WO2000001793A1 - A new improved enzyme containing granule - Google Patents
A new improved enzyme containing granule Download PDFInfo
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- WO2000001793A1 WO2000001793A1 PCT/DK1999/000364 DK9900364W WO0001793A1 WO 2000001793 A1 WO2000001793 A1 WO 2000001793A1 DK 9900364 W DK9900364 W DK 9900364W WO 0001793 A1 WO0001793 A1 WO 0001793A1
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- enzyme
- coating
- granule
- granule according
- enzyme containing
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/02—Enzymes or microbial cells immobilised on or in an organic carrier
- C12N11/04—Enzymes or microbial cells immobilised on or in an organic carrier entrapped within the carrier, e.g. gel or hollow fibres
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/16—Organic compounds
- C11D3/38—Products with no well-defined composition, e.g. natural products
- C11D3/386—Preparations containing enzymes, e.g. protease or amylase
- C11D3/38672—Granulated or coated enzymes
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- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/10—Salts
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D7/00—Compositions of detergents based essentially on non-surface-active compounds
- C11D7/02—Inorganic compounds
- C11D7/04—Water-soluble compounds
- C11D7/10—Salts
- C11D7/16—Phosphates including polyphosphates
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N11/00—Carrier-bound or immobilised enzymes; Carrier-bound or immobilised microbial cells; Preparation thereof
- C12N11/14—Enzymes or microbial cells immobilised on or in an inorganic carrier
-
- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/96—Stabilising an enzyme by forming an adduct or a composition; Forming enzyme conjugates
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12N—MICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
- C12N9/00—Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
- C12N9/98—Preparation of granular or free-flowing enzyme compositions
-
- C—CHEMISTRY; METALLURGY
- C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
- C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
- C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
- C11D3/39—Organic or inorganic per-compounds
Definitions
- the high humidity constant coating will inhibit moisture from entering the granule at a broader ranger of humidity conditions (% RH) of the surrounding matrix.
- % RH a ranger of humidity conditions
- the rate of moisture absorption, and thus the damaging affects on the enzyme is believed to be further increased if the core material also readily absorbs the incoming moisture, which is the case for many known core materials.
- the moisture absorption process may thus be accelerated by swelling or expansion of the core materials forming cracks, holes or disruptions in the coating, thus making moisture access to the enzyme in the core even easier.
- Choosing a coating with a constant humidity value higher than the expected % RH of the surrounding air thus effectively reduces this process.
- a coating with a high constant humidity value is believed to inhibit entry of microorganisms thus reducing the possibility of microbial growth within the granule.
- a water soluble compound benefits release and/or dissolution of the enzyme upon introduction of the granule in an aqueous medium (e.g. a cleaning or washing liquor) much more than insoluble salts such as calcium carbonate and minerals or inorganic compounds such as kaolin and/or titandioxide .
- a preferred water soluble compound is an inorganic salt, e.g. salts of sulfate, sulfite, phosphate, phosphonate, nitrate, chloride or carbonate or salts of simple organic acids (less than 10 carbon atoms e.g. 6 or less carbon atoms) such as citrate, malonate or acetate.
- Sodium sulfate and sodium citrate are the most preferred water soluble compounds as they are cheap chemicals .
- the coating comprises as said at least 60% w/w, e.g. 65% w/w or 70% w/w of the water soluble compound, which preferably may be at least 75% w/w, e.g. at least 80% w/w, at least 85% w/w, e.g.
- the coating may even essentially consist of the water soluble compound.
- minor amounts of other feasible compounds may be present in the coating such as conventional coating materials. Examples of are, inter alia, described in the paragraph "additional coatings" given below.
- the coating should encapsulate the enzyme containing core by forming a substantially continuous layer.
- the layer or coating is preferably homogenous in thickness and by substantially continuous is meant that the core surface should have few or none uncoated areas .
- the core contains the enzyme (s) .
- the core may be constructed in any way or of any material which provides the desired functional properties of the core material, e.g. the core may consist of materials which allows readily release of the enzyme (s) upon introduction to an aqueous medium.
- the core is constructed of a particulate carrier (I) with the enzyme absorbed and/or an enzyme containing layer (II) applied on the carrier surface, optionally comprising an enzyme protecting reducing agent. There may even be additional coating within the core material providing desired functional properties of the core material.
- Another preferred core is the so called T-granulate wherein enzyme and granulation material is mixed to form granules incorporating the enzyme distributed throughout the core such as described in US 4,106,991 e.g. Example 1. Any conventional methods and non-enzyme materials may be used to prepare the core.
- the core may through the coating absorb moisture from the surrounding environment, a process which may cause the core to swell resulting in crack formation in the coating and further moisture absorbance .
- the core may even in at high relative humidity dissolve and become fluid.
- the core should preferably be a non absorbing core, i.e. the should only be able of absorbing less moisture than 20% w/w of it own dry weight, preferably less than 10% w/w, e.g. less than 8% w/w or less than 5% w/w, measured at 75% RH at 20°C.
- Preferred oxidoreductases in the context of the invention are peroxidases (EC 1.11.1), laccases (EC 1.10.3.2) and glucose oxidases (EC 1.1.3.4)], while preferred transferases are transferases in any of the following sub-classes:
- a most preferred type of transferase in the context of the 35 invention is a transglutaminase (protein-glutamine ⁇ - glutamyltransferase; EC 2.3.2.13).
- oxidoreductases examples include GluzymeTM (enzyme available from Novo Nordisk A/S) . Further oxidoreductases are available from other suppliers .
- proteases examples include EsperaseTM, AlcalaseTM, NeutraseTM, DurazymTM, SavinaseTM, Kannase, PyraseTM, Pancreatic Trypsin NOVO (PTN) , Bio-FeedTM Pro and Clear-LensTM Pro (all available from Novo Nordisk A/S, Bagsvaerd, Denmark) .
- lipases examples include LipolaseTM, LipolaseTM Ultra, LipoPrime, LipozymeTM, PalataseTM, NovozymTM 435 and LecitaseTM (all available from Novo Nordisk A/S) .
- Other commercially available lipases include LumafastTM
- LipomaxTM Ps . pseudoalcaligenes lipase from Gist- brocades/Genencor Int. Inc.; and Bacillus sp . lipase from Solvay enzymes. Further lipases are available from other suppliers.
- carbohydrases examples include Alpha-GalTM, Bio-FeedTM Alpha, Bio-FeedTM Beta, Bio-FeedTM Plus Bio-FeedTM Plus, NovozymeTM 188, CelluclastTM, CellusoftTM CeremylTM, CitrozymTM, DenimaxTM, DezymeTM, DextrozymeTM FinizymTM, FungamylTM, GamanaseTM, GlucanexTM, LactozymTM MaltogenaseTM, PentopanTM, PectinexTM, PromozymeTM, PulpzymeTM NovamylTM, TermamylTM, AMGTM (Amyloglucosidase Novo) MaltogenaseTM, SweetzymeTM and AquazymTM (all available from Novo Nordisk A/S) . Further carbohydrases are available from other suppliers . The amount of enzyme to be incorporated in a granule of the invention will depend on the intended use of the granulate. For many applications, the
- the content of enzyme (calculated as pure enzyme protein) in a granule of the invention will typically be in the range of from about 0.5% to 20% by weight of the core.
- the granules of the present invention may comprise one, two or more additional coating layers on the inside or outside surface of the protective coating according to the invention.
- the additional coating layers may perform any of a number of functions in the granule, depending on the intended use of the granule.
- an additional coating may achieve one or more of the following effects:
- Suitable pigments include, but are not limited to, finely divided whiteners, such as titanium dioxide or kaolin, coloured pigments, water soluble colorants, as well as combinations of one or more pigments and water soluble colorants.
- Lubricants can also play a related role in improving the coating process, by reducing the tackiness of binders in the coating.
- a lubricant is applied as additional coating.
- the composition of 1) an enzyme containing core, 2) a coating and 3) and an additional lubricant coating has shown particularly good properties with respect to enzyme stability.
- the invention also relates to a method for manufacture/production of the enzyme containing granule described herein.
- Conventional coating methods may be used to apply the coating according to the invention as described by the references stated in the previous section (above) .
- a method for production of the enzyme containing granule may comprise the following steps: a) mixing an enzyme containing core material with a liquid medium comprising the water soluble compound of the invention and, b) removing volatile components of the liquid medium from the mixture, so as to deposit the nonvolatile components of the liquid medium as solid coating layer on the core material.
- the enzyme containing granule is produced by a fluid bed process comprising : a) fluidising an enzyme containing core material in a fluid bed apparatus , b) introducing a liquid medium comprising the water soluble compound of the invention by atomization of the liquid medium into the fluid bed, so as to deposit nonvolatile components of the liquid medium as a solid coating layer on the core material and, c) removing volatile components of the liquid medium from the coated core material .
- additional enzyme may be absorbed on the particulate carrier prior to applying the enzyme layer (II)
- This absorption may be achieved by: a) absorbing the enzyme (s) into the surface of the carrier by contacting the particulate carrier with a liquid comprising the enzyme in a mixer, b) mixing the composition by means of mixing blades, and c) drying the enzyme loaded carrier by fluidising it in a fluid bed apparatus,
- the mixing equipment can satisfactorily be used to mix the particulate carrier with the enzyme-containing liquid medium.
- the mixing equipment can be a batch mixer or a continuous mixer, such as a convective mixer [see, e.g., Harnby et al., Mixing in the Process Industries, pp. 39-53 (ISBN 0-408- 11574-2)].
- Non-convective mixing equipment e.g. rotating drum mixers or so-called pan-granulators, may also be employed.
- Drying of enzyme-loaded particulate carrier, application of the enzyme containing layer (II) the coating (III) and any additional coatings may be performed in any type of fluidising equipment (such as in a fluid-bed apparatus or other form of fluidizing equipment, such as a H ⁇ ttlin-type fluidizer) .
- suitable fluid-bed equipment see, e.g., Harnby et al . , Mixing in the Process Industries, pp. 54-77 (ISBN 0-408- 11574-2) .
- the enzyme containing granule according to the invention is useful where ever enzymes are to be stored alone or to be incorporated in another dry product, and an improved enzyme stability is needed to enable good storage properties (improved shelf life) of the granule.
- relatively humid conditions i.e. under an atmosphere with a % RH of more than 55% RH, preferably more than 60% RH, e.g. more than 70% RH.
- oxidative compounds such as peroxides or superoxides, e.g. bleach (e.g.
- a detergent composition of the invention comprises the enzyme containing granule of the invention and a surfactant. Additionally, it may optionally comprise a builder, another enzyme, a suds suppresser, a softening agent, a dye-transfer inhibiting agent and other components conventionally used in detergents such as soil -suspending agents, soil-releasing agents, optical brighteners, abrasives, bactericides, tarnish inhibitors, coloring agents, and/or encapsulated or non- encapsulated perfumes.
- the surfactant system may comprise nonionic, anionic, cationic, ampholytic, and/or zwitterionic surfactants.
- the surfactant system preferably consists of anionic surfactant or a combination of anionic and nonionic surfactant, e.g. 50-100% of anionic surfactant and 0-50% nonionic.
- the laundry detergent compositions may also contain cationic, ampholytic, zwitterionic, and semi -polar surfactants, as well as the nonionic and/or anionic surfactants other than those already described herein.
- the surfactant may comprise polyalkylene oxide (e.g. polyethylene oxide) condensates of alkyl phenols.
- the alkyl group may contain from about 6 to about 14 carbon atoms, in a straight chain or branched-chain.
- the ethylene oxide may be present in an amount equal to from about 2 to about 25 moles per mole of alkyl phenol .
- the surfactant may also comprise condensation products of primary and secondary aliphatic alcohols with about 1 to about 25 moles of ethylene oxide.
- the alkyl chain of the aliphatic alcohol can either be straight or branched, and generally contains from about 8 to about 22 carbon atoms.
- Suitable anionic surfactants include the alkyl sulfate surfactants which are water soluble salts or acids of the formula ROS03M wherein R preferably is a C10-C24 hydrocarbyl , preferably an alkyl or hydroxyalkyl having a C10-C20 alkyl component, more preferably a C12-C18 alkyl or hydroxyalkyl, and M is H or a cation, e.g., an alkali metal cation (e.g. sodium, potassium, lithium) , or ammonium or substituted ammonium.
- R preferably is a C10-C24 hydrocarbyl , preferably an alkyl or hydroxyalkyl having a C10-C20 alkyl component, more preferably a C12-C18 alkyl or hydroxyalkyl
- M is H or a cation, e.g., an alkali metal cation (e.g. sodium, potassium, lithium) , or ammoni
- Alkylbenzene sulfonates are suitacble, especially linear (straight-chain) alkyl benzene sulfonates (LAS) wherein the alkyl group preferably contains from 10 to 18 carbon atoms.
- the laundry detergent compositions typically comprise from about 1% to about 40%, preferably from about 3% to about 20% by weight of such anionic surfactants.
- compositions according to the present invention may further comprise a builder system.
- a builder system Any conventional builder system is suitable for use herein including aluminosilicate materials, silicates, polycarboxylates and fatty acids, materials such as ethylenediamine tetraacetate (EDTA) , metal ion sequestrants such as aminopolyphosphonates .
- Phosphate builders can also be used herein.
- Suitable builders can be an inorganic ion exchange material, commonly an inorganic hydrated aluminosilicate material, more particularly a hydrated synthetic zeolite such as hydrated zeolite A, X, B, HS or MAP.
- Detergency builder salts are normally included in amounts of from 5% to 80% by weight of the composition. Preferred levels of builder for liquid detergents are from 5% to 30%.
- the detergent composition may also comprise a bleaching agents, e.g. an oxygen bleach or a halogen bleach.
- the oxygen bleach may be a hydrogen peroxide releasing agent such as a perborate (e.g. PB1 or PB4) or a percarbonate, or it may e.g. be a percarboxylic acid.
- the particle size of a bleaching agent may be 400-800 microns. When present, oxygen bleaching compounds will typically be present at levels of from about 1% to about 25%.
- the hydrogen peroxide releasing agent can be used in combination with bleach activators such as tetra- acetylethylenediamine (TAED) , nonanoyloxybenzene-sulfonate
- NOBS 5-trimethyl-hexsanoloxybenzene-sulfonate
- PAG pentaacetylglucose
- the halogen bleach may be, e.g. a hypohalite bleaching agent, for example, trichloro-isocyanuric acid and the sodium and potassium salt of dichloroisocyanurates and N-chloro and N- bromo alkane sulfonamides .
- a hypohalite bleaching agent for example, trichloro-isocyanuric acid and the sodium and potassium salt of dichloroisocyanurates and N-chloro and N- bromo alkane sulfonamides .
- Such materials are normally added at 0.5-10% by weight of the finished product, preferably 1-5% by weight .
- compositions of the invention may for example, be formulated as hand and machine laundry detergent compositions including laundry additive compositions and compositions suitable for use in the pretreatment of stained fabrics, rinse added fabric softener compositions, and compositions for use in general household hard surface cleaning operations and dishwashing operations.
- the enzyme containing granules of the invention may be incorporated in the detergent compositions described in WO 97/04079, WO 97/07202, WO 97/41212, and PCT/DK 97/00345.
- carrier material Portions of carrier material was prepared by spraying 3.0 kg of fibrous cellulose (ArbocelTM FTC200) , 3.0 kg of kaolin (SpeswhiteTM, English China Clay) and 20.5 kg of finely ground sodium sulfate with 9.5 kg of a 21% w/w aqueous solution of carbohydrate binder (GlucidexTM 21D, from Roquette Freres) .
- This mixtures was granulated and dried as described in Example 1 in US 4,106,991.
- the dry granulated carrier material was sieved, and the fraction between 0.3 and 1.0 mm was separated and used for further processing.
- the granulated and fractionated carrier material was transferred to a L ⁇ diger mixer equipped with a multiple chopper head, and sprayed with a liquid SavinaseTM enzyme concentrate solution approximately 33 KNPU/g containing 0.4% w/w g of a nonionic surfactant (Softanol 50) .
- the enzyme containing solution was sprayet onto the carrier at dosage of 0.15 kg solution per kg carrier material .
- the nonionic surfactant was added to the enzyme concentrate to enhance the absorption of the enzyme onto the carrier.
- the SavinaseTM concentrate was applied using a pressure nozzle submerged in the carrier and spraying directly into the chopper.
- the carrier and the SavinaseTM concentrate was mixed by means of mixing blades and the mixing blades and the chopper were operated continuously during the spraying.
- the resulting product was transferred to a Glatt WSG 15 fluid-bed apparatus (Glatt, Germany) with an air- inlet temperature of 62°C, and dried for 30 minutes, or until the product temperature exceeded 50°C, and then sieved on a 1.2 mm mesh screen, leaving only 0.8% w/w of residual, oversized particles on the sieve.
- the enzyme assay used herein is a protease activity assay, and the unit for protease activity herein is Kilo Novo Protease Units per gram of sample (KNPU/g) .
- the activity is determined relatively to an enzyme standard (SavinaseTM) of known activity.
- SavinaseTM enzyme standard
- the enzyme standard is standardized by measuring for a given amount of enzyme the formation rate ( ⁇ mol/minute) of free amino groups liberated from digestion of di-methyl -casein (DMC) in solution by the enzyme.
- the formation rate is monitored by recording the linear development of absorbance at 420 nm of the simultaneous reaction between the formed free amino groups and added 2 , 4 , 6-tri-nitro-benzene- sulfonic acid (TNBS) .
- alfa-amylase activity e.g. Natalase ®
- any conventional alfa-amylase assay may be used (such as the method described in AF318/1-GB available upon request from Novo Nordisk A/S - Denmark) .
- Alfa-amylases cleaves 1-6 alfa bonds between adjacent glucose units.
- the substrae may be completely digested into monosaccharides and 2-chlor-4-nitrophenol , which form a detectable colour. Kits for performing these assays are commercially available.
- the constant humidity of water soluble compound coating materials were measured by preparing a saturated aqueous solution with excess of solid phase of the compound in an open beaker. After equilibrium has been reached and no more of the compound dissolves in the liquid phase, and solid particles of the compound are still visible, the beaker is placed in a sealed thermostated humidity measuring device (e.g. a Novasina apparatus) , which measures the % RH at the chosen temperature of the atmosphere over the saturated solution.
- a sealed thermostated humidity measuring device e.g. a Novasina apparatus
- a sample of the dry enzyme-loaded granular carrier was transferred to a Glatt WSG5 conventional fluid bed apparatus.
- a conventional top spray coating technique with an air inlet temperature of 70 °C, air outlet temperature of 42 °C and with air volume of 600 m3/h the following steps were carried out in sequence :
- an enzyme containing layer was applied onto the carrier by spraying an enzyme containing aqueous solution containing SavinaseTM, PVP/VA co-polymer (Luviscol VA64) and titaniumdioxide
- an additional coating layer of 50 g titaniumdioxide (Kronos 5 2044) , 50 g kaolin (ECC Supreme) , 55 g Glascol LS27 (46% suspension from Allied Colloids Ltd.- GB) , 30 g PEG 4000 and 1.67 g Softanol 50 per kg carrier was applied by spraying an aqueous solution of these components onto the product of b) , at a spraying rate for the coating solution of 100 g/min, and 0 d) a final coating was applied by spraying a solution of 7.5 g PEG 4000 per kg carrier onto the product of c) , at a spraying rate for the coating solution of 100 g/min.
- the finished enzyme containing granule was dried for 5 minutes and then cooled to 30°C, where after it was removed from the fluid bed and sifted between 300 and 1200 ⁇ m
- the first type of granule was prepared by repeating 0 steps a) -d) with the exception that the coating described in b) was replaced by a 80 g ammonium sulfate per kg carrier coating layer by spraying a 37% w/w aqueous solution of ammonium sulfate onto the product of a) , at a spraying rate for the coating solution of 100 g/min.
- the second type of granule was also 5 prepared by repeating steps a) -d) , but with the exception that the coating described in b) was replaced by a 80 g sodium formiate per kg carrier coating layer by spraying a 37% w/w aqueous solution of sodium formiate onto the product of a) , at a spraying rate for the coating solution of 100 g/min. 0
- the storage stability of the enzyme containing granulates from Example 1 were tested in one powder detergent (A) containing perborate bleach and TAED and one powder detergent 5 (B) containing percarbonate bleach. 100 mg samples of the enzyme containing granulates and 10.0 g samples of the detergents were mixed to constitute test samples. The samples were incubated in open jars at air conditions 35°C and 55% RH in a thermostated and humidity controlled cupboard. Identical samples were taken out from the cupboard after 2 and 4 weeks and analyzed for enzyme (SavinaseTM) activity together with identical reference samples, which had been stored in sealed jars below -18 °C. The results are given in Example 1, wherein the enzyme activities of the samples are given as a percentage of the corresponding reference samples.
- Example 2 The hygroscopicity of the samples from Example 1 were tested including a reference sample which was identical to the granulates of Examples 1 to 3 except that it did not contain any salt coating of ammonium sulfate, sodium citrate or sodium formiate. All samples were incubated for 1 week in open jars at 3 different conditions: 55% RH and 35°C, 60% RH and 30°C and 74% RH and 37°C. Subsequently the water absorption of the samples were determined by weighing the samples before and after the incubation. Further after the incubation the samples were examined under a microscope. The results are given in Table 2, which shows the water absorption of the samples at different humidities.
- Table 2 further lists the results of the microscope examination, which showed that the coating of some of the samples were damaged (cracks had developed) which was most clearly observed when the water absorption of the coating (absorption of the sample minus the absorption of the reference) had reached a level of approximately 50% of the salt layer weight (which constitutes 6% of total formula) .
- An enzyme containing granule was produced as in Example 4 with the exception that the coating of pure sodium citrate was replaced by a mixture of sodium citrate and sodium thiosulfate in the weight ratio 9:1. Thus a coating consisting of 72 g sodium citrate and 8 g thiosulfate per kg carrier was applied.
- a comparative base granulate was prepared as described in
- Example 16 This example was prepared as Example 16 with the exception that the solution for the coating (b) was reduced to 7.35 kg.
- This example was produced according to Example 16 step (a) , i.e. without the salt coating and the dust suppressing film.
- the granulate was conventionally coated as described in US 106,991 Example 22 by applying a solution of 7.2% w/w PEG 4000 and 13,0% w/w of a 1:1 mixture of Ti02 and kaolin.
- the enzyme concentrate was an aqueous suspension of crystalline enzyme which was also used as the granulating liquid containing also a binder (Glucidex) .
- the granulate had furthermore an addition of 0.4% w/w sodium thiosulfate (calculated as % of the uncoated granulate) .
- the granulate was conventionally coated as described in US 106,991 Example 22 by applying a solution of 7% of PEG 4000 and 12.5% of a 1:1 mixture of Ti02 and kaolin.
- Example 25 A Natalase ® containing granulate was produced as described in Example 24. 1300 g of the Natalase containing base granulate was transferred to a UniGlatt fluid bed where coated with a salt coating by spraying it with a 50°C salt solution at consisting of:
- the non-coated granules was coated with a salt layer using a fluid bed according to the following procedure:
- Example 28 The enzyme stability in the granules were tested in a model powder detergent containing Sodium Perborate at 35°C and 55% relative humidity in open boxes according to Example 9.
- the % salt was calculated as % w/w salt of the uncoated granules under the condition that all water was evaporated. From Example 10 it was concluded that the enzyme stability in the Savinase ® granules were significantly improved by the salt coating and that increasing the amount of salt improves the stability.
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Abstract
Description
Claims
Priority Applications (6)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP99927738A EP1092007B1 (en) | 1998-06-30 | 1999-06-28 | A new improved enzyme containing granule |
AT99927738T ATE255158T1 (en) | 1998-06-30 | 1999-06-28 | NEW, IMPROVED ENZYME CONTAINING GRANULES |
DE69913146T DE69913146T2 (en) | 1998-06-30 | 1999-06-28 | New, improved, enzyme-containing granules |
JP2000558184A JP2002519052A (en) | 1998-06-30 | 1999-06-28 | New and improved enzyme-containing particles |
DK99927738T DK1092007T3 (en) | 1998-06-30 | 1999-06-28 | New improved enzyme-containing granule |
AU44992/99A AU4499299A (en) | 1998-06-30 | 1999-06-28 | A new improved enzyme containing granule |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DKPA199800876 | 1998-06-30 | ||
DKPA199800876 | 1998-06-30 |
Publications (1)
Publication Number | Publication Date |
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WO2000001793A1 true WO2000001793A1 (en) | 2000-01-13 |
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Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/DK1999/000364 WO2000001793A1 (en) | 1998-06-30 | 1999-06-28 | A new improved enzyme containing granule |
Country Status (9)
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EP (1) | EP1092007B1 (en) |
JP (1) | JP2002519052A (en) |
CN (1) | CN1192087C (en) |
AT (1) | ATE255158T1 (en) |
AU (1) | AU4499299A (en) |
DE (1) | DE69913146T2 (en) |
DK (1) | DK1092007T3 (en) |
ES (1) | ES2212568T3 (en) |
WO (1) | WO2000001793A1 (en) |
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Also Published As
Publication number | Publication date |
---|---|
EP1092007B1 (en) | 2003-11-26 |
DE69913146D1 (en) | 2004-01-08 |
EP1092007A1 (en) | 2001-04-18 |
AU4499299A (en) | 2000-01-24 |
ATE255158T1 (en) | 2003-12-15 |
CN1312853A (en) | 2001-09-12 |
DK1092007T3 (en) | 2004-04-05 |
ES2212568T3 (en) | 2004-07-16 |
JP2002519052A (en) | 2002-07-02 |
CN1192087C (en) | 2005-03-09 |
DE69913146T2 (en) | 2004-09-16 |
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