Patent Application
20180370941
The invention relates to a configurational stereoisomer of flocoumafen, to a composition and a rodenticidal bait comprising such a configurational stereoisomer and to a process for controlling target rodent pests. The invention also relates to a process for obtaining such a configurational stereoisomer of flocoumafen. The invention thus relates to the technical field of controlling populations of target rodent pests.
It is known practice to use poisons in the form of rodenticidal baits against target rodent pests. WO 2005/072524 discloses a rodenticidal bait comprising a proportion of 50 ppm of flocoumafen in the bait and a proportion of 40 ppm of fipronil.
Such a bait is liable to be consumed by animals other than target rodent pests when it is made available to target rodent pests. It may be consumed directly (primary consumption) by domestic animals or pets. It may also be consumed accidentally by humans. Such consumption may result in poisoning, which may be lethal, of these domestic animals, pets or humans.
In addition, a fraction of the flocoumafen of these rodenticidal baits may be ingested (secondary consumption) by animals—especially by birds—which prey or carrion-feed on rodent pests and especially weakened target rodent pests that have consumed such a rodenticidal bait. This secondary consumption is liable in the long term to result in the death by secondary intoxication of these predatory or carrion-feeding animals, which may be animals—especially birds—belonging to protected species.
The invention is thus directed towards overcoming these drawbacks by proposing a configurational stereoisomer of flocoumafen, a composition and a rodenticidal bait comprising such a configurational stereoisomer and a process for controlling target rodent pests, which are effective for controlling the populations of target rodent pests and can also limit the risks of poisoning of non-target animals—especially domestic or reared animals, pets or humans—which accidentally consume such a rodenticidal bait.
The invention is thus directed towards overcoming these drawbacks by proposing a configurational stereoisomer of flocoumafen, a composition and a rodenticidal bait comprising such a configurational stereoisomer and a process for controlling target rodent pests, which are not only effective for controlling the populations of target rodent pests but can also limit the risks of secondary poisoning of wild animals—for example foxes or birds—which prey on weakened target rodent pests that have consumed the rodenticidal bait or of wild animals which carrion-feed on target rodent pests that died from being poisoned.
The invention is also directed towards proposing a configurational stereoisomer of flocoumafen, a composition and a rodenticidal bait comprising such a configurational stereoisomer and a process for controlling target rodent pests, which are environmentally friendly and friendly to human health and to the health of non-target animals, especially birds, and in particular birds of prey.
The invention is also directed towards proposing a configurational stereoisomer of flocoumafen, a composition and a rodenticidal bait comprising such a configurational stereoisomer and a process for controlling target rodent pests, the use of which is in accordance with the rules of good practice, especially with respect to the protection of birds, and in particular birds of prey.
The invention is also directed towards proposing a configurational stereoisomer of flocoumafen, a composition and a rodenticidal bait comprising such a configurational stereoisomer and a process for controlling target rodent pests, which are able to be used for controlling target rodent pests that are liable to have become resistant to known baits for controlling target rodent pests.
The invention is thus directed towards proposing an alternative to known rodenticidal baits.
To do this, the invention relates to a configurational stereoisomer, named enantiomer E1, of flocoumafen, said enantiomer E1 having, by chromatographic analysis of a flocoumafen composition comprising four configurational stereoisomers of flocoumafen performed under conditions described hereinbelow, a retention time t1 having a value such that t1<t2<t3<t4; t2, t3 and t4 representing the retention times of the configurational stereoisomers of flocoumafen different from said enantiomer E1, said analysis being performed at a temperature of 23.5° C. and under the following conditions:
Throughout the text:
in which are represented the numbers of carbons 1 and 3 of the 1,2,3,4-tetrahydronaphthalene group;
The invention thus relates to said enantiomer E1 in isolated form, which has the property of being able to be eluted first, under the chromatography conditions described above, relative to the four configurational stereoisomers of flocoumafen.
The inventors have observed that analysis of flocoumafen by high-pressure liquid chromatography under the conditions described above reveals four signals or peaks corresponding to four compounds of the same chemical structural formula and corresponding to formula (I) of flocoumafen. They determined, by analysis of flocoumafen preparations comprising variable proportions of the two diastereoisomers of flocoumafen, that:
The retention time values t1, t2, t3 and t4 are liable to vary, especially with the temperature of the chromatography column. However, under these chromatographic conditions, the order of elution of the flocoumafen enantiomers remains unchanged.
One of the two diastereoisomers of flocoumafen is a configurational stereoisomer of flocoumafen in which carbons 1 and 3 of the 1,2,3,4-tetrahydronaphthalene group of flocoumafen have the same absolute configuration and the other of the two diastereoisomers of flocoumafen is a configurational stereoisomer of flocoumafen in which carbons 1 and 3 of the 1,2,3,4-tetrahydronaphthalene group of flocoumafen have different absolute configurations, the absolute configurations being determined according to the Cahn-Ingold-Prelog sequential priority and nomenclature rules.
The inventors performed such a separation of the configurational stereoisomers, i.e. of the enantiomers of the two diastereoisomers, of flocoumafen by high-pressure liquid chromatography on a LUX® Cellulose-4 chiral column (00F-4490-B0, Phenomenex, Le Pecq, France). Where appropriate, it is possible successively to perform several high-pressure liquid chromatography steps on a chiral column for the purposes of obtaining the desired amount of said enantiomer E1 in the desired purity. It is also possible to perform such a separation by high-pressure liquid chromatography on a preparative chiral column of larger dimensions—especially with an inside diameter of greater than 2 mm—and in which the stationary phase has a particle size of greater than 3 μm. The inventors obtained said enantiomer E1 purified and separated from enantiomer E4 of said diastereoisomer D1,4 of flocoumafen and from the enantiomers E2 and E3 of said diastereoisomer D2,3 of flocoumafen by removing the mobile phase from the collected fraction containing said enantiomer E1.
A method for separating the enantiomers of said diastereoisomer D1,4 of flocoumafen was not previously known. Under these experimental conditions, the enantiomers (E1 and E4) of said diastereoisomer D1,4 are efficiently separated and purified by high-pressure liquid chromatography. Under these chromatographic conditions, the enantiomers of said diastereoisomer D2,3 of flocoumafen are also separated.
The invention thus relates to said enantiomer E1 of said diastereoisomer D1,4 which is the least retained (which has the shortest retention time) of the four enantiomers of the flocoumafen diastereoisomers separated by chromatography under the abovementioned conditions.
The invention thus relates to said enantiomer E1 separated from enantiomer E4 of said diastereoisomer D1,4 and separated from each enantiomer of said diastereoisomer D2,3.
The invention also relates to a chromatographic process for separating the configurational stereoisomers—especially said enantiomers E1 and E4 of said diastereoisomer D1,4 and said enantiomers E2 and E3 of said diastereoisomer D2,3. The invention also relates to a chromatographic process for obtaining said enantiomer E1 according to the invention.
The invention thus relates to such a chromatographic process for obtaining said enantiomer E1 according to the invention, in which:
The invention also relates to said enantiomer E1 obtained via a process according to the invention.
The invention also relates to a composition comprising said enantiomer E1 according to the invention, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4.
The invention thus relates to a composition comprising a configurational stereoisomer, named enantiomer E1, of flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of a configurational stereoisomer, named enantiomer E4, of flocoumafen;
The invention thus relates to such a composition comprising said enantiomer E1, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4, i.e. with the exclusion of a composition in which said enantiomer E1 and said enantiomer E4 are in equimolar mixture and not optically active.
Said enantiomer E1 and said enantiomer E4 of any composition comprising flocoumafen are assayed by chromatographic analysis and separation using a chiral stationary phase and a liquid mobile phase as described above for the analysis of the configurational stereoisomers of flocoumafen, by performing quantitative detection of the enantiomers of the flocoumafen diastereoisomers at the outlet of the separating column, for example by absorption photometry or spectrophotometry, adjusting the flocoumafen concentration and the injection volume for the purposes of obtaining optimum detection and measuring the value of the area under the peak for each enantiomer E1 and E4. It is also possible to assay said enantiomer E1 and said enantiomer E4 of any composition comprising flocoumafen by performing detection by mass spectrometry at the outlet of the separating column.
Advantageously and according to the invention, the amount of said enantiomer E1 is greater than the amount of said enantiomer E4 in the composition. In the composition, said diastereoisomer D1,4 is predominantly in the form of said enantiomer E1. The composition according to the invention comprises said diastereoisomer D1,4 predominantly in the form of said enantiomer E1.
Throughout the text, the term “said diastereoisomer D1,4 is predominantly in the form of said enantiomer E1” means that the ratio of the amount (on a mass, molar or volume basis) of said enantiomer E1 to the amount (on a corresponding mass, molar or volume basis) of said diastereoisomer D1,4 (in all its enantiomeric forms) is greater than 50%.
Thus, in particular, in a composition according to the invention:
Advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the sum of the amount of said enantiomer E1 and of the amount of said enantiomer E4 present in the composition is greater than 50%, especially greater than 60%, in particular greater than 70%, more particularly greater than 80%, preferably greater than 90%, more preferentially greater than 95%, particularly preferentially greater than 98%, even more preferentially greater than 99% or about 1000/o.
In a particular embodiment, advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the sum of the amount of said enantiomer E1 and of the amount of said enantiomer E4 present in the composition is greater than 75%, preferably between 85% and 100% and more preferentially between 90% and 98%.
In another embodiment, advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the sum of the amount of said enantiomer E1 and of the amount of said enantiomer E4 present in the composition is between 98% and 100%.
The composition may also comprise an amount of said enantiomer E4 such that the ratio of this amount to the sum of the amount of said enantiomer E1 and of the amount of said enantiomer E4 present in the composition is less than 50%, especially less than 25%, preferentially between 0%/o and 25%, in particular less than 100/o.
Advantageously and according to the invention, flocoumafen is predominantly in the form of said enantiomer E1 in the composition. The composition thus comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is greater than the ratio of the amount of said enantiomer E4 to the amount of flocoumafen in the composition and greater than the ratio of the amount of each enantiomer of said diastereoisomer D2,3 to the amount of flocoumafen in the composition.
Thus, in particular, in a composition according to the invention:
Advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is greater than 25%, especially greater than 50%, in particular greater than 70%, more particularly greater than 80%, preferably greater than 90%, particularly preferentially greater than 95%, more preferentially greater than 98%, even more preferentially greater than 99% or about 100%.
In a particular embodiment, advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is greater than 70%, preferably between 80% and 100% and more preferentially between 90% and 100%.
In another embodiment, advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is between 95% and 99%.
In another particular embodiment, advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is greater than 95%.
In another embodiment, advantageously and according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is between 98% and 100%, limits inclusive.
In another particularly advantageous embodiment according to the invention, the composition comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the composition is substantially about 100%.
A composition according to the invention may be substantially free of said enantiomer E4, i.e. said enantiomer E4 may optionally be present in the composition but only in trace amount. A composition according to the invention may also be substantially free of said diastereoisomer D2,3, i.e. said diastereoisomer D2,3 may optionally be present in the composition but only in trace amount.
Advantageously and according to the invention, the composition may be in liquid form and may comprise a liquid solvent for flocoumafen. It may be a solution of flocoumafen in a solvent for flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4. It may also be a solution comprising flocoumafen in a solvent for flocoumafen and in which the amount of said enantiomer E1 is greater than the amount of said enantiomer E4. It may also be a solution comprising flocoumafen in a solvent for flocoumafen and in which the flocoumafen is predominantly in the form of said enantiomer E1.
Advantageously and according to the invention, the composition may be in solid form. It may also be a solid comprising flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4. It may also be a solid comprising flocoumafen and in which the amount of said enantiomer E1 is greater than the amount of said enantiomer E4. It may also be a solid comprising flocoumafen and in which the flocoumafen is predominantly in the form of said enantiomer E1.
The invention thus also relates to a composition according to the invention comprising flocoumafen, the flocoumafen of the composition being optically active. However, it is not excluded for the flocoumafen of the composition according to the invention to be optically inactive.
The invention also relates to the use of a composition according to the invention for the preparation of a rodenticidal bait for target rodent pests.
The invention also relates to a rodenticidal bait comprising a composition according to the invention, and at least one excipient that is edible for target rodent pests.
A rodenticidal bait according to the invention comprises:
Advantageously, a rodenticidal bait according to the invention comprises an excipient that is edible for target rodent pests and said enantiomer E1 in which the amount of said enantiomer E1 is greater than the amount of said enantiomer E4. It may also be a rodenticidal bait comprising flocoumafen and in which the flocoumafen is predominantly in the form of said enantiomer E1.
The inventors who succeeded in separating said enantiomer E1 and said enantiomer E4 and in isolating said enantiomer E1 also discovered, entirely surprisingly and unexpectedly, that:
They also found that it is thus possible to control a population of target rodent pests by selectively targeting the female target rodent pests, limiting the number of litters of target rodent pests.
Thus, said enantiomer E1 according to the invention allows the production of rodenticidal baits with high rodenticidal efficacy against female target rodent pests, making it possible to limit the number of litters of target rodent pests that may be generated by these female target rodent pests.
Such a rodenticidal bait thus makes it possible to limit the residual amount of flocoumafen in the liver of male rats while maintaining in the liver of female rats an amount of flocoumafen that is rodenticidal for said female target rodent pests. Such a rodenticidal bait is thus less toxic to the environment, and in particular to animals—especially to birds belonging to protected species—which prey or carrion-feed on rodent pests and especially on weakened male target rodent pests that have consumed such a rodenticidal bait, but conserves sufficient anticoagulant activity, in particular on female target rodent pests, so that the rodenticidal bait makes it possible to control the populations of target rodent pests.
A rodenticidal bait according to the invention is able to be used to control populations of target rodent pests that are resistant to known rodenticidal treatments.
Advantageously, a rodenticidal bait according to the invention comprises a mass amount of flocoumafen such that the ratio of this mass amount of flocoumafen to the mass amount of rodenticidal bait is less than 200 ppm, i.e. less than 200 mg of flocoumafen per kilogram of rodenticidal bait. Advantageously, it comprises a mass amount of flocoumafen such that the ratio of this mass amount of flocoumafen to the mass amount of rodenticidal bait is greater than 1 ppm. Advantageously, a rodenticidal bait according to the invention comprises a mass amount of flocoumafen such that the ratio of this mass amount of flocoumafen to the mass amount of rodenticidal bait is between 1 ppm and 200 ppm (1 mg to 200 mg of flocoumafen per kilogram of rodenticidal bait). Advantageously, the ratio of this mass amount of flocoumafen to the mass amount of rodenticidal bait is between 1 ppm and 100 ppm (1 mg to 100 mg of flocoumafen per kilogram of rodenticidal bait), especially between 1 ppm and 50 ppm (1 mg to 50 mg of flocoumafen per kilogram of rodenticidal bait), preferably between 5 ppm and 25 ppm (5 mg to 25 mg of flocoumafen per kilogram of rodenticidal bait).
Advantageously, a rodenticidal bait according to the invention comprises an amount of said enantiomer E1 such that the ratio of this amount to the amount of flocoumafen in the rodenticidal bait is greater than 70%, more particularly greater than 80%, preferably greater than 90%, particularly preferentially greater than 95%, more preferentially greater than 98%, even more preferentially greater than 99% or about 100%, and of flocoumafen as a mass amount in the rodenticidal bait such that the ratio of this mass amount to the mass amount of rodenticidal bait is less than 200 ppm, especially less than 50 ppm.
Advantageously and according to the invention, the excipient that is edible for target rodent pests is chosen to allow consumption of the rodenticidal bait by target rodent pests. Advantageously and according to the invention, each edible excipient is non-lethal to target rodent pests. The edible excipient is not in itself rodenticidal.
Advantageously and according to the invention, the edible excipient comprises at least one food chosen from the group formed from cereal seeds—especially hulled cereal seeds—cereal seed meals, cereal seed flours, cereal seed flakes, cereal bran and non-cereal seeds, for example alfalfa seeds—especially in hulled form, in the form of meal, in the form of flour, or in the form of flakes or bran. The edible excipient may comprise any support that can be consumed by target rodent pests.
Advantageously, the edible excipient comprises at least one food chosen from the group formed from foods of plant origin and foods of animal origin. Advantageously, the edible excipient comprises at least one food chosen to be able to stimulate the appetite of the target rodent pests. In particular, this food is chosen from the group formed from seeds of one or more cereals, hulled seeds of one or more cereals, meals of seeds of one or more cereals, flakes of seeds of one or more cereals, bran of one or more cereals and flour of seeds of one or more cereals. By way of example, the cereals are chosen from the group formed from oat, wheat, barley, corn, soybean and rice.
Advantageously, the food is chosen from the group formed from sweetened foods. For example, they may be foods comprising at least one sugar chosen from the group formed from sucrose, lactose, fructose and glucose. It may be a sugar syrup—for example a sugar syrup obtained by hydrolysis of starch—or a sugar syrup obtained by hydrolysis of sucrose (invert sugar syrup), or a beet sugar syrup, or a maple syrup or a sugarcane syrup, or a syrup obtained from a plant of the Stevia genus.
Advantageously, the food is chosen from the group formed from coconut albumen (copra) flakes and flour. Advantageously, the food is chosen from the group formed from walnuts, hazelnuts and almonds—in grated and/or powder form.
Advantageously, the food is chosen from the group formed from plant fats, plant oils (for example rapeseed oil, soybean fat, sunflower oil, cocoa butter, groundnut oil, groundnut butter, corn oil, palm oil), animal fats and animal oils (butter, lard, fish oil).
Advantageously, the food is chosen from the group formed from proteins of plant origin and proteins of animal origin. By way of example, examples that may be mentioned include powdered milk—especially powdered skimmed milk—eggs—especially powdered eggs—protein hydrolysates of animal origin and protein hydrolysates of plant origin.
Advantageously and according to the invention, the rodenticidal bait is chosen from the group formed from solid baits comprising flocoumafen and a solid edible excipient. Advantageously, the rodenticidal bait is a solid in divided form, for example in the form of balls or granules. Advantageously, the rodenticidal bait may be a solid in block or paste form that may be consumed by the target rodent pests or a solid material that may be nibbled by the target rodent pests. Advantageously, the solid rodenticidal bait according to the invention may be in the form of a rigid block, a semi-rigid block, a foam, a powder or a gel.
Advantageously, the rodenticidal bait which is in the form of a powder, in the form of a foam or in the form of a gel is suitable for soiling the fur of the target rodent pest(s) and for being ingested by said pest(s) during their grooming.
It may be a solid rodenticidal bait comprising flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4. It may also be a solid rodenticidal bait comprising flocoumafen and in which the amount of said enantiomer E1 is greater than the amount of said enantiomer E4 in the rodenticidal bait. It may also be a solid rodenticidal bait comprising flocoumafen predominantly in the form of said enantiomer E1.
Advantageously and according to the invention, the rodenticidal bait is chosen from the group formed from liquid baits comprising flocoumafen and a liquid edible excipient. The rodenticidal bait is then a drink for target rodent pests.
Advantageously and according to the invention, the rodenticidal bait is chosen from the group formed from liquid baits comprising flocoumafen and a liquid edible excipient. The rodenticidal bait is then a drink for target rodent pests. It may be a solution of flocoumafen in a solvent for flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4. It may also be a solution of flocoumafen in a solvent for flocoumafen and in which the amount of said enantiomer E1 is greater than the amount of said enantiomer E4 in the rodenticidal bait. It may also be a solution of flocoumafen in a solvent for flocoumafen and in which the flocoumafen is predominantly in the form of said enantiomer E1.
It may also be a suspension of flocoumafen in solid form in a liquid medium. It may also be an emulsion of flocoumafen in a liquid medium.
The invention thus also relates to a rodenticidal bait comprising said enantiomer E1, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4, the flocoumafen of the rodenticidal bait being optically active. However, it is not excluded for the flocoumafen of the rodenticidal bait according to the invention comprising said enantiomer E1, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4, to itself be optically inactive.
Advantageously, the rodenticidal bait comprises at least one dye. Such a dye makes it possible in particular to give said rodenticidal bait a colour that is readily detectable and identifiable by a person handling the rodenticidal bait.
Advantageously, the rodenticidal bait comprises at least one preserving agent capable of ensuring its conservation during its storage. Advantageously, the rodenticidal bait comprises at least one bittering compound such as denatonium benzoate, also known as Bitrex®, which is intended to reduce the risks of accidental consumption by non-target organisms.
Advantageously, in a particular variant, the composition and the rodenticidal bait according to the invention exclusively comprise flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4, as rodenticidal substance. In particular, the composition and the rodenticidal bait according to the invention are free of any other anticoagulant substance for rodenticidal use different from flocoumafen. However, in this variant according to the invention, the composition and the rodenticidal bait may comprise any pest-control substance other than a rodenticide, such as an insecticidal and/or acaricidal substance.
Advantageously, in another particular variant, the composition and the rodenticidal bait according to the invention comprise flocoumafen, with the exclusion of a racemic mixture of said enantiomer E1 and of said enantiomer E4, and at least one other substance different from flocoumafen as rodenticidal substance. This other rodenticidal substance different from flocoumafen may be another anticoagulant substance—especially of the anti-vitamin K type or not—or any other non-anticoagulant rodenticidal substance.
The invention also relates to a process for controlling—in particular a process for selectively controlling—target rodent pests, in which there is spread an amount of rodenticidal bait comprising:
The invention also relates to a process for controlling target rodent pests, especially a process for selectively controlling female target rodent pests, in which there is spread an amount of rodenticidal bait according to the invention, said amount of bait being sufficient to be rodenticidal, especially for female target rodent pests.
In such a process, advantageously and according to the invention, a rodenticidal bait is chosen in which the amount of said enantiomer E1 is greater than the amount of said enantiomer E4 in the rodenticidal bait. In such a process, advantageously and according to the invention, flocoumafen is predominantly in the form of said enantiomer E1.
Advantageously and as a variant according to the invention, the following are chosen in combination:
A rodenticidal bait according to this variant of the invention is a rodenticidal bait that is mortal in a single intake, or a “one-shot” bait. Advantageously and according to this variant of the invention, the mass proportion of flocoumafen in the rodenticidal bait is less than 200 ppm, especially between 2 ppm and 200 ppm, preferably between 2 ppm and 100 ppm, more preferentially between 2 ppm and 50 ppm and in particular between 15 ppm and 50 ppm.
Advantageously and in another variant according to the invention, the following are chosen in combination:
Advantageously and according to the invention, said 24-hour periods are consecutive.
This other variant of the invention is thus also directed towards a process for selectively controlling target rodent pests, in which there is spread an amount of rodenticidal bait that is lethal for female target rodent pests which durably consume this rodenticidal bait and generally non-lethal for non-target rodents or animals which accidentally consume this rodenticidal bait. This is then referred to as a “multi-dose” or “multi-feeding” control process. In such a process according to the invention, the consumption of rodenticidal bait by a female target rodent pest over a period of 24 hours is insufficient to result in the death of the target rodent pest, whereas repeated consumption of rodenticidal bait over at least two consecutive days is sufficient to result in the death of the female target rodent pest.
This other variant of the invention is thus directed towards a process for selectively controlling a population of target rodent pests, in which target rodent pests are provided with an amount of rodenticidal bait that is liable to be ingested by the target rodent pests, said amount of rodenticidal bait being sufficient to kill female target rodent pests which consume said rodenticidal bait over several days.
Advantageously, in this other variant of a process according to the invention, the amount of rodenticidal bait spread, the mass proportion of flocoumafen relative to the rodenticidal bait and the proportion of said enantiomer E1 relative to said diastereoisomer D1,4 are adapted so that the consumption of the rodenticidal bait is lethal to female target rodent pests which daily consume rodenticidal bait over at least two 24-hour periods, especially from 3 to 7 periods, said periods possibly being consecutive.
Advantageously, in this other variant of a process according to the invention, since the proportion of said enantiomer E1 is greater than 95%—especially about 100%—relative to the flocoumafen in the rodenticidal bait, the mass proportion of flocoumafen relative to the rodenticidal bait is between 2 ppm and 100 ppm, especially between 2 ppm and 50 ppm, preferably between 2 ppm and 15 ppm, in particular about 10 ppm.
In a process according to the invention, target rodent pests are provided with an amount of rodenticidal bait that is sufficient to satisfy the daily appetite of the female target rodent pests, said rodenticidal bait predominantly comprising said enantiomer E1 relative to said diastereoisomer D1,4 and/or relative to the flocoumafen.
In a process according to the invention, the amount of rodenticidal bait spread, the proportion of said enantiomer E1 relative to said diastereoisomer D1,4 and the mass proportion of flocoumafen relative to the rodenticidal bait are adapted so as to allow consumption of rodenticidal bait for several days by female target rodent pests, while at the same time limiting:
The invention also relates to a configurational stereoisomer of flocoumafen, to a process for obtaining this configurational stereoisomer, to a composition and a rodenticidal bait comprising this configurational stereoisomer and to a process for controlling target rodent pests, which are characterized in combination by all or some of the characteristics mentioned hereinabove or hereinbelow.
Other aims, characteristics and advantages of the invention will emerge on reading the following description and the examples, which are given for purely non-limiting purposes and which refer to the attached figures, in which:
Homogenization of the Liver Sample
About 0.525 g (+0.025 g) of rat liver is weighed out accurately and placed in a 50 mL polypropylene tube. 10 mL of acetone are added and the suspension is homogenized using an Ultra-Turrax® homogenizer/disperser for a time of about 30 seconds. The homogenizer/disperser shaft is rinsed with hot water and then twice with 20 mL of acetone in a polypropylene tube. The homogenate is centrifuged for 5 minutes at a centrifugation speed of 3000 rpm (revolutions per minute). The supernatant is collected and transferred into a test tube. The sample is subjected to evaporation under a stream of nitrogen (N2) at a temperature of 40° C. so as to form a dry extract.
Lipid Removal
1 mL of acetonitrile is added to the tube containing the dry extract so as to dissolve it. The acetonitrile solution is washed twice successively with 1 mL of hexane. The lipid-free extract is dried under a stream of nitrogen (N2) at a temperature of 40° C. and is then taken up in 0.5 mL of methanol and dissolved by vortex stirring. 0.5 mL of ultra-pure (Milli-Q) water is then added. The sample is vortex-homogenized.
Solid-Phase Extraction (SPE) of Flocoumafen
1 mL of dichloromethane (CH2Cl2), then 1 mL of methanol (CH3OH), then 1 mL of ultra-pure (Milli-Q) water are passed through an Oasis HLB 1 cc cartridge (WAT094225, Waters). The lipid-free liver extract (1 mL CH3OH/Milli-Q H2O) containing flocoumafen is then loaded onto the top of the preconditioned cartridge. The liver extract penetrates through the cartridge by gravity on contact with the solid phase of the cartridge. 1 mL of washing solution formed from methanol (CH3OH) and ultra-pure water (H2O) in a 90/10 volume proportion is loaded onto the top of the cartridge. The cartridge is dried by suction under vacuum connected to the bottom of the cartridge. 1 mL of eluting solution formed from dichloromethane (CH2Cl2) and methanol (CH3OH) in a 90/10 volume proportion is then loaded onto the top of the cartridge and an eluate comprising flocoumafen is collected at the bottom of the cartridge. The solvent of the eluate is evaporated off under a stream of nitrogen (N2) at a temperature of 40° C. The sample is taken up in 0.5 mL of acetonitrile (NC—CH3) and the acetonitrile solution containing flocoumafen is filtered through a 0.2 μm porosity filter.
Analysis of the Configurational Stereoisomers of Flocoumafen
The configurational stereoisomers of flocoumafen are separated by high-pressure liquid chromatography using a LUX® Cellulose-4 chiral column (00F-4490-B0, Phenomenex, Le Pecq, France) as stationary phase and a mixture formed from acetonitrile (A) and water comprising 0.1% by volume of formic acid (B), with an A/B volume ratio of 92/8, as mobile phase with a flow rate of the liquid mobile phase in the chromatography column of 0.25 mL/minute. 1 μL of the rat liver extract prepared beforehand as described above is injected. Detection is performed by tandem mass spectrometry (MS/MS) in negative electrospray ionization (ESI) mode. The temperature of the nebulizer gas is 350° C. and its flow rate is 8 L/minute. The pressure of the nebulizer gas is brought to 2700 hPa. In particular, the MRM (“Multiple Reaction Monitoring”) transitions m/z 541.1→382.1 and m/z 541.1→161, corresponding to the flocoumafen signals, are detected.
The retention time values for each of the configurational stereoisomers of flocoumafen are, under the conditions described:
The retention time values t1, t2, t3 and t4 are liable to vary, especially with the temperature of the chromatography column. However, under these chromatographic conditions, the order of elution of the flocoumafen enantiomers remains unchanged. As a guide, for a temperature variation of a few degrees Celsius, the retention time value (t1) of said enantiomer E1 according to the invention may range between 4.4 min and 4.6 min. The retention time value (t2) of enantiomer E2 of said diastereoisomer D2,3 of flocoumafen may range between 5.9 min and 6.4 min. The retention time value (t3) of enantiomer E3 of said diastereoisomer D2,3 of flocoumafen may range between 6.4 min and 6.9 min. The retention time value (t4) of enantiomer E4 of said diastereoisomer D1,4 of flocoumafen may range between 8.9 min and 9.4 min.
Hepatic Persistence of the Configurational Stereoisomers of Flocoumafen in Male Rats and in Female Rats
A solution comprising flocoumafen in a mixture of vegetable oil and 5% of DMSO so that the amount of flocoumafen ingested by each rat is about 2.3 mg per kilogram of rat is administered orally (per os) to 8-week-old male and female laboratory rats (Sprague-Dawley rats, Charles River, Saint-Germain-sur-l'Arbresle, France) weighing between 180 and 200 g. The tube-fed rats are treated daily by subcutaneous administration of a dose of vitamin K1 at a rate of 1 U per rat so as to keep the rats alive for the duration of the experiment.
The ratio of the sum of the amounts of said enantiomer E2 and of said enantiomer E3 (diastereoisomer D2,3) to the amount of flocoumafen in the tube-feeding solution is 59% and the ratio of the sum of the amounts of said enantiomer E1 and of said enantiomer E4 (diastereoisomer D1,4) to the amount of flocoumafen in the tube-feeding solution is 41%.
At 1 day (D+1), 3 days (D+3) and 7 days (D+7) after tube-feeding, six rats anaesthetized beforehand with isoflurane are euthanized, the liver of the euthanized rats is removed and the amounts of enantiomer E1 of flocoumafen according to the invention present in the liver of the tube-fed rats are then extracted from the liver and assayed. The results are given in table 1 below, in which the values of the concentration of each of the flocoumafen enantiomers in the liver are the mean of the values measured on the three rats and expressed in nanograms (ng) per gram of liver and represented in
The mean content of said enantiomer E1 in the liver of male rats is lower than the mean content of said enantiomer E1 in the liver of female rats. A rodenticidal bait and a process for selectively controlling a population of target rodent pests according to the invention makes it possible to target the female target rodent pests, killing said female target rodent pests and limiting the reproduction of the target rodent pests, while at the same time limiting the risks of poisoning animals—especially birds—which prey or carrion-feed on rodent pests, especially weakened target rodent pests which have consumed such a rodenticidal bait (secondary consumption). It is, however, not excluded that certain male target rodent pests may be poisoned in the case of high and repeated consumption of rodenticidal bait according to the invention.
It goes without saying that the invention may be the subject of numerous implementation variants and applications. In particular, a composition, a rodenticidal bait and a process for controlling target rodent pests are subject to an infinite number of variants both in the formulation of the rodenticidal bait and in the embodiments of the process.
| Number | Date | Country | Kind |
|---|---|---|---|
| 15.62164 | Dec 2015 | FR | national |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2016/079860 | 12/6/2016 | WO | 00 |
