Highly wettable, water dispersible, granules including two pesticides

Information

  • Patent Grant
  • 8968757
  • Patent Number
    8,968,757
  • Date Filed
    Wednesday, October 12, 2011
    13 years ago
  • Date Issued
    Tuesday, March 3, 2015
    9 years ago
Abstract
The present disclosure relates to water dispersible granular pesticide compositions, and methods of making and using the compositions. The pesticide compositions include an inner layer including a first pesticide coated on to a substrate, and an outer layer comprising a second pesticide coated on the inner layer. The outer layer increases the water dispersibility of the granular composition, and protects the first pesticide against hydrolysis and photolysis.
Description
FIELD

The present disclosure relates generally to the field of pesticides. In particular, the present disclosure relates to highly wettable, water dispersible granules that include at least two pesticide compositions. The present disclosure also relates to methods of making and using such pesticide granules.


BACKGROUND

Left unattended, pests such as insects and rodents can quickly infest enclosed structures, such as restaurants and homes. Examples of pests which can infest areas in and around enclosed structures include cockroaches, ants, ground beetles and spiders. In addition to being a nuisance, some of these pests can also bring pathogens into the restaurant or home, creating unsanitary eating and living conditions. The use of pesticide compositions has aided in decreasing the infestation of insects in and around residential and commercial structures.


Various types of pesticide compositions and methods of repelling or terminating crawling pests are currently available, including gel baits, glue pads and poisons. Because the pests can enter walls through small cracks and crevices and inhabit relatively inaccessible areas, such as within floors and behind walls, various tools can be used to “flush” the pests from the wall. For example, flushing agents can be sprayed into the areas to irritate or agitate the pests and cause them to leave the inaccessible areas and come out into the open and expose themselves. Once the pests enter the open environment, they are exposed to a pesticide composition that terminates them.


There is an ongoing need to provide effective pesticides.


SUMMARY

In some aspects, the present disclosure relates to a granular pesticide composition comprising an inner layer comprising a first pesticide, and an outer layer comprising a second pesticide. In some embodiments, the first pesticide comprises a reduced risk pesticide. In other embodiments, a substrate is selected from the group consisting of silica particles. In other embodiments, the substrate is selected from the group consisting of soluble inerts, for example, salts and carbohydrates.


In other embodiments, the second pesticide comprises a surfactant pesticide. In some embodiments, the composition comprises a water dispersible granule. In other embodiments, the composition is substantially free of phosphorous.


In other aspects, the present disclosure relates to methods for eliminating pests comprising applying a pesticide composition to an enclosed or partially enclosed area in a structure inhabited by insects, wherein the pesticide composition comprises a water dispersible granule having an inner layer comprising a first pesticide coated on to a substrate and an outer layer comprising a second pesticide coated on the inner layer.


In some embodiments, the methods further comprise diluting the pesticide composition with a diluent before applying the pesticide composition to the enclosed or partially enclosed area. In other embodiments, the diluent comprises water.







DETAILED DESCRIPTION

In some aspects, the present disclosure relates to highly wettable, water dispersible pesticide compositions that include at least two layers, e.g., an inner layer and an outer layer, coated onto a solid substrate. Each layer includes a pesticide composition. The outer layer of pesticide is selected such that it provides an increased water wettability and dispersibility to the granules. The outer layer also aids in preventing degradation, viz., hydrolysis and/or photolysis of the inner layer of pesticide. The outer layer also improves the grease compatibility of the inner layer pesticide, and can further provide cleaning benefits. That is, in some embodiments, the outer layer can act as both a cleaning agent and an insecticide. In some embodiments, the outer layer provides pesticidal properties on contact. In some embodiments, the inner layer provides residual pesticidal properties.


So that the invention may be more readily understood certain terms are first defined.


As used herein, “weight percent,” “wt-%,” “percent by weight,” “% by weight,” and variations thereof refer to the concentration of a substance as the weight of that substance divided by the total weight of the composition and multiplied by 100. It is understood that, as used here, “percent,” “%,” and the like are intended to be synonymous with “weight percent,” “wt-%,” etc.


As used herein, the term “about” refers to variation in the numerical quantity that can occur, for example, through typical measuring and liquid handling procedures used for making concentrates or use solutions in the real world; through inadvertent error in these procedures; through differences in the manufacture, source, or purity of the ingredients used to make the compositions or carry out the methods; and the like. The term “about” also encompasses amounts that differ due to different equilibrium conditions for a composition resulting from a particular initial mixture. Whether or not modified by the term “about”, the claims include equivalents to the quantities.


It should be noted that, as used in this specification and the appended claims, the singular forms “a,” “an,” and “the” include plural referents unless the content clearly dictates otherwise. Thus, for example, reference to a composition containing “a compound” includes a composition having two or more compounds. It should also be noted that the term “or” is generally employed in its sense including “and/or” unless the content clearly dictates otherwise.


Compositions


In some aspects, the present disclosure relates to pesticide compositions including at least two layers. The pesticide compositions can include an inner layer, and an outer layer coated on the inner layer. The inner layer includes a first pesticide composition, and the outer layer includes a second pesticide composition. In some embodiments, the first and second pesticide compositions are not the same. In some embodiments, the first and second pesticide compositions are the same. In some embodiments, the first, second, or both the first and the second pesticide compositions are substantially free of phosphorous.


The pesticide compositions include those that kill or control a variety of pests. Pests killed or controlled by the pesticides include, but are not limited to, arthropods, e.g., insects, arachnids, crustaceans, and others. Arthropods killed or controlled by the pesticide composition include, but are not limited to, cockroaches, and any other crawling pests, for example, ants, ground beetles, spiders, bed bugs, and the like, and flying pests, and their larvae and eggs.


The inner layer includes a first pesticide composition. In some embodiments, a reduced or minimum risk pesticide, as defined by the Environmental Protection Agency (“EPA”) is included as the first inner layer pesticide, but other pesticides can be used as well. Reduce risk pesticides include pesticides with characteristics such as very low toxicity to humans and non target organisms, including fish and birds, low risk of ground water contamination or runoff, and low potential for pesticide resistance. Exemplary active ingredients for reduced risk pesticides include but are not limited to, castor oil, cedar oil, cinnamon and cinnamon oil, citric acid, citronella and citronella oil, cloves and clove oil, corn gluten meal, corn oil, cottonseed oil, dried blood, eugenol, garlic and garlic oil, geraniol, geranium oil, lauryl sulfate, lemon grass oil, linseed oil, malic acid, mint and mint oil, peppermint and peppermint oil, 2-phenethyl propionate (2-phenyethyl propionate), potassium sorbate, putrescent whole egg solids, rosemary and rosemary oil, sesame and sesame oil, sodium chloride, sodium lauryl sulfate, soybean oil, thyme and thyme oil, white pepper, zinc metal strips, and combinations thereof. Examples of other pesticides that can be used in the inner layer include TEMPO® Ultra WP and TEMPO Ultra SC, commercially available from Bayer Professional Care, Suspend SC, available from Bayer Environmental Science, Phantom, available from BASF, Talstar Pro, available from FMC, and Demand CS, available from Syngenta.


In some embodiments, the inner layer includes an effective amount of a pesticide, viz., an amount effective to kill or control a targeted pest, e.g., insect. In some embodiments, the first inner layer includes about 1 wt % to about 90 wt %, about 20 wt % to about 80 wt %, or about 30 wt % to about 60 wt % of a pesticide.


In some embodiments, the first pesticide composition includes a pesticide that has poor grease compatibility. As used herein the term “poor grease compatibility” refers to compounds and compositions that are hydrophobic and lipophilic, and tend to migrate into the grease layer that they come into contact with. Thus, they are not as efficacious against pests as those pesticides which have higher grease compatibilities. In some embodiments, the first pesticide composition is a residual kill pesticide.


The inner layer can be coated onto a substrate. Any substrate capable of being coated with a first pesticide composition can be used. For example, in some embodiments, an insoluble material, e.g., silica particles can be used as the substrate for coating a first pesticide composition on to. In other embodiments, a soluble material, e.g., salts and/or carbohydrates can be used as the substrate. Examples include sodium chloride, sodium acetate, sodium bicarbonate, sodium sesquicarbonate, sodium carbonate, sodium sulfate, trisodium phosphate, disodium phosphate, monosodium phosphate, sodium tripolyphosphate, potassium chloride, potassium acetate, potassium carbonate, sugar, sucrose, and the like. Any material capable of having the first pesticide applied to it can be used as a substrate. Preferred substrates are about 50 microns in diameter or smaller for insoluble substrates.


In other embodiments, the inner layer can be formed by an agglomeration or granulation process.


In other embodiments, a pre-formed first pesticide composition is used as the inner layer already coated on a substrate. For example, a commercially available pesticide available for use in a solid form can be used. In some embodiments, the first pesticide composition comprises a solid form of a reduced risk pesticide as defined by the EPA, but pesticides that do not qualify as reduced risk can also be used.


In some aspects, the outer layer of the pesticide composition includes a second pesticide composition. In some embodiments, the second pesticide composition is a contact kill pesticide when dissolved in water that kills pests or insects on contact. In some embodiments, the second pesticide composition includes a surfactant pesticide. As used herein, the term “surfactant pesticide” refers to a pesticide which also has surfactant properties. That is, a surfactant pesticide refers to a chemical substance which has the ability to kill or control pests, e.g., insects, and also has the ability to reduce or lower the surface tension of a liquid with which the surfactant pesticide comes into contact with. Preferred surfactant pesticides include sodium lauryl sulfate, alcohol ethoxylates, quaternary ammonium compounds, fatty acids, fatty acid soaps, twin-tailed surfactants such as dioctylsulfosuccinate, and mixtures thereof. Preferred surfactant pesticides include a hydrophobic portion with from about 6 to about 16 carbon atoms, or about 8 to 14, or about 10 to 12 carbon atoms. In some embodiments, the surfactant pesticide includes sodium lauryl sulfate. Sodium lauryl sulfate is a surfactant pesticide that is highly soluble in water, e.g., 250 g/L at 20° C.


In other embodiments, the second pesticide composition includes a combination of surfactant pesticide and water. The combination of surfactant pesticide and water can be sprayed on to the inner layer to form the outer layer of the composition, and upon drying form granules. For example, in some embodiments, the second pesticide composition can include a combination of a solid form of surfactant pesticide and water. Suitable component concentrations for a concentrate of the second pesticide composition include between about 40% and about 100%, between about 50% and about 100%, between about 60% and 100%, between about 70% and between about 100%, between about 80% and 100%, between about 90% and about 100%, between about 93% and about 100%, or between about 95% and about 100% surfactant pesticide by weight and balance water.


Examples of suitable solid forms of sodium lauryl sulfate include, but are not limited to, powder, pellet and block forms. An example of a particularly suitable pellet form of sodium lauryl sulfate is needle form sodium lauryl sulfate. An example of a suitable commercially available needle form sodium lauryl sulfate includes Stepanol DX®, CAS number 151-21-3, available from Stephan Company, Northfield, Ill. While both powder form and pellet form sodium lauryl sulfate may be used to form the pesticide composition of the present invention, pellet form sodium lauryl sulfate is generally easier to handle and does not become airborne as easily as other solid forms.


In other embodiments, a commercially available aqueous solution of a surfactant can be used, for example, a 30% sodium lauryl sulfate.


In further embodiments, the pesticide composition may also include additional components or agents, such as additional functional materials. In other embodiments, the first and second pesticides of the pesticide composition may provide a large amount, or even all of the total weight of the pesticide composition, for example, in embodiments having few or no additional functional materials disposed therein.


The functional materials provide desired properties and functionalities to the pesticide composition. For the purpose of this application, the term “functional materials” includes a material that when dispersed or dissolved in a use and/or concentrate solution, such as an aqueous solution, or when included in granules of the present invention, provides a beneficial property in a particular use. Some particular examples of functional materials are discussed in more detail below, although the particular materials discussed are given by way of example only, and a broad variety of other functional materials may be used.


The pesticide compositions may include attractants such as cockroach pheromones (e.g., sex attractants, aggregation pheromones) or food-based attractants (e.g., methylcyclopentenalone, maltol, fenugreek and other flavorings). When an attractant is included in the pesticide compositions, the attractant may constitute between about 0.1% and about 5% by weight of the pesticide composition. The pesticide compositions may also optionally include humectants such as glycerol to slow evaporation and maintain wetness of the pesticide composition after application. When a humectant is included in the pesticide composition, the humectant may constitute between about 0.5% and about 10% by weight of the pesticide composition.


In some embodiments, the pesticide compositions can also include a co-surfactant. Without wishing to be bound by any particular theory, it is thought that the inclusion of a co-surfactant composition can reduce the drying of the second pesticide composition, and prolong the activity of the pesticide composition. Further, it is thought that the inclusion of a co-surfactant can increase the insecticidal efficacy of the compositions. When a co-surfactant composition is included, the co-surfactant composition can be present at a ratio of up to about 1:0.03, 1:0.5, 1:1, or 1:3 of the surfactant pesticide to the co-surfactant composition. Exemplary co-surfactants include long-chain alcohols, amine oxides, guerbet alcohols, guerbet alcohol ethoxylates, protonated fatty acids, and twin-tailed surfactants such as dioctylsulfosuccinate. The co-surfactants preferably have a hydrophobic tail with a carbon chain length of from about 6 to 16, about 8 to 14, or about 10 to 12.


The compositions can also include additional inert ingredients. In some embodiments, the compositions include only additional inert ingredients that can be included in reduced/minimum risk pesticide products exempted under Section 25(b) of the Federal Insecticide, Fungicide, and Rodenticide Act (“FIFRA”).


Methods of Making and Using


The water dispersible granules may be made by a variety of processes. In some aspects, the outer layer can be sprayed or melted on to the inner layer. In some aspects, the water dispersible granules may be made using an agglomeration process, or a fluidized bed process. For example, a substrate, e.g., silica particles or a water soluble salt, can be suspended in a fluidized bed. A solution of the first pesticide composition in a carrier can then be sprayed on to the suspended substrate particles. After the first pesticide composition is coated on to the substrate, the second pesticide composition is sprayed on to the coated substrate. In some embodiments, the second pesticide composition includes sodium lauryl sulfate and water.


In other aspects, a first pesticide composition already pre-formed can be used. That is, a commercially available pesticide composition in a solid form, e.g., granules or powders, can be used. To make compositions according to embodiments of the present invention, a second pesticide composition, e.g., sodium lauryl sulfate can be coated on to the first pesticide composition.


In some aspects, the present disclosure relates to methods for eliminating pests. The methods include applying the pesticide compositions to an enclosed or partially enclosed area in a structure inhabited by pests.


The pesticide compositions can be applied to the area to be treated in a variety of ways. In some embodiments, the granules are applied to the area using a drop type, rotary type, or hand held type applicator. In other embodiments, the pesticide composition granules can be dissolved in a carrier, e.g., water, at the location of use to provide a use solution. Once the pesticide composition has been thoroughly dispersed in the carrier to form a substantially homogeneous or uniform solution, the pesticide composition may be applied onto a surface as a spray or foam. The use solution is applied onto the surface for an amount of time sufficient to terminate the pests.


The pesticide compositions may be employed at any of a wide variety of locations in which it is desired to eliminate pest infestation. The pesticide compositions are effective in killing pests, including crawling and flying pests, and in particular cockroaches. In addition, the pesticide compositions are generally more ecologically sustainable than traditional pesticides, making it particularly useful where it is desired to use an environmentally friendly pesticide. Such applications include using the pesticide compositions in and around restaurants, stores, homes, or other generally enclosed structures in which humans and animals are present.


The pesticide compositions can be applied in and around areas such as apartment buildings, bakeries, beverage plants, bottling facilities, breweries, cafeterias, candy plants, canneries, cereal processing and manufacturing plants, cruise ships, dairy barns, poultry facilities, flour mills, food processing plants, frozen food plants, homes hospitals, hotels, houses, industrial buildings, kennels, kitchens, laboratories, manufacturing facilities, mausoleums, meat processing and packaging plants, meat and vegetable canneries, motels, nursing homes, office buildings, organic facilities, restaurants, schools, stores, supermarkets, warehouses and other public buildings and similar structures. In particular, the pesticide compositions can be applied to surfaces, such as floors, where pests may harbor, including cracks, crevices, niches, dark areas, drains, and other harborage sites.


The pesticide compositions can also be used in methods for controlling insects, arachnids, and mites. The method includes allowing an effective amount of the pesticide compositions to act on the insects, arachnids, and/or mites.


The present disclosure may be better understood with reference to the following examples. These examples are intended to be representative of specific embodiments of the disclosure, and are not intended as limiting the scope of the disclosure.


EXAMPLES
Example 1

Example 1 tested the pesticidal efficacy of a granule with an inner layer pesticide and an outer layer pesticide. The example first looked at the pesticidal properties in a wet panel forced exposure test to determine the efficacy of the pesticide on contact. Then the example looked at the pesticidal properties in a dry panel forced exposure test to determine the residual efficacy of the pesticide.


For the wet panel forced test, 20 adult male German cockroaches are placed on a stainless steel panel. The panel with the cockroaches are placed in a spray tower and sprayed with the pesticide for 60 seconds, starting when the spray comes into contact with the surface of the panel. The cockroaches are removed from the panel and placed in a jar with food and water. The jar is then observed for mortality at certain time intervals post-exposure.


For the dry panel test, panels are prepared by spraying the pesticide on the panel and allowing the panel to dry. Then 20 adult male German cockroaches are placed on the panel and allowed to remain on the panel for 60 seconds. The cockroaches are removed from the panel and placed in a jar with food and water. The jars are observed for mortality at certain time intervals post-exposure. The dry forced exposure tests suggests how the pesticides would perform as a residual pesticide.









TABLE 1







Mortality Over Time Using the Wet Forced Exposure Test















1
5
15
30
1
2
24



min.
min.
min.
min.
hour
hours
hours


















Dried up
83.33
100
100
100
100
100
100


Finito +


Tempo WP


SLS + decyl
31.67
65
100
100
100
100
100


alcohol +


Tempo WP


Tempo WP
8.33
25
100
100
100
100
100


Water
0
0
0
0
0
0
0










Table 1 shows that a granule with dried up Finito as the outer layer (Finito is an aqueous pesticide commercially available from Ecolab Inc., St. Paul, Minn.) plus Tempo WP as the inner layer (a pesticide commercially available from Bayer Professional Care) (final dried composition is 98.8% dried Finito Solid and 5.2% Tempo WP; test solution was made by dispersing 9.45 grams of the dried composition in 90.55 grams of deionized water) was effective against 83.33% of the cockroaches within 1 minute, and 100% within 5 minutes. Also, a granule with SLS and decyl alcohol as the outer layer and Tempo WP as the inner layer (final dried composition was 48.61% SLS, 2.93% decyl alcohol, and 48.46% Tempo WP; test solution was made by dispersing 0.6 gram of the dried composition in 99.4 grams of deionized water) was effective against 31.67% of the cockroaches within 1 minute, and 65% within 5 minutes. Both are providing significantly improved contact kill in comparison to Tempo WP, which was effective against 0% of the cockroaches within 1 minute, and 25% within 5 minutes.









TABLE 2







Mortality Over Time Using the Dry Forced Panel Test














24
48
72




1 Min
Hour
Hour
Hour
1 Week















Dried up Finito +
48.33
33.33
30.00
51.67
51.67


Tempo WP







SLS + decyl
100.00
100.00
100.00
100.00
100.00


alcohol + Tempo







WP







Tempo WP
100.00
100.00
100.00
100.00
100.00


Water
0.00
0.00
0.00
0.00
0.00









Other Embodiments

It is to be understood that while the invention has been described in conjunction with the detailed description thereof, the foregoing description is intended to illustrate, and not limit the scope of the invention, which is defined by the scope of the appended claims. Other aspects, advantages, and modifications are within the scope of the following claims.


In addition, the contents of all patent publications discussed supra are incorporated in their entirety by this reference.


It is to be understood that wherever values and ranges are provided herein, all values and ranges encompassed by these values and ranges, are meant to be encompassed within the scope of the present invention. Moreover, all values that fall within these ranges, as well as the upper or lower limits of a range of values, are also contemplated by the present application.

Claims
  • 1. A method for eliminating pests comprising: applying a pesticide composition to an enclosed or partially enclosed area in a structure inhabited by insects, wherein the pesticide composition comprises a water dispersible granule comprising a substrate,an inner layer comprising a residual kill first pesticide coated on to the substrate andan outer layer comprising a contact kill second pesticide coated on the inner layer, the second pesticide comprising sodium lauryl sulfate and optionally an additional surfactant pesticide selected from the group consisting of alcohol ethoxylates, quaternary ammonium compounds, fatty acids, fatty acid soaps, dioctylsulfosuccinate, and mixtures thereof and the surfactant pesticide has a hydrophobic portion with a carbon chain length of from about 6 to 16,wherein the first pesticide comprises about 20-80 wt-% of the inner layer and the second pesticide comprises at least about 40 wt-% of the outer layer.
  • 2. The method of claim 1, wherein the first pesticide comprises a reduced risk pesticide.
  • 3. The method of claim 1, wherein the substrate is selected from the group consisting of silica particles.
  • 4. The method of claim 1, wherein the pesticide composition is substantially free of phosphorous.
  • 5. The method of claim 2, wherein the reduced risk pesticide comprises an active ingredient selected from the group consisting of castor oil, linseed oil, cedar oil, malic acid, cinnamon, cinnamon oil, mint, mint oil, citric acid, peppermint, peppermint oil, citronella, citronella oil, 2-phenethyl propionate, cloves, clove oil, potassium sorbate, corn gluten meal, putrescent whole egg solids, corn oil, rosemary, rosemary oil, cottonseed oil, sesame, sesame oil, dried blood, sodium chloride, eugenol garlic, garlic oil, soybean oil, geraniol, thyme, thyme oil, geranium oil, white pepper, lauryl sulfate, lemongrass oil, and mixtures thereof.
  • 6. The method of claim 1, wherein the second pesticide further comprises an active ingredient selected from the group consisting of castor oil, linseed oil, cedar oil, malic acid, cinnamon, cinnamon oil, mint, mint oil, citric acid, peppermint, peppermint oil, citronella, citronella oil, 2-phenethyl propionate, cloves, clove oil, potassium sorbate, corn gluten meal, putrescent whole egg solids, corn oil, rosemary, rosemary oil, cottonseed oil, sesame, sesame oil, dried blood, sodium chloride, eugenol garlic, garlic oil, soybean oil, geraniol, thyme, thyme oil, geranium oil, white pepper, lauryl sulfate, lemongrass oil, and mixtures thereof.
  • 7. The method of claim 1, further comprising diluting the pesticide composition with a diluent before applying the pesticide composition to the enclosed or partially enclosed area.
  • 8. The method of claim 7, wherein the diluent comprises water.
  • 9. A method for eliminating pests comprising: applying a pesticide composition to an enclosed or partially enclosed area in a structure inhabited by insects, wherein the pesticide composition comprises a water dispersible granule comprising a silica particle substrate,an inner layer comprising a residual kill first pesticide coated on to the substrate, the first pesticide selected from the group consisting of castor oil, linseed oil, cedar oil, malic acid, cinnamon, cinnamon oil, mint, mint oil, citric acid, peppermint, peppermint oil, citronella, citronella oil, 2-phenethyl propionate, cloves, clove oil, potassium sorbate, corn gluten meal, putrescent whole egg solids, corn oil, rosemary, rosemary oil, cottonseed oil, sesame, sesame oil, dried blood, sodium chloride, eugenol garlic, garlic oil, soybean oil, geraniol, thyme, thyme oil, geranium oil, white pepper, lauryl sulfate, lemongrass oil, and mixtures thereof; andan outer layer comprising a contact kill second pesticide coated on the inner layer, the second pesticide comprising a surfactant pesticide selected from the group consisting of sodium lauryl sulfate, alcohol ethoxylates, quaternary ammonium compounds, fatty acids, fatty acid soaps, dioctylsulfosuccinate, and mixtures thereof and the surfactant pesticide has a hydrophobic portion with a carbon chain length of from about 6 to 16.
  • 10. The method of claim 9, wherein the outer layer provides the granule with increased water wettability.
  • 11. The method of claim 9, wherein the outer layer aids in preventing degradation of the inner layer by hydrolysis or photolysis.
  • 12. The method of claim 9, wherein the outer layer improves the grease compatibility of the inner layer pesticide.
  • 13. The method of claim 9, wherein the inner layer includes about 20 to about 80 wt-% of pesticide.
  • 14. The method of claim 9, wherein the pesticide composition further comprises an attractant.
  • 15. The method of claim 9, wherein the pesticide composition further comprises a humectant.
  • 16. The method of claim 9, wherein the outer layer further comprises a co-surfactant and wherein the ratio of the surfactant pesticide to the co-surfactant is from about 1:0.03 to about 1:3.
  • 17. The method of claim 16, wherein the surfactant pesticide is sodium lauryl sulfate.
  • 18. The method of claim 9, wherein the pesticide is applied in an area where humans are present.
CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority to Provisional Application Ser. No. 61/392,353 filed on Oct. 12, 2010, which is incorporated by reference herein in its entirety.

US Referenced Citations (344)
Number Name Date Kind
3808339 Bordenca Apr 1974 A
3873725 Skinner et al. Mar 1975 A
3920442 Albert et al. Nov 1975 A
4181734 D'Silva Jan 1980 A
4191773 Dorn Mar 1980 A
4194001 Ruscoe et al. Mar 1980 A
4195080 Herrera et al. Mar 1980 A
4198397 Gillings et al. Apr 1980 A
4198782 Kydonieus et al. Apr 1980 A
4200644 Engel Apr 1980 A
4206230 Paul Jun 1980 A
4215138 Ozawa et al. Jul 1980 A
4218468 Paul Aug 1980 A
4226881 Barer Oct 1980 A
4235872 Tocker Nov 1980 A
4235927 Engel Nov 1980 A
4237168 Reifschneider Dec 1980 A
4243677 Engel Jan 1981 A
4255435 Watkins et al. Mar 1981 A
4263287 Dennis Apr 1981 A
4264606 Ozawa et al. Apr 1981 A
4265906 Kasamatsu et al. May 1981 A
4265907 Paul May 1981 A
4268520 Grantham May 1981 A
4268521 Knabke May 1981 A
4268525 Paul May 1981 A
4271181 Eastburg Jun 1981 A
4279895 Carle Jul 1981 A
4291055 Chen Sep 1981 A
4291058 Suchy Sep 1981 A
4299258 Brite Nov 1981 A
4303640 Fuyama et al. Dec 1981 A
4308279 Smeltz Dec 1981 A
4313941 Duinker et al. Feb 1982 A
4320139 Takei et al. Mar 1982 A
4320140 Crounse et al. Mar 1982 A
4335118 Fischer et al. Jun 1982 A
4335252 Engel Jun 1982 A
4342778 Drabek et al. Aug 1982 A
4346091 Sanborn Aug 1982 A
4346092 Sanborn Aug 1982 A
4357348 Kasamatsu et al. Nov 1982 A
4359580 Grasso Nov 1982 A
4361554 Saunders Nov 1982 A
4370346 Punja Jan 1983 A
4375476 Cardis Mar 1983 A
4376785 Matsuo et al. Mar 1983 A
4380537 Monroe Apr 1983 A
4382927 Sherman May 1983 A
4386071 Carle May 1983 A
4391820 Holan et al. Jul 1983 A
4391823 Boxler et al. Jul 1983 A
4393074 Middleton Jul 1983 A
4399152 Brouwer et al. Aug 1983 A
4405353 Angyan et al. Sep 1983 A
4415748 Scharpf et al. Nov 1983 A
4419350 Letchworth et al. Dec 1983 A
4423028 Walker et al. Dec 1983 A
4423042 Dorn et al. Dec 1983 A
4426379 Edwards Jan 1984 A
4436719 Lindaberry Mar 1984 A
4438137 Allan Mar 1984 A
4439430 Reifschneider Mar 1984 A
4447413 Rippstein, Jr. May 1984 A
4450169 Nezot et al. May 1984 A
4457923 Fahmy Jul 1984 A
4461758 Brite Jul 1984 A
4461764 Magee Jul 1984 A
4470966 Costanza et al. Sep 1984 A
4481215 Tocker Nov 1984 A
4490380 Redemann Dec 1984 A
4490390 Priester et al. Dec 1984 A
4496586 Matsui et al. Jan 1985 A
4501742 Harris Feb 1985 A
4504483 Ozawa et al. Mar 1985 A
4510133 Evans Apr 1985 A
4518593 Juvin et al. May 1985 A
4536506 Marcoux et al. Aug 1985 A
4540710 Holan et al. Sep 1985 A
4551546 Punja Nov 1985 A
4562062 Shinjo et al. Dec 1985 A
4564631 Elbert et al. Jan 1986 A
4564639 Nagase et al. Jan 1986 A
4567199 Crowley Jan 1986 A
4568541 Dorn et al. Feb 1986 A
4568670 Reifschneider et al. Feb 1986 A
4582825 Baumann et al. Apr 1986 A
4595679 Broadbent Jun 1986 A
4596890 Kisida et al. Jun 1986 A
4596892 Plummer Jun 1986 A
4602945 Graber et al. Jul 1986 A
4604971 Baker et al. Aug 1986 A
4617316 Plummer Oct 1986 A
4632936 Boase et al. Dec 1986 A
4636523 Plummer Jan 1987 A
4650792 Underwood Mar 1987 A
4659703 Chavdarian Apr 1987 A
4662103 Cheng May 1987 A
4666747 Quinn May 1987 A
4680294 Shiokawa et al. Jul 1987 A
4685423 Baker et al. Aug 1987 A
4688349 Renth Aug 1987 A
4696822 Matsumura et al. Sep 1987 A
4709068 Sieburth Nov 1987 A
4725589 Tsuboi et al. Feb 1988 A
4737509 Plummer Apr 1988 A
4767773 Ayad Aug 1988 A
4780457 Tsuboi et al. Oct 1988 A
4786650 Drabek Nov 1988 A
4796381 Kauth et al. Jan 1989 A
4798839 Ayad Jan 1989 A
4803956 Corrigan et al. Feb 1989 A
4805341 Maeda Feb 1989 A
4808762 Meier et al. Feb 1989 A
4818525 Kamada Apr 1989 A
4822613 Rodero Apr 1989 A
4826682 Sakharova May 1989 A
4833159 Bushell et al. May 1989 A
4837209 Chavdarian Jun 1989 A
4851438 Flashinski Jul 1989 A
4860488 Shigetoyo Aug 1989 A
4861762 Puritch et al. Aug 1989 A
4863718 Bernardo Sep 1989 A
4867972 Girardeau et al. Sep 1989 A
4868209 Punja Sep 1989 A
4873264 Chou et al. Oct 1989 A
4879117 Rombi Nov 1989 A
4888174 Farquharson et al. Dec 1989 A
4888340 Neh et al. Dec 1989 A
4889719 Ohtsubo et al. Dec 1989 A
4889872 Naumann et al. Dec 1989 A
4892732 Parconagian et al. Jan 1990 A
4895871 Lutomski et al. Jan 1990 A
4900758 Fisher Feb 1990 A
4904464 Albanese Feb 1990 A
4904696 Sakamoto et al. Feb 1990 A
4911913 Hostetter et al. Mar 1990 A
4925657 Den Braber et al. May 1990 A
4933181 Brown et al. Jun 1990 A
4936901 Surgant, Sr. et al. Jun 1990 A
4944950 Sakharova Jul 1990 A
4945088 Okamoto et al. Jul 1990 A
4945107 Minetti Jul 1990 A
4956353 Dowd Sep 1990 A
4963584 Hidasi et al. Oct 1990 A
4975425 Barnett, Jr. Dec 1990 A
4975451 Cullen et al. Dec 1990 A
4980373 Kisida et al. Dec 1990 A
4983391 Muneyuki et al. Jan 1991 A
4992275 Lush Feb 1991 A
4997592 Woogerd Mar 1991 A
5017615 Workman May 1991 A
5026727 Bushnell Jun 1991 A
5034404 Uneme et al. Jul 1991 A
5049585 Robson et al. Sep 1991 A
5061489 Bernier et al. Oct 1991 A
5068229 Benoit et al. Nov 1991 A
5091416 Bushell Feb 1992 A
5100667 Chan et al. Mar 1992 A
5106872 Alder et al. Apr 1992 A
5110594 Morita May 1992 A
5122364 Portas Jun 1992 A
5122518 Vrba Jun 1992 A
5128329 Minagawa et al. Jul 1992 A
5152096 Rudolph Oct 1992 A
5153182 Tozzi Oct 1992 A
5166425 Tsushima et al. Nov 1992 A
5223270 Jones Jun 1993 A
5225443 Murphy et al. Jul 1993 A
5238949 Shiokawa et al. Aug 1993 A
5262323 Baird et al. Nov 1993 A
5266324 Stendel et al. Nov 1993 A
5300503 Peake et al. Apr 1994 A
5320855 Roche et al. Jun 1994 A
5326560 Henderson Jul 1994 A
5338544 Donovan Aug 1994 A
5352674 Cummings Oct 1994 A
5369027 Lambert et al. Nov 1994 A
5389662 Pap et al. Feb 1995 A
5401771 Demassey et al. Mar 1995 A
5427794 Miles Jun 1995 A
5446019 Ely et al. Aug 1995 A
5455256 Kamochi et al. Oct 1995 A
5457178 Jackson et al. Oct 1995 A
5476869 Murai et al. Dec 1995 A
5510363 Thirugnanam Apr 1996 A
5516747 Lachut May 1996 A
5521192 Henrie, II et al. May 1996 A
5531981 Kuwazuru et al. Jul 1996 A
5571829 Thirugnanam Nov 1996 A
5578250 Thomas et al. Nov 1996 A
5595749 Rascher et al. Jan 1997 A
5614558 James et al. Mar 1997 A
5620678 Burke Apr 1997 A
5631276 Kern May 1997 A
5641499 Bencsits Jun 1997 A
5646133 Sanders Jul 1997 A
5674846 Johnson et al. Oct 1997 A
5676959 Heitz et al. Oct 1997 A
5683971 Rose et al. Nov 1997 A
5702703 Schnepf et al. Dec 1997 A
5705193 Bourgogne et al. Jan 1998 A
5709890 Sanders et al. Jan 1998 A
5712281 Cullen et al. Jan 1998 A
5712295 Mencke et al. Jan 1998 A
5756459 Jackson et al. May 1998 A
5773016 Nelson Jun 1998 A
5783203 Schutte et al. Jul 1998 A
5792755 Sagenmüller et al. Aug 1998 A
5849870 Warren et al. Dec 1998 A
5860266 Martinet et al. Jan 1999 A
5885598 Knauf et al. Mar 1999 A
5888989 Kern Mar 1999 A
5910323 Lajoie et al. Jun 1999 A
5925670 Silverman et al. Jul 1999 A
5935943 Asai et al. Aug 1999 A
5939438 Yeager et al. Aug 1999 A
5942542 Killick et al. Aug 1999 A
5945114 Ogawa et al. Aug 1999 A
5977186 Franklin Nov 1999 A
5994331 Erdelen et al. Nov 1999 A
5998330 Felton Dec 1999 A
5998475 James et al. Dec 1999 A
5998484 Zobitne et al. Dec 1999 A
6022881 Asai et al. Feb 2000 A
6060489 Erdelen et al. May 2000 A
6074656 Katsuda et al. Jun 2000 A
6090398 Schroder et al. Jul 2000 A
6093413 Matson Jul 2000 A
6103763 Horst Aug 2000 A
6110866 Walker Aug 2000 A
6153181 Nelson et al. Nov 2000 A
6162825 Silverman et al. Dec 2000 A
6218407 Erdelen et al. Apr 2001 B1
6258369 Pullen Jul 2001 B1
6277389 Pullen Aug 2001 B1
6296865 Dujardin et al. Oct 2001 B1
6429180 Wisniewski et al. Aug 2002 B1
6444690 Erdelen et al. Sep 2002 B2
6482863 Munagavalasa et al. Nov 2002 B2
6492357 Nakakura et al. Dec 2002 B1
6534529 Uhr et al. Mar 2003 B2
6541448 Isaac et al. Apr 2003 B2
6544538 Caine Apr 2003 B1
6548085 Zobitne et al. Apr 2003 B1
6564502 Barcay et al. May 2003 B2
6576661 Brück et al. Jun 2003 B1
6582712 Pullen Jun 2003 B2
6582732 Bender et al. Jun 2003 B1
6585990 Huang Jul 2003 B1
6588374 Cottrell et al. Jul 2003 B1
6593293 Baum et al. Jul 2003 B1
6596271 Hammock et al. Jul 2003 B2
6662491 Flinn et al. Dec 2003 B2
6814030 Cottrell et al. Nov 2004 B2
6849633 Okui et al. Feb 2005 B2
6855330 Sirinyan et al. Feb 2005 B2
6855348 Ahn et al. Feb 2005 B2
6867223 Cottrell et al. Mar 2005 B2
6900190 Fischer et al. May 2005 B2
6919090 Fischer et al. Jul 2005 B2
6984662 Cottrell et al. Jan 2006 B2
6986898 Bessette Jan 2006 B1
7019036 Hiromoto Mar 2006 B2
7084138 Fischer et al. Aug 2006 B2
7091233 Fischer et al. Aug 2006 B2
7125565 Sugishita et al. Oct 2006 B2
7132448 Cottrell et al. Nov 2006 B2
7192600 Barcay et al. Mar 2007 B2
7201926 Fried et al. Apr 2007 B2
7205289 Fischer et al. Apr 2007 B2
7208474 Bermudez et al. Apr 2007 B2
7214788 Guzov et al. May 2007 B2
7232845 Fischer et al. Jun 2007 B2
7247756 Theodoridis et al. Jul 2007 B2
7282492 Wengel et al. Oct 2007 B2
7288572 Konze et al. Oct 2007 B2
7297351 Hiromoto Nov 2007 B2
7312204 Erdelen et al. Dec 2007 B2
7326704 Selby Feb 2008 B2
7341735 Pullen Mar 2008 B2
7341736 Flashinski Mar 2008 B2
7345092 Cottrell et al. Mar 2008 B2
7354595 Cottrell et al. Apr 2008 B2
7371768 Okui et al. May 2008 B2
7384647 Ferko, IV Jun 2008 B2
7384927 Iori Jun 2008 B2
7416880 Park et al. Aug 2008 B2
7423062 Tsushima Sep 2008 B2
7435411 Park et al. Oct 2008 B2
7439280 Lu et al. Oct 2008 B2
8110608 Herrera et al. Feb 2012 B2
20010014654 Davister et al. Aug 2001 A1
20030073667 Endris et al. Apr 2003 A1
20030092710 Nakakura et al. May 2003 A1
20030170341 Goodman et al. Sep 2003 A1
20040142903 Femia et al. Jul 2004 A1
20040175405 Mohamed Mahgoub et al. Sep 2004 A1
20050003001 Yamaguchi et al. Jan 2005 A1
20050038094 Warrington Feb 2005 A1
20050058681 Johnson Mar 2005 A1
20050112165 Taylor May 2005 A1
20050152937 Lin Jul 2005 A1
20050169954 Cottrell et al. Aug 2005 A1
20050196416 Kipp et al. Sep 2005 A1
20050233986 Clough Oct 2005 A1
20050244387 Grewal Nov 2005 A1
20050244445 Anderson Nov 2005 A1
20050266036 Awada et al. Dec 2005 A1
20060034898 Amodt et al. Feb 2006 A1
20060063829 Andersch et al. Mar 2006 A1
20060083764 Hernandez et al. Apr 2006 A1
20060093637 Stock et al. May 2006 A1
20060115506 Harmer et al. Jun 2006 A1
20060135564 Kim et al. Jun 2006 A1
20060257440 Asai et al. Nov 2006 A1
20070003586 Homoelle, Jr. et al. Jan 2007 A1
20070009563 Hataipitisuk Jan 2007 A1
20070048346 Ido Mar 2007 A1
20070071785 Craven et al. Mar 2007 A1
20070178128 Bessette Aug 2007 A1
20070202089 Bermudez et al. Aug 2007 A1
20070254927 Cottrell et al. Nov 2007 A1
20070254951 Cottrell et al. Nov 2007 A1
20070259015 Patterson et al. Nov 2007 A1
20070264297 Scialdone et al. Nov 2007 A1
20070275971 Erdelen et al. Nov 2007 A1
20070276014 Cottrell et al. Nov 2007 A1
20080003185 Valpey et al. Jan 2008 A1
20080038214 Cottrell et al. Feb 2008 A1
20080038383 Bessette et al. Feb 2008 A1
20080064603 Pullen Mar 2008 A1
20080070787 Pullen Mar 2008 A1
20080112992 Mohamed Mahgoub et al. May 2008 A1
20080118461 Boucher, Jr. et al. May 2008 A1
20080214400 Pullen Sep 2008 A1
20080214502 Smogoleski et al. Sep 2008 A1
20080214634 Konze et al. Sep 2008 A1
20080233159 Katsuda et al. Sep 2008 A1
20080300225 Marrone Dec 2008 A1
20090057442 Nguyen Mar 2009 A1
20090082204 Royalty et al. Mar 2009 A1
20120087987 Man et al. Apr 2012 A1
20120088828 Man et al. Apr 2012 A1
Foreign Referenced Citations (17)
Number Date Country
101326918 Dec 2008 CN
0 008 880 Mar 1980 EP
0 582 065 Feb 1994 EP
0 936 859 Aug 2002 EP
1 158 964 Apr 2004 EP
1 490 025 Feb 2008 EP
1 572 357 Jul 1980 GB
1 604 860 Dec 1981 GB
2 144 994 Mar 1985 GB
2 145 086 Mar 1985 GB
2 150 565 Jul 1985 GB
WO 9322915 Nov 1993 WO
WO 9422311 Oct 1994 WO
WO 9702748 Jan 1997 WO
WO 0195726 Dec 2001 WO
WO 2008032328 Mar 2008 WO
WO 2009147648 Dec 2009 WO
Non-Patent Literature Citations (7)
Entry
Jakasa, I. et al., “Increased permeability for polyethylene glycols through skin compromised by sodium lauryl sulphate,” Experimental Dermatology, vol. 15, pp. 801-807 (2006).
Longman, G.F., “The analysis of detergents,” Talanta, vol. 22, pp. 621-636 (1975).
Sinniah, B., “Insecticidal effect of aliphatic alcohols against aquatic stages of Aedes mosquitoes,” Transactions of the Royal Society of Tropical Medicine and Hygiene, vol. 77, No. 1, pp. 35-38 (1983).
Sodium Lauryl Sulfate; Exemption From the Requirement of a Tolerance, Federal Register, vol. 74, No. 154, pp. 40503-40509 (Aug. 12, 2009).
van der Merwe, D. et al., “Effect of vehicles and sodium lauryl sulphate on xenobiotic permeability and stratum corneum partitioning in porcine skin,” Toxicology, vol. 206, pp. 325-335 (2005).
Wadaan, M. et al., “Skin Lesions Induced by Sodium Lauryl Sulfate (SLS) in Rabbits,” J. Med. Sci., vol. 5, No. 4, pp. 320-323 (Oct.-Dec. 2005).
International Search Report and Written Opinion cited in International Application No. PCT/US2011/055999 mailed May 18, 2012.
Related Publications (1)
Number Date Country
20120087964 A1 Apr 2012 US
Provisional Applications (1)
Number Date Country
61392353 Oct 2010 US