 2002-04-29 | 2012-05-15 | Piedmont Pharmaceuticals, Llc | Methods and compositions for treating ectoparasite infestation |
| US8815270B2 (en) | 2002-04-29 | 2014-08-26 | Piedmont Pharmaceuticals, Llc | Methods and compositions for treating ectoparasite infestation |
| WO2007143298A3 (fr) * | 2006-04-28 | 2009-04-30 | Summit Vetpharm Llc | Insecticides topiques à concentration élevée contenant des pyréthroïdes |
| AU2007257076B2 (en) * | 2006-04-28 | 2012-04-12 | Ceva Animal Health, Llc | High concentration topical insecticides containing pyrethroids |
| AU2012203409B2 (en) * | 2006-04-28 | 2012-09-06 | Ceva Animal Health, Llc | High concentration topical insecticides containing pyrethroids |
| EP2015636A4 (fr) * | 2006-04-28 | 2013-04-10 | Summit Vetpharm Llc | Insecticides topiques à concentration élevée contenant des pyréthroïdes |
Also Published As
| Publication number | Publication date |
|---|---|
| NZ332213A (en) | 2000-04-28 |
| GB9821315D0 (en) | 1998-11-25 |
| EP0901321A1 (fr) | 1999-03-17 |
| GB2326341A (en) | 1998-12-23 |
| ZA974164B (en) | 1998-05-14 |
| AU3186997A (en) | 1997-12-05 |
| AR007143A1 (es) | 1999-10-13 |
| AU718950B2 (en) | 2000-05-04 |
| IE960347A1 (en) | 1997-11-19 |
| GB2326341B (en) | 2000-04-12 |
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