US20120128597A1 - Composition for prevention and treatment of allergic and/or inflammatory diseases - Google Patents
Composition for prevention and treatment of allergic and/or inflammatory diseases Download PDFInfo
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- US20120128597A1 US20120128597A1 US13/059,406 US200913059406A US2012128597A1 US 20120128597 A1 US20120128597 A1 US 20120128597A1 US 200913059406 A US200913059406 A US 200913059406A US 2012128597 A1 US2012128597 A1 US 2012128597A1
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- arabinogalactan
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K38/00—Medicinal preparations containing peptides
- A61K38/16—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof
- A61K38/168—Peptides having more than 20 amino acids; Gastrins; Somatostatins; Melanotropins; Derivatives thereof from plants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/70—Carbohydrates; Sugars; Derivatives thereof
- A61K31/715—Polysaccharides, i.e. having more than five saccharide radicals attached to each other by glycosidic linkages; Derivatives thereof, e.g. ethers, esters
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/02—Medicinal preparations containing materials or reaction products thereof with undetermined constitution from inanimate materials
- A61K35/10—Peat; Amber; Turf; Humus
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K35/00—Medicinal preparations containing materials or reaction products thereof with undetermined constitution
- A61K35/66—Microorganisms or materials therefrom
- A61K35/74—Bacteria
- A61K35/741—Probiotics
- A61K35/744—Lactic acid bacteria, e.g. enterococci, pediococci, lactococci, streptococci or leuconostocs
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K36/00—Medicinal preparations of undetermined constitution containing material from algae, lichens, fungi or plants, or derivatives thereof, e.g. traditional herbal medicines
- A61K36/18—Magnoliophyta (angiosperms)
- A61K36/88—Liliopsida (monocotyledons)
- A61K36/899—Poaceae or Gramineae (Grass family), e.g. bamboo, corn or sugar cane
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P11/00—Drugs for disorders of the respiratory system
- A61P11/06—Antiasthmatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P17/00—Drugs for dermatological disorders
- A61P17/06—Antipsoriatics
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P19/00—Drugs for skeletal disorders
- A61P19/02—Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
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- A—HUMAN NECESSITIES
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- A61P5/00—Drugs for disorders of the endocrine system
- A61P5/48—Drugs for disorders of the endocrine system of the pancreatic hormones
- A61P5/50—Drugs for disorders of the endocrine system of the pancreatic hormones for increasing or potentiating the activity of insulin
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- A—HUMAN NECESSITIES
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- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K39/00—Medicinal preparations containing antigens or antibodies
- A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
- A61K2039/55511—Organic adjuvants
- A61K2039/55516—Proteins; Peptides
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- A61K2039/57—Medicinal preparations containing antigens or antibodies characterised by the type of response, e.g. Th1, Th2
Definitions
- the present invention refers to an antiallergenic composition
- an antiallergenic composition comprising at least one arabinogalactan or arabinogalactan protein and/or humic acid.
- Allergic reactions of type I involve e.g. bronchial asthma, atopic dermatitis, urticaria, hay fever and food allergy.
- bronchial asthma atopic dermatitis
- urticaria urticaria
- hay fever atopic dermatitis
- food allergy atopic dermatitis
- the number of persons suffering from allergic disorders, chronic inflammatory disorders and/or autoimmune diseases is steadily increasing. The latest statistics show that about 30% of the European citizens suffer from allergies.
- Allergic reactions of type I are mediated by IgE antibodies, of which the production is regulated by Th2 cells.
- Th2 cells are present with an increased frequency compared to Th1 cells during allergic diseases.
- Th2 mediated immune response predominates, whereas during the first year of life Th1 mediated response increases and thereafter dominates the immune response (non-allergic response).
- the polysaccharide arabinogalactan, particularly arabinogalactan from larch is known to have immune modulating effects.
- G. S. Kelly describes in Altern Med Rev, 1999; 4:96-103 and N. L. Currier et al. in Phytomedicine, 2002; 10:145-153 immune enhancing properties of larch arabinogalactan by activation of NK cells.
- L. S. Kim et al. found in Altern Med Rev, 2002; 7:138-149 a stimulation of the components of the immune response in patients after taking larch arabinogalactan, particularly in combination with Echinacea.
- arabinogalactan differs dependent from the source for isolation. J. Duan et al. disclose in Carbohydr Res, 2003; 338:1291-1297 structural features of arabinogalactan with immunological activity from Diospyros kaki and I. Taguchi et al. in Carbohydr Res, 2004; 339:763-770 the structure of an immune modulating arabinogalactan from rhizomes of Atractylodes lancea. In all the prior literature the effect of arabinogalactan is described as increasing the immediate immune reactions.
- WO 01/49319 and EP-A 1 637 147 describe a composition or an extract of stable dust for prevention or treatment of allergic diseases.
- Lactococcus species primarily is described for oral uptake for probiotic approaches (e.g. Kimoto et al., Microbiol Immunol, 2004; 4:75-82; Perdigon, G. et al., Int J Immunopathol Pharmacol, 1999; 12:97-102; Villamil, L. et al., Clin Diagn Lab Immunol, 2002; 9:1318-1323; Vitini E. et al., Biocell, 2000; 24:223-32; Perdigon, G. et al.
- Lactococcus sp. for prevention and treatment of a disease is disclosed in connection with overweight or diabetes (KR1020010106068), stomach diseases (KR1020040044300) and rheumatic arthritis (EP-A 762 881).
- An antigen-antitoxin-mixture for preparation of a homeopathic composition for use in the area of heart diseases, hypertension and allergic diseases is described in DE-A 100 07 771.
- the object of the present invention was to provide a means or remedy for prevention and/or protection against and/or treatment of allergic and/or inflammatory diseases.
- a prophylactic antiallergenic composition comprising at least one arabinogalactan or arabinogalactan protein and/or humic acid.
- arabinogalactan primarily means the arabinogalactan polysaccharide unit which is part of an arabinogalactan protein or arabinogalactan peptide naturally occurring in e.g. various plants.
- the arabinogalactan can be isolated from said plants by isolating the arabinogalactan protein or peptide and thereafter separating the sugar from the protein/peptide or by using an isolation technique where the arabinogalactan immediately is separated and can be isolated as such.
- the isolated arabinogalactan is preferred, however, the effect of the arabinogalactan is not significantly decreased when the arabinogalactan protein or peptide is used. Therefore it is not relevant to separate the arabinogalactan from the protein/peptide, as long as the arabinogalactan is present in the composition according to the invention.
- the composition contains at least one arabinogalactan.
- Arabinogalactans of different plants may have different structures, particularly concerning the sugar composition, sequence and bonding type. Thus, different 3D structures of the arabinogalactans result depending on the preparation pathways of the plant which is the source for isolation.
- any arabinogalactan can be used, however, preferably the arabinogalactan is one isolatable from any grass.
- isolated is meant that the arabinogalactan is either isolated from a natural source, which is preferably a grass, or the arabinogalactan is isolated from any other source or is artificially prepared (e.g. synthesized), however has the same structure as an arabinogalactan isolated from the natural source (preferably grass).
- One preferred arabinogalactan is isolatable from Meadow Foxtail ( Alopecurus pratensis ), another preferred one can be isolated from timothy grass and timothy grass pollen ( Phleum pratense L) or Cock's Foot ( Dactylis glomerata ) or England Fog ( Holcus lannatus ) or English Raygrass ( Lolium perenne ) or Smooth Meadow grass ( Poa pratense ) or Rye ( Secale cereale ) or grasses from related species as well as mixtures of at least two of these preferred arabinogalactans can be used.
- an arabinogalactan having a structure shown in FIG. 1 is particularly preferred.
- An arabinogalactan having a structure as shown in FIG. 1 according to the present invention can be used as a means or remedy or medicament as such without any further active ingredient for the prevention, protection against or treatment of any of the diseases mentioned below, since such an arabinogalactan has a particularly high effect already alone.
- a mixture of at least one of the preferred arabinogalactans with at least one further arabinogalactan can be used without any further active ingredient.
- Humic acid is one product of decomposition of organic material and has a structure shown in FIG. 3 .
- Humic acid has an immunomodulating effect in living organisms as it is shown in the examples below and therefore can be used alone for prevention, protection or treatment of the diseases discussed herein.
- humic acid is used in combination with at least one arabinogalactan, particularly preferred with at least one of the arabinogalactans which are mentioned above as preferred.
- composition of the present invention comprises (a) at least one arabinogalactan or arabinogalactan protein and at least one further active ingredient selected from the group of (b) naturally occurring, isolated bacteria of the genus Lactococcus or fragments thereof and/or (c) humic acid.
- naturally occurring bacteria means, that the bacterium/bacteria is/are not genetically engineered and is/are isolatable from any natural source.
- isolated as well is meant that the bacteria can be isolated from a natural source, however, as well they can be grown and cultivated under defined conditions, e.g. as cell cultures.
- the present invention involves the use of bacteria of the genus Lactococcus as naturally occurring, non-genetically engineered, particularly non-transgenic microbe.
- bacteria Preferably said bacteria are used in isolated form. This means that either at least one Lactococcus species, preferably L. lactis, or a mixture of Lactococcus species in isolated and optionally purified form are added to the pharmaceutical composition. Further fragments of the bacteria can be used.
- fragments is used here for membrane parts and membrane ingredients, cell wall proteins, particularly glycosylated proteins (others than arabinogalactan proteins), polysaccharides (others than arabinogalactan), lipopolysaccharides (endotoxines), cytosolic proteins, molecules and/or compounds and/or metabolites expressed or synthesized by the bacteria, nucleic acids and/or any other ingredient which is part of the original bacterium.
- glycosylated proteins others than arabinogalactan proteins
- polysaccharides others than arabinogalactan
- lipopolysaccharides endotoxines
- cytosolic proteins molecules and/or compounds and/or metabolites expressed or synthesized by the bacteria, nucleic acids and/or any other ingredient which is part of the original bacterium.
- a mixture of bacteria fragments and undestroyed bacteria can be used.
- the non-fragmented bacteria can be used as living organisms or after any denaturation step. Since the mentioned bacteria themselves are harmless for mammal organisms the use in vital form corresponds to natural occurrence and is a preferred embodiment of the invention.
- a method for sterilisation of the composition can be applied like e.g. using an autoclave, cooking or heating the organisms, use of bactericides, bacteriastatica, fungicides, fungistatica, viricides and/or viristatica, UV rays or use of organic solutions which are toxic for bacteria like e.g. alcohols, particularly ethanol, propanol, isopropanol etc., lyophilisation or sterilisation by coldness.
- the combination of (a) at least one arabinogalactan or arabinogalactan protein with at least one of the components (b) and (c) increases the effect of the application of arabinogalactan alone. Whereas (a) induces a significant proinflammatory response and a tolerization of the immunological T-cell response by downregulating both Th1 and Th2 activation as demonstrated by suppression of cytokines in stimulated spleen cells from mice and downregulation of all antibody responses, (b) also activates proinflammatory cytokines and selectively activates Th1 response. Instead, (c) does not activate proinflammation but at the same time leads to a tolerance effect.
- composition of the present application is that all the ingredients themselves are absolutely harmless for mammals, however, according to the present invention it has been found that they can be used for long term prevention or protection against allergic or inflammatory diseases.
- Arabinogalactan, the mentioned bacteria as well as humic acid can be found anywhere in the environment and no negative influence for good health is known.
- Application of at least arabinogalactan, preferably the composition of the present invention before any onset of an allergic or an inflammatory disease can prevent such a disease or can alleviate the violence of outbreak. This is what is meant with “prevention” or “protection”.
- the origin of the ingredients (a), (b) and/or (c) is not relevant for the present invention as long as they fulfill the requirements that they are harmless, and they correspond to the definition given above for the ingredients (a), (b) and (c).
- Sources for isolation of the arabinogalactan preferably is grass and for the bacteria preferably are grass, hay, dust of houses, dust of cowsheds, food, fruits and similar. After isolation the ingredients may be purified or cultivated (bacteria). However, as well the ingredients can be commercially obtained.
- each of the components (a), (b) and/or (c) can be isolated from any suitable source and optionally purified or can be commercially obtained.
- at least one of the preferred arabinogalactans e.g. as shown in FIG. 1
- the carrier either can be a dissolvent like e.g. water or an alcohol, without being limited to these, or a solution as mentioned above, or can be any suitable dry carrier like e.g. ground silicate, starch, cellulose and cellulose derivatives and similar without being limited to these.
- each of the components (a), (b) and/or (c) to result in the composition is not relevant and depends only on their availability and the comfort of the preparing person or device.
- a liquid composition containing at least component (a) and optionally at least one of the components (b) and (c) are prepared by addition of at least one arabinogalactan to an aqueous or aqueous-alcoholic solution, thereafter optionally either adding one of the components (b) and (c) or adding both sequentially or both together.
- Addition of the bacteria (b) may be employed either directly after isolation and optional purification or they can be denaturated and/or fragmented before they are added to the other ingredients or the carrier. Furthermore any sterilisation step can be carried out or any sterilizing agent can be added to the composition, e.g. any of the sterilizing methods or agents mentioned above.
- Humic acid as component (c) as well can be added directly after isolation or as a commercially available product.
- Either each of the components or the ready-prepared composition can be lyophilized after preparation to provide a storage stable product for direct application or for uptake with water or any other suitable solvent before use.
- At least one arabinogalactan or the composition can be applied already immediately after birth of a child or during the first life period.
- the composition is suitable for application for infants (babies) or pregnant women, e.g. for whom is known due to a positive family anamnesis that they have an increased risk to develop any allergic or chronic inflammatory disease or which show first signs of such disease. Prevention for the infants may already be obtained by application of the arabinogalactan or the composition according to the invention to the pregnant mother.
- the composition is suitable and can serve for modification of the infant and adult immune system. Therefore the composition or the ingredients (a), (b) and/or (c) can be applied to pregnant women, infants (babies), children during the first years of life (up to 8-10 years) and adults for treatment preferably repetitively. Preferably the composition or the ingredients are applied to pregnant women, infants, children or adults who have due to several diagnostic features an increased risk to develop any allergic or chronic inflammatory disease. The composition or the ingredients (a), (b) and/or (c) can also be applied to pregnant women, infants, children or adults who already show first signs of an allergic or chronic inflammatory disease. An increased risk as well can be determined by genetic analysis.
- One advantage of the present invention is high efficacy whereas the inventive composition can be applied by any easy conventional route.
- Application can be via oral, nasal, conjunctival, inhalative, subcutaneous, intra-articular, intraperitoneal, rectal or vaginal route. Oral, nasal or inhalative application is preferred.
- the composition is provided as a pharmaceutical composition in form of an aerosol, solution, preferably aqueous or aqueous-alcoholic solution, suspension, lyophilisate, powder, tablet or suppository.
- a pharmaceutical composition in form of an aerosol, solution, preferably aqueous or aqueous-alcoholic solution, suspension, lyophilisate, powder, tablet or suppository.
- Most of these embodiments are particularly suitable for nasal, oral or inhalative application.
- An aerosol according to the invention comprises small solid or liquid particles, which can be prepared by an inhalator, a fogging device or respiratory device.
- the particles of the aerosol can consist of the composition or can contain the composition in combination with a suitable supporting material.
- the aerosol can have a particle size e.g. of up to 100 ⁇ m for nasal application.
- the aerosol preferably has a particle size of up to 10 ⁇ m, preferred of up to 5 ⁇ m.
- a solution according to the invention can contain at least one arabinogalactan and optionally at least one of components (b), preferably soluble fragments of components (b), and/or component (c) preferably in form of an aqueous solution or an aqueous-alcoholic solution.
- components (b), preferably soluble fragments of components (b), and/or component (c) preferably in form of an aqueous solution or an aqueous-alcoholic solution.
- Said solution can be buffered or can contain further optional ingredients like salt, preferably salt in isotonic amounts (e.g. physiological isotonic NaCl solution).
- Further said solution can contain further harmless ingredients, e.g. natural or synthetic additives like conserving agents, stabilizers, flavours like sugar, pharmaceutically suitable carriers, emulsifiers, diluents and if desired natural dying agents.
- the composition can be in form of a suspension.
- a solution can be used as described above.
- composition can be a lyophilisate or a powder or can be mixed with a pharmaceutically applicable powder.
- a lyophilisate or powder can be combined with any further pharmaceutically acceptable ingredients, e.g. for application with a powder inhalator.
- the powder or lyophilisate can be used to prepare a tablet or suppository for oral, anal or vaginal application.
- the composition or the active ingredients are applied to pregnant women, infants or children within the first five years of life, more preferably within the first two years of life or to adults with a risk of respective diseases.
- the composition may be applied by any commonly known route, preferably by an inhalator, evaporator, fogging device, atomizer or respiratory device. It can be applied periodically over a longer time period to obtain a continued stimulation in the organism.
- the composition or the active ingredients can be applied up to 10 years once up to 21 times per week, preferably 7 times to 14 times per week.
- Application can be obtained by injection of a spray in the nose or by inhalation. In the last case the duration can be between 1 and 120 minutes, preferably between 5 and 60 minutes.
- composition can be carried out by any suitable means.
- the components (a), (b), and (c) alone or in combination are applied in a concentration of 1 ng to 100 g/day or 10 2 to 10 11 cfu/day, respectively.
- the components (a), (b,) and (c) are applied in a concentration of 1 ⁇ g to 10 g/day or 10 4 to 10 10 cfu/day, respectively.
- the present invention further provides a prophylactic antiallergenic, i.e. health-improving indoor air product.
- a prophylactic antiallergenic i.e. health-improving indoor air product.
- the composition described above is provided in a form suitable to be distributed in the indoor air and forms part of an indoor air product.
- the present invention further provides a composition comprising at least one arabinogalactan or arabinogalactan protein and/or humic acid, as described above, for the prophylaxis and/or treatment of allergic or chronic inflammatory diseases, that does not have to be administered via conventional pharmaceutical routes, i.e. oral, subcutaneous, intra-articular, intra-peritoneal, rectal, vaginal, conjunctival, nasal or inhalative routes using an inhaler, nebulizer or vaporizer equipped with a mouthpiece/facemask.
- the indoor product of the present invention comprises the composition of the present invention in a form suitable to be distributed in the indoor air.
- the composition forming part of the indoor air product can be simply distributed in the indoor air to generate a health-improving indoor air, thus simulating the healthy air in natural farming environments.
- the indoor air product of the present invention has several advantages over conventional pharmaceutical compositions.
- the composition comprised therein may be easily administered to very young children, and even newborn babies.
- all persons present in the room participate on the health-improving effect.
- the composition may also be sprayed on items the child often comes into contact with, such as soft toys, upholstery, bed linen, mattresses, pillows, blankets, and the like.
- indoor air is the (breathing) air inside a closed or closable space usually occupied by human beings, for example a residence, an office or a public building or a vehicle, a plane, a train and the like.
- the composition may be prepared as explained above, i.e. any of the aforementioned functional ingredients may be obtained by harvesting from natural sources, chemical synthesis, or biotechnological procedures and mixing them afterwards. If the composition comprises more than one functional ingredient, each of said ingredients may be independently harvested from a natural source, chemically synthesized, or biotechnologically produced. If two or more functional ingredients present in one composition are obtained in the same way, i.e. both harvested from natural sources, they may be obtained in the same procedure, i.e. simultaneously harvested from the same origin, or may be harvested from different origins and thereafter mixed together.
- the arabinogalactan may be used in an isolated from, i.e. separated from any further organic (plant or bacterial) material of its natural origin, but in particular in the indoor air product of the present invention it may as well be used in a form in which it is bound or otherwise associated to organic material of its natural origin.
- the composition comprises the functional ingredients, i.e. the arabinogalactan, arabinogalactan protein and/or humic acid and further active ingredients, in the form of a stable dust extract, a hay extract, or a grass extract, or a mixture thereof.
- these extracts usually comprise more than one functional ingredient in the sense of the present invention.
- the use of an extract offers the possibility for simultaneously obtaining more than one functional ingredient in one single process step.
- non-pathologic, non-transgenic isolated bacteria said bacteria preferably being selected from the group consisting of Lactococcus and Acinetobacter, or fragments thereof, or mixtures thereof may be added.
- Extracts from stable dust samples may be obtained by any method known to a person skilled in the art for this purpose. It is, however, preferred to use the following procedure: At first the dust samples are optionally homogenized, for example using a mortar, a triturator or a mill. The dust is then suspended in water or isotonic saline (0.9% aqueous solution of sodium chloride) at room temperature (20 to 25° C.), preferably 22° C., after which a certain amount of glass beads, preferably having a diameter of 0.1 to 2 mm, more preferably 0.4 to 0.6 mm, are added and the mixture is mechanically disintegrated, for example by using a homogenizer or a shaking apparatus for several hours. After disintegration is judged completed, the sample components are separated by centrifugation, the supernatant is collected, dialyzed against water and then lyophilized.
- isotonic saline (0.9% aqueous solution of sodium chloride
- Stable dust samples may also be collected using an impactor, as described for example in WO 01/49319.
- Microorganisms, in particular bacteria, may be obtained from such samples using cell culture.
- Specific strains may be collected from such cultivated samples, isolated and further cultivated, as described for example in EP 1 964 570 A1.
- the extraction solvent preferably is water, more preferably isotonic saline.
- the solution obtained may be lyophilized in order to obtain a dry powdered substance, or the extract may be directly processed further.
- the one or more functional ingredients preferably are dispersed or dissolved in a solvent, preferably in water, more preferably in isotonic saline.
- the composition comprised in the indoor air product of the present invention may additionally comprise a finely divided excipient, preferably a solid excipient, more preferably selected from the group consisting of lactose, sodium chloride, acetate, citrate, lactate, sulfite or benzoate. Said excipient acts as an inert carrier substance, improving the suspension stability, dosing precision, and chemical stability of the functional ingredient.
- composition comprised in the indoor air product of the present invention additionally may comprise a propellant, preferably selected from the group consisting ofbutane, propane, carbon dioxide or compressed air.
- a propellant preferably selected from the group consisting ofbutane, propane, carbon dioxide or compressed air.
- the propellant preferably is free from any fluorochlorinated hydrocarbons (CFC).
- said composition additionally may comprise a surface-active agent or emulsifier.
- a surface-active agent or emulsifier Any suitable agent can be used without any restriction of the invention, however, preferably the surface-active agent or emulsifier is selected from the group consisting of commonly known phosphates, polysorbates, lecithine, mono- or diglycerides or other fatty acid derivatives.
- the amount of functional ingredients in the composition preferably is in the range of 0.001 to 20 mg/ml, more preferred 0.01 to 15 mg/ml and even more preferred 0.1 to 10 mg/ml.
- the indoor air product composition of the present invention preferably additionally comprises (1) a container for storing the composition and (2) a dispenser for distributing the composition in the indoor air, wherein the composition preferably is distributed in the indoor air in the form of a plurality of spray droplets or finely divided particles.
- Said spray droplets or particles preferably have a diameter in the range of from 1 to 500 ⁇ m, preferably 5 to 300 ⁇ m
- the size and shape of the container are not particularly limited. Any container for storing a room spray composition known in the state of the art may be used.
- the propellant and at least one functional ingredient may be comprised in the same storage container or may be comprised in separate containers, and mixed only upon the process of distributing the composition in the indoor air.
- the container is equipped with a fixing device for fixation at the wall, room ceiling or rod of a bed or other furniture.
- the shape of the container is adapted to the type and shape of dispenser, which is well-known to a person skilled in the art.
- the dispenser preferably is selected from the group consisting of foggers, nebulizers, or sprayers. Any type of dispenser suitable for distributing/spraying liquids is usable according to the present invention and doesn't restrict the inventive concept.
- a refillable and reusable container and dispenser is a preferred embodiment wherein the liquid composition comprising the functional ingredient(s) can be refilled in the container.
- the inventive composition can be distributed in the indoor air by an air humidifier.
- composition comprised in the indoor air product of the present invention can be used for generating a health-improving indoor air.
- the present invention also comprises a method of generating a health-improving indoor air, comprising the step of distributing the composition of the indoor air product of the present invention in form of a plurality of spray droplets or particles in the indoor air.
- the composition is preferably distributed in the indoor air by using a dispenser as described above.
- FIG. 1 Structure of arabinogalactan isolatable from timothy grass pollen ( Phleum pratense L.). According to NMR spectroscopical analyses (see FIG. 2-4 and Table 1), the arabinogalactan from Meadow foxtail ( Alopecurus pratensis ) comprises very similar structures.
- FIG. 1 a Structural detail of arabinogalacan 1 of Phleum pratense. L. Brecker et al. Carbohydr Res, 2005; 340:657-663
- FIG. 1 b Structural detail of arabinogalacan 2 of Phleum pratense. L. Brecker et al. Carbohydr Res, 2005; 340:657-663
- FIG. 2 Concentration of arabinogalactan isolated from A. pratensis (AGP PB320) compared to known concentrations of arabinogalactan from gum Arabic by means of radial diffusion assay.
- FIG. 3 1 D 1 H NMR spectrum of the arabinogalactan from Alopecurus pratensis.
- FIG. 4 2 D 1 H, 1 H correlation spectrum (COSY) of the arabinogalactan from Alopecurus pratensis.
- FIG. 5 2 D 1 H, 1 H total correlation spectrum (TOCSY) of the arabinogalactan from Alopecurus pratensis.
- FIG. 6 Structure of humic acid
- FIG. 7 Sensitization and treatment protocol for eliciting asthma in mice and treatment with arabinogalactan or humic acid. See example 2.1
- FIG. 8 Number of eosinophilic granulocytes in airways of mice that were sensitized with ovalbumin and treated with either arabinogalactan or humic acid. See Example 2.2.
- FIG. 9 Infiltration of eosinophilic granulozytes in mice that were treated with Lactococcus lactis during sensitization. See Example 2.2.
- FIG. 10 Interleukin-5 production of splenocytes of mice that were treated with arabinogalactan or humic acid. See Example 2.2.
- FIG. 11 Measurement of local IgE production in mice that were treated with arabinogalactan or humic acid during sensitization. See Example 2.3.
- FIG. 12 Number of eosinophilic granulocytes in airways of mice that were sensitized with ovalbumin and treated with combinations of Lactococcus lactis and arabinogalactan during sensitization. See Example 2.4.
- FIG. 13 Measurement of local IgE production in mice that were sensitized with ovalbumin and treated with combinations of Lactococcus lactis and arabinogalactan during sensitization. See Example 2.4.
- FIG. 14 Number of eosinophilic granulocytes in airways of mice that were sensitized with ovalbumin and treated with combinations of arabinogalactan and humic acid during sensitization. See Example 2.5.
- FIG. 15 Measurement of local IgE production in mice that were treated with combinations of Lactococcus lactis and arabinogalactan during sensitization. See Example 2.5.
- FIG. 16 Number of eosinophilic granulocytes in airways of mice that were sensitized with ovalbumin and treated with arabinogalactan from gum arabic, larch (Larix) or hay during sensitization. See Example 2.6.
- FIG. 17 Number of eosinophilic granulocytes in airways of mice that were sensitized with ovalbumin and treated with arabinogalactan from Yorkshire Fog ( Holcus lanatus ) during sensitization. See Example 2.7.
- Ovalbumin Ovalbumin
- mice were sensitized by intraperitoneal injection of 20 ⁇ g ovalbumin (OVA; GradeV; Sigma, St. Louis, Mo.) emulsified in 2.2 mg aluminum hydroxide (Imject Alum; Pierce, Rockford, Ill.) in a total volume of 200 ⁇ l on days 1 and 14. On days 28 and 38 mice were challenged via the airways with 1% OVA aerosol for 20 min ( FIG. 7 ) using a PARI-Boy aerosol generator. Controls were injected with aluminum hydroxide alone and challenged with PBS aerosol (non-sensitized).
- OVA ovalbumin
- PBS aerosol non-sensitized
- mice Treatment of mice was done by intranasal application of arabinogalactan (0.5 ⁇ g or 5 ⁇ g) or humic acid (1 ⁇ g or 10 ⁇ g) in 50 ⁇ l volume or by intranasal application of 10 8 cfu lyophilized bacteria, respectively. Mice were treated for a total of 14 times starting on day 1 of sensitization with the last application 10 days before the final challenge. For this procedure mice were anesthetized with a mixture of Ketamin and Xylazin. The sensitization and treatment protocol is shown in FIG. 7 .
- mice After treatment of mice with arabinogalactan, humic acid or Lactococcus lactis during sensitization eosinophilic infiltration of cells in the airways were analyzed. Since eosinophilia depends on IL-5 production of Th2 cells production of this cytokine after restimulation of cells with allergen was also studied.
- IgE Since one major characteristic of atopic disease is production of IgE said IgE production was measured in mice that were treated with arabinogalactan or humic acid or Lactococcus lactis during sensitization ( FIG. 11 ).
- mice were treated with a submaximal dose (10 6 or 10 7 cfu) of Lactococcus lactis in combination with a submaximal dose (1 ⁇ g) of arabinogalactan from Meadow foxtail ( Alopecurus pratensis ) according to the protocol shown in FIG. 7 and the description in examples 2.2 and 2.3.
- a submaximal dose 10 6 or 10 7 cfu
- a submaximal dose (1 ⁇ g) of arabinogalactan from Meadow foxtail ( Alopecurus pratensis ) according to the protocol shown in FIG. 7 and the description in examples 2.2 and 2.3.
- Table 2 as well as FIG. 12 and FIG. 13 , respectively, the combination resulted in less eosinophilic granulocytes ( FIG. 12 ) and less OVA specific IgE ( FIG. 13 ) in the bronchoalveolar lavage of treated mice compared to accordant controls.
- mice were treated with 1 ⁇ g or 5 ⁇ g arabinogalactan from Meadow foxtail ( Alopecurus pratensis ) and 10 ⁇ g humic acid simultaneously according to the protocol shown in FIG. 7 and the description in examples 2.2 and 2.3.
- the combination resulted in less eosinophilic granulocytes ( FIG. 14 ) and less total IgE ( FIG. 15 ) in the bronchoalveolar lavage of treated mice compared to controls.
- mice were also treated with 5 ⁇ g arabinogalactan from gum arabic, larch ( Larix ), hay or Yorkshire Fog ( Holcus lanatus ), respectively, in order to compare the effects of arabinogalactans from different sources.
- Experiments were conducted according to the protocol shown in FIG. 7 and the description in example 2.2.
- arabinogalactans isolated from hay or grass species reduced the number of eosinophilic granulocytes considerably more than the arabinogalactans isolated from other plants.
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Also Published As
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WO2010020379A1 (fr) | 2010-02-25 |
US20160296596A1 (en) | 2016-10-13 |
EP2346512A1 (fr) | 2011-07-27 |
US9375444B2 (en) | 2016-06-28 |
US20140154290A1 (en) | 2014-06-05 |
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