GB2344997A - Iodine-releasing disinfectant solution - Google Patents
Iodine-releasing disinfectant solution Download PDFInfo
- Publication number
- GB2344997A GB2344997A GB9828519A GB9828519A GB2344997A GB 2344997 A GB2344997 A GB 2344997A GB 9828519 A GB9828519 A GB 9828519A GB 9828519 A GB9828519 A GB 9828519A GB 2344997 A GB2344997 A GB 2344997A
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- United Kingdom
- Prior art keywords
- ppm
- iodine
- surfactant
- acid
- disinfectant
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Classifications
-
- A—HUMAN NECESSITIES
- A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
- A01N—PRESERVATION 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
- A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds
- A01N59/12—Iodine, e.g. iodophors; Compounds thereof
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- Life Sciences & Earth Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Agronomy & Crop Science (AREA)
- Inorganic Chemistry (AREA)
- Pest Control & Pesticides (AREA)
- Plant Pathology (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Dentistry (AREA)
- General Health & Medical Sciences (AREA)
- Wood Science & Technology (AREA)
- Zoology (AREA)
- Environmental Sciences (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
An aqueous iodine-releasing disinfectant solution comprises an iodophor, a disinfectant active organic acid and an anionic alkyl diphenyl ether disulphonate surfactant. The preferred composition is a concentrated solution which, on dilution with water, yields 15-30 ppm of available iodine, 300-700 ppm of acid and 300-700 ppm of surfactant. Alternatively, the composition can be in ready-to-use form with the active ingredients present in the aforementioned amounts.
Description
IMPROVEMENTS IN ORGANIC CHEMICAL COMPOSITIONS
This invention relates to disinfectant iodinereleasing cleaning compositions for hard surfaces. More particularly, it relates to such compositions in which the amount of iodine has been reduced to a level at which the iodine does not present a staining problem, and yet the disinfectant properties of the compositions remain as high as those with considerably larger amounts of. available iodine.
Iodine was discovered in the early years of the 19th century and has long been used for a wide variety of germicidal and disinfecting purposes for both medical and non-medical uses. Iodine is an effective antiseptic but has certain drawbacks, such as an unpleasant smell and the tendency to produce dark coloured stains on surfaces.
Furthermore, it is only sparingly soluble.
In order to overcome the drawbacks associated with the use of iodine, the iodophors were developed.
Iodophors are generally defined as complexes of iodine and surface active agents, particularly nonionic detergents, which act as carriers and solubilizing agents for the iodine. Iodophors generally enhance the bactericidal activity of iodine, reduce its odour and reduce its staining characteristics. Typical surfactants used in the preparation of iodophors are polyvinyl pyrrolidone (povidone), polyether glycols, polyvinyl alcohols, polyacrylic acids, polyamides, polyoxyalkylenes and the like. The most commonly used surface active agents include polyvinyl pyrrolidone and its iodine complex generally referred to as"povidone-iodine".
Other commonly used surface active agents in iodophors include long chain alkyl phenol/ethylene oxide condensates. Although nonionic, anionic and cationic surface active agents can be used as complexing agents for iodine, nonionic surfactants are preferred and most of the commercially available iodophors are nonionic in nature. There is an extensive amount of patent literature which discusses iodophors; and more details on the chemistry of iodophors can be found in W. Gottardi, "Iodine and Iodine Compounds", which is chapter 8 of
Block, Disinfection. Sterilization and Preservation (1983), pertinent portions of which are incorporated herein by reference.
The use of iodophors in disinfectant compositions for hard surface cleaning is well known in the art, as exemplified in Bakka U. S. Patent No. 3,650,966, Morlock et al. U. S. Patent No. 4,088,597, Langford U. S. Patent
No. 4,207,310, and Gartner U. S. Patent No. 4,526,751. It is generally believed that, in order to provide effective "hospital strength"disinfection, iodophor-containing cleaning/disinfectant compositions must provide at least 75 parts per million (ppm) of available iodine. However, the use of iodine at this level produces dark stains, particularly on porous surfaces. Of course, reducing the level of available iodine will reduce staining but iodine levels below 75 ppm do not generally produce acceptable disinfection.
Kolstad U. S. Patent No. 4,867,897 discloses a germicidal composition comprising iodine, a solvent for the iodine, and one or more anionic detergents. The preferred anionic detergents are sodium lauryl sulphate and nonylphenoxytetra (ethyleneoxy) ethanol sulphates. The stated purpose of these compositions is to provide a level of available iodine which is higher than what would ordinarily be attainable with the use of iodophcrs. It is readily apparent that such compositions, because of their high iodine level, would be likely to cause severe staining on porous surfaces.
There is therefore a need to provide an iodine releasing detergent/disinfecting composition in which iodine levels can be reduced to the point where there is no significant staining of porous surfaces whilst, at the same time, providing an iodine-releasing composition which exhibits hospital strength disinfection.
The invention significantly reduces the staining of surfaces by iodine-based disinfectant compositions.
The compositions of this invention comprise a nonioni=e- iodophor, an organic acid such as citric acid, and an anionic surfactant which is an alkyl phenoxybenzene disulphonate. The presence of the organic acid and this type of anionic surfactant permits a significant reduction in the amount of iodophor, whilst still maintaining hospital strength disinfectant activity. The reduction in the amount of the iodophor, and hence in the amount of available iodine, results in reduced staining whilst still maintaining a level of disinfection achieved with higher levels of iodine. Typically, iodine levels can be reduced from the 75 ppm thought to be required for hospital strength disinfection to a level of about 25 ppm or even lower in some circumstances.
More particularly, this invention provides a concentrated aqueous iodine releasing disinfectant solution comprising (a) an iodophor, (b) a disinfectant active organic acid in sufficient amount to provide from about 300 to about 700 ppm of said acid, and (c) an anionic alkyR diphenyl ether disulphonate surfactant in sufficient amo 4 to provide from about 3QO to about 700 ppm of said surfactant; this solution yields, on dilution with water, from about 15 to about 30 ppm of available iodine.
The invention also provides an aqueous iodinereleasing disinfectant composition which comprises (a) a nonionic'iodophor in sufficient amount to provide the composition with from about 15 to about 30 ppm of available iodine, (b) 300 to 70 ; ppm of a disinfectant active organic acid, and (c) 300 to 700 ppm of an anionic alkyl diphenyl ether disulphonate surfactant.
The iodophors preferred for use in the present invention are complexes of iodine with nonionic surface active agents such as povidone, alkylphenol ethoxylates-, secondary alcohol ethoxylates, ethylene oxide/propylene oxide block copolymers and butoxy-ethylene oxide/propylene oxide block copolymers. A preferred commercially available iodophor is a-(p-nonylphenyl)-X- hydroxypoly (oxyethylene)-iodine complex sold under the trademark Clean Front Concentrate by West Agro which provides 20% titratable iodine. Other commercially available iodophors include Biopal NR-20 from Rhone
Poulenc, a nonylphenoxypoly (ethyleneoxy) ethanol-iodine complex having 20-24% titratable iodine and Bio-Surf I20, an iodine complex of similar chemical structure from
Lonza Inc. Also available from West Agro are MS/DS
Concentrate, a polyethoxy/polypropoxy/polyethoxyethanol- iodine complex having 12.9% titratable-odine, and Lo
Foam Concentrate, a mixture of butoxy polypropoxy/polyethoxyethanol-iodine cor. plex and polyethoxyJpolypropoxy/polyethoxyethano~-iodine complex having 12% titratable iodine.
The term"titratable iodine", sometimes referred to as"available iodine", is determined by titration with a standard thiosulphate solution and microbial activity is related directly to this value. In iodine complexes, the available iodine usually amounts to from about 80% to about 850 of the iodine originally added.
The purpose of the acid is to promote the germicidal activity of the iodophor in order to provide additional sanitizing effect and also to provide a pH in the acid range. Any suitable acid can be used for this purpose; these include hydrochloric acid, lactic acid, hydroxyacetic acid, phosphoric acid, acetic acid, boric acid, citric acid, oxalic acid and the like. Organic acids are preferred and, of these, citric acid is particularly preferred. A pH in the acid range functions to maintain the availability of iodine in the solution.
Generally, the pH of the solution should be below 6 and preferably bRtween 2.0 and 5.0.
Although anionic detergents in general have been previously known as possible ingredients in iodinereleasing disinfectant solutions, it has now been discovered that the use of anionic detergents which have two aromatic rings, particularly phenyl rings, provides a level of effectiveness not attained by other anionic surfactants. Preferred anionic surfactants for use in connection with this invention include the disulphonates such as Dowfax 2A1 (or 2EP or XDS 30599 or XU 40333.00) sold Wy the Dow Chemical Corporation and Poly-Tergent 2A1 (or 2EP) sold by Olin Corporation, both of which comprise principally sodium dodecyldiphenyl ether disulphonate.
Other suitable surfactants include: disodium mono-and di-dodecyl diphenyl oxide disulphonate (Aerosol DPOS-45,
American Cyanamid); sodium alkyl diphenyl oxide disulphonate (Calfax DB-45,10L-45 and 16L-35, Pilot
Chemicals Co.); sodium hexyl diphenyloxide disulphonate (Dowfax XDS 8292.00, Dow Chemical Corp.); sodium n-decyl diphenyloxide disulphonate (Dowfax 3B2 or 8390 or
XU40340.00, Dow Chemical Corp.); sodium n-hexadecyl diphenyloxide disulphonate (Dowfax XU 40341.00, Dow
Chemical Corp.); n-decyl diphenyloxide disulphonate (Dowfax 3BO, Dow Chemical Corp.) ; sodium alkyl diphenyl oxide disulphonate (Larosol NRL-40, PPG Industries); sodium decyl diphenyl ether disulphonate (Poly-Tergent 3B2, Olin Corp.); alkyl diphenyl ether disulphonate sodium salt (Poly-Tergent 4C3, Olin Corp.); and sodium dodecyl diphenyloxide disulphonate (Sandoz Sulfonate 2A1,
Sandoz Chemicals Corp.).
In addition to the foregoing three ingredients, the compositions of the present invention may also include one or more nonionic surfactants to help solubilize the iodine. Suitable surfactants include fatty alcohol alkoxylates, for example, ethoxylated and propoxylated linear fatty alcohols such as Olin Corp.'s
SL series surfactants and Plurafac-D25 by BASF, linear primary alcohol. ethoxylStef such as Shell Chemical's Neodols, secondary alcohol ethoxylates such as Union Carbide's Tergit. bl 15-S series, ethylene oxide/propylene oxidt-block copolymers such as BASF's Pluronics and
Tetronics, and alkylphenol ethoxylates such as Union Carbide's Tergitol NP series and Triton X and N series.
The compositions of this invention include disinfectant/detergent compositions which comprise a sufficient amount of an iodophor to provide, under conditions of use, from about 15 to about 30 ppm of available iodine. By"available iod'ney is meant the amount of I2 which is available to function as a disinfectant agent. This amount will, of course, vary according to the particular iodophor used in the composition, and also according to the amounts of the other ingredients present in the composition. The appropriate level of iodophor to use can be easily determined by persons skilled in the art. It has been found that, in order to produce hospital strength disinfection comparable to what would ordinarily be provided by an aqueous solution of an iodophor--i. e., about 75 ppm--this invention requires that the iodophor be present in sufficient amount to yield only approximately 25 ppm of available iodine. If disinfection at a level somewhat lower than hospital strength is all that is necessary for desired use, an iodine availability level of 15 ppm can be sufficient.
In ready-to-use disinfectant/detergent compositions of this invention, the amounts of organic acid and anionic detergent should desirably be from about 300 to about 700 ppm, preferably from 400 to 600 ppm.
With a iodine availability of 25 ppm, suitable levels o. f organic acid and anionic detergent are each about 500 ppm.
Although the invention includes ready-to-use aqueous compositions of the type described above, it will in most cases be more convenient to supply the disinfectant/detergent composition in concentrated form, for example in a concentration which, on 1: 100 dilution in water, would yield the above-described ready-to-use compositions. Alternatively, where a user is likely to be satisfied with a lower level of disinfection, concentrated solutions can be provided with directions for use which would yield different levels of disinfective activity.
A further reason for formulating the compositions of this invention as dilutable concentrates is that, in concentrated form, the iodine is more stable.
This invention will be better understood by reference to the following examples, which are included here for purposes of illustration and are not intended to be limitations.
Example1 Procedure for Potentiometri Titration of Available
Iodine
This method is intended to give an accurate titration by using a potentiometer and graphing the millivolt readings to obtain a potential curve. The curve in turn is used to find the end point of the titration and the milliliters of titrant.
Equipment:Beckman zeromatic pH meter or equivalent, burette and magnetic stirrer.
Reagents : 0.025 N Na2S203, 99% Acetic Acid, 2% starch indicator solution (potato starch) and KI crystals.
Procedure: Set up of Beckman meter-remove reference electrode and plug in platinum electrode.
Press button marked + 700. millivolts. Press read button when you have the electrodes in the sample.
Weigh approximately 0.3 grams of concentrated
Iodofor or equivalent amount in formulation to the nearest milligram. Dissolve the sample in 200 ml of distilled water, put on stirrer and immerse the electrodes, then press READ button on pH meter. Add 1 ml of acetic acid, 1 ml of starch indicator and sprinkle KI crystals until the millivolt reading is approximately80mv. Begin titrating and plot the points on linear graph paper. Continue till there is a sharp change in potential, then do two more points to be sure this is the . end point. For very low concentrations, use 0.001 N Na2S2 3- Calculations k available 12 = ml of titrant x N of titrant x 12.692
wt. of sample
Example 2
A concentrated iodophor-containing detergent/ disinfectant composition was prepared having the following ingredients, in their indicated percentages by weight
Table I
%
Poly-Tergent Sol-62 3. 00
Poly-Tergent 2A1 (45%) 11. 12
Clean Front Concentrate 1.25
Deionized Water 79.63
Citric Acid 5.00
This formulation was diluted 1 part to 100 with' tap water and tested against Staphylococcus aureus,
Salmonella cholerasuis and Pseudomonas aeruqinosa in the
AOAC use dilution test specified by the United States
Environmental Protection Agency. In this test, the bacteria in question are dried on a surface, then subjected to the test liquid at the specified dilution.
The bacteria are then incubated in a nutrient bath. To pass the test, only one in 60 samples of bacteria is allowed to grow when put into the nutrient broth. If the formula is effective against all three organisms, it is considered a"hospital strength disinfectant". The formulation was tested twice and the results are as follows:
Table II Staph. Salmonella Pseud.
Test #1 1/60 0/60 0/60 Test #2 1/60 1/60 0/60
1 Poly (oxyethylene/oxypropylene) - (monohexyl/
monooctyl/monodecyl) ether; nonionic detergent, Olin
Corporation
2 Sodium dodecyldiphenyloxide disulphonate; anionic
detergent, Olin Corporation 3 a- (p-nonylphenyl)-U-hydroxypoly (oxyethylene)-iodine,
West Agro
These results indicate that this formula provides hospital strength disinfection with only 25 ppm available iodine instead of the recommended 75 ppm iodine. The iodine availability was measured according to the method of Example 1.
Example 3
A formulation similar to the composition of
Example 2 was prepared but with sodium dodecylbenzene sulfonate (Bio-Soft D-40, Stepan Co.) used as the anionic surfactant. Tests were-run against Staphylococcus aureus and Pseudomonas aeruginosa. The results are shown in the following Table III.
Table III
Staph. Pseud.
3/60 8/60
These data show that the formulation is essentially ineffective against the species tested and cannot be regarded as providing hospital strength disinfection.
Example 4
A formulation similar to the composition of
Example 2 was prepared except that the iodine level was adjusted downward to 0.72% at 1: 100 dilution. The tested solution had only 15 ppm of available iodine as measured by the method of Example 1. Testing, again done in accordance with the method of Example 2, showed effectiveness against the Staphylococcus and Salmonella species but unsatisfactory results against the
Pseudomonas species--Test #1. In a subsequent test-
Test #2--the dilution level was adjusted to 1: 64, thereby increasing the level of available iodine to 25 ppm, and the composition was tested against the
Pseudomonas species. In this case, the result was successful. The data are shown in the attached Table IV:
Table IV
Staph. Salmonella Pseud.
Test #1 1/60 0/60 4/60
Test #2 1/60
Claims (12)
- Claims: 1. A concentrated aqueous iodine-releasing disinfectant solution which, on dilution with water, yields from 15 to 30 ppm of available iodine, said solution comprising (a) an iodophor, (b) a disinfectant active organic acid in sufficient amount to provide from 300 to 700 ppm of said acid, and (c) an anionic alkyl diphenyl ether disulphonate surfactant in sufficient amount to provide from 300 to 700 ppm of said surfactant.
- 2. A disinfectant solution according to Claim 1 which, on dilution with water, yields from 15 to 25 ppm of available iodine, in which the organic acid is present in sufficient amount to provide from 400 to 600 ppm of said acid, and in which the surfactant is present in sufficient amount to provide from 400 to 600 ppm of said surfactant.
- 3. A disinfectant solution according to Claims 1 or 2 in which, on dilution with water, the available iodine is about 25 ppm, the organic acid is present in sufficient amount to provide about 500 ppm of said acid and the surfactant is present in sufficient amount to provide about 500 ppm of said surfactant.
- 4. A disinfectant solution according to any of claims 1-3 in which the acid is citric acid.
- 5. A disinfectant solution according to any of claims 1-4 in which the surfactant is an alkyl diphenyloxide disulphonate.
- 6. A disinfectant solution according to Claim 5 in which the surfactant is Sodium dodecyldiphenyloxide disulphonate.
- 7. A disinfectant solution according to any of claims 1-6 in whCh the pH is below 6.0.
- 8. A disinfectant solution according to Claim 7 in which the pH ranges from 2.0 to 5.0.
- 9. An aqueous iodine-releasing disinfectant composition which comprises (a) a nonionic iodophor in sufficient amount to provide the composition with from 15 to 30 ppm of available iodine, (b) 300 to 700 ppm of a disinfectant active organic acid, and (c) 300 to 700 ppm of an anionic diphenyl # disulphonate surfactant.
- 10. A composition according to Claim 9 in which the acid is citric acid.
- 11. A composition according to Claims 8 or 9 in which the surfactant is an alkyldiphenyloxide disulphonate.
- 12. A composition according to Claim 11 in which the surfactant is sodium dodecyldiphenyloxide disulphonate.
Priority Applications (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9828519A GB2344997A (en) | 1998-12-24 | 1998-12-24 | Iodine-releasing disinfectant solution |
AU18673/00A AU1867300A (en) | 1998-12-24 | 1999-12-17 | An aqueous iodine containing disinfectant composition |
PCT/GB1999/004205 WO2000038525A1 (en) | 1998-12-24 | 1999-12-17 | An aqueous iodine containing disinfectant composition |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB9828519A GB2344997A (en) | 1998-12-24 | 1998-12-24 | Iodine-releasing disinfectant solution |
Publications (2)
Publication Number | Publication Date |
---|---|
GB9828519D0 GB9828519D0 (en) | 1999-02-17 |
GB2344997A true GB2344997A (en) | 2000-06-28 |
Family
ID=10844950
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB9828519A Withdrawn GB2344997A (en) | 1998-12-24 | 1998-12-24 | Iodine-releasing disinfectant solution |
Country Status (3)
Country | Link |
---|---|
AU (1) | AU1867300A (en) |
GB (1) | GB2344997A (en) |
WO (1) | WO2000038525A1 (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003061389A1 (en) * | 2002-01-16 | 2003-07-31 | 3M Innovative Properties Company | Antiseptic compositions and methods |
US6838078B2 (en) | 2002-01-16 | 2005-01-04 | 3M Innovative Properties Company | Film-forming compositions and methods |
WO2008045135A3 (en) * | 2006-10-11 | 2008-07-03 | Biolargo Life Technologies Inc | Systems providing antimicrobial activity to an environment |
US8021610B2 (en) | 2006-09-07 | 2011-09-20 | Biolargo Life Technologies, Inc. | Systems providing antimicrobial activity to an environment |
US9414601B2 (en) | 2006-09-07 | 2016-08-16 | Biolargo Life Technologies, Incorporated | Material having antimicrobial activity when wet |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2017204727A1 (en) * | 2016-05-27 | 2017-11-30 | Delaval Holding Ab | Teat dip with residual efficacy |
Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4867897A (en) * | 1987-08-03 | 1989-09-19 | Mdt Corporation | Germicidal iodophor composition |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3274116A (en) * | 1963-08-05 | 1966-09-20 | Dow Chemical Co | Iodine detergent solution |
US3650966A (en) * | 1969-08-20 | 1972-03-21 | Economics Lab | Iodine detergent composition |
JPH072646B2 (en) * | 1987-12-10 | 1995-01-18 | 明治製菓株式会社 | Disinfectant composition |
-
1998
- 1998-12-24 GB GB9828519A patent/GB2344997A/en not_active Withdrawn
-
1999
- 1999-12-17 AU AU18673/00A patent/AU1867300A/en not_active Abandoned
- 1999-12-17 WO PCT/GB1999/004205 patent/WO2000038525A1/en active Application Filing
Patent Citations (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4867897A (en) * | 1987-08-03 | 1989-09-19 | Mdt Corporation | Germicidal iodophor composition |
Cited By (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2003061389A1 (en) * | 2002-01-16 | 2003-07-31 | 3M Innovative Properties Company | Antiseptic compositions and methods |
US6838078B2 (en) | 2002-01-16 | 2005-01-04 | 3M Innovative Properties Company | Film-forming compositions and methods |
AU2002367455B2 (en) * | 2002-01-16 | 2006-07-27 | 3M Innovative Properties Company | Antiseptic compositions and methods |
US7323163B2 (en) | 2002-01-16 | 2008-01-29 | 3M Innovative Properties Company | Film-forming compositions and methods |
EP1955594A1 (en) * | 2002-01-16 | 2008-08-13 | 3M Innovative Properties Company | Antiseptic compositions and methods |
US8840932B2 (en) | 2002-01-16 | 2014-09-23 | 3M Innovative Properties Company | Antiseptic compositions and methods |
US9277750B2 (en) | 2002-01-16 | 2016-03-08 | 3M Innovative Properties Company | Antiseptic compositions and methods |
EP3064065A1 (en) * | 2002-01-16 | 2016-09-07 | 3M Innovative Properties Company | Antiseptic compositions and methods |
US8021610B2 (en) | 2006-09-07 | 2011-09-20 | Biolargo Life Technologies, Inc. | Systems providing antimicrobial activity to an environment |
US9414601B2 (en) | 2006-09-07 | 2016-08-16 | Biolargo Life Technologies, Incorporated | Material having antimicrobial activity when wet |
WO2008045135A3 (en) * | 2006-10-11 | 2008-07-03 | Biolargo Life Technologies Inc | Systems providing antimicrobial activity to an environment |
Also Published As
Publication number | Publication date |
---|---|
AU1867300A (en) | 2000-07-31 |
WO2000038525A1 (en) | 2000-07-06 |
GB9828519D0 (en) | 1999-02-17 |
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Legal Events
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