NZ535808A

NZ535808A - Micronized crystalline tiotropium bromide

Info

Publication number: NZ535808A
Application number: NZ535808A
Authority: NZ
Inventors: Helmut Bender; Hagen Graebner; Konrad Schindler; Michael Josef Friedrich Trunk; Michael Walz
Original assignee: Boehringer Ingelheim Pharma
Priority date: 2002-03-20
Filing date: 2003-03-10
Publication date: 2005-09-30
Also published as: NO20044003L; TW200305421A; HRP20040855A2; EA007064B1; EP1785422A1; EP1487832B9; CN101220025A; UY27725A1; KR20050008662A; RS57551B1; HUE031876T2; AR039017A1; ZA200405636B; DK1487832T3; CA2479652A1; DE10212264A1; UA78295C2; EP1487832A1; DE50307883D1; HRP20040855B1

Abstract

Micronized crystalline tiotropium bromide, processes for preparing it and its use for preparing a pharmaceutical composition, particularly for preparing a pharmaceutical composition with an anticholinergic activity are described. In particular, crystalline tiotropium bromide micronisate, characterized by a particle size X50 of between 1.0 um and 3.5 um at a Q(5.8) value of more than 60%, by a specific surface value in the range between 2m2/g and 5m2/g, by a specific heat of solution of more than 65 Ws/g and by a water content from about 1% to about 4.5%, is disclosed. The described pharmaceutical composition may be in the form of an inhalable powder and is useful in treating asthma or COPD.

Description

<div class="application article clearfix" id="description"> New Zealand Paient Spedficaiion for Paient Number 535808 WO 03/078429 PCT/EP03/02422 80280pct.210 MICRONIZED CRYSTALLINE TIOTROPIUM BROMIDE 535 8 08 The invention relates to a crystalline micronisate of (1a,2p,4p,5a,7P)-7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02'4]nonane-bromide, processes for preparing it and its use for preparing a pharmaceutical composition, particularly for preparing a pharmaceutical composition with an anticholinergic activity. Background to the invention The compound (1a,2p,4p,5a,7P)-7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02'4]nonane-bromide, is known from European Patent Application EP 418 716 A1 and has the following chemical structure: Br (I) The compound has valuable pharmacological properties and is known by the name tiotropium bromide (BA679). Tiotropium bromide is a highly effective anticholinergic and can therefore provide therapeutic benefit in the treatment of asthma or COPD (chronic obstructive pulmonary disease). Tiotropium bromide is preferably administered by inhalation. Suitable inhalable powders packed into appropriate capsules (inhalettes) and administered by suitable powder inhalers may be used. Alternatively, it may be administered by the use of suitable inhalable aerosols. These also include powdered inhalable aerosols which contain, for example, HFA134a, HFA227 or mixtures thereof as propellant gas. In view of the administration of tiotropium bromide by inhalation it is necessary to provide the active substance in a finely divided (or micronised) form. Preferably, the active substance has an average particles size of 0.5 to 10|jm, preferably from 1 to 6|jm, most preferably from 1.5 to 5|jm. (intellectual property office! of iuz 1 - JUL 2005 2 The above particle sizes are generally achieved by grinding (so-called micronisation) of the active substance. As breakdown of the pharmaceutical^ active substance must be prevented as far as possible as a side-effect of the micronisation, in spite of the hard conditions required for the process, high stability of the active substance during the grinding process is absolutely essential. It should be borne in mind that in some cases, during the grinding process, changes may occur to the solid properties of the active substance, which may influence the pharmacological properties of the formulation which is to be inhaled. Methods of micronising pharmaceutically active substances are known as such in the prior art. The aim of the present invention is to provide a method which makes micronised tiotropium bromide available in a form which satisfies the stringent requirements imposed on an active substance intended for inhalation and thus takes account of the specific properties of tiotropium bromide, or which at least provides a useful alternative. Detailed description of the invention It has been found that, depending on the choice of conditions which can be used when purifying the crude product obtained after industrial manufacture, tiotropium bromide occurs in various crystalline modifications, so-called polymorphs. It has also been found that these different modifications can be deliberately produced by selecting the solvents used for the crystallisation as well as by a suitable choice of the process conditions used in the crystallisation process. For the purposes of the present invention, namely to provide tiotropium bromide in a micronised form suitable for inhalation, it has proved suitable to use the crystalline monohydrate of tiotropium bromide, which can be obtained in crystalline form by choosing specific reaction conditions. In order to prepare this crystalline monohydrate, it is necessary to take up tiotropium bromide which has been obtained, for example, according to the instructions disclosed in EP 418 716 A1, in water, heat it, purify it with activated charcoal and after removing the activated charcoal slowly crystallise out the tiotropium bromide monohydrate by slow cooling. The method described below is preferably used according to the invention. intellectual 9r0pertv office of i\!.z 1 - JUL 2005 RECE!VFP 3 0.4 to 1.5 kg, preferably 0.6 to 1 kg, most preferably about 0.8 kg of water are used as solvent per mole of tiotropium bromide used. The mixture obtained is heated with stirring, preferably to more than 50°C, most preferably to more than 60°C. The maximum temperature which can be selected will be determined by the boiling point of the solvent used, i.e. water. Preferably the mixture is heated to a range from 80-90°C. Activated charcoal, dry or moistened with water, is added to this solution. Preferably, 10 to 50 g, more preferably 15 to 35 g, most preferably about 25 g of activated charcoal are put in per mole of tiotropium bromide used. If desired, the activated charcoal is suspended in water before being added to the solution containing the tiotropium bromide. 70 to 200 g, preferably 100 to 160 g, most preferably about 135 g water are used to suspend the activated charcoal, per mole of tiotropium bromide used. If the activated charcoal is suspended in water prior to being added to the solution containing the tiotropium bromide, it is advisable to rinse with the same amount of water. After the activated charcoal has been added, stirring is continued at constant temperature for between 5 and 60 minutes, preferably between 10 and 30 minutes, most preferably about 15 minutes, and the mixture obtained is filtered to remove the activated charcoal. The filter is then rinsed with water. 140 to 400 g, preferably 200 to 320 g, most preferably about 270 g of water are used for this, per mole of tiotropium bromide used. The filtrate is then slowly cooled, preferably to a temperature of 20-25°C. The cooling is preferably carried out at a cooling rate of 1 to 10°C per 10 to 30 minutes, preferably 2 to 8°C per 10 to 30 minutes, more preferably 3 to 5°C per 10 to 20 minutes, most preferably 3 to 5°C roughly per 20 minutes. If desired, the cooling to 20 to 25°C may be followed by further cooling to below 20°C, most preferably to 10 to 15°C. Once the filtrate has cooled, it is stirred for between 20 minutes and 3 hours, preferably between 40 minutes and 2 hours, most preferably about one hour, to complete the crystallisation. The crystals formed are finally isolated by filtering or suction filtering the solvent. If it proves necessary to subject the crystals obtained to another washing step, it is advisable to use water or acetone as the washing solvent. 0.1 to 1.0 I, preferably 0.2 to 0.5 I, most preferably about 0.31 solvent are used, per mole of tiotropium bromide, to wash the tiotropium bromide monohydrate crystals obtained. If desired the washing step may be repeated. The product obtained is dried in vacuo or using circulating hot air until a water content of 2.5 - 4.0 % is obtained. 4 The resulting crystalline tiotropium bromide monohydrate is used in the grinding process (micronisation) described below. This process may be carried out using conventional mills. Preferably, the micronisation is carried out with the exclusion of moisture, more preferably, using a corresponding inert gas such as nitrogen, for example. It has proved particularly preferable to use air jet mills in which the material is comminuted by the impact of the particles on one another and on the walls of the grinding container. According to the invention, nitrogen is preferably used as the grinding gas. The material for grinding is conveyed by the grinding gas under specific pressures (grinding pressure). Within the scope of the present invention, the grinding pressure is usually set to a value between about 2 and 8 bar, preferably between about 3 and 7 bar, most preferably between about 3.5 and 6.5 bar. The material for grinding is fed into the air jet mill by means of the feed gas under specific pressures (feed pressure). Within the scope of the present invention a feed pressure of between about 2 and 8 bar, preferably between about 3 and 7 bar and most preferably between about 3.5 and 6 bar has proved satisfactory. The feed gas used is also preferably an inert gas, most preferably nitrogen again. The material to e ground (crystalline tiotropium bromide monohydrate) may be fed in at a rate of about 5-35 g/min, preferably at about 10-30 g/min. For example, without restricting the subject of the invention thereto, the following apparatus has proved suitable as a possible embodiment of an air jet mill: a 2-inch Microniser with grinding ring, 0.8 mm bore, made by Messrs Sturtevant Inc., 348 Circuit Street, Hanover, MA 02239, USA. Using the apparatus, the grinding process is preferably carried out with the following grinding parameters: grinding pressure: about 4.5 - 6.5 bar; feed pressure: about 4.5 - 6.5 bar; supply of grinding material: about 17-21 g/min. The ground material thus obtained is then further processed under the following specific conditions. The micronisate is exposed to a water vapour at a relative humidity of at least 40% at a temperature of 15-40°C, preferably 20-35°C, most preferably 25-30°C . Preferably, the humidity is set to a value of 50 - 95% r. h., preferably 60 - 90% r.h., most preferably 70 - 80% r.h. By relative humidity (r.h.) is meant, within the scope of the present invention, the quotient of the partial steam pressure and the steam pressure of the water at the temperature in question. Preferably, the micronisate obtained from the grinding process described above is subjected to the chamber conditions mentioned above for a period of at least 6 hours. Preferably, however, the micronisate is subjected to the chamber conditions 5 mentioned above for about 12 to 48 hours, preferably about 18 to 36 hours, more preferably about 20 to 28 hours. In one aspect the invention relates to tiotropium bromide micronisate which may be obtained by the process described above. The micronisate of tiotropium bromide obtainable by the above method has a characteristic particle size X50of between 1.0 pm and 3.5 pm, preferably between 1.1 |jm and 3.3 pm, most preferably between 1.2 pm and 3.0pm and Q(5.8) of more than 60%, preferably more than 70 %, most preferably more than 80%. The characteristic value X50 denotes the median value of the particle size below which 50% of the particles fall, with regard to the distribution by volume of the individual particles. The characteristic value Q(58) corresponds to the quantity of particles below 5.8 pm , based on the volume distribution of the particles. The particle sizes were determined within the scope of the present invention by laser diffraction (Fraunhofer diffraction). More detailed information on this subject can be found in the experimental descriptions of the invention. Also characteristic of the tiotropium micronisate according to the invention which was prepared by the above process are Specific Surface Area values in the range between 2 m2/g and 5 m2/g, more particularly between 2.5 m2/g and 4.5 m2/g and most outstandingly between 3.0 m2/g and 4.0 m2/g. Carrying out the process according to the invention leads to the micronisate of tiotropium bromide according to the invention which is characterised by specific enthalpies of solution. These preferably have a value of more than 65 Ws/g, preferably more than 71 Ws/g. Most preferably the heat 6f solution of the micronisate according to the invention is in excess of 74 Ws/g. Detailed information on determining the enthalpies of solution can be found in the experimental descriptions of the invention. The tiotropium bromide micronisate which may be obtained using the above process is further characterised in that the water content of the micronisate is between about 1 % and about 4.5 %, preferably between about 1,4% and 4,2%, more preferably between about 2.4% and 4.1%. Particularly preferred tiotropium bromide micronisate according to the invention is characterised in that the water content of the micronisate is between about 2.6 % and about 4.0 %, most preferably between about 2.8% and 3.9%, particularly between about 2.9% and 3.8%. 6 One aspect of the present invention therefore relates to tiotropium bromide micronisate which has the above characteristics. Within the scope of the present invention, unless otherwise stated, any reference to tiotropium bromide micronisate is to be taken as a reference to the crystalline micronisate of tiotropium bromide which has the above characteristics and which can be obtained by the method according to the invention as described above (micronisation followed by further treatment in accordance with the parameters described above). In another aspect the present invention relates to the use of the tiotropium bromide micronisate according to the invention as a pharmaceutical composition in view of the pharmaceutical efficacy of the micronisate according to the invention. In another aspect the present invention relates to inhalable powders characterised in that they contain tiotropium bromide micronisate according to the invention. In view of the anticholinergic effects of tiotropium bromide a further aspect of the present invention relates to the use of the tiotropium bromide micronisate according to the invention for preparing a pharmaceutical composition for treating diseases in which the use of an anticholinergic agent may have a therapeutic benefit. It is preferably used for preparing a pharmaceutical composition for treating asthma or COPD. The tiotropium bromide micronisate which may be obtained by the process according to the invention is exceptionally suitable for the preparation of pharmaceutical formulations. It may be used particularly for preparing inhalable powders. Accordingly, the present invention relates to inhalable powders containing at least about 0.03 %, preferably less than 5 %, more preferably less than 3 % of the tiotropium bromide micronisate obtainable by the process described above in admixture with a physiologically acceptable excipient, characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 15 to 80|jm and finer excipient with an average particle size of 1 to 9 pm, the proportion of finer excipient in the total amount of excipient being from 1 to 20%. The percentages specified are percent by weight. 7 According to the invention, inhalable powders are preferred which contain about 0.05 to about 1%, preferably about 0.1 to about 0.8%, more preferably about 0.2 to about 0.5% tiotropium bromide micronisate, which may be obtained by the method described above and has the characteristics of the micronisate which may be obtained according to the invention. The inhalable powders containing the micronisate according to the invention are preferably characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 17 to 50|jm, more preferably 20 to 30pm and finer excipient with an average particle size of 2 to 8pm, more preferably 3 to 7pm . The average particle size here denotes the 50% value from the volume distribution measured by laser diffraction by the dry dispersion method. Preferred powders for inhalation are those wherein the proportion of finer excipient in the total amount of excipient is from 3 to 15%, more preferably 5 to 10%. Where the present invention refers to a mixture, this always means a mixture obtained by mixing together components which have previously been clearly defined. Accordingly an excipient mixture of coarser and finer ingredients can only refer to mixtures obtained by mixing a coarser excipient component with a finer one. The coarser and finer excipient fractions may consist of the same chemical substance or chemically different substances, while inhalable powders in which the coarser excipient fraction and the finer excipient fraction consist of the same chemical compound are preferred. Examples of physiologically acceptable excipients which may be used to prepare the inhalable powders according to the invention include, for example, monosaccharides (e.g. glucose or arabinose), disaccharides (e.g. lactose, saccharose, maltose or trehalose), oligo- and polysaccharides (e.g. dextrane), polyalcohols (e.g. sorbitol, mannitol, xylitol), salts (e.g. sodium chloride, calcium carbonate) or mixtures of these excipients with one another. Preferably, mono- or disaccharides are used, while the use of lactose, glucose or trehalose is preferred, preferably lactose or glucose, particularly, but not exclusively, in the form of their hydrates. For the purposes of the invention, lactose is the particularly preferred excipient, while lactose monohydrate is most particularly preferred. The inhalable powders containing the micronisate according to the invention may for example be administered using inhalers which meter a single dose from a reservoir by means of a measuring chamber (e.g. according to US 4570630A) or by other 8 means (e.g. according to DE 36 25 685 A). Preferably, however, the inhalable powders are packed into capsules (to make so-called inhalettes), which are used in inhalers such as those described in WO 94/28958, for example. If the inhalable powder according to the invention is to be packed into capsules (inhalettes) or other packages which provide single doses in accordance with the preferred application mentioned above, it is advisable to fill the capsules with amounts of from 1 to 15 mg, preferably 3 to 10 mg, most preferably from 4 to 6 mg of inhalable powder per capsule. The inhalable powders containing the tiotropium bromide micronisate according to the invention are characterised by a high degree of homogeneity in terms of the accuracy of measuring a single dose. This is in the range from < 8%, preferably <6%, most preferably <4%. The inhalable powders containing the tiotropium bromide micronisate according to the invention may be obtained by the method described below. After the starting materials have been weighed out, first of all the excipient mixture is prepared from the defined fractions of coarser excipient and finer excipient. Then the inhalable powders according to the invention are prepared from the excipient mixture and the active substance. If the inhalable powder is to be administered using inhalettes in suitable inhalers the preparation of the inhalable powder is followed by the manufacture of the capsules containing the powder. In the preparation methods described below, the abovementioned components are used in the proportions by weight described in the abovementioned compositions of the inhalable powders according to the invention. The inhalable powders according to the invention are prepared by mixing the coarser excipient fractions with the finer excipient fractions and then mixing the resulting excipient mixture with the active substance. To prepare the excipient mixture the coarser and finer excipient fractions are placed in a suitable mixing container. The two components are preferably added through a screening granulator with a mesh size of 0.1 to 2 mm, most preferably 0.3 to 1 mm, even more preferably 0.3 to 0.6 mm. Preferably, the coarser excipient is put in first, and then the finer and coarser excipient are added alternately. It is particularly preferred when preparing the excipient mixture to screen in the two components in alternate layers. Preferably, the two components are screened in alternately in 15 to 45, most preferably 20 to 40 layers each. The two excipients may be mixed while the two components are being added. Preferably, however, the two ingredients are not mixed until after they have been screened in in layers. 9 After the preparation of the excipient mixture, this and the active substance, the tiotropium bromide micronisate according to the invention, are placed in a suitable mixing container. The active substance used has an average particle size of 0.5 to 10 pm, preferably 1 to 6 pm, more preferably 1.5 to 5 pm. The two components are preferably added through a screening granulator with a mesh size of 0.1 to 2 mm, most preferably 0.3 to 1 mm, even more preferably 0.3 to 0.6 mm. Preferably, the excipient mixture is put in and then the active substance is added to the mixing container. Preferably, in this mixing process, the two components are added in batches. In the preparation of the excipient mixture it is particularly preferred to screen in the two components alternately in 25 to 65, preferably 30 to 60 layers each. The operation of mixing the excipient mixture with the active substance may be carried out while the two components are being added. Preferably, however, the two ingredients are not mixed until after they have been screened in in layers. The powder mixture obtained by if desired by passed through a screening granulator once more or repeatedly and then subjected to another mixing process. In another aspect the present invention relates to an inhalable powder which contains the tiotropium bromide micronisate according to the invention and may be obtained by the methods described above. The following detailed experimental descriptions serve to illustrate the present invention more fully without restricting the scope of the invention to the embodiments described by way of example hereinafter. Experimental section A) Preparation of crystalline tiotropium bromide monohydrate 15.0 kg of tiotropium bromide, which may be prepared by the experimental procedure disclosed in European Patent Application EP 418 716 A1, are added to 25.7 kg of water in a suitable reaction vessel. The mixture is heated to 80-90°C and stirred at constant temperature until a clear solution is formed. Activated charcoal (0.8 kg), moistened with water, is suspended in 4.4 kg of water, this mixture is added to the solution containing the tiotropium bromide and rinsed with 4.3 kg of water. The mixture thus obtained is stirred for at least 15 min at 80-90°C and then filtered through a heated filter into an apparatus which has been preheated to an outer temperature of 70°C . The filter is rinsed with 8.6 kg of water. The contents of the apparatus are cooled at 3-5°C every 20 minutes to a temperature of 20-25°C. The apparatus is further cooled to 10-15°C using cold water and crystallisation is 10 completed by stirring for at least one hour. The crystals are isolated using a suction drier, the crystal slurry isolated is washed with 9 litres of cold water (10-15°C) and cold acetone (10-15°C). The crystals obtained are dried in a nitrogen current at 25°C over 2 hours. Yield : 13.4 kg of tiotropium bromide monohydrate (86 % of theory) Characterisation of crystalline tiotropium bromide monohydrate The tiotropium bromide monohydrate obtainable using the method described above was investigated by DSC (Differential Scanning Calorimetry). The DSC diagram shows two characteristic signals. The first, relatively broad, endothermic signal between 50-120°C can be attributed to the dehydration of the tiotropium bromide monohydrate into the anhydrous form. The second, relatively sharp, endothermic peak at 230 ± 5°C can be put down to the melting of the substance. This data was obtained using a Mettler DSC 821 and evaluated using the Mettler STAR software package. The data was recorded at a heating rate of 10 K/min. Since the substance melts with decomposition (= incongruent melting process), the melting point observed depends to a great extent on the heating rate. At lower heating rates, the melting/decomposition process is observed at significantly lower temperatures, e.g. at 220 ± 5 °C at a heating rate of 3 K/min. It is also possible that the melting peak may be split. The split is all the more apparent the lower the heating rate in the DSC experiment. The crystalline tiotropium bromide monohydrate was characterised by IR spectroscopy. The data was obtained using a Nicolet FTIR spectrometer and evaluated with the Nicolet OMNIC software package, version 3.1. The measurement was carried out with 2.5 pmol of tiotropium bromide monohydrate in 300 mg of KBr. Table 1 shows some of the essential bands of the IR spectrum. 11 Table 1: Attribution of specific bands Wave number (cm"1) Attribution Type of oscillation 3570, 3410 O-H elongated oscillation 3105 Aryl C-H elongated oscillation 1730 C=0 elongated oscillation 1260 Epoxide C-0 elongated oscillation 1035 Ester C-OC elongated oscillation 720 Thiophene cyclic oscillation The crystalline tiotropium bromide monohydrate was characterised by X-ray structural analysis. The measurements of X-ray diffraction intensity were carried out on an AFC7R- 4-circuit diffractometer (Rigaku) using monochromatic copper Ka radiation. The structural resolution and refinement of the crystal structure were obtained by direct methods (SHELXS86 Program) and FMLQ-refinement (TeXsan Program). Experimental details of the crystalline structure, structural resolution and refinement are collected in Table 2. Table 2: Experimental data on the analysis of the crystalline structure of tiotropium bromide monohydrate. A. Crystal data Empirical formula Weight of formula colour and shape of crystals dimensions of crystals crystal system lattice type space group lattice constants formula units per elementary cell [C19H22N04S2] Br ■ H20 472.43 + 18.00 colourless, prismatic 0.2 x 0.3 x 0.3 mm monoclinic primitive P21/n a = 18.0774 A, b = 11.9711 A c = 9.9321 A 0 = 102.691° V = 2096.96 A3 4 12 B. Measurements of intensity Diffractometer X-ray generator wavelength current, voltage take-off angle crystal assembly crystal-detector gap detector opening temperature determining the lattice constants Scan Type Scan speed Scan width 2©max measured independent reflexes corrections C. Refinement Reflections (I > 3al) Variable ratio of reflections/parameters R-values: R, Rw Rigaku AFC7R Rigaku RU200 A=1.54178A (monochromatic copper Ka-radiation) 50kV, 100mA 6° steam-saturated capillary 235mm 3.0 mm vertical and horizontal 18° 25 reflexes (50.8° < 20 < 56.2°) w-20 8.0 32.0°/min in w (0.58 + 0.30 tan 0)0 120° 5193 3281 ( Rint=0.051) Lorentz polarisation Absorption (Transmission factors 0.56 - 1.00) crystal decay 10.47% decay 1978 254 7.8 0.062, 0.066 The X-ray structural analysis carried out showed that crystalline tiotropium bromide hydrate has a simple monoclinic cell with the following dimensions: a = 18.0774 A, b = 11.9711 A, c = 9.9321 A, |3 = 102.691 °, V = 2096.96 A3. The atomic coordinates described in Table 3 were determined by the above X-ray structural analysis: 3: Coordinates 13 Atom X V z u (ea) Br(1) 0.63938(7) 0.0490(1) 0.2651(1) 0.0696(4) S(1) 0.2807(2) 0.8774(3) 0.1219(3) 0.086(1) S(2) 0.4555(3) 0.6370(4) 0.4214(5) 0.141(2) 0(1) 0.2185(4) 0.7372(6) 0.4365(8) 0.079(3) 0(2) 0.3162(4) 0.6363(8) 0.5349(9) 0.106(3) 0(3) 0.3188(4) 0.9012(5) 0.4097(6) 0.058(2) 0(4) 0.0416(4) 0.9429(6) 0.3390(8) 0.085(3) 0(5) 0.8185(5) 0.0004(8) 0.2629(9) 0.106(3) N(1) 0.0111(4) 0.7607(6) 0.4752(7) 0.052(2) C(1) 0.2895(5) 0.7107(9) 0.4632(9) 0.048(3) C(2) 0.3330(5) 0.7876(8) 0.3826(8) 0.048(3) 0(3) 0.3004(5) 0.7672(8) 0.2296(8) 0.046(3) 0(4) 0.4173(5) 0.7650(8) 0.4148(8) 0.052(3) 0(5) 0.1635(5) 0.6746(9) 0.497(1) 0.062(3) 0(6) 0.1435(5) 0.7488(9) 0.6085(9) 0.057(3) 0(7) 0.0989(6) 0.6415(8) 0.378(1) 0.059(3) 0(8) 0.0382(5) 0.7325(9) 0.3439(9) 0.056(3) 0(9) 0.0761(6) 0.840(1) 0.315(1) 0.064(3) 0(10) 0.1014(6) 0.8974(8) 0.443(1) 0.060(3) 0(11) 0.0785(5) 0.8286(8) 0.5540(9) 0.053(3) 0(12) -0.0632(6) 0.826(1) 0.444(1) 0.086(4) 0(13) -0.0063(6) 0.6595(9) 0.554(1) 0.062(3) 0(14) 0.4747(4) 0.8652(9) 0.430(1) 0.030(2) 0(15) 0.2839(5) 0.6644(9) 0.1629(9) 0.055(3) 0(16) 0.528(2) 0.818(2) 0.445(2) 0.22(1) 0(17) 0.5445(5) 0.702(2) 0.441(1) 0.144(6) 0(18) 0.2552(6) 0.684(1) 0.019(1) 0.079(4) 0(19) 0.2507(6) 0.792(1) -0.016(1) 0.080(4) H(1) -0.0767 0.8453 0.5286 0.102 H(2) -0.0572 0.8919 0.3949 0.102 H(3) -0.1021 0.7810 0.3906 0.102 H(4) -0.0210 0.6826 0.6359 0.073 H(5) -0.0463 0.6178 0.4982 0.073 H(6) 0.0377 0.6134 0.5781 0.073 H(7) 0.1300 0.7026 0.6770 0.069 H(8) 0.1873 0.7915 0.6490 0.069 14 Table 3 continued: Coordinates H(9) 0.1190 0.6284 0.2985 0.069 H(10) 0.0762 0.5750 0.4016 0.069 H(11) 0.1873 0.6082 0.5393 0.073 H(12) -0.0025 0.7116 0.2699 0.066 H(13) 0.1084 0.8383 0.2506 0.075 H(14) 0.1498 0.9329 0.4626 0.071 H(15) 0.0658 0.8734 0.6250 0.063 H(16) 0.2906 0.5927 0.2065 0.065 H(17) 0.2406 0.6258 -0.0469 0.094 H(18) 0.2328 0.8191 -0.1075 0.097 H(19) 0.4649 0.9443 0.4254 0.037 H(20) 0.5729 0.8656 0.4660 0.268 H(21) 0.5930 0.6651 0.4477 0.165 H(22) 0.8192 -0.0610 0.1619 0.084 H(23) 0.7603 0.0105 0.2412 0.084 x, y, z: fractional coordinates; U(eq) mean quadratic amplitude of atomic movement in the crystal C) Preparation of the tiotropium bromide micronisate according to the invention The tiotropium bromide monohydrate obtainable by the process described above is micronised with an air jet mill of the 2-inch microniser type with grinding ring, 0.8 mm bore, made by Messrs Sturtevant Inc., 348 Circuit Street, Hanover, MA 02239, USA. Using nitrogen as the grinding gas the following grinding parameters are set, for example: grinding pressure: 5.5 bar; feed pressure: 5.5 bar; supply (of crystalline monohydrate) or flow speed: 19 g/min. The ground material obtained is then spread out on sheet metal racks in a layer thickness of about 1 cm and subjected to the following climatic conditions for 24 -24.5 hours: temperature: 25 - 30 °C; relative humidity: 70-80%. D) Measuring techniques for characterising the tiotropium bromide micronisate according to the invention The parameters mentioned in the description which characterise the tiotropium bromide micronisate according to the invention were obtained by the measuring techniques and methods described below: 15 D.1) Determining the water content according to Karl-Fischer (tiotropium bromide): Type Mettler DL 18 with disodium tartrate dihydrate Hydranal-Titrant 5 (Riedel-deHaen) Hydranal Solvent (Riedel-deHaen) Titrator Calibrating substance: Titrant: Solvent: Measuring method: Sample amount: 50-100mg Stirring time: 60 s The stirring time before the start of titration ensures that the sample is fully dissolved. The water content of the sample is calculated by the apparatus in percent and indicated. D.2) Determining particle size by laser diffraction (Fraunhofer diffraction) Measuring method: To determine the particle size the powder is fed into a laser diffraction spectrometer by means of a dispersing unit. Measuring equipment: Laser diffraction spectrometer (HELOS), Messrs. Sympatec Software: WINDOX Version 3.3/REL 1 Dispersing unit: RODOS / Dispersing pressure: 3 bar Equipment parameters: Detector: Multielement detector (31 semicircular rings) Method: Air dispersal Focal length: 100 mm Measuring range: RS 0.5/0.9 - 175 |im Evaluation mode: HRLD-Mode Rodos Dry Disperser: Injector: 4 mm Pressure: 3 bar Injector vacuum: maximum (~ 100 mbar) Suction: Nilfilsk (advance 5 s) Metering device: Vibri Feed rate: 40 % (manually increased to 100 %) Bed height: 2 mm Speed of rotation: 0 16 D.3) Determining the Specific Surface Area (1-bundle B.E.T. method): Measuring method: The specific surface is determined by exposing the powder sample to a nitrogen/helium atmosphere at different pressures. Cooling the sample causes the nitrogen molecules to be condensed on the surface of the particles. The quantity of condensed nitrogen is determined by means of the change in the thermal heat conductivity of the nitrogen/helium mixture and the surface of the sample is calculated by means of the surface nitrogen requirement. Using this value and the weight of the sample, the specific surface is calculated. Equipment and materials: Measuring equipment: Heater: Measuring and drying gas: Adsorbate: Coolant: Measuring cell: Calibration peak; Analytical scale: Monosorb, Messrs Quantachrome Monotektor, Messrs Quantachrome nitrogen (5.0) / helium (4.6) 70/30, Messer Griesheim 30% nitrogen in helium liquid nitrogen with capillary tube, Messrs. W. Pabisch GmbH&Co.KG 1000 |jl, Fa. Precision Sampling Corp. R 160 P, Fa. Satorius Calculating the specific surface: The measured values are indicated by the equipment in [m2] and are usually converted into [cm2/g] on weighing (dry mass): ^spez MW mtr 10000 = specific surface [cm2/g] = Measured value [m^] = dry mass [g] = conversion factor [cm^/m^] D.4) Determining the heat of solution (enthalpy of solution) Ec: The solution enthalpy is determined using a solution calorimeter 2225 Precision Solution Calorimeter made by Messrs. Thermometric. The heat of solution is calculated by means of the change in temperature occurring (as a result of the dissolving process) and the system-related change in temperature calculated from the base line. 17 Before and after the ampoule is broken, electrical calibration is carried out with an integrated heating resistor of a precisely known power. A known heat output is delivered to the system over a set period and the jump in temperature is determined. Method and equipment parameters: Solution calorimeter: 2225 Precision Solution Calorimeter, Messrs Thermometric Reaction cell: 100 ml Thermistor resistance: 30.0 kH (at 25 °C) Speed of stirrer: 600 U/min Thermostat: Thermostat of 2277 Thermal Activity Monitor TAM, Messrs Thermometric Temperature: 25 °C ± 0.0001 °C (over 24h) Measuring ampoules: Crushing ampoules 1 ml, Messrs Thermometric Seal: Silicon stopper and beeswax, Messrs. Thermometric Weight: 40 to 50 mg Solvent: Chemically pure water Volume of solvent: 100 ml Bath temperature: 25°C Temperature resolution: High Starting temperature: -40mK (+ 10mK) temperature-offset Interface: 2280-002 TAM accessory interface 50 Hz, Messrs Thermometric Software: SolCal V 1.1 for WINDOWS Evaluation: Automatic evaluation with Menu point CALCULATION/ ANALYSE EXPERIMENT. (Dynamics of base line ; calibration after breakage of ampoule). Electrical calibration: The electrical calibration takes place during the measurement, once before and once after the breakage of the ampoule. The calibration after the breakage of the ampoule is used for the evaluation. Amount of heat: 2.5Ws Heating power: 250 mW Heating time: 10 s Duration of base lines: 5 min (before and after heating) 18 Evaluation for tiotropium bromide micronisate: As the mass of the tiotropium bromide micronisate weighed out has to be corrected by the water content of the material, the unsealed ampoules together with about 1 g of the test substance are left to stand open for at least 4 hours. After this equilibration time the ampoules are sealed with the silicon stoppers and the water content of the bulk sample is determined by Karl-Fischer titration. The filled and sealed ampoule is weighed on the scale again. The sample mass is corrected according to the following formula: .100%-x. m„ = ( ) • rti 100% where: mc is the corrected mass mw is the sample mass weighed into the ampoule x is the water content in percent (determined in parallel by Karl-Fischer titration) The corrected mass mc determined by this calculation is used as the input value (= weight) to calculate the solution enthalpy measured. E) Preparation of the powder formulation containing the tiotropium bromide micronisate according to the invention In the Examples which follow, lactose-monohydrate (200M) is used as the coarser excipient. It may be obtained, for example, from Messrs DMV International, 5460 Veghel/NL under the product name Pharmatose 200M. In the Examples which follow, lactose-monohydrate (5|j) is used as the finer excipient. It may be obtained from lactose-monohydrate 200M by conventional methods (micronising). Lactose-monohydrate 200M may be obtained, for example, from Messrs DMV International, 5460 Veghel/NL under the product name Pharmatose 200M. Apparatus The following machines and equipment, for example, may be used to prepare the inhalable powders containing the tiotropium bromide micronisate according to the invention: 19 Mixing container or powder mixer: Gvrowheel mixer 200 L; type: DFW80N-4; made by: Messrs Engelsmann, D-67059 Ludwigshafen. Granulating sieve: Quadro Comil; type: 197-S; made by: Messrs Joisten & Kettenbaum, D-51429 Bergisch-Gladbach. E.1) Preparation of the excipient mixture: 31.82 kg of lactose monohydrate for inhalation (200M) are used as the coarser excipient component. 1.68 kg of lactose monohydrate (5pm) are used as the finer excipient component. In the resulting 33.5 kg of excipient mixture the proportion of the finer excipient component is 5%. About 0.8 to 1.2 kg of lactose monohydrate for inhalation (200M) are added to a suitable mixing container through a suitable granulating sieve with a mesh size of 0.5 mm. Then alternate layers of lactose monohydrate (5pm) in batches of about 0.05 to 0.07 kg and lactose monohydrate for inhalation (200M) in batches of 0.8 to 1.2 kg are sieved in. Lactose monohydrate for inhalation (200M) and lactose monohydrate (5pm) are added in 31 and 30 layers, respectively (tolerance: ±6 layers). The ingredients sieved in are then mixed together (mixing at 900 rpm). E.2) Preparation of the final mixture To prepare the final mixture, 32.87 kg of the excipient mixture (1.1) and about 0.13 kg of the tiotropium bromide micronisate according to the invention are used. The content of active substance in the resulting 33.0 kg of inhalable powder is 0.4%. About 1.1 to 1.7 kg of excipient mixture (E.1) are added to a suitable mixing container through a suitable granulating sieve with a mesh size of 0.5 mm. Then alternate layers of tiotropium bromide micronisate in batches of about 0.003 kg and excipient mixture (E.1) in batches of 0.6 to 0.8 kg are sieved in. The excipient mixture and the active substance are added in 46 and 45 layers, respectively (tolerance: ±9 layers). The ingredients sieved in are then mixed together The final mixture is passed twice more through a granulating sieve and then mixed (mixing at 900 rpm). E.3) Inhalation capsules: 20 Inhalation capsules (inhalettes) having the following composition were produced using the mixture obtained according to E.2: tiotropium bromide monohydrate: 0.0225 mg lactose monohydrate (200 M): 5.2025 mg lactose monohydrate (5 pm): 0.2750 mg hard gelatine capsule: 49.0 mg Total: 54.5 mg Analogously to the method described in E.2 inhalation capsules (inhalettes) of the following composition are obtained: a) tiotropium bromide monohydrate: 0.0225 mg lactose monohydrate (200 M): 4.9275 mg lactose monohydrate (5 pm): 0.5500 mg hard gelatine capsule: 49.0 mg Total: 54.5 mg b) tiotropium bromide monohydrate: 0.0225 mg lactose monohydrate (200 M): 5.2025 mg lactose monohydrate (5 pm): 0.2750 mg polyethylene capsule: 100.0 mg Total: 105.50 mg F) Measuring techniques for determining the particle sizes of the excipient components used in E) The average particle size of the various excipient ingredients of the formulation containing the tiotropium bromide micronisate according to the invention which may be prepared according to E) was determined as follows: 21 F.1) Determining the particle size of finely divided lactose: Measuring equipment and settings: The equipment is operated according to the manufacturer's instructions. HELOS Laser-diffraction spectrometer, (SympaTec) RODOS dry disperser with suction funnel, (SympaTec) from 100 mg Vibri Vibrating channel, Messrs. Sympatec Frequency of vibrating channel: 40 rising to 100 % Duration of sample feed: 1 to 15 sec. (in the case of 100 mg) Measuring equipment: Dispersing unit: Sample quantity: Product feed: Focal length: Measuring time: Cycle time: Start/stop at: Dispersing gas: Pressure: Vacuum: Evaluation method: 100 mm (measuring range: 0.9 -175 pm) about 15 s (in the case of 100 mg) 20 ms 1 % on channel 28 compressed air 3 bar maximum HRLD Sample preparation /product feed: At least 100 mg of the test substance are weighed onto a piece of card. Using another piece of card all the larger lumps are broken up. The powder is then sprinkled finely over the front half of the vibrating channel (starting about 1 cm from the front edge). After the start of the measurement the frequency of the vibrating channel is varied from about 40 % up to 100 % (towards the end of the measurement). The time taken to feed in the entire sample is 10 to 15 sec. </div>

Claims

<div class="application article clearfix printTableText" id="claims"> 22 F.
2) Determining the particle size of lactose 200M : Measuring equipment and settings: The equipment is operated according to the manufacturer's instructions. Measuring equipment: Dispersing unit: Sample quantity: Product feed: Laser diffraction spectrometer (HELOS), Sympatec RODOS dry disperser with suction funnel, Sympatec 500 mg VIBRI Vibrating channel, Messrs. Sympatec Frequency of vibrating channel: 18 rising to 100 % Focal length (1): Focal length (2): Measuring time: Cycle time: Start/stop at: Pressure: Vacuum: Evaluation method: 200 mm (measuring range: 1.8 - 350 pm) 500 mm (measuring range: 4.5 - 875 pm) 10s 10 ms 1 % on channel 19 3 bar maximum HRLD Sample preparation /product feed: About 500 mg of the test substance are weighed onto a piece of card. Using another piece of card all the larger lumps are broken up. The powder is then transferred into the funnel of the vibrating channel. A gap of 1.2 to 1.4 mm is set between the vibrating channel and funnel. After the start of the measurement the amplitude setting of the vibrating channel is increased from 0 to 40 % until a continuous flow of product is obtained. Then it is reduced to an amplitude of about 18%. Towards the end of the measurement the amplitude is increased to 100%. 23 Patent Claims 1) Crystalline tiotropium bromide micronisate, characterised by a particle size X5o of between 1.0 pm and 3.5 |jm at a Q(5.8) value of more than 60%, by a specific surface value in the range between 2 m2/g and 5 m2/g, by a specific heat of solution of more than 65 Ws/g and by a water content from about 1 % to about 4.5 %. 2) Crystalline tiotropium bromide micronisate according to claim 1, characterised in that the particle size X50 has a value of 1.1 pm to 3.3 pm, at a Q(5.8) value of more than 70 %. 3) Crystalline tiotropium bromide micronisate according to either one of claims 1 or 2, characterised in that it has a specific surface value in the range from 2.5 m2/g to 4.5 m2/g. 4) Crystalline tiotropium bromide micronisate according to any one of claims 1, 2 or 3, characterised by a specific heat of solution of more than 71 Ws/g. 5) Crystalline tiotropium bromide micronisate according to any one of claims 1 to 4, characterised by a water content from about 1.4 % to about 4.2 % . 6) Process for preparing the tiotropium micronisate according to any one of claims 1 to 5, characterised in that a) crystalline tiotropium bromide monohydrate, which when thermally analysed by DSC has an endothermic maximum at 230 ± 5°C at a heating rate of 10K/min, which is characterised by an IR spectrum which has bands inter alia at wavelengths 3570, 3410, 3105, 1730, 1260, 1035 and 720 cm"1 and which is characterised by a simple monoclinic cell with the following dimensions: a = 18.0774 A, b = 11.9711 A, c = 9.9321 A, p = 102.691 °,V= 2096.96 A3. is micronised and b) then at a temperature of 15 - 40 °C exposed to water vapour with a relative humidity of at least 40% for a period of at least 6 hours. 7) Process according to claim 6, characterised in that in order to carry out step a) the micronisation is carried out under inert gas. intellectual pwi^fv0frce'l OF N.Z. 1 - JUL 2005 8) 24 Process according to claim 7, characterised in that in order to carry out step a) the micronisation is carried out under the inert gas nitrogen. 9) Process according to any one of claims 6 to 8, characterised in that to carry out step a) an air jet mill is used with the following grinding parameters: grinding pressure: about 2-8 bar; feed pressure: about 2-8 bar; grinding gas/feed gas: nitrogen; product supply: about 5 - 35 g/min. 10) Process according to any one of claims 6 to 9, characterised in that in order to carry out step b) the product obtained from step a) at a temperature of 20 -35°C is exposed to water vapour at a relative humidity of 50 - 95% for a period of about 12 to 48 hours. 11) Process according to any one of claims 6 to 10, characterised in that the crystalline tiotropium bromide monohydrate used as starting product is obtained by the following steps: a) taking up tiotropium bromide in water; b) heating the resulting mixture; c) adding activated charcoal and d) after removing the activated charcoal, slowly crystallising the tiotropium bromide monohydrate while slowly cooling the aqueous solution. 12) Process according to claim 11, characterised in that a) 0.4 to 1.5 kg of water are used per mol of tiotropium bromide used, b) the mixture obtained is heated to more than 50°C, c) 10 to 50 g of activated charcoal are used per mol of tiotropium bromide used and after the activated charcoal has been added the mixture is stirred for between 5 and 60 minutes, d) the mixture obtained is filtered, the filtrate obtained is cooled to a temperature of 20-25°C at a cooling rate of from 1 to 10°C per 10 to 30 minutes and the tiotropium bromide monohydrate is crystallised. 13) Crystalline tiotropium bromide micronisate obtainable by a process according to any one of claims 6 to 12. 14) Use of the crystalline tiotropium bromide micronisate according to any one of claims 1-5 or 13 for preparing a pharmaceutical composition. I INTELLECT UAL HfiGPERTY OFFIPF" 1 OF NZ. j ii ii 25 16) 17) 19) 20) 21) 22) 23) Use according to claim 14, for preparing an inhalable pharmaceutical composition. Use of crystalline tiotropium bromide micronisate according to any one of claims 1-5 or 13 for preparing a pharmaceutical composition for treating diseases in which the administration of an anticholinergic may have a therapeutic benefit. Use according to claim 16, characterised in that the diseases are asthma or COPD. Pharmaceutical composition, characterised in that it contains crystalline tiotropium bromide micronisate according to any one of claims 1-5 or 13. Pharmaceutical composition according to claim 18, characterised in that it is an inhalable powder. Inhalable powder according to claim 19, characterised in that it contains at least about 0.03 % of tiotropium bromide micronisate according to any one of claims 1-5 or 13 in admixture with a physiologically acceptable excipient and further characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 15 to 80|jm and finer excipient with an average particle size of 1 to 9 pm, wherein the proportion of finer excipient in the total quantity of excipient is from 1 to 20%. Inhalable powder according to claim 20, characterised in that it contains between about 0.05 and about 1% of tiotropium bromide micronisate according to any one of claims 1-5 or 13. Inhalable powder according to claim 21, characterised in that it contains between about 0.1 and about 0.8% of tiotropium bromide micronisate. Inhalable powder according to any one of claims 20 to 22, characterised in that the excipient consists of a mixture of coarser excipient with an average particle size of 17 to 50pm and finer excipient with an average particle size of 2 to 8pm. 26 24) Inhalable powder according to any one of claims 20 to 23, characterised in that the proportion of finer excipient in the total quantity of excipient is from 3 to 15%. 25) Inhalable powder according to any one of claims 20 to 24, characterised in that monosaccharides, disaccharides, oligo- and polysaccharides, polyalcohols, salts or mixtures of these excipients with one another may be used as excipients. 26) Inhalable powder according to claim 25, characterised in that glucose, arabinose, lactose, saccharose, maltose, trehalose, dextrane, sorbitol, mannitol, xylitol, sodium chloride, calcium carbonate or mixtures of these excipients with one another may be used as excipients. 27) Inhalable powder according to claim 26, characterised in that glucose or lactose or mixtures of these excipients with one another may be used as excipients. 28) Process for preparing the inhalable powders according to any one of claims 20 to 27, characterised in that in a first step the coarser excipient fractions are mixed with the finer excipient fractions and in a subsequent step the excipient mixture thus obtained is mixed with the tiotropium bromide micronisate according to one of claims 1-5 or 13. 29) Capsule (inhalette), characterised in that it contains an inhalable powder according to any one of claims 19-28. 30) Crystalline tiotropium bromide micronisate according to claim 1, as substantially herein described in the Experimental Section. 31) Crystalline tiotropium bromide micronisate according to any one of claims 1 to 5 or 13, as substantially herein described. 32) Process according to claim 6, as substantially herein described in Experimental Sections A to C. 33) Process according to any one of claims 6 to 12, as substantially herein described. "iNTELLECTUAp^RGPFRfro^Fn Or i\!„> • ' j 1 - JUL 2005 27 34) Use according to either of claims 14 or 16, in which the pharmaceutical composition is as substantially herein described in Experimental Section E. 35) Pharmaceutical composition according to claim 18, as substantially herein described. 36) Inhalable powder according to claim 20, as substantially herein described. 37) Process for according to claim 28, as substantially herein described in Experimental Sections E.1, E.2 and F. 38) Process according to claim 28, as substantially herein described. 39) Capsule (inhalette) according to claim 29, as substantially herein described in Experimental Section E.3. 40) Capsule (inhalette) according to claim 29, as substantially herein described. fintellectual property OFFICEl of m.z 1 - JUL 2005 </div>