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WO2000047048A1 - Pesticide treatment - Google Patents

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Publication number
WO2000047048A1
WO2000047048A1 PCT/AU2000/000071 AU0000071W WO0047048A1 WO 2000047048 A1 WO2000047048 A1 WO 2000047048A1 AU 0000071 W AU0000071 W AU 0000071W WO 0047048 A1 WO0047048 A1 WO 0047048A1
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WO
WIPO (PCT)
Prior art keywords
composition
active
actives
residue
level
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
Application number
PCT/AU2000/000071
Other languages
French (fr)
Inventor
Paul John Martin
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Virbac Australia Pty Ltd
Original Assignee
Virbac Australia Pty Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Virbac Australia Pty Ltd filed Critical Virbac Australia Pty Ltd
Priority to AU27837/00A priority Critical patent/AU2783700A/en
Priority to NZ513186A priority patent/NZ513186A/en
Publication of WO2000047048A1 publication Critical patent/WO2000047048A1/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N47/00Biocides, 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
    • A01N47/08Biocides, 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
    • A01N47/28Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N<
    • A01N47/34Ureas or thioureas containing the groups >N—CO—N< or >N—CS—N< containing the groups, e.g. biuret; Thio analogues thereof; Urea-aldehyde condensation products
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/90Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having two or more relevant hetero rings, condensed among themselves or with a common carbocyclic ring system
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION 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
    • A01N61/00Biocides, pest repellants or attractants, or plant growth regulators containing substances of unknown or undetermined composition, e.g. substances characterised only by the mode of action

Definitions

  • This invention relates to pesticidal compositions having the particular, but not sole,
  • MRLs act as a
  • MRLs are specific for tissue type and pesticide. They are generally determined on a per molecule of pesticide residue basis. Lower
  • Substitute Sheet levels of residue equate to shorter WHP. If the pesticide residue levels of a tissue are below the
  • composition for the control of pests and plants and animals or one which provides the public
  • the invention relates to a composition including two or more actives where each
  • the combination of actives provide a high kill rate.
  • composition is suitable for administration to warm blooded animals.
  • the actives are selected from the group comprising anthelmintics, miticides,
  • tickicides tickicides, antibiotics and insecticides, and other compounds used to treat pests of plants and
  • the actives are selected from the group comprising avermectins, synthetic
  • the actives selected for the composition share the same mode of action.
  • the invention relates to a method of devising a composition, including
  • the invention relates to a method of manufacturing a pesticidal
  • composition containing two or more actives including taking a first active which is known to
  • determining the LD 90 of a second active for said target pest combining the LD 90 quantity of the first and second actives with a suitable carrier to provide an effective pesticidal composition.
  • the invention relates to a method of treating a warm blooded animal by administering to that animal the compositions of the present invention or compositions made by
  • the invention in another related aspect relates to a method of treating a warm blooded animal by administering to the animal simultaneously or within a relatively short period of time at least
  • This invention may also broadly be said to consist in the parts, elements and features referred to
  • Pesticides can be classed in different groups on the basis of their mode of action.
  • the mode of action of the avermectins is thought to be by inhibition of the neuron transmitter
  • GABA gamma amino butyric acid
  • ivermectin eprinomectin.
  • moxidectin act by this mode.
  • the synthetic pyrethroids are a different class of nerve poisons but all synthetic pyrethroids work the same way.
  • composition consists of two or more
  • pesticidally active compounds each present in lower levels than would individually give rise to
  • the total activity of the composition is at least the sum of that of the
  • composition which is a component of the composition means that the residue levels for each active should
  • compositions of the present invention may be arrived at in a number of ways.
  • a first active is selected and the maximum of allowable residue level is determined. This will be described
  • the amount of the fist active added should be less
  • a second active is selected and the maximum residue level should be determined.
  • the kill rate of the composition can be estimated by comparing amount of each active added
  • a more accurate kill rate can be determined by
  • composition can be arrived at by taking a first active which is known to kill the
  • LD 90 amount exceeds the maximum residue level a lower kill rate, eg LD 80 will need to
  • each active is selected and perhaps a third active added.
  • the selected quantities of each active are
  • composition with a LD 99 or greater effective kill rate of the target pest may be achieved with
  • pesticidal composition may be any suitable pesticidal composition.
  • the target pest may contain more than two actives, where this is the case the amount of each of the independent actives required to give a combined LD 99 or greater effective kill rate of the target pest may be less than the levels indicated in the paragraph above.
  • composition is prepared by dissolving the actives in the oily carrier.
  • the final volume is
  • compositions were administered to beef cattle as at a rate of 1 ml per 10
  • the milk residue levels were tested every 12 hours for 7 days from administration.
  • the milk residue levels were tested every 12 hours for 7 days from administration.
  • abamectin or a combination of abamectin and ivermectin As can be clearly seen the abamectin and ivermectin residues remained low throughout the test period, both levels remaining below
  • the invention provides the advantage of limiting the WHP to which valuable commodities are subjected, whilst maintaining an effective level of control of pests.
  • This has advantages for primary and secondary industries. For example, decreased periods before cows can be milked or

Landscapes

  • Life Sciences & Earth Sciences (AREA)
  • Agronomy & Crop Science (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Health & Medical Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Dentistry (AREA)
  • General Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
  • Environmental Sciences (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)

Abstract

Many pesticidal treatments involve the use of pesticides which break down to harmful residues. Withholding periods apply where the level of residue in the relevant plant or animal tissue exceeds maximum residue level allowed for that pesticide by the regulatory bodies. The invention relates to a composition which avoids the imposition of a withholding period while conferring effective relief from infestations of pests, by incorporating 2 or more active pesticidal compounds. Each pesticidally active compound is present in a sufficiently small amount so as not to give exceed the allowable residue level thereby avoiding imposition of a withholding period, whilst the combined effect of the actives is such as to give the required pesticidal kill rate.

Description

PESTICIDE TREATMENT
FIELD OF THE INVENTION:
This invention relates to pesticidal compositions having the particular, but not sole,
characteristic of reduced withholding periods for food and animal products.
BACKGROUND:
Many primary and secondary industries rely on plants and animals to produce goods that are
then modified and processed for sale.
The yields produced by such plants and animals are often detrimentally affected by their
infestation with pests. This has necessitated the use of pesticides to curb infection rates and pest
loads on primary producers. However, the compounds used may cause detrimental effects on
humans and other animals, and therefore various Administrative Bodies, including the
Australian National Registration Authority, impose 'withholding periods' on the goods of so-
treated plants and animals.
Withholding periods (WHPs) for plant and animal products are the periods following treatment
with a pesticide, during which so-treated plant and animal products cannot be used or consumed
by humans or other animals. These periods are based on the level of pesticide residue in plant or
animal tissue following treatment. Maximum Residue Levels (MRLs) are the maximum
acceptable level of pesticide residue in tissues at the time of slaughter or harvest. MRLs act as a
safety threshold, above which a WHP must be imposed. MRLs are specific for tissue type and pesticide. They are generally determined on a per molecule of pesticide residue basis. Lower
Substitute Sheet levels of residue equate to shorter WHP. If the pesticide residue levels of a tissue are below the
MRL then no WHP will be imposed.
Current methods of pesticide treatment result in tissue residue levels in excess of the MRLs and
therefore necessitate a WHP. A typical example would be the treatment of cattle with 200
μg/kg of abamectin by subcutaneous injection or 500 μg/kg by pour on application. This results
in a residue level well above the MRL of 0.005 mg/kg in milk after treatment.
The situation is similar for the wool industry with there being a maximum acceptable residue
level for the handling of wool. This necessitates wool being subjected to a WHP after treatment
before it can be collected or otherwise handled. The wool WHPs in Australia, are still under
discussion between various Registry Bodies, but the current recommendation is not to use
products within 2 to 6 months of harvesting the wool.
The use of chemicals on crop species necessitates a withholding period for consumption of the
products by humans or other animals.
The imposition of a WHP may lead to delays in processing of products which can be expensive
and inconvenient. Accordingly a number of solutions have been addressed. The majority of the
solutions to date have centered on finding new pesticidal compounds which are without the
harmful residues or at least have decreased the levels of residues, eliminating or at least decreasing the period of the applicable WHP. This approach has had varying levels of success,
however is expensive and requires the discovery and registration of new parasiticidal compounds. OBJECT:
It is an object of this invention to provide an improved pesticidal composition for the control of
pests of plants and animals, or one which provides the public with a useful choice.
It is a further object of this invention to provide an improved method of designing a pesticidal
composition for the control of pests and plants and animals, or one which provides the public
with a useful choice.
STATEMENT OF INVENTION:
In one aspect the invention relates to a composition including two or more actives where each
active is present in the amount which is less than the amount of that active which would give
rise to a residue which exceeds the maximum residue level.
Preferably the combination of actives provide a high kill rate.
Preferably the composition is suitable for administration to warm blooded animals.
Preferably the actives are selected from the group comprising anthelmintics, miticides,
tickicides, antibiotics and insecticides, and other compounds used to treat pests of plants and
animals.
More preferably the actives are selected from the group comprising avermectins, synthetic
pyrethroids, benzimidizoles, benzophenol ureas, insect group regulators, antibodies, and
pyrazoles.
Preferably the actives selected for the composition share the same mode of action. In another related aspect the invention relates to a method of devising a composition, including
two or more active ingredients, wherein the amount of each active included is less than the
amount giving rise to a level of residue which exceeds the maximum residue level.
In a further related aspect the invention relates to a method of manufacturing a pesticidal
composition containing two or more actives, including taking a first active which is known to
kill a target pest and to determine the LD 90 quantity of the first active for said target pest and
determining the LD 90 of a second active for said target pest, combining the LD 90 quantity of the first and second actives with a suitable carrier to provide an effective pesticidal composition.
In another related aspect the invention relates to a method of treating a warm blooded animal by administering to that animal the compositions of the present invention or compositions made by
the method of the present invention.
In another related aspect the invention relates to a method of treating a warm blooded animal by administering to the animal simultaneously or within a relatively short period of time at least
two actives, the dose of each active administered being less than results in a residue exceeding
the maximum residue levels or at least in a reduced withholding period or export slaughter
interval.
This invention may also broadly be said to consist in the parts, elements and features referred to
or indicated in the specification of the application, individually or collectively, and any or all
combinations of any two or more of the parts, elements or features, and where specific features
are mentioned herein which have known equivalents such equivalents are deemed to be
incorporated herein as individually set forth. PREFERRED EMBODIMENT:
The following examples are given by way of illustration only and shall not be taken as being in
any way limiting as to the spirit or scope of the invention.
Pesticides can be classed in different groups on the basis of their mode of action. The mode of
action is the pharmacological or pharmacokinetic actions of the active ingredient. For example,
the mode of action of the avermectins is thought to be by inhibition of the neuron transmitter,
gamma amino butyric acid (GABA). All the members of this class of molecule, eg abamectin,
ivermectin, eprinomectin. moxidectin act by this mode. The synthetic pyrethroids are a different class of nerve poisons but all synthetic pyrethroids work the same way.
Where pesticides with the same mode of action are chosen for the composition it is likely that
there will be synergy between those products in dealing with a particular pest (although synergy
is not a necessary feature of this invention). It is preferable although not vital for the different
actives to share the same mode of action. The proviso being that a composition which is
suitable for each of the active compounds can be arrived at. It may be that the use of a mixture
of compounds with different modes of action may confer advantage in a given composition
which compensate for any potential loss in kill rate, for example through overlap of susceptible and resistant individuals.
It has been discovered that effective control of pests of plants and animals may be achieved by
treatment with a composition which contains two or more actives each present in a level which
results in residue levels which are less than the Maximum Residue Level. The important feature of the invention is that the composition consists of two or more
pesticidally active compounds each present in lower levels than would individually give rise to
an effective kill rate. The total activity of the composition is at least the sum of that of the
individual pesticidally active compounds but the residue (and consequently the withholding
period) is calculated on the basis of individual molecules. For example if two actives with the
same mode of action are used at the LD 90 level for a target pest one after the other then active
A will kill 90% of the pests. Active B will kill 90 % of the remaining 10%, of the combined
effect will be a kill rate of 99% - known as a combined LD 99. Similarly if A and B are
administered together. Giving a lower dose of each individual pesticidally active compound
which is a component of the composition means that the residue levels for each active should
fall below the maximum residue level, therefore we expect a decreased or nil withholding period
for products of plants and animals treated with these compositions.
The compositions of the present invention may be arrived at in a number of ways. Some
examples are given below:
A first active is selected and the maximum of allowable residue level is determined. This will
usually be set by from the government departments responsible for registration of veterinary
formations or health and safety regulations. The amount of the fist active added should be less
than will give rise to a level of residue which exceeds the maximum residue level.
A second active is selected and the maximum residue level should be determined. In addition
the maximum amount of this second active which will give rise to a residue level below the
allowable maximum should be determined and the amount of the second active added to the composition should not exceed this amount. The kill rate of the composition can be estimated by comparing amount of each active added
with the LD 99 levels of each of the actives. A more accurate kill rate can be determined by
trials.
If the kill rate is less than is desired a third or fourth active can be added following the same
process as set out above for the second active.
Alternatively the composition can be arrived at by taking a first active which is known to kill the
target pests and determining the quantity of the first active necessary for achieving LD 99 and
LD 90, kill rates. Likewise the LD 99 and LD 90 quantity of a second active should be
determined. A check should be made to ensure that the LD 90 amounts of the active do not give
rise to a residue level which exceeds the maximum residue level.
If the LD 90 amount exceeds the maximum residue level a lower kill rate, eg LD 80 will need to
be selected and perhaps a third active added. The selected quantities of each active are
combined in suitable carriers and excipients to provide a stable composition. Those skilled in
the art will know suitable carriers for use with each active.
It will be understood that different combinations of actives will interact differently so that a
composition with a LD 99 or greater effective kill rate of the target pest may be achieved with
quantities of actives, which are below the quantity required to attain a LD 90 kill rate, lower or higher than an LD 90 level.
Further it will be understood by those skilled in the art that the pesticidal composition may
contain more than two actives, where this is the case the amount of each of the independent actives required to give a combined LD 99 or greater effective kill rate of the target pest may be less than the levels indicated in the paragraph above.
It is envisaged that the combination of active may have an additive if not synergistic effect on
reduction of pest numbers.
In addition it is desirable but not essential that each of the actives selected behaves
independently with respect to metabolism, excretion and detoxification of the active Obviously
the selection of actives which break down to give the same residue should not be used together.
It is hoped that the use of the compositions the subject of this invention will lead to a decreased
incidence of resistance pesticides, due to the reliance on a combination of pesticides together giving the effective kill rate.
TRIALS/EXAMPLES
These and other aspects of this invention, which should be considered an in all it's novel
aspects, will be apparent from the following examples.
Examples
Anthelmintic Pour On for treatment and control of internal and external pests of beef cattle. Dose rate is 1 mL/lOkg.
Example 1
Abamectin 2.5 g/L
Ivermectin 2.5 g/L N-propyl gallate 0.2 g/L
Thiodipropionic acid 0.15 g/L
Icinol PM l O mL
Butyl icinol lO mL
Butyl diicinol to 1 L
Dissolve the preservatives in the icinol PM. Add the butyl icinol and dissolve the actives. Add
and dissolve the dye. Make up the final volume with butyl diicinol.
Example 2
Abamectin 2.5 g/L
Ivermectin 2.5 g/L
Oily Carrier 640 g/L
Isopropyl alcohol to 1 L
The composition is prepared by dissolving the actives in the oily carrier. The final volume is
made up with HDPE containers.
Topical lousicide for treatment and control of the sheep body louse. Dose rate 1 mL/2.55 kg
Example 3
Triflumuron 12.5 g/L
Diflubenzuron 12.5 g/L Methyl pyrolidinone 250 mL
FDC Blue NO 1 0.05 g/L
Icinol DPN to 1 L
Dissolve the actives in methyl pyrolidinone. Add and dissolve the dye in 300 ml make up with 200 mL of icinol.
Example 4: Dose rate 1 mL/5 kg
Cypermethrin 12.5 g/L
Deltamethrin 5 g/L
Sudan Blue 0.25 g/L
Dowanol to 1 L
In addition it is possible to use a low amount of active ingredients from two or more different classes. This may reduce the residue levels even further, and result in a nil or much reduced
WHP. This would depend on the composition requirements of the different actives.
TRIAL
Trials were conducted using the compositions in Example 1 (ABA/IVM-ICI) and Example 2
(ABA/IVM-OIL). The compositions were administered to beef cattle as at a rate of 1 ml per 10
kg.
The milk residue levels were tested every 12 hours for 7 days from administration. The milk
was tested for the presence of residues of abamectin (see table 1 and figure 1) and for the presence of residues of ivermectin (table 2, and figure 2). The data obtained is summarized on table 1 and table 2 entitled "Milk residue levels in nanograms per mL from animals treated with
abamectin or a combination of abamectin and ivermectin". As can be clearly seen the abamectin and ivermectin residues remained low throughout the test period, both levels remaining below
the maximum residue level. The data clearly shows that the abamectin alone gives a high level
of residue, peaking at around 7.3 mg/mL at day 3, whereas when half the level is given in combination with ivermectin the peak is less defined and reaches a level of around 2.4, less than half the level of abamectin alone.
The data illustrates that the use of lower levels of a combination of parasiticially active compounds will provide decreased residue levels. These decreased residue levels will in turn
allow reduction or elimination of withholding periods of animals so-treated.
e r- © o
© o
<
H U ft* IMilk Residue Levels in nanograms per milliliter from animals treated with abamectin or a combination of abamectin and ivermectin. Table 1. Abamectin Biang/mL
Figure imgf000014_0001
Table 2. Ivermectin ng/mL
(
o
ADVANTAGES
The invention provides the advantage of limiting the WHP to which valuable commodities are subjected, whilst maintaining an effective level of control of pests. This has advantages for primary and secondary industries. For example, decreased periods before cows can be milked or
slaughtered after treatment. Obviously the longer the cows are not producing commercial grade
milk the longer the dairy farmer is not making money from the sale of that milk. The costs in
other primary industries may not be so direct. However they will centre around costs of storage
for goods during the WHP lost production time, and also the restriction placed on pest control strategies.
The elimination or reduction of WHPs for these products will be of great economic benefit to those involved in our primary industries.
In addition shorter export slaughter levels may be achieved.

Claims

CLAIMS:
1. A composition including two or more actives where each active is present in the amount which is less than the amount of that active which would give rise to a residue which exceeds the maximum residue level.
2. A composition as claimed in claim 1 , wherein the combination of actives provide a high kill
rate.
3. A composition as claimed in any of claims 1 or 2 which is further suitable for administration
to warm blooded animals.
4. A composition as claimed in any of claims 1 to 3, wherein the actives are selected from the
group comprising anthelmintics, miticides, tickicides, antibiotics and insecticides, and other compounds used to treat pests of plants and animals.
5. A composition as claimed in any of claims 1 to 4, wherein the actives are selected from the group comprising avermectins, synthetic pyrethroids, benzimidizoles, benzophenol ureas, insect group regulators, antibodies, and pyrazoles.
6. A composition as claimed in any of claims 1 to 4, wherein the actives selected for the composition share the same mode of action.
7. A method of devising a composition, including two or more active ingredients, wherein the amount of each active included is less than the amount giving rise to a level of residue which exceeds the maximum residue level.
8. A method of manufacturing a pesticidal composition containing two or more actives, including taking a first active which is known to kill a target pest and to determine the LD 90 quantity of the first active for said target pest and determining the LD 90 of a second
active for said target pest, combining the LD 90 quantity of the first and second actives with a suitable carrier to provide an effective pesticidal composition.
9. A method of treating a warm blooded animal by administering to that animal a composition
as claimed in any of claims 1 to 6 or made by the method of claims 7 to 8.
10. A method of treating a warm blooded animal by administering to the animal simultaneously or within a relatively short period of time at least two actives, the dose of each active
administered being less than results in a residue exceeding the maximum residue levels or at
least in a reduced withholding period or export slaughter interval.
PCT/AU2000/000071 1999-02-08 2000-02-08 Pesticide treatment Ceased WO2000047048A1 (en)

Priority Applications (2)

Application Number Priority Date Filing Date Title
AU27837/00A AU2783700A (en) 1999-02-08 2000-02-08 Pesticide treatment
NZ513186A NZ513186A (en) 1999-02-08 2000-02-08 Pesticide treatment containing two pesticides from the same chemical class

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
AUPP8582 1999-02-08
AUPP8582A AUPP858299A0 (en) 1999-02-08 1999-02-08 Pesticidal compositions

Publications (1)

Publication Number Publication Date
WO2000047048A1 true WO2000047048A1 (en) 2000-08-17

Family

ID=3812784

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/AU2000/000071 Ceased WO2000047048A1 (en) 1999-02-08 2000-02-08 Pesticide treatment

Country Status (4)

Country Link
AU (1) AUPP858299A0 (en)
NZ (1) NZ513186A (en)
WO (1) WO2000047048A1 (en)
ZA (1) ZA200107362B (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004026033A1 (en) * 2002-09-20 2004-04-01 Artpharm Pty Ltd Plant pesticides and uses thereof
WO2025024908A1 (en) * 2023-07-28 2025-02-06 Elanco Saude Animal Ltda Antiparasitic compositions of macrocyclic lactones

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986007525A1 (en) * 1985-06-19 1986-12-31 Robert Young & Company Limited Pyrethroid-containing parasiticidal composition
EP0327467A2 (en) * 1988-02-05 1989-08-09 CHINOIN Gyogyszer és Vegyészeti Termékek Gyára RT. Arthropodicidal compositions
GB2220856A (en) * 1988-07-18 1990-01-24 Merck & Co Inc Novel synergistic agricultural insecticidal and acaricidal combinations containing avermectin derivatives
WO1992012634A1 (en) * 1991-01-25 1992-08-06 Fmc Corporation Novel pyrethroid composition
WO1995005812A1 (en) * 1993-08-24 1995-03-02 Ashmont Holdings Limited Anthelmintic formulations

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1986007525A1 (en) * 1985-06-19 1986-12-31 Robert Young & Company Limited Pyrethroid-containing parasiticidal composition
EP0327467A2 (en) * 1988-02-05 1989-08-09 CHINOIN Gyogyszer és Vegyészeti Termékek Gyára RT. Arthropodicidal compositions
GB2220856A (en) * 1988-07-18 1990-01-24 Merck & Co Inc Novel synergistic agricultural insecticidal and acaricidal combinations containing avermectin derivatives
WO1992012634A1 (en) * 1991-01-25 1992-08-06 Fmc Corporation Novel pyrethroid composition
WO1995005812A1 (en) * 1993-08-24 1995-03-02 Ashmont Holdings Limited Anthelmintic formulations

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2004026033A1 (en) * 2002-09-20 2004-04-01 Artpharm Pty Ltd Plant pesticides and uses thereof
WO2025024908A1 (en) * 2023-07-28 2025-02-06 Elanco Saude Animal Ltda Antiparasitic compositions of macrocyclic lactones

Also Published As

Publication number Publication date
NZ513186A (en) 2004-02-27
AUPP858299A0 (en) 1999-03-04
ZA200107362B (en) 2002-09-18

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