CA2452386C - Granulates containing liposoluble substances and a process for the preparation thereof - Google Patents
Granulates containing liposoluble substances and a process for the preparation thereof Download PDFInfo
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- CA2452386C CA2452386C CA2452386A CA2452386A CA2452386C CA 2452386 C CA2452386 C CA 2452386C CA 2452386 A CA2452386 A CA 2452386A CA 2452386 A CA2452386 A CA 2452386A CA 2452386 C CA2452386 C CA 2452386C
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0087—Galenical forms not covered by A61K9/02 - A61K9/7023
- A61K9/0095—Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
- A61K9/1605—Excipients; Inactive ingredients
- A61K9/1617—Organic compounds, e.g. phospholipids, fats
- A61K9/1623—Sugars or sugar alcohols, e.g. lactose; Derivatives thereof; Homeopathic globules
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P15/00—Drugs for genital or sexual disorders; Contraceptives
- A61P15/18—Feminine contraceptives
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P35/00—Antineoplastic agents
Abstract
A process is described for the preparation of granulates that contain liposoluble and hydrophobic substances, preferably steroidal substances, and that exhibit rapid and excellent water-dispersibility. The process comprises:
a) the dispersion of substance (A) in water in the presence of a surfactant (B), b) the incorporation of a water-soluble polyhydroxylated solid excipient (C) in the aqueous dispersion until a granulable pasty mass is obtained and c) the granulation of the mass. The granulates so obtained are suitable for the preparation, at the time of use, of stable and homogeneous aqueous suspensions that are used for nutritional, cosmetic or, preferably, pharmaceutical purposes.
a) the dispersion of substance (A) in water in the presence of a surfactant (B), b) the incorporation of a water-soluble polyhydroxylated solid excipient (C) in the aqueous dispersion until a granulable pasty mass is obtained and c) the granulation of the mass. The granulates so obtained are suitable for the preparation, at the time of use, of stable and homogeneous aqueous suspensions that are used for nutritional, cosmetic or, preferably, pharmaceutical purposes.
Description
GRANULATES CONTAINING LIPOSOLUBLE SUBSTANCES AND A PROCESS FOR THE
PREPARATION THEREOF
The present invention relates to a process for the preparation of granulates con-taining liposoluble substances and, more especially, relates to a process for prepar-ing granulates that contain liposoluble substances and that exhibit immediate dis-persibility in water and that are therefore suitable for the preparation, at the time of use, of stable and homogeneous aqueous suspensions that are used for nutri-tional, cosmetic or, preferably, pharmaceutical purposes.
TECHNICAL FIELD OF THE INVENTION
The poor water-solubility of some hydrophobic substances can make the prepara-tion of their stable aqueous dispersions particularly problematic, regardless of whether this is in the field of nutrition, cosmetics or pharmaceuticals.
In the pharmaceutical sector in particular, the marked liposolubility of some classes of compound sometimes prevents the study and development of some formulations which could be produced in order to offer the drug to patients under improved conditions and with improved pharmacological properties, with great advantages in therapeutic practice. The improvement in the solubility of an active substance generally corresponds both to the achievement of higher blood levels ih vivo, perhaps obtainable in even shorter times, and to a lower absorption variabil-ity, which occurs above all when the drug has poor bio-availability.
Using surface-active agents, which help to reduce the stuface tension of particles, it is generally possible to disperse liposoluble substances in water to give rela-tively stable pseudo-solutions, suspensions or emulsions.
However, some classes of compound, for example, steroidal substances and, in particular, megestrol acetate, exhibit distinctive hydrophobic characteristics.
The above-mentioned megestrol acetate is a progestin which is widely used both in the field of contraceptives and as an anti-tumour agent and which is distributed by Bristol Myers Squibb under the mark Megace~ (Merck Index, 1996, no. 5849).
Megestrol acetate, like various other substances for therapeutic, cosmetic or nutri-tional use, is a hydrophobic compound which, in addition to exhibiting extremely poor water-solubility (2 pg/ml), is characterised by a high contact tension and is therefore difficult to wet.
Another disadvantage is the fact that the surface of the particles tends to absorb and trap air, thereby causing the product to float on the surface of the water.
Owing to those characteristics, the dispersion in aqueous medium of megestrol acetate and, more generally, substances having similar properties, constitutes a problem which is difficult to solve. Tn fact, it is usually impossible to obtain satis-factory and sufficiently stable dispersions in water either by the simple addition of surfactants or by micronisation: in the latter case, a deterioration in solubility is in fact observed, which is due to the fact that the micronisation of the compound greatly increases the surface area of the particles and, therefore, the enclosed air and the tendency to float.
All those disadvantages generally male it necessary to abandon the preparation of aqueous formulations of said substances, whereas, in various applications, it would be particularly advantageous to succeed in dispersing them adequately in water.
For example, in the pharmaceutical field it would be useful to be able to adminis-ter certain particularly hydrophobic substances, such as rnegestrol acetate, by the oral route, in the form of aqueous liquid formulations, especially in situations in which the patient has difficulty in swallowing solid forms or when the treatment provides for a high dosage which would require the ingestion of a large number of tablets or capsules.
For example, the treatment of cachexy, which is manifested by patients suffering from AmS, is a typical form of therapy using a high dosage of rnegestrol acetate (EP338404).
Various formulation studies have been undertaken to improve the dissolvability in water of poorly water-soluble substances but, as far as we know, the only known examples of aqueous formulations for the oral administration of megestrol acetate are the syrups referred to in EP519351 and US6028065.
Those syrups are defined by the inventors as being "flocculated aqueous suspen-sions", prepared by dispersing in water a mixture of megestrol acetate, a surfac-tant, such as polysorbate 80, and a hydrophilic polymer at concentrations of from 5% to 30%, such as polyethylene glycol, propylene glycol, glycerol or sorbitol.
However, the suspensions described above, in which the megestrol acetate is partly suspended and partly flocculated and in a layer at the bottom of the bottle, are definitely not the ideal form for correct oral administration because, even if they are suitably agitated, they do not ensure homogeneous distribution of the ac-tive substance and therefore reliable and repeatable dosage.
We have now surprisingly found that it is possible to granulate and then to dis-perse in water liposoluble substances that are not wettable and that float on water, such as megestrol acetate, in a complete, rapid and homogeneous manner and thus to prepare at the time of use stable aqueous formulations that are unquestionably useful in the field of nutrition, cosmetics and, in particular, pharmaceuticals.
The granulates of the present invention are particularly advantageous compared with the syrups of the prior art because they are stable over time, easy to handle and transport and are non-bulky. They also advantageously enable the compound to be dispersed in water at the moment of use, thus providing at the time of use homogeneous stable aqueous preparations with a precise and, if necessary, high dosage of the liposoluble substance.
DESCRIPTION OF THE INVENTION
The present invention therefore relates to a process for preparing granulates that exhibit rapid and excellent water-dispersibility and that contain liposoluble and hydrophobic substances, which process comprises:
a) the dispersion of substance (A) in water in the presence of a surfactant (B), b) the incorporation of a water-soluble polyhydroxylated solid excipient (C) in the aqueous dispersion until a granulable pasty mass is obtained and c) the granulation of the mass.
The present invention permits the preparation of solid and stable granulates which, once placed in an aqueous mediurn~, ensure not only that the liposoluble compound is immediately wetted but that it is diffused in an excellent manner in the water to provide a stable lactescent microsuspension.
PREPARATION THEREOF
The present invention relates to a process for the preparation of granulates con-taining liposoluble substances and, more especially, relates to a process for prepar-ing granulates that contain liposoluble substances and that exhibit immediate dis-persibility in water and that are therefore suitable for the preparation, at the time of use, of stable and homogeneous aqueous suspensions that are used for nutri-tional, cosmetic or, preferably, pharmaceutical purposes.
TECHNICAL FIELD OF THE INVENTION
The poor water-solubility of some hydrophobic substances can make the prepara-tion of their stable aqueous dispersions particularly problematic, regardless of whether this is in the field of nutrition, cosmetics or pharmaceuticals.
In the pharmaceutical sector in particular, the marked liposolubility of some classes of compound sometimes prevents the study and development of some formulations which could be produced in order to offer the drug to patients under improved conditions and with improved pharmacological properties, with great advantages in therapeutic practice. The improvement in the solubility of an active substance generally corresponds both to the achievement of higher blood levels ih vivo, perhaps obtainable in even shorter times, and to a lower absorption variabil-ity, which occurs above all when the drug has poor bio-availability.
Using surface-active agents, which help to reduce the stuface tension of particles, it is generally possible to disperse liposoluble substances in water to give rela-tively stable pseudo-solutions, suspensions or emulsions.
However, some classes of compound, for example, steroidal substances and, in particular, megestrol acetate, exhibit distinctive hydrophobic characteristics.
The above-mentioned megestrol acetate is a progestin which is widely used both in the field of contraceptives and as an anti-tumour agent and which is distributed by Bristol Myers Squibb under the mark Megace~ (Merck Index, 1996, no. 5849).
Megestrol acetate, like various other substances for therapeutic, cosmetic or nutri-tional use, is a hydrophobic compound which, in addition to exhibiting extremely poor water-solubility (2 pg/ml), is characterised by a high contact tension and is therefore difficult to wet.
Another disadvantage is the fact that the surface of the particles tends to absorb and trap air, thereby causing the product to float on the surface of the water.
Owing to those characteristics, the dispersion in aqueous medium of megestrol acetate and, more generally, substances having similar properties, constitutes a problem which is difficult to solve. Tn fact, it is usually impossible to obtain satis-factory and sufficiently stable dispersions in water either by the simple addition of surfactants or by micronisation: in the latter case, a deterioration in solubility is in fact observed, which is due to the fact that the micronisation of the compound greatly increases the surface area of the particles and, therefore, the enclosed air and the tendency to float.
All those disadvantages generally male it necessary to abandon the preparation of aqueous formulations of said substances, whereas, in various applications, it would be particularly advantageous to succeed in dispersing them adequately in water.
For example, in the pharmaceutical field it would be useful to be able to adminis-ter certain particularly hydrophobic substances, such as rnegestrol acetate, by the oral route, in the form of aqueous liquid formulations, especially in situations in which the patient has difficulty in swallowing solid forms or when the treatment provides for a high dosage which would require the ingestion of a large number of tablets or capsules.
For example, the treatment of cachexy, which is manifested by patients suffering from AmS, is a typical form of therapy using a high dosage of rnegestrol acetate (EP338404).
Various formulation studies have been undertaken to improve the dissolvability in water of poorly water-soluble substances but, as far as we know, the only known examples of aqueous formulations for the oral administration of megestrol acetate are the syrups referred to in EP519351 and US6028065.
Those syrups are defined by the inventors as being "flocculated aqueous suspen-sions", prepared by dispersing in water a mixture of megestrol acetate, a surfac-tant, such as polysorbate 80, and a hydrophilic polymer at concentrations of from 5% to 30%, such as polyethylene glycol, propylene glycol, glycerol or sorbitol.
However, the suspensions described above, in which the megestrol acetate is partly suspended and partly flocculated and in a layer at the bottom of the bottle, are definitely not the ideal form for correct oral administration because, even if they are suitably agitated, they do not ensure homogeneous distribution of the ac-tive substance and therefore reliable and repeatable dosage.
We have now surprisingly found that it is possible to granulate and then to dis-perse in water liposoluble substances that are not wettable and that float on water, such as megestrol acetate, in a complete, rapid and homogeneous manner and thus to prepare at the time of use stable aqueous formulations that are unquestionably useful in the field of nutrition, cosmetics and, in particular, pharmaceuticals.
The granulates of the present invention are particularly advantageous compared with the syrups of the prior art because they are stable over time, easy to handle and transport and are non-bulky. They also advantageously enable the compound to be dispersed in water at the moment of use, thus providing at the time of use homogeneous stable aqueous preparations with a precise and, if necessary, high dosage of the liposoluble substance.
DESCRIPTION OF THE INVENTION
The present invention therefore relates to a process for preparing granulates that exhibit rapid and excellent water-dispersibility and that contain liposoluble and hydrophobic substances, which process comprises:
a) the dispersion of substance (A) in water in the presence of a surfactant (B), b) the incorporation of a water-soluble polyhydroxylated solid excipient (C) in the aqueous dispersion until a granulable pasty mass is obtained and c) the granulation of the mass.
The present invention permits the preparation of solid and stable granulates which, once placed in an aqueous mediurn~, ensure not only that the liposoluble compound is immediately wetted but that it is diffused in an excellent manner in the water to provide a stable lactescent microsuspension.
The process of the invention relates to the granulation of liposoluble and hydro-phobic substances (A), regardless of whether they are for nutritional, cosmetic or, preferably, pharmaceutical use.
In the present context, liposoluble substances are to be understood as meaning those substances, especially those active substances, which exhibit very poor wa-ter-solubility, preferably lower than 20 ~tg/ml, at 20°C. In addition, these sub-stances are particularly hydrophobic, that is to say, practically non-wettable.
According to the present invention, the substances that can be formulated are gen-erally any substances characterised by poor water-solubility and wettability, irre-spective of whether they are used in the field of nutrition, cosmetics or pharma-ceuticals.
In the pharmaceutical field, the classes of the steroids and, preferably, megestrol acetate, may be mentioned by way of non-limiting example.
The process to which the present invention relates comprises initially the disper-sion of the water=insoluble substmce in water in the presence of a surfactant (B).
The surfactants used are generally non-ionic surfactants, such as, for example, poloxamers, polyoxyethylene alkyl ethers, polyoxyethylene stearates, poly-oxyethylene glycol hydroxy stearates and the fatty acid esters of polyoxyethylene sorbitans or polysorbates. A preferred group of non-ionic surfactants comprises the polysorbates, such as polysorbate 20, 40, 60, 65, 80 and 85, more preferably polysorbate 80 (Tween 80°).
In addition to ensuring that the water-insoluble substalice is distl-ibuted uniformly in the selected soluble polyalcohols, those surfactants make it possible to obtain a finished granulate which is compact and heavy but which has the characteristic of dispersing the liposoluble substance uniformly as soon as the granulate is placed in water.
The dispersion of the liposoluble substance in water is generally carned out at a temperature of from 20°C to 60°C, preferably from 25°C to 40°C.
According to the present invention, the lipsoluble substance, preferably megestrol acetate, is dispersed in an excellent manner in the aqueous solvent in the presence of a surfactant, and then a water-soluble polyhydroxylated solid excipient (C) is added to it until a granulable pasty mass is obtained.
The excipient is generally a solid water-soluble polyhydroxylated compound se-lected from soluble polyalcohols, such as mannitol or sorbitol, andlor sugars, such as, for example, lactose or fructose, and mixtures thereof. In the present context, rnannitol is particularly preferred.
The polyhydroxylated compounds (C) selected as solubilisers and dispersants of the water-insoluble substance, especially megestrol acetate, are used in an amount by weight, relative to the substance to be solubilised (A), of generally from 1:1 to 6:1 and, preferably, from 3:1 to 5:1, while the amount of selected surfactant (B) used, still calculated relative to the water-insoluble substance (A), ranges from 0.013:1 to 0.7:1, more advantageously from 0.02:1 to 0.33:1.
The process to which the present invention relates requires initially the dispersion of the water-insoluble substance in water in the presence of a surfactant.
The amount of water used is not a particularly important parameter because it can vary fairly freely, bearing in mind the necessity to ensure both good dispersion of the active substance and, subsequently, by gradual incorporation of the polyhy-droxylated excipient, the production of a pasty mass which is neither too fluid nor excessively solid and which is suitable for granulation. Generally, the operation is carried out with quantities of water, expressed by weight relative to the water-insoluble substance (A), of from 0.2:1 to 1:1, preferably from 0.5:1 to 0.7:1.
The incorporation of the water-soluble polyhydroxylated solid excipient is gener-ally carried out in portions and while agitating, in accordance with the method of successive dilutions, in order to confer the best possible dispersion and to obtain a pasty mass having the desired consistency.
Finally, the mass so prepared is subjected to granulation, preferably in a suitable mesh granulator.
The present invention relates also to the granulates obtainable using the above-described process and to the pharmaceutical forms that can be prepared using those granulates.
The granulates of the invention can be used as such or, preferably, can be utilised for the preparation, at the time of use, of oral aqueous dispersions characterised by stability and a precise posological content, or the granulates can be otherwise for-mulated.
These granulates for preparing, at the time of use, solutions for oral administration generally have a content of liposoluble substance, preferably megestrol acetate, in the final granulate of from 5 to 50% by weight, preferably from 15 to 25% by weight, and a particle size of from 5 to 180 pm, preferably from 30 to 160 p.m.
The aqueous dispersions according to the present invention prepared at the time of use are generally prepared by mixing the granulate with an amount of water equal to at least 80 ml per gram of granulate and by agitating until the granulate has completely dissolved.
These granulates are particularly suitable for the oral administration of even large amounts of liposoluble substances.
In the specific case of megestrol acetate, for example, it is possible to use the ac-tive substance in a single administration, in amounts of generally up to 320 mg, optionally even higher, and preferably approximately 160 mg.
The granulates of the invention can be formulated, optionally with the addition of other pharmaceutically acceptable excipients, such as, for example, effervescent mixtures, disintegrators, lubricants, sweeteners and flavourings, which improve the palatability of. the suspensions or facilitate disintegration, in the form of pack-ets, effervescent packets, syrups prepared at the time of use, tablets, effervescent tablets, quick-dissolving sublingual tablets.
For example, sweeteners, preferably synthetic sweeteners, such as saccharine, ace-sulfame, aspartame, cyclamate or_mixtures thereof, are generally used in the oral formulations of the invention.
It is, however, important to emphasise that the above-mentioned additional ex-cipients are not absolutely necessary to confer on the granulate the distinctive wa-ter-dispersibilitywhich characterises it.
In a preferred embodiment of the present invention the predetermined amounts of water and polysorbate 80 are introduced into a suitable mixer and are agitated un-til the whole has been completely mixed and solubilised in the water at a tempera-ture of from 25°C to 40°C.
At that point, the megestrol acetate is added in portions, with agitation, to give a completely uniform suspension.
When the megestrol acetate has been completely suspended, the introduction of mannitol in small portions is initiated.
While still agitating slowly, the addition of mannitol is continued until a consis-tent finished mass capable of being granulated is obtained.
The mass is transferred to the granulator and is granulated on a mesh.
Finally, the granulate obtained is dried in an air bath.
The following Examples are now given for the puyose of better illustrating the present invention, but without limiting it.
Example 1 Preparation of the~ranulate The standard procedure used for preparing the granulate based on megestrol ace-tate is sub-divided into the stages described hereinafter.
STAGE I
Approximately 2.5 litres of water, and polysorbate 80 (100 g) were introduced into a suitable mixer provided with counter-rotating scraping blades and a turbilze and having a capacity of 20 litres, and the whole was agitated until complete solu-bilisation in the water had occurred.
At that point 3 kg of megestrol acetate (Farmabios, particle size: <150 ~,m 88.21%; <36 ~,m 49.66%) were introduced in portions, with agitation, to give a completely uniform suspension. When the megestrol acetate had been completely suspended, introduction of the mannitol (4 kg, Carlo Erba)in small portions was initiated.
Agitation was continued until a homogeneous mixture was obtained which, how-ever, had a density such that it could be readily transferred to a mixer of a size suf ficient to contain the amount of mannitol which it was desired to add in order to obtain a suitable finished granulate.
STAGE II
The mixture obtained in STAGE I was placed in the mixer provided. A fw-ther I3 kg of mannitol were added while agitating slowly. Agitation was continued for approximately 1 hour until a finished mass was obtained which was consistent and capable of being granulated.
STAGE III
The mixture obtained in STAGE II was removed and was granulated on a 0.63 mm mesh or, altomatively, in a suitable granulator, for example with extrusion by rotating blades or a screw.
STAGE IV
The granulate obtained was dried in an air bath.
The distribution of the megestrol acetate was checl~ed (HPLC, standard method pharmacopoeia USP 24, ed. 2000, pages 1030-1032) and was found to be from 98.5% to 101.5%.
Example 2 Preparation of an adueous dispersion at the time of use The granulate prepared according to Example 1 (900 mg) was placed in a beaker containing water (100-150 ml) and agitated rapidly. An immediate and uniform dispersion of the granulate was observed, with the formation of a lactescent mi-crosuspension suitable for oral use.
The dispersion so prepared demonstrates that the granulate of the invention is ideal for rapidly and homogeneously suspending liposoluble and hycliophobic substances in water. Unlilce the syrups of the prior art, no separation or floccula-tion of the active substance is observed.
Example 3 Dissolving test A comparative dissolving test was carried out between the granulate prepared ac-cording to Example 1 and the megestrol acetate powder (particle size: <150 ~m 88.21%; <36 pm 49.66%) The operating conditions were as follows:
Medium: water (900 ml) Apparatus: paddle Rate of rotation of the blades: 100 rpm Temperature: 37°C
Reading wavelength: 280 iun The following Figure 1 shows that the granulate is characterised by optimum and rapid dispersibility in aqueous medium and is therefore particularly suitable for the preparation of aqueous formulations at the time of use.
Examples 4 - 7 given hereinafter illustrate the preparation, in accordance with conventional methods, of solid pharmaceutical forms that comprise the granulates of Example 1 and that are suitable for the oral administration of megestrol acetate.
Example 4 Normal paclcets .
Each packet, having a total weight of 900 mg, has the following composition:
Megestrol acetate:160.0 mg Polysorbate 80: 5.0 mg Mannitol: 640.0 mg Aspartame: 45.0 mg Strawberry flavouring:50.0 mg (3.51 distillable essence supported on dextrose, maltodextrin,4 gum arabic) Effervescent pacl~ets Each packet lowing composition:
has the fol Megestrol acetate:160.0 mg Polysorbate: 5.0 mg Mannitol: 640.0 mg Aspartame: 40.0 m~
Citric acid: 292.5 mg Sodium bicarbonate: 309.0 mg Lemon flavouring: 100.0 mg Example 6 Effervescent tablets Each effervescent tablet has the following composition:
Megestrol acetate: 160.0 mg Polysorbate 5.0 mg 80:
Mannitol: 640.0 mg Aspartame: 43.0 mg Citric acid: 390.0 mg Sodium bicarbonate:412.0 mg Lemon flavouring:100.0 mg Ea~ample 7 uick-dissolving subling<.ial tablets Each tablet has the following composition:
Megestrol acetate:160.0 mg Mannitol: 390.0 mg Aspartame: 45.0 mg Strawberry flavouring50.0 mg Polysorbate 80: 5.0 mg
In the present context, liposoluble substances are to be understood as meaning those substances, especially those active substances, which exhibit very poor wa-ter-solubility, preferably lower than 20 ~tg/ml, at 20°C. In addition, these sub-stances are particularly hydrophobic, that is to say, practically non-wettable.
According to the present invention, the substances that can be formulated are gen-erally any substances characterised by poor water-solubility and wettability, irre-spective of whether they are used in the field of nutrition, cosmetics or pharma-ceuticals.
In the pharmaceutical field, the classes of the steroids and, preferably, megestrol acetate, may be mentioned by way of non-limiting example.
The process to which the present invention relates comprises initially the disper-sion of the water=insoluble substmce in water in the presence of a surfactant (B).
The surfactants used are generally non-ionic surfactants, such as, for example, poloxamers, polyoxyethylene alkyl ethers, polyoxyethylene stearates, poly-oxyethylene glycol hydroxy stearates and the fatty acid esters of polyoxyethylene sorbitans or polysorbates. A preferred group of non-ionic surfactants comprises the polysorbates, such as polysorbate 20, 40, 60, 65, 80 and 85, more preferably polysorbate 80 (Tween 80°).
In addition to ensuring that the water-insoluble substalice is distl-ibuted uniformly in the selected soluble polyalcohols, those surfactants make it possible to obtain a finished granulate which is compact and heavy but which has the characteristic of dispersing the liposoluble substance uniformly as soon as the granulate is placed in water.
The dispersion of the liposoluble substance in water is generally carned out at a temperature of from 20°C to 60°C, preferably from 25°C to 40°C.
According to the present invention, the lipsoluble substance, preferably megestrol acetate, is dispersed in an excellent manner in the aqueous solvent in the presence of a surfactant, and then a water-soluble polyhydroxylated solid excipient (C) is added to it until a granulable pasty mass is obtained.
The excipient is generally a solid water-soluble polyhydroxylated compound se-lected from soluble polyalcohols, such as mannitol or sorbitol, andlor sugars, such as, for example, lactose or fructose, and mixtures thereof. In the present context, rnannitol is particularly preferred.
The polyhydroxylated compounds (C) selected as solubilisers and dispersants of the water-insoluble substance, especially megestrol acetate, are used in an amount by weight, relative to the substance to be solubilised (A), of generally from 1:1 to 6:1 and, preferably, from 3:1 to 5:1, while the amount of selected surfactant (B) used, still calculated relative to the water-insoluble substance (A), ranges from 0.013:1 to 0.7:1, more advantageously from 0.02:1 to 0.33:1.
The process to which the present invention relates requires initially the dispersion of the water-insoluble substance in water in the presence of a surfactant.
The amount of water used is not a particularly important parameter because it can vary fairly freely, bearing in mind the necessity to ensure both good dispersion of the active substance and, subsequently, by gradual incorporation of the polyhy-droxylated excipient, the production of a pasty mass which is neither too fluid nor excessively solid and which is suitable for granulation. Generally, the operation is carried out with quantities of water, expressed by weight relative to the water-insoluble substance (A), of from 0.2:1 to 1:1, preferably from 0.5:1 to 0.7:1.
The incorporation of the water-soluble polyhydroxylated solid excipient is gener-ally carried out in portions and while agitating, in accordance with the method of successive dilutions, in order to confer the best possible dispersion and to obtain a pasty mass having the desired consistency.
Finally, the mass so prepared is subjected to granulation, preferably in a suitable mesh granulator.
The present invention relates also to the granulates obtainable using the above-described process and to the pharmaceutical forms that can be prepared using those granulates.
The granulates of the invention can be used as such or, preferably, can be utilised for the preparation, at the time of use, of oral aqueous dispersions characterised by stability and a precise posological content, or the granulates can be otherwise for-mulated.
These granulates for preparing, at the time of use, solutions for oral administration generally have a content of liposoluble substance, preferably megestrol acetate, in the final granulate of from 5 to 50% by weight, preferably from 15 to 25% by weight, and a particle size of from 5 to 180 pm, preferably from 30 to 160 p.m.
The aqueous dispersions according to the present invention prepared at the time of use are generally prepared by mixing the granulate with an amount of water equal to at least 80 ml per gram of granulate and by agitating until the granulate has completely dissolved.
These granulates are particularly suitable for the oral administration of even large amounts of liposoluble substances.
In the specific case of megestrol acetate, for example, it is possible to use the ac-tive substance in a single administration, in amounts of generally up to 320 mg, optionally even higher, and preferably approximately 160 mg.
The granulates of the invention can be formulated, optionally with the addition of other pharmaceutically acceptable excipients, such as, for example, effervescent mixtures, disintegrators, lubricants, sweeteners and flavourings, which improve the palatability of. the suspensions or facilitate disintegration, in the form of pack-ets, effervescent packets, syrups prepared at the time of use, tablets, effervescent tablets, quick-dissolving sublingual tablets.
For example, sweeteners, preferably synthetic sweeteners, such as saccharine, ace-sulfame, aspartame, cyclamate or_mixtures thereof, are generally used in the oral formulations of the invention.
It is, however, important to emphasise that the above-mentioned additional ex-cipients are not absolutely necessary to confer on the granulate the distinctive wa-ter-dispersibilitywhich characterises it.
In a preferred embodiment of the present invention the predetermined amounts of water and polysorbate 80 are introduced into a suitable mixer and are agitated un-til the whole has been completely mixed and solubilised in the water at a tempera-ture of from 25°C to 40°C.
At that point, the megestrol acetate is added in portions, with agitation, to give a completely uniform suspension.
When the megestrol acetate has been completely suspended, the introduction of mannitol in small portions is initiated.
While still agitating slowly, the addition of mannitol is continued until a consis-tent finished mass capable of being granulated is obtained.
The mass is transferred to the granulator and is granulated on a mesh.
Finally, the granulate obtained is dried in an air bath.
The following Examples are now given for the puyose of better illustrating the present invention, but without limiting it.
Example 1 Preparation of the~ranulate The standard procedure used for preparing the granulate based on megestrol ace-tate is sub-divided into the stages described hereinafter.
STAGE I
Approximately 2.5 litres of water, and polysorbate 80 (100 g) were introduced into a suitable mixer provided with counter-rotating scraping blades and a turbilze and having a capacity of 20 litres, and the whole was agitated until complete solu-bilisation in the water had occurred.
At that point 3 kg of megestrol acetate (Farmabios, particle size: <150 ~,m 88.21%; <36 ~,m 49.66%) were introduced in portions, with agitation, to give a completely uniform suspension. When the megestrol acetate had been completely suspended, introduction of the mannitol (4 kg, Carlo Erba)in small portions was initiated.
Agitation was continued until a homogeneous mixture was obtained which, how-ever, had a density such that it could be readily transferred to a mixer of a size suf ficient to contain the amount of mannitol which it was desired to add in order to obtain a suitable finished granulate.
STAGE II
The mixture obtained in STAGE I was placed in the mixer provided. A fw-ther I3 kg of mannitol were added while agitating slowly. Agitation was continued for approximately 1 hour until a finished mass was obtained which was consistent and capable of being granulated.
STAGE III
The mixture obtained in STAGE II was removed and was granulated on a 0.63 mm mesh or, altomatively, in a suitable granulator, for example with extrusion by rotating blades or a screw.
STAGE IV
The granulate obtained was dried in an air bath.
The distribution of the megestrol acetate was checl~ed (HPLC, standard method pharmacopoeia USP 24, ed. 2000, pages 1030-1032) and was found to be from 98.5% to 101.5%.
Example 2 Preparation of an adueous dispersion at the time of use The granulate prepared according to Example 1 (900 mg) was placed in a beaker containing water (100-150 ml) and agitated rapidly. An immediate and uniform dispersion of the granulate was observed, with the formation of a lactescent mi-crosuspension suitable for oral use.
The dispersion so prepared demonstrates that the granulate of the invention is ideal for rapidly and homogeneously suspending liposoluble and hycliophobic substances in water. Unlilce the syrups of the prior art, no separation or floccula-tion of the active substance is observed.
Example 3 Dissolving test A comparative dissolving test was carried out between the granulate prepared ac-cording to Example 1 and the megestrol acetate powder (particle size: <150 ~m 88.21%; <36 pm 49.66%) The operating conditions were as follows:
Medium: water (900 ml) Apparatus: paddle Rate of rotation of the blades: 100 rpm Temperature: 37°C
Reading wavelength: 280 iun The following Figure 1 shows that the granulate is characterised by optimum and rapid dispersibility in aqueous medium and is therefore particularly suitable for the preparation of aqueous formulations at the time of use.
Examples 4 - 7 given hereinafter illustrate the preparation, in accordance with conventional methods, of solid pharmaceutical forms that comprise the granulates of Example 1 and that are suitable for the oral administration of megestrol acetate.
Example 4 Normal paclcets .
Each packet, having a total weight of 900 mg, has the following composition:
Megestrol acetate:160.0 mg Polysorbate 80: 5.0 mg Mannitol: 640.0 mg Aspartame: 45.0 mg Strawberry flavouring:50.0 mg (3.51 distillable essence supported on dextrose, maltodextrin,4 gum arabic) Effervescent pacl~ets Each packet lowing composition:
has the fol Megestrol acetate:160.0 mg Polysorbate: 5.0 mg Mannitol: 640.0 mg Aspartame: 40.0 m~
Citric acid: 292.5 mg Sodium bicarbonate: 309.0 mg Lemon flavouring: 100.0 mg Example 6 Effervescent tablets Each effervescent tablet has the following composition:
Megestrol acetate: 160.0 mg Polysorbate 5.0 mg 80:
Mannitol: 640.0 mg Aspartame: 43.0 mg Citric acid: 390.0 mg Sodium bicarbonate:412.0 mg Lemon flavouring:100.0 mg Ea~ample 7 uick-dissolving subling<.ial tablets Each tablet has the following composition:
Megestrol acetate:160.0 mg Mannitol: 390.0 mg Aspartame: 45.0 mg Strawberry flavouring50.0 mg Polysorbate 80: 5.0 mg
Claims (22)
1. A process for preparing a granulate that exhibits rapid and excellent water-dispersibility and that contains liposoluble and hydrophobic substances, having a water-solubility at 20°C of less than 20 µml, which process comprises:
a) the dispersion of substance (A) in water in the presence of a surfactant (B), b) the incorporation of a water-soluble polyhydroxylated solid excipient (C) in the aqueous dispersion until a granulable pasty mass is obtained and c) the granulation of the mass, wherein the surfactant (B) and the polyhydroxylated solid excipient (C) are present in amounts by weight of, respectively, from 0.013 to 0.7 of (B) and from 1 to 6 of (C), per unit of liposoluble substance (A).
a) the dispersion of substance (A) in water in the presence of a surfactant (B), b) the incorporation of a water-soluble polyhydroxylated solid excipient (C) in the aqueous dispersion until a granulable pasty mass is obtained and c) the granulation of the mass, wherein the surfactant (B) and the polyhydroxylated solid excipient (C) are present in amounts by weight of, respectively, from 0.013 to 0.7 of (B) and from 1 to 6 of (C), per unit of liposoluble substance (A).
2. A process according to claim 1, wherein the substance (A) is a steroidal substance, preferably megestrol acetate.
3. A process according to claim 1, wherein the surfactant (B) is a polysorbate, preferably polysorbate 80.
4. A process according to claim 1, wherein the dispersion of the liposoluble substance (A) in water is effected at a temperature of from 20°C to 60°C, preferably from 25°C to 40°C.
5. A process according to claim 1, wherein the water-soluble polyhydroxylated solid excipient (C) is selected from mannitol, sorbitol, lactose and fructose and mixtures thereof.
6. A process according to claim 1, wherein the surfactant (B) and the polyhydroxylated solid excipient (C) are present, in amounts by weight, of from 0.02 to 0.33 of (B) and from 3 to 5 of (C), per unit of liposoluble substance (A).
7. A process according to claim 1, wherein the amount of water, by weight, relative to substance (A), is from 0.2 to 1, preferably from 0.5 to 0.7.
8. A granulate obtainable according to claims 1 to 7.
9. A granulate according to claim 8, having a content of substance (A) of from 5 to 50% by weight, preferably from 15 to 25% by weight.
10. A pharmaceutical composition comprising a granulate according to claim 8.
11. A pharmaceutical composition according to claim 10, in the form of an aqueous dispersion.
12. A pharmaceutical composition according to claim 10, in the form of a packet, an effervescent packet, a syrup prepared at the time of use, a tablet, an effervescent tablet and a quick-dissolving sublingual tablet.
13. A process for the preparation of an aqueous dispersion according to claim 11, characterized in that the granulate is mixed with at least 80 ml of water per gram of granulate and is agitated until complete dispersion has occurred.
14. A granulate comprising a liposoluble and hydrophobic substance (A), having a water-solubility at 20°C of less than 20 µg/ml, a surfactant (B), and a water soluble polyhydroxylated solid excipient (C) in amounts by weight of, respectively, from 0.013 to 0.7 of (B) and from 1 to 6 of (C), per unit of liposoluble substance (A).
15. A granulate according to claim 14 characterized in that said liposoluble substance (A) is a steroidal substance.
16. A granulate according to claim 14 characterized in that said liposoluble substance (A) is megestrol acetate.
17. A granulate according to claims 14 to 16 characterized in that the surfactant (B) is a polysorbate, preferably polysorbate 80.
18. A granulate according to claims 14 to 17 characterized in that water-soluble polyhydroxylated solid excipient (C) is selected from mannitol, sorbitol, lactose and fructose and mixtures thereof.
19. A granulate according to claims 14 to 18 wherein the surfactant (B) and the polyhydroxylated solid excipient (C) are present, in amounts by weight, of from 0.02 to 0.33 of (B) and from 3 to 5 of (C), per unit of liposoluble substance (A).
20. A granulate according to claims 14 to 19 characterized by further containing pharmaceutically acceptable excipients.
21. A granulate according to claims 14 to 20 characterized in that said liposoluble substance (A) is present in amounts of 5 to 50% by weight.
22. A granulate according to claim 21 characterized in that said liposoluble substance (A) is present in amounts of 15 to 25% by weight.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP01202657A EP1275377B1 (en) | 2001-07-11 | 2001-07-11 | Granulates containing liposoluble substances and process of preparation thereof |
EP01202657.1 | 2001-07-11 | ||
PCT/EP2002/007636 WO2003005989A2 (en) | 2001-07-11 | 2002-07-09 | Granulates containing liposoluble substances and a process for the preparation thereof |
Publications (2)
Publication Number | Publication Date |
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CA2452386A1 CA2452386A1 (en) | 2003-01-23 |
CA2452386C true CA2452386C (en) | 2011-01-18 |
Family
ID=8180628
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
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CA2452386A Expired - Fee Related CA2452386C (en) | 2001-07-11 | 2002-07-09 | Granulates containing liposoluble substances and a process for the preparation thereof |
Country Status (21)
Country | Link |
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US (1) | US7615547B2 (en) |
EP (1) | EP1275377B1 (en) |
JP (1) | JP2004536118A (en) |
KR (1) | KR100877628B1 (en) |
AT (1) | ATE243028T1 (en) |
AU (1) | AU2002328866B2 (en) |
BR (1) | BR0211081A (en) |
CA (1) | CA2452386C (en) |
DE (1) | DE60100389T2 (en) |
DK (1) | DK1275377T3 (en) |
ES (1) | ES2199202T3 (en) |
HR (1) | HRP20040010A2 (en) |
IL (1) | IL159346A0 (en) |
MX (1) | MXPA04000211A (en) |
NO (1) | NO20040043L (en) |
NZ (1) | NZ530473A (en) |
PL (1) | PL204963B1 (en) |
PT (1) | PT1275377E (en) |
RU (1) | RU2288704C2 (en) |
WO (1) | WO2003005989A2 (en) |
ZA (1) | ZA200309680B (en) |
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Publication number | Priority date | Publication date | Assignee | Title |
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US20050080486A1 (en) | 2000-11-29 | 2005-04-14 | Fallin T. Wade | Facet joint replacement |
US6579319B2 (en) | 2000-11-29 | 2003-06-17 | Medicinelodge, Inc. | Facet joint replacement |
US7753937B2 (en) | 2003-12-10 | 2010-07-13 | Facet Solutions Inc. | Linked bilateral spinal facet implants and methods of use |
CA2630304C (en) | 2005-12-09 | 2012-04-10 | Teva Pharmaceutical Industries Ltd. | Aqueous dispersions and solutions of difficult to dissolve compounds and methods of their preparation |
ES2496166T3 (en) * | 2006-12-22 | 2014-09-18 | Yuhan Corporation | Solid dispersion containing revaprazan and its preparation process |
EP3702442A1 (en) * | 2011-12-22 | 2020-09-02 | Life Technologies Corporation | Cell culture media and methods |
US10328087B2 (en) | 2015-07-23 | 2019-06-25 | Therapeuticsmd, Inc. | Formulations for solubilizing hormones |
US10286077B2 (en) | 2016-04-01 | 2019-05-14 | Therapeuticsmd, Inc. | Steroid hormone compositions in medium chain oils |
BR112018070199A2 (en) | 2016-04-01 | 2019-01-29 | Therapeuticsmd Inc | pharmaceutical composition of steroid hormone |
EP3641726A1 (en) * | 2017-06-23 | 2020-04-29 | MedCan Pharma A/S | Cannabinoid pouch |
CN108309933A (en) * | 2018-03-19 | 2018-07-24 | 青岛国海生物制药有限公司 | A kind of oral megestrol acetate nanosuspension and preparation method thereof |
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DE3610037A1 (en) * | 1986-03-21 | 1987-09-24 | Schering Ag | NIFEDIPINE COMBINATION PRODUCT |
JPH0449232A (en) | 1990-06-15 | 1992-02-18 | Fujisawa Pharmaceut Co Ltd | Composition of suspension or suspension and preparation therefrom |
US5338732A (en) | 1991-06-18 | 1994-08-16 | Bristol-Myers Squibb Company | Megestrol acetate formulation |
US5395627A (en) * | 1992-09-04 | 1995-03-07 | Akzo N.V. | Pharmaceutical granulate |
FR2702968B1 (en) | 1993-03-23 | 1995-06-23 | Lafon Labor | Process for the preparation of particles containing an active ingredient by extrusion and lyophilization. |
BR9407728A (en) | 1993-10-01 | 1997-02-12 | Syntex Inc | Oral suspensions of high doses of microfenolate mofetil |
US5976570A (en) * | 1993-12-21 | 1999-11-02 | Applied Analytical Industries, Inc. | Method for preparing low dose pharmaceutical products |
FR2730163B1 (en) | 1995-02-03 | 1997-04-04 | Jouveinal Lab | NOVEL PHARMACEUTICAL COMPOSITION CONTAINING TRIMEBUTINE AND PROCESS FOR THE PREPARATION THEREOF |
US20020028248A1 (en) | 1996-03-14 | 2002-03-07 | Takayuki Tsukada | Rapid-release microdispersible ecadotril preparation |
US5985309A (en) * | 1996-05-24 | 1999-11-16 | Massachusetts Institute Of Technology | Preparation of particles for inhalation |
DE19637082A1 (en) * | 1996-09-12 | 1998-03-19 | Boehringer Mannheim Gmbh | Rapidly disintegrating pellets |
TW486370B (en) * | 1996-12-25 | 2002-05-11 | Yamanouchi Pharma Co Ltd | Rapidly disintegrable pharmaceutical composition |
US6028065A (en) * | 1998-04-20 | 2000-02-22 | Pharmaceutical Resources, Inc. | Flocculated suspension of megestrol acetate |
ID29270A (en) | 1998-11-20 | 2001-08-16 | Rtp Pharma Inc | MICRO PARTICLES THAT ARE STABILIZED BY PHOSPHOLIPIDS THAT CAN SPREAD |
US6316029B1 (en) * | 2000-05-18 | 2001-11-13 | Flak Pharma International, Ltd. | Rapidly disintegrating solid oral dosage form |
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2001
- 2001-07-11 AT AT01202657T patent/ATE243028T1/en active
- 2001-07-11 PT PT01202657T patent/PT1275377E/en unknown
- 2001-07-11 DE DE60100389T patent/DE60100389T2/en not_active Expired - Lifetime
- 2001-07-11 EP EP01202657A patent/EP1275377B1/en not_active Expired - Lifetime
- 2001-07-11 ES ES01202657T patent/ES2199202T3/en not_active Expired - Lifetime
- 2001-07-11 DK DK01202657T patent/DK1275377T3/en active
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2002
- 2002-07-09 JP JP2003511797A patent/JP2004536118A/en active Pending
- 2002-07-09 PL PL369294A patent/PL204963B1/en not_active IP Right Cessation
- 2002-07-09 NZ NZ530473A patent/NZ530473A/en not_active IP Right Cessation
- 2002-07-09 CA CA2452386A patent/CA2452386C/en not_active Expired - Fee Related
- 2002-07-09 WO PCT/EP2002/007636 patent/WO2003005989A2/en active IP Right Grant
- 2002-07-09 AU AU2002328866A patent/AU2002328866B2/en not_active Ceased
- 2002-07-09 BR BR0211081-4A patent/BR0211081A/en not_active Application Discontinuation
- 2002-07-09 US US10/258,004 patent/US7615547B2/en not_active Expired - Fee Related
- 2002-07-09 KR KR1020047000280A patent/KR100877628B1/en not_active IP Right Cessation
- 2002-07-09 MX MXPA04000211A patent/MXPA04000211A/en active IP Right Grant
- 2002-07-09 RU RU2004103853/15A patent/RU2288704C2/en not_active IP Right Cessation
- 2002-07-09 IL IL15934602A patent/IL159346A0/en not_active IP Right Cessation
- 2002-07-09 ZA ZA200309680A patent/ZA200309680B/en unknown
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2004
- 2004-01-06 NO NO20040043A patent/NO20040043L/en unknown
- 2004-01-07 HR HR20040010A patent/HRP20040010A2/en not_active IP Right Cessation
Also Published As
Publication number | Publication date |
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CA2452386A1 (en) | 2003-01-23 |
EP1275377A1 (en) | 2003-01-15 |
WO2003005989A2 (en) | 2003-01-23 |
BR0211081A (en) | 2004-12-14 |
EP1275377B1 (en) | 2003-06-18 |
KR100877628B1 (en) | 2009-01-07 |
PL369294A1 (en) | 2005-04-18 |
PL204963B1 (en) | 2010-02-26 |
JP2004536118A (en) | 2004-12-02 |
RU2004103853A (en) | 2005-03-27 |
DE60100389D1 (en) | 2003-07-24 |
MXPA04000211A (en) | 2005-03-07 |
DE60100389T2 (en) | 2004-05-19 |
ZA200309680B (en) | 2004-12-22 |
HRP20040010B1 (en) | 2007-01-31 |
NO20040043L (en) | 2004-01-06 |
US20040009232A1 (en) | 2004-01-15 |
PT1275377E (en) | 2003-11-28 |
AU2002328866B2 (en) | 2007-02-15 |
IL159346A0 (en) | 2004-06-01 |
NZ530473A (en) | 2006-02-24 |
HRP20040010A2 (en) | 2004-06-30 |
ATE243028T1 (en) | 2003-07-15 |
KR20040018440A (en) | 2004-03-03 |
US7615547B2 (en) | 2009-11-10 |
ES2199202T3 (en) | 2004-02-16 |
WO2003005989A3 (en) | 2003-05-01 |
RU2288704C2 (en) | 2006-12-10 |
DK1275377T3 (en) | 2003-10-06 |
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