Patent Application
20160136112
The present invention relates to a composition comprising tapentadol in dissolved form and oral dosage forms comprising said composition. The invention further relates to a process for producing the composition comprising tapentadol in a dissolved form and to the corresponding process of producing an oral dosage form containing the composition of the invention. Finally, the invention relates to the use of a saturated tapentadol solution for the preparation of a solid oral dosage form.
Tapentadol is an analgesic whose effect is reported to be based on two molecular mechanisms. Firstly, like opioids, tapentadol may activate μ-receptors and thus presynaptically and postsynaptically attenuates the transmission of pain stimuli in the spinal cord and brain. Secondly, tapentadol may act as a noradrenalin re-uptake inhibitor and thus increases the concentration of that nerve messenger in the synaptic gap.
In the context of this invention, the term “tapentadol” refers to 3-[1R,2R)-(3-dimethylamino)-1-ethyl-2-methylpropyl]phenol according to Formula (1).
Generally, the term “tapentadol” refers to tapentadol in form of the free base or in form of a pharmaceutically acceptable salt. In a particularly preferred embodiment of the present invention tapentadol is present in from of its free base. In another particularly preferred embodiment tapentadol is present in the form of the HCl salt according to Formula (1a)
Synthesis pathways for tapentadol and its use as an analgesic have been described in EP 0 693 475 A1.
Further, EP 1 612 203 discloses crystalline forms of tapentadol hydrochloride, namely Form A reported to belong to the monoclinic system (P21) and Form B reported to belong to the orthorhombic system (P212121), which can be distinguished by X-ray diffraction. It is further reported that the crystalline polymorph A converts to Form B in the temperature range between 40 and 50° C. The result is reversible since Form B is changing into Form A at a lower temperature.
EP 2 240 431 discloses crystalline forms of tapentadol base, namely Form A, Form B and Form C. It is disclosed that mixtures of form A and B are obtained when tapentadol base is crystallised under ambient conditions.
However, such a behaviour (occurrence of morphological changes) can be unfavourable for example for dosage forms such as tablets, since it may cause solid state changes in the dosage form, often resulting in different dissolution and pharmacokinetic properties. Such changes hence may require a strict temperature control of the dosage forms, especially in summer and/or in climate zones III and IV. Additionally, such solid state changes may lead to regulatory and commercial disadvantages.
Hence, it was an object of the present invention to overcome the above drawbacks of the above-mentioned formulation.
In particular, it was an object of the present invention to provide tapentadol hydrochloride in a form in which does not require a specific temperature control during storage or when used in climate zones III and IV.
Further, a form of tapentadol hydrochloride should be provided that shows advantageous dissolution and pharmacokinetic properties, in particular when used after storage or in in climate zones III and IV.
Further, a form of tapentadol hydrochloride should be provided that shows improved properties with regard to processability.
Additionally, it was an object to provide a pharmaceutical composition containing tapentadol in a form not being protected by the scope of EP 1 612 203 and EP 2 240 431. Further, said composition should show in-vitro and/or in-vivo pharmacokinetic properties being similar to the ones of the compositions as disclosed in EP 1 612 203 and EP 2 240 431.
All the above-mentioned objectives should preferably be solved for a dosage form designed for immediate release (“IR”) and for modified release (“MR”).
According to the present invention, the above objectives can be achieved by a pharmaceutical composition comprising dissolved tapentadol, organic solvent with a high boiling point and carrier. In the composition of the present invention tapentadol is present in a dissolved form in an organic solvent with a high boiling point and may adhere to said carrier or is preferably adsorbed on said carrier in dissolved form. The composition can advantageously be processed into oral dosage forms and can be used under hot environmental conditions without undergoing any solid state changes.
Thus, the subject of the invention is a pharmaceutical composition, preferably a pharmaceutical composition having a solid appearance, comprising
Atmospheric pressure, 1013 mbar and 760 mm Hg are equivalent values and refer to standard pressure.
A further subject of the present invention is an oral dosage form comprising the composition of the invention and optionally further pharmaceutical excipient(s).
Another subject of the present invention is a method of producing the composition according to the invention comprising the steps of
Further, the subject of the present invention relates to a process for producing an oral dosage form comprising the steps of
Finally, a subject of the present invention relates to the use of saturated tapentadol solution for producing a solid oral dosage form wherein said dosage form is free of crystalline tapentadol.
The above-illustrated subjects of the present invention are alternative solutions to the above-outlined problems.
The present invention concerns a pharmaceutical composition, which is mixture of a solid state carrier and tapentadol in dissolved state. Preferably, the physical appearance of the entire composition is solid, at 25° C. The same applies for the dosage form of the present invention.
The organic solvent (b) has a boiling point of 110° C. to 350° C., wherein the boiling point is measured at 1013 mbar. However, this does not imply that the tapentadol has to be dissolved at 1013 mbar in the organic solvent (b).
The term “tapentadol” as used in the present application preferably can refer to tapentadol according to the above formula (1) or tapentadol hydrochloride according to the above formula (1a). Alternatively, it can refer to pharmaceutically acceptable solvates, hydrates and mixtures thereof.
In a particularly preferred embodiment the composition of the present invention as well as the oral dosage form of the present invention comprise tapentadol as the sole pharmaceutical active agent.
In an alternative embodiment the composition of the present invention as well as the oral dosage form of the present invention can comprise tapentadol in combination with further pharmaceutical active agent(s).
In the present invention tapentadol is present in a dissolved form.
The term “dissolved tapentadol” can be used in the context of this invention to designate the above compound in which the components (atoms, ions or molecules) do not exhibit a periodic arrangement over a great range (=long-range order), such as usually known from crystalline substances. Consequently, the present tapentadol hydrochloride for example does not show any clear interferences determined by means of X-ray diffraction. The present tapentadol hydrochloride components (atoms, ions or molecules, preferably ions) each are preferably surrounded by a solvate shell. This solvate shell can be composed of several layers of solvent molecules wherein the molecules of the various layers of the solvate shell interact with the core molecule the more the closer they are to said core molecule. Solvated molecules can preferably be regarded as a flexible entity whose solvate shell is in interaction with solvent molecules.
In a preferred embodiment dissolved tapentadol hydrochloride can be regarded as non-solid tapentadol hydrochloride or in other words tapentadol hydrochloride in a non-solid form.
In a preferred embodiment of the composition the organic solvent (b) has a melting point between −80° C. and 25° C., preferably between −75° C. and 10° C., more preferably between −72° C. and 5° C., especially between −70° and −5° C. at 1013 mbar. Thus, the organic solvent used in the present invention is liquid at room temperature (25° C.).
It is further preferred that the organic solvent (b) has a boiling point of 110° C. to 350° C., preferably at 1013 mbar. Further preferred, the organic solvent can have a boiling point of at least 120° C., 130° C., 140° C., 150° C., 160° C., 170° C., 180° C. or 190° C. Further preferred, the organic solvent can have a boiling point of up to 345° C., 340° C., 335° C., 330° C., 325° C., 320° C., 315° C. or 310° C. All possible combinations (e.g. 170 to 340° C.) of the above lower and upper limits are also preferred. Preferably, the temperature is determined at 1013 mbar. In this application a “boiling point of 110 to 350° C.” also encompasses those organic solvents (b) that undergo decomposition in said temperature range. Further, the boiling point is not related to a single temperature but can also refer to a temperature interval, for example when a mixture of organic solvents is used.
Preferably, the boiling point is determined according to Pharm. Eur. 4.0, Chapter 2.2.12.
In a further embodiment of the invention the organic solvent (b) has a density of 0.95 to 1.30 g/ml.
It is further preferred that the organic solvent (b) has a density of 1.00 to 1.20 g/ml at 25° C., even more preferably 1.02 to 1.17 g/ml, especially 1.03 to 1.13 g/ml. The density can be determined the following formula:
m=the mass of the solvent
V=volume of the solvent
In a further embodiment of the invention the organic solvent (b) has a vapour pressure of less than 10 hPa or mbar at 20° C., preferably less than 1 hPa or mbar at 20° C.
The vapour pressure is the vapour exerted by a vapour P in a thermodynamic equilibrium with its liquid phase at a given temperature in a closed system. According to the Antoine equation the estimated vapour pressures can be calculated.
wherein A, B and C are substance-specific coefficients (i.e., constants or parameters) and
T is the temperature of the liquid.
It is preferred that the organic solvent (b) comprises one to three hydroxy groups, preferably two or three hydroxy groups, especially two hydroxy groups.
For example, organic solvent (b) can be polyethylene glycols such as tetraethylene glycol- and, pentaethylene glycol, alcohol, polyethyleneglycol ether, such as diethyleneglycol monoethylether, glycerol, propylene glycol such as 1,2-propylene glycol, alkyl diols such as 2,3-butanediol, triols such as 1,2,6-hexantriol, dimethylisosorbid, Glycofurol (tetrahydrofufuryl polyethylene glycol), polydimethyl siloxane and mixtures thereof. Especially preferred are 1,2-propylene glycol, 2,3-butanediol, glycerol, dimethylisosorbid, Glycofurol and diethyleneglycol monoethylether. Dimethylisosorbid is particularly preferred.
The composition of the present invention can preferably have a weight ratio of dissolved tapentadol (a) to organic solvent (b) of 1:1 to 1:15, preferably of 1:1 to 1:10, more preferably of 1:1 to 1:7, most preferably of 1:1 to 1:5.
It turned out that with the above ratio it can be particularly assured that the complete amount of tapentadol remains in the dissolved state and does not precipitate as a solid (crystalline) substance.
The present composition further comprises a carrier (c). The carrier is preferably solid, wherein “solid” refers to the appearance at 25° C. The term “carrier (c)” may refer to a single carrier (c) or a mixture of more than one carrier (c). The carrier (c) can be regarded as a substance to which dissolved tapentadol (a) and organic solvent (b) can be adhered/adsorbed, wherein it is assured that the tapentadol maintains its dissolved state. Thus, the carrier (c) can be regarded as a stabilizer of dissolved tapentadol (a) in organic solvent (b). Generally, the solid carrier (c) can be a substance which is capable of inhibiting the transformation of dissolved, preferably dissolved, tapentadol to any solid state (e.g. amorphous or crystalline) of tapentadol.
Further, due to the solid carrier (c) the physical composition can be provided in a state suitable for further processing, such as filling in a capsule.
In a preferred embodiment the present composition can have a Carr's Index of 5 to 21. In alternative more preferred embodiment the present composition can have a Carr's Index of 12 to 16. In alternative even more preferred embodiment the present composition can have a Carr's Index of 5 to 15. The Carr's Index (%) can be determined by the following equation
The tapped density and poured density is determined according Pharm. Eur. 4.0, 2.9.15. The tapped density is determined after 1250 stamps (V1250).
In a preferred embodiment the composition of the invention can comprise tapentadol (a) and carrier (c), wherein the weight ratio of dissolved tapentadol (a) to carrier (c) can be from 1:1 to 1:20, preferably from 1:1 to 1:15, more preferably from 1:1 to 1:10 and particularly from 1:1 to 1:7.
Generally, the carrier (c) can be a non-brittle or brittle substance.
Pharmaceutical excipients, such as carriers, can generally be classified with regard to the change in the shape of the particles under compression pressure (compaction): plastic excipients are characterised by plastic deformation, whereas when compressive force is exerted on brittle substances, the particles tend to break into smaller particles. Brittle behaviour on the part of the substrate can be quantified by the increase in the surface area in a moulding. In the art, it is customary to classify the brittleness in terms of the “yield pressure”. According to a simple classification, the values for the “yield pressure” are low for plastic substances but high in the case of friable substances (Duberg, M., Nyström, C., 1982, “Studies on direct compression of tablets VI. Evaluation of methods for the estimation of particle fragmentation during compaction”, Acta Pharm. Suec. 19, 421-436; Humbert-Droz P., Mordier D., Doelker E., “Méthode rapide de détermination du comportement á la compression pour des études de préformulation.”, Pharm. Acta Helv., 57, 136-143 (1982)). The “yield pressure” describes the pressure that has to be reached for the excipient (i.e. preferably the vehicle) to begin to flow plastically.
The “yield pressure” is preferably calculated by using the reciprocal of the gradient of the Heckel plot, as described in York, P., Drug Dev. Ind. Pharm. 18, 677 (1992). The measurement in this case is preferably made at 25° C. and at a deformation rate of 0.1 mm/s.
In the context of the present invention, an excipient (especially a carrier) is deemed to be a non-brittle excipient when it has a “yield pressure” of not more than 120 MPa, preferably not more than 100 MPa, in particular 5 to 80 MPa. An excipient is usually described as a brittle excipient when it has a “yield pressure” of more than 80 MPa, preferably more than 100 MPa, particularly preferably more than 120 MPa, especially more than 150 MPa. Brittle excipients may exhibit a “yield pressure” of up to 300 MPa or up to 400 MPa or even up to 500 MPa.
Examples of non-brittle excipients (vehicles) are mannitol or starch.
In a preferred embodiment the non-brittle substance is not povidone.
Examples of brittle excipients (vehicles) are silicates or aluminosilicates, preferably magnesium aluminosilicates.
In a particularly preferred embodiment, brittle substances are used as a carrier (c) in the oral dosage form of the present invention.
It is further preferred that the carrier (c) is a non-water-soluble substance. A non-water-soluble substance generally is a pharmaceutical excipient as specified in the European Pharmacopoeia, with a water solubility of less than 33 mg/ml, measured at 25° C. Preferably, the non-water-soluble substance has a solubility of 10 mg/ml or less, more preferably 5 mg/ml or less, especially 0.01 to 2 mg/ml (determined according to Column Elution method pursuant to EU Directive RL67-548-EWG, Appendix V Chapt. A6).
In a preferred embodiment of the invention the carrier can be an organic polymer or an inorganic substance.
In a preferred alternative embodiment of the invention the carrier (c) can preferably be an organic polymer. In addition, the carrier (c) can also include substances which behave like polymers. Examples of these substances are fats and waxes. Furthermore, the carrier (c) can also include solid, non-polymeric compounds, which preferably can contain polar side groups. Examples of these compounds are sugar alcohols or disaccharides.
In a preferred embodiment the carrier (c) can be a polymer. The polymer to be used for the preparation of the pharmaceutical composition preferably may have a glass transition temperature (Tg) of more than 45° C., more preferably of 50° C. to 150° C., in particular of 55° C. to 120° C. A respective Tg can be important for achieving the desired properties of the resulting dosage form.
In the present invention the term “glass transition temperature” (Tg) describes the temperature at which amorphous or partially crystalline polymers change from the solid state to the liquid state. In the process a distinct change in physical parameters, e.g. hardness and elasticity, occurs. Beneath the Tg a polymer is usually glassy and hard, whereas above the Tg it changes into a rubber-like to viscous state. The glass transition temperature is determined in the context of this invention by means of dynamic differential scanning calorimetry (DSC).
For this purpose, a Mettler Toledo® DSC 1 apparatus can be used. The work is performed at a heating rate of 1-20° C./min, preferably 10° C./min, and at a cooling rate of 5° C. to 50° C./min, preferably 50° C./min.
In general, the organic polymer to be used as carrier (c) preferably can have a weight-average molecular weight of 1,000 to 500,000 g/mol, more preferably from 1,500 to 100,000 g/mol and particularly from 2,000 to 50,000 g/mol. The weight-average molecular weight is preferably determined by means of gel permeation chromatography.
If the organic polymer used as carrier (c) is dissolved in water in an amount of 2% by weight, the resulting solution preferably can have a viscosity of 1 to 50 mPa·s, more preferably 1.5 to 20 mPa·s, and even more preferably from 2 to 12 mPa·s or (especially in the case of HPMC) from 12 to 18 mPa·s, measured at 25° C., and determined in accordance with Ph. Eur. 6.0, Chapter 2.2.10.
In the present invention, hydrophilic polymers can preferably be used as carrier (c). The term “hydrophilic polymers” generally refers to polymers which possess hydrophilic groups. Examples of suitable hydrophilic groups can be hydroxy, sulfonate, carboxylate and quaternary ammonium groups.
The carrier (c) may, for example, comprise the following polymers: microcrystalline cellulose, polysaccharides, such as hydroxypropyl methyl cellulose (HPMC), ethyl cellulose, methyl cellulose, hydroxyethyl cellulose, ethyl hydroxyethyl cellulose, hydroxypropyl cellulose (HPC), polyvinyl alcohol, and mixtures thereof.
In a preferred embodiment the carrier does not comprise polyvinylpyrrolidone.
Likewise, it can preferably be possible to use sugar alcohols such as mannitol, sorbitol or xylitol as carriers (c).
Alternatively, also a silicone, preferably further mixed with silicon dioxide such as simethicone, can be used as carrier (c).
In a more preferred embodiment of the invention the carrier (c) can be an inorganic substance. An inorganic substance can preferably be regarded as a compound that does not contain a hydrocarbon group. It is further preferred that the carrier (c) can be a phosphate or a silicate, preferably a silicate, more preferably an aluminosilicate.
Examples for inorganic substances suitable to be used as carriers are phosphates, such dicalcium phosphate, silicium dioxides such as aerosil, silica gel or Aeroperl 300, clay minerals, such as kaolinite, bentonite and montmorillonite, kieselguhr (celite), zeolites, mesoporous silica, such as MSU-G, MSU-F, MCM-48 and SBA-15, and magnesium aluminosilicates, such as Al2O3.MgO.1.7SiO2.xH2O (Neusilin), or mixtures therefrom.
Further, active coal (i.e. activated carbon) can be preferably used as carrier (c).
In a preferred embodiment the carrier (c), in particular the inorganic carrier (c), has a specific surface area of 50 to 450 m2/g, more preferably 75 to 400 m2/g, in particular 100 to 300 m2/g. The specific surface area preferably is determined by gas adsorption according to Ph. Eur., 6th edition, Chapter 2.9.26. For this purpose, an ASAP® 2020 (Micrometrics) and an ‘outgasing’ temperature of 40° C. is used. It has surprisingly been found that the above-mentioned specific surface area might be beneficial for achieving the above-mentioned objects (e.g. stabilisation of the dissolved state of tapentadol hydrochloride).
In a preferred embodiment the carrier (c) is selected from simethicone, activated carbon, microcrystalline cellulose, starch, polysaccharides, sugar alcohols, phosphates, silicium dioxides, clay minerals, kieselguhr, zeolites, mesoporous silica and magnesium aluminosilicates, or mixtures thereof.
In a more preferred embodiment the carrier (c) is selected from simethicone, active coal, microcrystalline cellulose, phosphates, silicium dioxides, clay minerals, kieselguhr, zeolites, mesoporous silica and magnesium aluminosilicates, or mixtures thereof.
Most preferred as carrier (c) are silicates, in particular magnesium aluminosilicates, especially Al2O3.MgO.1.7SiO2.xH2O (neusilin) and bentonite.
Most preferred as carrier (c) are further mesoporous silica, especially Aeroperl® 300, celite, MSU-G, MSU-F, MCM-48 and SBA-15.
The composition of the present invention can be applied in form of an oral dosage form, in particular in form of a solid oral dosage form. Thus, another object of the present invention is a solid oral dosage form comprising a tapentadol hydrochloride composition according to the present invention and further pharmaceutical excipient(s).
The pharmaceutical excipients are excipients with which the person skilled in the art is familiar, such as those which are described in the European Pharmacopoeia (Ph. Eur.) and/or in the US Pharmacopoeia (USP).
In a preferred embodiment of the present invention the oral dosage form can further comprise one or more excipients(s) selected from surfactants (d), fillers (e), binders (f), disintegrants (g), lubricants (h), and glidants (j).
Surfactants (d) can be regarded as substances lowering the interfacial tension between two phases, thus enabling or supporting the formation of dispersions or working as a solubilizer. Common surfactants are alkylsulfates (for example sodium lauryl sulfate), alkyltrimethylammonium salts, alcohol ethoxylates and the like. Surfactants can be used in an amount of 0 to 2% by weight, preferably of 0.1 to 1.5% by weight, based on the total weight of the oral dosage form.
It is particularly preferred that the oral dosage form of the present invention does not contain a surfactant.
Fillers (e) or diluents can be used to increase the bulk volume and weight of a low-dose drug to a limit at which a pharmaceutical dosage form can be formed. Fillers should fulfil several requirements, such as being chemically inert, non-hygroscopic, biocompatible, easily processable and possessing good biopharmaceutical properties. Examples of fillers are lactose, sucrose, glucose, mannitol, calcium carbonate, cellulose and others. Fillers (e) can be used in an amount of 0 to 25% by weight, preferably 1 to 20% by weight, based on the total weight of the dosage form.
Binders (f) may be added to the pharmaceutical formulation in order to ensure that oral dosage forms, preferably tablets, can be formed with the required mechanical strength. The binder can, for example, be starch, polyvinyl pyrrolidone or cellulose derivatives. The binding agent can be present in an amount of 0 to 20% by weight, preferably 1 to 18% by weight, more preferably 2 to 15% by weight, in particular 3 to 12% by weight, based on the total weight of the pharmaceutical formulation.
Disintegrants (g) are compounds which enhance the ability of the dosage form, preferably the ability of the tablet to break into smaller fragments when in contact with a liquid, preferably water. Preferred disintegrants are sodium carboxymethyl starch, cross-linked polyvinyl pyrrolidone (crospovidone), sodium carboxymethyl glycolate (for example Explotab®), swelling polysaccharide, for example soy polysaccharide, carrageenan, agar, pectin, starch and derivatives thereof, protein, for example formaldehyde-casein, sodium bicarbonate or mixtures thereof. More preferred are sodium carboxymethyl cellulose and cross-linked polyvinyl pyrrolidone (crospovidone). Disintegrants can be used in an amount of 0 to 15% by weight, preferably of 1 to 12% by weight, more preferably 3 to 10% by weight, based on the total weight of the dosage form.
The function of lubricants (h) is reported to ensure that tablet formation and ejection can occur with low friction between the solid and the die wall. Further, lubricants can generally increase the powder flowability. The lubricant is preferably a stearate or fatty acid, more preferably an earth alkali metal stearate, such as magnesium stearate. The lubricant is suitably present in an amount of 0 to 2% by weight, preferably of about 0.1 to 1.0% by weight, based on the total weight of the dosage form.
Glidants (j) can also be used to improve the flowability. Traditionally, talc was used as glidant, but is nowadays nearly fully replaced by colloidal silica (for example Aerosil®). Preferably, the glidant can be present in an amount of 0 to 3% by weight, more preferably 0.1 to 2.5% by weight, in particular 0.25 to 2.0% by weight based on the total weight of the dosage form.
It lies in the nature of pharmaceutical excipients that they sometimes can perform more than one function in a pharmaceutical formulation. In this regard it is generally noted that due to the nature of pharmaceutical excipients it cannot be excluded that a certain compound meets the requirements of more than one of the components (b) or (c) and (d) to (j). Therefore, colloidal silica (Aerosil) may function as a carrier for forming the composition according to the invention as well as a pharmaceutical excipient (j), i.e. the fact that colloidal silica is used as component for forming the composition according to the invention does not mean that it cannot also be acting as a glidant (j).
However, in order to enable an unambiguous distinction, it is preferred in the present application that one and the same pharmaceutical compound can only function as one of the compounds (b) or (c) and (d) to (j). For example, if microcrystalline cellulose functions as a carrier (c), it cannot additionally function as a disintegrant (g), even though microcrystalline cellulose also exhibits a certain disintegrating effect.
The oral dosage form of the present invention can preferably comprise the following amounts of components:
10 to 300 mg tapentadol, preferably 25 to 250 mg tapentadol, particularly 50, 100 or 250 mg tapentadol,
50 to 750 mg organic solvent, preferably 100 to 650 mg organic solvent, particularly 200 to 500 mg organic solvent,
40 to 650 mg carrier, preferably 80 to 550 mg carrier, particularly 125 to 450 mg carrier,
0 to 20 mg surfactant, preferably 2 to 15 mg surfactant, particularly 4 to 10 mg surfactant,
0 to 250 mg filler, preferably 25 to 200 mg filler, particularly 40 to 100 mg filler,
0 to 125 mg binder, preferably 15 to 100 mg binder, particularly 25 to 75 mg binder,
0 to 100 mg disintegrant, preferably 5 to 75 mg disintegrant, particularly 10 to 50 mg disintegrant,
0 to 25 mg glidant, preferably 1 to 15 mg glidant, particularly 2 to 7 mg glidant, 0 to 15 mg lubricant, preferably 1 to 10 mg lubricant, particularly 2 to 8 mg lubricant.
In a preferred embodiment the oral dosage form of the present invention can preferably comprise:
1 to 25 wt. % tapentadol, preferably 3 to 22 wt. % tapentadol, particularly 5 to 20 wt. % tapentadol,
5 to 50 wt. % organic solvent, preferably 10 to 55 wt. % organic solvent, particularly 20 to 50 wt. % organic solvent,
5 to 40 wt. % carrier, preferably 10 to 38 wt. % carrier, particularly 20 to 35 wt. % carrier,
0 to 2 wt. % surfactant, preferably 0.05 to 1.6 wt. % surfactant, particularly 0.1 to 1.5 wt. % surfactant,
0 to 25 wt. % filler, preferably 1 to 20 wt. % filler, particularly 3 to 10 wt. % filler,
0 to 20 wt. % binder, preferably 2 to 15 wt. % binder, particularly 3 to 12 wt. % binder,
0 to 15 wt. % disintegrant, preferably 1 to 12 wt. % disintegrant, particularly 3 to 10 wt. % disintegrant
0 to 2 wt. % lubricant, preferably 0.1 to 1.0 wt. % lubricant, particularly 0.2 to 0.8 wt. % lubricant,
0 to 3 wt. % glidant, preferably 0.1 to 2.5 wt. % glidant, particularly 0.25 to 2.0 wt. % glidant,
based on the total weight of the oral dosage form.
In a still further embodiment of the present invention the oral dosage form can be a capsule or a tablet, more preferably a tablet, for peroral use. Alternatively, the solid oral dosage form can be filled as powder or granulate into devices like sachets or stick-packs.
The present invention further relates to a method for producing a composition according to the invention. Hence, a further subject of the present invention is a method for producing a composition comprising dissolved tapentadol (a), organic solvent (b), and carrier (c) comprising the steps of
Generally, the comments made above for tapentadol, organic solvent and carrier can also apply to the method of the present invention.
In step i) of the method of the invention tapentadol is dissolved in organic solvent (b).
The term “dissolving” means that a substance, such as tapentadol, is brought into contact with the solvent, preferably with a solvent or solvent mixture as defined above for compound (b), e.g. a mixture of polyethylene glycols having an average molar weight of 190 to 210 g/mol (PEG 200) or 1,2-propyleneglycol, wherein the solvent wets the surface of the substance or the substance can be completely dissolved in the solvent. When a clear solution is obtained and no tapentadol (crystals) can be detected by visual control, this can be regarded as a complete dissolving of tapentadol in an organic solvent.
In a preferred embodiment tapentadol is preferably added to organic solvent. It is further preferred that the organic solvent is preferably stirred and/or heated, preferably to a temperature of about 80° C.
In a preferred embodiment tapentadol can be dissolved in organic solvent (b), preferably under stirring during the dissolving step, preferably at a stirring speed of 300 to 450 rpm (rotations per minute). Additionally, it is preferred that the solvent is at an elevated temperature, preferably at about 80° C., during the dissolving step. Further, tapentadol is preferably added in crystalline form.
Further, to support the formation of the solution of step i) tapentadol in organic solvent can be subjected to a mechanical treatment, such as ultrasonic treatment. Generally, ultrasonic treatment can be carried out by immersing tapentadol and organic solvent into an ultrasonic device, for example an ultrasonic bath. Examples of ultrasonic treatment are hydrodynamic cavitation, sono-fragmentation and/or sono-cavitation or co-grinding. For example, ultrasonic treatment can be carried out with Tesla ultrasonic equipment.
Ultrasonic treatment can preferably be performed by using ultrasonic waves having a frequency of 5 to 100 kHz, more preferably of 10 to 80 kHz. Furthermore, ultrasonic treatment is preferably performed by using ultrasonic waves having an intensity of 50 to 5000 W, more preferably 500 to 1000 W. As an example, 1000 W and 20 kHz or 500 W and 58 kHz can be used.
Usually, the mechanical treatment can be carried out for 1 to 30 minutes, preferably for 5 to 20 minutes.
Once the tapentadol is completely dissolved in organic solvent (b) in step ii), carrier (c) and the solution of step i) can be mixed.
In a preferred embodiment carrier (c) is added to the solution of step i). It is preferred that the solution of step i) is at elevated temperature, preferably about 80° C., when the mixing with carrier (c) is carried out. Further, the solution is preferably stirred, preferably at a stirring speed of 300 to 550 rpm (rotations per minute) during the mixing step ii).
In a preferred embodiment the mixture of step ii), preferably after being allowed to cool to 23° C., can be obtained as a powder-like material.
In an alternative embodiment further pharmaceutical active agent can be added to the mixture between step ii) and optional step iii).
In optional step iii) the mixture of step ii) can preferably be milled and/or sieved.
The milling can preferably be performed in conventional milling apparatuses, such as in a ball mill, air jet mill, pin mill, classifier mill, cross beater mill, disk mill, mortar grind-er or a rotor mill. A planetary ball mill is preferably used.
The milling time is preferably 0.5 minutes to 30 minutes, preferably 1 to 15 minutes, more preferably 3 to 7 minutes.
It is preferred that the sieving of the mixture of step ii) can be carried out with a sieve having a mesh size of 25 to 1000 μm, preferably 50 to 800 μm, especially 100 to 600 μm.
Further, the subject of the present invention relates to a method for preparing the oral dosage of the invention comprising the steps:
In steps i) to iii) a composition according to the present invention is provided, i.e. all the above process steps i), ii) and iii) leading to the present composition also apply to the process for preparing the present oral dosage form.
In step iv) additional further excipient(s) and/or further pharmaceutically active agent can optionally be added to the mixture of step ii) or step iii). During or after the addition of the optional excipients and/or further pharmaceutically active agent the resulting mixture can preferably be blended. The excipients can preferably be selected from the excipients (d), (e), (f), (g), (h) and (j) as described above.
In step v) the mixture of step ii), step iii) or step iv) is processed into a solid oral dosage form. Processing the mixture of step ii), step iii) or step iv) into a solid oral dosage form can preferably comprise filling said mixture into capsules, preferably hard gelatine capsules. Optionally, processing the mixture of step ii), step iii) or step iv) into tablets can be carried out by compressing said formulation on a rotary press, e.g. on a Fette® (Fette GmbH, Germany) or a Riva® piccola (Riva, Argentina). If a rotary press is applied, the main compression force can range from 1 to 50 kN, preferably 3 to 40 kN. The resulting tablets can have a hardness of 30 to 400 N, more preferred of 50 to 250 N, particularly preferably of 30 to 180 N, more preferably 40 to 150 N, wherein the hardness can be measured according to Ph. Eur. 6.0, Chapter 2.9.8. For the optional filling of the formulation into capsules, dependent dosing systems (for example an auger) or preferably independent dosing systems (for example MG2, Matic (IMA)) can be used.
Further, the dosage form, preferably the tablet, of the invention preferably has a content uniformity, i.e. a content of active agent(s), which lies within the concentration of 90 to 110%, preferably 95 to 105%, especially preferred from 98 to 102% of the average content of the active agents(s). The “content uniformity” is determined with a test in accordance with Ph. Eur., 6.0, Chapter 2.9.6. According to that test, the content of the active agents of each individual tablet out of 20 tablets must lie between 90 and 110%, preferably between 95 and 105%, especially between 98 and 102% of the average content of the active agents(s). Therefore, the content of the active drugs in each tablet of the invention differs from the average content of the active agent by at most 10%, preferably at most 5% and especially at most 2%.
In addition, the resulting tablet preferably has a friability of less than 5%, particularly preferably less than 2%, especially less than 1%. The friability is determined in accordance with Ph. Eur., 6.0, Chapter 2.9.7. The friability of tablets generally refers to tablets without coating.
The pharmaceutical formulation of the invention may be a peroral tablet which can be swallowed unchewed. The tablet can preferably be film coated.
Generally, film coatings that do not affect the release of the active agent(s) and film coatings affecting the release of the active agent(s) can be employed with tablets according to invention. The film coatings that do not affect the release of the active agent(s) are preferred.
Preferred examples of film coatings which do not affect the release of the active ingredient can be those including poly(meth)acrylate, methylcellulose (MC), hydroxypropyl methylcellulose (HPMC), hydroxypropyl cellulose (HPC), hydroxyethyl cellulose (HEC), polyvinylpyrrolidone (PVP) and mixtures thereof. These polymers can have a weight-average molecular weight of 10,000 to 150,000 g/mol.
In an alternative preferred embodiment, the film coating can affect the release of the active agent. Examples for film coatings affecting the release of the active agent are gastric juice-resistant film coatings and retard coatings.
In the preferred embodiment the film can have a thickness of 2 μm to 150 μm, preferably from 10 to 100 μm, more preferably from 20 to 60 μm.
In a preferred embodiment the dosage form of the invention is for modified release. In that case the release profile of the pharmaceutical formulation, preferably of the tablet, according to USP method (USP paddle apparatus, 900 ml test medium, in phosphate buffer at pH 6.8 and 37° C., 100 rpm) after 2 hours indicates a content release of 0 to 90%, preferably of 10 to 80%, further preferably 15 to 75%, more preferably 20 to 50% and particularly of 25 to 40%.
In an alternatively preferred embodiment of the invention the dosage form is for immediate release. In that case the release profile of the pharmaceutical formulation, preferably of the tablet, according to USP method (USP paddle apparatus, 900 ml test medium, in phosphate buffer at pH 6.8 and 37° C., 100 rpm) after 15 minutes indicates a content release of at least 50%, preferably at least 70%, especially at least 90%.
Further, the invention relates to the use of a saturated tapentadol solution for producing a solid oral dosage form, wherein said dosage form is free of crystalline tapentadol.
A saturated tapentadol solution is a solution containing as much tapentadol without forming a precipitate that the maximum of dissolved tapentadol is reached. The saturation of a solution may depend on its temperature.
The compositions were examined by X-ray powder diffraction.
The measurements were performed as follows: The samples were measured on a D8 Advance powder X-ray diffractometer (Bruker-AXS, Karlsruhe, Germany) in a PMMA sample holder rotating at 20 rpm during the measurement (Bragg-Brentano geometry). Further conditions for the measurements are summarized below. The raw data were analysed with the program EVA (Bruker-AXS, Karlsruhe, Germany).
Instrument: Agilent 1200 coupled with Esquire HCT (Bruker Daltonics)
Column: Interchim Uptishere Strategy 2.2 Pro 920212;
Detection: UV/DAD (κ=274.4 nm)
Column temp.: 40° C.
Flow [mL/min]: 0.8
Injection volume: 3 μL
Solvent A: acetonitrile
Solvent B: 0.2% formic acid and 0.1% HFBA, pH 2.8
Gradient
MS parameters:
Tapentadol hydrochloride was dissolved in solvent at 80° C. To the clear solution Neusilin® was added portionwise with stirring at 80° C., then the mixture was allowed to cool down to room temperature. A powder-like material was obtained. The employed amounts and the resulting solid state of the formulations are specified in Table 1.
Samples were stored in open and closed glass vials at 40° C./75% relative humidity. XRPD analysis was performed after two weeks and three months, respectively.
The above results show that even after storage over a period of three months the compositions of the present invention do not show any amounts of crystalline phase. Thus, the tapentadol hydrochloride is maintained in dissolved state.
Preparation of Tapentadol HCl and Neusilin corresponding to example 1a of WO2011/138037
0.2 g of crystalline Tapentadol hydrochloride was dissolved in 2 mL water and 12 mL isopropanol under stirring at RT. 0.2 g Neusilin US2 was added and the mixture was stirred for 5 min at RT. The solvent was evaporated to yield a white, free-flowing powder.
Preparation of Tapentadol HCl and povidone corresponding to example 4 of US2010272815
0.5 g of crystalline Tapentadol hydrochloride was dissolved in 20 mL Methanol under stirring at RT. 0.5 g Povidone was added, the solution was filtrated through 0.45 micron filter, and the solvent evaporated at 50° C. under vacuum for 4 h. The resulting mass was cooled to RT to yield a pasty gum.
Chemical purity was analysed for most of the samples with LC-MS. Chemical purity stayed constant during experiments.
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1,2-propanediol has a boiling point of 187° C. at atmospheric pressure and a vapour pressure constant of 0.1 mbar at 20° C. Although a highest possible concentration of Tapentadol HCl in solution was obtained, there is no indication that Tapentadol HCl crystallises in the present sample, i.e. tapentadol hydrochloride stays dissolved.
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| Number | Date | Country | Kind |
|---|---|---|---|
| 13179047.9 | Aug 2013 | EP | regional |
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/EP2014/066583 | 8/1/2014 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 61861473 | Aug 2013 | US |
