NZ526024A

NZ526024A - Inhalative propellant-free solution formulation containing a tiotropium salt

Info

Publication number: NZ526024A
Application number: NZ526024A
Authority: NZ
Inventors: Karin Drechsel; Barbara Niklaus-Humke; Christel Schmelzer; Petra Barth
Original assignee: Boehringer Ingelheim Pharma
Priority date: 2000-10-31
Filing date: 2001-10-24
Publication date: 2005-10-28
Also published as: UY26991A1; SK288031B6; WO2002036591A2; AU2174102A; ZA200303045B; NO20031914L; HUP0301377A2; WO2002036591A3; IL155676A0; HUP0301377A3; AR038765A1; HRP20030337A2; UA76435C2; ME00242B; EA009068B1; MEP40708A; EE200300202A; KR100983208B1; KR20040010552A; BG66425B1

Abstract

A liquid propellant-free pharmaceutical preparation comprises a tiotropium salt as one active substance, in a concentration based on tiotropium of between 0.0005 and 5 % by weight, a second active substance selected from antiallergics, antihistamines, steroids and/or leukotriene antagonists, water or a water/ethanol mixture as solvent, in which at least the tiotropium salt is dissolved, an acid for achieving a pH between 2.0 and 3.1, a preservative, and optionally a complexing agent, stabilizer, cosolvent and/or other adjuvants and additives in addition to the preservative. The pharmaceutical preparation can be used as a medicament for the treatment of asthma and/or COPD for administration by inhalation.

Description

<div class="application article clearfix" id="description"> WO 02/36591 PCT/EP01/12296 526024 76653pct.207 Inhalable formulation of a solution containing a tiotropium salt The present invention relates to a propellant-free inhalable formulation of a pharmaceutically acceptable salt of tiotropium dissolved in water or a mixture of water and ethanol, in conjunction with at least one other active substance preferably administered by inhalation, and propellant-free inhalable aerosols resulting therefrom. The formulation according to the invention is particularly suitable for administering the active substance by inhalation, especially for treating asthma and COPD. Tiotropium, chemically (1a,2p,4(3,5a,7p)-)-7-[(hydroxydi-2-thienylacetyl)oxy]-9,9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane, is known as tiotropium bromide from European Patent Application EP 418 716 A1. The bromide salt of tiotropium has the following chemical structure: The compound has valuable pharmacological properties and is known by the name tiotropium bromide. Tiotropium and its salts are highly effective anticholinergics and can provide therapeutic benefit in the treatment of asthma or COPD (chronic obstructive pulmonary disease). The monohydrate of tiotropium bromide is also pharmacologically valuable. Both compounds are a preferred object of the present invention. Br (I) The present invention relates to liquid active substance formulations of these compounds which can be administered by inhalation; the liquid formulations according to the invention have to meet high quality standards. WO 02/36591 2 PCT/EP01/12296 To achieve an optimum distribution of active substances in the lung it makes sense to use a liquid formulation without propellant gases administered using suitable inhalers. Those inhalers which are capable of nebulising a small amount of a liquid formulation in the dosage needed for therapeutic purposes within a few seconds into an aerosol suitable for therapeutic inhalation are particularly suitable. Within the scope of the invention, preferred nebulisers are those in which an amount of less than 100 microlitres, preferably less than 50 microlitres, most preferably less than 20 microlitres of active substance solution can be nebulised preferably in one puff to form an aerosol having an average particle size of less than 20 microns, preferably less than 10 microns, so that the inhalable part of the aerosol already corresponds to the therapeutically effective quantity. An apparatus of this kind for the propellant-free administration of a metered amount of a liquid pharmaceutical composition for inhalation is described in detail for example in International Patent Application WO 91/14468 "Atomizing Device and Methods" and also in WO 97/12687, cf. Figures 6a and 6b and the accompanying description. In a nebuliser of this kind a pharmaceutical solution is converted by means of a high pressure of up to 500 bar into an aerosol destined for the lungs, which is sprayed. Within the scope of the present specification reference is expressly made to the entire contents of the literature mentioned above. In inhalers of this kind the formulations of solutions are stored in a reservoir. It is essential that the active substance formulations used are sufficiently stable when stored and at the same time are such that they can be administered directly, if possible without any further handling, in accordance with their medical purpose. Moreover, they must not contain any ingredients which might interact with the inhaler in such a way as to damage the inhaler or the pharmaceutical quality of the solution or of the aerosol produced. To nebulise the solution a special nozzle is used as described for example in WO 94/07607 or WO 99/16530. Reference is expressly made here to both these publications. WO 02/36591 PCT/EP01/12296 WO 98/27959 discloses formulations of solutions for the inhaler described above which contain as additive the disodium salt of editic acid (sodium edetate). For aqueous formulations of solutions which are to be converted into inhalable aerosols using the inhaler described above, the specification favours a minimum concentration of sodium edetate of 50 mg/100 ml, in order to reduce the incidence of spray anomalies. Among the Examples disclosed there is a formulation containing tiotropium bromide. In this formulation the active substance is dissolved in water. The proportion of sodium edetate is again 50 mg/100 ml. Surprisingly, it has now been found that formulations of solutions of tiotropium salts in water or a water-ethanol mixture wherein the proportion of the additive sodium edetate is significantly less than 50 mg/100 ml show a reduction in the scattering of the composition delivered, compared with the formulation containing tiotropium bromide known from the prior art. In addition, the spray quality is very good. The resulting aerosol has very good properties for administration by inhalation. Another advantage of the formulation is that, thanks to the absence of or reduction in the additive sodium edetate in the active substance formulation, the pH of the solution formulation can be lowered. Low pH levels are necessary for the long-term stability of the tiotropium salts in the formulation. It is therefore an aim of the present invention to provide an aqueous active substance formulation containing a pharmaceutically acceptable tiotropium salt which meets the high standards needed in order to be able to achieve optimum nebulisation of a solution using the inhalers mentioned hereinbefore. The active substance formulations according to the invention must be of sufficiently high pharmaceutical quality, i.e. they should be pharmaceutically stable over a storage time of some years, preferably at least one year, more preferably two years. Another aim is to provide propellant-free formulations of solutions containing tiotropium salts which are nebulised under pressure using an inhaler, the composition delivered by the aerosol produced falling reproducibly within a specified range. WO 02/36591 PCT/EP01/12296 4 Another aim is to provide formulations of solutions with tiotropium and another active substance which can be administered by inhalation. These aims should be read disjunctively with the further aim of at least providing a useful alternative. According to the invention, any pharmaceutically acceptable salts of tiotropium may be used for the formulation. When the term tiotropium salt is used within the scope of the present invention, this is to be taken as a reference to tiotropium. According to the invention a reference to tiotropium, which is the free ammonium cation, corresponds to a reference to tiotropium in the form of a salt (tiotropium salt) which contains an anion as counter-ion. Tiotropium salts which may be used within the scope of the present invention are preferably compounds which contain, in addition to tiotropium as counter-ion (anion), chloride, bromide, iodide, methanesulphonate, para-toluenesulphonate and/or methylsulphate. Within the scope of the present invention tiotropium bromide is preferred as the salt. References to tiotropium bromide within the scope of the present invention must always be taken as references to all possible amorphous and crystalline modifications of tiotropium bromide. These may for example contain molecules of solvent in their crystalline structure. Of all the crystalline modifications of tiotropium bromide those which also contain water (hydrates) are preferred according to the invention. It is particularly preferred within the scope of the present invention to use tiotropium bromide monohydrate. In the formulations according to the invention combinations with a tiotropium salt and only one other active substance are preferred. In the formulations according to the invention the tiotropium salts are dissolved in a solvent. The solvent may be exclusively water, or it may be a mixture of water and ethanol. Ethanol may be added to the formulation in order to increase the solubility of additives or other active substances apart from the tiotropium salt, preferably tiotropium bromide or tiotropium bromide monohydrate. The relative proportion of ethanol to water is not limited; it may be 90 % by volume, for example. Preferably, the maximum limit of ethanol is 70 % by volume, particularly 60 % by volume and most preferably 30 % by volume. The remaining % by volume consists of water. The preferred solvent is water without the addition of ethanol. I fNT£u£. 2 « AUG 2005 RPPCii/cn WO 02/36591 PCT/EP01/12296 5 The concentration of the tiotropium salt based on the proportion of tiotropium in the finished pharmaceutical preparation depends on the therapeutic effect sought. For most of the complaints which respond to tiotropium the concentration of tiotropium is between 0.0005 and 5 % by weight, preferably between 0.001 and 3 % by weight. The pH of the formulation according to the invention is between 2.0 and 4.5, preferably between 2.5 and 3.5 and more preferably between 2.7 and 3.5 and particularly preferably between 2.7 and 3.2. Most preferred are pHs with an upper limit of 3.1. The pH is adjusted by the addition of pharmacologically acceptable acids. Examples of inorganic acids which are preferred for this purpose include: hydrochloric acid, hydrobromic acid, nitric acid, sulphuric acid and/or phosphoric acid. Examples of particularly suitable organic acids are: ascorbic acid, citric acid, malic acid, tartaric acid, maleic acid, succinic acid, fumaric acid, acetic acid, formic acid and/or propionic acid, etc. Preferred inorganic acids are hydrochloric acid and sulphuric acid. It is also possible to use acids which form an acid addition salt with the active substance or, in the case of combined preparations, with one of the active substances. Of the organic acids, ascorbic acid, fumaric acid and citric acid are preferred, especially citric acid. If desired, mixtures of the abovementioned acids may also be used, particularly in the case of acids which have other properties in addition to their acidifying properties, e.g. those which act as flavourings or antioxidants, such as for example citric acid or ascorbic acid. Hydrochloric acid deserves special mention as an inorganic acid. If desired, pharmacologically acceptable bases may be used to titrate the pH precisely. Suitable bases include for example alkali metal hydroxides and alkali metal carbonates. The preferred alkali ion is sodium. If bases of this kind are used, care must be taken to ensure that the resulting salts, which are then contained in the WO 02/36591 6 PCT/EP01/12296 finished pharmaceutical formulation, are pharmacologically compatible with the abovementioned acid. According to the invention, there is no need to add editic acid (EDTA) or one of the known salts thereof, sodium edetate, to the present formulation as a stabiliser or complexing agent. Another preferred embodiment contains editic acid and/ or the salts thereof. In a preferred embodiment with sodium edetate the content based on sodium edetate is less than 10 mg /100 ml. In this case, there is one preferred range from 5 mg/100 ml to less than 10 mg/100 ml or another from greater than 0 to 5 mg/100ml. In another embodiment the content of sodium edetate is 10 to 30 mg/100 ml, preferably not more than 25 mg/100 ml. In a preferred embodiment this additive is omitted entirely. The remarks made concerning sodium edetate also apply analogously to other comparable additives which have complexing properties and can be used instead, such as for example nitrilotriacetic acid and the salts thereof. By complexing agents is preferably meant within the scope of the present invention molecules which are capable of entering into complex bonds. Preferably, these compounds should have the effect of complexing cations, most preferably metal cations. The other active substances apart from the tiotropium salt in the combined preparation are selected in particular from among the antihistamines, antiallergic agents, leukotriene antagonists and/or steroids. These active substances include: As steroids: Case 1/1162 FF Boehringer Ingelheim Pharma KG Alclomethasone, Alclomethasone-dipropionate, Alisactide, Amcinonide Aminoglutethimide, Aristocort-diacetate, Beclomethasone, Beclomethasone, Douglas, Beclomethasone-17,21-dipropionate, Betamethasone valerate, Betamethasone adamantoate, Budesonide, Butixocort, Canesten-HC, Ciclometasone, Clobetasol, Clobetasone, Cloprednol, Cloprednol Fluocortin butyl, Cortivazol, Deflazacort, Deflazacort, Demetex, Deprodone, Deprodone Propionate, Dexamethasone, Dexamethasone-21 -isonicotinate, Dexamethasone isonicotinate, Diflorasone, Difluprednate, Endrisone, Fluazacort, Fluclorolone acetonide, Flunisolide, Fluocinolone acetonide, Fluocinonide, Fluocortin, Fluocortolone capronate, Fluodexan, Fluorometholone, Fluticasone, Fluticasone-propionate, Formebolone, Formocortal, Halcinonide, Halometasone, Halopredone-acetate, Hydrocortisone, Hydrocortisone-17-Butyrate, Hydrocortisone-aceponate, Hydrocortisone-butyrate propionate, Icomethasone enbutate Ciclometasone, Lotrisone, Mazipredone, Medrysone, Meprednisone, Methylprednisolone-Aceponate, Mometasone, Mometasone furoate, Mycophenolate mofetil Pranlukast, Paramethasone-acetate, Prednicarbate, Promedrol, Seratrodast, Tipredan, Case 1/1162 FF Boehririger Ingelheim Pharma KG 8 Tixocortol-pivalate, Triamcinolone, T riamcinolone-Hexacetonide, Trilostan, Trimacinolone Benetonide, Ulobetasol-propionate, Zileuton methyl 9-alpha-chloro-6-alpha-fluoro-11 -beta-17-alpha-dihydroxy-16-alpha-methyl-3-oxo-l ,4-androstadiene-17-beta-carboxylate-17-propionate, Particularly preferred are the combinations of tiotropium bromide, or tiotropium bromide-monohydrate and budesonide, flunisolide, beclomethasone dipropionate or fluticasone, as well as the pharmacologically acceptable (possibly other) salts thereof. The preferred combination comprises tiotropium bromide, or tiotropium bromide monohydrate and budesonide. The concentration of the steroid, e.g. budesonide, flunisolide, beclomethasone dipropionate or fluticasone, in the formulations according to the invention is preferably 0.05 to 10 wt.%, preferably up to 5 wt.%, more preferably 0.1 to 2.5 wt.%, particularly preferably 0.2 to 2.5 wt.%. When the formulation is used with the inhaler mentioned hereinbefore the concentration of steroid is preferably adjusted so that 12.5 to 250 micrograms of steroid are delivered per spray. Particularly preferred are concentrations in which the pharmacologically active dose is administered in one or two sprays. If the combined formulation contains a leukotriene antagonist, this is preferably selected from among montelukast, pranlukast, zafiriukast, 1 -(((R)-(3-(2-(6,7-difluoro-2-quinolinyl)ethenyl)phenyl)-3-(2-(2-hydroxy-2-propyl)phenyl)thio)-methylcyclopropane-acetic acid, 1 -(((R)-3-(3-(2-(2,3-dichlorothieno[3,2-b]pyridin-5-yl)-(E)-ethenyl)phenyl)-3-(2-(1-hydroxy-1-methylethyl)phenyl)propyl)thio)methyl)-cyclopropane-acetic acid or [2-[[2-(4-tert-butyI-2-thiazoIyI)-5 -benzofuranyl]oxymethyl]phenyl]acetic acid. Montelukast, pranlukast and/or zafiriukast are preferred. Case 1/1162 FF 9 Boehringer Ingelheim Pharma KG The concentration of the leukotriene antagonist is from 0.05 to 10 wt.%, preferably up to 5 wt.%, more preferably 0.1 to 3.5 wt.%. The following are mentioned as examples of antihistamines and antiallergic agents: Azelastine, Astemizole, Bamipine, Carbinoxamine hydrogen maleate, Cetirizine, Cexchlorpheniramine, Chlorphenoxamine, Clemastine, Clemastine hydrogen fumarate, Desloratidine, Dimenhydrinate, Dimetindene, Disodium cromoglycate, Diphenhydramine, Doxylamine, Ebastine, Emedastine, Epinastine, Fexofenadine, Ketotifen, Levocabastine, Loratadine, Meclozine, Mequitazine, Mizolastine, Nedocromil, Pheniramine and/or Promethazine. Case 1/1162 FF Boehringer Ingelheim Pharma KG 10 Epinastine, nedocromil, disodium cromogiycate, astemizole, mequitazine, carbinoxamine and/or clemastine and/or the corresponding pharmaceutically acceptable salts are preferred. In the combined preparation, the concentration of the antiallergic agents and/or antihistamines is preferably 0.05 to 15 wt.%, preferably up to 10 wt.%, more preferably 0.1 to 10 wt.%, most preferably 0.1 to 7 wt.%. All the abovementioned active substances may optionally also be used in the form of their pharmacologically acceptable salts thereof. The combined preparations are preferably formulations in which tiotropium is present in solution. The other active substance may be dissolved or suspended; this is generally determined by the other active substance and the particular solvent used. If the additional active substance is one which is vulnerable at low pHs, it is preferably formulated as a suspension. The advantage of a suspended form is that the pH can be made more acidic, which is to the benefit of the stability of the dissolved tiotropium. The preferred pH range of tiotropium bromide is between 2. 0 and 4.5, preferably 2.5 and 3.5, most preferably between 2.7 and 3.2. In the case of steroids, these are preferably used in suspended form, especially fluticasone. This is particularly true if the solvent used is only water without ethanol. If ethanol is added, the steroid may also be formulated as a solution. However, it has been found that budesonide, for example, is also sufficiently stable at a pH of 3.5 if it is dissolved in a mixture of water and ethanol. With regard to the use of the formulations according to the invention in the inhaler described within the scope of the present invention, it may be advantageous if all the ingredients of the formulation are present in solution. Case 1/1162 FF Boehringer Ingelheim Pharma KG 11 As well as ethanol, other cosolvents and/or other adjuvants may be added to the formulation according to the invention. Other preferred cosolvents are those which contain hydroxyl groups or other polar groups, for example alcohols - especially isopropylalcohol, glycols - especially propyleneglycol, polyethyleneglycol, polypropyleneglycol, glycolether, glycerol, polyoxyethylene alcohols and polyoxyethylene fatty acid esters. By adjuvants and additives are meant, in this context, any pharmacologically acceptable and therapeutically useful substance which is not an active substance, but can be formulated together with the active substance(s) in the pharmacologically suitable solvent, in order to improve the qualities of the active substance formulation. Preferably, these substances have no pharmacological effects or no appreciable or at least no undesirable pharmacological effects in the context of the desired therapy. The adjuvants and additives include, for example, surfactants such as e.g. soya lecithin, oleic acid, sorbitan esters such as sorbitan trioleate, polyvinylpyrrolidone, other stabilisers, complexing agents, antioxidants and/or preservatives which prolong the shelf life of the finished pharmaceutical formulation, flavourings, vitamins and/or other additives known in the art. The additives also include pharmacologically acceptable salts such as sodium chloride, for example. Suitable surfactants or suspension-stabilising agents include all the pharmacologically acceptable substances which have a lipophilic hydrocarbon group and one or more functional hydrophilic groups, especially Cs-20-fatty alcohols, C5-20-fatty acids, Cs-20-fatty acid esters, lecithin, glycerides, propyleneglycol esters, polyoxyethylenes, polysorbates, sorbitan esters and/or carbohydrates. Cs-20-fatty acids, propyleneglycol diesters and/or triglycerides and/or sorbitans of the Cs-2o-fatty acids are preferred, while oleic acid and sorbitan mono-, di- or trioleates are particularly preferred. Alternatively, toxicologically and pharmaceutically acceptable polymers and/or block polymers may be used as suspension stabilising agents. The quantity of surfactant may be up to 1:1 based on the proportion by weight of the suspended active substances; amounts of 0.0001 ;1 to 0.5:1 are preferred while amounts of from 0.0001:1 to 0.25:1 are especially preferred. Case 1/1162 FF 12 Boehringer Ingelheim Pharma KG The preferred excipients include antioxidants such as ascorbic acid, for example, provided that it has not already been used to adjust the pH, vitamin A, vitamin E, tocopherols and similar vitamins or provitamins occurring in the human body. Preservatives can be added to protect the formulation from contamination with pathogenic bacteria. Suitable preservatives are those known from the prior art, particularly benzalkonium chloride or benzoic acid or benzoates such as sodium benzoate in the concentration known from the prior art. Preferred formulations contain only benzalkonium chloride, an acid for adjusting the pH and sodium edetate, in addition to the solvent water and/or water/ethanol and the tiotropium salt. In another preferred embodiment, sodium edetate is omitted. These embodiments may optionally also contain sodium chloride. As already mentioned a number of times, tiotropium bromide is described in EP 418 716 A1 and crystalline tiotropium bromide monohydrate may be obtained using a process which is described in more detail below. In order to prepare the crystalline monohydrate according to the present invention, the tiotropium bromide obtained by the method disclosed in EP 418 716 A1, for example, first has to be taken up in water, heated, purified with activated charcoal and, after removal of the activated charcoal, the tiotropium bromide-monohydrate is slowly crystallised while cooling slowly. The following procedure is preferably followed: In a reaction vessel of suitable dimensions, the solvent is mixed with tiotropium bromide, which has been obtained by the method disclosed in EP 418 716 A1, for example. For each mol of tiotropium bromide put in, 0.4 to 1.5 kg, preferably 0.6 to 1 kg, most preferably about 0.8 kg of water are used as solvent. The mixture obtained is heated with stirring, preferably to above 50°C, most preferably to above 60°C. The maximum temperature which can be selected is determined by the boiling point of the solvent used. Preferably, the mixture is heated to a range from 80-90°C. Case 1/1162 FF Boehringer Ingelheim Pharma KG 13 Activated charcoal, either 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 mol of tiotropium bromide used. If desired the activated charcoal is suspended in water before being added to the solution containing tiotropium bromide. 70 to 200 g, preferably 100 to 160 g, more preferably about 135 g of water are used, per mol of tiotropium bromide put in, in order to suspend the activated charcoal. If the activated charcoal is suspended in water beforehand, before being added to the solution containing tiotropium bromide, it is advisable to rinse again 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, more preferably for 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 mol of tiotropium bromide used. The filtrate is then slowly cooled, preferably to a temperature of 20-25°C. The cooling preferably takes place at a cooling rate of 1 to 10°C every 10 to 30 minutes, preferably 2 to 8°C every 10 to 30 minutes, more preferably 3 to 5°C every 10 to 20 minutes, most preferably 3 to 5°C about every 20 minutes. If desired, the cooling to 20 to 25°C may be followed by further cooling to below 20°C, more preferably to 10 to 15°C. After cooling is complete, stirring is continued for between 20 minutes and 3 hours, preferably between 40 minutes and 2 hours, more preferably for about one hour to complete the crystallisation. The crystals obtained are then isolated by filtering or suction filtering to remove the solvent. If it should prove necessary to subject the crystals obtained to a further washing step, it is advisable to use water or acetone as the washing solvent. 0.1 to 1.0 L, preferably 0.2 to 0.5 L, more preferably about 0.3 L of solvent may be used per mol of tiotropium bromide put in, in order to wash the tiotropium bromide monohydrate crystals obtained. If necessary the washing step may be repeated. The product obtained is dried in vacuo or using circulating heated air until a water content of 2.5 - 4.0 % is obtained. According to one aspect the present invention therefore also relates to formulations of solutions of the type described above using crystalline tiotropium bromide monohydrate which may be obtained by the procedure described above. Case 1/1162 FF 14 Boehringer Ingelheim Pharma KG The pharmaceutical formulations containing tiotropium salts according to the invention are preferably used in an inhaler of the kind described hereinbefore in order to produce the propellant-free aerosols according to the invention. At this point we should once again expressly mention the patent documents described hereinbefore, to which reference is hereby made. As described at the beginning, a further developed embodiment of the preferred inhaler is disclosed in WO 97/12687 and Figure 6 thereof. This nebuliser (Respimat®) can advantageously be used to produce the inhalable aerosols according to the invention containing a tiotropium salt as active substance. Because of its cylindrical shape and handy size of less than 9 to 15 cm long and 2 to 4 cm wide, the device can be carried anywhere by the patient. The nebuliser sprays a defined volume of the pharmaceutical formulation out through small nozzles at high pressures, so as to produce inhalable aerosols. The preferred atomiser essentially consists of an upper housing part, a pump housing, a nozzle, a locking clamp, a spring housing, a spring and a storage container, characterised by - a pump housing fixed in the upper housing part and carrying at one end a nozzle body with the nozzle or nozzle arrangement, - a hollow piston with valve body, - a power take-off flange in which the hollow body is fixed and which is located in the upper housing part, - a locking clamping mechanism located in the upper housing part, - a spring housing with the spring located therein, which is rotatably mounted on the upper housing part by means of a rotary bearing, - a lower housing part which is fitted onto the spring housing in the axial direction. The hollow piston with valve body corresponds to a device disclosed in WO 97/12687. It projects partially into the cylinder of the pump housing and is disposed to be axially movable in the cylinder. Reference is made particularly to Figures 1-4 -especially Figure 3 - and the associated parts of the description. At the moment of release of the spring the hollow piston with valve body exerts, at its high pressure Case 1/1162 FF 15 Boehringer Ingelheim Pharma KG end, a pressure of 5 to 60 Mpa (about 50 to 600 bar), preferably 10 to 60 Mpa (about 100 to 600 bar) on the fluid, the measured amount of active substance solution. Volumes of 10 to 50 microlitres are preferred, volumes of 10 to 20 microlitres are more preferable, whilst a volume of 15 microlitres per actuation is particularly preferred. The valve body is preferably mounted at the end of the hollow piston which faces the nozzle body. The nozzle in the nozzle body is preferably microstructured, i.e. manufactured by micro-engineering. Microstructured nozzle bodies are disclosed for example in WO-94/07607 and in WO 99/16530; reference is hereby made to the contents thereof, especially Figure 1 of WO-94/07607 and the associated description. The nozzle body consists for example of two sheets of glass and/or silicon securely fixed together, at least one of which has one or more microstructured channels which connect the nozzle inlet end to the nozzle outlet end. At the nozzle outlet end there is at least one round or non-round opening 2 to 10 microns deep and 5 to 15 microns wide, the depth preferably being 4.5 to 6.5 microns and the length being 7 to 9 microns. If there is a plurality of nozzle openings, preferably two, the directions of spraying of the nozzles in the nozzle body may run parallel to each other or may be inclined relative to one another in the direction of the nozzle opening. In the case of a nozzle body having at least two nozzle openings at the outlet end, the directions of spraying may be inclined relative to one another at an angle of 20 degrees to 160 degrees, preferably at an angle of 60 to 150 degrees, most preferably 80 to 100°. The nozzle openings are preferably arranged at a spacing of 10 to 200 microns, more preferably at a spacing of 10 to 100 microns, still more preferably 30 to 70 microns. A spacing of 50 microns is most preferred. The directions of spraying therefore meet in the region of the nozzle openings. As already mentioned, the liquid pharmaceutical preparation hits the nozzle body at an entry pressure of up to 600 bar, preferably 200 to 300 bar and is atomised through the nozzle openings into an inhalable aerosol. The preferred particle sizes of the aerosol are up to 20 microns, preferably 3 to 10 microns. Case 1/1162 FF 16 Boehringer Ingelheim Pharma KG The locking clamping mechanism contains a spring, preferably a cylindrical helical compression spring as a store for the mechanical energy. The spring acts on the power take-off flange as a spring member the movement of which is determined by the position of a locking member. The travel of the power take-off flange is precisely limited by an upper stop and a lower stop. The spring is preferably tensioned via a stepping-up gear, e.g. a helical sliding gear, by an external torque which is generated when the upper housing part is turned relative to the spring housing in the lower housing part. In this case, the upper housing part and the power take-off flange contain a single- or multi-speed spline gear. The locking member with the engaging locking surfaces is arranged in an annular configuration around the power take-off flange. It consists for example of a ring of plastics or metal which is inherently radially elastically deformable. The ring is arranged in a plane perpendicular to the axis of the atomiser. After the locking of the spring, the locking surfaces of the locking member slide into the path of the power take-off flange and prevent the spring from being released. The locking member is actuated by means of a button. The actuating button is connected or coupled to the locking member. In order to actuate the locking clamping mechanism the actuating button is moved parallel to the annular plane, preferably into the atomiser, and the deformable ring is thereby deformed in the annular plane. Details of the construction of the locking clamping mechanism are described in WO 97/20590. The lower housing part is pushed axially over the spring housing and covers the bearing, the drive for the spindle and the storage container for the fluid. When the atomiser is operated, the upper part of the housing is rotated relative to the lower part, the lower part taking the spring housing with it. The spring meanwhile is compressed and biased by means of the helical sliding gear, and the clamping mechanism engages automatically. The angle of rotation is preferably a whole-number fraction of 360 degrees, e.g. 180 degrees. At the same time as the spring is tensioned, the power take-off component in the upper housing part is moved along by a given amount, the hollow piston is pulled back inside the cylinder in the pump Case 1/1162 FF 17 Boehringer Ingelheim Pharma KG housing, as a result of which some of the fluid from the storage container is sucked into the high pressure chamber in front of the nozzle. If desired, a plurality of replaceable storage containers containing the fluid to be atomised can be inserted in the atomiser one after another and then used. The storage container contains the aqueous aerosol preparation according to the invention. The atomising process is initiated by gently pressing the actuating button. The clamping mechanism then opens the way for the power take-off component. The biased spring pushes the piston into the cylinder in the pump housing. The fluid emerges from the nozzle of the atomiser in the form of a spray. Further details of the construction are disclosed in PCT applications WO 97/12683 and WO 97/20590, to which reference is hereby made. The components of the atomiser (nebuliser) are made of a material suitable for their function. The housing of the atomiser and - if the function allows - other parts as well are preferably made of plastics, e.g. by injection moulding. For medical applications, physiologically acceptable materials are used. Figures 1a/b, which are identical to Figures 6 a/b of WO 97/12687, show the Respimat® nebuliser with which the aqueous aerosol preparations according to the invention can advantageously be inhaled. Figure 1 a shows a longitudinal section through the atomiser with the spring under tension, Figure 1 b shows a longitudinal section through the atomiser with the spring released. The upper housing part (51) contains the pump housing (52), on the end of which is mounted the holder (53) for the atomiser nozzle. In the holder is the nozzle body (54) and a filter (55). The hollow piston (57) fixed in the power take-off flange (56) of the locking clamping mechanism projects partly into the cylinder of the pump housing. At its end the hollow piston carries the valve body (58). The hollow piston is sealed off Case 1/1162 FF Boehringer Ingelheim Pharma KG 18 by the gasket (59). Inside the upper housing part is the stop (60) on which the power take-off flange rests when the spring is relaxed. Located on the power take-off flange is the stop (61) on which the power take-off flange rests when the spring is under tension. After the tensioning of the spring, the locking member (62) slides between the stop (61) and a support (63) in the upper housing part. The actuating button (64) is connected to the locking member. The upper housing part ends in the mouthpiece (65) and is closed off by the removable protective cap (66). The spring housing (67) with compression spring (68) is rotatably mounted on the upper housing part by means of the snap-fit lugs (69) and rotary bearings. The lower housing part (70) is pushed over the spring housing. Inside the spring housing is the replaceable storage container (71) for the fluid (72) which is to be atomised. The storage container is closed off by the stopper (73), through which the hollow piston projects into the storage container and dips its end into the fluid (supply of active substance solution). The spindle (74) for the mechanical counter is mounted on the outside of the spring housing. The drive pinion (75) is located at the end of the spindle facing the upper housing part. On the spindle is the slider (76). The nebuliser described above is suitable for nebulising the aerosol preparations according to the invention to form an aerosol suitable for inhalation. If the formulation according to the invention is nebulised using the method described above (Respimat®), the mass expelled, in at least 97%, preferably at least 98% of all the actuations of the inhaler (puffs), should correspond to a defined quantity with a range of tolerance of not more than 25%, preferably 20% of this quantity. Preferably, between 5 and 30 mg, more preferably between 5 and 20 mg of formulation are delivered as a defined mass per puff. The proportion of the mass delivered which is outside a tolerance limit of not more than 25% in relation to the desired mass should be less than 1.5%, preferably less than 1.2%. Case 1/1162 FF Boehringer Ingelheim Pharma KG 19 However, the formulation according to the invention can also be nebulised using inhalers other than those described above, for example jet-stream inhalers. Case 1/1162 FF 20 Boehringer Ingelheim Pharma KG Examples I. Example of the synthesis of tiotropium bromide monohydrate 15.0 kg of tiotropium bromide 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 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 to a temperature of 20-25°C at a rate of 3-5°C every 20 minutes. Using cold water the apparatus is cooled further to 10-15°C and crystallisation is completed by stirring for at least another hour. The crystals are isolated using a suction filter drier, the crystal slurry isolated is washed with 9 L of cold water (10-15°C) and cold acetone (10-15°C). The crystals obtained are dried at 25°C for 2 hours in a nitrogen current. Yield: 13.4 kg of tiotropium bromide monohydrate (86 % of theory). Case 1/1162 FF Boehringer Ingelheim Pharma KG 21 II. Examples of formulations 100 g of pharmaceutical preparation contain: Example Amount of Amount of Amount of Amount of pH, tiotropium tiotropium benzalkonium sodium adjusted bromide, based bromide chloride edetate with HCI on tiotropium: monohydrate, based on tiotropium: (1N) 1 0.099 g — 10 mg 25 mg 3.0 2 0.006 g — 10 mg 25 mg 3.0 3 0.099 g — 10 mg 10 mg 3.0 4 0.006 g — 10 mg 10 mg 3.0 5 0.099 g 10 mg 25 mg 3.0 6 0.006 g 10 mg 25 mg 3.0 7 0.099 g 10 mg 10 mg 3.0 8 —- 0.006 g 10 mg 10 mg 3.0 The remainder is water or water/ethanol and one of the abovementioned substances in an amount known from the prior art. active Examples 9 to 12: Budesonide Each of Examples 1 to 8 may additionally contain: Example 9a: budesonide: 0.3 g, pH, adjusted with HCI:3.0, solvent water only, no ethanol; Example 9b: budesonide: 0.3 g, pH, adjusted with HCI:3,5; Example 9c: budesonide: 0.3 g, pH, adjusted with HCI:4.0; Example 10: analogous to Example 9a to 9c with budesonide: 0.6 g, Example 11: analogous to Example 9a to 9c with budesonide: 1.3 g, Example 12: analogous to Example 9a to 9c with budesonide: 2.0 g. In Examples 9 to 12 the steroid is present in the formulation in suspension. Sorbitan trioleate may be used as a surfactant. Case 1/1162 FF 22 Boehringer Ingelheim Pharma KG Examples 13 to 15 Analogous to Examples 9 to 12. Benzalkonium chloride is exchanged for sodium benzoate. Examples 16 to 19 Analogous to Examples 9 to 12. Instead of hydrochloric acid, citric acid is exclusively used to adjust the pH. Examples 20 to 30 The ingredients and amounts are analogous to Examples 9 to 19. Instead of water, a mixture of water (10 vol.%) and ethanol (90 vol.%) is used. Budesonide is present in solution. Other Examples Analogously to Examples 9 to 30 described above, the same amount of flunisolide, beclomethasone dipropionate or fluticasone is used instead of budesonide. In the case of fluticasone, lecithin is preferably added instead of sorbitan trioleate in the case of the suspension formulation. The steroids are formulation as a suspension if the solvent used is water on its own. In the case of a mixture of water and ethanol the steroid may be in solution. Example 31 Epinastine: 0.2 g EDTA: 25 mg Tiotropium bromide monohydrate: 29 mg, 0.1 N hydrochloric acid to adjust the pH to 3.0, water ad 100 ml. </div>

Claims

<div class="application article clearfix printTableText" id="claims"> Case 1/1162 FF 23 Boehringer Ingelheim Pharma KG Patent Claims 1. Liquid, propellant-free pharmaceutical preparation comprising at least two combinable active substances containing • a tiotropium salt as one of the active substances, in a concentration based on tiotropium of between 0.0005 and 5 % by weight, • another active substance selected from among the antiallergics, antihistamines, steroids and/or leukotriene antagonists, • water or a water/ethanol mixture as solvent, in which at least the tiotropium salt is dissolved, • acid for achieving a pH between 2.0 and 3.1, • a pharmacologically acceptable preservative, • optionally a pharmacologically acceptable complexing agent and/or stabiliser and/or a pharmacologically acceptable cosolvent and/or other pharmacologically acceptable adjuvants and additives in addition to the preservative. 2. Pharmaceutical preparation according to claim 1, wherein the tiotropium salt is a salt selected from chloride, bromide, iodide, methanesulphonate, para-toluenesulphonate, and/or methylsulphate. 3. Pharmaceutical preparation according to claim 1, wherein the active substance is tiotropium bromide. 4. Pharmaceutical preparation according to claim 1, wherein the active substance is tiotropium bromide monohydrate. INTELLECTUAL PROPERTY OFFICE OF N.Z. 2 6 AUG 2005 RECEIVED Case 1/1162 FF Boehringer Ingelheim Pharma KG 24 5. Pharmaceutical preparation according to any one of claims 1 to 4, wherein the solvent is water. 6. Pharmaceutical preparation according to any one of claims 1 to 4, wherein the solvent is a water-ethanol mixture with up to 90 vol.% of ethanol. 7. Pharmaceutical preparation according to claim 6, wherein the solvent is a water-ethanol mixture with up to 70 vol.% of ethanol. 8. Pharmaceutical preparation according to claim 7, wherein the solvent is a water-ethanol mixture with up to 30 vol.% of ethanol. 9. Pharmaceutical preparation according to any one of claims 1 to 8, wherein it does not contain a complexing agent. 10. Pharmaceutical preparation according to any one of claims 1 to 9, wherein it does not contain a stabiliser. 11. Pharmaceutical preparation according to any one of claims 1 to 8, wherein an editic acid salt is present in an amount of greater than 0 up to 25 mg /100 ml. 12. Pharmaceutical preparation according to claim 11, wherein an editic acid salt is present in an amount from 5 to less than 10 mg/100 ml. 13. Pharmaceutical preparation according to claim 11 or claim 12, wherein the editic acid salt is sodium edetate. 14. Pharmaceutical preparation according to any one of claims 1 to 13, wherein the pH is between 2.5 and 3.1. 15.Pharmaceutical preparation according to claim 14, wherein the pH is between 2.7 and 3.1. INTELLECTUAL PROPERTY OFFICE 'OF N.Z. 26 AUG 2005 RECEIVED Case 1/1162 FF 25 Boehringer Ingelheim Pharma KG 16. Pharmaceutical preparation according to claim 15, wherein the pH is between 2.7 and 3.0. 17. Pharmaceutical preparation according to any one of claims 1 to 16, wherein the concentration of tiotropium is between 0.0005 and 5 % by weight. 18. Pharmaceutical preparation according to claim 17, wherein the concentration of tiotropium is up to 3% by weight. 19. Pharmaceutical preparation according to any one of claims 1 to 18, wherein the preparation contains benzalkonium chloride as preservative. 20. Pharmaceutical preparation according to any one of claims 1 to 8 and 11 to 19, wherein cosolvents and/or pharmacologically acceptable adjuvants and additives are used in addition to the preservative. 21. Pharmaceutical preparation according to claim 20, wherein the preparation contains an antioxidant as adjuvant. 22. Pharmaceutical preparation according to any one of claims 1 to 21, wherein no cosolvents and/or pharmacologically acceptable adjuvants and additives are used apart from the preservative. 23. Pharmaceutical preparation according to any one of claims 1 to 22, wherein the concentration of tiotropium is between 0.001 and 3 wt.%. 24. Pharmaceutical preparation according to any one of claims 1 to 23, wherein the concentration of tiotropium is between 0.0005 to 0.5 wt.%. 25. Pharmaceutical preparation according to claim 24, wherein the concentration of tiotropium is between 0.0005 to 0.25 wt.%. INTELLECTUAL PROPERTY OFFICE 7 2 6 AUG 2005 RECEIVED Case 1/1162 FF 26 Boehringer Ingelheim Pharma KG 26. Pharmaceutical preparation according to claim 25, wherein the concentration of tiotropium is between 0.001 to 1 wt.%. 27. Pharmaceutical preparation according to any one of claims 1 to 26, wherein all the ingredients are dissolved in the solvent. 28. Pharmaceutical preparation according to any one of claims 1 to 27, wherein the additional active substance is in suspension in the solvent. 29. Pharmaceutical preparation according to any one of claims 1 to 28, wherein the additional active substance is a steroid. 30. Pharmaceutical preparation according to claim 29, wherein the concentration of the steroid is 0.05 to 5 wt.%. 31. Pharmaceutical preparation according to claim 30, wherein the concentration of the steroid is 0.1 to 2.5 wt.%. 32. Pharmaceutical preparation according to any one of claims 29 to 31, wherein the steroid is budesonide, beclomethasone dipropionate, fluticasone and/or flunisolide. 33. Pharmaceutical preparation according to any one of claims 1 to 28, wherein the additional active substance is an antiallergic and/or an antihistamine. 34. Pharmaceutical preparation according to claim 33, wherein the concentration of the antiallergic and/or antihistamine is 0.05 to 15 wt.%. 35. Pharmaceutical preparation according to claim 34, wherein the concentration of the antiallergic and/or antihistamine is up to 10 wt.%. 36. Pharmaceutical preparation according to claim 35, wherein the concentration of the antiallergic and/or antihistamine is 0.1 to 10 wt.%. INTELLECTUAL PROPERTY OFFICE OF N.Z. 2 6 AUG 2005 RECEIVED Case 1/1162 FF 27 Boehringer Ingelheim Pharma KG 37. Pharmaceutical preparation according to claim 36, wherein the concentration of the antiallergic and/or antihistamine is 0.1 to 7 wt.%. 38. Pharmaceutical preparation according to any one of claims 33 to 38, wherein the additional active substance is epinastine, nedocromil, disodium cromoglycate, astemizole, mequitazine, carbinoxamine and/or clemastine and/or a corresponding pharmaceutically acceptable salt thereof. 39. Pharmaceutical preparation according to any one of claims 1 to 28, wherein the additional active substance is a leukotriene antagonist. 40. Pharmaceutical preparation according to claim 39, wherein the concentration of the leukotriene antagonist is 0.05 to 10 wt.%. 41. Pharmaceutical preparation according to claim 40, wherein the concentration of the leukotriene antagonist is up to 5 wt.%. 42. Pharmaceutical preparation according to claim 41, wherein the concentration of the leukotriene antagonist is 0.1 to 3.5 wt.%. 43. Pharmaceutical preparation according to any one of claims 39 to 42, wherein the leukotriene antagonist is montelukast, pranlukast, zafiriukast, 1-(((R)-(3-(2-(6,7-difluoro-2-quinolinyl)ethenyl)phenyl)-3-(2-(2-hydroxy-2-propyl)phenyl)thio)methylcyclopropane-acetic acid, 1-(((R)-3-(3-(2-(2,3-dichlorothieno[3,2-b]pyridin-5-yl)-(E)-ethenyl)phenyl)-3-(2-(1-hydroxy-1-methylethyl)phenyl)propyl)thio)methyl)cyclopropane-acetic acid, [2-[[2-(4-tert-butyl-2-thiazolyl)-5-benzofuranyl]oxymethyl]phenyl]acetic acid. 44. Pharmaceutical preparation according to claim 1, containing water, a surfactant, 0.1 wt.% of tiotropium bromide, another active substance selected from among the antiallergics, antihistamines, steroids and/or leukotriene antagonists, 0.01 wt.% of benzalkonium chloride, 0.05 wt.% of sodium edetate, the preparation being adjusted to 3.0 with hydrochloric acid or citric acid. intellectual property office OF N.Z. 2 6 AUG 2005 Dcr>cu/crt Case

1/1162 FF 28 Boehringer Ingelheim Pharma KG 45. Pharmaceutical preparation according to any one of claims 1 to 44 for use as a pharmaceutical composition for administration by inhalation. 46. Use of a pharmaceutical preparation according to any one of claims 1 to 44 in the preparation of a medicament, for the treatment of asthma and/or COPD. 47. Process for preparing a pharmaceutical preparation according to any one of claims 1 to 45 by mixing the individual components. 48. Pharmaceutical preparation as claimed in any one of claims 1 to 45, substantially as herein described with reference to any one of the Figures and/or Examples. 49. Pharmaceutical preparation as claimed in any one of claims 1 to 45, substantially as herein described. 50. Use of a pharmaceutical preparation as claimed in claim 46, substantially as herein described with reference to any one of the Figures and/or Examples. 51. Use of a pharmaceutical preparation as claimed in claim 46, substantially as herein described. 52. Process for preparing a pharmaceutical preparation as claimed in claim 47, substantially as herein described with reference to any one of the Figures and/or Examples. 53. Process for preparing a pharmaceutical preparation as claimed in claim 47, substantially as herein described. INTELLECTUAL PROPERTY OFFICE OF N.Z. 2 6 AUG 2005 RECEIVED </div>