Patent Grant
9510597
This invention relates to a synergistic combination of selected microbicides having greater activity than would be observed for the individual microbicides.
In some cases, commercial microbicides cannot provide effective control of microorganisms, even at high use concentrations, due to weak activity against certain types of microorganisms, e.g., those resistant to some microbicides, or due to aggressive environmental conditions. Combinations of different microbicides are sometimes used to provide overall control of microorganisms in a particular end use environment. For example, U.S. Pat. App. Pub. No. 2007/0078118 discloses synergistic combinations of N-methyl-1,2-benzisothiazolin-3-one (MBIT) with other biocides. However, there is a need for additional combinations of microbicides having enhanced activity against various strains of microorganisms to provide effective control of the microorganisms. Moreover, there is a need for combinations containing lower levels of individual microbicides for environmental and economic benefit. The problem addressed by this invention is to provide such additional combinations of microbicides.
The present invention is directed to a synergistic microbicidal composition comprising: (a) N-methyl-1,2-benzisothiazolin-3-one; and (b) at least one microbicide selected from the group consisting of dodecylguanidine, poly(hexamethylene biguanide hydrochloride), sodium pyrithione, sodium ortho-phenylphenate, terbutryn, dimethoxane and 2-(hydroxymethyl)-2-nitropropane-1,3-diol.
As used herein, the following terms have the designated definitions, unless the context clearly indicates otherwise. “MBIT” is N-methyl-1,2-benzisothiazolin-3-one. “Dimethoxane” is 2,6-dimethyl-1,3-dioxan-4-ol acetate. The term “microbicide” refers to a compound capable of killing, inhibiting the growth of or controlling the growth of microorganisms at a locus; microbicides include bactericides, fungicides and algaecides. The term “microorganism” includes, for example, fungi (such as yeast and mold), bacteria and algae. The term “locus” refers to an industrial system or product subject to contamination by microorganisms. The following abbreviations are used throughout the specification: ppm=parts per million by weight (weight/weight), mL=milliliter, ATCC=American Type Culture Collection, MBC=minimum biocidal concentration, and MIC=minimum inhibitory concentration. Unless otherwise specified, temperatures are in degrees centigrade (° C.), and references to percentages are by weight (wt %). Amounts of organic microbicides are given on an active ingredient basis in ppm (w/w).
The compositions of the present invention unexpectedly have been found to provide enhanced microbicidal efficacy at a combined active ingredient level lower than that of the individual microbicides. Additional microbicides beyond those listed in the claims may be present in the composition.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and dodecylguanidine, and a ratio of N-methyl-1,2-benzisothiazolin-3-one to dodecylguanidine is from 1:1 to 1:650, preferably from 1:1 to 1:30 or from 1:50 to 1:650, preferably from 1:3 to 1:30 or from 1:80 to 1:650, preferably from 1:3.5 to 1:28 or from 1:80 to 1:640.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and poly(hexamethylene biguanide hydrochloride), and a ratio of N-methyl-1,2-benzisothiazolin-3-one to poly(hexamethylene biguanide hydrochloride) is from 4:1 to 2:1 or from 1:533 to 1:1067.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and sodium pyrithione, and a ratio of N-methyl-1,2-benzisothiazolin-3-one to sodium pyrithione is from 21:1 to 1:40, preferably from 5:1 to 1:40, preferably from 3.3:1 to 1:35.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and sodium ortho-phenylphenate, and a ratio of N-methyl-1,2-benzisothiazolin-3-one to sodium ortho-phenylphenate is from 1:60 to 1:135, preferably from 1:60 to 1:130, preferably from 1:62.5 to 1:125.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and terbutryn, and a ratio of N-methyl-1,2-benzisothiazolin-3-one to terbutryn is from 1:100 to 1:110,000, preferably from 1:104 to 1:106,667.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and dimethoxane, and a ratio of N-methyl-1,2-benzisothiazolin-3-one to dimethoxane is from 1:1 to 1:650, preferably from 1:1 to 1:30 or from 1:50 to 1:650, preferably from 1:3 to 1:30 or from 1:80 to 1:650, preferably from 1:3.5 to 1:28 or from 1:80 to 1:640.
In one preferred embodiment of the invention, the antimicrobial composition comprises N-methyl-1,2-benzisothiazolin-3-one and 2-(hydroxymethyl)-2-nitropropane-1,3-diol. Preferably, a weight ratio of a ratio of N-methyl-1,2-benzisothiazolin-3-one to 2-(hydroxymethyl)-2-nitropropane-1,3-diol is from 3:1 to 1:5, preferably from 2:1 to 1:4.
The microbicides in the composition of this invention may be used “as is” or may first be formulated with a solvent or a solid carrier. Suitable solvents include, for example, water; glycols, such as ethylene glycol, propylene glycol, diethylene glycol, dipropylene glycol, polyethylene glycol, and polypropylene glycol; glycol ethers; alcohols, such as methanol, ethanol, propanol, phenethyl alcohol and phenoxypropanol; ketones, such as acetone and methyl ethyl ketone; esters, such as ethyl acetate, butyl acetate, triacetyl citrate, and glycerol triacetate; carbonates, such as propylene carbonate and dimethyl carbonate; and mixtures thereof. It is preferred that the solvent is selected from water, glycols, glycol ethers, esters and mixtures thereof. Suitable solid carriers include, for example, cyclodextrin, silicas, diatomaceous earth, waxes, cellulosic materials, alkali and alkaline earth (e.g., sodium, magnesium, potassium), montmorillonite, zeolite, layered double hydroxide metal salts (e.g., chloride, nitrate, bromide, sulfate) and charcoal.
A microbicide component can be formulated in the form of an emulsion, dispersion or solution. The solvent component can be an organic solvent or water, preferably water. Such mixtures can contain adjuvants, co-solvents, thickeners, anti-freeze agents, emulsifiers, dispersants, fillers, pigments, surfactants, biodispersants, defoamers, sulfosuccinates, terpenes, furanones, polycations, stabilizers, scale inhibitors and anti-corrosion additives.
When both microbicides are each first formulated with a solvent, the solvent used for the first microbicide may be the same as or different from the solvent used to formulate the other commercial microbicide, although water is preferred for most industrial biocide applications. It is preferred that the two solvents are miscible.
Those skilled in the art will recognize that the microbicide components of the present invention may be added to a locus sequentially, simultaneously, or may be combined before being added to the locus. It is preferred that the first microbicide and the second microbicide component be added to a locus simultaneously or sequentially. When the microbicides are added simultaneously or sequentially, each individual component may contain adjuvants, solvent, thickeners, anti-freeze agents, colorants, sequestrants (such as ethylenediamine-tetraacetic acid, ethylenediaminedisuccinic acid, iminodisuccinic acid and salts thereof), dispersants, surfactants, biodispersants, sulfosuccinates, terpenes, furanones, polycations, stabilizers, scale inhibitors and anti-corrosion additives.
The microbicidal compositions of the present invention can be used to inhibit the growth of microorganisms or higher forms of aquatic life (such as protozoans, invertebrates, bryozoans, dinoflagellates, crustaceans, mollusks, etc.) by introducing a microbicidally effective amount of the compositions onto, into, or at a locus subject to microbial attack. Suitable loci include, for example: industrial process water; electrocoat deposition systems; cooling towers; air washers; gas scrubbers; mineral slurries; wastewater treatment; ornamental fountains; reverse osmosis filtration; ultrafiltration; ballast water; evaporative condensers; heat exchangers; pulp and paper processing fluids and additives; starch; plastics; emulsions; dispersions; paints; latices; coatings, such as varnishes; construction products, such as mastics, caulks, and sealants; construction adhesives, such as ceramic adhesives, carpet backing adhesives, and laminating adhesives; industrial or consumer adhesives; photographic chemicals; printing fluids, colorants; household products, such as bathroom and kitchen cleaners and sanitary wipes; cosmetics; toiletries; shampoos; soaps; detergents; industrial cleaners; floor polishes; laundry rinse water; metalworking fluids; conveyor lubricants; hydraulic fluids; leather and leather products; textiles; textile products; wood and wood products, such as plywood, chipboard, wallboard, flakeboard, laminated beams, oriented strandboard, hardboard, and particleboard; petroleum processing fluids; fuel; oilfield fluids, such as injection water, fracture fluids, and drilling muds; agriculture adjuvant preservation; preservation of agricultural products, surfactant preservation; medical devices; diagnostic reagent preservation; food preservation, such as plastic or paper food wrap; food, beverage, and industrial process pasteurizers; toilet bowls; recreational water; pools; and spas.
Preferably, the microbicidal compositions of the present invention are used to inhibit the growth of microorganisms at a locus selected from one or more of mineral slurries, pulp and paper processing fluids and additives, starch, emulsions, dispersions, paints, latices, coatings, construction adhesives, such as ceramic adhesives, carpet backing adhesives, photographic chemicals, printing fluids, colorants, household products such as bathroom and kitchen cleaners and sanitary wipes, cosmetics, toiletries, shampoos, soaps, detergents, industrial cleaners, floor polishes, laundry rinse water, metal working fluids, textile products, wood and wood products, preservation of agricultural products and agricultural adjuvants, surfactant preservation, diagnostic reagent preservation, food preservation, and food, beverage, and industrial process pasteurizers.
The specific amount of the composition of this invention necessary to inhibit or control the growth of microorganisms and higher aquatic life forms in a locus depends upon the particular locus to be protected. Typically, the amount of the composition of the present invention to control the growth of microorganisms in a locus is sufficient if it provides from 0.1 to 1,000 ppm of the isothiazoline ingredient of the composition in the locus. It is preferred that the isothiazolone ingredients of the composition be present in the locus in an amount of at least 0.5 ppm, preferably at least 4 ppm, preferably at least 10 ppm. It is preferred that the isothiazolone ingredients of the composition be present in the locus in an amount of no more than 1000 ppm, preferably no more than 500 ppm, preferably no more than 200 ppm, preferably no more than 100 ppm.
The synergism of the biocides combination of the present invention was determined using the method described by Kull, F. C, et. all in Applied Microbiology 9:538-541 (1961). The formula to calculate the synergistic index (SI) is
Qa/QA+Qb/QB=SI
Where
QA=concentration of compound A in ppm, acting alone produced an end point or if end point could not be established, the highest concentration tested will be used the as the end point for the calculation and the SI will be recorded in “less than or <” values
Qa=concentration of compound A in ppm, in the mixture, which produced an end point
QB=concentration of compound B in ppm, acting alone produced an end point or if end point could not be established, the highest concentration tested will be used the as the end point for the calculation and the SI will be recorded in “less than or <” values
Qb=concentration of compound B in ppm, in the mixture, which produced an end point Synergism within two biocides is demonstrated when the SI has a value less than 1. The mixtures showed an additive effect if SI is equal to 1 and antagonistic if SI is greater than 1. In this invention, two different approaches of synergistic study were conducted. One synergistic study is determined based on the minimum inhibitory concentration (MIC), the lowest concentration of a biocide prevents the growth of tested microorganism under a specific set of conditions. The second study was based on three to four consecutive challenge testing. This test was conducted to take biocide mode of action and speed of kill into a consideration. The data for synergistic effect was depicted at any point of in each challenge testing where the synergistic effect was observed and showed the most activities.
The microorganisms tested are Escherichia coli (E. coli, ATCC #8739), yeast, Candida albicans (c. albicans, ATCC #10231) and mold, Aspergillus niger (a. niger, ATCC #16404). The final concentration of microorganisms in the tested media is about 104 cfu/mL
MBIT synergy with a secondary biocide was determined by evaluating the minimum biocide or biocide blend concentration required to inhibit microbial growth. All studies were conducted using a 96 well microtiter plate format. For all studies, 200 μl of microbial growth media, containing various concentrations of MBIT alone, the secondary biocide alone, or combinations of both biocide chemistries, was added to individual wells of a microtiter plate. Specifically, Tryptic Soy Broth (TSB) was utilized for bacteria (E. coli, ATCC #8739), Yeast Malt Extract Broth (YMB) for yeast (Candida albicans, ATCC #10231) and Potato Dextrose Broth (PDB) for mold (Aspergillus niger, ATCC #16404). Test organisms, at a final concentration of 104 CFU/mL or 104 spores/mL, were applied to each well in parallel experiments to initiate the MIC evaluations. Growth medium containing no biocide was utilized as a control in each experimental setup to confirm the growth viability of each organism. Eight concentrations (2-fold dilutions) of each individual biocide were evaluated in the microbial growth inhibition studies in addition to the 64 possible combinations of these biocide concentrations. Evaluation of the individual biocide concentrations is required to achieve an inhibitory concentration end point for synergy index calculation. Following organism addition the 96-well microtiter plates were incubated at 25° C. for 48 hours or until growth was observed in the control wells containing no biocide. Individual wells were scored as growth or no growth based on visual organism growth turbidity. The lowest single active biocide concentrations resulting in no organism growth, for both MBIT and the secondary biocide, were recorded for synergy index calculations in addition to the combined biocide concentrations which resulted in an inhibition of microbial growth.
Ratios of the two biocides exhibiting synergy are presented in Tables 1-6.
E. coli
C. albicans
A. niger
E. coli
C. albicans
A. niger: No synergy at any ratio
E. coli
C. albicans: No synergy at any ratio
A. niger
E. coli: No synergy at any ratio
C. albicans: No synergy at any ratio
A. niger
E. coli: No synergy at any ratio
C. albicans
E. coli: No synergy at any ratio
C. albicans: No synergy at any ratio
A. niger: No synergy at any ratio
MKC evaluations were utilized to determine the synergy of MBIT with the co-biocides DXN (6-Acetoxy-2,4-dimethyl-m-dioxane) and THNM (2-Hydroxymethyl-2-nitro-1,3-propanediol) due to the inability to evaluate these particular biocide chemistries in MIC evaluations. The following test methods were designed for the evaluation of the aforementioned synergistic combinations. The results can be found in Tables 7 and 8.
Bacteria
Testing began (day 0) by applying sterile water, supplemented with 2.0% TSB, to each well of a 96-well microtiter plate. Various concentrations of MBIT alone, the co-biocide alone, or combinations of both biocide chemistries, were added to individual wells of the microtiter plate followed by addition of Escherichia coli (ATCC #8739) at a final concentration of 5×104 CFU/mL. Equivalent inoculations were applied on days 7, 14 and 21 of the study. To determine the extent of bacterial kill, an aliquot (20 μl) of each sample was taken on days 1, 7, 8, 14, 15, 21, 22 and transferred to tryptic soy broth (180 μl). After 48 hours of incubation at 30° C., bacterial kill (to a maximum detection limit of 5×101 CFU/mL) was visually determined by the presence or lack of turbidity within the TSB.
Yeast
Testing began (day 0) by applying sterile water, supplemented with 2.0% yeast malt extract broth, to each well of a 96-well microtiter plate. Various concentrations of MBIT alone, the co-biocide alone, or combinations of both biocide chemistries, were added to individual wells of the microtiter plate followed by addition of Candida albicans (ATCC #10231) at a final concentration of 5×104 CFU/mL. Equivalent inoculations were applied on days 7, 14 and 21 of the study. To determine the extent of yeast kill, an aliquot (20 μl) of each sample was taken on days 1, 7, 8, 14, 15, 21, 22 and transferred to yeast malt extract broth (180 μl). After 48 hours of incubation at 30° C., yeast kill (to a maximum detection limit of 5×101 CFU/mL) was visually determined by the presence or lack of turbidity within the YMB.
Mold
Testing began (day 0) by applying sterile water, supplemented with 2.0% potato dextrose broth, to each well of a 96-well microtiter plate. Various concentrations of MBIT alone, the co-biocide alone, or combinations of both biocide chemistries, were added to individual wells of the microtiter plate followed by addition of Aspergillus niger (ATCC #16404) at a final concentration of 5×104 spores/mL. Equivalent inoculations were applied on days 7 and 14 of the study. To determine the extent of mold kill, an aliquot (20 μl) of each sample was taken on days 1, 7, 8, 14, 15, 21 and transferred to potato dextrose broth (180 μl). After 48-96 hours of incubation at 30° C., mold kill (to a maximum detection limit of 5×101 spores/mL) was visually determined by the presence or lack of turbidity within the PDB.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US2013/042185 | 5/22/2013 | WO | 00 |
| Publishing Document | Publishing Date | Country | Kind |
|---|---|---|---|
| WO2013/177258 | 11/28/2013 | WO | A |
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| 20150164077 A1 | Jun 2015 | US |
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| 61651170 | May 2012 | US |
