EP1317533A1 - Durch eine schmierschicht charakterisiertes granulat - Google Patents

Durch eine schmierschicht charakterisiertes granulat

Info

Publication number
EP1317533A1
EP1317533A1 EP01964946A EP01964946A EP1317533A1 EP 1317533 A1 EP1317533 A1 EP 1317533A1 EP 01964946 A EP01964946 A EP 01964946A EP 01964946 A EP01964946 A EP 01964946A EP 1317533 A1 EP1317533 A1 EP 1317533A1
Authority
EP
European Patent Office
Prior art keywords
granule
lubricant
active
granules
enzyme
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
EP01964946A
Other languages
English (en)
French (fr)
Inventor
Ole Simonsen
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Novozymes AS
Original Assignee
Novozymes AS
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Novozymes AS filed Critical Novozymes AS
Publication of EP1317533A1 publication Critical patent/EP1317533A1/de
Ceased legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C12BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
    • C12NMICROORGANISMS OR ENZYMES; COMPOSITIONS THEREOF; PROPAGATING, PRESERVING, OR MAINTAINING MICROORGANISMS; MUTATION OR GENETIC ENGINEERING; CULTURE MEDIA
    • C12N9/00Enzymes; Proenzymes; Compositions thereof; Processes for preparing, activating, inhibiting, separating or purifying enzymes
    • C12N9/98Preparation of granular or free-flowing enzyme compositions
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/0039Coated compositions or coated components in the compositions, (micro)capsules
    • CCHEMISTRY; METALLURGY
    • C11ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11DDETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/16Organic compounds
    • C11D3/38Products with no well-defined composition, e.g. natural products
    • C11D3/386Preparations containing enzymes, e.g. protease or amylase
    • C11D3/38672Granulated or coated enzymes

Definitions

  • the present invention relates to a granule comprising an active component and an outer lubrication layer which inhibits forma- tion of dusting of active component from the granule.
  • Granules containing active components, such as enzymes have been used for decades in various industries. Several technologies have been developed to provide such granules.
  • One object of providing actives in the form of granules is to prevent or inhibit formation of active, because actives may cause health damage to persons handling the actives. Conventionally this has been achieved by providing active-containing granules comprising an active-containing core and various coating layers.
  • An active-containing granule typically consist of a core and a coating, where an important feature of the coating is to reduce the formation of dust when handling the granulate.
  • WO 96/16151 relates to enzyme granules coated with a non aqueous liquid or a unctuous mixture and an anti-caking agent WO 01/04279 and WO 00/01793 (unpublished at the date of priority) also disclose granules comprising a lubricant.
  • the present invention relates to an active- containing granule comprising a lubricant on the outer surface of the granule, characterized by (a) the lubricant is in liquid form at 25°C and has a viscosity of less than 5000 centipoise at 25°C or
  • the lubricated granules have a relative friction coefficient which is less than 80% when compared to unlubricated granules when measured by a rheometer by using a tip speed of 50 rpm, a helix angle of 3° (compaction mode) , using the 46 mm rotor and weighing 170 g granulate into a 50 mm testing container or
  • the lubricant is a mineral oil
  • the invention relates to a process for producing a granule of the invention, compositions comprising the granule of the invention and to use of the granule of the invention.
  • Granules containing actives, such as enzymes are dry particles which upon handling, are subjected to wear and tear (collision and friction) because individual granules collide with each other and cause "grinding" of the granule surface. This is believed to cause breakage of coating or even disintegration of the granule, where upon dry active, e.g. enzyme protein, may be liberated and form health damaging dust.
  • actives such as enzymes
  • lubricants as herein defined can serve as anti-agglomeration agents and wetting agents as well as reducing dust formation and granule breakage.
  • the active-containing granule of the invention suitably comprises an active-containing core and one or more coating layers as known in the art.
  • lubricant is to be understood as any non-aqueous compound or mixture of compounds, which forms a liquid at 25°C and atmospheric pressure. Preferably it has a viscosity of less than 5000 centipoise at these conditions.
  • the core of the core is the core of the core
  • the core contains the active (s), preferably 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 actives (s) upon introduction to an aqueous medium.
  • Preferred constructions of the core includes: Spray dried core particles, prepared by spray drying a liquid enzyme containing solution whereby small droplets of active-containing solution dry up to form an active-containing particulate material. Very small particles can be pro- prised this way (Michael S. Showell (editor); Powdered detergents; Surfactant Science Series; 1998; vol. 71; page 140- 142; Marcel Dekker) .
  • Layered core particles wherein an active is coated as a layer around a preformed core particle or adsorbed into the surface of the core particle. Particles of a desired size can be obtained this way if a useful core particle of the desired size can be found.
  • This type of product is described in e.g. WO 97/23606 and WO 97/39116 incorporated by refer- ence.
  • Extruded or pelletized core particles wherein an active- containing paste is pressed to pellets or under pressure is extruded through a small opening and cut into particles which is subsequently dried.
  • Such particles usually have a considerable size because of the material in which the extrusion opening is made (usually a plate with bore holes) sets a limit on the allowable pressure drop over the extrusion opening.
  • very high extrusion pressures when using a small opening increases heat generation in the active-containing paste which may be harmful to the active.
  • Prilled core particles wherein an active-containing powder is immobilised in a solidified wax matrix.
  • Prilled particles are usually prepared by suspending active powder in molten wax and spraying the suspension, e.g. through a rotating disk atomizer, into a cooling chamber where the droplets quickly solidify (Michael S. Showell (editor); Powdered detergents; Surfactant Science Series; 1998; vol. 71; page 140-142; Marcel Dekker) .
  • Mixer granulation particles prepared by adding active, liquid and a dry powder composition of granulating components.
  • the liquid and the powder in a suitable proportion is mixed and as the moisture of the liquid is absorbed in the dry powder, the components of the dry powder will start to adhere and agglomerate and particles will build up forming granules comprising the active.
  • Such a process is described in 4,106,991 (NOVO NORDISK) and related documents EP 170360 Bl (NOVO NORDISK), EP 304332 Bl (NOVO NORDISK), EP 304331 (NOVO NORDISK) , WO 90/09440 (NOVO NORDISK) and WO 90/09428 (NOVO NORDISK), all incorporated by reference.
  • the components of the core may be those known to the art including but not limited to:
  • the active may be any active component, which use benefits from being formulated into a granule.
  • Such actives may be a pharmaceutical
  • active is meant to encompass all components, which when released from the granule in application of the granule in a process, serves a purpose of improving the process. Suitable actives are those which are either subjects of deactiva- tion and/or causing deactivation to other components in the a composition comprising the granule.
  • the active may be inorganic of nature, such as bleach components, or organic.
  • Preferred actives are biologically active materials, such as catalytically active materials such as enzymes, pharmaceutical materials active in the human or ani- mal body or agricultural chemicals such as herbicides, pesticides, bactericides and/or fungicides. Such compounds are usually very sensitive to the surrounding environment and may suitably be obtained from chemical processes or from fermenting microorganisms. Most preferred actives are peptides or polypetides such as enzymes.
  • An enzyme in the context of the present invention may be any enzyme or combination of different enzymes, which benefits from being granulated in order to be applicable for a specific use. Accordingly, when reference is made to "an enzyme” this will in general be understood to include combinations of one or more enzymes .
  • enzyme variants are included within the meaning of the term "enzyme” .
  • examples of such enzyme variants are disclosed, e.g., in EP 251,446 (Genencor) , WO 91/00345 (Novo Nordisk) , EP 525,610 (Solvay) and WO 94/02618 (Gist-Brocades NV) .
  • oxidoreductases EC 1.-.-.-
  • transferases EC 2.-.-.-
  • hydrolases EC 3.-.-.-
  • lyases EC 4.-.-.-
  • isomerases EC 5.-.-.-
  • ligases EC 6.-.-.-
  • 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)]
  • preferred transferases are transferases in any of the following sub-classes:
  • a most preferred type of transferase in the context of the invention is a transglutaminase (protein-glutamine ⁇ - glutamyltransferase; EC 2.3.2.13).
  • transglutaminases are described in WO 96/06931 (Novo Nordisk A/S) .
  • Preferred hydrolases in the context of the invention are: Carboxylic ester hydrolases (EC 3.1.1.-) such as lipases (EC 3.1.1.3); phytases (EC 3.1.3.-), e.g. 3-phytases (EC 3.1.3.8) and 6-phytases (EC 3.1.3.26); glycosidases (EC 3.2, which fall within a group denoted herein as "carbohydrases”) , such as ⁇ - amylases (EC 3.2.1.1); peptidases (EC 3.4, also known as proteases) ; and other carbonyl hydrolases] .
  • Carboxylic ester hydrolases EC 3.1.1.-
  • lipases EC 3.1.1.3
  • phytases EC 3.1.3.-
  • 3-phytases EC 3.1.3.8
  • 6-phytases EC 3.1.3.26
  • glycosidases EC 3.2, which fall within a group denoted herein as "
  • carbohydrase is used to denote not only enzymes capable of breaking down carbohydrate chains (e.g. starches) of especially five- and six-membered ring structures (i.e. glycosidases, EC 3.2), but also enzymes capable of isomerizing carbohydrates, e.g. six- membered ring structures such as D-glucose to five-membered ring structures such as D-fructose.
  • Carbohydrases of relevance include the following (EC numbers in parentheses) : ⁇ -amylases (3.2.1.1), ⁇ -amylases (3.2.1.2), glucan 1,4- ⁇ - glucosidases (3.2.1.3), cellulases (3.2.1.4), endo-1, 3 (4) - ⁇ - glucanases (3.2.1.6), endo-1, 4- ⁇ -xylanases (3.2.1.8), dextranases (3.2.1.11), chitinases (3.2.1.14), polygalacturonases (3.2.1.15), lysozymes (3.2.1.17), ⁇ - glucosidases (3.2.1.21), ⁇ -galactosidases (3.2.1.22), ⁇ - galactosidases (3.2.1.23), amylo-1, 6-glucosidases (3.2.1.33), xylan 1, 4- ⁇ -xylosidases (3.2.1.37),
  • oxidoreductases examples include GluzymeTM (enzyme available from Novo Nordisk
  • proteases examples include KannaseTM, EverlaseTM, EsperaseTM, AlcalaseTM, NeutraseTM, DurazymTM, SavinaseTM, PyraseTM, Pancreatic Trypsin NOVO (PTN) , Bio-FeedTM Pro and Clear-LensTM Pro (all available from Novo Nordisk A/S, Bagsvaerd, Denmark) .
  • Other commercially available proteases include MaxataseTM, MaxacalTM, MaxapemTM, OpticleanTM and PurafectTM (available from Genencor International Inc. or Gist-Brocades).
  • Examples of commercially available upases include LipoprimeTM LipolaseTM, LipolaseTM Ultra, LipozymeTM, PalataseTM, NovozymTM 435 and LecitaseTM (all available from Novo Nordisk A/S) .
  • LipomaxTM Ps . pseudoalcaligenes lipase from Gist-
  • 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, Sweetzy eTM and AquazymTM (all available from Novo Nordisk A/S) .
  • 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 enzyme content will be as high as possible or practicable.
  • the content of enzyme (calculated as percent pure enzyme protein per granule weight) in a granule of the invention will typically be in the range of from about 0.5% to 50% by weight of the enzyme-containing granule, but higher amounts such as 50-90% w/w are also suitable.
  • the enzyme activity (proteolytic activity) of the finished granules will typically be in the range of 1-20 KNPU/g.
  • This unit for protease activity is Kilo Novo Protease Units per gram of sample (KNPU/g) .
  • the activity is determined relatively to an enzyme standard of known activity in KNPU/g.
  • 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) .
  • TNBS 2,4,6- tri-nitro-benzene-sulfonic acid
  • the digestion of DMC and the color reaction is carried out at 50°C in a pH 8.3 boric acid buffer with a 9 min. reaction time followed by a 3 min. measuring time.
  • a folder AF 220/1 is available upon request to Novo Nordisk A/S, Denmark, which folder is hereby included by reference.
  • an activity of 10-500 KNU/g will be typical.
  • the activity is determined relatively to an enzyme standard of known activity in KNU/g.
  • the enzyme standard is standardized by measuring for a given amount of enzyme the formation rate ( ⁇ mol/minute) of 2-chlor-4-nitrophenol liberated from digestion of 2-chlor-4- nitrophenyl-b-D-maltoheptaosid substrate by the enzyme and auxiliary alfa- and beta-glucosidase enzymes in solution. Kits for performing ⁇ -amylase assays are commercially available.
  • ⁇ -amylase assay may be found in the leaflet AF318/1-GB available upon request from Novo Nordisk A/S, Denmark.
  • an activity in the range of 50-400 KLU/g will normally be suitable.
  • the enzyme will be applied to the granulation process as an enzyme containing liquid.
  • the enzyme containing liquid may be applied as a purified product in which the en- zyme is dissolved or dispersed as crystalline and/or amorphous protein in an aqueous liquid in the form of an enzyme concentrate or the enzyme containing liquid may be in the form of a fermentation broth.
  • the water in the liquid may be used as a liquid agent for the granulation process ( supra) .
  • the preformed core particles are preferably carbohydrate based core particles such as particles formed from plant flours or products (cassava, manioc, cereal flours, sugars, dextrins etc.) or salt based core particles made from salts such as, alkali or earth alkali metal salts of sulfate, sulfite, phosphate, phosphonate, nitrate, chloride or carbonate or salts of simple organic acids such as citrate, malonate or acetate are preferred.
  • carbohydrate based core particles such as particles formed from plant flours or products (cassava, manioc, cereal flours, sugars, dextrins etc.) or salt based core particles made from salts such as, alkali or earth alkali metal salts of sulfate, sulfite, phosphate, phosphonate, nitrate, chloride or carbonate or salts of simple organic acids such as citrate, malonate or acetate are preferred.
  • Suitable fillers are water soluble and/or insoluble inorganic salts such as finely ground alkali sulphate, alkali carbonate and/or alkali chloride), clays such as kaolin (e.g. SpeswhiteTM, English China Clay) , bentonites, talcs, zeolites, and/or silicates .
  • kaolin e.g. SpeswhiteTM, English China Clay
  • Binders are binders with a high melting point or no melting point at all and of a non waxy nature e.g. polyvinyl pyrrolidon, dextrins, polyvinylalkohol, cellulose derivatives, for example hydroxypropyl cellulose, methyl cellulose or CMC.
  • a suitable binder is a carbohydrate binder such as Glucidex 21D available from Roquette Freres, France.
  • Pure or impure cellulose in fibrous form can be sawdust, pure fibrous cellulose, cotton, or other forms of pure or impure fibrous cellulose. Also, filter aids based on fibrous cellulose can be used. Several brands of cellulose in fibrous form are on the market, e.g. CEPO and ARBOCELL. In a publication from Sven- ska Tramjolsfabrikerna AB, "Cepo Cellulose Powder" it is stated that for Cepo S/20 cellulose the approximate maximum fiber length is 500 ⁇ m, the approximate average fibre length is 160 ⁇ m, the approximate maximum fibre width is 50 ⁇ m and the approximate average fibre width is 30 ⁇ m.
  • CEPO SS/200 cellulose has an approximate maximum fibre length of 150 ⁇ m, an approximate average fibre length of 50 ⁇ m, an ap- proximate maximum fiber width of 45 ⁇ m and an approximate average fiber width of 25 ⁇ m.
  • Cellulose fibers with these dimensions are very well suited for the purpose of the invention.
  • the words "Cepo” and "Arbocel” are Trade marks.
  • a preferred fibrous cellulose is ArbocelTM BFC200.
  • synthetic fibres may be used as described in EP 304331 Bl and typical fibres may be made of polyethylene, polypropylene, polyester, especially nylon, polyvinylformat , poly (meth) acrylic compounds.
  • Liquid agent Liquid agent
  • a liquid agent is used in conventional mixer granulation processes for enabling the build up or agglomeration of the conventional granulating component particles into granules.
  • the liquid agent is water and/or a waxy substance.
  • the liquid agent is always used in a liquid phase in the granulation process but may later on solidify; the waxy substance if present, therefore, is either dissolved or dispersed in the water or melted.
  • waxy substance as used herein is meant a substance which possesses all of the following characteristics 1) the melting point is between 30 and 100°C, preferably between 40 and 60°C, 2) the substance is of a tough and not brittle nature, and 3) the substance possesses a certain plasticity at room temperature.
  • Both water and waxy substance are liquid agents, i.e. they are both active during the formation of the granules; the waxy substance stays as a constituent in the finished granules, whereas the majority of the water is removed during a drying step.
  • waxy substances are polyglycols, fatty alcohols, ethoxylated fatty alcohols, mono-, di- and triglycerolesters of higher fatty, acids, e.g. glycerol monostearate, alkylarylethoxylates, and coconut monoethanolamide .
  • the liquid agent can be either water alone, waxy substance alone or a mixture of water and waxy substance .
  • the water and the waxy substance can be added in any sequence, e.g. first the water and then the waxy substance, or first the waxy substance and then the water or a solution or suspension of the waxy substance in the water.
  • the waxy substance can be soluble or insoluble (but dispersible) in water. If water is used a liquid agent it may not be a part of the finished mixer granule as usually most of the water is dried off off at a subsequent drying of the mixer granules.
  • alkaline or neutral materials examples include alkali metal silicates, -carbonates or bicarbonates which provide a chemical scavenging effect by actively neutralizing e.g. oxidants.
  • alkaline protective agents examples include alkali metal silicates, -carbonates or bicarbonates which provide a chemical scavenging effect by actively neutralizing e.g. oxidants.
  • reducing protective agents examples include salts of sulfite, thiosulfite or thiosulfate
  • antioxidants examples include methionine, butylated hydrox toluene (BHT) or butylated hy- droxyanisol (BHA) .
  • enzyme stabilizers may be borates, borax, formates, di- and tricarboxylic acids and reversible enzyme inhibitors such as organic compounds with sulfhydryl groups or alkylated or arylated boric acids.
  • Crosslinking agents may be active-compatible surfactants eg ethoxylated alcohols, especially ones with 10 to 80 ethoxy groups .
  • Further suspension agents, mediators (for boosting bleach action upon dissolution of the granule in e.g. a washing application) and/or solvents may be incorporated in the granule core .
  • Coatings One or more coating may be applied to the granule of the invention to provide desired properties of the granule, e.g. protection of the active in the core.
  • the components of a coating may suitably be components, supra, used in the core, preferably with the exception of enzymes.
  • Conventional coatings as known to the art may suitably be used such as the coatings described in WO 89/08694, WO 89/08695, 270 608 Bl and/or PA 1998 00876 (Danish priority application unpublished at the priority date of this invention) .
  • the coating may comprise minor amounts of a protective agent capable of reacting with a component capable of inactivating (being hostile to) the active, said component entering the granule from a surrounding matrix, i.e. before the component come into contact and inactivate the active.
  • the protective agent may thus e.g. be capable of neutralizing, reducing or otherwise reacting with the component rendering it harmless to the active.
  • Typical components capable of inactivating the active are oxidants such as perbo- rates, percarbonates, organic peracids and the like.
  • Protective agents may fall into several categories : alkaline or neutral materials, reducing agents, antioxidants and/or salts of first transition series metal ions. Each of these may be used in conjunction with other protective agents of the same or different categories.
  • alkaline protective agents are alkali metal silicates, -carbonates or bi- carbonates which provide a chemical scavenging effect by actively neutralizing e.g. oxidants.
  • reducing protective agents are salts of sulfite, thiosulfite or thiosul- fate, while examples of antioxidants are methionine, butylated hydroxytoluene (BHT) or butylated hydroxyanisol (BHA) .
  • Most preferred agents are salts of thiosulfates, e.g. sodium thi- osulfate.
  • the amounts of protective agent in the coating may be 5-40% w/w of the coating, preferably 5-30%, e.g. 10-20%.
  • the coating should encapsulate the active-containing granule by forming a substantially continuous homogenous layer.
  • the coating may perform any of a number of functions in the granule, depending on the intended use of the granule.
  • a coating may achieve one or more of the following effects: (i) some reduction of the active dust formation of an active- containing granule;
  • the coating may further comprise one or more of the following: anti-oxidants, chlorine scavengers, plasticizers, pigments, additional enzymes and fragrances.
  • Plasticizers useful in coating layers in the context of the present invention include, for example: polyols such as sugars, sugar alcohols, or polyethylene glycols (PEGs) having a molecular weight less than 1000; urea, phthalate esters such as dibutyl or dimethyl phthalate; and water.
  • polyols such as sugars, sugar alcohols, or polyethylene glycols (PEGs) having a molecular weight less than 1000
  • PEGs polyethylene glycols having a molecular weight less than 1000
  • urea, phthalate esters such as dibutyl or dimethyl phthalate
  • water water
  • 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 .
  • the granule of the invention is coated with a protective coating having a high constant humidity such as described in the Danish patent application WO 00/01793 pages 5-9 and examples hereby incorporated by reference.
  • the core and coating constituting the active-containing granulate to be lubricated are suitably spherical or near spherical and may suitable have an average diameter in their longest dimension in the range of 50-2000 ⁇ m, preferably 200-
  • the lubricant 1200 ⁇ m, more preferably 400-800 ⁇ m or 50-200 ⁇ m.
  • the lubricant of the invention is a compound or a mixture of compounds forming a non-aqueous liquid at 25°C and which preferably has a viscosity of less than 5000 centipoises at 25°C, such as 500-5000 cP, preferably less than 4000 centipoises such as 500-4000 cP, more preferably less than 3000 centipoises such as 500-3000 cP and most preferably less than 2500 centipoises such as 500-2500 cP.
  • lubricants having a low viscosity are considerably easier to apply as a thin layer in small amounts on a granule and that a homogenous distribution of the small amounts of lubricant on the entire granules surface of a granules is facilitated by a low viscosity.
  • lubricants having a higher viscosity the lubricant tends to adhere inhomogenously to the granule surface in the form of sticky lumps.
  • Another advantage of low viscosity lubricants is that especially low viscosity lubricants reduces the friction of granules when the lubricant is applied to the outer surface of said granules.
  • Reduction of granule friction may suitable be measured by a rheometer.
  • one aspect of the invention relates to active-containing granules comprising a lubricant on the outer surface of the granule, wherein the lubricated granules have a relative friction coefficient which is less than 80%, e.g. 5-80%, when compared to unlubricated granules when measured by a rheometer by using a tip speed of 50 rpm, a helix angle of 3° (compaction mode) , using the 46 mm rotor and weighing 170 g granulate into a 50 mm testing container.
  • the relative friction coefficient is less than 78%, e.g. 5-78%, more preferably less than 75%, e.g. 5-75%, most preferably less than 70%, e.g. 5-70%, com- pared to unlubricated granules.
  • the lubricant is preferably an organic compound or a mixture of organic compounds that satisfy the low viscosity re- quirements.
  • Preferred lubricants are nonionic surfactants such as Softanol (e.g. Softanol 50) and/or Dobanol, natural refined mineral oils such as Whiteway T15 (an alkane oil) , synthetic mineral oils, such as silicone oils, animal oils, plant oil or any suitable mixture.
  • a lubricant which as a further feature are substantially not soluble in the granule material on which it is applied.
  • the lubricant will not dissolve in and/or mix with the granule surface on which it is applied and disappear, e.g. by absorption, from the granule surface where it serves it function.
  • the lubricant and the coating material may be mixed prior to the application of lubricant and coating to the granules. This mixture or dispersion may thus be applied simultaneously to the granule and because of the insolubility of the lubricant in the coating material the lubricant may separate from the coating material to form an outer lubrication layer.
  • substantially not soluble in this context means that less than 1 g lubricant can be dissolved in 1 kg of the granule material on which it is applied.
  • the granule material such as a coating layer on which the lubricant is applied is usually a hydrophilic water soluble material.
  • preferred lubricants are hydrophobic.
  • mineral oil lubricants are suitable and hence in one aspect the invention relates to active-containing granules comprising a mineral oil lubricant on the outer surface of the granules.
  • Most preferred lubricants are mineral oil lubricants having a viscosity of less than 5000 centipoises which reduces the rela- tive friction coefficient of lubricated granules to less than 80% when compared to unlubricated granules. While lubrication of active-containing granules will grease and reduce friction between granules, rendering them less dusting and lowering the risk of breakage, we have also found that in some instances the greasing properties of the lu- bricant, also may cause the dry granules to become sticky and agglomerate if too much lubricant is applied.
  • Agglomeration may be inhibited by powdering the granule with a dry particulate material, such as Ti0 2 , such as described in US 4,106,991 example 22.
  • a dry particulate material such as Ti0 2 , such as described in US 4,106,991 example 22.
  • this will counter act or even cancel the lubrica- tion effect and we have found that lowering the amount of lubricant preferably to less than 1% w/w of the lubricated granule will prevent significant agglomeration, while maintaining the beneficiary greasing effect.
  • the lubricant should preferably be applied in a very thin layer constituting less than 1% of the granule by weight, such as between 0.01% to 1% preferably less than 0.75% w/w, such as be- tween 0.1% to 0.75%, more preferably about 0.5% w/w such as between 0.1% to 0.5% of the granule.
  • Applying a very thin lubrication layer will be facilitated by using a low viscosity lubricant and/or a lubricant which is substantially not soluble in the granule material on which it is applied as described su- pra .
  • the use of an anti- caking agent to prevent agglomeration during manufacture or storage of granules may successfully be omitted.
  • the granules of the invention are free of anti-caking agents applied on the lubrication layer.
  • the lubricant may suitably be applied to an enzyme granule by adding the lubricant to the granule in suitable amounts and mixing this composition until the lubricant deposited and distrib- uted on the surface of the granules .
  • the mixing may be achieved by spraying the lubricant onto the enzyme granule in a high speed mixer or in a fluid bed coater.
  • the process of preparing granules of the invention is conveniently free of any steps adding anti-agglomera ion agents onto the lubrication layer.
  • compositions for use in industry or household may suitably be incorporated in compositions for use in industry or household.
  • Such compositions include cleaning and/or disinfecting compo- sitions such as detergent composition further comprising a surfactant.
  • cleaning and/or disinfecting compo- sitions such as detergent composition further comprising a surfactant.
  • Such compositions are described e.g. in WO 00/01793 in the section "Detergent discosure” .
  • Other compositions are antimicrobial compositions, wherein the enzyme is optionally an antimicrobial oxidoreductase and compositions for treatment of microbial biofilm, wherein the enzyme is optionally an antimicrobial oxidoreductase and the composition optionally further comprises a hydrolase enzyme.
  • Other composition may be feed or food compositions such as animal feed or bakers flour.
  • the enzyme concentrate was an aqueous suspension of crys- talline enzyme containing also a carbohydrate binder
  • the granulate was coated as described in US 4,106,991 Example 22 by applying a solution of 6.9% PEG 4000 and 12.5% of a 1:1 Ti0 2 /Kaolin mixture.
  • the granulate was further coated in a L ⁇ dige mixer with 2.0% PEG4000 followed, by powdering the granulate with 1.5% Kaolin.
  • a part of the granulate was lubricated by adding a nonionic surfactant in a L ⁇ dige mixer (mixing for 5 minutes at room temperature) as given in the table below.
  • the final granulates were tested for dust using the conventional Heubach attrition method which is known to the art, (see e.g. WO 93/07263), measuring both the total dust created (as mg dust per 20 g granulate) and the enzyme dust (as nanogram protein per g granulate) .
  • the values given in the table is the mean of three measurements .
  • Uncoated enzyme granulate was produced as in example 1.
  • the granulate was coated as described in example 1 by applying a solution of 5.0% PEG 4000 and 12.5% of a 1:1 Ti0 2 /Kaolin mixture.
  • the granulate was further coated with 1.5% PEG4000 in a L ⁇ dige mixer, followed by powdering the granulate with 1.5% Kaolin.
  • Uncoated enzyme granulate was produced as in example 1.
  • the granulate was coated as described in example 1 by applying a solution of 4.5% PEG 4000 and 12.5% of a 1:1 Ti0 2 /Kaolin mixture.
  • the granulate was further coated in a L ⁇ dige mixer with a pre-blended mixture of PEG4000 and lubricant (see table below) , followed by powdering the granulate with 1.5% Kaolin.
  • a lubricant soluble in PEG4000 Softanol 50
  • a lubri- cant not soluble in PEG4000 Whiteway T15
  • the relative friction coefficient of the lubricated granulates from example 1 were measured using a powder rheometer from Manumit Powder Rheometer (Freeman Technology FT3 Powder Rheometer) .
  • the friction coefficient is proportional to the FORCE divided by the TORQUE measured by the rheometer (tip speed 50 rpm, helix angle 3° (compaction mode), using the 46 mm rotor and weighing 170 g granulate into the 50 mm container.
  • the relative friction coefficients are calculated by dividing with the friction coefficient from the un-lubricated granulate:

Landscapes

  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Zoology (AREA)
  • General Health & Medical Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Genetics & Genomics (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Engineering & Computer Science (AREA)
  • Biomedical Technology (AREA)
  • Molecular Biology (AREA)
  • Microbiology (AREA)
  • Biotechnology (AREA)
  • Biochemistry (AREA)
  • Epidemiology (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Detergent Compositions (AREA)
  • Enzymes And Modification Thereof (AREA)
EP01964946A 2000-09-08 2001-09-07 Durch eine schmierschicht charakterisiertes granulat Ceased EP1317533A1 (de)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
DKPA200001340 2000-09-08
DK200001340 2000-09-08
PCT/DK2001/000582 WO2002020746A1 (en) 2000-09-08 2001-09-07 Lubricated granules

Publications (1)

Publication Number Publication Date
EP1317533A1 true EP1317533A1 (de) 2003-06-11

Family

ID=8159703

Family Applications (1)

Application Number Title Priority Date Filing Date
EP01964946A Ceased EP1317533A1 (de) 2000-09-08 2001-09-07 Durch eine schmierschicht charakterisiertes granulat

Country Status (5)

Country Link
EP (1) EP1317533A1 (de)
JP (1) JP2004508040A (de)
CN (1) CN1452657A (de)
AU (1) AU2001285723A1 (de)
WO (1) WO2002020746A1 (de)

Families Citing this family (16)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US7960332B2 (en) 2003-01-27 2011-06-14 Novozymes A/S Stabilization of granules
PT1729797E (pt) 2004-03-22 2008-12-17 Solvay Pharm Gmbh Composições farmacêuticas orais de produtos contendo lipase, em particular de pancreatina, contendo tensioactivos
EP2258209B1 (de) 2004-09-27 2015-06-24 Novozymes A/S Phytasegranulate in der Tierernährung
EP1913138B1 (de) 2005-07-29 2016-08-24 Abbott Laboratories GmbH Verfahren zur herstellung von pankreatin-pulver mit einem niedrigen virusgehalt
US11266607B2 (en) 2005-08-15 2022-03-08 AbbVie Pharmaceuticals GmbH Process for the manufacture and use of pancreatin micropellet cores
US9198871B2 (en) 2005-08-15 2015-12-01 Abbott Products Gmbh Delayed release pancreatin compositions
AU2007224464A1 (en) * 2006-03-10 2007-09-20 Basf Se Solid enzyme formulations and process for their preparation
US10072256B2 (en) 2006-05-22 2018-09-11 Abbott Products Gmbh Process for separating and determining the viral load in a pancreatin sample
WO2008017661A1 (en) 2006-08-07 2008-02-14 Novozymes A/S Enzyme granules for animal feed
CN101505611B (zh) 2006-08-07 2013-03-27 诺维信公司 用于动物饲料的酶团粒
US10557108B2 (en) 2008-03-28 2020-02-11 Novozymes A/S Triggered release system
WO2011000924A1 (en) 2009-07-03 2011-01-06 Abbott Products Gmbh Spray-dried amylase, pharmaceutical preparations comprising the same and use
EP2575447B1 (de) * 2010-05-27 2015-07-01 Exosect Limited Flüssige zusammensetzungen enthaltend ein system zur anhaltenden freisetzung eines insektizids
EP2537918A1 (de) 2011-06-20 2012-12-26 The Procter & Gamble Company Verbraucherprodukte mit lipasenhaltigen beschichteten Partikeln
CN112469825A (zh) 2018-09-11 2021-03-09 诺维信公司 用于饲料组合物的稳定颗粒
US20230364203A1 (en) 2020-10-07 2023-11-16 Novozymes A/S New Granules for Animal Feed

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3737376A (en) * 1970-08-05 1973-06-05 Pabst Brewing Co Non-dusting and moisture-resistant enzyme compositions

Family Cites Families (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE2628976A1 (de) * 1975-06-30 1977-01-27 Procter & Gamble Klares, stabiles, einphasiges und fluessiges wasch- und reinigungsmittel
US4129515A (en) * 1976-09-13 1978-12-12 The Procter & Gamble Company Heavy-duty liquid detergent and process
NZ234587A (en) * 1989-08-04 1991-11-26 Mcneil Ppc Inc A chewable pharmaceutical tablet of compressed coated granules
US5324649A (en) * 1991-10-07 1994-06-28 Genencor International, Inc. Enzyme-containing granules coated with hydrolyzed polyvinyl alcohol or copolymer thereof
ATE210723T1 (de) * 1991-10-07 2001-12-15 Genencor Int Umhüllte enzym enthaltende körnchen
EP0804532B1 (de) 1994-11-18 2001-01-17 Genencor International, Inc. Umhüllte enzymgranulate
AU4499299A (en) * 1998-06-30 2000-01-24 Novozymes A/S A new improved enzyme containing granule
EP1889904A3 (de) * 1999-10-01 2008-07-09 Novozymes A/S Enzymgranulat

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3737376A (en) * 1970-08-05 1973-06-05 Pabst Brewing Co Non-dusting and moisture-resistant enzyme compositions

Non-Patent Citations (3)

* Cited by examiner, † Cited by third party
Title
JAN H VAN EE, ONNO MISSET AND ERIK J BAAS: "enzymes in detergency", MARCEL DEKKER INC *
MICHAEL S SHOWELL: "powdered detergents", 1998, MARCEL DEKKER INC *
See also references of WO0220746A1 *

Also Published As

Publication number Publication date
AU2001285723A1 (en) 2002-03-22
WO2002020746A1 (en) 2002-03-14
CN1452657A (zh) 2003-10-29
JP2004508040A (ja) 2004-03-18

Similar Documents

Publication Publication Date Title
EP1198562B1 (de) Verfahren zur herstellung eines ein enzym enthaltendes granulat
US7632799B2 (en) Process for preparing coated enzyme granules with salt coatings
EP1224273B1 (de) Enzymgranulat
US6136772A (en) Enzyme-containing granules and process for the production thereof
US20080292883A1 (en) Granules With Filamentous Coatings
JP4944036B2 (ja) 活性化合物を含んでなる顆粒の安定化
EP1317533A1 (de) Durch eine schmierschicht charakterisiertes granulat
EP1324751B1 (de) Einen wirkstoff enthaltende, beschichtete teilchen
EP1590455B1 (de) Enzymstabilisierung
EP1490485B1 (de) Granulate mit filamentösen schichten
US20020119201A1 (en) Lubricated granules
DE60117028T3 (de) Wirkstoffe und viskoelastische flüssigkeiten enthaltende partikel
EP1606381B1 (de) Umhüllte enzymkörnchen

Legal Events

Date Code Title Description
PUAI Public reference made under article 153(3) epc to a published international application that has entered the european phase

Free format text: ORIGINAL CODE: 0009012

17P Request for examination filed

Effective date: 20030408

AK Designated contracting states

Designated state(s): AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE TR

AX Request for extension of the european patent

Extension state: AL LT LV MK RO SI

17Q First examination report despatched

Effective date: 20061211

STAA Information on the status of an ep patent application or granted ep patent

Free format text: STATUS: THE APPLICATION HAS BEEN REFUSED

18R Application refused

Effective date: 20091111