(19)
(11)EP 2 531 036 B1

(12)EUROPEAN PATENT SPECIFICATION

(45)Mention of the grant of the patent:
07.06.2017 Bulletin 2017/23

(21)Application number: 11707213.2

(22)Date of filing:  03.02.2011
(51)International Patent Classification (IPC): 
A01P 1/00(2006.01)
A01N 59/06(2006.01)
A61K 33/20(2006.01)
A01N 59/00(2006.01)
A01N 59/08(2006.01)
(86)International application number:
PCT/GB2011/050180
(87)International publication number:
WO 2011/095809 (11.08.2011 Gazette  2011/32)

(54)

DISINFECTANT MATERIALS AND METHODS

DESINFEKTIONSMATERIALIEN UND METHODEN

MATÉRIAUX DE DÉSINFECTANT ET MÉTHODES


(84)Designated Contracting States:
AL AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO RS SE SI SK SM TR

(30)Priority: 09.12.2010 GB 201020901
03.02.2010 GB 201001717

(43)Date of publication of application:
12.12.2012 Bulletin 2012/50

(73)Proprietor: Mauve Technology Ltd.
Wimborne Dorset BH21 1QU (GB)

(72)Inventor:
  • NORTON, David
    Wimborne, Dorset BH21 3AE (GB)

(74)Representative: chapman + co 
18 Staple Gardens
Winchester, Hampshire SO23 8SR
Winchester, Hampshire SO23 8SR (GB)


(56)References cited: : 
CA-A1- 2 028 930
JP-A- 57 111 363
JP-A- 2008 036 020
GB-A- 2 422 545
JP-A- 2001 259 652
KR-A- 2001 044 875
  
      
    Note: Within nine months from the publication of the mention of the grant of the European patent, any person may give notice to the European Patent Office of opposition to the European patent granted. Notice of opposition shall be filed in a written reasoned statement. It shall not be deemed to have been filed until the opposition fee has been paid. (Art. 99(1) European Patent Convention).


    Description


    [0001] The present invention is concerned with disinfectant materials and with methods of disinfecting.

    [0002] Chlorine and chlorine-based disinfectants have been widely used in the medical field as early as the 18th century. Chlorine-based chemicals, such as sodium hypochlorite, have also been used for many years in water and sewage treatment, and for sterilising equipment subject to contamination. Other chlorine donors, such as calcium hypochlorite, have also been used as disinfectants or sterilising agents. Several bacteriological studies have demonstrated that the effectiveness and efficacy of such hypochlorites depends chiefly on the concentration of hypochlorous acid present in solution when the chemicals are put into use.

    [0003] The concentration of hypochlorous acid depends on the amount and concentration of the hypochlorite, and also on the pH of the solution. Specifically, the more alkaline the solution, the less hypochlorous acid is present, and consequently the less effective the solution is as a disinfectant or sterilant. At near neutral pH (such as pH 7.5) only 50% of the chlorine is present as hypochlorous acid (HOCl) and the remaining is present as hypochlorite ions (OCl-). As the pH of the solution increases further (to a pH of greater than 7.5), the relative concentration of hypochlorite ions increases, relative to hypochlorous acid content and the germicidal efficacy decreases still further.

    [0004] On the other hand, as the solution is acidified to a pH of less than 7.5, the relative concentration of hypochlorous acid increases and the germicidal efficacy increases significantly. At a pH of 6.5, approximately 90% of the chlorine will be available as hypochlorous acid. It is in the pH range of 5 to 6 that such solutions are at their most potent because at these pH values, hypochlorous acid provides greater than 98% of the free available chlorine.

    [0005] Hypochlorous acid is known to be highly active against a range of pathogens such as Mycobacterium tuberculosis, Mycobacterium avium intracellulare, Mycobacterium chelonae, methicillin-resistant Staphylococcus aureus, Candida albicans, Escherichia coli, Pseudomonas aeruginosa, Enterococcus faecalis, Bacillus subtilis and human immunodeficiency virus HIV-1.

    [0006] Accordingly, it could be expected that hypochlorites would be widely used, particularly in the medical field, as potent germicides. However, this is not currently the case because their solutions are generally commercially available only at relatively high pH values, which in turn is because they are only adequately stable in alkaline conditions. However, although stable, they are not very effective as disinfecting or sterilising solutions at such high pH values. Also, at these relatively high pH values the solutions cause significant skin irritation and corrosion of equipment.

    [0007] Hypochlorites at their most potent pH (pH 5 to 7 or slightly acidic) have a very short life cycle (usually a few days at most) and consequently cannot be stored for extended time periods.

    [0008] GB2437489 discloses the use of at least one of sodium hypochlorite (NaOCl) and calcium hypochlorite [Ca(OCl)2] as a chlorine donor together with one or more acids, such as dicarboxylic or tricarboxylic acids, for example, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, suberic acid, and citric acid. The hypochlorite and the acids can be provided in solid (typically powdered or granular) form to be made up in water when required, or stored in aqueous solution.

    [0009] While such an aqueous solution has reasonable storage stability, deterioration over time is inevitable. For maximum efficacy, therefore, the disinfectant solution may be made up shortly before use by mixing together separate supplies of the hypochlorite and the acid.

    [0010] For example, WO00/51434 discloses a weak acid disinfectant comprising a first agent (which may contain e.g. sodium or calcium hypochlorite) and a second agent (which may contain e.g. succinic acid). The two agents may be packaged separately, or composed into one package. The disinfectant is provided in the form of an aqueous solution.

    [0011] CA2028930 discloses a method of providing a hypochlorous acid sterilant solution by combining a first solution containing a hypochlorite salt with a second component that may be e.g. acetic acid or formic acid.

    [0012] WO98/21308 discloses an acid bleaching composition prepared from a first aqueous containing succinic acid and a second aqueous solution containing hypochlorite.

    [0013] However, when separate solutions of hypochlorite and acids are used, it can frequently be difficult to ensure complete dissolution.

    [0014] The present inventionconcerns a disinfectant combination, which comprises;
    1. (a) a first sealed or closed packcontaining a water-soluble hypochlorite, the hypochlorite being in aqueous solution at an alkaline pH;
    2. (b) a second sealed or closed pack containing at least one saturated, water-soluble, physiologically acceptable carboxylic acid.


    [0015] According to the invention, the carboxylic acid in the second pack is in solution in an alcoholic solvent which comprises 40 to 60% ethanol and the balance of the solvent is water.

    [0016] The ethanol acts as an effective solvent for the carboxylic acid and allows the provision of separate liquid concentrates, which are to be mixed together in water before the combination is used as a disinfectant. The materials used in the disinfectant system are simple to use by untrained personnel and do not necessitate the use of special equipment; they are environmentally friendly and do not necessitate special ventilation or disposal equipment. Each of the two components is easy to package and distribute, with good storage stability and a long shelf life.

    [0017] GB 2422545 discloses a dispenser for a two part disinfectant solution, one part being typically hypochlorite and the other part being typically an acid solution. The document discloses that the two parts are combined and dispensed in the form ot a foam The document further discloses that either or both parts may contain other 'solvents' such as ethanol or glycerol (provided that a sufficiently stable foam can be achieved. There is no hint or suggestion that an acid should be pre-dissolved in alcoholic solvent that comprises ethanol and optionally water, and consequently no hint or suggestion of advantages stemming from the use of the acid in solution in such an alcoholic solvent.

    [0018] The hypochlorite used in the disinfectant combination according to the present invention may be initially in dry form, to be mixed in water for the first pack.

    [0019] Surprisingly, it has also been found that the use of a disinfectant combination according to the present invention may cause less damage to medical apparatus, such as endoscopes, than conventional disinfectants. Effectively, the lifetime of the apparatus such as endoscopes may be significantly increased, since they have been found to be able to withstand a greater number of disinfection cycles using the combination according to the invention.

    [0020] Traditionally, glutaraldehyde has been the most commonly used disinfectant in endoscopy units, because it is relatively inexpensive, and does not damage endoscopes, accessories or automated processing equipment. However, glutaraldehyde is asthamagenic, and adverse reactions to glutaraldehyde are common among endoscopy personnel,. The use of glutaraldehyde has therefore been significantly curtailed (and in some countries glutaraldehyde has been withdrawn from use for this reason). Various alternative disinfectants have therefore been proposed for endoscopes, such as ortho-phthalaldehyde, succinic dialdehyde, peracetic acid and chlorine-containing disinfectants. Chlorine-containing disinfectants are known to cause damage to the lacquer coating of some endoscopes, and therefore have not hitherto been considered to be entirely satisfactory for this purpose.

    [0021] It is therefore surprising that endoscopes can be disinfected 50 to 100 times using the combination according to the invention, while maintaining the lacquer in pristine, undamaged condition.

    [0022] The carboxylic acid used in the disinfectant combination according to the invention may be mono-, di- or tri- functional; it is preferably a saturated (alkanoic) acid. Optionally, the acid may have one or more substituents which are substantially inert in the presence of a chlorine donor. The acid is preferably a solid (when in pure, isolated form at 20°C, although of course according to the invention, the acid is provided in alcoholic solution). The acid is typically an alkane dioic acid with up to 7 carbon atoms in a saturated chain, or a hydroxyl substituted acid such as citric acid.

    [0023] As the length of the carbon chain increases, the solubility of the acid in water and alcohol decreases, so the carbon chain length should not be such that the acid is no longer soluble in the alcoholic solvent.

    [0024] Typical such carboxylic acids for use according to the invention include one or more of oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid and suberic acid. An especially preferred such acid is adipic acid.

    [0025] The alcoholic solvent for the carboxylic acid comprises 40 to 60% by weight of ethanol, with the balance being water. It is particularly preferred that the solvent consists of substantially equal amounts by weight of ethanol and water (that is, each is preferably present in an amount of 45 to 55% by weight). The ethanol may be pure, but more usually an Industrial denatured alcohol or a trade specific denatured alcohol will be used. These are 99.9% pure ethanol and they are regularly used in the preparation of medical biocidal reagents and external medical applications such as creams and ointments.

    [0026] The hypochlorite used in the first pack may be sodium hypochlorite and/or calcium hypochlorite. The first pack is a sealed or closed pack containing the hypochlorite in aqueous solution at an alkaline pH such that the solution has prolonged storage life. The closed pack may provide a unit dose of the hypochlorite solution, or it may be a dispenser arranged to dispense predetermined amounts of the hypochlorite solution.

    [0027] The preferred amount of hypochlorite such as calcium hypochlorite [Ca(OCl)2] depends on the end use of the combination according to the invention. For example, for a free available chlorine content of 250 mg/l, approximately 300 mg of calcium hypochlorite [Ca(OCl)2] would be required per litre of aqueous solution. For a free available chlorine level of 50 mg/l, approximately 60 mg of calcium hypochlorite [Ca(OCl)2] would be required per litre of aqueous solution.

    [0028] In either case, an equivalent amount of an acid such as adipic acid and/or succinic acid is required to obtain the necessary pH and subsequent efficacy. The former concentration [250 mg/l] is strong enough for disinfection and sterilisation of medical devices, for example, flexible endoscopes, orthopaedic instruments and the like. It is also suitable for use in complete room remediation and the removal of biofilms from water lines, for example, in dental units.

    [0029] Typically the hypochlorite solution contains about 30 to 40 grams of hypochlorite per litre of water.

    [0030] The aqueous solvent for the hypochlorite may, for example, be of potable tap water, deionised water or distilled water.

    [0031] The second sealed or closed pack containing the carboxylic acid in solution in the ethanolic solvent may provide a unit dose of carboxylic acid solution, or it may be a dispenser arranged to dispense predetermined amounts of the solution of the carboxylic acid. Typically the carboxylic acid solution contains about 30 to 40 grams of acid per litre of 50/50 ethanol/water.

    [0032] The first and second packs may be separate containers (such as sachets or vials each containing the desired amount of the required ingredients); alternatively, a duplex container may be provided such that both can be opened simultaneously when it is desired to dispense the respective contents.

    [0033] Both the hypochlorite solution and the carboxylic acid solution may contain acceptable non-deleterious additives, such as buffers, detergents or the like. When the carboxylic acid solution contains water, the latter may, for example, be .potable tap water, de-ionised water or distilled water. By "acceptable" we mean herein physiologically acceptable when the solutions are to be used to disinfect articles or surfaces intended to contact a human or animal body.

    [0034] The combination according to the invention is preferably employed in a method of disinfection, in which a disinfectant is formed in situ. The present invention further comprises a non-therapeutical method of disinfection of a surface or article, which method comprises dissolving at least one saturated, water-soluble, physiologically acceptable carboxylic acid, in an alcoholic solvent which comprises 40 to 60% ethanol, the balance of the solvent being water, mixing the resulting solution with a dosed amount of a water-soluble hypochlorite (typically in aqueous solution), and applying the resultant disinfectant mixture to the surface or article. The mixture of the alcoholic solution and the hypochlorite is preferably diluted in water (typically using water in an amount of at least 20 times the volume of the concentrates).

    [0035] The present invention further comprises a method of disinfecting a body of water, which comprises dissolving at least one saturated, water-soluble, physiologically acceptable carboxylic acid, in an alcoholic solvent which comprises 40 to 60% ethanol, the balance of the solvent being water, and mixing the solution with a dosed amount of a water-soluble hypochlorite in the body of water.

    [0036] The body of water in the method of disinfection may, for example, be in a container such as a barrel, drum, bottle or the like, or it may be in the form of an open body such as a well, pool, or water course, or water in a pipeline. By this means, potable water may be obtained from a body of water which was previously unfit for consumption.

    [0037] Preferably a dosed amount of the alcoholic solution is mixed with a dosed amount of the water-soluble hypochlorite, and the resulting combined solution, optionally diluted with further water, applied to a surface, material or article to be disinfected, or applied to the body of water. The diluted combined solution may be applied to the surface, material or article by spraying or by the use of an applicator, or by dipping, immersing or submerging the surface to be disinfected in the diluted combined solution.

    [0038] It is particularly preferred to immerse an entire article to be disinfected in a reservoir containing a freshly prepared combined solution which has preferably been diluted with further water (again, typically of potable tap water, deionised water or distilled water).

    [0039] The article to be disinfected may, for example, be an item for personal or medical use, such as an endoscopic device suitable for use in endoscopic inspection or surgery, typically using a disinfectant at solution strengths of about 200 to 300 ppm. The disinfection according to the invention may be carried out in automatic endoscopy reprocessing (AER) apparatus.

    [0040] When used for this purpose, the disinfection cycle is preferably after a cleaning cycle (such as the manual removal of blood, secretions or other debris).

    [0041] Disinfection according to the invention is then to substantially destroy vegetative microorganisms, mycobacteria, viruses, fungal spores and most bacterial spores to a level such that the disinfected article is suitable for safe use in a patient.

    [0042] Other applications of the combination according to the invention include the disinfection of water lines, typically in dental surgeries so as to remove biofilm from within the lines, which could otherwise lead to cross contamination. Further applications are for a weaker solution (typically about 40 to 60 ppm) for general hospital ward and theatre hard surface cleaning. Still further applications include disinfection of surfaces in abattoirs and the like (where of course the level of destruction of microorganisms, viruses and the like is not as stringent as for apparatus such as endoscopes which come into intimate contact with vulnerable patients.

    [0043] Even lower concentrations of the combination according to the invention, say, for example, around 5 mg/l free available chlorine, may be employed for supplying bacteria-free water to dental unit water lines and water for misting of comestible produce such as salad, vegetable and fruit products, to enhance the appearance and shelf life thereof, in supermarkets or the like. Approximately 6 mg of calcium hypochlorite [Ca (OCl)2] would be required for each litre of aqueous solution for such an application.

    [0044] In a typical mode of operation, dosed amounts (such as about 200 ml) of each supply, in the form of a concentrate, may be separately dispensed and mixed with typically 25 to 27 litres of water to create a disinfecting solution, typically of pH about 6.0. The disinfecting solution thus formed is applied to the surface to be disinfected as indicated above.

    [0045] The final pH of the disinfecting solution and its free available chlorine level in the form of hypochlorous acid can be varied or controlled by selecting the amounts and ratios of the respective ingredients. Thus an optimum pH can be selected so as to maximise the concentration of free available chlorine in the form of hypochlorous acid.

    [0046] Preferred features and aspects of the present invention will now be illustrated with reference to the following worked Examples, which are of course of an illustrative rather than limiting nature.

    Example 1



    [0047] 7.5g of powdered calcium hypochlorite was dissolved in 200ml of de-ionised water and 7.5g of adipic acid was dissolved separately in 200ml of 50/50 ethanol/deionised water. The two solutions were then mixed and diluted into 25L [62.5 fold] in deionised water, which produced an active chlorine content of approx. 250 ppm at a pH of 6-7. The mixed solution was pumped into a suitably sized receptacle where an endoscopic inspection device was submerged therein for a period of 5 minutes, after which it was tested and found to be substantially free of surface microorganisms.

    [0048] The solution was also tested in standard test EN 13727 under simulated Clean Conditions: 0.03% Bovine albumin (final concentration) and Dirty Conditions: 0.3% Bovine albumin (final concentration) plus 0.3% sheep erythrocytes. The EN 13727 test method involves mixing 1 ml of the test bacteria with 1 ml of interfering substance (0.3% or 3% albumin with 0.3% sheep erythrocytes), and then adding 8 ml of the test disinfectant. After the required contact time, 1 ml is removed to 9 ml of recovery broth (8ml neutralizer and 1 ml water) for 5 minutes after which it is plated onto Tryptone Soya Agar to detect surviving test bacteria.

    [0049] When tested in this manner under simulated clean conditions, the solution resulted in a 5 log10 reduction in under one minute, easily meeting the requirements of test EN 13727. A 5 log10 reduction in under 60 minutes was also achieved under simulated dirty conditions. The results of such tests, carried out in duplicate, are summarised in the following table.
    Test organismContact timeLog10 initial countMean log10 reduction
    Clean conditionsDirty conditions
    Test 1Test 2MeanTest 1 Test 2 Mean
    Staphylococcus aureus 1 min 8.23 >7.23 >7.23 >7.23 2.91 3.38 3.15
    2 min >7.23 >7.23 >7.23 3.35 3.75 3.55
    5 min >7.23 >7.23 >7.23 3.35 3.85 3.60
    60 min >7.23 >7.23 >7.23 >7.23 >7.23 >7.23
    Pseudomonus aeruginosa 1 min 7.69 >6.69 >6.69 >6.69 3.21 3.43 3.32
    2 min >6.69 >6.69 >6.69 4.31 4.90 4.61
    5 min >6.69 >6.69 >6.69 4.39 4.61 4.50
    60 min >6.69 >6.69 >6.69 >6.69 >6.69 >6.69
    Enterococcus hirae 1 min 7.65 >6.65 6.16 >6.41 2.86 2.61 2.74
    2 min >6.65 >6.65 >6.65 3.02 3.31 3.17
    5 min >6.65 >6.65 >6.65 2.61 3.22 2.92
    60 min >6.65 >6.65 >6.65 >6.65 >6.65 >6.65


    [0050] Similar results for clean conditions were also achieved in other tests relevant to chemical disinfectants in relation to the European Standards for chemical disinfectants [EN14885]. These are as follows Tuberculoidal Efficacy Tests EN14348, and Assessment of Sporicidal Activity & Virucidal Efficacy of a disinfectant using EN 14476.

    Example 2



    [0051] Example 1 was repeated with a similar amount of succinic acid instead of adipic acid. Similar results were obtained.

    Example 3



    [0052] 7.5g of powdered calcium hypochlorite was dissolved in 200ml of deionised water. Separately, 3.75g of adipic acid was mixed with 3.75g of succinic acid and dissolved in 200ml of 50/50 ethanol/deionised water. The two solutions were then mixed and further diluted into 25L [62.5 fold] of deionised water which produced an active chlorine content of approx. 250 ppm at a pH of 6-7.

    [0053] The mix was pumped into a suitably sized receptacle where an endoscopic inspection device was submerged therein for a period of 5 minutes, after which it was tested and found to be substantially free of surface microorganisms.

    Example 4



    [0054] 1.5g of powdered calcium hypochlorite was dissolved in 100ml of de-ionised water and 1.5g of adipic acid was dissolved separately in 100ml of 50/50 ethanol/deionised water. The two solutions were then mixed & diluted into 25L [125 fold] in sealed container. This solution was then used to clean a laboratory hard-surface, after which the surface was immediately tested and found to be substantially free of surface microorganisms.

    Example 5



    [0055] Example 4 was repeated with a similar amount of succinic acid instead of adipic acid. Similar results were obtained.

    Example 6



    [0056] 1.5g of powdered calcium hypochlorite was dissolved in 100ml of de-ionised water. Separately, 0.75g of adipic acid was mixed with 0.75g of succinic acid and dissolved in 100ml of 50/50 ethanol/deionised water. The two solutions were then mixed and diluted into 25L [125 fold] in a sealed container. This solution was then used to clean a laboratory hard-surface, after which it was immediately tested and found to be substantially free of surface microorganisms.

    Example 7



    [0057] A mixed solution as made up in Example 1 was used to disinfect a range of cleaned endoscopes in an Automated Endoscope Reprocessing apparatus in an accelerated 300 cycle test (equivalent to 12 months normal usage). All endoscopes were examined pre- and post-disinfection; no corrosion, build or cracks were observed, and exposed metal parts were unaffected. The disinfection method therefore provides a significant advantage relative to prior art techniques, where damage is frequently noted.


    Claims

    Claims for the following Contracting State(s): AT, BE, CH, DE, DK, ES, FR, GR, IT, LI, LU, MC, NL, SE

    1. A two pack disinfectant combination, which comprises:

    a first sealed or closed pack containing a water-soluble hypochlorite in aqueous solution at an alkaline pH; and

    a second sealed or closed pack containing at least one saturated, water-soluble, physiologically acceptable carboxylic acid, characterised in that the carboxylic acid in the second pack is in solution in an alcoholic solvent which comprises 40 to 60% ethanol, the balance of the solvent being water.


     
    2. A combination according to claim 1, wherein the hypochlorite is in aqueous solution.
     
    3. A combination according to claim 1 or 2, wherein the carboxylic acid is a mono-, di- or tri- functional, saturated alkanoic acid optionally having one or more substituents which are substantially inert in the presence of a chlorine donor.
     
    4. A combination according to claim 3, wherein the acid is a solid when in pure isolated form at 20°C, and is an alkane dioic acid with up to 7 carbon atoms in a saturated chain, or a hydroxyl substituted alkanoic acid.
     
    5. A non-therapeutical method of disinfection of a surface or article, which comprises dissolving at least one saturated, water-soluble, physiologically acceptable carboxylic acid in a solvent, mixing the resultant solution with a dosed amount of a water-soluble hypochlorite, and applying the resultant disinfectant mixture to the surface or article, characterised in that the solvent comprises 40 to 60% ethanol, the balance of the solvent being water.
     
    6. A method according to claim 5, in which the disinfectant mixture is diluted with water before application to the surface or article.
     
    7. A method according to claim 6, wherein the disinfectant mixture is applied to the surface or article by spraying; by the use of an applicator; or by dipping, immersing or submerging the surface or article into the diluted disinfectant mixture.
     
    8. A method according to claim 6 or 7, wherein the article is a cleaned endoscopic device.
     
    9. A method of disinfecting a body of water, which comprises dissolving at least one saturated, water-soluble, physiologically acceptable carboxylic acid, in a solvent, and mixing the resulting solution with a dosed amount of a water-soluble hypochlorite in the body of water characterised in that the carboxylic acid is dissolved in solution in an alcoholic solvent which comprises 40 to 60% ethanol, the balance of the solvent being water.
     
    10. A method according to any of claims 5 to 9, in which the hypochlorite is provided in aqueous solution.
     
    11. A method according to any of claims 5 to 10, wherein the carboxylic acid is a mono-, di- or tri- functional, saturated alkanoic acid optionally having one or more substituents which are substantially inert in the presence of a chlorine donor.
     
    12. A method according to any of claims 5 to 11, wherein the acid is a solid in isolated form at 20°C, and is an alkane dioic acid with up to 7 carbon atoms in a saturated chain, or a hydroxyl substituted alkanoic acid.
     


    Claims

    Claims for the following Contracting State(s): GB

    1. A method of disinfecting a body of water, which comprises dissolving at least one saturated, water-soluble, physiologically acceptable carboxylic acid, in a solvent, and mixing the solution with a dosed amount of a water-soluble hypochlorite in the body of water, characterised in that the solvent for the carboxylic acid is an alcoholic solvent which comprises 40 to 60% by weight of ethanol, the balance of the solvent being water.
     
    2. A method according to claim 1, in which the hypochlorite is provided in aqueous solution.
     
    3. A method according to claim 1 or 2, wherein the carboxylic acid is a mono-, di- or tri- functional, saturated alkanoic acid optionally having one or more substituents which are substantially inert in the presence of a chlorine donor.
     
    4. A method according to any of claims 1 to 3, wherein the acid is a solid in isolated form at 20°C, and is an alkane dioic acid with up to 7 carbon atoms in a saturated chain, or a hydroxyl substituted alkanoic acid.
     


    Ansprüche

    Patentansprüche für folgende(n) Vertragsstaat(en): AT, BE, CH, DE, DK, ES, FR, GR, IT, LI, LU, MC, NL, SE

    1. Desinfektionskombination mit zwei Packungen, die umfasst:

    eine erste versiegelte oder geschlossene Packung, die ein wasserlösliches Hypochlorit in wässriger Lösung mit einem alkalischen pH-Wert enthält; und

    eine zweite versiegelte oder geschlossene Packung, die mindestens eine gesättigte, wasserlösliche, physiologisch annehmbare Carbonsäure enthält, dadurch gekennzeichnet, dass die Carbonsäure in der zweiten Packung gelöst in einem alkoholischen Lösungsmittel vorliegt, das 40 bis 60 % Ethanol umfasst, wobei der Rest des Lösungsmittels Wasser ist.


     
    2. Kombination nach Anspruch 1, wobei das Hypochlorit in wässriger Lösung ist.
     
    3. Kombination nach Anspruch 1 oder 2, wobei die Carbonsäure eine mono-, di- oder trifunktionale gesättigte Alkancarbonsäure ist, die gegebenenfalls einen oder mehrere Substituenten aufweist, die in Gegenwart eines Chlordonors im Wesentlichen inert sind.
     
    4. Kombination nach Anspruch 3, wobei die Säure in reiner isolierter Form bei 20 °C ein Feststoff ist und eine Alkandicarbonsäure mit bis zu 7 Kohlenstoffatomen in einer gesättigten Kette oder eine hydroxylsubstituierte Alkansäure ist.
     
    5. Nicht-therapeutisches Verfahren zur Desinfektion einer Oberfläche oder eines Artikels, welches Auflösen von mindestens einer gesättigten, wasserlöslichen, physiologisch annehmbaren Carbonsäure in einem Lösungsmittel, Mischen der resultierenden Lösung mit einer dosierten Menge eines wasserlöslichen Hypochlorits und Aufbringen der resultierenden Desinfektionsmittelmischung auf eine Oberfläche oder einen Artikel umfasst, dadurch gekennzeichnet, dass das Lösungsmittel 40 bis 60 % Ethanol umfasst, wobei der Rest des Lösungsmittels Wasser ist.
     
    6. Verfahren nach Anspruch 5, wobei die Desinfektionsmittelmischung vor Aufbringung auf die Oberfläche oder den Artikel mit Wasser verdünnt wird.
     
    7. Verfahren nach Anspruch 6, wobei die Desinfektionsmittelmischung durch Sprühen auf die Oberfläche oder den Artikel; durch Verwendung eines Applikators oder durch Tauchen, Eintauchen oder Untertauchen der Oberfläche oder des Artikels in die verdünnte Desinfektionsmittelmischung aufgebracht wird.
     
    8. Verfahren nach Anspruch 6 oder 7, wobei der Artikel ein gereinigtes Endoskopiegerät ist.
     
    9. Verfahren zum Desinfizieren eines Wasserkörpers, welches Auflösen von mindestens einer gesättigten, wasserlöslichen, physiologisch annehmbaren Carbonsäure in einem Lösungsmittel und Mischen der resultierenden Lösung mit einer dosierten Menge eines wasserlöslichen Hypochlorits in dem Wasserkörper umfasst, dadurch gekennzeichnet, dass die Carbonsäure in einer Lösung in einem alkoholischen Lösungsmittel gelöst wird, das 40 bis 60 % Ethanol umfasst, wobei der Rest des Lösungsmittels Wasser ist.
     
    10. Verfahren nach einem der Ansprüche 5 bis 9, wobei das Hypochlorit in wässriger Lösung bereitgestellt wird.
     
    11. Verfahren nach einem der Ansprüche 5 bis 10, wobei die Carbonsäure eine mono-, di- oder trifunktionale gesättigte Alkancarbonsäure ist, die gegebenenfalls einen oder mehrere Substituenten aufweist, die in Gegenwart eines Chlordonors im Wesentlichen inert sind.
     
    12. Verfahren nach einem der Ansprüche 5 bis 11, wobei die Säure in isolierter Form bei 20 °C ein Feststoff ist und eine Alkandicarbonsäure mit bis zu 7 Kohlenstoffatomen in einer gesättigten Kette oder eine hydroxylsubstituierte Alkansäure ist.
     


    Ansprüche

    Patentansprüche für folgende(n) Vertragsstaat(en): GB

    1. Verfahren zum Desinfizieren eines Wasserkörpers, welches Auflösen von mindestens einer gesättigten, wasserlöslichen, physiologisch annehmbaren Carbonsäure in einem Lösungsmittel und Mischen der resultierenden Lösung mit einer dosierten Menge eines wasserlöslichen Hypochlorits in den Wasserkörper umfasst, dadurch gekennzeichnet, dass das Lösungsmittel für die Carbonsäure ein alkoholisches Lösungsmittel ist, das 40 bis 60 % Ethanol umfasst, wobei der Rest des Lösungsmittels Wasser ist.
     
    2. Verfahren nach Anspruch 1, wobei das Hypochlorit in wässriger Lösung bereitgestellt wird.
     
    3. Verfahren nach Anspruch 1 oder 2, wobei die Carbonsäure eine mono-, di- oder trifunktionale gesättigte Alkancarbonsäure ist, die gegebenenfalls einen oder mehrere Substituenten aufweist, die in Gegenwart eines Chlordonors im Wesentlichen inert sind.
     
    4. Verfahren nach einem der Ansprüche 1 bis 3, wobei die Säure in isolierter Form bei 20 °C ein Festoff ist und eine Alkandicarbonsäure mit bis zu 7 Kohlenstoffatomen in einer gesättigen Kette oder eine hydroxylsubstituierte Alkansäure ist.
     


    Revendications

    Revendications pour l'(les) Etat(s) contractant(s) suivant(s): AT, BE, CH, DE, DK, ES, FR, GR, IT, LI, LU, MC, NL, SE

    1. Combinaison désinfectante à deux emballages, qui comprend :

    un premier emballage scellé ou fermé contenant un hypochlorite hydrosoluble en solution aqueuse à pH alcalin ; et

    un second emballage scellé ou fermé contenant au moins un acide carboxylique saturé, soluble dans l'eau, physiologiquement acceptable, caractérisé en ce que l'acide carboxylique dans le second emballage en solution dans un solvant alcoolique qui comprend 40 à 60% d'éthanol, le reste du solvant étant composé d'eau.


     
    2. Combinaison selon la revendication 1, dans laquelle l'hypochlorite est en solution aqueuse.
     
    3. Combinaison selon les revendications 1 ou 2, dans laquelle l'acide carboxylique est un acide alcanoïque saturé mono, di ou trifonctionnel comportant éventuellement un ou plusieurs substituants qui sont sensiblement inertes en présence d'un donneur de chlore.
     
    4. Combinaison selon la revendication 3, dans laquelle l'acide est un solide lorsqu'il est sous forme isolée pure à 20°C et est un acide alcane dioïque avec jusqu'à 7 atomes de carbone dans une chaîne saturée ou un acide alcanoïque substitué par un hydroxyle.
     
    5. Procédé non-thérapeutique de désinfection d'une surface ou d'un article, qui comprend la dissolution d'au moins un acide carboxylique saturé, soluble dans l'eau, physiologiquement acceptable dans un solvant, le mélange de la solution résultante avec une quantité dosée d'un hypochlorite hydrosoluble et en appliquant le mélange désinfectant résultant sur la surface ou l'article, caractérisé en ce que le solvant comprend 40 à 60% d'éthanol, le reste du solvant étant composé d'eau.
     
    6. Procédé selon la revendication 5, dans lequel le mélange désinfectant est dilué avec de l'eau avant application sur la surface ou l'article.
     
    7. Procédé selon la revendication 6, dans lequel le mélange désinfectant est appliqué sur la surface ou l'article par pulvérisation ; par l'utilisation d'un applicateur ; ou par trempage, immersion ou submersion de la surface ou l'article dans le mélange désinfectant dilué.
     
    8. Procédé selon les revendications 6 ou 7, dans lequel l'article est un dispositif endoscopique nettoyé.
     
    9. Procédé de désinfection d'une masse d'eau qui comprend la dissolution d'au moins un acide carboxylique saturé, hydrosoluble, physiologiquement acceptable, dans un solvant et le mélange de la solution résultante avec une quantité dosée d'un hypochlorite hydrosoluble dans la masse d'eau, caractérisé en ce que l'acide carboxylique est dissout dans la solution dans un solvant alcoolique qui comprend 40 à 60% d'éthanol, le reste du solvant étant composé d'eau.
     
    10. Procédé selon l'une quelconque des revendications 5 à 9, dans lequel l'hypochlorite est fourni en solution aqueuse.
     
    11. Procédé selon l'une quelconque des revendications 5 à 10, dans laquelle l'acide carboxylique est un acide alcanoïque saturé mono, di ou trifonctionnel comportant éventuellement un ou plusieurs substituants qui sont sensiblement inertes en présence d'un donneur de chlore.
     
    12. Procédé selon l'une quelconque des revendications 5 à 11, dans laquelle l'acide est un solide sous forme isolée à 20°C et est un acide alcane dioïque avec jusqu'à 7 atomes de carbone dans une chaîne saturée ou un acide alcanoïque substitué par un hydroxyle.
     


    Revendications

    Revendications pour l'(les) Etat(s) contractant(s) suivant(s): GB

    1. Procédé de désinfection d'une masse d'eau qui comprend la dissolution d'au moins un acide carboxylique saturé, hydrosoluble, physiologiquement acceptable, dans un solvant et le mélange de la solution résultante avec une quantité dosée d'un hypochlorite hydrosoluble dans la masse d'eau, caractérisé en ce que l'acide carboxylique est dissout dans la solution dans un solvant alcoolique qui comprend 40 à 60% d'éthanol, le reste du solvant étant composé d'eau.
     
    2. Procédé selon la revendication 1, dans lequel l'hypochlorite est fourni en solution aqueuse.
     
    3. Procédé selon l'une des revendications 1 ou 2, dans lequel l'acide carboxylique est un acide alcanoïque saturé mono, di ou trifonctionnel comportant éventuellement un ou plusieurs substituants qui sont sensiblement inertes en présence d'un donneur de chlore.
     
    4. Procédé selon l'une quelconque des revendications 1 à 3, dans lequel l'acide est un solide sous forme isolée à 20°C et est un acide alcane dioïque avec jusqu'à 7 atomes de carbone dans une chaîne saturée ou un acide alcanoïqe substitué par un hydroxyle.
     






    Cited references

    REFERENCES CITED IN THE DESCRIPTION



    This list of references cited by the applicant is for the reader's convenience only. It does not form part of the European patent document. Even though great care has been taken in compiling the references, errors or omissions cannot be excluded and the EPO disclaims all liability in this regard.

    Patent documents cited in the description