US20190037846A1 - Insecticidal Polymer Matrix Comprising PBO and DM - Google Patents

Insecticidal Polymer Matrix Comprising PBO and DM Download PDF

Info

Publication number
US20190037846A1
US20190037846A1 US16/157,145 US201816157145A US2019037846A1 US 20190037846 A1 US20190037846 A1 US 20190037846A1 US 201816157145 A US201816157145 A US 201816157145A US 2019037846 A1 US2019037846 A1 US 2019037846A1
Authority
US
United States
Prior art keywords
insecticidal
pbo
matrix
polymer
content
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Abandoned
Application number
US16/157,145
Inventor
Mikkel Vestergaard Frandsen
Michael Stanley Pedersen
Matthieu Zellweger
Sebastien Gouin
Sicco Dirk Roorda
Thi Quynh Chi Phan
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
VESTERGAARD SA
Original Assignee
VESTERGAARD SA
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by VESTERGAARD SA filed Critical VESTERGAARD SA
Priority to US16/157,145 priority Critical patent/US20190037846A1/en
Publication of US20190037846A1 publication Critical patent/US20190037846A1/en
Abandoned legal-status Critical Current

Links

Images

Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N43/00Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
    • A01N43/02Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms
    • A01N43/24Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms
    • A01N43/26Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings
    • A01N43/28Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3
    • A01N43/30Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds having rings with one or more oxygen or sulfur atoms as the only ring hetero atoms with two or more hetero atoms five-membered rings with two hetero atoms in positions 1,3 with two oxygen atoms in positions 1,3, condensed with a carbocyclic ring
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/08Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests containing solids as carriers or diluents
    • A01N25/10Macromolecular compounds
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N25/00Biocides, pest repellants or attractants, or plant growth regulators, characterised by their forms, or by their non-active ingredients or by their methods of application, e.g. seed treatment or sequential application; Substances for reducing the noxious effect of the active ingredients to organisms other than pests
    • A01N25/34Shaped forms, e.g. sheets, not provided for in any other sub-group of this main group
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N53/00Biocides, pest repellants or attractants, or plant growth regulators containing cyclopropane carboxylic acids or derivatives thereof
    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N2300/00Combinations or mixtures of active ingredients covered by classes A01N27/00 - A01N65/48 with other active or formulation relevant ingredients, e.g. specific carrier materials or surfactants, covered by classes A01N25/00 - A01N65/48

Definitions

  • the present invention relates to an insecticidal polymer matrix comprising piperonyl butoxide and deltamethrin.
  • insecticides can be integrated in polymer material in order to prevent insects to work their way through the material.
  • release rates of insecticides in a polymer matrix this is regarded as a difficult issue, because a release that is too rapid exhausts the matrix quickly with regard to insecticidal effect, and a too slow release does not have the desired efficiency or suitable regeneration properties in case the insecticide falls off or is removed, for instance, by washing.
  • the insecticidal dose on the surface of the material should be sufficiently high for killing insects
  • the release should last for more than a year in the case of LLIN, and should allow regeneration of the net's activity in case of washing of the net
  • the overall content of the insecticide and synergist should be low in order to keep the cost for LLIN at a minimum, as well as to minimize the potential exposure of an end-user to the active ingredients contained in the net.
  • the latter are important factors, because the largest markets for LLIN are regions with low income, and the primary end-users are infants and young children.
  • an insecticidal polymer matrix made of a material containing Piperonyl Butoxide (PBO) and deltamethrin (DM) as part of the material for migration of the PBO and the DM from inside the material to the surface of the matrix.
  • PBO Piperonyl Butoxide
  • DM deltamethrin
  • the PBO content is higher than 3 times the content of the DM in the polymer matrix in terms of weight.
  • the PBO content is higher than 4 times or 5 times the content of the DM in the polymer matrix, for example between 5 and 10 times or between 8 and 10.
  • the above mentioned minimum ratios between the PBO and the pyrethroid are much higher than the ratio of 2 as disclosed in WO 00/40084.
  • the invention is highly suitable for producing insecticidal fibres for LLIN and other insecticidal fabrics.
  • the polymer may advantageously be a polyolefin, for example polypropylene or polyethylene.
  • the example states the content of fine silica powder, zinc stearate, and other ingredients affecting the migration rate of permethrin.
  • the effective insecticidal amount needed on the surface of the substrate is generally different for the two insecticides permethrin and DM.
  • the conclusion is that the ratio should be much smaller than the stated 12.1 for permethrin.
  • a ratio of 5 in a HDPE/LDPE matrix without other ingredients corresponds to 83% HDPE and 17% HDPE if no other ingredients are included in the matrix, and a ratio of 20 corresponds to 95% HDPE and 5% LDPE.
  • the apparent broad interval of 5 to 20 corresponds to the relatively narrow interval of 83% to 95%.
  • the amount of LDPE in a polymer matrix with HDPE should not be too high, in order to assure an optimal migration rate of the PBO and the DM, whilst concomitantly achieving optimal mechanical properties of the polymer matrix.
  • both substances migrate to the surface of the material, preferably a mosquito net, and expose the insect to PBO and DM instantaneously. This is a different strategy than for the micro capsules in the above mentioned International patent application WO 2006/111553 with a sequential exposure of PBO followed by DM.
  • the two polymers HDPE and LDPE may be mixed with other polymers, experiments did show good results with only these two polymers constituting the polymer matrix.
  • the matrix is free from fine silica powder, or zinc stearate, or both of them in contrast to the matrix as disclosed in the above mentioned WO 2008/004711.
  • the surface content of PBO and DM on the surface of a polymer matrix depends on the migration rate of PBO and DM in the polymer but also on the thickness of the polymer substrate (i.e. the distance to the surface).
  • the migration rate is influenced by, amongst other factors, the proportion of amorphous phase in the polymer (i.e. the percentage of crystallinity), the diffusion coefficient, which, in turn, is affected by the temperature and the degree of affinity between the additives and the polymer. Therefore, the surface content of DM and PBO at any moment in time is determined by a combination of various thermodynamic effects but also by the shape of the polymeric substrate being in the form of a yarn, a foil, or a bulk product.
  • the above ratios were verified as being especially useful for an insecticidal matrix in the form of a fully drawn monofilament yarn with a diameter of between 0.05 mm and 0.3 mm, preferably between 0.1 mm and 0.15 mm.
  • the HDPE and LDPE ratio of between 5 and 11, 5 and 10, or between 8 and 10, was suitable for such filaments.
  • the above figures are also useful for multifilaments having a linear density in the same range.
  • the content of deltamethrin preferably, is less than 1.5%, more preferably less than 1%, of the weight of the polymer matrix.
  • a useful amount of DM in a matrix according to the invention is between 1 g and 6 g per kg polymer, for example, between 1 g and 5 g or between 2 g and 6 g or between 3 g and 5 g per kg polymer.
  • Another preferred combination is
  • a highly preferred use of the filament matrix according to the invention is a monofilament yarn as part of a woven net, especially bed nets against mosquitoes.
  • the entire net may be made of such insecticidal matrices according to the invention, but in some cases, it is preferred that only the roof is made thereof.
  • the side walls could then be made of polymer containing DM but not PBO, for example a polyethylene matrix with DM.
  • the side walls are made of another material, for example polyethylene terephthalate (PET), also called polyester (PES).
  • One of the ways to slow down chemical or photochemical degradation of PBO and DM on the surface of the matrix uses an antioxidant distributed, preferably homogenously distributed, in the polymeric substrate.
  • Such antioxidants is used to decompose as fast as possible any reactive species, for example radicals and peroxides, formed with time on order to prevent reaction with and changing of the chemical nature of DM or PBO in such a way that their bioactivities is detrimentally affected.
  • promotors or inhibitors may be used to adjust the migration speed.
  • some promotors or inhibitors may work more or less on DM than on PBO, by which the migration speed of these two components can be adjusted relatively.
  • the matrix according to the invention is primarily intended for extrusion, however, it may as well be used in moulding processes.
  • the DM and the PBO are incorporated into the molten polymer.
  • ingredients for a matrix according to the invention are found among UV protectors, plasticizers, colorants, preservatives, detergents, fillers, impact modifiers, antifogging agents, blowing agents, clarifiers, nucleating agents, coupling agents, conductivity-enhancing agents to prevent static electricity, stabilizers, for example, carbon and oxygen radical scavengers, flame retardants, mould release agents, optical brighteners, spreading agents, antiblocking agents, foam-forming agents, anti-soiling agents, thickeners, further biocides, wetting agents, plasticizers adhesive or anti-adhesive agents, fragrance, pigments and dyestuffs and other liquids including water or organic solvents.
  • UV protectors for example, carbon and oxygen radical scavengers, flame retardants, mould release agents, optical brighteners, spreading agents, antiblocking agents, foam-forming agents, anti-soiling agents, thickeners, further biocides, wetting agents, plasticizers adhesive or anti-adhesive agents, fragrance,
  • the matrix may be coated with other insecticidal agents, for example Carbamates or Organophosphates. This can be used as a measure against insecticidal resistance. However, in this case, it should be assured that the coating is configured for migration of the DM and PBO through the coating.
  • insecticidal agents for example Carbamates or Organophosphates.
  • the matrix may also be used for tarpaulins, foils, flat yarns and bulk material.
  • Such different materials may be combined by different kind of bonding techniques or sewing techniques.
  • materials with an insecticidal polymer matrix according to the invention may be combined with materials containing other insecticides.
  • a net or fabric with a polymer matrix according to the invention may be combined with a different net, fabric, foil, flat yarn or tarpaulin containing a different insecticide in order to combat insecticidal resistance.
  • the extrusion should be relatively mild, with a temperature lower than 240° C., and with minimal residence time, water quenching of the yarns, and in-line drawing of the yarn to a draw ratio of 5 to 10, rather 8 to 10, thus, achieving the crystallinity of the yarn/matrix associated with the state of “fully drawn yarn” and the desired migration rate and as well as other suitable physical properties.
  • an insecticidal polymer matrix is selected with HDPE (high density polyethylene), LDPE (low density polyethylene), wherein the ratio of the contents of HDPE and LDPE is between 3 and 30, preferably between 5 and 20 or between 5 and 11 or between 8 and 10.
  • HDPE high density polyethylene
  • LDPE low density polyethylene
  • the ratio of the contents of HDPE and LDPE is between 3 and 30, preferably between 5 and 20 or between 5 and 11 or between 8 and 10.
  • Such a matrix is advantageous also for other insecticides than DM and other synergists than PBO.
  • the insecticide, and optionally the synergist should be able to migrate in the matrix.
  • a non limiting appropriate content of DM is larger than 1 g/kg, preferably larger than or at least 2 g/kg.
  • the content of DM is lower than 5 g/kg, preferably at most or lower than 4 g/kg.
  • an interval of between 1 and 5 g/kg or, preferably, between 2 and 4 g/kg has been experienced as a good interval for such fibres in mosquito nets.
  • the end points of all stated intervals may be part of the intervals.
  • FIG. 1 illustrates the influence of time lag on the efficacy of PBO exposure and DM
  • FIG. 2 illustrates the effect of the content ratio between PBO and DM
  • FIG. 3 shows a first embodiment of a bed net according to the invention with a roof that contains PBO and DM;
  • FIG. 4 shows a second embodiment of a bed net according to the invention, the bed net having a skirt
  • FIG. 5 illustrates a rectangular net
  • the path leading to the invention did comprise a number of intermediate steps, in as much as the solution, despite its simplicity is not straightforward.
  • One of the corner stones of the invention is the fact that experiments revealed that the bioefficacy of PBO and DM treatment is highest when mosquitoes were exposed to PBO and DM simultaneously. As described above, this is against the teaching in the field of insecticidal nets. A proof for this is illustrated in FIG. 1 , showing that for different dosages, there was a remarkable increase in efficacy when DM and PBO were provided to the mosquito at the same time.
  • polyester has a very slow migration rate, which was not sufficient to release enough DM and PBO through migration of polyester yarn of 100 Denier, even when used a multifilament with 35 filaments.
  • HDPE had a release rate which was higher than for polyester, but not high enough for sufficient insecticidal efficacy or regeneration at a rate suitable for mosquito netting materials, despite good mechanical properties making it suitable for knitting into netting material.
  • LDPE has a migration rate, which is far too high for a LLIN, and yarns made of pure LDPE have low mechanical properties that make them unsuitable for knitting into netting material.
  • a mixture of LDPE and HDPE was envisaged, and it was found empirically, that for sufficient but also long lasting release of DM and PBO, a mixture of HDPE and LDPE was optimum, where the weight ratio between HDPE and LDPE was between 30 and 3 and rather between 20 and 5.
  • the ratio depends on the thickness of the matrix.
  • the HDPE/LDPE weight ratio was best between 15 and 25 and for yarns with a thickness of 0.25 mm, the ratio was best between 4 and 7.
  • the ratio may be interpolated.
  • Examples of successful yarns had diameters of between 0.10 mm and 0.15 mm, for example around 0.12 mm, and a content of HDPE and LDPE in terms of weight at a ratio between 8 and 10, for example around 9, and containing 4 g DM per kg polymer and 25 g PBO per kg polymer. Due to necessary initial migration before a sufficient content is reached at the surface of the matrix, the yarn had to be stored for a certain time to reach sufficient efficacy, for example a week to reach 80% efficacy.
  • the content of DM and PBO may be varied.
  • the content of DM in the yarn with a thickness of between 0.10 mm and 0.15 mm, and a HDPE and LDPE weight content ratio of between 8 and 10, the content of DM may be selected between 2 g and 6 g DM per kg polymer and correspondingly 4 to 10 times as much PBO, preferably between 5 and 7 times as much PBO, for example 6 times as much PBO.
  • the monofilament polyethylene yarns may successfully be used for bed nets, where the entire net is provided with such material.
  • the extruded HDPE/LDPE monofilament yarn may be used for the top part of the net.
  • the efficacy will in most cases still be high, because mosquitoes typically attack their potential victims from above and tend to land on the roof of bed nets, especially rectangular bed nets.
  • migration promoters may be included in the molten matrix prior to extrusion of the insecticidal polyethylene blend.
  • FIG. 3 illustrates a conical canopy net 1 above a bed 6 to protect humans on the bed 6 from being attacked by insects, primarily mosquitoes.
  • the roof 4 of the net 1 is provided as a material according to the invention with PBO and DM incorporated in a polymer matrix, and the side walls 5 of the canopy 1 comprise an insecticide but no PBO.
  • a stabilising ring 9 is inserted between the roof 4 and the side walls 5 .
  • FIG. 4 illustrates a conical canopy insecticidal barrier according to another embodiment of the invention, wherein the roof 4 and the side wall 5 are provided as a material according to the invention with PBO and DM incorporated in a polymer matrix.
  • the side wall 5 extends to the lower edge 30 of the barrier and has an upper part 2 and a lower part 3 .
  • the canopy insecticidal barrier is intended to cover a space for human beings or animals, for example a bed 6 as illustrated in FIG. 4 .
  • the lower part 3 of the barrier 1 is exposed to surface touch and, therefore, exposed to abrasion of insecticide from the surface of the material.
  • the lower part 3 is has a material with higher abrasion resistance and mechanical strength, for example a stronger net, a fabric or a tarpaulin or a combination of these. Also, the lower part 3 may be provided with higher insecticidal content in order to take into account the higher abrasion of the insecticide from the surface of the material.
  • the thickness of the filaments for bed nets may vary in dependency of the actual requirements for the net.
  • yarns with a weight of between 50 Denier and 100 Denier are used.
  • FIG. 5 shows a rectangular shape for a net, which may substitute the shapes of the nets in FIG. 4 and FIG. 3 .
  • the net in FIG. 5 has a roof 4 with a polymer matrix according to the invention, whereas the side walls 5 are multifilament polyester in order for the side walls to have soft, cotton like feeling.
  • the net has a tighter knit in this part 3 .
  • the walls of the net are provided without PBO but with DM impregnation complying with WHO specification 333/TC and being wash resistant and largely in line with the impregnation method in the disclosure of International patent application WO 01/37662, which also is used for the well known bed net under the trademark PermaNet®.
  • the side wall 5 is provided with between 2.5 g and 3.5 g DM per kg of the matrix, which mainly is the polymer.
  • the amount per square meter is higher.
  • the DM level is 115 mg/m 2 of the lower part 3 of the side wall 5 and 85 mg/m 2 in the remaining part of the side wall 5 .
  • the preferred net had a minimum of 24 holes per cm 2 .
  • the preferred amount of DM in the roof net with 100 Denier was chosen to be between 3 and 5 g/kg cooperating with a PBO content between 5 to 7 times, rather around 6 times, as large as the DM content.

Abstract

An insecticidal polymer matrix containing Piperonyl Butoxide (PBO) and deltamethrin (DM), wherein the ratio between the content of PBO and the content of DM in terms of weight is higher than 3.

Description

    FIELD OF THE INVENTION
  • The present invention relates to an insecticidal polymer matrix comprising piperonyl butoxide and deltamethrin.
  • BACKGROUND OF THE INVENTION
  • In connection with insecticide control, it is well known that insecticides can be integrated in polymer material in order to prevent insects to work their way through the material. However, when it comes to the control of release rates of insecticides in a polymer matrix, this is regarded as a difficult issue, because a release that is too rapid exhausts the matrix quickly with regard to insecticidal effect, and a too slow release does not have the desired efficiency or suitable regeneration properties in case the insecticide falls off or is removed, for instance, by washing.
  • For crop sheets, as disclosed in U.S. Pat. No. 4,888,174, it is known to mix LDPE with other polymers in order to reduce the migration speed. This is in line with the disclosure of International Patent Application WO 02/34487, stating that “the selection of the polymers depends on the desired release rate”, where the disclosure proposes a pesticideretaining layer of LDPE (low density polyethylene) bonded to a layer of HDPE (high density polyethylene), where the HDPE layer prevents a too fast release of the insecticide.
  • For cables, it is known from U.S. Pat. No. 4,680,328 to extrude insecticidal polymer blends with LDPE, HDPE and LLDPE (linear low density polyethylene) and a preferred insecticide halopyridyl phosphate.
  • Apart from the difficulty of achieving a suitable migration speed of insecticide in polymer matrices, the combination of an insecticide, for example DM (Deltamethrin), and a synergist, for example PBO (piperonyl butoxide), incorporated in a polymer matrix implies additional challenges. Despite the fact that incorporation of a pyrethroid and PBO has been reported in connection with pet collars, for example in International patent application WO 00/40084 or WO 06/127407, the migration speed for long lasting insecticidal nets (LLIN) or fabrics is still an unresolved problem in practice. This is due to the fact that several parameters have to be fitted together to yield a product that is satisfactory. The parameters have to be found such that, firstly, the insecticidal dose on the surface of the material should be sufficiently high for killing insects, secondly, the release should last for more than a year in the case of LLIN, and should allow regeneration of the net's activity in case of washing of the net, and thirdly, the overall content of the insecticide and synergist should be low in order to keep the cost for LLIN at a minimum, as well as to minimize the potential exposure of an end-user to the active ingredients contained in the net. The latter are important factors, because the largest markets for LLIN are regions with low income, and the primary end-users are infants and young children.
  • Especially, for insecticidal polymer matrices containing DM and PBO, the optimal ratio between the content of DM relative to the content of PBO in terms of weight is still an open questions.
  • International patent application WO 2006/111553 discloses microcapsules with a solution of an insecticide, for example DM, and a synergist, for example PBO, in an aqueous suspension inside a polyurea capsule. The ingredients of the microcapsule are released due to breakage of the microcapsule wall when it dries after spraying. The background for this disclosure is the assumption that release of the insecticide should be several hours delayed as compared to the release of the synergist. In the disclosed Example 5, the amount of synergist PBO relatively to the insecticide DM is a factor of 2 in the premix A. As shown in FIG. 1, this premix is then surrounded by an emulsion containing a premix B containing 81% PBO. When used in connection with FIG. 2 of WO 2006/111553, the blend of Premix A and premix B with 5.9% DM and 23.9% PBO yields a ratio of 4.1 between PBO and DM which is further surrounded by premix B containing PBO. Although stating precise figures for containment of PBO and DM in an aqueous suspension inside a microcapsule for delayed release of DM relative to PBO, this disclosure does not give any hint as to the content of PBO relative to DM in a polymer matrix, for example a polyethylene matrix, where the insect shall be exposed to PBO and DM simultaneously by DM and PBO migrated to the surface of the matrix.
  • OBJECT OF THE INVENTION
  • Therefore, it is the object of the invention to provide an insecticidal polymer matrix with DM and PBO, where the ratio between DM and PBO is optimised.
  • DESCRIPTION OF THE INVENTION
  • This purpose is achieved with an insecticidal polymer matrix made of a material containing Piperonyl Butoxide (PBO) and deltamethrin (DM) as part of the material for migration of the PBO and the DM from inside the material to the surface of the matrix. The PBO content is higher than 3 times the content of the DM in the polymer matrix in terms of weight. Preferably, the PBO content is higher than 4 times or 5 times the content of the DM in the polymer matrix, for example between 5 and 10 times or between 8 and 10. The above mentioned minimum ratios between the PBO and the pyrethroid are much higher than the ratio of 2 as disclosed in WO 00/40084.
  • The invention is highly suitable for producing insecticidal fibres for LLIN and other insecticidal fabrics.
  • The polymer may advantageously be a polyolefin, for example polypropylene or polyethylene.
  • International patent application WO 2008/004711 discloses an insecticidal resin containing HDPE and LDPE. Deltamethrin is one of the possibilities of insecticides, however, no relation is stated for the ratio between HDPE and LDPE in this resin with deltamethrin. A ratio of 12.1 is implicitly stated in a single example for an HDPE/LDPE matrix containing 87.23% HDPE and 7.2% LDPE, permethrin, fine silica powder and a number of other ingredients. Although permethrin is also a pythroid, this ratio of 12.1 contains no information about advantageous ratios of HDPE/LDPE for deltamethrin (DM). This is so, because
      • DM has a much higher molecular weight than permethrin, which influences the diffusion coefficient;
      • DM has a higher polarity than permethrin which results in DM having a lower affinity in the non-polar PE; and
      • DM has a vapour pressure an order of magnitude lower than permethrin.
  • Furthermore, the example states the content of fine silica powder, zinc stearate, and other ingredients affecting the migration rate of permethrin. In addition, the effective insecticidal amount needed on the surface of the substrate, is generally different for the two insecticides permethrin and DM. Using this above information about the difference between DM and permethrin, the conclusion is that the ratio should be much smaller than the stated 12.1 for permethrin. However, it is desirable to have a more precise indication for the ratio between HDPE and LDPE in an insecticidal matrix useful in connection with DM.
  • Experimentally, there have been achieved good results for polyethylene matrices containing HDPE and LDPE, wherein the ratio of the contents of HDPE and LDPE is between 3 and 30, preferably between 5 and 20, for example between 5 and 11 or between 8 and 10.
  • Having regard to the interval of between 5 and 20 when containing DM, this result is surprising relative to the disclosure of a ratio of 12.1 for permethrin in International patent application WO 2008/004711, because one should expect the optimal ratio for DM be substantially different from 12.1, for example a ratio equal to a value around 2 or less due to the entirely different nature of DM, which is in solid form with entirely different parameters than the liquid permethrin.
  • The argument becomes more illustrative when using percentages. A ratio of 5 in a HDPE/LDPE matrix without other ingredients corresponds to 83% HDPE and 17% HDPE if no other ingredients are included in the matrix, and a ratio of 20 corresponds to 95% HDPE and 5% LDPE. Thus, the apparent broad interval of 5 to 20 corresponds to the relatively narrow interval of 83% to 95%. Having regard to the entire different nature of permethrin, one would expect the advantageous content of HDPE in the case of deltamethrin be much smaller than the than the 87.23% as disclosed for permethrin in WO 2008/004711. However, surprisingly, this is not the case.
  • As experiments have shown, the amount of LDPE in a polymer matrix with HDPE should not be too high, in order to assure an optimal migration rate of the PBO and the DM, whilst concomitantly achieving optimal mechanical properties of the polymer matrix. In this case, both substances migrate to the surface of the material, preferably a mosquito net, and expose the insect to PBO and DM instantaneously. This is a different strategy than for the micro capsules in the above mentioned International patent application WO 2006/111553 with a sequential exposure of PBO followed by DM.
  • Though, the two polymers HDPE and LDPE may be mixed with other polymers, experiments did show good results with only these two polymers constituting the polymer matrix. Also, preferably, the matrix is free from fine silica powder, or zinc stearate, or both of them in contrast to the matrix as disclosed in the above mentioned WO 2008/004711.
  • The surface content of PBO and DM on the surface of a polymer matrix depends on the migration rate of PBO and DM in the polymer but also on the thickness of the polymer substrate (i.e. the distance to the surface). The migration rate is influenced by, amongst other factors, the proportion of amorphous phase in the polymer (i.e. the percentage of crystallinity), the diffusion coefficient, which, in turn, is affected by the temperature and the degree of affinity between the additives and the polymer. Therefore, the surface content of DM and PBO at any moment in time is determined by a combination of various thermodynamic effects but also by the shape of the polymeric substrate being in the form of a yarn, a foil, or a bulk product.
  • The above ratios were verified as being especially useful for an insecticidal matrix in the form of a fully drawn monofilament yarn with a diameter of between 0.05 mm and 0.3 mm, preferably between 0.1 mm and 0.15 mm. Especially, the HDPE and LDPE ratio of between 5 and 11, 5 and 10, or between 8 and 10, was suitable for such filaments. However, the above figures are also useful for multifilaments having a linear density in the same range.
  • The content of deltamethrin, preferably, is less than 1.5%, more preferably less than 1%, of the weight of the polymer matrix.
  • A useful amount of DM in a matrix according to the invention is between 1 g and 6 g per kg polymer, for example, between 1 g and 5 g or between 2 g and 6 g or between 3 g and 5 g per kg polymer.
  • A preferred combination of parameters is the following,
      • the insecticidal matrix is in the form of a monofilament, preferably fully drawn, with a diameter of between 0.05 mm and 0.30 mm, or an insecticidal matrix in the form of monofilaments of the type between 50 and 100 Denier,
      • the weight content of DM is between 2 g and 6 g, for example between 3 g and 5 g, per kg polymer,
      • the weight content of PBO is more than 3 times, or rather more than 5 times, the weight content of the DM.
  • Another preferred combination is
      • the insecticidal matrix is in the form of a monofilament, preferably fully drawn, with a diameter of between 0.05 mm and 0.30 mm, or an insecticidal matrix in the form of monofilaments of the type between 50 and 100 Denier,
      • the ratio between the content of HDPE relative to the content of LDPE in the matrix is between 8 and 10, for example the content of LDPE is between 9% and 11%;
        • the weight content of DM is between 2 g and 6 g, for example between 3 g and 5 g, per kg polymer,
        • the weight content of PBO is more than 3 times, or rather more than 5 times, the weight content of the DM.
  • A preferred combination of parameters were the following,
      • the insecticidal matrix is in the form of a monofilament, preferably fully drawn, with a diameter of between 0.10 mm and 0.15 mm, or an insecticidal matrix in the form of monofilaments of the type between 50 and 100 Denier,
      • the ratio between the content of HDPE relative to the content of LDPE in the matrix is between 8 and 10, for example the content of LDPE is between 9% and 11%;
      • the weight content of DM is between 3 g and 5 g per kg polymer,
      • the weight content of PBO is between 5 and 7 times the weight content of the DM.
  • At this point, it should be emphasized that the content of DM is in the sub-percent range and the content of PBO is in the range of a few % only, whereas in International application WO 00/40084 the content of Pyrethroid is in the range of up to 10% and the content of PBO is in the range up to 20%. By including vast amounts of insecticide and synergist in a matrix, high insecticidal efficiency and also relatively long lasting effect can, indeed, be achieved. However, for LLIN, this must withstand the additional constraint of regeneration of insecticidal activity after washing in an interval that is relevant for the end product, typically less than seven days. Furthermore, the risk to end users and the production costs should be low, which requires an as low content as possible, though still enough for sufficient long lasting effect and multiple regenerations following repeated washings at regular intervals.
  • A highly preferred use of the filament matrix according to the invention is a monofilament yarn as part of a woven net, especially bed nets against mosquitoes. For bed nets, the entire net may be made of such insecticidal matrices according to the invention, but in some cases, it is preferred that only the roof is made thereof. The side walls could then be made of polymer containing DM but not PBO, for example a polyethylene matrix with DM. Alternatively, the side walls are made of another material, for example polyethylene terephthalate (PET), also called polyester (PES).
  • One of the ways to slow down chemical or photochemical degradation of PBO and DM on the surface of the matrix uses an antioxidant distributed, preferably homogenously distributed, in the polymeric substrate. Such antioxidants is used to decompose as fast as possible any reactive species, for example radicals and peroxides, formed with time on order to prevent reaction with and changing of the chemical nature of DM or PBO in such a way that their bioactivities is detrimentally affected.
  • In addition, special migration promotors or inhibitors may be used to adjust the migration speed. For example, some promotors or inhibitors may work more or less on DM than on PBO, by which the migration speed of these two components can be adjusted relatively.
  • The matrix according to the invention is primarily intended for extrusion, however, it may as well be used in moulding processes. Thus, the DM and the PBO are incorporated into the molten polymer.
  • Other ingredients for a matrix according to the invention are found among UV protectors, plasticizers, colorants, preservatives, detergents, fillers, impact modifiers, antifogging agents, blowing agents, clarifiers, nucleating agents, coupling agents, conductivity-enhancing agents to prevent static electricity, stabilizers, for example, carbon and oxygen radical scavengers, flame retardants, mould release agents, optical brighteners, spreading agents, antiblocking agents, foam-forming agents, anti-soiling agents, thickeners, further biocides, wetting agents, plasticizers adhesive or anti-adhesive agents, fragrance, pigments and dyestuffs and other liquids including water or organic solvents.
  • Apart from the incorporation of DM and PBO in the matrix, the matrix may be coated with other insecticidal agents, for example Carbamates or Organophosphates. This can be used as a measure against insecticidal resistance. However, in this case, it should be assured that the coating is configured for migration of the DM and PBO through the coating.
  • Apart from using the matrix according to the invention for bednets and fabrics, the matrix may also be used for tarpaulins, foils, flat yarns and bulk material. Such different materials may be combined by different kind of bonding techniques or sewing techniques. Also, materials with an insecticidal polymer matrix according to the invention may be combined with materials containing other insecticides. For example, a net or fabric with a polymer matrix according to the invention may be combined with a different net, fabric, foil, flat yarn or tarpaulin containing a different insecticide in order to combat insecticidal resistance.
  • The extrusion should be relatively mild, with a temperature lower than 240° C., and with minimal residence time, water quenching of the yarns, and in-line drawing of the yarn to a draw ratio of 5 to 10, rather 8 to 10, thus, achieving the crystallinity of the yarn/matrix associated with the state of “fully drawn yarn” and the desired migration rate and as well as other suitable physical properties.
  • Generally, it seems that an advantage over the prior art is achieved, if an insecticidal polymer matrix is selected with HDPE (high density polyethylene), LDPE (low density polyethylene), wherein the ratio of the contents of HDPE and LDPE is between 3 and 30, preferably between 5 and 20 or between 5 and 11 or between 8 and 10. Such a matrix is advantageous also for other insecticides than DM and other synergists than PBO. However, the insecticide, and optionally the synergist, should be able to migrate in the matrix.
  • For mosquito nets, for example with fibres of 75 or 100 Denier, a non limiting appropriate content of DM is larger than 1 g/kg, preferably larger than or at least 2 g/kg. Optionally, the content of DM is lower than 5 g/kg, preferably at most or lower than 4 g/kg. Thus, an interval of between 1 and 5 g/kg or, preferably, between 2 and 4 g/kg has been experienced as a good interval for such fibres in mosquito nets.
  • Optionally, the end points of all stated intervals may be part of the intervals.
  • DESCRIPTION OF THE DRAWING
  • The invention will be explained in more detail with reference to the drawing, where
  • FIG. 1 illustrates the influence of time lag on the efficacy of PBO exposure and DM;
  • FIG. 2 illustrates the effect of the content ratio between PBO and DM;
  • FIG. 3 shows a first embodiment of a bed net according to the invention with a roof that contains PBO and DM;
  • FIG. 4 shows a second embodiment of a bed net according to the invention, the bed net having a skirt;
  • FIG. 5 illustrates a rectangular net.
  • DETAILED DESCRIPTION OF THE INVENTION
  • The path leading to the invention did comprise a number of intermediate steps, in as much as the solution, despite its simplicity is not straightforward.
  • In the teaching in the field of insecticidal nets, it has hitherto been assumed that PBO has to be transferred to the mosquito well in advance to the exposure to DM, because the PBO was believed to need a certain time in the mosquito before it temporarily breaks down the resistance mechanism. This is reflected in the above mentioned International patent application WO 2006/11155. As the degradation of PBO by sunlight/visible light creates radicals leading to a degradation of the DM, it has hitherto been believed that a provision of PBO and DM at the surface of the net at the same time and at the same position is a hinder for an efficient insecticidal net, because the time lapse between the necessary PBO exposure to the mosquito before the DM exposure leads to a degradation of the DM in the mean time. This implied a conclusion that a polymer having incorporated DM as well as PBO for migration to the surface of the material is not a proper material for insecticidal nets. It should be mentioned here that no LLIN with incorporated PBO and DM have found way to the market yet, despite a great demand for a feasible solution. Instead, encapsulation of synergist and insecticide together with an antioxidant into UV protected microcapsules has been proposed in U.S. Pat. No. 4,056,610 as one of the measures to overcome this problem.
  • One of the corner stones of the invention is the fact that experiments revealed that the bioefficacy of PBO and DM treatment is highest when mosquitoes were exposed to PBO and DM simultaneously. As described above, this is against the teaching in the field of insecticidal nets. A proof for this is illustrated in FIG. 1, showing that for different dosages, there was a remarkable increase in efficacy when DM and PBO were provided to the mosquito at the same time.
  • Having recognised this, there was a new motivation for providing a polymer matrix containing PBO and DM, where both can be found on the surface of the matrix and migrate at a similar rate so as to replenish the surface after depletion (by washing, for instance) in order to expose insects to DM and PBO at the same time. As long as there is a steady release of these two substances, the efficacy against mosquitoes is optimal. Of course, this is compounded by the added constraint for LLINs that the said polymer matrix, once knitted into a netting material, should have suitable migration properties so that PBO and DM be regenerated at the surface of the yarn/fabric following washing.
  • The question then arises, which material should be chosen for the matrix. Studies revealed that polyester has a very slow migration rate, which was not sufficient to release enough DM and PBO through migration of polyester yarn of 100 Denier, even when used a multifilament with 35 filaments. HDPE had a release rate which was higher than for polyester, but not high enough for sufficient insecticidal efficacy or regeneration at a rate suitable for mosquito netting materials, despite good mechanical properties making it suitable for knitting into netting material. On the other hand, LDPE has a migration rate, which is far too high for a LLIN, and yarns made of pure LDPE have low mechanical properties that make them unsuitable for knitting into netting material. Thus, according to the invention, a mixture of LDPE and HDPE was envisaged, and it was found empirically, that for sufficient but also long lasting release of DM and PBO, a mixture of HDPE and LDPE was optimum, where the weight ratio between HDPE and LDPE was between 30 and 3 and rather between 20 and 5. The ratio depends on the thickness of the matrix. For monofilament yarns with a thickness of 0.06 mm, the HDPE/LDPE weight ratio was best between 15 and 25 and for yarns with a thickness of 0.25 mm, the ratio was best between 4 and 7. For yarn thickness in between these two numbers, the ratio may be interpolated. These parameters seem to give the said monofilament yarns adequate crystallinity at a given draw ratio and therefore an appropriate migration rate at the typical temperature these products are used.
  • In the experiments, no other polymers were introduced into the matrix. The above ratios corresponded in these experiments to a LDPE weight content of between 3.5% and 35% in the HDPE/LDPE matrix, whereas, however, the preferred content of LDPE in terms of weight was between 5% and 17%, better between 8% and 12%.
  • A successful monofilament yarn with a diameter of 0.10 mm to 0.15 mm, for example around 0.12 mm, the content of HDPE and LDPE in terms of weight was at a ratio between 8 and 10, rather around 9, corresponding to an LDPE content of around 10%, when no other polymers were introduced.
  • However, as it turned out, not only the ratio between the content of HDPE and LDPE could be used to optimise the yarn with respect to long lasting high efficiency. Also the content of the PBO content relative to the DM content proves to be crucial.
  • In this connection, FIG. 2 shows the PBO/DM ratio as abscissa and a percentage Functional Mortality of resistant Culex quinquefasciatus as ordinate for two different DM dosages, namely dosage DM1=1.32 mg/m2 and dosage DM2=1.76 mg/m2 in a WHO cone test with a mixture of DM and PBO. From FIG. 2, it is apparent that the ratio between PBO and DM in terms of weight should be above 4, or rather above 5, in order to yield a high efficacy against mosquitoes. However, a ratio far above 5 does not improve the effect.
  • Examples of successful yarns had diameters of between 0.10 mm and 0.15 mm, for example around 0.12 mm, and a content of HDPE and LDPE in terms of weight at a ratio between 8 and 10, for example around 9, and containing 4 g DM per kg polymer and 25 g PBO per kg polymer. Due to necessary initial migration before a sufficient content is reached at the surface of the matrix, the yarn had to be stored for a certain time to reach sufficient efficacy, for example a week to reach 80% efficacy.
  • The content of DM and PBO may be varied. For example, in the yarn with a thickness of between 0.10 mm and 0.15 mm, and a HDPE and LDPE weight content ratio of between 8 and 10, the content of DM may be selected between 2 g and 6 g DM per kg polymer and correspondingly 4 to 10 times as much PBO, preferably between 5 and 7 times as much PBO, for example 6 times as much PBO.
  • The monofilament polyethylene yarns may successfully be used for bed nets, where the entire net is provided with such material. However, in case that the side walls of the nets are preferred to be produced in polyester multifilament due to the relatively higher softness and cotton like feeling, the extruded HDPE/LDPE monofilament yarn may be used for the top part of the net. The efficacy will in most cases still be high, because mosquitoes typically attack their potential victims from above and tend to land on the roof of bed nets, especially rectangular bed nets.
  • As a further addition, migration promoters may be included in the molten matrix prior to extrusion of the insecticidal polyethylene blend.
  • FIG. 3 illustrates a conical canopy net 1 above a bed 6 to protect humans on the bed 6 from being attacked by insects, primarily mosquitoes. The roof 4 of the net 1 is provided as a material according to the invention with PBO and DM incorporated in a polymer matrix, and the side walls 5 of the canopy 1 comprise an insecticide but no PBO. A stabilising ring 9 is inserted between the roof 4 and the side walls 5.
  • FIG. 4 illustrates a conical canopy insecticidal barrier according to another embodiment of the invention, wherein the roof 4 and the side wall 5 are provided as a material according to the invention with PBO and DM incorporated in a polymer matrix. The side wall 5 extends to the lower edge 30 of the barrier and has an upper part 2 and a lower part 3. The canopy insecticidal barrier is intended to cover a space for human beings or animals, for example a bed 6 as illustrated in FIG. 4. In order to enter the space underneath the canopy, the lower part 3 of the barrier 1 is exposed to surface touch and, therefore, exposed to abrasion of insecticide from the surface of the material. In order to increase the strength of the net, the lower part 3 is has a material with higher abrasion resistance and mechanical strength, for example a stronger net, a fabric or a tarpaulin or a combination of these. Also, the lower part 3 may be provided with higher insecticidal content in order to take into account the higher abrasion of the insecticide from the surface of the material.
  • The thickness of the filaments for bed nets may vary in dependency of the actual requirements for the net. Typically, yarns with a weight of between 50 Denier and 100 Denier are used.
  • FIG. 5 shows a rectangular shape for a net, which may substitute the shapes of the nets in FIG. 4 and FIG. 3. However, the net in FIG. 5 has a roof 4 with a polymer matrix according to the invention, whereas the side walls 5 are multifilament polyester in order for the side walls to have soft, cotton like feeling. In order to provide additional strength to the lower part 3 of the side walls 5, the net has a tighter knit in this part 3. The walls of the net are provided without PBO but with DM impregnation complying with WHO specification 333/TC and being wash resistant and largely in line with the impregnation method in the disclosure of International patent application WO 01/37662, which also is used for the well known bed net under the trademark PermaNet®. The side wall 5 is provided with between 2.5 g and 3.5 g DM per kg of the matrix, which mainly is the polymer. As the yarn density is different in the lower part 3 of the side walls 5, the amount per square meter is higher. For example, if the value is chosen to 2.8 g/kg in a 75 Denier yarn, for example with about 40 g/m2 for the lower part of the side walls and 30 g/m2 for the remaining part of the side walls, the DM level is 115 mg/m2 of the lower part 3 of the side wall 5 and 85 mg/m2 in the remaining part of the side wall 5. The preferred net had a minimum of 24 holes per cm2. The preferred amount of DM in the roof net with 100 Denier was chosen to be between 3 and 5 g/kg cooperating with a PBO content between 5 to 7 times, rather around 6 times, as large as the DM content.

Claims (15)

1-20. (canceled)
21. An insecticidal polymer matrix being made of a material with Piperonyl Butoxide (PBO) and deltamethrin (DM) as part of the material for migration of the PBO and the DM from inside the material to the surface of the matrix, wherein the ratio between the content of PBO and the content of DM in terms of weight is higher than 4, and wherein the amount of DM in the polymer is between 1 g and 6 g per kg polymer.
22. An insecticidal polymer matrix according to claim 21, wherein the ratio between the content of PBO and the content of DM is higher than 5.
23. An insecticidal polymer matrix according to claim 22, wherein the ratio between the content of PBO and the content of DM is between 5 and 10.
24. An insecticidal polymer matrix according to claim 21, wherein the polymer is a thermoplastic polymer.
25. An insecticidal polymer matrix according to claim 24, wherein the polymer is a polyolefin.
26. An insecticidal polymer matrix according to claim 25, wherein the polymer is polyethylene.
27. An insecticidal matrix according to claim 21, wherein the insecticidal matrix contains at least one of UV protectors and antioxidants for slowing down chemical or photochemical degradation of PBO and DM.
28. An insecticidal polymer matrix according to claim 21, wherein the insecticidal matrix is in the form of a monofilament with a diameter of between 0.05 mm and 0.35 mm.
29. An insecticidal polymer matrix according to claim 21, wherein the insecticidal matrix is in the form of a yarn.
30. An insecticidal matrix according to claim 29, wherein the yarn is an extruded and water quenched yarn drawn with a draw ratio of 5 to 10.
31. An insecticidal matrix according to claim 29, wherein the insecticidal matrix contains at least one of UV protectors and antioxidants for slowing down chemical or photochemical degradation of PBO and DM.
32. An insecticidal matrix according to claim 29, wherein the insecticidal matrix is in the form of a yarn as part of a bed net.
33. An insecticidal matrix according to claim 21, wherein the insecticidal matrix is in the form of a tarpaulin, a foil, or a flat yarn.
34. An insecticidal matrix according to claim 33, wherein the insecticidal matrix contains at least one of UV protectors and antioxidants for slowing down chemical or photochemical degradation of PBO and DM.
US16/157,145 2008-08-06 2018-10-11 Insecticidal Polymer Matrix Comprising PBO and DM Abandoned US20190037846A1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US16/157,145 US20190037846A1 (en) 2008-08-06 2018-10-11 Insecticidal Polymer Matrix Comprising PBO and DM

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DKPA200801073 2008-08-06
US14/562,905 US10111430B2 (en) 2008-08-06 2014-12-08 Insecticidal polymer matrix comprising PBO and DM
US16/157,145 US20190037846A1 (en) 2008-08-06 2018-10-11 Insecticidal Polymer Matrix Comprising PBO and DM

Related Parent Applications (1)

Application Number Title Priority Date Filing Date
US14/562,905 Continuation US10111430B2 (en) 2008-08-06 2014-12-08 Insecticidal polymer matrix comprising PBO and DM

Publications (1)

Publication Number Publication Date
US20190037846A1 true US20190037846A1 (en) 2019-02-07

Family

ID=41479597

Family Applications (3)

Application Number Title Priority Date Filing Date
US13/057,776 Active 2030-05-02 US8906400B2 (en) 2008-08-06 2009-07-23 Insecticidal polymer matrix comprising PBO and DM
US14/562,905 Active US10111430B2 (en) 2008-08-06 2014-12-08 Insecticidal polymer matrix comprising PBO and DM
US16/157,145 Abandoned US20190037846A1 (en) 2008-08-06 2018-10-11 Insecticidal Polymer Matrix Comprising PBO and DM

Family Applications Before (2)

Application Number Title Priority Date Filing Date
US13/057,776 Active 2030-05-02 US8906400B2 (en) 2008-08-06 2009-07-23 Insecticidal polymer matrix comprising PBO and DM
US14/562,905 Active US10111430B2 (en) 2008-08-06 2014-12-08 Insecticidal polymer matrix comprising PBO and DM

Country Status (11)

Country Link
US (3) US8906400B2 (en)
EP (1) EP2326183B1 (en)
JP (1) JP5539984B2 (en)
KR (1) KR20110042186A (en)
CN (1) CN102202512A (en)
AP (1) AP3009A (en)
BR (1) BRPI0916403A8 (en)
DK (1) DK2326183T3 (en)
TW (1) TW201028088A (en)
WO (1) WO2010015257A2 (en)
ZA (1) ZA201100533B (en)

Families Citing this family (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8936801B2 (en) * 2011-05-02 2015-01-20 Vestergaard Frandsen Sa Retention of PBO in polymer matrices by phthalocyanines
WO2012164080A1 (en) * 2011-06-03 2012-12-06 Intelligent Insect Control Insecticidal polyethylene fiber, yarn or textile products with improved migration profiles and washing resistance
GB201319336D0 (en) * 2013-11-01 2013-12-18 Liverpool School Tropical Medicine Mosquito bed net assembly
WO2018037094A1 (en) 2016-08-24 2018-03-01 Vestergaard Sa Fenazaquin and indoxacarb in a product for killing insects, especially mosquitoes
WO2018037093A1 (en) 2016-08-24 2018-03-01 Vestergaard Sa A method and substrate with abamectin and fenpyroximate for killing mosquitoes
IT202100014189A1 (en) 2021-05-31 2022-12-01 Sachim Srl POLYETHYLENE SUPPORT TO WHICH A HYDROGEL LOADED WITH A NATURAL PESTICIDE ACTIVE INGREDIENT IS BOUND

Family Cites Families (18)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2811477A (en) * 1955-02-18 1957-10-29 Thomas L Cunningham Moth-proofing composition
US4680328A (en) 1984-11-29 1987-07-14 The Dow Chemical Company Insect resistant polyethylene composition suitable for wire and cable applications
US4888174A (en) 1987-10-19 1989-12-19 The Dow Chemical Company Insecticidal polymeric compositions
US5230843A (en) * 1987-12-21 1993-07-27 Entek Manufacturing Inc. Process of forming microporous fibers and filaments
AU666399B2 (en) 1992-09-21 1996-02-08 Virbac (Australia) Pty Limited Pesticidal compositions
JP3535258B2 (en) 1995-04-28 2004-06-07 フクビ化学工業株式会社 Olefin-based insect repellent resin composition having durability and molded product thereof
AU2961000A (en) 1999-01-08 2000-07-24 Y-Tex Corporation Pet medallion
CN1479572A (en) * 2000-12-03 2004-03-03 ��̩�ռ����о��� Barrier preventing wood pest access to wooden structures
ATE302546T1 (en) 2001-10-25 2005-09-15 Siamdutch Mosquito Netting Com TREATMENT OF TISSUES WITH AN INSECTICIDE
MY132793A (en) 2002-12-30 2007-10-31 Institute For Medical Res Malaysia Insecticidal paint composition
US7610757B2 (en) * 2004-07-30 2009-11-03 Komatsu Ltd. Intake controller of internal combustion engine
ITMI20050728A1 (en) * 2005-04-22 2006-10-23 Endura Spa INNOVATIVE FORMULATION
US20060288955A1 (en) 2005-05-24 2006-12-28 Wyeth Device and method for controlling insects
JP2008013508A (en) * 2006-07-07 2008-01-24 Sumitomo Chemical Co Ltd Insect pest control material
CN101511177A (en) * 2006-09-11 2009-08-19 住友化学株式会社 Insect-repellent fiber and insect-repellent net
WO2008032844A2 (en) * 2006-09-11 2008-03-20 Sumitomo Chemical Company, Limited Insect-repellent fiber
TW201018757A (en) * 2008-08-06 2010-05-16 Vestergaard Frandsen Sa Insecticidal polymer matrix comprising HDPE and LDPE
AP3032A (en) 2008-10-21 2014-11-30 Intelligent Insect Control Textile product for killing insects

Also Published As

Publication number Publication date
JP2011529927A (en) 2011-12-15
US20150093427A1 (en) 2015-04-02
US20120121681A1 (en) 2012-05-17
WO2010015257A2 (en) 2010-02-11
DK2326183T3 (en) 2017-03-06
US10111430B2 (en) 2018-10-30
AP2011005560A0 (en) 2011-02-28
AP3009A (en) 2014-10-31
BRPI0916403A8 (en) 2017-05-09
WO2010015257A3 (en) 2010-08-26
EP2326183A2 (en) 2011-06-01
EP2326183B1 (en) 2016-03-09
JP5539984B2 (en) 2014-07-02
US8906400B2 (en) 2014-12-09
TW201028088A (en) 2010-08-01
BRPI0916403A2 (en) 2015-08-04
CN102202512A (en) 2011-09-28
KR20110042186A (en) 2011-04-25
ZA201100533B (en) 2016-08-31

Similar Documents

Publication Publication Date Title
US20110165213A1 (en) Insecticidal Polymer Matrix Comprising HDPE and LDPE
US20190037846A1 (en) Insecticidal Polymer Matrix Comprising PBO and DM
EP2170048B1 (en) Insecticidal thread
JP5307805B2 (en) Insecticidal barrier with partial synergist
EP2417287B1 (en) A textile product (e.g. an insecticide net)
KR20100038402A (en) Insecticidal barrier with a durable lower part
WO2010046348A1 (en) Textile product for killing insects
US20120034285A1 (en) Mosquito Net with Dinotefuran and PBO for Killing Mosquitoes, Especially Mosquitoes with Pyrethroid Resistance
WO2013171118A2 (en) A strong insecticidal net
OA16566A (en) Insecticidal polymer matrix comprising PBO and DM.
KR100438020B1 (en) Preparation of Insect repel-lent fabric containing Permethrin
WO2012069049A1 (en) A product with low density polymer resin releasing fipronil in a controlled way and use of such a product
EP2704564B1 (en) Retention of pbo in polymer matrices by a phtalocyanine
BRPI0916403B1 (en) POLYMERIC MATRIX INSECTICIDAL
WO2012149933A1 (en) Method for regulating migration of insecticide or acaricide in a polymer fibre by stretching

Legal Events

Date Code Title Description
STPP Information on status: patent application and granting procedure in general

Free format text: DOCKETED NEW CASE - READY FOR EXAMINATION

STPP Information on status: patent application and granting procedure in general

Free format text: NON FINAL ACTION MAILED

STPP Information on status: patent application and granting procedure in general

Free format text: RESPONSE TO NON-FINAL OFFICE ACTION ENTERED AND FORWARDED TO EXAMINER

STPP Information on status: patent application and granting procedure in general

Free format text: FINAL REJECTION MAILED

STCB Information on status: application discontinuation

Free format text: ABANDONED -- FAILURE TO RESPOND TO AN OFFICE ACTION