EP3128839A1 - Neuartige biozide produkte - Google Patents

Neuartige biozide produkte

Info

Publication number
EP3128839A1
EP3128839A1 EP15720212.8A EP15720212A EP3128839A1 EP 3128839 A1 EP3128839 A1 EP 3128839A1 EP 15720212 A EP15720212 A EP 15720212A EP 3128839 A1 EP3128839 A1 EP 3128839A1
Authority
EP
European Patent Office
Prior art keywords
formulation
biocidal
concentrated
weight
proportion
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP15720212.8A
Other languages
English (en)
French (fr)
Inventor
Stephan AUBERGER
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.)
SALVECO
Original Assignee
SALVECO
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 SALVECO filed Critical SALVECO
Priority to EP20166050.3A priority Critical patent/EP3725154A1/de
Publication of EP3128839A1 publication Critical patent/EP3128839A1/de
Ceased legal-status Critical Current

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Classifications

    • AHUMAN NECESSITIES
    • A01AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
    • A01NPRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/36Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing at least one carboxylic group or a thio analogue, or a derivative thereof, and a singly bound oxygen or sulfur atom attached to the same carbon skeleton, this oxygen or sulfur atom not being a member of a carboxylic group or of a thio analogue, or of a derivative thereof, e.g. hydroxy-carboxylic acids
    • 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
    • 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
    • A01N25/30Biocides, 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 characterised by the surfactants
    • 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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/02Saturated carboxylic acids or thio analogues thereof; Derivatives thereof
    • A01N37/04Saturated carboxylic acids or thio analogues thereof; Derivatives thereof polybasic
    • 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
    • A01N37/00Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids
    • A01N37/42Biocides, pest repellants or attractants, or plant growth regulators containing organic compounds containing a carbon atom having three bonds to hetero atoms with at the most two bonds to halogen, e.g. carboxylic acids containing within the same carbon skeleton a carboxylic group or a thio analogue, or a derivative thereof, and a carbon atom having only two bonds to hetero atoms with at the most one bond to halogen, e.g. keto-carboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/361Carboxylic acids having more than seven carbon atoms in an unbroken chain; Salts or anhydrides thereof
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/33Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing oxygen
    • A61K8/36Carboxylic acids; Salts or anhydrides thereof
    • A61K8/365Hydroxycarboxylic acids; Ketocarboxylic acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/60Sugars; Derivatives thereof
    • A61K8/602Glycosides, e.g. rutin
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q17/00Barrier preparations; Preparations brought into direct contact with the skin for affording protection against external influences, e.g. sunlight, X-rays or other harmful rays, corrosive materials, bacteria or insect stings
    • A61Q17/005Antimicrobial preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • A61Q19/10Washing or bathing preparations
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K2800/00Properties of cosmetic compositions or active ingredients thereof or formulation aids used therein and process related aspects
    • A61K2800/40Chemical, physico-chemical or functional or structural properties of particular ingredients
    • A61K2800/59Mixtures
    • A61K2800/596Mixtures of surface active compounds

Definitions

  • the present invention relates to a new generation of biocidal products that do not present chronic risks and very few acute impacts to health and the environment.
  • the active substances and adjuvants that make up the biocidal formulations according to the invention are of plant origin, preferably agricultural, and renewable, and are otherwise totally, naturally and rapidly biodegradable.
  • Biocidal products are commonly used in a wide variety of products, including household and / or industrial disinfectants, insecticides, wood treatment products, etc.
  • Biocidal products are intended to destroy, repel or render ineffective undesirable organisms, considered harmful or not, such as bacteria, viruses, fungi, to prevent the action or to fight in any other way by a chemical action or biological.
  • a biocide is generally characterized by its field of application: bactericidal, fungicidal, antiviral and / or insecticide.
  • Bactericides have an action against certain Gram + and / or Gram- bacteria.
  • Fungicides have an action against certain fungi and some yeasts.
  • antivirals they have an action against some viruses.
  • Biocidal assets can therefore present a major risk for human and animal health, but also for the environment; Moreover, from an etymological point of view “bios” means “the life “and” -cide “means” who kills ". Indeed, biocidal assets can act for a long time, spread, be partially degraded, or not be degraded at all according to their nature, and they are then considered as (bio) accumulable and toxic.
  • the active substances that make up biocides are generally active ingredients of petrochemical origin.
  • biocides may also comprise a mixture of the last two categories of components, that is to say, active ingredients of petrochemical origin and substances of plant origin, in order to achieve the desired efficiency.
  • quaternary ammonium derivatives which represent a major class of biocidal substances of chemical origin which are used in surface disinfectants and for hand hygiene.
  • biocidal products for Europe represents a volume of 300 000 to 750 000 tonnes per year (impact study of the Biocides Directive 98/8 / EC - 2007) which corresponds to an annual global market of 7 billion euros.
  • Biocides Directive 98/8 / EC - 2007 impact study of the Biocides Directive 98/8 / EC - 2007
  • These biocides must have the capacity to be fully degraded in a natural way after their use, so as to reduce the risks for humans, animals and the environment, while limiting the induced resistance.
  • biocidal products must be effective at low concentrations so as to offer industrial and economic solutions in line with the economic positioning of the health markets.
  • biocides of natural origin have been developed.
  • biocidal solutions contain a washing base combined with a disinfecting base.
  • these products do not exhibit the same biocidal efficacy or the same ease of use (dose / time ratio / action spectrum) as the biocidal solutions containing active agents and / or chemical-synthetic adjuvants.
  • Patent document WO 2012/114039 already discloses a biocidal composition comprising:
  • nonionic surfactants of the polyol type between 0.03% and 25% of nonionic surfactants of the polyol type and preferably between 0.03% and 25% of nonionic surfactants of the glycoside, polyglycerol ester or sorbitan ester type; between 0.03% and 25% of anionic surfactants, preferably of the carboxylate or polycarboxylate type;
  • composition although having a plant origin and having a biocidal activity on certain pathogens, can be further improved.
  • composition described in this document does not have optimal efficacy against undesirable organisms and likely to be pathogenic, for example certain strains of fungi or some undesirable viruses or pathogens.
  • the present invention thus relates to a new generation of biocidal formulations for cleaning and disinfecting all types of surfaces.
  • biocidal formulations are derived from renewable plant resources, preferably agricultural resources, and they are fully biodegradable over the entire formulation.
  • the active substance of the biocidal formulations according to the invention consists of at least one organic acid of plant origin.
  • This organic acid can be derived directly from a plant resource, preferably agricultural, or from a transformed agricultural resource.
  • the present invention describes a concentrated biodegradable biocidal formulation comprising compounds derived from renewable plant resources, said formulation being characterized in that it comprises at least the following compounds:
  • At least one organic acid in a proportion of between 76 and 98% by weight, relative to the total weight of the formulation; at least one anionic surfactant in a proportion of between 2 and 24% by weight, relative to the total weight of the formulation.
  • the proportion of organic acid is between 76 and 92%, and more preferably between 76 and 84%.
  • the proportion of anionic surfactant it is preferably between 3 and 15%, preferably between 5 and 10%.
  • the biocidal formulation according to the invention comprises compounds derived from vegetable resources, in particular agricultural resources, which are entirely renewable. As a result, said biocidal formulation is fully biodegradable.
  • composition is 100% biodegradable according to the results of the tests of the OECD experimental protocol.
  • the biocidal formulations according to the invention have an innovative effect of providing biological provision of the biocidal active through adapted surfactant structures. and under the effect of physicochemical changes of the mixture, which results in a sought combination between the constituents and performance to substitute, equi-concentration, chemicals and dangerous market.
  • the present biocidal formulation has an effective action against certain undesirable or pathogenic organisms, and an improved effect over biocidal formulations known from the prior art.
  • the action of the formulation is illustrated in the examples below.
  • this biocidal formulation makes it possible to control fungi belonging to the species Aspergillus niger, which is likely to be toxic and pathogenic, in particular by causing pulmonary mycoses in humans.
  • the formulation according to the invention also has a biocidal activity, in particular virucidal, against strains of virus belonging to the family of adenoviruses, which may be responsible for diseases such as pharyngitis, pneumonia, or still conjunctivitis.
  • the virucidal effect has also been demonstrated against rotaviruses, particularly those responsible for gastroenteritis.
  • the choice of the organic acid is made according to the field of application of the biocidal formulations and the target organisms to eliminate or whose development is desired to slow down.
  • the organic acid or acids are lactic acid and citric acid.
  • lactic acid is used.
  • lactic acid is one of the essential elements of human metabolism, but also the metabolism of animals and micro-organisms. Lactic acid inherently exhibits interference properties on microorganisms because it acts directly on their pH as well as their energy cycle. Moreover, it also has an antimicrobial action by inhibiting their growth (for Escherichia Coli among others).
  • the concentrated biocidal formulation according to the invention also comprises at least one anionic surfactant.
  • This is advantageously chosen from sodium carboxylates comprising a number of carbon atoms of between 5 and 16.
  • the anionic surfactant may also consist of a potassium carboxylate comprising a number of carbon atoms of between 5 and 16.
  • the carbon chain of the anionic surfactants is derived from fatty alcohol or vegetable fatty acid.
  • the anionic surfactant is an alkyl carboxylate of sodium caprate, sodium caprylate, sodium laurate, C 8 -C 16 alkyl sulfate of ammonium, or potassium, a carboxylated fatty acid ester.
  • the anionic surfactant may also consist of the acidic species derived from these salts.
  • the concentrated biocidal formulation according to the invention may also comprise other ingredients.
  • said formulation may comprise, in addition to the organic acid and the anionic surfactant, at least one nonionic surfactant and / or at least one natural perfume and / or at least one chelating agent.
  • nonionic surfactants or other components of the essential oil or chelating type that can be used in the composition of the biocidal product according to the invention are selected according to the type of performance and application required: a judicious mixture is necessary so as not to disturb or modify the biocidal properties initially sought. Effectively, for example, effective disinfecting and / or degreasing properties are necessary in the restaurant or agribusiness world with products that have little or no toxicity in order to avoid any worrying chemical contamination, in particular by the presence of chemical residues on the surfaces after the disinfection procedure.
  • the biocidal formulation according to the invention may comprise at least one nonionic surfactant, preferably in a proportion of between 2 and 15% by weight relative to the total mass of the formulation.
  • this nonionic surfactant is chosen from glycosides and alkyl polyglycosides whose carbon chain comprises between 5 and 20 carbon atoms, more advantageously still between 5 and 18 carbon atoms, and the hydrophilic group is preferably composed of residues. pentose or hexose.
  • the formulation according to the invention may comprise a nonionic surfactant selected from octyl glucosides, decyl glucosides, lauryl glucosides, coco glucosides, D-glucopyranose, D-xylopyranose C10-C16 alkylpolyglycosides.
  • a nonionic surfactant selected from octyl glucosides, decyl glucosides, lauryl glucosides, coco glucosides, D-glucopyranose, D-xylopyranose C10-C16 alkylpolyglycosides.
  • the chelating agents that can be used in the composition of the biocidal formulation according to the invention are conventional agents in the field of cleaning and disinfection of surfaces for domestic or professional use.
  • chelants commonly used in biocidal products, such as citric acid, derived from lemon juice or fermentation of simple or complex plant sugars, including glucose, fructose, and sucrose, or sorbic acid, derived from the mountain ash, or oxalic acid, derived from the roots or rhizomes of many plants (sorrel, beetroot, etc.), sequestering monomers or polymers such as chicory extracts, or amino acid derivatives.
  • citric acid derived from lemon juice or fermentation of simple or complex plant sugars, including glucose, fructose, and sucrose
  • sorbic acid derived from the mountain ash
  • oxalic acid derived from the roots or rhizomes of many plants (sorrel, beetroot, etc.)
  • sequestering monomers or polymers such as chicory extracts, or amino acid derivatives.
  • the chelating agent may also, in one embodiment, be derived from the fermentation of agricultural equipment.
  • This basic agricultural equipment may for example consist of molasses residues to obtain complexing agents of the gluconate type.
  • the chelating agent (s) are present in a proportion of 0.1% to 10% by weight relative to the total mass of the formulation.
  • the olfactory properties of the biocidal products according to the invention can be conferred by the presence of at least one natural perfume derived from a renewable and biodegradable natural resource.
  • This natural perfume can be advantageously chosen from essential oils, vegetable essences or plant extracts.
  • Examples include mint A, mint N or eucalyptus G.
  • the natural perfume (s) are present in the concentrated biocidal formulation in a proportion of 0.01% to 10% by weight relative to the total mass of the formulation.
  • a formulation containing the biocidal product according to the invention can be diluted 1 to 500 times in water depending on the intended use.
  • the formulations according to the invention comply with European regulations in terms of effectiveness. They meet the standards EN1040, EN1276, EN1656, EN 1275, EN 13697, EN1650 and EN14476 + A1 in dirty or clean conditions.
  • biocidal formulations according to the invention may be used at dilution rates and in times of action comparable to those required by the professional market. In addition, they comply with the biocidal efficacy requirements required, without any particular danger to the application, biodegradable and without ecotoxicity after elimination.
  • the biocidal formulations according to the invention are provided in concentrated liquid form. They can be very diluted, for example 50 to 500 times, especially in water, and keep their activities as well depending on the intended application.
  • the present invention also relates to an aqueous liquid composition
  • an aqueous liquid composition comprising at least the biocide formulation described above and water, and all the dilutions in water of said composition to a minimum concentration of 0.2% of said composition.
  • the remainder of the composition comprises at least water.
  • the aqueous liquid composition according to the invention may also comprise other ingredients so as to improve the cleaning and / or organoleptic properties, without however modifying the biocidal activity of said formulation.
  • the biocidal formulation according to the invention is present in said aqueous liquid composition in a proportion of between 0.2 and 2% by weight, relative to the total mass of said composition.
  • said formulation can be advantageously diluted between 50 and 500 times and still be active on unwanted organisms that it is desired to eliminate.
  • the biocidal formulation according to the invention is present in said aqueous liquid composition in a proportion of between 1 and 2% by weight, more advantageously between 1.5 and 2% by weight, relative to the total mass. of said composition.
  • biocidal formulations are particularly interesting because they are still effective even at high dilution rates, and have an efficiency comparable to more concentrated formulations but are less interesting from an economic point of view.
  • biocidal formulations according to the invention are based on a disinfecting action but also a detergent, degreasing, emollient, olfactory, etc.
  • an application of the formulations according to the invention to anti-foam products for cleaning masonry works products for cleaning the pontoons and hulls of the mosses and algae that colonize them; disinfectant detergent solutions for all types of surfaces; solutions for hand hygiene by washing or friction; food disinfection solutions; solutions for the disinfection of premises, buildings and transport and livestock equipment; surface disinfection solutions for the food, cosmetics or pharmaceutical industry; disinfection solutions for premises and / or transport of household waste, solutions for disinfecting milking equipment, teats, litter of animals.
  • biocidal formulations according to the invention are used for hand hygiene, by washing or friction, in liquid or semi-liquid form, with or without rinsing with water.
  • the present invention also relates to a substrate impregnated with a concentrated biocidal formulation according to the invention, allowing the application of said formulation on a surface to be cleaned and disinfected.
  • This substrate may consist of a fabric, a wipe or a towel.
  • the formulation according to the invention can be pure and dehydrated and be activated once in the presence of water or be already diluted and ready for use.
  • the substrate may also be impregnated with the aqueous liquid composition as described above, said composition comprising at least the biocidal formulation and water, said formulation being present in a proportion of between 0.2 % and 2% by weight relative to the total mass of said composition.
  • the biocidal formulation according to the invention has the following compounds, in the following proportions:
  • This formula is only classified as irritating according to the regulations in force, in the same way as the lactic acid used in said formulation. Such a classification enables him to pass through heavy and expensive instruction files for marketing. In addition, this formulation presents no danger to humans or the environment compared to substances of chemical origin which are marketed on the market.
  • This formulation is diluted according to the surfaces to be cleaned, sanitized and the desired disinfecting effectiveness.
  • the active diluted formula for surface disinfection does not present any known and / or regulated hazard.
  • biocidal formulation according to the invention is composed as follows:
  • anionic surfactants of the fatty acid salt type with a chain containing 8 to 10 carbon atoms of sodium alkyl carboxylate type 24% of anionic surfactants of the fatty acid salt type with a chain containing 8 to 10 carbon atoms of sodium alkyl carboxylate type.
  • biocidal formulation according to the invention is composed as follows:
  • anionic surfactants of sodium coconut type fatty acid salts type
  • biocidal formulation according to the invention is composed as follows:
  • biocidal formulation which has been tested is that which is specified above and which comprises:
  • This quantitative suspension test for the evaluation of the basic yeasticidal activity of the formulation according to the invention is carried out by a Microbiology Laboratory. This test is carried out in conditions of dirt and in additional conditions.
  • a dilution / neutralization method is applied to a formulation according to the invention.
  • the neutralizer consists of sodium chloride (0.85% w / v), Na 2 CO 3 (0.1%), supplemented with distilled water.
  • the formulation according to the invention is diluted in physiological saline at the following concentrations: 1%, 1.2%, 1.5% and 2%.
  • the tests are carried out on a strain of Candida albicans (ATCC 90028) at a temperature of 20 ° C ( ⁇ 1 ° C).
  • the contact time is limited to 5 minutes ( ⁇ 10 seconds).
  • the interfering substance is bovine albumin (fraction V) at 3.00 g / l. This is the condition of dirt.
  • the tests are incubated at a temperature of 25.0 ° C ( ⁇ 0.2 ° C) for 48h.
  • the formula according to the invention has a yeast activity in soil conditions (3.00 g / l of bovine albumin) after 5 minutes of contact at 20 ° C against a reference strain of Candida albicans for the concentration of 1.2%.
  • the biocidal formulation is diluted to a concentration of 2% in water.
  • the tests were conducted at a temperature of 20 ° C ( ⁇ 1 ° C). Two contact times were tested: 15 min and 30 min.
  • the interfering substance is bovine albumin (fraction V) at a rate of 0.30 g / l. This is the condition of cleanliness.
  • the tests are incubated at a temperature of 30 ° C for a duration of 2 days.
  • the formulation diluted to 2% has a fungicidal activity against the Aspergillus niger strain after a contact time of 30 min at a temperature of 20 ° C and cleanliness conditions (0.30 g / l of albumin bovine).
  • This virucidal efficacy test is carried out according to the methodology of standard NF EN 14476 + A1 (January 2007) on two viruses.
  • the first virus tested is a Rotavirus (strain ATCC VR-1290) and the tests were conducted on 3 samples of disinfectant product ready for use, according to the formulation of the present invention diluted to 2% in water.
  • the test is carried out at 20 ° C ( ⁇ 1 ° C). The contact time is 15 minutes. The samples are diluted in sterile distilled water. The interfering substance is bovine albumin (BSA 3.00 g / l).
  • the viral strain was tested on MA-104 cells at 36.5 ° C under 5% CO 2 .
  • the technique for stopping the virucidal action is the addition of a solution containing Na 2 CO 3 , at the rate of 70 g / l, pH 10.85 and 10 ml of stopping solution for 10 ml of solution of trial. Such a solution makes it possible to stop the action of the disinfectant on the virus and to measure the effectiveness of the biocide formulation tested.
  • the virus is titrated in PFU / ml (plaque-forming units), ie in number of infectious viral particles per ml and more commonly in logarithm of the viral titre.
  • the second virus tested is an Adenovirus (adenoid strain 75 ATCC VR-5).
  • biocidal formulation according to the invention is diluted to 2% in water and the test method is the same as that used on Rotavirus and described above.
  • the contact time is 60 min.
  • the viral strain was tested on HEp-2 cells at 36.5 ° C under 5% CO 2 .
  • results The three samples of biocidal formulation according to the invention have a virucidal activity on the Adenovirus strain at a concentration of 2% for 60 min of contact.
  • Adenovirus 0395A / 2013 2% 60 min R 4, 125 YES 0.3
  • the present biocidal formulation is effective at a concentration of 1% on enveloped DNA genome viruses, such as those belonging to the family Herpesviridae.
  • the biocidal formulation is also 1% effective on influenza viruses.
  • This quantitative suspension assay for the evaluation of the bactericidal activity of the formulations according to the present invention is carried out by a Microbiology Laboratory.
  • a dilution / neutralization method is applied to a formulation according to the invention.
  • the neutralizer consists of sodium chloride (0.85% w / v), Na 2 CO 3 (0.1%), supplemented with distilled water. This dilution / neutralization method makes it possible to stop the biocidal action of the product at the end of the contact time tested.
  • the formulation according to the invention is diluted in physiological saline at the following concentrations: 0.5%, 1.2% and 1.5%.
  • the tests are performed on strains of Staphylococcus aureus (ATCC 6538), Escherichia coli (ATCC 10536), Enterococcus hirae (ATCC 10541) and Pseudomonas aeruginosa (ATCC 15442) at a temperature of 20 ° C ( ⁇ 1 ° C).
  • the contact time is limited to 5 minutes ( ⁇ 10 seconds).
  • the interfering substance is bovine albumin (fraction V) at 3.00 g / l. This is the condition of dirt.
  • the incubation is carried out at a temperature of 37.0 ° C ( ⁇ 0.2 ° C) for 24 hours.
  • a concentrated disinfection formula according to the formulation of the present invention exhibits a bactericidal activity in soil conditions (3.00 g / l of bovine albumin) after 5 minutes of contact at 20 ° C to view the 4 strains of reference tested for the test concentration of 1%.
  • the limiting microorganism is Staphylococcus aureus (ATCC 6538).
  • Tests are also carried out according to a standardized method (EN13697) so as to demonstrate the bactericidal and / or yeasticidal effect by application to surfaces.
  • control surfaces used are stainless steel discs on which a solution of bacteria and / or yeasts is deposited. It is more particularly the microbial strains exposed above.
  • the discs are then immersed in the biocidal solution at 20 ° C (+/- 0.2 ° C) for a contact time of 5 minutes. Residual microbial concentration is determined after incubation at 37 ° C (+/- 2 ° C) for bacteria or at 25 ° C (+/- 0.2 ° C) for yeasts.
  • a concentrated disinfection formula according to the formulation of the present invention has a bactericidal and yeasticidal activity under dirty conditions (3.00 g / l bovine albumin) after 5 minutes of contact at 20 ° C with respect to the 4 reference bacterial strains tested and the yeast strain for the test concentration of 1%.
  • This test is an evaluation in aqueous medium of the ultimate aerobic biodegradability of a sample of the concentrated formulation according to the invention.
  • Figure 1 shows the decomposition result curves for dissolved organic carbon after 28 days.
  • the reference substance is sodium acetate.
  • concentration disinfection corresponds to the tested biocidal formulation described above and the “inhibition test” sample corresponds to a mixture between the formulation according to the invention and the sodium acetate.
  • the percentage degradation of the reference substance is greater than 70% (99%) on the fourteenth day;
  • the degree of DOC removal in the inhibitory test containing the test compound and the reference substance, being greater than 35% after 14 days (98%), the sample is not considered as poisonous to seeding.
  • the biodegradation time (corresponding to 90% of the maximum biodegradation rate) is about 25 days;
  • the tested sample "concentrated disinfection” is considered to be readily biodegradable (70% DOC threshold level being acquired within 10 days after 10% biodegradability is reached (94% at the end of the interval of 10 days to ll t test day).
  • the degree of biodegradability measured takes into account the totality of the formulation actually there is no by-product of degradation because the formulation is exclusively composed of carbon atoms, oxygen and hydrogen from plant extracts . It is a true measure of ultimate biodegradability.

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  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Veterinary Medicine (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental Sciences (AREA)
  • Pest Control & Pesticides (AREA)
  • Plant Pathology (AREA)
  • Agronomy & Crop Science (AREA)
  • Dentistry (AREA)
  • Wood Science & Technology (AREA)
  • Zoology (AREA)
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  • Epidemiology (AREA)
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  • Dermatology (AREA)
  • Toxicology (AREA)
  • Agricultural Chemicals And Associated Chemicals (AREA)
EP15720212.8A 2014-04-10 2015-04-09 Neuartige biozide produkte Ceased EP3128839A1 (de)

Priority Applications (1)

Application Number Priority Date Filing Date Title
EP20166050.3A EP3725154A1 (de) 2014-04-10 2015-04-09 Neuartige biozide produkte

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
FR1453179A FR3019714B1 (fr) 2014-04-10 2014-04-10 Nouveaux produits biocides
PCT/FR2015/050954 WO2015155485A1 (fr) 2014-04-10 2015-04-09 Nouveaux produits biocides

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EP3128839A1 true EP3128839A1 (de) 2017-02-15

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EP15720212.8A Ceased EP3128839A1 (de) 2014-04-10 2015-04-09 Neuartige biozide produkte

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EP (2) EP3725154A1 (de)
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US20200101185A1 (en) * 2017-06-16 2020-04-02 Orbital Systems Ab A method for disinfection and cleaning of at least one part of a device intended for recycling of water
FR3147071A1 (fr) 2023-03-27 2024-10-04 Hypred Composition désinfectante et ses utilisations.

Family Cites Families (10)

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Publication number Priority date Publication date Assignee Title
US4430381A (en) * 1982-06-25 1984-02-07 The Buckeye Cellulose Corporation Monocarboxylic acid antimicrobials in fabrics
US5143720A (en) * 1990-11-28 1992-09-01 Microcide, Inc. Disinfecting and sanitizing compositions
GB9419668D0 (en) * 1994-09-28 1994-11-16 Diversey Corp Disinfectant compositions
CA2397496C (en) * 2000-02-28 2007-07-24 The Procter & Gamble Company Acidic antimicrobial compositions for treating food and food contact surfaces and methods of use thereof
US20040001797A1 (en) * 2002-06-21 2004-01-01 Abel Saud Antimicrobial compositions, products and methods employing same
US20050271711A1 (en) * 2004-04-26 2005-12-08 The Procter & Gamble Company Therapeutic antimicrobial compositions and methods
US20050260243A1 (en) * 2004-04-26 2005-11-24 The Procter & Gamble Company Method of treating microbial plant diseases
WO2008045860A2 (en) * 2006-10-10 2008-04-17 Michael Lynch Methods of inactivating viruses
US8541356B2 (en) * 2009-11-23 2013-09-24 S.C. Johnson & Son, Inc. Water-activated “green” multi-functional wipe
FR2971913B1 (fr) * 2011-02-25 2013-07-26 Salveco Nouveaux produits biocides

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See also references of WO2015155485A1 *

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FR3019714A1 (fr) 2015-10-16
EP3725154A1 (de) 2020-10-21
FR3019714B1 (fr) 2017-07-07
WO2015155485A1 (fr) 2015-10-15
US20170035049A1 (en) 2017-02-09

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