US20020081327A1

US20020081327A1 - Direct pour-on antiparasitic skin solution and methods for treating, preventing and controlling myasis

Info

Publication number: US20020081327A1
Application number: US09/450,186
Authority: US
Inventors: Jean-Pierre Etchegaray; Philippe Jeannin
Original assignee: Individual
Current assignee: Boehringer Ingelheim Animal Health USA Inc
Priority date: 1996-03-29
Filing date: 1999-11-29
Publication date: 2002-06-27
Anticipated expiration: 2016-08-05
Also published as: US20020155147A1; US6413542B1; US6797724B2

Abstract

The direct pour-on skin solution intended to eliminate parasites, in particular Boophilus microplus, from cattle and sheep comprises from 0.05 to 25%, preferably from 0.05 to 10%, and in particular from 0.1 to 2% weight/volume, relative to the total solution, of a compound of formula (I):

in a formulation at low volume, designed to release the compound (I) onto the skin and the hairs for a contact action against parasites.

Description

The present invention relates to a direct pour-on skin solution which contains an antiparasitic product and is intended to be applied topically to cattle and sheep.

The invention also relates to the use of antiparasitic compounds for the preparation of this skin solution, as well as to a treatment process relating thereto.

Cattle and sheep are affected by a large number of parasites.

The main ones are ticks of the genus Boophilus, among which mention may be made of the species microplus (cattle tick), decoloratus and anulatus.

The other main parasites of cattle and sheep are indicated in order of decreasing importance:

myiases such as Dermatobia hominis (known as Berne in Brazil) and Cochlyomia hominivorax (greenbottle); sheep myiases such as Lucilia sericata, Lucilia cuprina (known as blowfly strike in Australia, New Zealand and South Africa). These are flies whose larva constitutes the animal parasite.

flies proper, namely those whose adult constitutes the parasite, such as Haematobia irritans (horn fly).

lice such as Linognathus vitulorum, etc.

galls such as Sarcoptes scabiei and Psoroptes ovis.

Ticks, in particular Boophilus microplus, are very closely attached to the pasture in which they live and are particularly difficult to control.

There is at the present time no truly effective method for controlling ticks, and less still an effective way of controlling the set of parasites indicated above.

WO-A-87/3781, EP-A-295,117 and EP-A-500,209 describe a class of insecticides which are N-phenyl-pyrazole derivatives. These compounds are given as having activity against a very large number of parasites, including Boophilus microplus, in fields as varied as agriculture, public health and veterinary medicine. The general teaching of these documents indicates that these insecticidal compounds may be administered via different routes; oral, parenteral, percutaneous and topical routes. Topical administration comprises, in particular, oral formulations, baits, dietary supplements, skin solutions (pour-on), solutions for spraying (sprays), baths, showers, jets, powders, greases, shampoos, creams, etc. The pour-on type skin solutions are designed for percutaneous administration. Example 9 of EP-A-295,117 and Example 29I of EP-A-500,209 describe a pour-on type skin solution containing 15% insecticide and 85% dimethyl sulphoxide, for percutaneous administration of the insecticide.

EP-A-296,381 also describes pyrazole compounds having insecticidal activity in the field of agriculture, public health and veterinary medicine. Boophilus microplus is one of the very many targets mentioned. There are very many forms of administration here also, and these include, for example, solutions, emulsions, suspensions, powders, pastes, granules and aerosols.

The problem which is posed is to find an effective means which is entirely suitable for controlling the parasites of cattle and sheep, in particular ticks, most particularly Boophilus microplus in cattle and in particular lice and blowfly in sheep, under the conditions in which these animals are reared.

The Applicant has found that it is possible to effectively control Boophilus microplus for cattle using a specific topical formulation. The Applicant has also found that this formulation is effective against sheep lice and sheep flies known as “blowfly”.

The aim of the present invention is thus to provide a novel composition which is entirely effective against Boophilus microplus and also against all of the other parasites described above such as, in particular, sheep lice and “blowfly”, this composition being entirely suitable for controlling these parasites under the conditions in which these animals are reared.

Another aim of the invention is to provide such a formulation which has a long period of efficacy, preferably longer than or equal to two months.

Another aim of the invention is to provide such a formulation which is quick and easy to use and entirely compatible with use on herds or flocks containing a large number of animals.

Another aim of the invention is to provide such a formulation which is particularly suitable for extensive pasture rearing and for use intended to protect animals during the period of rounding up and finishing (Feed Lot in USA), namely the final period of rearing in which a large number of animals are herded into a small enclosure over an average period of two months preceding slaughter.

The subject of the present invention is thus a direct pour-on skin solution, intended to eliminate parasites from cattle and sheep, most particularly ticks, especially Boophilus microplus in cattle and lice and blowfly in sheep, comprising from 0.05 to 25% weight/volume, relative to the total solution, of a compound of formula (I)

in which:

R ₁is CN or methyl or a halogen atom;

R ₂is S(O)_nR₃or 4,5-dicyanoimidazol-2-yl or haloalkyl;

R ₃is alkyl or haloalkyl;

R ₄represents a hydrogen or halogen atom; or a radical NR₅R₆, S(O)_mR₇, C(O)R₇, C(O)O—R₇, alkyl, haloalkyl or OR₈or a radical —N═C(R₉)(R₁₀) ;

R ₅and R₆independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl, alkoxycarbonyl or S(O)_rCF₃radical; or R₅and R₆may together form a divalent alkylene radical which may be interrupted by one or two divalent hetero atoms, such as oxygen or sulphur;

R ₇represents an alkyl or haloalkyl radical;

R ₈represents an alkyl or haloalkyl radical or a hydrogen atom;

R ₉represents an alkyl radical or a hydrogen atom;

R ₁₀represents a phenyl or heteroaryl group optionally substituted with one or more halogen atoms or groups such as OH, —O-alkyl, —S-alkyl, cyano or alkyl;

R ₁₁and R₁₂represent, independently of each other, a hydrogen or halogen atom, or optionally CN or NO₂;

R ₁₃represents a halogen atom or a haloalkyl, haloalkoxy, S(O)_qCF₃or SF₅group;

m, n, q, and r represent, independently of each other, an integer equal to 0, 1 or 2;

X represents a trivalent nitrogen atom or a radical C—R ₁₂, the other three valency positions of the carbon atom forming part of the aromatic ring;

with the proviso that, when R ₁is methyl, either R₃is haloalkyl, R₄is NH₂, R₁₁is Cl, R₁₃is CF₃and X is N; or R₂is 4,5-dicyanoimidazol-2-yl, R₄is Cl, R₁₁is Cl, R₁₃is CF₃and X is ═C—C1;

Preferably, in formula (I),

R ₁is CN or methyl;

R ₂is S(O)_nR₃;

R ₃is alkyl or haloalkyl;

R ₄represents a hydrogen or halogen atom; or a radical NR₅R₆, S(O)_mR₇, C(O)R₇, alkyl, haloalkyl or OR₈or a radical —N═C(R₉)(R₁₀);

R ₅and R₆independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl or S(O)_rCF₃radical; or R₅and R₆may together form a divalent alkylene radical which may be interrupted by one or two divalent hetero atoms, such as oxygen or sulphur;

R ₇represents an alkyl or haloalkyl radical;

R ₈represents an alkyl or haloalkyl radical or a hydrogen atom;

R ₉represents an alkyl radical or a hydrogen atom;

R ₁₁and R₁₂represent, independently of each other, a hydrogen or halogen atom;

with the proviso that, when R ₁is methyl, then R₃is haloalkyl, R₄is NH₂, R₁₁is Cl, R₁₃is CF₃and X is N.

However, low concentrations of from 0.05 to 10% weight/volume, more particularly from 0.1 to 2%, are preferred. Optimally, the value is between 0.25 and 1.5%, in particular in the region of 1%.

The expression pour-on skin solution is understood to refer to a ready-to-use solution intended to be applied topically and locally on the animal, preferably on the animal's back and at several points or along the line of the back, and applied in low volume, preferably of 5 to 20 ml per 100 kg, preferably about 10 ml per 100 kg, with a total volume of from 10 to 150 ml per animal, preferably limited to 50 ml.

The compound acts by simple contact, the parasite becoming impregnated with the compound on contact with the hairs and the skin.

This thereby affords, in a noteworthy manner, a both perfect compatibility with the restrictions of use in extensive grazing, in terms of ease of use in particular, and a spectrum of activity and of efficacy, as well as a period of efficacy, which are suited to this type of rearing.

By working on the concentration of compound (I), in particular of compound A, solutions having noteworthy activities are obtained with, in particular, two months of efficacy against Boophilus microplus, this result never before having been achieved. Moreover, the solution according to the invention allows Boophilus microplus to be totally eliminated from an infested animal in less than 2 days.

As has been stated above, the solution according to the present invention is applied topically, in low volume, to the animal's back. The compound of formula (I) then diffuses out in a noteworthy manner, this being reflected by a distribution of the compound over the animal's entire body. It has also been observed that the animals remained protected in the case of passage through water or exposure to rain.

The dose of compound of formula (I) is preferably between 0.1 and 2 mg/kg (animal weight), preferably between 0.25 and 1.5 mg/kg, and in particular about 1 mg/kg.

The compounds of formula (I) in which R ₁is CN will be selected most particularly. The compounds in which R₂is S(O)_nR₃, preferably with n=1, R₃preferably being CF₃or alkyl, for example methyl or ethyl, or alternatively n=0, R₃preferably being CF₃, as well as those in which X=C—R₁₂, R₁₂being a halogen atom, will also be selected. The compounds in which R₁₁is a halogen atom and those in which R₁₃is haloalkyl, preferably CF₃, are also preferred. In the context of the present invention, compounds combining two or more of these characteristics will advantageously be selected.

A preferred class of compounds of formula (I) consists of compounds such that R ₁is CN, R₃is haloalkyl, preferably CF₃, or ethyl, R₄is NH₂, R₁₁and R₁₂are, independently of each other, a halogen atom, and/or R₁₃is haloalkyl.

In the present invention, the alkyl radicals may contain generally from 1 to 6 carbon atoms. The cycle formed between the divalent alkylene radical representing R ₅and R₆, as well as with the nitrogen atom to which R₅and R₆are attached, may be generally a cycle of 5, 6 or 7 links.

A most particularly preferred compound of the formula (I) in the invention is 1-[2,6-Cl ₂4-CF₃phenyl]3-CN 4-[SO—CF₃]5-NH₂pyrazole, referred to hereinbelow as compound A. This compound A will be used in particular in a proportion of from 0.1 to 2% by weight, more particularly about 1%, relative to the total solution.

Mention may also be made of the two compounds which differ from the above by the following characteristics:

1−n=0,

2−n=1,

R ₃=CF₃

R ₃=ethyl.

The compounds of formula (I) may be prepared according to one or other of the processes described in patent applications WO-A-87/3781, 93/6089, 94/21606 or European patent application EP-A-0,295,117, or any other process which falls within the competence of a specialist skilled in the art of chemical synthesis. For the chemical preparation of the products of the invention, a person skilled in the art is considered as having at his or her disposal, inter alia, all the contents of “Chemical Abstracts” and the documents cited therein.

It is not departing from the scope of the present invention to incorporate other insecticides into the solution according to the present invention.

The solutions according to the invention, which are advantageously oily, generally comprise a diluent or vehicle and also a solvent (organic solvent) for the compound of formula (I) if the latter is not soluble in the diluent.

As organic solvent which can be used in the invention, mention may be made in particular of: acetyltributyl citrate, fatty acid esters such as the dimethyl ester, diisobutyl adipate, acetone, acetonitrile, benzyl alcohol, butyl diglycol, dimethylacetamide, dimethylformamide, dipropylene glycol n-butyl ether, ethanol, isopropanol, methanol, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, monomethylacetamide, dipropylene glycol monomethyl ether, liquid polyoxyethylene glycols, propylene glycol, 2-pyrrolidone, in particular N-methylpyrrolidone, diethylene glycol monoethyl ether, ethylene glycol and diethyl phthalate, or a mixture of at least two of these solvents.

As vehicle or diluent, mention may be made in particular of:

plant oils such as soybean oil, groundnut oil, castor oil, corn oil, cotton oil, olive oil, grape seed oil, sunflower oil, etc.; mineral oils such as petrolatum, paraffin, silicone, etc.; aliphatic or cyclic hydrocarbons or alternatively, for example, medium-chain (C8 to C12 in particular) triglycerides.

An emollient and/or spreading and/or film-forming agent will preferably be added, this agent being selected in particular from:

polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol, polyoxyethylenated sorbitan esters; lecithin, sodium carboxymethylcellulose, silicone oils, polydiorganosiloxane oils, in particular polydimethylsiloxane (PDMS) oils, for example those containing silanol functionalities, or a 45V2 oil,

anionic surfactants such as alkaline stearates, in particular sodium, potassium or ammonium stearates; calcium stearate, triethanolamine stearate; sodium abietate; alkyl sulphates, in particular sodium lauryl sulphate and sodium cetyl sulphate; sodium dodecylbenzenesulphonate, sodium dioctylsulphosuccinate; fatty acids, in particular those derived from coconut oil,

cationic surfactants such as water-soluble quaternary ammonium salts of formula N ⁺R′R″R″′R″″, Y⁻ in which the radicals R are optionally hydroxylated hydrocarbon radicals and Y⁻ is an anion of a strong acid such as the halide, sulphate and sulphonate anions; cetyltrimethylammonium bromide is among the cationic surfactants which can be used,

amine salts of formula N ⁺R′R″R′″ in which the radicals R are optionally hydroxylated hydrocarbon radicals; octadecylamine hydrochloride is among the cationic surfactants which can be used,

nonionic surfactants such as sorbitan esters, which are optionally polyoxyethylenated, in particular polysorbate 80, polyoxyethylenated alkyl ethers; polyoxypropylated fatty alcohols such as polyoxypropylene-styrol ether; polyethylene glycol stearate, polyoxyethylenated derivatives of castor oil, polyglycerol esters, polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids, copolymers of ethylene oxide and propylene oxide,

amphoteric surfactants such as the substituted lauryl compounds of betaine;

or a mixture of at least two of these agents.

The solvent will be used in proportion with the concentration of the compound I and its solubility in this solvent.

For example, compound A has a solubility of 4.3% m/V in acetyl tributyl citrate. It will be sought to have the lowest possible volume.

The vehicle makes up the difference to 100%.

The emollient is preferably used in a proportion of from 0.1 to 10%, in particular from 0.25 to 5%, by volume.

The subject of the present invention is also a process for the elimination of parasites, in particular Boophilus microplus, from cattle and sheep using a direct pour-on skin solution according to the present invention, so as obtain long-lasting and broad-spectrum efficacy, the solution being applied to the animal's back, preferably along the line of the back at one or more points.

According to a first embodiment, the process consists in applying the solution to the animals in pasture and/or before they arrive in pasture, the application preferably being repeated every month, preferably every two months.

According to a second embodiment, the process consists in applying the solution to the animals before they arrive in the “feed Lot”, it being possible for this application to be the final one before the animals are slaughtered.

Obviously, the process may also consist in combining these two embodiments, namely the first followed by the second.

In all cases, the efficacy advantageously makes it possible to stop any application 1 to 3 months before slaughter, in particular between 1.5 and 2.5 months, more particularly about two months before slaughter.

The solutions according to the invention may be applied using any means known per se, preferably using an applicator gun or a metering flask.

The aim of the method is not therapeutic and is, in particular, to cleanse the skin and the hairs of the animals by eliminating the parasites which are present thereon, as well as their residues and dejections. The result of this is that the animals are no longer stressed by the parasites and their bites, this having positive consequences, for example on their growth and on the use of their food ration.

Another subject of the invention is a therapeutic method using the external device according to the invention, intended for the treatment and prevention of parasitoses having pathogenic consequences.

The subject of the present invention is also the use of the compounds I, in particular compound A, for the manufacture of a direct pour-on skin solution comprising the compound (I) in a low volume and designed to release the compound (I) onto the skin and the hairs for a contact action against the parasites of cattle and sheep, in particular cattle ticks, such as Boophilus microplus, and sheep blowfly and lice.

The use according to the invention is directed towards producing skin solutions as described above.

The present invention will now be described in greater detail with the aid of non-limiting embodiment examples which demonstrate the activity of the solutions according to the present invention, with reference to the attached drawings in which: [0096]
FIG. 1 is a graph showing the efficacy, against [0097] Boophilus microplus, of skin solutions according to the invention, with a 0.25%, 0.5% and 1% content, relative to a control, this graph including, on the x-axis, the time in days after application of the skin solutions, and, on the y-axis to the left, the number of ticks counted on the animals on which the skin solutions according to the invention are applied, and, on the y-axis to the right, the number of ticks counted in the controls;
FIG. 2 is a graph showing the population of ticks in animals which have received the placebo according to Example 2, with, on the x-axis, the time in days, and, on the y-axis, the number of ticks; and [0098]
FIG. 3 compares the efficacy of a skin solution according to the invention containing 1% compound A (solid circles) with a skin solution containing 1% flumethrin (rings), with, on the x-axis, the time in days, and, on the y-axis, the number of ticks.[0099]

EXAMPLE 1

Preparation of the Solutions According to the Invention



Ingredient	Function	Amount

Compound A	active substance	x g
polyoxypropylene 15 stearyl ether	emollient	5 g
acetyl tributyl citrate	solvent	30 g
soybean oil	diluent	qs 100 ml

Compound A is dissolved in the solvent before being mixed with the other ingredients. [0101]

EXAMPLE 2

Study of the efficacy of skin solutions according to the invention containing, respectively, 0.25, 0.50 and 1% compound A to combat [0102] Boophilus microplus.
The study was performed on 16 young male castrated Herefords (weight ranging between 114 and 172 kg). [0103]
Three skin solutions according to Example 1 were prepared: [0104]
1. 1% compound A [0105]
2. 0.5% compound A [0106]
3. 0.25% compound A [0107]
A placebo was prepared, which differed from the skin solutions according to the invention in that it contained no compound A. [0108]
In the studies, 1 ml of skin solution or of placebo were used per 10 kg of animal weight. [0109]
The dose volume was applied along the line of the animal's back, from the head to the base of the tail. [0110]
Between days −24 and −1, the animals were artificially infested on 11 occasions with 2,500 [0111] Boophilus microplus larvae. The aim of 24-day infestation is to ensure that all of the stages of Boophilus microplus are present on the animal (eggs, larvae, adults).
On [0112] day 0, the animals receive one of the skin solutions or the placebo.
Before the skin solutions or the placebo are applied, the number of ticks present on the various animals in the different groups are counted. [0113]

The following table indicates the values recorded, the weight of the animals and the dose of skin solution or of placebo which will be applied to each of these animals.



		Number of	Weight
Group	Animal No.	ticks	(in kg)	Dose (ml)

1.00%	94	588	134	13.4
	43	470	140	14.0
	47	300	154	15.4
	39	254	160	16.0
0.50%	34	706	145	14.5
	99	452	143	14.3
	48	375	114	11.4
	45	201	153	15.3
0.25%	40	510	148	14.8
	92	453	144	14.4
	41	432	155	15.5
	36	236	171	17.1
Placebo	96	627	150	15.0
	44	482	144	14.4
	93	315	140	14.0
	97	292	172	17.2

The blood-engorged female ticks which become detached are included in the count. The results are indicated in FIG. 1. [0115]
A dose-dependent effect is obtained with 100% efficacy for the skin solution according to the invention containing 1% compound A. The less-concentrated solutions nevertheless give noteworthy results. [0116]
The great rapidity of action of the solutions according to the invention is also noted, the 1% solution allowing [0117] Boophilus microplus to be totally eliminated in less than 2 days.

EXAMPLE 3

Comparison of efficacy between a skin solution according to the invention containing 1% compound A and a skin solution containing 1% flumethrin. [0118]
Animals of the same breed as those in Example 1 were used. [0119]
On [0120] day 0, the groups are treated with:
skin solution containing 1% compound A [0121]
skin solution containing 1% flumethrin (mineral oil and ethylhexyl alcohol excipient) [0122]
placebo (excipient identical to the solution according to the invention) [0123]

Table 2 below indicates, for each group, the weight of the animals, the dose of skin solution received and the dose of active substance applied.



Group	Animal No.	Weight	Dose (ml)	Dose (mg/kg)⁻)

1%	719	141	14.1	1
Compound A	709	125	12.5	1
	713	150	15.0	1
	710	136	13.6	1
	703	138	13.8	1
1%	706	145	14.5	1
flumethrin	711	136	13.6	1
	715	132	13.2	1
	702	142	14.2	1
	701	127	12.7	1
Placebo	717	133	13.3	0
	707	133	13.3	0
	704	134	13.4	0
	718	132	13.2	0
	708	143	14.3	0

From [0125] day 2 to day 32, the animals receive 5,000 Boophilus microplus larvae three times a week. From day 18 to 64, the blood-engorged female ticks which become detached are collected and counted.
The results are indicated in FIGS. 2 and 3, which demonstrate the total efficacy of the skin solution according to the invention. [0126]

EXAMPLE 4

Study of efficacy over time. [0127]
Skin solutions according to the invention containing 0.25, 0.5 or 1% compound A where used in this example. [0128]
The composition of these solutions is the same as for the above examples. [0129]
The cattle were preinfested so as to have all of the stages of [0130] Boophilus microplus present (infestation with 5,000 larvae, 22 days, 15 days and 8 days before application of the skin solution).
After application of the skin solutions, the cattle are again infested with the larvae for 13 weeks, to determine the efficacy of the three concentrations. [0131]

The results are reported in Table 3 below:



		Efficacy index for each
	Weeks of infestation	concentration

	after treatment	0.25%	0.5%	1.0%

1	97.6	100	100
2	98.8	100	100
3	99.7	100	100
4	99.3	100	100
5	96.7	92.9	100
6	98.6	93.2	100
7	92.4	88.6	99.7
8	85.8	83.4	100
9	28.0	37.9	79.8
10	23.0	41.4	65.3
11	18.9	55.2	61.5
12	1.7	37.3	32.2
13	8.4	48.5	46.4

It is thus observed that noteworthy efficacy, which may last for two months or more, is obtained. [0133]

Claims

1. Direct pour-on skin solution intended to eliminate parasites from cattle and sheep, most particularly ticks, especially Boophilus microplus in cattle and lice and blowfly in sheep, comprising from 0.05 to 25% weight/volume, relative to the total solution, of a compound of formula (I):

in which:

R₁is CN or methyl or a halogen atom;

R₂is S(O)_nR₃or 4,5-dicyanoimidazol-2-yl or haloalkyl;

R₃is alkyl or haloalkyl;

R₄represents a hydrogen or halogen atom; or a radical NR₅R₆, S(O)_mR₇, C(O)R₇, C(O)O—R₇, alkyl, haloalkyl or OR₈or a radical —N═C (R₉) (R₁₀);

R₅and R₆independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl, alkoxycarbonyl, or S(O)_rCF₃radical; or R₅and R₆may together form a divalent alkylene radical which may be interrupted by one or two divalent hetero atoms, such as oxygen or sulphur;

R₇represents an alkyl or haloalkyl radical;

R₈represents an alkyl or haloalkyl radical or a hydrogen atom;

R₉represents an alkyl radical or a hydrogen atom;

R₁₀represents a phenyl or heteroaryl group optionally substituted with one or more halogen atoms or groups such as OH, —O-alkyl, —S-alkyl, cyano or alkyl;

R₁₁and R₁₂represent, independently of each other, a hydrogen or halogen atom or optionally CN or NO₂;

R₁₃represents a halogen atom or a haloalkyl, haloalkoxy, S(O)_qCF₃or SF₅group;

X represents a trivalent nitrogen atom or a radical C—R₁₂, the other three valency positions of the carbon atom forming part of the aromatic ring;

with the proviso that, when R₁is methyl, either R₃is haloalkyl, R₄is NH₂, R₁₁is Cl, R₁₃is CF₃and X is N; or R₂is 4,5-dicyanoimidazol-2-yl, R₄is Cl, R₁₁is Cl, R₁₃is CF₃and X is ═C—Cl;

2. Solution according to claim 1, wherein the compound of formula (I) is such that:

R₁is CN or methyl;

R₂is S(O)_nR₃;

R₃is alkyl or haloalkyl;

R₄represents a hydrogen or halogen atom; or a 1 radical NR₅R₆, S(O)_mR₇, C(O)R₇, alkyl, haloalkyl or OR₈or a radical —N═C(R₉) (R₁₀);

R₅and R₆independently represent a hydrogen atom or an alkyl, haloalkyl, C(O)alkyl or S(O)_rCF₃radical; or R₅and R₆may together form a divalent alkylene radical which may be interrupted by one or two divalent hetero atoms, such as oxygen or sulphur;

R₇represents an alkyl or haloalkyl radical;

R₈represents an alkyl or haloalkyl radical or a hydrogen atom;

R₉represents an alkyl radical or a hydrogen atom;

R₁₁and R₁₂represent, independently of each other, a hydrogen or halogen atom;

X represents a trivalent nitrogen atom or a radical C—R₂, the other three valency positions of the carbon atom forming part of the aromatic ring;

with the proviso that, when R₁is methyl, then R₃is haloalkyl, R₄is NH₂, R₁₁is Cl, R₁₃is CF₃and X is N.

3. Solution according to claim 2, wherein the compound of formula (I) is such that R₁is CN.

4. Solution according to claim 2, wherein the compound of formula (I) is such that R₁₃is haloalkyl.

5. Solution according to claim 2, wherein the compound of formula (I) is such that R₁₃is CF₃.

6. Solution according to claim 2, wherein the compound of formula (I) is such that R₂is S(O)_nR₃.

7. Solution according to claim 6, wherein n=1, R₃being chosen among the group consisting of CF₃, methyl and ethyl.

8. Solution according to claim 6, wherein n=0 and R₃is CF₃.

9. Solution according to claim 2, wherein the compound of formula (I) is such that X is C—R₁₂with R₁₂being a halogen atom.

10. Solution according to claim 2, wherein the compound of formula (I) is chosen from those in which R₁is CN, R₃is haloalkyl, R₄is NH₂, R₁₁and R₁₂are, independently of each other, a halogen atom and/or R₁₃is haloalkyl.

11. Solution according to claim 2, wherein the compound of formula (I) is chosen among the group consisting of the compound A:

1-[2,6-Cl₂4-CF₃phenyl]3-CN 4-[SO—CF₃] 5-NH₂pyrazole, and its derivatives with n=0, R₃=CF₃and n=1, R₃=ethyl.

12. Solution according to claim 2, wherein the compound of formula is present in a proportion of from 0.05 to 10% weight/volume.

13. Solution according to claim 2, wherein the compound of formula (I) is present in a proportion of from 0.1 to 2%.

14. Solution according to claim 2, wherein the compound of formula (I) is present in a proportion of from 0.25 to 1.5%.

15. Solution according to claim 2, wherein the compound of formula (I) is present in a proportion of about 1%.

16. Solution according to claim 11, wherein the compound of formula is present in a proportion of from 0.05 to 10% weight/volume.

17. Solution according to claim 11, wherein the compound of formula (I) is present in a proportion of from 0.1 to 2%.

18. Solution according to claim 11, wherein the compound of formula (I) is present in a proportion of from 0.25 to 1.5%.

19. Solution according to claim 11, wherein the compound of formula (I) is present in a proportion of about 1%.

20. Solution according to claim 2, wherein it comprises a solvent for the compound (I) and a diluent, optionally an emollient.

21. Solution according to claim 20, wherein the solvent is selected from the group consisting of:

acetyl tributyl citrate, fatty acid esters such as the dimethyl ester, diisobutyl adipate, acetone, acetonitrile, benzyl alcohol, butyl diglycol, dimethylacetamide, dimethylformamide, dipropylene glycol n-butyl ether, ethanol, isopropanol, methanol, ethylene glycol monoethyl ether, ethylene glycol monomethyl ether, monomethylacetamide, dipropylene glycol monomethyl ether, liquid polyoxyethylene glycols, propylene glycol, 2-pyrrolidone, in particular N-methylpyrrolidone, diethylene glycol monoethyl ether, ethylene glycol and diethyl phthalate, or a mixture of at least two of these solvents.

22. Solution according to claim 20, wherein the diluent is selected from the group consisting of:

plant oils such as soybean oil, groundnut oil, castor oil, corn oil, cotton oil, olive oil, grape seed oil, sunflower oil, etc.; mineral oils such as petrolatum, paraffin, silicone, etc.; aliphatic or cyclic hydrocarbons or alternatively, medium-chain (C8 to C12 in particular).

23. Solution according to claim 20, wherein the emollient is selected from the group consisting of:

polyvinylpyrrolidone, polyvinyl alcohols, copolymers of vinyl acetate and vinylpyrrolidone, polyethylene glycols, benzyl alcohol, mannitol, glycerol, sorbitol, polyoxyethylenated sorbitan esters; lecithin, sodium carboxymethylcellulose, silicone oils,

cationic surfactants such as water-soluble quaternary ammonium salts of formula N⁺R′R″R′″R″″, Y⁻ in which the radicals R are optionally hydroxylated hydrocarbon radicals, and Y⁻ is an anion of a strong acid such as the halide, sulphate and sulphonate anions; cetyltrimethylammonium bromide is among the cationic surfactants which can be used,

amine salts of formula N⁻R′R″R′″ in which the radicals R are optionally hydroxylated hydrocarbon radicals; octadecylamine hydrochloride is among the cationic surfactants which can be used,

nonionic surfactants such as sorbitan esters, which are optionally polyoxyethylenated, in particular polysorbate 80, polyoxyethylenated alkyl ethers; polyoxypropylated fatty alcohols such as polyoxypropylene-15-stearyl ether; polyethylene glycol stearate, polyoxyethylenated derivatives of castor oil, polyglycerol esters, polyoxyethylenated fatty alcohols, polyoxyethylenated fatty acids, copolymers of ethylene oxide and propylene oxide,

amphoteric surfactants such as the substituted lauryl compounds of betaine;

or a mixture of at least two of these agents.

24. Solution according to claim 2, wherein it is an oily solution.

25. Solution according to claim 2, wherein it is designed to ensure protection over a period longer than or equal to 2 months.

26. Solution according to claim 2, wherein it is designed to ensure total elimination of Boophilus microplus in less than 2 days.

27. Process for the elimination of external parasites from cattle and sheep, most particularly ticks, especially Boophilus microplus in cattle and lice and blowfly in sheep, wherein one applies on the cattle or sheep a direct pour-on skin solution comprising from 0.05 to 25% weight/volume, relative to the total solution, of a compound of formula (I) below:

in which:

R₁is CN or methyl or a halogen atom;

R₂is S(O)_nR₃or 4,5-dicyanoimidazol-2-yl or haloalkyl;

R₃is alkyl or haloalkyl;

R₇represents an alkyl or haloalkyl radical;

R₈represents an alkyl or haloalkyl radical or a hydrogen atom;

R₉represents an alkyl radical or a hydrogen atom;

the compound (I) being formulated in a direct pour-on skin solution comprising the compound (I) in a low volume, designed to release the compound (I) onto the skin and the hairs for a contact action against the parasites.

28. Process according to claim 27, wherein the solution is applied in a volume of 5 to 20 ml per 100 kg of animal.

29. Process according to claim 27, wherein the solution is applied in a volume of about 10 ml per 100 kg of animal.

30. Process according to claim 27, wherein the solution is applied with a total volume of from 10 to 150 ml per animal.

31. Process according to claim 27, wherein the compound of formula (I) is such that:

R₁is CN or methyl;

R₂is S(O)_nR₃;

R₃is alkyl or haloalkyl;

R₄represents a hydrogen or halogen atom; or a radical NR R₆, S(O)_mR₇, C(O)R₇, alkyl, haloalkyl or OR₈or a radical —N═C (R₉) (R₁₀);

R₇represents an alkyl or haloalkyl radical;

R₈represents an alkyl or haloalkyl radical or a hydrogen atom;

R₉represents an alkyl radical or a hydrogen atom;

32. Process according to claim 31, wherein the compound of formula (I) is such that R₁is CN.

33. Process according to claim 31, wherein the compound of formula (I) is such that R₁₃is haloalkyl.

34. Process according to claim 31, wherein the compound of formula (I) is such that R₁₃is CF₃.

35. Process according to claim 31, wherein the compound of formula (I) is such that R₂is S(O)_nR₃.

36. Process according to claim 35, wherein n=1 and R₃is chosen among the group consisting of CF₃, methyl and ethyl.

37. Process according to claim 35, wherein n=0, R₃preferably being CF₃.

38. Process according to claim 31, wherein the compound of formula (I) is such that X is C—R₁₂with R₁₂being a halogen atom.

39. Process according to claim 31, wherein the compound of formula (I) is such that R₁is CN, R₃is haloalkyl, R₄is NH₂, R₁₁and R₁₂are, independently of each other, a halogen atom and/or R₁₃is haloalkyl.

40. Process according to claim 31, wherein the compound of the formula (I) is chosen among the group consisting of compound A:

41. Process according to claim 31, wherein the compound of formula is present in a proportion of from 0.05 to 10% weight/volume.

42. Process according to claim 31, wherein the compound of formula (I) is present in a proportion of from 0.1 to 2%.

43. Process according to claim 31, wherein the compound of formula (I) is present in a proportion of from 0.25 to 1.5%.

44. Process according to claim 31, wherein the compound of formula (I) is present in a proportion of about 1%.

45. Process according to claim 40, wherein the compound of formula is present in a proportion of from 0.05 to 10% weight/volume.

46. Process according to claim 40, wherein the compound of formula (I) is present in a proportion of from 0.1 to 2%.

47. Process according to claim 40, wherein the compound of formula (I) is present in a proportion of from 0.25 to 1.5%.

48. Process according to claim 40, wherein the compound of formula (I) is present in a proportion of about 1%.

49. Process according to claim 31, wherein one applies the solution in a proportion of from 0.1 to 2 mg/kg.

50. Process according to claim 31, wherein one applies the solution in a proportion of from 0.25 to 1.5 mg/kg.

51. Process according to claim 31, wherein one applies the solution in a proportion of about 0.1 mg/kg.

52. Process according to claim 40, wherein one applies the solution in a proportion of from 0.1 to 2 mg/kg.

53. Process according to claim 40, wherein one applies the solution in a proportion of from 0.25 to 1.5 mg/kg.

54. Process according to claim 40, wherein one applies the solution in a proportion of about 0.1 mg/kg.

55. Process according to claim 31, wherein one applies the solution to the animals in pasture or before they arrive in pasture.

56. Process according to claim 31, wherein one applies the solution every two months.

57. Process according to claim 31, wherein one applies the solution to the animals before they arrive in the Feed Lot, this application being the final one before the animal is slaughtered.

58. Process according to claim 31, wherein when applied topically locally onto the animal's skin, the solution is designed to ensure protection for at least two months, in particular against Boophilus microplus.

59. Process according to claim 31, wherein the solution is designed to ensure total elimination of Boophilus microplus in less than 2 days.