The present invention relates to isometric agglomerates of a nearly spherically shaped form, especially bath beads, and the cosmetic, therapeutic and hygienic use thereof. The invention is especially concerned with agglomerates on the basis of carriers of natural origin such as collagen, gelatine, starch, cellulose or urea, which comprise both lipids and vesicle forming agents as well as emulsifying components and optionally additives, without impairing the stability or activity thereof.
The agglomerates when contacting water, especially in a bathing, will form liposomal mono- up to multi-layer structures thereby enabling an improved transport of active compounds. This will result in an improved balneological/or therapeutic action as well as a caring effect in the sense of a reconstruction of the skin protection barrier function.
Heretofore bath products have been mostly liquid preparations in the form of surfactant (tenside) solutions with the addition of ethereal oils and other active components, gels, especially for shower purposes, or in the form of dissolved salts. Among the liquid preparations, those tenside products which contain a proportion, —possibly a very high proportion—of oils and other fat-like products, are in a class by themselves. In a specific embodiment such bath oils may further contain vesicle forming lipids and water dispersible tensids (having an HLB=hydrophilic-lipophilic balance value of 6-13). Such bath oils are capable of the spontaneous formation of liposomes (see German Patent application No. DE 42 05 548 A1). However it is known, that pure O/W-(oil-in-water) tensides may impair liposomal structures. Also known are solid bath additives, namely powders or granulates, comprising besides the CO2— releasing compounds lipid compounds, W/O-(water-in-oil) and optionally O/W-surfactants (tensides) as well as vesicle forming components, and optionally suitable additives, cf. European Patent EP B 0930 064 B1. Such compositions address the problem to transfer the combinations of surfactants and lipids known from fluid bath preparations to solid bath preparations such as effervescent bath tablets although such compressed products, in order to maintain stability, may contain only small amounts of fluids and lipids. In fact the addition of liquid or pasty lipids and tensides adversely affects the flow and tableting and the galenically relevant properties of the compressed products with regard to friability, strength and solubility. However such flow and stability problems are particularly relevant with regard to the production of individually measured solid forms just as very small particulate spherical micropellets (isometrical agglomerates). By the term “isometric agglomerate”, is usually intended a small, almost spherical solid form having an average particle size of about 0.5 up to 5 mm. Because of its condition it is difficult to achieve both a uniform application of substances as well as a continued stability while avoiding an undesired particle aggregation, particularly in case a specific delivering rate and—modus of desired compounds is intended. On the other hand there is a risk of hygroscopic changes in products containing salts.
The U.S. Pat. No. 4,093,745 discloses a non aggregating free-flowing bath bead composition by admixing urea prills with an oily emollient (emollients such as triglycerides or fatty acid alcohol esters). Optionally, in dependence of the desired purpose, powdered surfactants, especially sulphuric tensids, may be added. Additives such as colouring agents—which are especially desired because of the colouring of the bathing—may be applied in the form of a watery solution. In case additives are non-absorbable, they are first encapsulated into a water soluble powder such as starch or dextrin. However such material may lead to a sticky surface, which consequently may be covered by spraying coating surfactants onto that surface. However liposomal structures are not obtained.
Urea is a known substance which may also be used as moisturizing additive in smaller amounts, e.g. in water containing compositions, comprising specific lipids and active ingredients related thereto, optionally tensides as well as defined lipid transfer proteins, see DE 10 2005 056 538 A1.
However it were desirable if the aforementioned limitations and reductions in view of the stability or the flow properties of bath beads could be overcome and moreover liposomal structures within the bathing and with the application of water, respectively, were formed, in order to achieve an improvement of the skin caring as well as of optionally incorporated active ingredients, whereby in addition a highly comfortable management of the product were possible.
An object of the present invention therefore is to provide isometric agglomerates (such as spherical micropellets), in particular bath beads, especially on a natural basis, achieving an improvement concerning the active ingredient as well as skin caring effect without limitations concerning the stability and the application on the one hand and the activity on the other hand. Furthermore, when used these agglomerates shall produce liposomal structures spontaneously.
These objects are achieved by the following subjects:
According to the invention there are provided isometric agglomerates especially having a nearly spherical form, in particular bath beads, the carrier of which preferably being composed of a material selected from the group comprising collagen hydrolyzate originating from plants, animals or marine products; gelatine or gelatine hydrolyzate, cellulose, starch or urea. Within the agglomerate such carrier comprises a mixture of one or more, particularly natural, liquid lipids and solid to waxy lipids as well as at least one vesicle forming component and an emulsifier mixture of at least one dispersable (dispersion) compound(s) and at least one O/W-compound(s) as well as optionally active ingredients and/or additives, selected from the group comprising conditioning agents, perfumes, dyes. Such agglomerates may be prepared in a mixing apparatus usually known for the production of tablets. The invention insofar concerns isometric agglomerates having a nearly spherical form, and comprising:
80 to 97%, or 80 to 96%, by weight of a carrier, selected from the group comprising collagen hydrolyzate originating from plants, animals or marine sources; gelatine or gelatine hydrolyzate; cellulose; carbohydrates, starch or urea; as well as
It may also be preferred if the agglomerates comprise
Surprisingly, when introduced into water, stable liposomal-, especially mono- up to multi layer structures (vesicles) are formed by the agglomerates and bath beads, respectively as described above which liposomal structures (vesicles) especially being useful in the transport of active ingredients or lipidic components. This could not be expected, the more so as there is a great amount of O/W-emulsifiers, which are considered as not being favourable in regard to the formation of liposomal structures. Furthermore, also solid lipids are applied. Moreover, it could not be expected, that liposomal structures may be formed within the bathing, since the lipid is adsorbed or even absorbed within the core of the pellet, and since specific requirements concerning the emulsifiers are necessary to deliberate the vesicle forming lipids differing from those requirements to deliberate the lipids. It was therefore also especially surprising since—starting from vesicle forming granulates or powders—there is presently a completely different surface condition in the present agglomerates with respectively different conditions concerning adsorption and absorption.
In the present
The agglomerates according to the present invention in particular comprise at least 80% by weight, preferably 80 to 97% by weight, and more preferred 85 to 96% by weight of the carrier material. The carrier material is selected from natural, especially water-soluble base materials such as collagen hydrolyzate, e.g having a molecular mass of at most 50 000 D; which can be obtained from plant, animal or marine sources; gelatine/gelatine hydrolyzate, having a molecular mass of about 1 500 up to 250 000 D, preferably 50 000 D up to 250000 D; cellulose having an average molecular mass of 50 000 D up to 500 000 D, preferably 50 000 D up to 250 000 D; carbohydrates such as saccharose, fructose, dextrose; starch (e.g. rice starch, wheat starch, corn and potato starch), or else urea. A preferred carrier material is urea. The water-soluble carriers themselves are essentially anhydrous (with probably a very low amount resulting from the production) and are of an essentially spherical form.
Within the agglomerates according to the invention such carriers comprise a lipid phase (lipid layer). The lipids are selected from the group comprising liquid lipids a1) such as natural oils, as well as solid to semisolid (wax like) lipids a2) such as hydrogenated natural oils, or mixtures of a1) and a2). Preferred lipids are selected from mixtures of one or more lipids according to a1) and one or more lipids according to a2) (for example mixtures of one or more liquid lipids a1) and one or more solid/wax like lipids a2)), for example in a ratio of 1:1 to 1:7.
Preferred liquid lipids (oils) are selected from the group comprising:
Olive oil, sunflower oil, soy oil, peach pit oil, apricot pit oil, grape seed oil, castor bean oil, peanut oil, almond oil, mink oil, wheat germ oil, sesame oil, thistle oil, almond oil, avocado oil, shea butter or illipé butter; natural liquid waxes, e.g. jojoba oil or its substitute, oleyl erucate; coconut oil, borage oil, corn oil, walnut oil, palm (germ) oil, macademia nut oil, hazelnut oil, rosehip oil, cotton seed oil, papaya (paw paw) oil, or mixtures thereof.
Preferred liquid lipids (plant oils) are selected from (the group comprising) soy oil sunflower oil, wheat germ oil, olive oil, or mixtures thereof.
The preferred solid to wax like lipids a2) are preferably selected amongst hydrogenated soy oil, hydrogenated palm oil, hydrogenated caster oil, hydrogenated sunflower oil.
Also hydrogenated macademia nut oil, hydrogenated coconut oil may be suitable.
The lipids are preferably present in a total amount of from 0.1 up to 10% by weight, especially 0.5 up to 5% by weight. In case of mixtures of both liquid and solid lipids, an excess of the solid lipids vis a vis the liquid lipids is preferred.
Preferred solid lipids are particularly selected from (the group comprising) hydrogenated soy (bean) oil, hydrogenated palm oil and hydrogenated sunflower oil, or mixtures thereof.
The water-soluble carriers within the agglomerates according to the invention further comprise an emulsifier combination comprising (at least one) a dispersion component (agent) c) and (at least one) an O/W-emulsifier component d). Thereby an excess of the O/W-emulsifier is especially preferred.
Preferably, the ratio between the O/W-emulsifier(s) d) and the dispersion component(s) (agent) c) is greater > than 1, especially 1:2 up to 1:8, in particular 1:4 up to 1:7.
The dispersion components (agents) c) are preferably chosen amongst those substances, having an HLB-value of between 7 and 11, preferably 7.5 to 10. Such compounds are in particular non ionic substances such as fatty alcohols such as cetearyl alcohol, or monoglycerides such as glycerol stearate; furthermore lower polyethoxylated or lower polypropoxylated and mixed lower polyoxylated C8-22 fatty alcohols having an ethoxylation and/or propoxylation degree (EO-PO degree) of between 1 and 5 (EO/PO). Preferred compounds are low poly(eth)oxylated C8-22 fatty alcohols having an ethoxylation degree (EO-degree) of between 1 and 5. Such compounds may be selected from macrogollaurylethers having 1 to 4 EO units such as laureth-2, laureth 3, laureth-4 (polyoxyethylene lauryl ether having 2, 3 and 4 EO units, respectively), or mixtures thereof.
Suitable O/W emulsifiers d) may particularly be selected from those having an HLB value of preferred 13 and 40, preferably 13-25, more preferred 13.5 to 20, and especially 13.5 to 17. These are in particular higher polyethoxylated (EO) and/or higher polypropoxylated (PO) or higher mixed (BO/PO) polyoxylated C8-22-fatty alcohols, (especially alkyl-C10-18 fatty alcohol alkoxylates), or such ethoxylated and/or propoxylated C12-22 fatty acids having ethoxylation or propoxylation degrees of 8-25, or mixtures thereof, such as (HLB value in parentheses): polyoxypropylene-(15)stearylether, or polyoxyethylenesorbitane-monooleate (15,0), polyoxyethylene-sorbitan monostearate or—palmitate (15,0), polyoxyethylene stearylether (15,3), polyoxyethylene oleylether (15,3), polyoxyethylene-oxypropylene monostearat (15,7), poyloxyethylene-fatty alcohol ether (16,0), polyoxyethylene monostearat (HLB 15) and the like. Especially preferred emulsifiers are ethoxylated C12-22 fatty acids or ethoxylated C8-22 fatty alcohols having ethoxylation units of between 10 to 20 (HLB value e.g. 13-20, preferably 13.5 to 18).
Further suitable emulsifiers are sugar esters and sugar ethers of C12-22-fatty acids or of C8-22-fatty alcohols. These are for example sugar esters of saturated, unsaturated, partially saturated C12-18-fatty acids; polyoxyethylated and/or polyoxypropylated sugar esters of C12-18-fatty acids, with an EO and PO degree, respectively of between 8 and 25. Sugar ethers may be selected from those ethers of saturated, unsaturated, partially saturated C8-20-(or C8-22)-fatty alcohols; or of polyoxyethylated and/or polyoxypropylated sugar ethers of these C8-20-fatty alcohols. Thereby, the EO- and PO-degree respectively may be between 8 and 25. The sugar part may preferably be selected from the group comprising glucose, methyl glucose, saccharose and the acids and alcohols may preferably be selected from 16-18-fatty acids/and -alcohols. Preferred compounds are ethoxylated compounds. The acid- and alcohol components respectively, are specifically derived from aliphatic carboxylic acids/-alcohols. These are in particular caprylic acid, caprine acid, lauric acid, myristic acid, palmic acid, stearic acid, oleic acid, and mixtures thereof, as well as such fatty alcohols, respectively (oleylalcohol, laurylalcohol, stearylalcohol).
In a further especially preferred embodiment the O/W emulsifier components d) are selected amongst anionic compounds, especially such as (alkyl) C12-22-fatty alcohol-amino acid ester compounds, preferably an alkali salt thereof, whereby the amino acids are selected from the group comprising glycine, taurine, such as oleyl-, lauryl-taurate, sodium methyl oleyl-taurate and the like. These may be used in the form of their salts, such as the alkali salts.
The O/W emulsifier components d) may preferably be present in an amount of between 0.5 up to 6% by weight, the dispersion component (agent) c) may preferably be present in an amount of between 0.1% up to 5% by weight. The total amount of the emulsifier mixture (c)+d)) is between 0.6 and 11%, especially 0.6 up to 6% by weight.
Especially preferred dispersion components (agents) and O/W-emulsifier components c) and d) are selected from the group comprising low-polyethoxylated or low polypropoxylated and mixed low polyoxylated (PO/EO) C12-18-fatty alcohols having an EO/PO degree (ethoxylation/propoxylation degree) of between 1 and 5, preferably 2 to 4; especially having an EO degree of between 2 to 4 particularly such as the said lauryl ether compounds; as well as from C12-18-fatty alcohol-taurates, especially sodium-methyl oleyl-taurate.
The agglomerates according to the present invention do further comprise vesicle forming substances b). These are in particular phospholipids such as lecithin (e.g. egg or soy lecithin), or phosphatidyl-choline, -serine, or -diethanolamine, phosphatidylinosite, e.g. derived from soy, rape, cotton seed, egg; as well as mixtures thereof. Other suitable lipidic components utilizable for the forming of vesicles include sphingolipids (e.g. ceramides, cerebrosides, sphingosine, sphingomyelin), or ethoxylated sterols such as phytosterols (mixtures of sistosterol, camposterol and stigmasterol), for example the ethoxylated derivatives thereof such as PEG-(polyethyleneglykol)-5-soy bean sterol or PEG-(polyethyleneglykol)-5 rapeseed sterol=Generol® 122 E5 and Generol® R E5, respectively.
The amount of the vesicle forming substance(s) is preferably between 0.1 and 5% by weight, especially between 0.1 and 3% by weight.
Especially preferred vesicle forming substances are phospholipids, and amongst these lecithins, in particular soy lecithin, egg lecithin, or mixtures thereof.
The agglomerates according to the invention can further (optionally) contain an amount of active ingredients f) and optionally an amount of additives e), selected from the group comprising perfumes, dyes, conditioning agents.
Suitable active ingredients, which—if present—may be present in an amount of between 0.1 up to e.g. 5% by weight, especially include ethereal oils, plant extracts, or mixtures thereof. These active ingredients may representatively comprise ethereal oils/extracts suitable for cosmetic or optionally medical bath additives, preferably selected from kaki leaves, mango, figs, lavender, cedar, lotus flowers, chamomile flowers, ylang ylang, ginkgo, pine needles, cypress, orange, rose wood, extracts from plum, birch-leaf extract, aloe-vera extract, extracts from marigold, hibiscus, burdock, witch hazel-, march pennywort leaf, algae, quince, water lily and cinnamon, extracts from thyme, mint, limes, grapefruit, mandarin, juniper, valerian, lemon balm, eucalyptus, palma-rosa, rosemary, lemon grass, wild rose, spruce needles and pine needles, ginger, red-currant, lime-blossom, marigold, magnolia, pineapple, guava, Echinacea, ivy-leaf, blueberry, kaki (persimmon diospyros), melone-extract and the like or mixtures thereof.
These extracts can be produced, for example by steam distillation. Hereby there are obtained from the cited plants, for example, ethereal oils which are particularly preferred. The extracts can also be obtained by other known ways, for example by solvent extraction (with alcohols, triglycerides or hydrocarbons, water and mixtures thereof) and then be used as such.
Examples of analogous synthetically produced substances are terpenes and terpenoids such as camphor, menthol, cineol or mixtures thereof.
Other suitable active ingredients include for example, vitamins, such as Vitamin A, E, or others and suitable derivatives thereof, such as esters, e.g. palmitate, acetate, or phosphate. Also, essential unsaturated fatty acids and their esters may be used, such as linol- or linolen acid, glyceryl linoleate, glyceryl linolenate.
Furthermore, active substances that promote blood circulation, such as nicotinic acid derivatives such as methyl nicotinate or tocopheryl nicotinate, alpha- and beta-hydroxy acids and their derivatives, e.g. glycolic acid, malic acid, citric acid, tartaric acid, lactic acid, salicylic acid, isopropylbenzyl salicylate, C12-13 alkyl lactate (Cosmacol® ELI), or else antiphlogistic (anti-inflammatory) and antibacterial substances such as triterpenes, e.g. ursolic acid, glycyrrhizinic acid or glycyrrhetinic acid, and their derivatives, e.g. stearyl glycyrrhetinate, potassium glycyrrhinate; pantothenic acid derivatives, e.g. D-panthenol, panthenyl triacetate; or also polyphenols, flavonoids, e.g. rutine, ferulaic acid, and their esters, or isoflavones such as soybean isoflavones or co-enzyme Q 10, can be used as active substances.
Preferred active ingredients are selected amongst ethereal oils, plant extracts, vitamins or mixtures thereof.
A further group of active ingredients includes skin-care agents. These may be selected amongst glycerine, propylene glycol or polyethylene glycols, polypropylene glycol, butylenes glycol, sorbitol or polymers such as of polyquatemium types, collagen, the hydrolyzates thereof, amino acids.
Besides these active ingredients e) or together with these also further additives d) as mentioned above may be incorporated into the agglomerates according to the invention, preferably in an amount of between 0.1 and 10% by weight. These include conditioning agents, dyes and perfumes. The conditioning agents may be selected amongst mono- and dialkylphosphates or cetyl alcohol, or the like, or mixtures thereof. Especially suitable conditioning agents are colloids. These may be selected amongst polysaccharides (e.g. xanthan gum), dextrines, cyclodextrine or similar colloidal saccharides, furthermore high dispersible silica acid compounds such as silicium dioxide, or albumines, or mixtures thereof, or water-soluble (poly)(meth)acrylate polymers such as carbomers, or water-soluble cellulose derivatives such as methyl cellulose, hydroxypropyl cellulose or hydroxyethyl cellulose, hydroxypropyl methyl cellulose, whereby the colloids mentioned last, may have a molecular mass of more than 40 000 D, for example carbomers: 1.25 up to 4 millions D.
Another group of suitable conditioning agents includes pearlescent agents, glossing agents on a waxy base (wax glossing agents), e.g. beeswax, and solubilizing agents, respectively, such as ethanol, isopropanol, (poly)ethylene glycol, (poly)propylene glycol.
Dyes which can be used in compositions according to the invention may be selected amongst water-soluble compounds known in the art for that purpose.
Suitable perfumes may be selected amongst ethereal oils such as mentioned above or other analogous/synthetic compounds known in the art.
The amounts of dyes and perfumes are within the range usually applied for such compounds and are known in the art.
The conditioning agents may be applied in amounts of e.g. from 0.1 up to 5% by weight.
Preferred additives are selected from the group comprising dyes, perfumes colloids, especially silicium acid-(silicium dioxide) compounds, pearlescent agents, glossing agents on a waxy basis (e.g. beeswax), or mixtures thereof.
Especially preferred agglomerates are those wherein the carrier is selected from urea, especially spherically formed urea beads (prills).
Furthermore preferably:
A further advantage is a mixture of one or more lipids (e.g. above mentioned oils) a1) and one or more of the above mentioned lipids a2).
In another advantageous embodiment according to the invention the dispersion agent(s) c) is/are selected amongst non ionic low polyethoxylated or low polypropoxylated and low-mixed polyoxylated, preferably low ethoxylated C8-22-fatty-alcohols having an ethoxylation (and/or propoxylation degree) (EO/PO-degree) of between 1 and 5, ethoxylated glyceroles, being esteryfied with C12-22-fatty-acids and having an EO-degree of between 0.5 and 3.
In a further preferred embodiment, the O/W emulsifier(s) d) within the agglomerates as described is/are selected from the group comprising ethoxylated C12-22-fatty-acids or ethoxylated C8-22-fatty-alcohols having ethoxylation degrees of between 13 and 18 and an HLB-value of between 13 and 18, especially 14-18; sugar esters or sugar ethers of C12-22-fatty-acids or of C8-22-fatty-alcohols; polyoxyethylated sugar esters of C12-18-fatty-acids, having an EO-degree of between 8 and 25 and the sugar being derived from glucose, saccharose, methyl glucose; as well as alkyl C12-22-fatty-alcohol-amino acid ester-compounds, especially an alkali metal salt thereof, the amino acid being selected amongst glycine and taurine.
The ratio between the dispersion agent(s) c)/O/E-emulsifier(s) d) is preferably as indicated, in particular 1:2 to 1:8, and more specifically 1:3 to 1:7.
In another preferred embodiment according to the invention the amount of the solid to waxy like lipid(s) a2) is higher than die amount of the liquid lipid(s) a1), particularly 1, 5:1 to 5:1.
In another preferred embodiment the agglomerates comprise a vesicle forming lipid or lipids which is/are selected amongst phospholipids, such as lecithin (egg- or soy lecithin), phosphatidyl-cholin, -serin or -diethanolamine; phosphatidylinosit, e.g. derived from soy, rape, cotton seed, egg; furthermore sphingolipids (e.g. ceramides, cerebrosides, sphingosin, sphingomyelin); as well as mixtures thereof.
Also preferred are active ingredients f) preferably selected from the group comprising ethereal oils, plant extracts, skin care agents, or mixtures thereof; and/or additives e), especially selected amongst dyes, perfumes, colloids, pearlescent agents, solubilising agents or mixtures thereof.
Especially preferred embodiments include agglomerates comprising 87 to 96% by weight of urea (beads), and:
Further preferred embodiments include agglomerates comprising 87 to 96% by weight of urea (beads), and:
A specifically preferred embodiment includes agglomerates comprising 83 to 96% by weight of urea (or urea beads/prills);
The agglomerates according to the invention preferably have an average diameter of about 0.5 to 5 mm, in particular of 1 to 3 mm, and are preferably present in the form of bath beads.
The agglomerates according to the invention are prepared by treating a preferably spherically formed, essentially anhydrous carrier, especially urea, in a mixing vessel
1) with a part of a (separately prepared in a known manner) liquid to fluid mixture 1) of the liquid (if present) lipid a1), the vesicle forming lipid b), the dispersion agent c) and optional perfumes e), optional liquid compound d) and optional active ingredients e), preferably at room temperature (e.g. by applying, for example such as spraying, trickling);
2) contacting a mixture of the solid component(s) a2), O/W emulsifier d), optional solid active ingredients, optional solid additives such as colloids, in the mixing vessel with the carrier comprising the liquid mixture as obtained by step 1 and mixing the same; and then
3) applying the balance of the liquid to fluid mixture 1) onto the carrier obtained in step 2) and optionally treating the same with additives as far as present, selected from conditioning agents, especially colloids, pearlescent agents, wax glossing agents, dyes, solubilising agents, or mixtures thereof, in the mixing vessel (e.g. by application for example such as trickling, spraying).
Preferably, in step 1) also a liquid lipid a1) and in step 2) a lipid a2) is used.
Insofar component d) is liquid to fluid, or a mixture of liquid and solid substances, the liquid part is incorporated into the mixture 1.
It is preferred to apply about 50 to 80% by weight, especially 60-70% by weight, of the mixture 1 in step 1 and the balance in step 3).
By such a proceeding stable agglomerates are obtained, in particular bath beads having an essentially spherical form, which preferably do not comprise any preservation agents and which are essentially anhydrous.
Such agglomerates may easily be packed into suitable containers and transported in a most comfortable manner without loosing the agglomeration properties. As a consequence they may be easily applied to the bathing by adding the desired amount.
If added to a bathing area the agglomerates are rapidly solved, whereby surprisingly specific liposomal mono—to multilayer-structures are formed. These are shown in the electron photomicro-graphs (TEM photographs) according to
The agglomerates according to the invention consequently are usable as additives to full, part, aroma, refreshing or feet bath.
They may be applied in a cosmetic bath e.g. as a relaxing, or as a hygienic bathing or even therapeutic bathing. Insofar a sufficient amount of the agglomerates, preferably the beads, specifically the urea beads, which may comprise suitable active ingredients in view of the desired purpose, e.g. ethereal oil for refreshing, relaxing, ingredients for blood circulation, anti-bacterial/anti-inflammatory agents as described hereinabove, are applied to the desired bathing having a temperature suitable for the desired purpose, for example 35-38° C., or otherwise adapted (feet bathing).
The invention is further illustrated (without limitation) by the following examples 1-5. Thereby the agglomerates described have been prepared as indicated above.
Number | Date | Country | Kind |
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10 2008 045 280.7 | Sep 2008 | DE | national |
Filing Document | Filing Date | Country | Kind | 371c Date |
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PCT/EP2009/005971 | 8/18/2009 | WO | 00 | 4/8/2011 |