WO2001029164A1 - Reduced malto-oligosaccharide cleansing compositions - Google Patents

Reduced malto-oligosaccharide cleansing compositions Download PDF

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Publication number
WO2001029164A1
WO2001029164A1 PCT/US2000/029141 US0029141W WO0129164A1 WO 2001029164 A1 WO2001029164 A1 WO 2001029164A1 US 0029141 W US0029141 W US 0029141W WO 0129164 A1 WO0129164 A1 WO 0129164A1
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WO
WIPO (PCT)
Prior art keywords
cleansing
cleansing composition
oligosaccharide
composition according
malto
Prior art date
Application number
PCT/US2000/029141
Other languages
French (fr)
Inventor
Frank W. Barresi
Richard L. Antrim
Susan O. Freers
Original Assignee
Grain Processing Corporation
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 Grain Processing Corporation filed Critical Grain Processing Corporation
Priority to AU10998/01A priority Critical patent/AU1099801A/en
Priority to JP2001531951A priority patent/JP2003512508A/en
Priority to EP00972319A priority patent/EP1141193A1/en
Priority to CA002352269A priority patent/CA2352269A1/en
Priority to BR0007202-8A priority patent/BR0007202A/en
Priority to US09/801,352 priority patent/US6475979B2/en
Publication of WO2001029164A1 publication Critical patent/WO2001029164A1/en

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Classifications

    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/221Mono, di- or trisaccharides or derivatives thereof
    • 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
    • C11D17/0047Detergents in the form of bars or tablets
    • C11D17/006Detergents in the form of bars or tablets containing mainly surfactants, but no builders, e.g. syndet bar
    • 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
    • C11D17/08Liquid soap, e.g. for dispensers; capsuled
    • 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
    • C11D3/20Organic compounds containing oxygen
    • C11D3/22Carbohydrates or derivatives thereof
    • C11D3/222Natural or synthetic polysaccharides, e.g. cellulose, starch, gum, alginic acid or cyclodextrin
    • 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
    • C11D9/00Compositions of detergents based essentially on soap
    • C11D9/04Compositions of detergents based essentially on soap containing compounding ingredients other than soaps
    • C11D9/22Organic compounds, e.g. vitamins
    • C11D9/26Organic compounds, e.g. vitamins containing oxygen
    • C11D9/262Organic compounds, e.g. vitamins containing oxygen containing carbohydrates

Definitions

  • the present invention relates to cleansing compositions .
  • Carbohydrates are particularly useful when the cleansing bar includes a synthetic cleansing agent. Such cleansing agents often are more effective at dissolving dirt and oils than natural soap, but may be deemed too harsh on the skin or otherwise undesirable for use as a cleansing bar without the incorporation of a filler into the bar.
  • the use of carbohydrates such as starches and maltodextrins in laundry detergent also is known in the art
  • processing conditions for the production of cleansing compositions may expose the carbohydrate components to alkaline, thermal, and/or high shear conditions that may cause the carbohydrate to degrade.
  • the degradation of the carbohydrate can manifest itself in yellowing of the cleansing composition, or in an overall loss of performance of the cleansing composition. There is thus a need in the art for a carbohydrate material that can withstand the processing conditions used in the preparation of such cleansing compositions. There is also a need in the art for a cleansing composition that is resistant to yellowing and loss of performance due to degradation of the carbohydrate.
  • the present invention is based on the surprising discovery that a reduced malto-oligosaccharide may be used in connection with a cleansing composition to provide a cleansing composition that includes superior colorfastness, thickening ability, mildness, textural feel, and structural integrity, as well as increased billet density and enhanced shelf life stability.
  • the invention thus provides a cleansing composition that includes a cleansing agent and a structurant, filler, or thickener, the structurant, filler, or thickener comprising a reduced malto-oligosaccharide.
  • Other components such as modifiers, binders, water, fragrances, and other ingredients further may be included.
  • the cleansing composition takes the form of a bar soap.
  • the cleansing composition takes the form of a powdered laundry-type detergent.
  • the reduced malto-oligosaccharide preferably constitutes an encapsulating material for a carrier material, such as a perfume—containing material.
  • the cleansing composition takes the form of a liquid laundry detergent.
  • the liquid laundry detergent includes a reduced malto-oligosaccharide as a thickener or structurant (for instance, as a carrier for enzymes in the laundry detergent or as an encapsulant for other materials) .
  • FIGS. 1-4 graphically illustrate UV absorbance data presented in Example 3 and Comparative Example 1.
  • the invention incorporates reduced malto-oligosaccharides species. While the reduced malto-oligosaccharide species can be obtained by any suitable method, they are preferably prepared via reduction of readily available malto— oligosaccharide mixtures, e.g., as described in U.S. Patent
  • Maito- oligosaccharide mixtures suitable for reduction to form reduced malto—oligosaccharides are sold by Grain Processing Corporation of Muscatine, Iowa under the
  • MALTRIN® product designation these including, for example,
  • naturally occurring malto-oligosaccharides typically contain a mixture of a plurality of malto-oligosaccharide species.
  • the reduced malto-oligosaccharide species obtained by reduction of such naturally occurring precursors likewise will contain a plurality of reduced malto-oligosaccharide species.
  • Oligosaccharides can be prepared by the controlled hydrolytic cleavage of starches. In the production of such oligosaccharides, the glycoside linkages of the starch molecules are partially hydrolyzed to yield at least one oligosaccharide species, and more typically, a mixture of oligosaccharide species. Each oligosaccharide species in the mixture may be characterized by its degree of polymerization
  • DP refers to the number of saccharide units in the molecule.
  • Each oligosaccharide species also may be characterized by its dextrose equivalent (DE), which generally indicates the proportion of aldehyde, hemiacetal or ketone terminal groups in the molecule, and which is a measure of the reducing sugar content of the oligosaccharide, expressed as a percentage of the total dry substance.
  • DE dextrose equivalent
  • the DE value and DP profile for a given oligosaccharide mixture can vary substantially, depending, for example, upon the type of starch precursor used to obtain the mixture and the conditions employed for hydrolysis of the base starch.
  • the DP value of the reduced product may be different from the DP value of the precursor.
  • the malto- oligosaccharide preferably is reduced under conditions such that when a single reduced malto-oligosaccharide species is obtained by reduction of a malto-oligosaccharide precursor, the DP value of the reduced malto-oligosaccharide species preferably is substantially preserved.
  • the DP profile for the product preferably is substantially retained, e.g., as described in U.S. Patent Application Serial No. 09/366,065 (corresponding to PCT/US99/01098 ) .
  • the reduced malto-oligosaccharide species used in accordance with the present invention has a DE of less than about 1.
  • the reduced malto-oligosaccharide species used in conjunction with the invention can have any suitable DP value, preferably 2 or greater and typically greater than 2 (e.g., DP of 5 or greater) .
  • the preserving agent includes a mixture of a plurality of reduced alto- oligosaccharide species differing at least in DP value thus defining a DP profile for the mixture.
  • a mixture of a plurality of reduced malto-oligosaccharide species it is preferred that at least one of the reduced malto-oligosaccharide species has a DP greater than 5, more preferably greater than about DP 8, and most preferably greater than about DP 10.
  • At least about 80% of the reduced malto-oligosaccharide species have a DP greater than 5. More preferably at least about 60% of the reduced malto— oligosaccharide species have a DP greater than 8. Still more preferably, at least about 60% of the reduced malto- oligosaccharide species have a DP greater than 10. Most preferably, at least about 80% of the reduced malto- oligosaccharide species have a DP greater than 10. In a particularly preferred embodiment, at least about 75% of the reduced malto—oligosaccharide species m the mixture have a DP greater than 5 and at least about 40% of the reduced malto- oligosaccharide species in the mixture have a DP greater than 10.
  • the reduced malto-oligasaccharide species of the preserving agent of the present invention are comprised of sugar units having different glucose linkages (typically 1,4— and 1, 6—linkages) it is preferred that the ma ority of glucose units in the reduced malto—oligosaccharide species are 1,4- lmked.
  • the structurant may include other starches, maltodextrins, dext ⁇ ns, or sugars such as dextrose or sorbitol.
  • the reduced malto-oligosaccharides used in accordance with the present invention include modified reduced malto- oligosaccharides .
  • modified reduced malto- oligosaccharides can be found, for example, in PCT/US00/4068 , describing derivatized reduced malto-oligosaccharides .
  • Derivatized reduced malto-oligosaccharides can include, for example, reduced malto-oligosaccharides that incorporate one or more substituents or chemical modifications in one or more positions on one or more saccha ⁇ de units. Such substituents can be introduced, for example, by hydroxyalkylation, oxidation, etherification, and esterification reactions.
  • one or more primary alcohol positions in one or more saccharide units can be oxidized to form one or more carboxylic acids.
  • Etherification reactions can include, for example, ethoxylations, propoxylations and other alkylations, as well as reactions that can introduce a catiomc charge by using reagents such as, for example, 3-chloro-2- hydryoxypropyl-trimethylammonium chloride, or the like.
  • Esterification reactions can include, for example, acylation reactions in which an acyl group (e.g., having from about 2 to 20 carbon atoms) is introduced to one or more saccharide units. It is contemplated that enzymatically modified reduced malto-oligosaccharides may be used in conjunction with the invention, as well as reduced malto-oligosaccharides that have been otherwise modified.
  • the cleansing composition of the invention further includes a cleansing agent.
  • the cleansing composition of the invention takes the form of a soap bar
  • the cleansing composition preferably includes a natural soap, i.e., the saponification product resulting from alkaline treatment of triglycerides .
  • the cleansing agent preferably further includes a synthetic surfactant, such as an anionic, nonionic, or amphoteric surfactant.
  • the cleansing agent may include products such as sodium lauryl sulfate, stearic acid, sodium stearate, sodium methylcocoyltaurate, benzene sulfonate, sorbitan laurate, cocamidopropylbetaine, acylisethionate, and alkyl polyglucosides, and, in general, any surfactant or cleansing agent useful in connection with the preparation of a soap bar or a "non-soap" type bar.
  • Nonionic surf actants include ethoxylated fatty materials.
  • Amphoteric surfactants include cocoamidopropyl betaine and cocoamphoacetate . Further details concerning the cleansing agent may be found in "Soap,” in Kirk-Othmer Encyclopedia of Chemical Technology, 4th ed. , vol. 22 (1997).
  • the reduced malto- oligosaccharides are useful in conjunction with soaps in which the cleansing agent consists exclusively of natural soap, but the invention is contemplated to find greatest applicability in the case of cleansing bars in which some or all of the cleansing agent includes a synthetic surfactant.
  • the soap bar may include other soap additives as may be known in the art or otherwise found to be suitable in conjunction with the invention.
  • the soap may include a free fatty acid, such as coconut or palm kernel, for association with the cleansing agent to form soap crystals.
  • the soap may include a colorant, such as titanium dioxide, and/or a fragrance to improve the aesthetic properties of the soap bar.
  • An antioxidant such as EDTA (ethylene diamine tetraacetic acid) , EHDP (sodium etidronate) , or citric acid may be employed.
  • a chelant such as magnesium silicate, may be included.
  • the soap bar may include a humectant, such as glycerol, and may include a mildness additive, such as lanolin, vitamin E, aloe vera gel, mineral oil, or baking soda.
  • an antimicrobial agent such as TCC
  • TCS trichlorohydroxydiphenyl ether
  • Other ingredients such as abrasive agents (including such materials as pumice) and solvents (including glycerol), triethanolamine, ethyl alcohol, and sugars also may be incorporated.
  • Other suitable ingredients include waxes, glycerol stearate, and polyethyeneglycols, such as PEG 150, as well as emollients and other ingredients useful in connection with the preparation of a bar soap.
  • the foregoing optional ingredients may be incorporated in any amounts suitable to achieve their intended affect in the soap bar.
  • the reduced malto- oligosaccharide is used in conjunction with the production of a bar soap.
  • the bar soap has the following typical composition:
  • the reduced malto-oligosaccharide may be used in connection with the preparation of a laundry detergent.
  • U.S. Patent 5,656,584 purports to disclose a process for producing a particulate laundry additive composition, the process including mixing a porous carrier material, typically containing perfume, and an encapsulating material, typically a carbohydrate material, and then compacting the mixture to form agglomerates.
  • the process for producing a particulate laundry additive preferably includes encapsulating a carrier material with a reduced malto- oligosaccharide encapsulating material, and then compacting the material to form agglomerates.
  • the reduced malto-oligosaccharide may be used in other respects in connection with the preparation of laundry detergents, for instance, as a structurant.
  • the laundry detergent may be in the form of a liquid laundry detergent or a solid laundry detergent, such as a powdered detergent.
  • the detergent comprises a cleansing agent, preferably a synthetic surfactant as discussed hereinabove, and a reduced malto-oligosaccharide.
  • the laundry detergent may, of course, contain other additives as are known in the art or are otherwise may be found suitable in connection with the preparation of a laundry detergent.
  • Typical laundry detergents include builders, which are substances that augment the detersive effects of surfactants.
  • Such builders are added to remove hard water ions from the wash water, i.e., to soften the water.
  • Known builders include such ingredients as pentisodium triphosphate, tetrisodium pyrophosphate, trisodium phosphate, and glassy phosphates such as sodium polyinetaphosphate, sodium hexametaphosphate, and potassium phosphates.
  • Other builders include materials such as carbonates, silicates, zeolites, clays, NTA (nitrilotriacetic acid, trisodium salt) , and neutral soluble salts. Further details concerning suitable builders may be found in "Detergency, " in Kirk—Othmer Encyclopedia of Chemical Technology vol. 7 (1997)
  • the detergent may include other additives, such as antiredeposition agents, including sodium carboxymethycellulose and other cellulose derivatives, fluorescent whitening agents or blueing agents, or bleaching agents, such as sodium perborate trihydrate.
  • Other ingredients useful in connection with detergents include foam regulators and organic sequestering agents. Such optional ingredients may be present in any amount suitable for their intended purpose.
  • Many laundry detergents include enzymes, such as proteolytic enzymes and cellulase enzymes.
  • the reduced malto-oligosaccharide may be present in the detergent composition as a carrier for the enzymes.
  • the carrier may be prepared by introducing the enzyme onto a substrate, the substrate comprising the reduced malto- oligosaccharide. When used in this regard, the enzyme may be present in a ratio with respect to the reduced malto- oligosaccharide of about 1:1 to about 1:1000.
  • the cleansing composition may take any other suitable form, such as a liquid soap, a shampoo, a bath gel, a hand or automatic dishwashing detergent, a personal care product used for cleansing, or any other suitable form.
  • EXAMPLE 1 Preparation of a Cleansing Bar Polyethylene glycol 6000, 50 g; glycerol stearate, 25 g; stearic acid, 10 g; titanium dioxide, 0.1 g; and paraffin wax 2.5 g; are blended together to form a melt—like composition.
  • a reduced malto-oligosaccharide, 200 g; sodium lauryl sulfate, 20 g; and sodium cocoyl isethionate, 80 g; are then added and the moisture level is adjusted to 5 wt . % .
  • the temperature is brought to 100°C, and the mixture blended for 30 minutes.
  • the composition is then cooled on a chill roll and chipped.
  • the resultant chips are then plodded until a desired density is achieved, and the resulting extrudate is cut into billets.
  • the resulting billets are then compacted into bars.
  • EXAMPLE 2 This Example illustrates the preparation of a powdered soap.
  • Stearic acid, 50 g and canola oil, 5 g were dry blended together and heated to 75°C.
  • 50% Sodium Hydroxide, 15.0 g was added drop-wise during the heating process.
  • the blend was a 75°C, reduced malto-oligosaccharide, 20 g, was added to the blend.
  • the reduced malto-oligosaccharide had the same DP profile as MALTRIN M100.
  • Stirring continued for another 10 minutes and then the powder was removed from the heat and stirred manually for another 10 minutes. The resulting powder did not develop any color.
  • the powder was sifted through a 20 mesh screen.
  • Comparative Example 1 As a comparison with the soap of Example 2, stearic acid, 50 g and canola oil, 5 g, were dry blended together and heated to 75°C. 50% Sodium Hydroxide, 15.5 g, was added drop-wise during the heating process. Once the blend was at 75 C, MALTRIN M100, 20 g, was added to the blend. Stirring continued for another 10 minutes and then the powder was removed from the heat and stirred manually for another 10 minutes. The resulting powder became yellow. The powder was sifted through a 20 mesh screen. This soap was less homogeneous than the soap of Example 2.
  • Minolta color values were obtained using a Minoltachroma meter CR-300 from Minolta Corp. Ramsey, N.J. from the soap compositions of Example 2 and Comparative Example 1. The following results were determined.
  • EXAMPLE 3 This Example illustrates the advantages of using reduced malto-oligosaccharides in a liquid laundry detergent.
  • Reduced malto-oligosaccharide 10.4 g (4.1 moisture) with a carbohydrate profile that matches MALTRIN® M180 was added to a commercially available household liquid laundry detergent, 89.3 g. The mixture was stirred for approximately 30 minutes to allow the reduced malto-oligosaccharide to completely dissolve in the liquid detergent. Once completely dissolved, the pH of the solution was measured, and a 1.0 ml aliquot was removed for UV analysis. The mixture was then incubated in a 60° C water bath for 22 hours. The sample was again pH and UV analyzed. UV analysis was accomplished by diluting the 1.0 ml samples with 5 ml of water in a test tube and stirring the sample in a vortex mixer. The UV absorbance of the sample was then measured at several wavelengths . The data is shown m Table 1 and FIGS. 1-4.
  • Comparative Example 1 A commercially available household liquid laundry detergent, 100 g, was stirred in an Erlenmeyer flask for approximately 30 minutes. The pH of the solution was measured, and a 1.0 ml aliquot was removed for UV analysis. The liquid was then incubated in a 60° C water bath for 22 hours. The sample was again pH and UV analyzed. UV analysis was accomplished by diluting the 1.0 ml samples with 5 ml of water in a test tube and stirring the sample in a vortex mixer. The UV absorbance of the sample was then measured at several wavelengths. The data is shown in Table 1 and FIGS. 1-4.
  • the reduced malto—oligosaccharide product did not significantly increase the UV absorbance over time of the laundry detergent.
  • the reduced malto—oligosaccharide thus is particularly suitable for use as a filler or enzymatic carrier in connection with such laundry detergent.
  • the UV absorbance increased dramatically when unreduced MALTRIN ⁇ M180 was incorporated, thus indicating that color change and possibly cross-reactivity are more likely. It is thus seen that the reduced malto-oligosaccharides are more inert than are regular malto-oligosaccharides as indicated by less color formation and better pH stability.
  • Reduced malto-oligosaccharides thus may be used as an additive in laundry detergent formulation with less potential for cross-reactivity than regular malto-oligosaccharides .
  • Reduced malto-oligosaccharides also are more heat—stable than their unreduced counterparts, which may provide additional advantages in some cleansing applications.

Abstract

Disclosed are cleansing products that include reduced malto-oligosaccharides. In accordance with one embodiment of the invention, a cleansing product includes a surfactant and a reduced malto-oligosaccharide. In accordance with another embodiment, the reduced malto-oligosaccharide is an encapsulant for a product carrier in a powdered laundry-type detergent.

Description

REDUCED MALTO-OLIGOSACCHARIDE CLEANSING COMPOSITIONS
TECHNICAL FIELD OF THE INVENTION The present invention relates to cleansing compositions .
BACKGROUND OF THE INVENTION
It is known in the art that soluble starches, maltodextrins, and other carbohydrates can be used in the production of cleansing bars as structurants , fillers and thickening agents (see U.S. Patent 5,965,501; U.S. Patent
5,756,438, U.S. Patent 5,795,852, and U.S. Patent 5,520,840).
Carbohydrates are particularly useful when the cleansing bar includes a synthetic cleansing agent. Such cleansing agents often are more effective at dissolving dirt and oils than natural soap, but may be deemed too harsh on the skin or otherwise undesirable for use as a cleansing bar without the incorporation of a filler into the bar. The use of carbohydrates such as starches and maltodextrins in laundry detergent also is known in the art
(see U.S. Patent 5,656,584). However, processing conditions for the production of cleansing compositions may expose the carbohydrate components to alkaline, thermal, and/or high shear conditions that may cause the carbohydrate to degrade.
The degradation of the carbohydrate can manifest itself in yellowing of the cleansing composition, or in an overall loss of performance of the cleansing composition. There is thus a need in the art for a carbohydrate material that can withstand the processing conditions used in the preparation of such cleansing compositions. There is also a need in the art for a cleansing composition that is resistant to yellowing and loss of performance due to degradation of the carbohydrate. THE INVENTION
The present invention is based on the surprising discovery that a reduced malto-oligosaccharide may be used in connection with a cleansing composition to provide a cleansing composition that includes superior colorfastness, thickening ability, mildness, textural feel, and structural integrity, as well as increased billet density and enhanced shelf life stability. The invention thus provides a cleansing composition that includes a cleansing agent and a structurant, filler, or thickener, the structurant, filler, or thickener comprising a reduced malto-oligosaccharide. Other components, such as modifiers, binders, water, fragrances, and other ingredients further may be included. In one embodiment of the invention, the cleansing composition takes the form of a bar soap. In another embodiment, the cleansing composition takes the form of a powdered laundry-type detergent. In this embodiment, the reduced malto-oligosaccharide preferably constitutes an encapsulating material for a carrier material, such as a perfume—containing material. In another embodiment, the cleansing composition takes the form of a liquid laundry detergent. The liquid laundry detergent includes a reduced malto-oligosaccharide as a thickener or structurant (for instance, as a carrier for enzymes in the laundry detergent or as an encapsulant for other materials) .
BRIEF DESCRIPTION OF THE DRAWINGS FIGS. 1-4 graphically illustrate UV absorbance data presented in Example 3 and Comparative Example 1.
DESCRIPTION OF THE PREFERRED EMBODIMENTS
The invention incorporates reduced malto-oligosaccharides species. While the reduced malto-oligosaccharide species can be obtained by any suitable method, they are preferably prepared via reduction of readily available malto— oligosaccharide mixtures, e.g., as described in U.S. Patent
Application Serial No. 09/366,065 (corresponding to
PCT/US99/01098) . Maito- oligosaccharide mixtures suitable for reduction to form reduced malto—oligosaccharides are sold by Grain Processing Corporation of Muscatine, Iowa under the
MALTRIN® product designation, these including, for example,
MALTRIN® M040, MALTRIN® M050, MALTRIN® M100, MALTRIN® M150, and MALTRIN® M180. It will be appreciated that naturally occurring malto-oligosaccharides typically contain a mixture of a plurality of malto-oligosaccharide species. As such, the reduced malto-oligosaccharide species obtained by reduction of such naturally occurring precursors likewise will contain a plurality of reduced malto-oligosaccharide species.
Oligosaccharides can be prepared by the controlled hydrolytic cleavage of starches. In the production of such oligosaccharides, the glycoside linkages of the starch molecules are partially hydrolyzed to yield at least one oligosaccharide species, and more typically, a mixture of oligosaccharide species. Each oligosaccharide species in the mixture may be characterized by its degree of polymerization
(DP) , which refers to the number of saccharide units in the molecule. Each oligosaccharide species also may be characterized by its dextrose equivalent (DE), which generally indicates the proportion of aldehyde, hemiacetal or ketone terminal groups in the molecule, and which is a measure of the reducing sugar content of the oligosaccharide, expressed as a percentage of the total dry substance. The DE value and DP profile for a given oligosaccharide mixture can vary substantially, depending, for example, upon the type of starch precursor used to obtain the mixture and the conditions employed for hydrolysis of the base starch.
When a reduced malto-oligosaccharide species is obtained by reduction of a malto-oligosaccharide precursor, it will be appreciated that the DP value of the reduced product may be different from the DP value of the precursor. The malto- oligosaccharide preferably is reduced under conditions such that when a single reduced malto-oligosaccharide species is obtained by reduction of a malto-oligosaccharide precursor, the DP value of the reduced malto-oligosaccharide species preferably is substantially preserved. Similarly, when a mixture of a plurality of reduced malto-oligosaccharide species is obtained by reduction of a mixture of a plurality of malto-oligosaccharide species, the DP profile for the product preferably is substantially retained, e.g., as described in U.S. Patent Application Serial No. 09/366,065 (corresponding to PCT/US99/01098 ) . Preferably, the reduced malto-oligosaccharide species used in accordance with the present invention has a DE of less than about 1. The reduced malto-oligosaccharide species used in conjunction with the invention can have any suitable DP value, preferably 2 or greater and typically greater than 2 (e.g., DP of 5 or greater) . In a preferred embodiment, the preserving agent includes a mixture of a plurality of reduced alto- oligosaccharide species differing at least in DP value thus defining a DP profile for the mixture. When a mixture of a plurality of reduced malto-oligosaccharide species is utilized, it is preferred that at least one of the reduced malto-oligosaccharide species has a DP greater than 5, more preferably greater than about DP 8, and most preferably greater than about DP 10.
In a preferred embodiment, at least about 80% of the reduced malto-oligosaccharide species have a DP greater than 5. More preferably at least about 60% of the reduced malto— oligosaccharide species have a DP greater than 8. Still more preferably, at least about 60% of the reduced malto- oligosaccharide species have a DP greater than 10. Most preferably, at least about 80% of the reduced malto- oligosaccharide species have a DP greater than 10. In a particularly preferred embodiment, at least about 75% of the reduced malto—oligosaccharide species m the mixture have a DP greater than 5 and at least about 40% of the reduced malto- oligosaccharide species in the mixture have a DP greater than 10.
While the reduced malto-oligasaccharide species of the preserving agent of the present invention are comprised of sugar units having different glucose linkages (typically 1,4— and 1, 6—linkages) it is preferred that the ma ority of glucose units in the reduced malto—oligosaccharide species are 1,4- lmked. When a mixture of a plurality of reduced malto- oligosaccharide species is used in the preserving agent of the present invention, it is highly preferred that and at least about 80% of the species in the mixture have a DP greater than 5. The structurant may include other starches, maltodextrins, dextπns, or sugars such as dextrose or sorbitol.
The reduced malto-oligosaccharides used in accordance with the present invention include modified reduced malto- oligosaccharides . Examples of modified reduced malto- oligosaccharides can be found, for example, in PCT/US00/4068 , describing derivatized reduced malto-oligosaccharides . Derivatized reduced malto-oligosaccharides can include, for example, reduced malto-oligosaccharides that incorporate one or more substituents or chemical modifications in one or more positions on one or more sacchaπde units. Such substituents can be introduced, for example, by hydroxyalkylation, oxidation, etherification, and esterification reactions. By way of example, one or more primary alcohol positions in one or more saccharide units can be oxidized to form one or more carboxylic acids. Etherification reactions can include, for example, ethoxylations, propoxylations and other alkylations, as well as reactions that can introduce a catiomc charge by using reagents such as, for example, 3-chloro-2- hydryoxypropyl-trimethylammonium chloride, or the like. Esterification reactions can include, for example, acylation reactions in which an acyl group (e.g., having from about 2 to 20 carbon atoms) is introduced to one or more saccharide units. It is contemplated that enzymatically modified reduced malto-oligosaccharides may be used in conjunction with the invention, as well as reduced malto-oligosaccharides that have been otherwise modified.
The cleansing composition of the invention further includes a cleansing agent. When the cleansing composition of the invention takes the form of a soap bar, the cleansing composition preferably includes a natural soap, i.e., the saponification product resulting from alkaline treatment of triglycerides . The cleansing agent preferably further includes a synthetic surfactant, such as an anionic, nonionic, or amphoteric surfactant. Any suitable surfactant known in the art or otherwise found to be suitable may be used in conjunction with the invention, and thus the cleansing agent may include products such as sodium lauryl sulfate, stearic acid, sodium stearate, sodium methylcocoyltaurate, benzene sulfonate, sorbitan laurate, cocamidopropylbetaine, acylisethionate, and alkyl polyglucosides, and, in general, any surfactant or cleansing agent useful in connection with the preparation of a soap bar or a "non-soap" type bar. Other synthetic surf actants include sodium alkylsulfate and homologous ethoxylated versions and sulfonates, such as sodium cocoylisethionate. Nonionic surf actants include ethoxylated fatty materials. Amphoteric surfactants include cocoamidopropyl betaine and cocoamphoacetate . Further details concerning the cleansing agent may be found in "Soap," in Kirk-Othmer Encyclopedia of Chemical Technology, 4th ed. , vol. 22 (1997). It is contemplated that the reduced malto- oligosaccharides are useful in conjunction with soaps in which the cleansing agent consists exclusively of natural soap, but the invention is contemplated to find greatest applicability in the case of cleansing bars in which some or all of the cleansing agent includes a synthetic surfactant.
The soap bar may include other soap additives as may be known in the art or otherwise found to be suitable in conjunction with the invention. For instance, the soap may include a free fatty acid, such as coconut or palm kernel, for association with the cleansing agent to form soap crystals.
The soap may include a colorant, such as titanium dioxide, and/or a fragrance to improve the aesthetic properties of the soap bar. An antioxidant, such as EDTA (ethylene diamine tetraacetic acid) , EHDP (sodium etidronate) , or citric acid may be employed. A chelant, such as magnesium silicate, may be included. The soap bar may include a humectant, such as glycerol, and may include a mildness additive, such as lanolin, vitamin E, aloe vera gel, mineral oil, or baking soda. If desired, an antimicrobial agent, such as TCC
(trichlorocarbanalide) (or TCS ( trichlorohydroxydiphenyl ether) which have activity against a wide range of microorganisms may be used. Other ingredients, such as abrasive agents (including such materials as pumice) and solvents (including glycerol), triethanolamine, ethyl alcohol, and sugars also may be incorporated. Other suitable ingredients include waxes, glycerol stearate, and polyethyeneglycols, such as PEG 150, as well as emollients and other ingredients useful in connection with the preparation of a bar soap. The foregoing optional ingredients may be incorporated in any amounts suitable to achieve their intended affect in the soap bar.
In one embodiment of the invention, the reduced malto- oligosaccharide is used in conjunction with the production of a bar soap. The bar soap has the following typical composition:
Figure imgf000009_0001
In another embodiment, the reduced malto-oligosaccharide may be used in connection with the preparation of a laundry detergent. U.S. Patent 5,656,584 purports to disclose a process for producing a particulate laundry additive composition, the process including mixing a porous carrier material, typically containing perfume, and an encapsulating material, typically a carbohydrate material, and then compacting the mixture to form agglomerates. In accordance with an embodiment of the present invention, the process for producing a particulate laundry additive preferably includes encapsulating a carrier material with a reduced malto- oligosaccharide encapsulating material, and then compacting the material to form agglomerates. More generally, the reduced malto-oligosaccharide may be used in other respects in connection with the preparation of laundry detergents, for instance, as a structurant. The laundry detergent may be in the form of a liquid laundry detergent or a solid laundry detergent, such as a powdered detergent. In accordance with the invention, the detergent comprises a cleansing agent, preferably a synthetic surfactant as discussed hereinabove, and a reduced malto-oligosaccharide. The laundry detergent may, of course, contain other additives as are known in the art or are otherwise may be found suitable in connection with the preparation of a laundry detergent. Typical laundry detergents include builders, which are substances that augment the detersive effects of surfactants. Typically, such builders are added to remove hard water ions from the wash water, i.e., to soften the water. Known builders include such ingredients as pentisodium triphosphate, tetrisodium pyrophosphate, trisodium phosphate, and glassy phosphates such as sodium polyinetaphosphate, sodium hexametaphosphate, and potassium phosphates. Other builders include materials such as carbonates, silicates, zeolites, clays, NTA (nitrilotriacetic acid, trisodium salt) , and neutral soluble salts. Further details concerning suitable builders may be found in "Detergency, " in Kirk—Othmer Encyclopedia of Chemical Technology vol. 7 (1997)
The detergent may include other additives, such as antiredeposition agents, including sodium carboxymethycellulose and other cellulose derivatives, fluorescent whitening agents or blueing agents, or bleaching agents, such as sodium perborate trihydrate. Other ingredients useful in connection with detergents include foam regulators and organic sequestering agents. Such optional ingredients may be present in any amount suitable for their intended purpose. Many laundry detergents include enzymes, such as proteolytic enzymes and cellulase enzymes. In accordance with the invention, the reduced malto-oligosaccharide may be present in the detergent composition as a carrier for the enzymes. The carrier may be prepared by introducing the enzyme onto a substrate, the substrate comprising the reduced malto- oligosaccharide. When used in this regard, the enzyme may be present in a ratio with respect to the reduced malto- oligosaccharide of about 1:1 to about 1:1000.
The cleansing composition may take any other suitable form, such as a liquid soap, a shampoo, a bath gel, a hand or automatic dishwashing detergent, a personal care product used for cleansing, or any other suitable form.
The following examples further illustrate the present invention but, of course, should not be construed as in any way limiting its scope.
EXAMPLE 1 Preparation of a Cleansing Bar Polyethylene glycol 6000, 50 g; glycerol stearate, 25 g; stearic acid, 10 g; titanium dioxide, 0.1 g; and paraffin wax 2.5 g; are blended together to form a melt—like composition. A reduced malto-oligosaccharide, 200 g; sodium lauryl sulfate, 20 g; and sodium cocoyl isethionate, 80 g; are then added and the moisture level is adjusted to 5 wt . % . The temperature is brought to 100°C, and the mixture blended for 30 minutes. The composition is then cooled on a chill roll and chipped. The resultant chips are then plodded until a desired density is achieved, and the resulting extrudate is cut into billets. The resulting billets are then compacted into bars.
EXAMPLE 2 This Example illustrates the preparation of a powdered soap. Stearic acid, 50 g and canola oil, 5 g, were dry blended together and heated to 75°C. 50% Sodium Hydroxide, 15.0 g, was added drop-wise during the heating process. Once the blend was a 75°C, reduced malto-oligosaccharide, 20 g, was added to the blend. The reduced malto-oligosaccharide had the same DP profile as MALTRIN M100. Stirring continued for another 10 minutes and then the powder was removed from the heat and stirred manually for another 10 minutes. The resulting powder did not develop any color. The powder was sifted through a 20 mesh screen.
Comparative Example 1 As a comparison with the soap of Example 2, stearic acid, 50 g and canola oil, 5 g, were dry blended together and heated to 75°C. 50% Sodium Hydroxide, 15.5 g, was added drop-wise during the heating process. Once the blend was at 75 C, MALTRIN M100, 20 g, was added to the blend. Stirring continued for another 10 minutes and then the powder was removed from the heat and stirred manually for another 10 minutes. The resulting powder became yellow. The powder was sifted through a 20 mesh screen. This soap was less homogeneous than the soap of Example 2.
Minolta color values were obtained using a Minoltachroma meter CR-300 from Minolta Corp. Ramsey, N.J. from the soap compositions of Example 2 and Comparative Example 1. The following results were determined.
Figure imgf000012_0001
L values: L = 100 = white, L = 0 = black A = 100 = red, A = -80 = green
B = 70 = yellow. B = -70 = blue * From reference manual for Minoltachroma Meter CR-300, CR 310, and CR-331 (1991)
As demonstrated by these results, the soap of Example 2 had significantly greater white color and significantly less yellow color than the soap of Comparative Example 1
EXAMPLE 3 This Example illustrates the advantages of using reduced malto-oligosaccharides in a liquid laundry detergent.
Reduced malto-oligosaccharide 10.4 g (4.1 moisture) with a carbohydrate profile that matches MALTRIN® M180 was added to a commercially available household liquid laundry detergent, 89.3 g. The mixture was stirred for approximately 30 minutes to allow the reduced malto-oligosaccharide to completely dissolve in the liquid detergent. Once completely dissolved, the pH of the solution was measured, and a 1.0 ml aliquot was removed for UV analysis. The mixture was then incubated in a 60° C water bath for 22 hours. The sample was again pH and UV analyzed. UV analysis was accomplished by diluting the 1.0 ml samples with 5 ml of water in a test tube and stirring the sample in a vortex mixer. The UV absorbance of the sample was then measured at several wavelengths . The data is shown m Table 1 and FIGS. 1-4.
As a control, MALTRIN M180, 10.7 g (6.4% moisture) was added to a commercially available household liquid laundry detergent, 89.3 g. The mixture was stirred for approximately 30 minutes to allow the malto-oligosaccharide to completely dissolve in the liquid detergent. Once completely dissolved, the pH of the solution was measured, and a 1.0 ml aliquot was removed for UV analysis. The mixture was then incubated in a 60° C water bath for 22 hours. The sample was again pH and UV analyzed. UV analysis was accomplished by diluting the 1.0 ml samples with 5 ml of water in a test tube and stirring the sample in a vortex mixer. The UV absorbance of the sample was then measured at several wavelengths. The data is shown in Table 1 and FIGS. 1-4.
Comparative Example 1 A commercially available household liquid laundry detergent, 100 g, was stirred in an Erlenmeyer flask for approximately 30 minutes. The pH of the solution was measured, and a 1.0 ml aliquot was removed for UV analysis. The liquid was then incubated in a 60° C water bath for 22 hours. The sample was again pH and UV analyzed. UV analysis was accomplished by diluting the 1.0 ml samples with 5 ml of water in a test tube and stirring the sample in a vortex mixer. The UV absorbance of the sample was then measured at several wavelengths. The data is shown in Table 1 and FIGS. 1-4.
Figure imgf000014_0001
As is demonstrated by the foregoing data, the reduced malto—oligosaccharide product did not significantly increase the UV absorbance over time of the laundry detergent. The reduced malto—oligosaccharide thus is particularly suitable for use as a filler or enzymatic carrier in connection with such laundry detergent. On the other hand, the UV absorbance increased dramatically when unreduced MALTRINΘ M180 was incorporated, thus indicating that color change and possibly cross-reactivity are more likely. It is thus seen that the reduced malto-oligosaccharides are more inert than are regular malto-oligosaccharides as indicated by less color formation and better pH stability. Reduced malto-oligosaccharides thus may be used as an additive in laundry detergent formulation with less potential for cross-reactivity than regular malto-oligosaccharides . Reduced malto-oligosaccharides also are more heat—stable than their unreduced counterparts, which may provide additional advantages in some cleansing applications.
All of the references cited herein, including patents, patent applications, and publications, are hereby incorporated in their entireties by reference. While this invention has been described with an emphasis upon preferred embodiments, it will be apparent to those of ordinary skill in the art that variations of the preferred embodiments may be used and that it is intended that the invention may be practiced otherwise than as specifically described herein. Accordingly, this invention includes all modifications and equivalents encompassed within the spirit and scope of the invention as defined by the following claims.

Claims

WHAT IS CLAIMED IS:
1. A cleansing composition comprising: a cleansing agent; and a reduced malto-oligosaccharide.
2. A cleansing composition according to claim 1, further including a binder.
3. A cleansing composition according to claim 1, said reduced malto-oligosaccharide comprising a mixture of a plurality of malto-oligosaccharide species differing at least in DP value.
4. A cleansing composition according to claim 3, said reduced malto-oligosaccharide having been prepared by catalytically hydrogenating a plurality of malto- oligosaccharide species under reaction conditions suitable to substantially preserve the DP profile of said mixture.
5. A cleansing composition according to claim 1, said cleansing composition taking the form of a bar soap.
6. A cleansing composition according to claim 5, said cleansing composition including a humectant.
7. A cleansing composition according to claim 5, said cleansing composition including a fragrance.
8. A cleansing composition according to claim 5, said cleansing agent including an antioxidant.
9. A cleansing composition according to claim 5, said cleansing agent including a chelant.
10. A cleansing composition according to claim 5, said cleansing agent including an antimicrobial agent.
11. A cleansing composition according to claim 5, said cleansing agent consisting essentially of natural soap.
12. A cleansing composition according to claim 5, said cleansing agent including a synthetic surfactant.
13. A cleansing composition according to claim 5, including natural soap and a synthetic surfactant.
14. A cleansing composition according to claim 1, said cleansing composition taking the form of a powdered detergent.
15. A cleansing composition according to claim 14, said powdered detergent including an enzyme, said enzyme being carried on a carrier which comprises a reduced malto- oligosaccharide .
16. A cleansing composition according to claim 14, said powdered detergent comprising a plurality of spray dried particles .
17. A cleansing composition according to claim 1, said cleansing composition taking the form of a liquid soap.
18. A cleansing composition according to claim 17, said cleansing agent including a synthetic surfacant.
19. A cleansing agent according to claim 18, further including a detergent builder.
20. A cleansing agent according to claim 16, further including a bleaching agent .
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Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4336152A (en) * 1981-07-06 1982-06-22 American Cyanamid Company Disinfectant/cleanser compositions exhibiting reduced eye irritancy potential
EP0618286A1 (en) * 1993-03-30 1994-10-05 AUSIMONT S.p.A. Process for decreasing the build up of inorganic incrustations on textiles and detergent composition used in such process
US5520840A (en) * 1995-03-22 1996-05-28 Lever Brothers Company Detergent bars comprising water soluble starches
US5756438A (en) * 1996-03-26 1998-05-26 The Andrew Jergens Company Personal cleansing product
WO1998042814A1 (en) * 1997-03-21 1998-10-01 Unilever Plc Detergent bars comprising adjuvant powders for delivering benefit agent and process for manufacture of said bars
WO1998042818A1 (en) * 1997-03-20 1998-10-01 The Procter & Gamble Company Laundry additive particle having multiple surface coatings
WO1999011748A1 (en) * 1997-08-28 1999-03-11 Unilever Plc Soap bars
WO1999036442A1 (en) * 1998-01-20 1999-07-22 Grain Processing Corporation Reduced malto-oligosaccharides

Family Cites Families (65)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
NL50215C (en) 1938-03-26
US2280975A (en) 1938-08-17 1942-04-28 Atlas Powder Co Hydrogenation of invertible saccharides
US3639389A (en) 1968-05-15 1972-02-01 Cpc International Inc Low d.e. starch hydrolysate derivatives
FR2184454B1 (en) 1972-05-17 1975-06-20 Roquette Freres
US3876794A (en) 1972-12-20 1975-04-08 Pfizer Dietetic foods
US3935284A (en) 1973-10-19 1976-01-27 Ici United States Inc. Homogeneous hydrogenation of saccharides using ruthenium triphenyl phosphine complex
US4258110A (en) 1973-11-09 1981-03-24 Alvarez Mario Y Electrolytic device
US3963788A (en) 1974-08-20 1976-06-15 Kruse Walter M Polyhydric alcohol production using ruthenium zeolite catalyst
US4346116A (en) 1978-12-11 1982-08-24 Roquette Freres Non-cariogenic hydrogenated starch hydrolysate, process for the preparation and applications of this hydrolysate
FR2444080A1 (en) 1978-12-11 1980-07-11 Roquette Freres NON-CARIOGENIC HYDROGENIC STARCH HYDROLYSATE FOR CONFECTIONERY AND PROCESS FOR PREPARING THIS HYDROLYSATE
US4248895A (en) 1978-12-21 1981-02-03 Life Savers, Inc. Dehydrated higher polyalcohols, comestibles and chewing gum containing same and method
FR2445839A1 (en) 1979-01-08 1980-08-01 Roquette Freres HYDROLYSATE OF POSSIBLE HYDROGEN STARCH, PROCESS FOR THE PREPARATION THEREOF AND APPLICATIONS THEREOF
US4322569A (en) 1980-08-01 1982-03-30 Hydrocarbon Research, Inc. Catalytic hydrogenation of glucose to produce sorbitol
JPS57134498A (en) 1981-02-12 1982-08-19 Hayashibara Biochem Lab Inc Anhydrous crystalline maltitol and its preparation and use
JPS5882855A (en) 1981-11-05 1983-05-18 東洋製罐株式会社 Vessel cover with easily unsealed liner
FR2545834B1 (en) 1983-05-11 1985-08-30 Roquette Freres BEER WITH REDUCED ALCOHOL CONTENT AND PROCESS FOR PREPARING THE SAME
JPS6092239A (en) 1983-10-24 1985-05-23 Kawaken Fine Chem Co Ltd Preparation of gluconic acid
US4675293A (en) 1984-08-15 1987-06-23 Lonza Inc. Preparation of maltose and maltitol syrups
JPS61286318A (en) * 1985-06-13 1986-12-16 Ichiro Shibauchi Production of bathing agent
FR2597474B1 (en) 1986-01-30 1988-09-23 Roquette Freres PROCESS FOR THE OXIDATION OF ALDOSES, CATALYST IMPLEMENTED AND PRODUCTS THUS OBTAINED.
FR2597473B1 (en) 1986-01-30 1988-08-12 Roquette Freres PROCESS FOR THE OXIDATION OF DI-, TRI-, OLIGO- AND POLYSACCHARIDES TO POLYHYDROXYCARBOXYLIC ACIDS, CATALYST IMPLEMENTED AND PRODUCTS THUS OBTAINED.
DE68914401T2 (en) 1988-10-07 1994-08-25 Matsutani Kagaku Kogyo Kk Process for the production of fibrous food products containing dextrin.
GB8903593D0 (en) 1989-02-16 1989-04-05 Pafra Ltd Storage of materials
US5034231A (en) 1989-03-28 1991-07-23 Wm. Wrigly, Jr. Company Alitame stability using hydrogenated starch hydrolysate syrups
US5109128A (en) 1989-10-02 1992-04-28 Uop Continuous catalytic oxidation of alditols to aldoses
CA2034639C (en) 1990-05-29 2002-05-14 Alpha L. Morehouse Encapsulated products
US5200399A (en) 1990-09-14 1993-04-06 Boyce Thompson Institute For Plant Research, Inc. Method of protecting biological materials from destructive reactions in the dry state
JP3020583B2 (en) 1990-10-09 2000-03-15 日本食品化工株式会社 Method for removing bitterness of β-glucooligosaccharide
EP0572424B1 (en) 1991-02-20 1996-11-20 Pfizer Inc. Reduced polydextrose
IT1245063B (en) 1991-04-12 1994-09-13 Ferruzzi Ricerca & Tec PROCEDURE FOR OXIDATION OF CARBOHYDRATES
JPH0775515B2 (en) 1991-10-11 1995-08-16 日本食品化工株式会社 Frozen, freeze-dried denaturation-inhibiting substance, frozen and freeze-dried products containing the same, and method for producing the same
DE69122402T2 (en) 1991-12-23 1997-02-06 Cerestar Holding Bv Process for the production of oxygen acids from carbohydrates
FR2688792B1 (en) 1992-03-19 1994-06-10 Roquette Freres HYDROLYSATE OF STARCH HYDROGEN HYPOCARIOGENE, PROCESS FOR THE PREPARATION AND APPLICATION OF THIS HYDROLYSAT.
JPH05294837A (en) 1992-04-17 1993-11-09 Kao Corp Sebum-secretion promoting agent
CA2093499C (en) 1992-04-30 2003-07-01 Gerard J. Wansor Unsweetened, frozen, tea beverage concentrates
FR2693104B1 (en) 1992-07-03 1994-09-09 Oreal Cosmetic composition based on maltodextrin for maintaining and / or fixing the hairstyle.
FR2705207B1 (en) 1993-05-17 1995-07-28 Roquette Freres Hard coating process without sugar and products thus obtained.
JPH0770165A (en) 1993-06-28 1995-03-14 Hayashibara Biochem Lab Inc Nonreducing oligosaccharide, its production and use thereof
US5348737A (en) 1993-07-21 1994-09-20 Avlon Industries, Inc. Composition and process for decreasing hair fiber swelling
NL194919C (en) 1993-09-07 2003-07-04 Tno Process for oxidizing carbohydrates.
JP3533239B2 (en) 1994-03-01 2004-05-31 株式会社林原生物化学研究所 Maltohexaose / maltoheptaose-forming amylase, method for producing the same and use thereof
US5506353A (en) 1994-03-21 1996-04-09 Firmenich Sa Particulate hydrogenated starch hydrolysate based flavoring materials and use of same
US5955448A (en) 1994-08-19 1999-09-21 Quadrant Holdings Cambridge Limited Method for stabilization of biological substances during drying and subsequent storage and compositions thereof
FR2721823B1 (en) 1994-06-30 1996-08-02 Oreal Process for the permanent deformation of keratin materials
BR9408306A (en) 1994-10-17 1997-08-26 Firmenich & Cie Process for preparing particulate compositions particulate flavoring composition consumable edible material and process for flavoring tea leaves, tea powders or tea extracts
JP3625503B2 (en) 1994-11-11 2005-03-02 旭化成ファーマ株式会社 Composition-containing composition for clinical testing
US5641477A (en) 1994-11-28 1997-06-24 Avlon Industries, Inc. Reduction of hair damage during lanthionization with hair relaxers containing deswelling agents
FR2728436A1 (en) 1994-12-26 1996-06-28 Roquette Freres Sugar-free boiled sweets contg. polyol and with high water content
US5627273A (en) 1995-01-31 1997-05-06 National Starch And Chemical Investment Holding Corporation Method for preparing hydrophobically-terminated polysaccharide polymers and detergent compositions comprising the polysaccharide polymers
NL9500292A (en) 1995-02-16 1996-10-01 Stichting Nl Instituut Voor Ko Process for conversion of a starch material, and enzyme preparation useful therefor.
GB9514090D0 (en) * 1995-07-11 1995-09-13 Cerestar Holding Bv Non-catalysed oxidation of maltodextrin with an oxygen containing oxidant
US5690956A (en) 1995-09-27 1997-11-25 Sdg, Inc. Hair care perming agent
FR2740300B1 (en) 1995-10-30 1998-01-02 Roquette Freres SUGAR-FREE COATING OBTAINED BY HARD DRAGEIFICATION AND PROCESS FOR OBTAINING SAME
DE19542287A1 (en) 1995-11-14 1997-05-15 Suedzucker Ag Process for the preparation of di- and higher-oxidized carboxylic acids of carbohydrates, carbohydrate derivatives or primary alcohols
US5656584A (en) 1996-02-06 1997-08-12 The Procter & Gamble Company Process for producing a particulate laundry additive composition for perfume delivery
AU1675397A (en) 1996-02-09 1997-08-28 Cooperatie Cosun U.A. Modified inulin
DE69709794T2 (en) 1996-03-21 2002-05-02 Akzo Nobel Nv METHOD FOR THE OXIDATION OF DI-, TRI-, OLIGO- AND POLYSACCHARIDES TO POLYHYDROXYCARBOXYLIC ACIDS
US5795852A (en) 1996-04-24 1998-08-18 Lever Brothers Company, Division Of Conopco, Inc. Bar composition comprising nonionic polymeric surfacing as mildness enhancement agents
EP0839916B1 (en) 1996-05-15 2005-11-30 Nihon Shokuhin Kako Co., Ltd. Process for enzymatic preparation of nigerooligosaccharide
JP3634923B2 (en) 1996-07-19 2005-03-30 東和化成工業株式会社 Candy composition and method for producing candy using the same
DE19758788B4 (en) 1997-01-17 2007-12-13 Südzucker Aktiengesellschaft Mannheim/Ochsenfurt Stereo-selective hydrogenation of sugars to sugar alcohols with good purity - in aqueous solution, at high temperature and pressure, uses catalyst mixture of Raney metal and its alloy with inert core and active shell
US5965501A (en) 1997-03-28 1999-10-12 Lever Brothers Company, Division Of Conopco, Inc. Personal washing bar compositions comprising emollient rich phase/stripe
DE19751630A1 (en) 1997-11-21 1999-05-27 Bayer Ag Inclusion complexes of agrochemical agents
US5853487A (en) 1998-04-27 1998-12-29 Roquette Freres Process for producing low de starch hydrolysates by nanofiltration fractionation and blending of resultant products, preferably in liquid form, with other carbohydrates
AU1750500A (en) 1998-12-02 2000-06-19 Copa Distributors, Llc Gradual hair relaxation composition

Patent Citations (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4336152A (en) * 1981-07-06 1982-06-22 American Cyanamid Company Disinfectant/cleanser compositions exhibiting reduced eye irritancy potential
EP0618286A1 (en) * 1993-03-30 1994-10-05 AUSIMONT S.p.A. Process for decreasing the build up of inorganic incrustations on textiles and detergent composition used in such process
US5520840A (en) * 1995-03-22 1996-05-28 Lever Brothers Company Detergent bars comprising water soluble starches
US5756438A (en) * 1996-03-26 1998-05-26 The Andrew Jergens Company Personal cleansing product
WO1998042818A1 (en) * 1997-03-20 1998-10-01 The Procter & Gamble Company Laundry additive particle having multiple surface coatings
WO1998042814A1 (en) * 1997-03-21 1998-10-01 Unilever Plc Detergent bars comprising adjuvant powders for delivering benefit agent and process for manufacture of said bars
WO1999011748A1 (en) * 1997-08-28 1999-03-11 Unilever Plc Soap bars
WO1999036442A1 (en) * 1998-01-20 1999-07-22 Grain Processing Corporation Reduced malto-oligosaccharides

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