EP2296624A1 - New emulsions for producing medicinal products - Google Patents

New emulsions for producing medicinal products

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Publication number
EP2296624A1
EP2296624A1 EP09761683A EP09761683A EP2296624A1 EP 2296624 A1 EP2296624 A1 EP 2296624A1 EP 09761683 A EP09761683 A EP 09761683A EP 09761683 A EP09761683 A EP 09761683A EP 2296624 A1 EP2296624 A1 EP 2296624A1
Authority
EP
European Patent Office
Prior art keywords
amino
water
oil
salt
quinazoline
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
EP09761683A
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German (de)
French (fr)
Inventor
Regis Cartier
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Boehringer Ingelheim International GmbH
Original Assignee
Boehringer Ingelheim International GmbH
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Boehringer Ingelheim International GmbH filed Critical Boehringer Ingelheim International GmbH
Priority to EP09761683A priority Critical patent/EP2296624A1/en
Publication of EP2296624A1 publication Critical patent/EP2296624A1/en
Withdrawn legal-status Critical Current

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Classifications

    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/02—Inorganic compounds
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/30—Macromolecular organic or inorganic compounds, e.g. inorganic polyphosphates
    • A61K47/34—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyesters, polyamino acids, polysiloxanes, polyphosphazines, copolymers of polyalkylene glycol or poloxamers
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K9/00—Medicinal preparations characterised by special physical form
    • A61K9/10—Dispersions; Emulsions
    • A61K9/107—Emulsions ; Emulsion preconcentrates; Micelles
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00—Drugs for disorders of the respiratory system
    • A61P11/06—Antiasthmatics

Definitions

  • the invention relates to processes for the preparation of stable polymer-based emulsions and the emulsions obtainable by means of these processes and medicaments which can be prepared therefrom.
  • the invention relates to stable, polymer-based emulsions for pulmonary or nasal inhalation and the use of these drugs for the treatment of respiratory diseases, in particular for the treatment of COPD (chronic obstructive pulmonary disease) and asthma.
  • COPD chronic obstructive pulmonary disease
  • Emulsions are systems in which a divided liquid phase (oil or
  • Droplet diameter is usually present in the nanometer to micrometer range in a further liquid phase.
  • the two liquid phases are immiscible.
  • a W / O (water in oil) emulsion is a system in which the aqueous phase is finely dispersed in droplet form in an oil phase.
  • the high degree of fragmentation i.e., the very small droplets causes a very high surface area of the internal phase.
  • emulsions are thermodynamically stable and form a clear to opalescent, fluid system of oily consistency.
  • the special properties of the emulsions are closely related to their colloidal chemical structure, which is a consequence of the chemical composition and the production process of the emulsions.
  • emulsifiers for the preparation of emulsions so-called emulsifiers as
  • emulsifiers for the production of W / O (water in oil) emulsions consist chemically of a water-soluble and a lipophilic portion within the
  • the prior art mainly uses lipids and polymers.
  • the pharmaceutical performance of a drug containing an emulsion can thereby be improved by minimizing the hydrophilic portion of the emulsifier.
  • Under pharmaceutical performance are the physical properties, eg. B. stability, physicochemical properties, pharmacological properties, toxicological properties and pharmacokinetic properties. Among other things, these properties can be monitored by a high loading rate of the emulsion with an active ingredient, an improvement in a targeted release of an active ingredient over time, a reduction in toxicity or a delayed degradation of the formulation over time.
  • the emulsions can be used as a precursor for the production of solid particles, for example in the context of a spray-drying process.
  • the emulsion serves as a spray solution of the spray-drying process.
  • the emulsions are used as a precursor of solid drugs, it is advantageous if the emulsions are composed in such a way that the solid particles produced from the emulsion have a high glass transition temperature.
  • auxiliaries it is an object of the invention to provide stable emulsion with weak emulsifiers and methods for their preparation. It is also an object of the invention to provide stable emulsion with weak emulsifiers whose content of emulsifier is kept as low as possible. In addition, it is an object of the invention to provide medicaments containing emulsions according to the invention.
  • W / O (water in oil) emulsions according to the invention are further characterized in that the ionic strength of the aqueous phase used to prepare the emulsions of the invention has an ionic strength of greater than 10 mM (unit: milli-moles / liter). Preferred is an ionic strength of 15 mM, 20 mM, 30 mM and 50 mM.
  • aqueous phases having an ionic strength between 10 mM and 500 mM, between 15 mM and 500 mM, 20 mM and 500 mM, between 30 mM and 500 mM, between 10 mM and 400 mM, between 15 mM and 400 mM, between 20 mM and 400 mM, between 30 mM and 400 mM, between 10 mM and 300 mM, between 20 mM, 300 mM, between 30 mM and 300 mM, between 10 mM and 200 mM, between 20 mM, 200 mM, between 30 mM and 200 mM.
  • W / O (water in oil) emulsions according to the invention are further characterized in that emulsifiers from the group of co-polymers, in particular from the group of block co-polymers, are preferably used for their preparation.
  • emulsifiers from the group of co-polymers in particular from the group of block co-polymers, are preferably used for their preparation.
  • polymers from the substance class of PEG [poly (lactide-co-glycolides)] or the substance class of PEG [poly-lactides] are suitable as emulsifiers for the novel W / O (water in oil) emulsions, if these have the structure of block copolymers.
  • PEG stands for polyethylene glycol.
  • block copolymers polymers consisting of longer sequences or blocks of each monomer (e.g., aaaaaaaabbbbbbbbbbb ).
  • a diblock structure or triblock structure is to be understood as meaning that the polymer is composed of different units which are repeated regularly at the molecular level.
  • the emulsifiers can be selected from the class of block co-polymers. These contain at least one water-soluble block (block B) and at least one non-water-soluble block (block A).
  • blocks B water-soluble block
  • block A non-water-soluble block
  • compounds which have a diblock structure (AB) or a triblock structure (ABA) can be used as block co-polymers, block A consisting of successive monomer units aaaaaaaa... Of a first polymer and block B of successive monomer units bbbbbbbbb ... of the second polymer.
  • water-soluble block B PEG (polyethylene glycol) is used to a particular degree.
  • non-water-soluble block A a polyester compound is chosen in particular.
  • the polymer class of the poly (lactide-co-glycolides) or the polymer class of the poly-lactides is used as the polyester block.
  • emulsifiers selected from the class PEG- [poly (lactide-co-glycolides)] or the class of PEG- [poly-lactides].
  • PEG- poly (lactide-co-glycolides)
  • PEG- poly-lactides
  • Such substances are available under the name Resomer® (Boehringer Ingelheim Pharma GmbH & Co. KG, Germany).
  • polymers of these two classes of substances are suitable if they have the following properties (a), (b), (c), (d) and (e):
  • a lactide content of 50-100% (mass% based on molecular mass and 100% based on the molecular mass of polymer block A of the block co-polymer) and thereby the lactide content of the components L-lactide and may contain D-lactide and the D-lactide to the L-lactide is present in the ratio n ⁇ at most and n is a number less than or equal to 1, optionally the lactide portion consists exclusively of L-lactide.
  • substances from the class of PEG- [poly (lactide-co-glycolide)] 5 block co-polymers are suitable if they have the following properties (a), (b), (c), (d) and (e) include:
  • a lactide content of 50-99% (mass% based on molecular mass 15 and 100% based on the molecular mass of the polymer block A of the block co-polymer) and thereby the lactide content of the components L- Lactide and D-lactide may contain and the D-lactide to L-lactide maximally in the ratio n: ⁇ is present and n is a number less than or equal to 1, where appropriate, the lactide portion consists exclusively of L-lactide.
  • substances from the class of PEG [poly-lactide] block co-polymers are suitable if they have the following properties (a), (b), (c), and (f):
  • lactide portion may contain the components L-lactide and D-lactide and the D-lactide to L-lactide maximum in the ratio n ⁇ is present and n is a number less than or equal to 1, optionally the lactide portion exclusively made of L-lactide.
  • the emulsifiers are preferably used according to the invention in a concentration of 0.5%, 0.75%, 1%, 1.25% and 1.5%, preferably 0.75% used (mass% of the emulsifier based on the mass of the oil phase).
  • the emulsifiers for the production of W / O (water in oil) - emulsions in a concentration of 0.5% to 20%, 0.5% to 10%, 0.5% to 5%, preferably 0.5% to 2%, more preferably 0.75% to 1% are used (mass% of the emulsifier based on the mass of the oil phase).
  • the W / O (water in oil) emulsions in a specific embodiment are characterized in that the emulsion droplets have a hydrodynamic diameter between 200 nm and 3000 nm, preferably, 300 nm and 3000 nm, preferably, 300 nm and 2500 nm 500 nm and 2500 nm, preferably 500 nm and 2100 nm.
  • the hydrodynamic diameter is understood to mean the mean equivalent diameter, as can be determined by means of photon correlation spectroscopy (more details in the Experimental Section).
  • the invention relates to processes for the production of novel W / O (water in oil) emulsions, by means of which the objects according to the invention are achieved.
  • the preparation of W / O (water in oil) emulsions according to the invention can be carried out, for example, by adding an alkali metal salt, an alkaline earth metal salt, an acid addition salt of an active compound or a combination thereof before the preparation of the emulsion.
  • an acid addition salt of an active ingredient this acid addition salt is present in the aqueous phase in dissociated form.
  • the preparation of such a W / O (water in oil) emulsion comprises a process step characterized in that a salt is dissolved in the aqueous phase used to prepare the W / O (water in oil) emulsion ,
  • This salt may be an inorganic salt or an organic salt, for example the acid addition salt of an active ingredient.
  • the alkali metal salts and alkaline earth metal salts may be mentioned, wherein the anion may be selected from the group consisting of fluoride, chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate , Succinate, benzoate and p-toluenesulfonate.
  • the anion may be a single negatively charged anion selected from the group consisting of Fluoride, chloride, bromide, methanesulfonate and p-toluenesulfonate, most preferably bromide and chloride.
  • the cation may, for example, be selected from lithium, sodium, potassium, beryllium, magnesium, calcium, strontium and barium. Of particular importance are sodium, potassium, magnesium and calcium.
  • the process for producing W / O (water-in-oil) emulsions according to the invention comprises a process step which is characterized in that an organic phase contains an emulsifier from the substance class of PEG [poly (lactide-co-glycolides). ] or the PEG [poly-lactides] is added.
  • This organic phase is then processed in a further step together with an aqueous phase in which a salt is dissolved by intensive mixing to form a W / O (water in 01) emulsion.
  • This salt may be an inorganic salt or an organic salt, for example the acid addition salt of an active ingredient. Examples of possible salts are the alkali metal salts and alkaline earth metal salts, preferably sodium chloride.
  • the salts are considered equivalent to the use of active ingredients which, due to their ionic structure, have an ionic strength of more than 10 mM, also preferably 15 mM, 20 mM, 30 mM and 50 mM.
  • the emulsion is obtainable by homogenizing the organic and aqueous phases by intensive mixing.
  • the mixing process can also be carried out in an ultrasonic bath or an ultrasonic finger while ultrasound is applied to the mixture at the same time.
  • the invention relates to the use of W / O (water in oil) emulsions for the production of dry powder formulations for medicaments to be administered by inhalation.
  • the invention also relates to the use of the emulsions according to the invention as a spray solution for spray drying.
  • the spray-drying of pure active ingredients for inhalation purposes has been described in the prior art [for example: EP 0 072 046 A1; WO 2000 000176 A1; US 6019968; A. Chawla, K.M.G. Taylor, J.M. Newton, M.C.R. Johnson, Int. J. Pharm, 108 (3), (1994), 233-240].
  • the W / O (water in oil) emulsions according to the invention can be used for the preparation of a medicament. Preference is given to the production of a medicament for the treatment of respiratory diseases, in particular for the treatment of COPD and / or asthma.
  • the invention relates to the use the thus obtained W / O (water in oil) emulsions for the manufacture of a medicament for inhalation use in particular measure for the manufacture of a medicament for inhalation use, which allows a delayed release of the active ingredient.
  • W pharmacologically active agents
  • W Anticholinergics, corticosteroids, PDE4 inhibitors, LTD4 antagonists, EGFR inhibitors, dopamine agonists, HIV antihistamines, PAF antagonists and PI3 kinase inhibitors.
  • two- or three-fold combinations of W can be combined and used for application in the device according to the invention. Exemplary combinations of W would be:
  • W represents a betamimetics combined with an anticholinergic, corticosteroids, PDE4 inhibitors, EGFR inhibitors or LTD4 antagonists
  • W represents an anticholinergics combined with a betamimetics, corticosteroids, PDE4 inhibitors, EGFR inhibitors or LTD4 antagonists
  • W represents a corticosteroid combined with a PDE4 inhibitor, EGFR
  • W represents a PDE4 inhibitor combined with an EGFR inhibitor or LTD4
  • W represents an EGFR inhibitor combined with a LTD4 antagonist.
  • Preferred betamimetics for this purpose are compounds selected from the group consisting of albuterol, arformoterol, bambuterol, bitolterol, broxaterol, carbuterol, clenbuterol, fenoterol, formoterol, hexoprenaline, ibuterol, isoetharines, isoprenaline, levosalbutamol, mabuterol, meluadrine, metaproterenol , Orciprenaline, Pirbuterol, Procaterol, Reproterol, Rimiterol, Ritodrine, Salmefamol, Salmeterol, Soterenol, Sulphone terol, Terbutaline, Tiaramide, Tolubuterol, Zinterol, CHF-1035, HOKU-81, KUL-1248 and
  • the acid addition salts of the betamimetics are preferably selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro- toluenesulfonate.
  • anticholinergic compounds are preferably used here, which are selected from the group consisting of tiotropium salts, preferably the
  • the cations are the pharmacologically active ingredients.
  • the aforementioned salts may preferably contain chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate , Benzoate or p-toluenesulfonate, where chloride, bromide, Iodide, sulfate, methanesulfonate or p-toluenesulfonate are preferred as counterions.
  • the chlorides, bromides, iodides and methanesulfonates are particularly preferred.
  • anticholinergics are selected from the salts of the formula AC-I
  • X ⁇ is a single negatively charged anion, preferably an anion selected from the group consisting of fluoride, chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, lo nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate, benzoate and p-toluenesulfonate, preferably a singly negatively charged anion, more preferably an anion selected from the group consisting of fluoride, chloride, bromide, methanesulfonate and p-toluenesulfonate, most preferably bromide, optionally in the form of their racemates, enantiomers or hydrates , Of particular importance are those
  • X ⁇ can have the meanings given above.
  • 20 preferred anticholinergics are selected from the salts of the formula AC-2
  • R is either methyl or ethyl and in which X may have the abovementioned meanings.
  • the compound of the formula AC-2 may also be present in the form of the free base AC-2-base.
  • Preferred corticosteroids are compounds selected from the group consisting of beclomethasone, betamethasone, budesonide, butixocort, ciclesonide, deflazacort, dexamethasone, etiprednol, flunisolide, fluticasone, loteprednol, mometasone, prednisolone, prednisone, rofleponide, triamcinolone, RPR - 106541, NS-126, ST-26 and - 6,9-difluoro-17 - [(2-furanylcarbonyl) oxy] -1-hydroxy-16-methyl-3-oxo-androsta-1, 4-diene 17-carbothionic acid (S) -fluoromethyl ester
  • Examples of possible salts and derivatives of steroids may be: alkali metal salts, such as, for example, sodium or potassium salts, sulfobenzoates, phosphates, isonicotinates, acetates, dichloroacetates, propionates, dihydrogen phosphates, palmitates, pivalates or even furoates.
  • alkali metal salts such as, for example, sodium or potassium salts, sulfobenzoates, phosphates, isonicotinates, acetates, dichloroacetates, propionates, dihydrogen phosphates, palmitates, pivalates or even furoates.
  • Preferred PDE4 inhibitors here are compounds which are selected from the group consisting of enprofylline, theophylline, roflumilast,
  • the acid addition salts of the PDE4 inhibitors are preferably selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate,
  • Hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydrooxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate are Hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydrooxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
  • Preferred LTD4 antagonists here are compounds selected from the group consisting of montelukast, pranlukast, zafirlukast, MCC-847 (ZD-3523), MN-001, MEN-91507 (LM-1507), VUF-5078 , VUF-K-8707, L-733321 and
  • alkali metal salts such as, for example, sodium or potassium salts, alkaline earth salts, sulfobenzoates, phosphates, isonicotinates, acetates, propionates, dihydrogen phosphates, palmitates, pivalates or furoates.
  • the EGFR inhibitors used are preferably compounds selected from the group consisting of cetuximab, trastuzumab, ABX-EGF, Mab ICR-62 and - 4 - [(3-chloro-4-fluorophenyl) amino] -6- ⁇ [4- (morpholin-4-yl) -1-oxo-2-buten-1-yl] amino ⁇ -7-cyclopropylmethoxyquinazoline
  • these acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
  • Preferred dopamine agonists are compounds selected from the group consisting of bromocriptine, cabergoline, alpha-dihydroergocryptine, lisuride, pergolide, pramipexole, roxindole, ropinirole, talipexole, terguride and viozan, optionally in the form of their racemates, enantiomers , Diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates.
  • these acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
  • Hl antihistamines here preferably compounds are used, which are selected from the group consisting of epinastine, cetirizine, azelastine, fexofenadine, levocabastine, loratadine, mizolastine, ketotifen, emedastine, dimetindene, clemastine, bamipine, Cexchlorpheniramin, pheniramine, doxylamine, chlorphenoxamine , Dimenhydrinate, diphenhydramine, promethazine, ebastine, desloratidine and meclocine, optionally in the form of their racemates, enantiomers, diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates.
  • these acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
  • substance formulations or substance mixtures all inhalable compounds are used, such as, for example, inhalable macromolecules, as disclosed in EP 1 003 478.
  • substances, substance formulations or substance mixtures are used for the treatment of respiratory diseases, which are used in the inhalation area.
  • the compound may be derived from the group of derivatives of ergot alkaloids, triptans, CGRP inhibitors, phosphodiesterase V inhibitors, optionally in the form of their racemates, enantiomers or diastereomers, optionally in the form of their pharmacologically acceptable acid addition salts, their solvates and / or or hydrates.
  • the meter calculates the hydrodynamic diameter (Dh) of a suspension and gives the size distribution (volume-related determination mode).
  • the measurement results listed below correspond to the respective main peaks of the determined size distributions (for the purposes of this invention, the droplet size of the main peak corresponds to the hydrodynamic diameter).
  • the preparation of the emulsion solutions in the following Examples 1 to 4 was carried out such that the active ingredients or polymers were dissolved in a concentration of 0.75% (weight per volume in grams per 100 milli liters) in their respective phase.
  • the phases were combined and treated by means of an ultrasonic finger for 2 min at 30% power.
  • the tip is immersed 0.5 - 2 cm in the solution and the ultrasonic apparatus (manufacturer: Sonics & Materials Inc. (Darbury, CT, USA), type: "Vibra Cell", model: VC 50) at 30% of the maximum force Operated for 5 minutes. Influence of the ionic strength on the stability of the W / O (water in Q1) emulsions according to the invention
  • Example 1 Stability of W / O (water in oil) emulsions with different salts as a function of time
  • FIG. 1 shows W / O (water-in-oil) emulsions according to the invention which contain, as emulsifier, the polymer of the Resomer® type LGPt8546 (see legend of the figure and details according to Table 1).
  • DCM dichloromethane
  • the organic phase was then processed with an aqueous phase in a ratio of 1: 4 (volume: volume, i.e. one volume of aqueous phase to four volumes of organic phase) to form an emulsion by sonication.
  • the respective aqueous phase contained a different salt in an ionic strength of 20 mM.
  • the emulsions obtained are thus (W / O) water-in-oil emulsions (water / DCM emulsions).
  • Example 3 Stability of W / O (water in oil) Emulsion with different emulsifiers (polymers) as a function of time
  • the W / O (water-in-oil) emulsions according to the invention of the results shown in Figure 3 were obtained by dissolving as emulsifiers various Resomer® type polymers (in the organic phase (DCM)) in the inorganic (aqueous) phase Salbutamol sulphate salt was dissolved from these phases W / O 5 (water / DCM) emulsions, the amount of aqueous phase to the organic phase being 1: 4 (volume: volume, ie one volume of aqueous phase to four volumes of organic phase), produced by ultrasonic treatment.
  • DCM organic phase
  • Salbutamol sulphate salt was dissolved from these phases W / O 5 (water / DCM) emulsions, the amount of aqueous phase to the organic phase being 1: 4 (volume: volume, ie one volume of aqueous phase to four volumes of organic phase), produced by ultrasonic treatment.
  • all W / O (water / DCM) -10 emulsions according to the invention exhibit stable behavior.
  • the emulsion droplet size (hydrodynamic diameter of the emulsion) is in a suitable range between 300 nm and 3000 nm.
  • the emulsion droplet size remains stable at least within the measurement period of about 1 hour within this range suitable for the droplet size.
  • FIG. 4 Further examples of the stability behavior of W / O (water-in-oil) emulsions according to the invention are shown in Figure 4 (x-axis: measurement time of determining the hydrodynamic diameter, the zero value indicating the time of preparation of the emulsion, y-axis: hydrodynamic Diameter ie).
  • the W / O (water in oil) emulsions of the invention shown in FIG. 4 can be obtained in a comparable manner to Examples 1 to 3.
  • the composition was chosen such that
  • the emulsifier used was LGPt8546 (see legend of the figure and data according to Table 1).
  • all W / O (water / DCM) emulsions according to the invention exhibit stable behavior.
  • the emulsion droplet size (hydrodynamic oil diameter of the emulsion) is in a suitable range between 300 nm and 3000 nm.
  • the emulsion droplet size remains stable at least within the measurement period of about 1 hour within this range suitable for the droplet size.
  • Table 2 Composition of the emulsions prepared according to Examples 1 to 4 (% data corresponds to mass per volume (w / v) in grams per 100 milli liters).

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  • Health & Medical Sciences (AREA)
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  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
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  • Pharmacology & Pharmacy (AREA)
  • Animal Behavior & Ethology (AREA)
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  • Inorganic Chemistry (AREA)
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  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Engineering & Computer Science (AREA)
  • Dispersion Chemistry (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Medicinal Preparation (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Emulsifying, Dispersing, Foam-Producing Or Wetting Agents (AREA)
  • Colloid Chemistry (AREA)

Abstract

The invention relates to the provision of stable, polymer-based emulsions which in their aqueous phase have an ionic strength of more than 10 mM, and to processes for preparing them and also to the medicinal products obtainable using these emulsions.

Description

NEUE EMULSIONEN ZUR HERSTELLUNG VON ARZNEIMITTELN NEW EMULSIONS FOR THE MANUFACTURE OF MEDICAMENTS
Die Erfindung bezieht sich auf Verfahren zur Herstellung stabiler Polymer-basierten Emulsionen sowie der mit Hilfe dieser Verfahren erhältlichen Emulsionen und daraus herstellbaren Arzneimittel. In einer besonderen Ausführungsform betrifft die Erfindung stabile, polymer-basierte Emulsionen zur pulmonalen oder nasalen Inhalation sowie die Verwendung dieser Arzneimittel zur Behandlung von Atemwegserkrankungen, insbesondere zur Behandlung von COPD (chronic obstructive pulmonary disease = chronisch obstruktive Lungenerkrankung) und Asthma.The invention relates to processes for the preparation of stable polymer-based emulsions and the emulsions obtainable by means of these processes and medicaments which can be prepared therefrom. In a particular embodiment, the invention relates to stable, polymer-based emulsions for pulmonary or nasal inhalation and the use of these drugs for the treatment of respiratory diseases, in particular for the treatment of COPD (chronic obstructive pulmonary disease) and asthma.
Hintergrund der ErfindungBackground of the invention
Unter Emulsionen versteht man Systeme, bei denen eine zerteilte flüssige Phase (Öl oderEmulsions are systems in which a divided liquid phase (oil or
Wasser, je nachdem ob man W/O oder O/W Emulsionen betrachtet) mit einemWater, depending on whether one considers W / O or O / W emulsions) with one
Tröpfchendurchmesser üblicherweise im Nanometer- bis Mikrometerbereich in einer weiteren flüssigen Phase vorliegt. Die beiden flüssigen Phasen sind dabei nicht mischbar.Droplet diameter is usually present in the nanometer to micrometer range in a further liquid phase. The two liquid phases are immiscible.
Somit stellt eine W/O (Wasser in Öl)-Emulsion ein System dar, in dem die wässrige Phase fein verteilt in Tröpfchenform in einer Öl-Phase vorliegt. Der hohe Zerteilung sgrad (d.h. die sehr kleinen Tröpfchen) bedingt eine sehr hohe Oberfläche der inneren Phase.Thus, a W / O (water in oil) emulsion is a system in which the aqueous phase is finely dispersed in droplet form in an oil phase. The high degree of fragmentation (i.e., the very small droplets) causes a very high surface area of the internal phase.
Aufgrund der daraus folgenden hohen Grenzflächenenergien würde dies zu einer sofortigen Destabilisierung führen, was sich in einem Zusammenfließen der kleinenDue to the resulting high interfacial energies, this would lead to an immediate destabilization, resulting in a confluence of the small
Tröpfchen äußern müßte. Ein wesentliches Kennzeichen ist jedoch, dass Emulsionen thermodynamisch stabil sind und ein klares bis opaleszentes, dünnflüssiges System von ölartiger Konsistenz bilden.To express droplets. However, a key feature is that emulsions are thermodynamically stable and form a clear to opalescent, fluid system of oily consistency.
Die speziellen Eigenschaften der Emulsionen hängen dabei eng mit ihrem kolloidal- chemischen Aufbau zusammen, welche eine Folge der chemischen Zusammensetzung sowie des Herstellverfahrens der Emulsionen sind.The special properties of the emulsions are closely related to their colloidal chemical structure, which is a consequence of the chemical composition and the production process of the emulsions.
Allgemein werden zur Herstellung von Emulsionen sogenannte Emulgatoren alsGenerally, for the preparation of emulsions so-called emulsifiers as
Hilfsstoffe verwendet. Diese haben die Funktionen:Excipients used. These have the functions:
• Reduktion der Oberflächenspannung zwischen den nicht-mischbaren Flüssigkeiten • Stabilisierung der Emulsionströpfchen durch sterische Effekte und / oder elektro s tati sehe Ab stossung skr äf te .• reduction of the surface tension between the immiscible liquids • stabilization of the emulsion droplets by steric effects and / or electrostatic repulsion.
Aufgabe der ErfindungObject of the invention
Übliche Emulgatoren zur Herstellung von W/O (Wasser in Öl)-Emulsionen bestehen chemisch aus einem wasserlöslichen und einem lipophilen Anteil innerhalb derCommon emulsifiers for the production of W / O (water in oil) emulsions consist chemically of a water-soluble and a lipophilic portion within the
Molekülstruktur. Im Stand der Technik werden hauptsächlich Lipide und Polymere verwendet. Die pharmazeutische Performance eines Arzneimittels, welches eine Emulsion enthält, lässt sich dabei dadurch verbessern, dass der hydrophile Anteil des Emulgators minimiert wird. Unter pharmazeutischer Performance sind dabei die physikalischen Eigenschaften, z. B. die Stabilität, die physikochemische Eigenschaften, pharmakologische Eigenschaften, toxikologische Eigenschaften und pharmakokinetischen Eigenschaften zu verstehen. Beobachtet werden können diese Eigenschaften unter anderem an einer hohen Beladungsrate der Emulsion mit einem Wirkstoff, einer Verbesserung einer gezielten Freisetzung eines Wirkstoffes über die Zeit, einer Verringerung der Toxizität oder eines verzögerten Abbaus der Formulierung über die Zeit. Als eine spezifische Aufgabe der Erfindung kann aufgeführt werden, dass die Emulsionen als Vorstufe zur Herstellung von Feststoffpartikeln z.B. im Rahmen eines Sprühtrocknungsprozesses eingesetzt werden können. Hierbei dient die Emulsion als Sprühlösung des Sprühtrocknungsprozesses. Für den Fall dass die Emulsionen als Vorstufe von festen Arzneimitteln Verwendung finden, ist es von Vorteil, wenn die Emulsionen derart zusammengesetzt sind, dass die aus der Emulsion hergestellten Feststoffpartikel eine hohe Glasübergangstemperatur aufweisen.Molecular structure. The prior art mainly uses lipids and polymers. The pharmaceutical performance of a drug containing an emulsion can thereby be improved by minimizing the hydrophilic portion of the emulsifier. Under pharmaceutical performance are the physical properties, eg. B. stability, physicochemical properties, pharmacological properties, toxicological properties and pharmacokinetic properties. Among other things, these properties can be monitored by a high loading rate of the emulsion with an active ingredient, an improvement in a targeted release of an active ingredient over time, a reduction in toxicity or a delayed degradation of the formulation over time. As a specific object of the invention can be stated that the emulsions can be used as a precursor for the production of solid particles, for example in the context of a spray-drying process. Here, the emulsion serves as a spray solution of the spray-drying process. In the event that the emulsions are used as a precursor of solid drugs, it is advantageous if the emulsions are composed in such a way that the solid particles produced from the emulsion have a high glass transition temperature.
Es ist somit allgemeine Aufgabe der vorliegenden Erfindung stabile Emulsionen mit verbesserten Emulgatoren bereitzustellen sowie Verfahren zu deren Herstellung. Ein weiterer Aspekt der Erfindung ist es, stabile Emulsionen mit bioverträglichenIt is thus a general object of the present invention to provide stable emulsions with improved emulsifiers and processes for their preparation. Another aspect of the invention is stable, biocompatible emulsions
Hilfsstoffen bereit zu stellen. Insbesondere ist es Aufgabe der Erfindung, stabile Emulsion mit schwachen Emulgatoren bereitzustellen sowie Verfahren zu deren Herstellung. Auch ist es Aufgabe der Erfindung stabile Emulsion mit schwachen Emulgatoren bereitzustellen, deren Anteil an Emulgator möglichst gering gehalten wird. Darüber hinaus ist es Aufgabe der Erfindung, Arzneimittel, die erfindungsgemäße Emulsionen enthalten, bereit zu stellen.To provide auxiliaries. In particular, it is an object of the invention to provide stable emulsion with weak emulsifiers and methods for their preparation. It is also an object of the invention to provide stable emulsion with weak emulsifiers whose content of emulsifier is kept as low as possible. In addition, it is an object of the invention to provide medicaments containing emulsions according to the invention.
Detaillierte Beschreibung der ErfindungDetailed description of the invention
Überraschenderweise wurde gefunden, dass die erfindungsgemäßen W/O (Wasser in 01)- Emulsionen, die einen pharmakologisch aktiven Wirkstoff enthalten, dann die eingangs genannten Aufgaben lösen, wenn zu deren Herstellung eine wässrige Phase verwendet wird, die eine verdünnte Salzlösung darstellt.Surprisingly, it has been found that the W / O (water in 01) emulsions according to the invention, which contain a pharmacologically active agent, then solve the objects mentioned above, if an aqueous phase which is a dilute salt solution is used for their preparation.
Erfindungsgemäße W/O (Wasser in Öl)-Emulsionen sind ferner dadurch gekennzeichnet, dass die Ionenstärke der wässrigen Phase, die zur Herstellung der erfindungsgemäßen Emulsionen verwendet wird, eine Ionenstärke von mehr als 10 mM (Einheit: milli-mol / Liter) aufweist. Bevorzugt ist eine Ionenstärke von 15 mM, 20 mM, 30 mM und 50 mM. Desweiteren bevorzugt sind wässrige Phasen, die eine Ionenstärke zwischen 10 rnM und 500 rnM, zwischen 15 rnM und 500 rnM, 20 mM und 500 mM, zwischen 30 mM und 500 mM, zwischen 10 mM und 400 mM, zwischen 15 mM und 400 mM, zwischen 20 mM und 400 mM, zwischen 30 mM und 400 mM, zwischen 10 mM und 300 mM, zwischen 20 mM, 300 mM, zwischen 30 mM und 300 mM, zwischen 10 mM und 200 mM, zwischen 20 mM, 200 mM, zwischen 30 mM und 200 mM aufweisen.W / O (water in oil) emulsions according to the invention are further characterized in that the ionic strength of the aqueous phase used to prepare the emulsions of the invention has an ionic strength of greater than 10 mM (unit: milli-moles / liter). Preferred is an ionic strength of 15 mM, 20 mM, 30 mM and 50 mM. Also preferred are aqueous phases having an ionic strength between 10 mM and 500 mM, between 15 mM and 500 mM, 20 mM and 500 mM, between 30 mM and 500 mM, between 10 mM and 400 mM, between 15 mM and 400 mM, between 20 mM and 400 mM, between 30 mM and 400 mM, between 10 mM and 300 mM, between 20 mM, 300 mM, between 30 mM and 300 mM, between 10 mM and 200 mM, between 20 mM, 200 mM, between 30 mM and 200 mM.
Unter Ionenstärke / versteht manUnder ionic strength / is understood
2 / -, * "-S *— 1 mit n = Anzahl der Ionenarten c = molare Konzentration der jeweiligen Ionenart z = Ladung (Wertigkeit) des einzelnen Ions.2 / -, * "-S * - 1 with n = number of ionic species c = molar concentration of the respective ionic species z = charge (valency) of the single ion.
Erfindungsgemäße W/O (Wasser in Öl)-Emulsionen sind ferner dadurch gekennzeichnet, dass zu ihrer Herstellung bevorzugt Emulgatoren aus der Gruppe der Co-Polymere im besonderen aus der Gruppe der Block-Co-Polymere verwendet werden. Im besonderen eignen sich Polymere aus der Substanzklasse der PEG-[Poly-(Laktid-co- Glykolide)] oder der Substanzklasse der PEG-[Poly-Laktide] als Emulgatoren für die erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen, wenn diese die Struktur von Blockcopolymeren aufweisen. PEG steht hierbei für Polyethylenglykol.W / O (water in oil) emulsions according to the invention are further characterized in that emulsifiers from the group of co-polymers, in particular from the group of block co-polymers, are preferably used for their preparation. In particular, polymers from the substance class of PEG [poly (lactide-co-glycolides)] or the substance class of PEG [poly-lactides] are suitable as emulsifiers for the novel W / O (water in oil) emulsions, if these have the structure of block copolymers. PEG stands for polyethylene glycol.
Unter Blockcopolymeren versteht man Polymere, die aus längeren Sequenzen oder Blöcken jedes Monomers (z.B.: aaaaaaaabbbbbbbbbbbbb...) bestehen. Hierbei steht jederBy block copolymers is meant polymers consisting of longer sequences or blocks of each monomer (e.g., aaaaaaaabbbbbbbbbbbb ...). Everyone is here
Kleinbuchstabe für eine Monomereinheit. Je nach Anzahl der Blöcke spricht man auch vonLowercase letter for a monomer unit. Depending on the number of blocks one also speaks of
Diblock- und Triblock-Copolymeren.Diblock and triblock copolymers.
Unter einer Diblockstruktur beziehungsweise Triblockstruktur ist dabei zu verstehen, dass das Polymer aus unterschiedlichen Einheiten aufgebaut ist, welche sich auf molekularer Ebene regelmäßig wiederholen.A diblock structure or triblock structure is to be understood as meaning that the polymer is composed of different units which are repeated regularly at the molecular level.
Beispielsweise können für die erfindungegemäßen W/O (Wasser in Öl)-Emulsionen die Emulgatoren aus der Klasse der Block-Co-Polymere ausgewählt werden. Diese beinhalten mindestens einen wasserlöslichen Block (Block B) und mindestens einen nicht- wasserlöslichen Block (Block A). Erfindungsgemäß können als Block-Co-Polymere Verbindungen verwendet werden, die eine Diblockstruktur (A-B) oder eine Triblockstruktur (A-B-A) aufweisen, wobei der Block A aus aufeinander folgenden Monomereinheiten aaaaaaaaa... eines ersten Polymers und der Block B aus aufeinander folgenden Monomereinheiten bbbbbbbbbbbb... des zweiten Polymers besteht.For example, for the W / O (water in oil) emulsions according to the invention, the emulsifiers can be selected from the class of block co-polymers. These contain at least one water-soluble block (block B) and at least one non-water-soluble block (block A). According to the invention, compounds which have a diblock structure (AB) or a triblock structure (ABA) can be used as block co-polymers, block A consisting of successive monomer units aaaaaaaa... Of a first polymer and block B of successive monomer units bbbbbbbbbbb ... of the second polymer.
Als wasserlöslicher Block B wird in besonderem Maße PEG (Polyethylenglykol) verwendet. Als nicht- wasserlöslicher Block A wird in besonderem Maße eine Polyester- Verbindung gewählt. Beispielsweise wird als Polyester-Block die Polymer-Klasse der PoIy- (Laktid-co-Glykolide) beziehungsweise die Polymer-Klasse der Poly-Laktide verwendet.As water-soluble block B, PEG (polyethylene glycol) is used to a particular degree. As non-water-soluble block A, a polyester compound is chosen in particular. For example, the polymer class of the poly (lactide-co-glycolides) or the polymer class of the poly-lactides is used as the polyester block.
Folglich weisen die Monomereinheiten a des Blockes A im Falle derConsequently, the monomer units a of the block A in the case of
(i) PEG-[Poly-(Laktid-co-Glykolid)e] sowohl Laktid-Einheiten a1 als auch Glykolid-Einheiten a2 auf, wobei die Monomereinheiten „Laktid-Einheit a1" und „Glykolid-Einheit a2" entweder statistisch zufällig verteilt innerhalb des Blockes oder auch alternierend oder abwechselnd im Verlauf des Blockes vorkommen können oder im Falle der(i) PEG- [poly (lactide-co-glycolide) e] both lactide units a 1 and glycolide units a 2 , the monomer units "lactide unit a 1 " and "glycolide unit a 2 " either statistically randomly distributed within the block or even alternately or alternately in the course of the block or in the case of
(ii) PEG- [Poly-Laktide] ausschließlich Laktid-Einheiten a1 auf.(ii) PEG- [poly-lactides] exclusively lactide units a 1 on.
Zur Herstellung der erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen sind dabeiTo prepare the W / O (water in oil) emulsions according to the invention are thereby
Emulgatoren bevorzugt geeignet, die ausgewählt sind aus der Klasse PEG- [PoIy- (Laktid- co-Glykolide)] oder der Klasse der PEG- [Poly-Laktide]. Derartige Substanzen sind unter der Bezeichnung Resomer® (Boehringer Ingelheim Pharma GmbH & Co. KG, Deutschland) erhältlich. Im besonderen Maße sind Polymere aus diesen beiden Substanzklassen geeignet, wenn diese die folgenden Eigenschaften (a), (b), (c), (d) und (e) aufweisen:Preferably, emulsifiers selected from the class PEG- [poly (lactide-co-glycolides)] or the class of PEG- [poly-lactides]. Such substances are available under the name Resomer® (Boehringer Ingelheim Pharma GmbH & Co. KG, Germany). In particular, polymers of these two classes of substances are suitable if they have the following properties (a), (b), (c), (d) and (e):
(a) einen PEG- Anteil von 1 - 15 % (Massen-% bezogen auf die Gesamtmolekularmasse des Block-Co-Polymers),(a) a PEG content of 1-15% (mass% based on the total molecular weight of the block co-polymer),
(b) eine Molekularmasse zwischen 37.5 - 600 kDa, (c) eine Diblockstruktur oder Triblockstruktur,(b) a molecular mass between 37.5-600 kDa, (c) a diblock structure or triblock structure,
(d) einen Glykolid- Anteil von 0 - 50 % (Massen% bezogen auf die Molekularmasse, wobei 100% sich auf die Molekularmasse des Polymer-Block A des Block-Co- Polymers bezieht),(d) a glycolide fraction of 0-50% (mass% based on molecular mass, where 100% is based on the molecular mass of the polymer block A of the block co-polymer),
(e) einen Laktid- Anteil von 50 - 100% (Massen% bezogen auf die Molekularmasse und 100% sich auf die Molekularmasse des Polymer-Block A des Block-Co- Polymers bezieht) und dabei der Laktid- Anteil die Komponenten L-Laktid und D-Laktid enthalten kann und das D-Laktid zum L-Laktid maximal im Verhältnis n\\ vorliegt und n eine Zahl kleiner oder gleich 1 ist, gegebenenfalls der Laktid- Anteil ausschließlich aus L-Laktid besteht.(e) a lactide content of 50-100% (mass% based on molecular mass and 100% based on the molecular mass of polymer block A of the block co-polymer) and thereby the lactide content of the components L-lactide and may contain D-lactide and the D-lactide to the L-lactide is present in the ratio n \\ at most and n is a number less than or equal to 1, optionally the lactide portion consists exclusively of L-lactide.
Im speziellen sind Substanzen aus der Klasse der PEG- [PoIy- (Laktid-co-Glykolid)e] 5 Block-Co-Polymere geeignet, wenn diese die folgenden Eigenschaften (a), (b), (c), (d) und (e) aufweisen:In particular, substances from the class of PEG- [poly (lactide-co-glycolide)] 5 block co-polymers are suitable if they have the following properties (a), (b), (c), (d) and (e) include:
(a) einen PEG- Anteil von 1 - 15 % (Massen-% bezogen auf die Gesamtmolekularmasse des Block-Co-Polymers),(a) a PEG content of 1-15% (mass% based on the total molecular weight of the block co-polymer),
(b) eine Molekularmasse zwischen 37.5 - 600 kDa, l o (c) eine Diblockstruktur oder Triblockstruktur,(b) a molecular mass between 37.5-600 kDa, l o (c) a diblock structure or triblock structure,
(d) einen Glykolid- Anteil von 1 - 50 % (Massen% bezogen auf die Molekularmasse, wobei 100% sich auf die Molekularmasse des Polymer-Block A des Block-Co- Polymers bezieht),(d) a glycolide fraction of 1-50% (mass% based on molecular mass, where 100% is based on the molecular mass of the polymer block A of the block co-polymer),
(e) einen Laktid- Anteil von 50 - 99% (Massen% bezogen auf die Molekularmasse 15 und 100% sich auf die Molekularmasse des Polymer-Block A des Block-Co- Polymers bezieht) und dabei der Laktid- Anteil die Komponenten L-Laktid und D-Laktid enthalten kann und das D-Laktid zum L-Laktid maximal im Verhältnis n:\ vorliegt und n eine Zahl kleiner oder gleich 1 ist, gegebenenfalls der Laktid- Anteil ausschließlich aus L-Laktid besteht.(e) a lactide content of 50-99% (mass% based on molecular mass 15 and 100% based on the molecular mass of the polymer block A of the block co-polymer) and thereby the lactide content of the components L- Lactide and D-lactide may contain and the D-lactide to L-lactide maximally in the ratio n: \ is present and n is a number less than or equal to 1, where appropriate, the lactide portion consists exclusively of L-lactide.
2020
In einer weiteren speziellen Ausführungsform sind Substanzen aus der Klasse der PEG- [Poly-Laktide] Block-Co-Polymere geeignet, wenn diese die folgenden Eigenschaften (a), (b), (c), und (f) aufweisen:In a further specific embodiment, substances from the class of PEG [poly-lactide] block co-polymers are suitable if they have the following properties (a), (b), (c), and (f):
(a) einen PEG- Anteil von 1 - 15 % (Massen-% bezogen auf die 25 Gesamtmolekularmasse des Block-Co-Polymers),(a) a PEG content of 1-15% (mass% based on the total molecular weight of the block co-polymer),
(b) eine Molekularmasse zwischen 37.5 - 600 kDa,(b) a molecular mass between 37.5-600 kDa,
(c) eine Diblockstruktur oder Triblockstruktur,(c) a diblock structure or triblock structure,
(f) einen Laktid- Anteil von 85 - 99% (Massen% bezogen auf die Gesamtmolekularmasse des Block-Co-Polymers )(f) a lactide content of 85-99% (mass% based on the total molecular weight of the block co-polymer)
30 und dabei der Laktid- Anteil die Komponenten L-Laktid und D-Laktid enthalten kann und das D-Laktid zum L-Laktid maximal im Verhältnis n\\ vorliegt und n eine Zahl kleiner oder gleich 1 ist, gegebenenfalls der Laktid- Anteil ausschließlich aus L-Laktid besteht.30 and while the lactide portion may contain the components L-lactide and D-lactide and the D-lactide to L-lactide maximum in the ratio n \\ is present and n is a number less than or equal to 1, optionally the lactide portion exclusively made of L-lactide.
Von besonderer Bedeutung sind die in Tabelle 1 aufgeführten Polymere PEG-[PoIy- 35 (Laktid-co-Glykolide] und PEG-[Poly-Laktide] als Emulgatoren für erfindungsgemäße W/O (Wasser in Öl)-Emulsionen. Tabelle 1 : Für die Herstellung von Emulsionen verwendete Polymere (Hersteller:Of particular importance are the polymers PEG- [poly-35 (lactide-co-glycolides) and PEG- [poly-lactides] listed in Table 1 as emulsifiers for W / O (water in oil) emulsions according to the invention. Table 1: Polymers used for the preparation of emulsions (manufacturer:
Boehringer Ingelheim); Mw= Molekulargewicht in [kD] (theoretisch nach dem Herstellprozess berechnet auf Basis der verwendeten Monomer- Mengen); Tg = Glasübergangstemperatur in [0C]; die in der Spalte Composition angegebenen Prozentwerte stellen die Masse-bezogene %-Werte der Bausteine PEG, D/L- Laktide und Glykolide dar, wobei 100% sich auf die Gesamtmasse des Block- Co-Polymers bezieht.Boehringer Ingelheim); Mw = molecular weight in [kD] (calculated theoretically after the production process on the basis of the monomer amounts used); T g = glass transition temperature in [ 0 C]; the percentages given in the column Composition represent the mass-related% values of the building blocks PEG, D / L-lactides and glycolides, 100% being based on the total mass of the block co-polymer.
Zur Herstellung von W/O (Wasser in Öl) -Emulsionen werden die Emulgatoren erfindungsgemäß bevorzugt in einer Konzentration von 0,5%, 0,75%, 1%, 1,25% und 1,5%, bevorzugt 0,75% verwendet (Massen% des Emulgators bezogen auf die Masse der Öl-Phase).For the preparation of W / O (water in oil) emulsions, the emulsifiers are preferably used according to the invention in a concentration of 0.5%, 0.75%, 1%, 1.25% and 1.5%, preferably 0.75% used (mass% of the emulsifier based on the mass of the oil phase).
Erfindungsgemäß können die Emulgatoren zur Herstellung von W/O (Wasser in Öl)- Emulsionen in einer Konzentration von 0,5% bis 20%, 0,5% bis 10%, 0,5% bis 5%, bevozugt 0,5% bis 2%, besonders bevorzugt 0,75% bis 1% eingesetzt werden (Massen% des Emulgators bezogen auf die Masse der Öl-Phase).According to the invention, the emulsifiers for the production of W / O (water in oil) - emulsions in a concentration of 0.5% to 20%, 0.5% to 10%, 0.5% to 5%, preferably 0.5% to 2%, more preferably 0.75% to 1% are used (mass% of the emulsifier based on the mass of the oil phase).
Erfindungsgemäß sind die W/O (Wasser in Öl)-Emulsionen in einer spezifischen Ausführungsform dadurch gekennzeichnet, dass die Emulsionströpfchen einen hydrodynamischen Durchmesser zwischen 200 nm und 3000 nm, bevorzugt, 300 nm und 3000 nm , bevorzugt, 300 nm und 2500 nm, bevorzugt 500 nm und 2500 nm, bevorzugt 500 nm und 2100 nm aufweisen. Unter dem hydrodynamischen Durchmesser versteht man dabei den mittleren Äquivalenzdurchmesser, wie dieser mittels Photonenkorrelationsspektroskopie bestimmt werden kann (nähere Angaben dazu im Experimentellen Teil).According to the invention, the W / O (water in oil) emulsions in a specific embodiment are characterized in that the emulsion droplets have a hydrodynamic diameter between 200 nm and 3000 nm, preferably, 300 nm and 3000 nm, preferably, 300 nm and 2500 nm 500 nm and 2500 nm, preferably 500 nm and 2100 nm. The hydrodynamic diameter is understood to mean the mean equivalent diameter, as can be determined by means of photon correlation spectroscopy (more details in the Experimental Section).
Ferner betrifft die Erfindung Verfahren zur Herstellung erfindungsgemäßer W/O (Wasser in Öl)-Emulsionen, mit Hilfe deren die erfindungsgemäßen Aufgaben gelöst werden.Furthermore, the invention relates to processes for the production of novel W / O (water in oil) emulsions, by means of which the objects according to the invention are achieved.
Im Rahmen der Erfindung kann die Herstellung erfindungsgemäßer W/O (Wasser in Öl)- Emulsionen beispielsweise derart erfolgen, dass die wässrige Phase vor Herstellung der Emulsion mit einem Alkalisalz, einem Erdalkalisalz, einem Säureadditionssalzes eines Wirkstoffes oder einer Kombination derselben versetzt wird. Im Falle eines Säureadditionssalzes eines Wirkstoffes liegt dieses Säureadditionssalz in der wässrigen Phase in dissoziierter Form vor.In the context of the invention, the preparation of W / O (water in oil) emulsions according to the invention can be carried out, for example, by adding an alkali metal salt, an alkaline earth metal salt, an acid addition salt of an active compound or a combination thereof before the preparation of the emulsion. In the case of an acid addition salt of an active ingredient, this acid addition salt is present in the aqueous phase in dissociated form.
Die Herstellung einer solchen W/O (Wasser in Öl)-Emulsion umfasst einen Prozessschritt, der dadurch gekennzeichnet ist, dass in der wässrigen Phase, die zur Herstellung der W/O (Wasser in Öl)-Emulsion verwendet wird, ein Salz gelöst wird. Dieses Salz kann ein anorganisches Salz oder ein organisches Salz, beispielsweise das Säureadditionssalz eines Wirkstoffes sein. Als Beispiele möglicher Salze sind die Alkalisalze und Erdalkalisalze zu nennen, wobei das Anion ausgewählt sein kann aus der Gruppe bestehend aus Fluorid, Chlorid, Bromid, Iodid, Sulfat, Phosphat, Methansulfonat, Nitrat, Maleat, Acetat, Citrat, Fumarat, Tartrat, Oxalat, Succinat, Benzoat und p-Toluolsulfonat. Ebenso kann das Anion ein einfach negativ geladenes Anion sein, ausgewählt aus der Gruppe bestehend aus Fluorid, Chlorid, Bromid, Methansulfonat und p-Toluolsulfonat, insbesondere bevorzugt Bromid und Chlorid.The preparation of such a W / O (water in oil) emulsion comprises a process step characterized in that a salt is dissolved in the aqueous phase used to prepare the W / O (water in oil) emulsion , This salt may be an inorganic salt or an organic salt, for example the acid addition salt of an active ingredient. As examples of possible salts, the alkali metal salts and alkaline earth metal salts may be mentioned, wherein the anion may be selected from the group consisting of fluoride, chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate , Succinate, benzoate and p-toluenesulfonate. Similarly, the anion may be a single negatively charged anion selected from the group consisting of Fluoride, chloride, bromide, methanesulfonate and p-toluenesulfonate, most preferably bromide and chloride.
Das Kation kann beispielsweise ausgewählt sein aus Lithium, Natrium, Kalium, Beryllium, Magnesium, Calcium, Strontium und Barium. Von besonderer Bedeutung sind Natrium, Kalium, Magnesium und Calcium.The cation may, for example, be selected from lithium, sodium, potassium, beryllium, magnesium, calcium, strontium and barium. Of particular importance are sodium, potassium, magnesium and calcium.
Ebenso von besonderer Bedeutung ist das Natriumchlorid.Also of particular importance is sodium chloride.
Das Verfahren zur Herstellung erfindungsgemäßer W/O (Wasser in Öl)-Emulsionen umfasst in einer weiteren Ausführungsform einen Prozessschritt, der dadurch gekennzeichnet ist, dass einer organischen Phase ein Emulgator aus der Substanzklasse der PEG-[Poly-(Laktid-co-Glykolide)] oder der PEG-[Poly-Laktide] zugegeben wird. Diese organische Phase wird dann in einem weiteren Schritt zusammen mit einer wässrigen Phase, in der ein Salz gelöst ist, durch intensives Mischen zu einer W/O (Wasser in 01)- Emulsion verarbeitet. Dieses Salz kann ein anorganisches Salz oder ein organisches Salz, beispielsweise das Säureadditionssalz eines Wirkstoffes sein. Als Beispiele möglicher Salze sind die Alkalisalze und Erdalkalisalze, bevorzugt das Natriumchlorid zu nennen. Ebenso möglich ist es, in der wässrigen Phase eine Kombination von Salzen zu lösen. Erfindungsgemäß ist den Salzen gleichgestellt die Verwendung von Wirkstoffen, die aufgrund ihrer ionischen Struktur eine Ionenstärke von mehr als 10 mM, ebenso bevorzugt von 15 mM, 20 mM, 30 mM und 50 mM aufweisen.In a further embodiment, the process for producing W / O (water-in-oil) emulsions according to the invention comprises a process step which is characterized in that an organic phase contains an emulsifier from the substance class of PEG [poly (lactide-co-glycolides). ] or the PEG [poly-lactides] is added. This organic phase is then processed in a further step together with an aqueous phase in which a salt is dissolved by intensive mixing to form a W / O (water in 01) emulsion. This salt may be an inorganic salt or an organic salt, for example the acid addition salt of an active ingredient. Examples of possible salts are the alkali metal salts and alkaline earth metal salts, preferably sodium chloride. It is equally possible to dissolve a combination of salts in the aqueous phase. In accordance with the invention, the salts are considered equivalent to the use of active ingredients which, due to their ionic structure, have an ionic strength of more than 10 mM, also preferably 15 mM, 20 mM, 30 mM and 50 mM.
Die Emulsion ist erhältlich, indem die organische und die wässrige Phase durch intensives Mischen homogenisiert wird. Der Mischenvorgang ist auch in einem Ultraschallbad oder einem Ultraschallfinger unter zeitgleichem Einwirken von Ultraschall auf die Mischung durchführbar.The emulsion is obtainable by homogenizing the organic and aqueous phases by intensive mixing. The mixing process can also be carried out in an ultrasonic bath or an ultrasonic finger while ultrasound is applied to the mixture at the same time.
Desweiteren betrifft die Erfindung die Verwendung der W/O (Wasser in Öl)-Emulsionen zur Herstellung von Trockenpulverformulierungen für inhalativ zu applizierende Arzneimittel. Die Erfindung betrifft auch die Verwendung der erfindungsgemäßen Emulsionen als Sprühlösung für Sprühtrocknung s verfahren. Die Sprühtrocknung von reinen Wirkstoffen für inhalative Zwecke (Pulverinhalation) ist im Stand der Technik beschrieben [z.B.: EP 0 072 046 Al; WO 2000 000176 Al; US 6019968; A. Chawla, K.M.G. Taylor, J.M. Newton, M.C.R. Johnson, Int. J. Pharm, 108 (3), (1994), 233-240].Furthermore, the invention relates to the use of W / O (water in oil) emulsions for the production of dry powder formulations for medicaments to be administered by inhalation. The invention also relates to the use of the emulsions according to the invention as a spray solution for spray drying. The spray-drying of pure active ingredients for inhalation purposes (powder inhalation) has been described in the prior art [for example: EP 0 072 046 A1; WO 2000 000176 A1; US 6019968; A. Chawla, K.M.G. Taylor, J.M. Newton, M.C.R. Johnson, Int. J. Pharm, 108 (3), (1994), 233-240].
Erfindungsgemäß können die erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen verwendet werden zur Herstellung eines Arzneimittels. Bevorzugt dabei ist die Herstellung eines Arzneimittels zur Behandlung von Atemwegserkrankungen, insbesondere zur Behandlung von COPD und/oder Asthma. Ebenso betrifft die Erfindung die Verwendung der so erhaltenen W/O (Wasser in Öl)-Emulsionen zur Herstellung eines Arzneimittels zur inhalativen Anwendung im besonderen Maße zur Herstellung eines Arzneimittels zur inhalativen Anwendung, welches eine verzögerte Freisetzung des Wirkstoffes ermöglicht.According to the invention, the W / O (water in oil) emulsions according to the invention can be used for the preparation of a medicament. Preference is given to the production of a medicament for the treatment of respiratory diseases, in particular for the treatment of COPD and / or asthma. Likewise, the invention relates to the use the thus obtained W / O (water in oil) emulsions for the manufacture of a medicament for inhalation use in particular measure for the manufacture of a medicament for inhalation use, which allows a delayed release of the active ingredient.
Die im folgenden aufgeführten chemischen Verbindungen (pharmakologisch aktive Wirkstoffe, W) können dabei allein oder in Kombination als Arzneimittel-relevanter Bestandteil der erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen, bevorzugt als Komponente der wässrigen Phase Eingang finden. In den unten genannten Verbindungen ist W einen pharmakologisch aktiver Wirkstoff und (beispielsweise) ausgewählt aus der Gruppe bestehend aus Betamimetika,The chemical compounds listed below (pharmacologically active agents, W) can be used alone or in combination as a drug-relevant constituent of the W / O (water in oil) emulsions according to the invention, preferably as a component of the aqueous phase input. In the compounds mentioned below W is a pharmacologically active agent and (for example) selected from the group consisting of betamimetics,
Anticholinergika, Corticosteroiden, PDE4-Inhibitoren, LTD4- Antagonisten, EGFR- Hemmern, Dopamin-Agonisten, Hl -Antihistaminika, PAF-Antagonisten und PI3-Kinase Inhibitoren. Weiterhin können zwei- oder dreifach Kombinationen von W kombiniert werden und zur Anwendung in der erfindungsgemäßen Vorrichtung gelangen. Beispielhaft genannte Kombinationen von W wären:Anticholinergics, corticosteroids, PDE4 inhibitors, LTD4 antagonists, EGFR inhibitors, dopamine agonists, HIV antihistamines, PAF antagonists and PI3 kinase inhibitors. Furthermore, two- or three-fold combinations of W can be combined and used for application in the device according to the invention. Exemplary combinations of W would be:
W stellt ein Betamimetika dar, kombiniert mit einem Anticholinergika, Corticosteroide, PDE4-Inhibitore, EGFR-Hemmern oder LTD4- Antagonisten, W stellt ein Anticholinergika dar, kombiniert mit einem Betamimetika, Corticosteroiden, PDE4-Inhibitoren, EGFR-Hemmern oder LTD4- Antagonisten, - W stellt ein Corticosteroiden dar, kombiniert mit einem PDE4-Inhibitoren, EGFR-W represents a betamimetics combined with an anticholinergic, corticosteroids, PDE4 inhibitors, EGFR inhibitors or LTD4 antagonists, W represents an anticholinergics combined with a betamimetics, corticosteroids, PDE4 inhibitors, EGFR inhibitors or LTD4 antagonists, W represents a corticosteroid combined with a PDE4 inhibitor, EGFR
Hemmern oder LTD4- AntagonistenInhibitors or LTD4 antagonists
W stellt ein PDE4-Inhibitoren dar, kombiniert mit einem EGFR-Hemmern oder LTD4-W represents a PDE4 inhibitor combined with an EGFR inhibitor or LTD4
Antagonistenantagonists
W stellt ein EGFR-Hemmern dar, kombiniert mit einem LTD4- Antagonisten.W represents an EGFR inhibitor combined with a LTD4 antagonist.
Als Betamimetika gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Albuterol, Arformoterol, Bambuterol, Bitolterol, Broxaterol, Carbuterol, Clenbuterol, Fenoterol, Formoterol, Hexoprenaline, Ibuterol, Isoetharine, Isoprenaline, Levosalbutamol, Mabuterol, Meluadrine, Metaproterenol, Orciprenaline, Pirbuterol, Procaterol, Reproterol, Rimiterol, Ritodrine, Salmefamol, Salmeterol, Soterenol, Sulphonterol, Terbutaline, Tiaramide, Tolubuterol, Zinterol, CHF-1035, HOKU-81, KUL-1248 undPreferred betamimetics for this purpose are compounds selected from the group consisting of albuterol, arformoterol, bambuterol, bitolterol, broxaterol, carbuterol, clenbuterol, fenoterol, formoterol, hexoprenaline, ibuterol, isoetharines, isoprenaline, levosalbutamol, mabuterol, meluadrine, metaproterenol , Orciprenaline, Pirbuterol, Procaterol, Reproterol, Rimiterol, Ritodrine, Salmefamol, Salmeterol, Soterenol, Sulphone terol, Terbutaline, Tiaramide, Tolubuterol, Zinterol, CHF-1035, HOKU-81, KUL-1248 and
3-(4-{6-[2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-hexyloxy}- butyl) -benzyl- Sulfonamid - 5-[2-(5,6-Diethyl-indan-2-ylamino)-l-hydroxy-ethyl]-8-hydroxy-lH-quinolin-2-on3- (4- {6- [2-Hydroxy-2- (4-hydroxy-3-hydroxymethyl-phenyl) -ethyl-amino] -hexyloxy} -butyl) -benzyl-sulfonamide - 5- [2- (5,6- diethyl-indan-2-ylamino) -l-hydroxy-ethyl] -8-hydroxy-lH-quinolin-2-one
4-Hydroxy-7-[2-{ [2-{ [3-(2-phenylethoxy)propyl]sulphonyl}ethyl]-amino}ethyl]-4-Hydroxy-7- [2- {[2- {[3- (2-phenylethoxy) propyl] sulphonyl} ethyl] amino} ethyl] -
2(3H)-benzothiazolon 1 - (2-Fluor-4-hydroxyphenyl) -2- [4- ( 1 -benzimidazolyl) -2-methyl-2-butylamino] ethanol l-[3-(4-Methoxybenzyl-amino)-4-hydroxyphenyl]-2-[4-(l-benzimidazolyl)-2-methyl- 2-butylamino] ethanol l-[2H-5-hydroxy-3-oxo-4H-l,4-benzoxazin-8-yl]-2-[3-(4-N,N-dimethylaminophenyl)- 2-methyl-2-propylamino]ethanol2 (3H) -benzothiazolone 1- (2-Fluoro-4-hydroxyphenyl) -2- [4- (1-benzimidazolyl) -2-methyl-2-butylamino] ethanol 1- [3- (4-methoxybenzylamino) -4-hydroxyphenyl] - 2- [4- (1-benzimidazolyl) -2-methyl-2-butylamino] ethanol 1- [2H-5-hydroxy-3-oxo-4H-1,4-benzoxazin-8-yl] -2- [3 - (4-N, N-dimethylaminophenyl) -2-methyl-2-propylamino] ethanol
- l-[2H-5-hydroxy-3-oxo-4H-l,4-benzoxazin-8-yl]-2-[3-(4-methoxyphenyl)-2-methyl-2- propylamino] ethanol- 1- [2H-5-hydroxy-3-oxo-4H-1,4-benzoxazin-8-yl] -2- [3- (4-methoxyphenyl) -2-methyl-2-propylamino] ethanol
- l-[2H-5-hydroxy-3-oxo-4H-l,4-benzoxazin-8-yl]-2-[3-(4-n-butyloxyphenyl)-2-methyl- 2-propylamino]ethanol - l-[2H-5-hydroxy-3-oxo-4H-l,4-benzoxazin-8-yl]-2-{4-[3-(4-methoxyphenyl)-l,2,4- triazol-3-yl]-2-methyl-2-butylamino Jethanoi- 1- [2H-5-hydroxy-3-oxo-4H-1,4-benzoxazin-8-yl] -2- [3- (4-n-butyloxyphenyl) -2-methyl-2-propylamino] ethanol - 1- [2H-5-hydroxy-3-oxo-4H-1,4-benzoxazin-8-yl] -2- {4- [3- (4-methoxyphenyl) -l, 2,4-triazole-3-one yl] -2-methyl-2-butylamino Jethanoi
5-Hydroxy-8-(l-hydroxy-2-isopropylaminobutyl)-2H-l,4-benzoxazin-3-(4H)-on l-(4-Amino-3-chlor-5-trifluoπnethylphenyl)-2-tert.-butylamino)ethanol5-hydroxy-8- (1-hydroxy-2-isopropylaminobutyl) -2H-1,4-benzoxazine-3- (4H) -on- (4-amino-3-chloro-5-trifluoromethylphenyl) -2-tert .-butylamino) ethanol
6-Hydroxy-8- { 1 -hydroxy-2- [2-(4-methoxy-phenyl)- 1 , 1 -dimethyl-ethylamino]-ethyl } - 4H-benzo[l,4]oxazin-3-on6-Hydroxy-8- {1-hydroxy-2- [2- (4-methoxyphenyl) -1,1-dimethylethylamino] -ethyl} -4H-benzo [1,4] oxazin-3-one
6-Hydroxy-8-{ l-hydroxy-2-[2-(4-phenoxy-essigsäureethylester)-l,l-dimethyl- ethylamino] -ethyl } -4H-benzo [1,4] oxazin-3-on6-Hydroxy-8- {1-hydroxy-2- [2- (4-phenoxy-acetic acid ethyl ester) -l, l-dimethyl-ethylamino] -ethyl} -4 H -benzo [1,4] oxazin-3-one
6-Hydroxy-8- { 1 -hydroxy-2- [2-(4-phenoxy-essigsäure)- 1 , 1 -dimethyl-ethylamino] - ethyl}-4H-benzo[l,4]oxazin-3-on - 8- { 2- [ 1 , 1 -Dimethyl-2-(2,4,6-trimethylphenyl)-ethylamino]- 1 -hydroxy-ethyl } -6- hydroxy-4H-benzo[l,4]oxazin-3-on6-Hydroxy-8- {1-hydroxy-2- [2- (4-phenoxyacetic acid) -1,1-dimethylethylamino] ethyl} -4H-benzo [1,4-oxazin-3-one 8- {2- [1,1-dimethyl-2- (2,4,6-trimethylphenyl) ethylamino] -1-hydroxyethyl} -6-hydroxy-4H-benzo [1,4-oxazine-3-] on
6-Hydroxy-8- { 1 -hydroxy-2- [2-(4-hydroxy-phenyl)- 1 , 1 -dimethyl-ethylamino] -ethyl } -6-hydroxy-8- {1-hydroxy-2- [2- (4-hydroxyphenyl) -1,1-dimethyl-ethylamino] -ethyl} -
4H-benzo[l,4]oxazin-3-on4H-benzo [l, 4] oxazin-3-one
6-Hydroxy- 8- { 1 -hydroxy-2- [2-(4-isopropyl-phenyl)- 1 , 1 dimethyl-ethylamino] -ethyl } - 4H-benzo[l,4]oxazin-3-on6-Hydroxy-8- {1-hydroxy-2- [2- (4-isopropylphenyl) -1,1-dimethyl-ethylamino] -ethyl} -4H-benzo [1,4-oxazin-3-one
8- { 2- [2-(4-Ethyl-phenyl)- 1 , 1 -dimethyl-ethylamino] - 1 -hydroxy-ethyl } -6-hydroxy-4H- benzo[ 1 ,4] oxazin-3-on8- {2- [2- (4-ethylphenyl) -1,1-dimethylethylamino] -1-hydroxyethyl} -6-hydroxy-4H-benzo [1,4] oxazin-3-one
8- { 2- [2-(4-Ethoxy-phenyl)- 1 , 1 -dimethyl-ethylamino] - 1 -hydroxy-ethyl } -6-hydroxy-4H- benzo[ 1 ,4] oxazin-3-on - 4-(4-{2-[2-Hydroxy-2-(6-hydroxy-3-oxo-3,4-dihydro-2H-benzo[l,4]oxazin-8-yl)- ethylamino] -2-methyl-propyl } -phenoxy)-buttersäure8- {2- [2- (4-Ethoxy-phenyl) -l, 1-dimethyl-ethylamino] -1-hydroxy-ethyl} -6-hydroxy-4H-benzo [1,4] oxazin-3-one 4- (4- {2- [2-Hydroxy-2- (6-hydroxy-3-oxo-3,4-dihydro-2H-benzo [l, 4] oxazin-8-yl) ethylamino] -2- methyl-propyl} -phenoxy) -butyric acid
8- { 2- [2- (3 ,4-Difluor-phenyl)- 1 , 1 -dimethyl-ethylamino] - 1 -hydroxy-ethyl } -6-hydroxy-8- {2- [2- (3,4-difluorophenyl) -1,1-dimethylethylamino] -1-hydroxyethyl} -6-hydroxy
4H-benzo[l,4]oxazin-3-on l-(4-Ethoxy-carbonylamino-3-cyano-5-fluorophenyl)-2-(tert.-butylamino)ethanol - 2-Hydroxy-5-( 1 -hydroxy-2- { 2- [4-(2-hydroxy-2-phenyl-ethylamino)-phenyl]- ethylamino } -ethyl)-benzaldehyd N- [2-Hydroxy-5- ( 1 -hydroxy-2- { 2- [4- (2-hydroxy-2-phenyl-ethylamino)-phenyl] - ethylamino } -ethyl)-phenyl] -formamid4H-benzo [1,4] oxazin-3-one 1- (4-ethoxycarbonylamino-3-cyano-5-fluorophenyl) -2- (tert -butylamino) ethanol - 2-hydroxy-5- (1 - hydroxy-2- {2- [4- (2-hydroxy-2-phenyl-ethylamino) -phenyl] -ethylamino} -ethyl) -benzaldehyde N- [2-hydroxy-5- (1-hydroxy-2- {2- [4- (2-hydroxy-2-phenyl-ethylamino) -phenyl] -ethylamino} -ethyl) -phenyl] -formamide
8-Hydroxy-5-(l-hydroxy-2-{2-[4-(6-methoxy-biphenyl-3-ylamino)-phenyl]- ethylamino}-ethyl)-lH-quinolin-2-on - 8-Hydroxy-5-[l-hydroxy-2-(6-phenethylamino-hexylamino)-ethyl]-lH-quinolin-2-on8-Hydroxy-5- (1-hydroxy-2- {2- [4- (6-methoxy-biphenyl-3-ylamino) -phenyl] -ethylamino} -ethyl) -1H-quinolin-2-one - 8- hydroxy-5- [(6-phenethylamino-hexylamino) -ethyl l-hydroxy-2-] -lH-quinolin-2-one
5- [2- (2- { 4- [4- (2- Amino-2-methyl-propoxy)-phenylamino] -phenyl } -ethylamino)- 1 - hydroxy-ethyl]-8-hydroxy-lH-quinolin-2-on5- [2- (2- {4- [4- (2-amino-2-methyl-propoxy) -phenyl-amino] -phenyl} -ethyl-amino) -1-hydroxy-ethyl] -8-hydroxy-1H-quinoline 2-one
[3-(4- { 6- [2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino] -hexyloxy } - butyl) - 5 -methyl-phenyl] -harnstof f - 4-(2- { 6-[2-(2,6-Dichloro-benzyloxy)-ethoxy] -hexylamino } - 1 -hydroxy-ethyl)-2- hydroxymethyl-phenol[3- (4- {6- [2-Hydroxy-2- (4-hydroxy-3-hydroxymethylphenyl) -ethylamino] -hexyloxy} -butyl) -5-methylphenyl] -urea f - 4- ( 2- {6- [2- (2,6-dichloro-benzyloxy) -ethoxy] -hexylamino} -1-hydroxy-ethyl) -2-hydroxymethyl-phenol
3-(4-{6-[2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-hexyloxy}- butyl)-benzylsulfonamid3- (4- {6- [2-Hydroxy-2- (4-hydroxy-3-hydroxymethylphenyl) -ethylamino] -hexyloxy} -butyl) -benzylsulfonamide
3-(3-{7-[2-Hydroxy-2-(4-hydroxy-3-hydroxymethyl-phenyl)-ethylamino]-heptyloxy}- propyl)-benzylsulfonamid3- (3- {7- [2-Hydroxy-2- (4-hydroxy-3-hydroxymethylphenyl) -ethylamino] -heptyloxy} -propyl) -benzylsulfonamide
4-(2- { 6- [4-(3-Cyclopentanesulfonyl-phenyl)-butoxy]-hexylamino } - 1 -hydroxy-ethyl)-2- hydroxymethyl-phenol4- (2- {6- [4- (3-Cyclopentanesulfonylphenyl) -butoxy] -hexylamino} -1-hydroxyethyl) -2-hydroxymethyl-phenol
N-Adamantan-2-yl-2-(3-{2-[2-hydroxy-2-(4-hydroxy-3-hydroxymethyl-phenyl)- ethylamino] -propyl } -phenyl)-acetamidN-Adamantan-2-yl-2- (3- {2- [2-hydroxy-2- (4-hydroxy-3-hydroxymethylphenyl) ethylamino] -propyl} -phenyl) -acetamide
gegebenenfalls in Form ihrer Racemate, Enantiomere, Diastereomere und gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, Solvate oder Hydrate. Erfindungsgemäß bevorzugt sind die Säureadditionssalze der Betamimetika ausgewählt aus der Gruppe bestehend aus Hydrochlorid, Hydrobromid, Hydroiodid, Hydrosulfat, Hydrophosphat, Hydromethansulfonat, Hydronitrat, Hydromaleat, Hydroacetat, Hydro- citrat, Hydrofumarat, Hydrotartrat, Hydrooxalat, Hydro succinat, Hydrobenzoat und Hydro- p-toluolsulfonat.optionally in the form of their racemates, enantiomers, diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates. According to the invention, the acid addition salts of the betamimetics are preferably selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro- toluenesulfonate.
Als Anticholinergika gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Tiotropiumsalzen, bevorzugt dasAs anticholinergic compounds are preferably used here, which are selected from the group consisting of tiotropium salts, preferably the
Bromidsalz, Oxitropiumsalzen, bevorzugt das Bromidsalz, Flutropiumsalzen, bevorzugt das Bromidsalz, Ipratropiumsalzen, bevorzugt das Bromidsalz, Glycopyrroniumsalzen, bevorzugt das Bromidsalz, Trospiumsalzen, bevorzugt das Chloridsalz, Tolterodin. In den vorstehend genannten Salzen stellen die Kationen die pharmakologisch aktiven Bestandteile dar. Als Anionen können die vorstehend genannten Salze bevorzugt enthalten Chlorid, Bromid, Iodid, Sulfat, Phosphat, Methansulfonat, Nitrat, Maleat, Acetat, Citrat, Fumarat, Tartrat, Oxalat, Succinat, Benzoat oder p-Toluolsulfonat, wobei Chlorid, Bromid, Iodid, Sulfat, Methansulfonat oder p-Toluolsulfonat als Gegenionen bevorzugt sind. Von allen Salzen sind die Chloride, Bromide, Iodide und Methansulfonate besonders bevorzugt.Bromide salt, oxitropium salts, preferably the bromide salt, flutropium salts, preferably the bromide salt, ipratropium salts, preferably the bromide salt, glycopyrronium salts, preferably the bromide salt, trospium salts, preferably the chloride salt, tolterodine. In the above-mentioned salts, the cations are the pharmacologically active ingredients. As anions, the aforementioned salts may preferably contain chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate , Benzoate or p-toluenesulfonate, where chloride, bromide, Iodide, sulfate, methanesulfonate or p-toluenesulfonate are preferred as counterions. Of all the salts, the chlorides, bromides, iodides and methanesulfonates are particularly preferred.
Ebenfalls bevorzugte Anticholinergika sind ausgewählt aus den Salzen der Formel AC-ILikewise preferred anticholinergics are selected from the salts of the formula AC-I
worin X ~ ein einfach negativ geladenes Anion, bevorzugt ein Anion ausgewählt aus der Gruppe bestehend aus Fluorid, Chlorid, Bromid, Iodid, Sulfat, Phosphat, Methansulfonat, l o Nitrat, Maleat, Acetat, Citrat, Fumarat, Tartrat, Oxalat, Succinat, Benzoat und p-Toluol- sulfonat, bevorzugt ein einfach negativ geladenes Anion, besonders bevorzugt ein Anion ausgewählt aus der Gruppe bestehend aus Fluorid, Chlorid, Bromid, Methansulfonat und p- Toluolsulfonat, insbesondere bevorzugt Bromid, bedeutet gegebenenfalls in Form ihrer Racemate, Enantiomere oder Hydrate. Von besonderer Bedeutung sind solchewherein X ~ is a single negatively charged anion, preferably an anion selected from the group consisting of fluoride, chloride, bromide, iodide, sulfate, phosphate, methanesulfonate, lo nitrate, maleate, acetate, citrate, fumarate, tartrate, oxalate, succinate, benzoate and p-toluenesulfonate, preferably a singly negatively charged anion, more preferably an anion selected from the group consisting of fluoride, chloride, bromide, methanesulfonate and p-toluenesulfonate, most preferably bromide, optionally in the form of their racemates, enantiomers or hydrates , Of particular importance are those
15 Arzneimittelkombinationen, die die Enantiomere der Formel AC-l-en15 drug combinations containing the enantiomers of the formula AC-l-en
enthalten, worin X ~ die vorstehend genannten Bedeutungen aufweisen kann. Weiterhin 20 bevorzugte Anticholinergika sind ausgewählt aus den Salzen der Formel AC-2contain, wherein X ~ can have the meanings given above. Furthermore, 20 preferred anticholinergics are selected from the salts of the formula AC-2
worin R entweder Methyl oder Ethyl bedeuten und worin X die vorstehend genannte Bedeutungen aufweisen kann. In einer alternativen Ausführungsform kann die Verbindung der Formel AC-2 auch in Form der freien Base AC-2-base vorliegen. wherein R is either methyl or ethyl and in which X may have the abovementioned meanings. In an alternative embodiment, the compound of the formula AC-2 may also be present in the form of the free base AC-2-base.
Weiterhin genannte Verbindungen sind:Further named compounds are:
2,2-Diphenylpropionsäuretropenolester-Methobromid 2,2-Diphenylpropionsäurescopinester-Methobromid - 2-Fluor-2,2-Diphenylessigsäurescopinester-Methobromid 2-Fluor-2,2-Diphenylessigsäuretropenolester-Methobromid 3,3',4,4'-Tetrafluorbenzilsäuretropenolester-Methobromid 3,3',4,4'-Tetrafluorbenzilsäurescopinester-Methobromid 4,4'-Difluorbenzilsäuretropenolester-Methobromid - 4,4'-Difluorbenzilsäurescopinester-Methobromid 3,3'-Difluorbenzilsäuretropenolester-Methobromid 3,3'-Difluorbenzilsäurescopinester-Methobromid 9-Hydroxy-fluoren-9-carbonsäuretropenolester-Methobromid 9-Fluor-fluoren-9-carbonsäuretropenolester-Methobromid - 9-Hydroxy-fluoren-9-carbonsäurescopinester-Methobromid 9-Fluor-fluoren-9-carbonsäurescopinester-Methobromid 9-Methyl-fluoren-9-carbonsäuretropenolester-Methobromid 9-Methyl-fluoren-9-carbonsäurescopinester-Methobromid Benzilsäurecyclopropyltropinester-Methobromid - 2,2-Diphenylpropionsäurecyclopropyltropinester-Methobromid2,2-Diphenylpropionic acid-tropol ester-methobromide 2,2-diphenylpropionic acid copolester-methobromide - 2-fluoro-2,2-diphenylacetic acid-co-ester methobromide 2-fluoro-2,2-diphenylacetic acid-tropol ester-methobromide 3,3 ', 4,4'-tetrafluorobenzilic acid-tropol ester-methobromide 3,3 ', 4,4'-Tetrafluorobenzilic Acid Copoester Methobromide 4,4'-Difluorobenzilic Acid-Sterol Ester Methobromide - 4,4'-Difluorobenzilic Acid Copoester Methobromide 3,3'-Difluorobenzilic Acid-Sterol Ester Methobromide 3,3'-Difluorobenzilic Acid Copoprene Ester Methobromide 9-Hydroxy fluorene-9-carboxylic acid tropol ester methobromide 9-fluoro-fluorene-9-carboxylic acid-tropol ester-methobromide - 9-hydroxy-fluorene-9-carboxylic acid-co-ester methobromide 9-fluoro-fluoren-9-carboxylic acid-co-ester methobromide 9-methyl-fluorene-9-carboxylic acid-tropol ester Methobromide 9-Methyl-fluorene-9-carboxylic Acid Copinester Methobromide Benzyl Acid Cyclopropyl Tropin Ester Methobromide - 2,2-Diphenylpropionic Acid Cyclopropyl Methacrylate
9-Hydroxy-xanthen-9-carbonsäurecyclopropyltropinester-Methobromid 9-Methyl-fluoren-9-carbonsäurecyclopropyltropinester-Methobromid 9-Methyl-xanthen-9-carbonsäurecyclopropyltropinester-Methobromid 9-Hydroxy-fluoren-9-carbonsäurecyclopropyltropinester-Methobromid - 4,4'-Difluorbenzilsäuremethylestercyclopropyltropinester-Methobromid 9-Hydroxy-xanthen-9-carbonsäuretropenolester-Methobromid 9-Hydroxy-xanthen-9-carbonsäurescopinester-Methobromid 9-Methyl-xanthen-9-carbonsäuretropenolester-Methobromid9-Hydroxy-xanthene-9-carboxylic acid cyclopropyltropine ester methobromide 9-methyl-fluorene-9-carboxylic acid cyclopropyltropine ester methobromide 9-methyl-xanthene-9-carboxylic acid cyclopropyltropine ester methobromide 9-hydroxy-fluorene-9-carboxylic acid cyclopropyltropine ester methobromide - 4,4'- Methyl difluorobenzilate cyclopropyltropine ester methobromide 9-hydroxy-xanthene-9-carboxylic acid-tropol ester-methobromide 9-hydroxy-xanthene-9-carboxylic acid-co-ester methobromide 9-methyl-xanthene-9-carbonsäuretropenolester methobromide
9-Methyl-xanthen-9-carbonsäurescopinester-Methobromid9-methyl-xanthene-9-carbonsäurescopinester methobromide
9-Ethyl-xanthen-9-carbonsäuretropenolester-Methobromid9-ethyl-xanthene-9-carbonsäuretropenolester methobromide
9-Difluoπnethyl-xanthen-9-carbonsäuretropenolester-Methobromid - 9-Hydroxymethyl-xanthen-9-carbonsäurescopinester-Methobromid9-Difluoromethyl-xanthene-9-carboxylic acid-tropol ester-methobromide - 9-hydroxymethyl-xanthene-9-carboxylic acid-co-ester methobromide
Die vorstehend genannten Verbindungen sind im Rahmen der vorliegenden Erfindung auch als Salze einsetzbar, in denen statt des Methobromids, die Salze Metho-X zur Anwendung gelangen, wobei X die vorstehend für X" genannten Bedeutungen haben kann.The abovementioned compounds can also be used in the context of the present invention as salts in which, instead of the methobromide, the salts Metho-X are used, where X may have the meanings given above for X " .
Als Corticosteroide gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Beclomethason, Betamethason, Budesonid, Butixocort, Ciclesonid, Deflazacort, Dexamethason, Etiprednol, Flunisolid, Fluticason, Loteprednol, Mometason, Prednisolon, Prednison, Rofleponid, Triamcinolon, RPR- 106541, NS- 126, ST-26 und - 6,9-Difluor-17-[(2-furanylcarbonyl)oxy]-l l-hydroxy-16-methyl-3-oxo-androsta-l,4- dien-17-carbothionsäure (S)-fluoromethylesterPreferred corticosteroids here are compounds selected from the group consisting of beclomethasone, betamethasone, budesonide, butixocort, ciclesonide, deflazacort, dexamethasone, etiprednol, flunisolide, fluticasone, loteprednol, mometasone, prednisolone, prednisone, rofleponide, triamcinolone, RPR - 106541, NS-126, ST-26 and - 6,9-difluoro-17 - [(2-furanylcarbonyl) oxy] -1-hydroxy-16-methyl-3-oxo-androsta-1, 4-diene 17-carbothionic acid (S) -fluoromethyl ester
6,9-Difluor- 11 -hydroxy- 16-methyl-3-oxo- 17-propionyloxy-androsta- 1 ,4-dien- 17- carbothionsäure (S)-(2-oxo-tetrahydro-furan-3S-yl)ester,6,9-Difluoro-11-hydroxy-16-methyl-3-oxo-17-propionyloxy-androsta-1,4-diene-17-carbothionic acid (S) - (2-oxo-tetrahydrofuran-3S-yl) esters,
6α,9α-difluoro-llß-hydroxy-16α-methyl-3-oxo-17α-(2,2,3,3-tertamethylcyclo- propylcarbonyl)oxy-androsta-l,4-diene-17ß-carbonsäure cyanomethyl ester gegebenenfalls in Form ihrer Racemate, Enantiomere oder Diastereomere und gegebenenfalls in Form ihrer Salze und Derivate, ihrer Solvate und/oder Hydrate. Jede Bezugnahme auf Steroide schließt eine Bezugnahme auf deren gegebenenfalls existierende Salze oder Derivate, Hydrate oder Solvate mit ein. Beispiele möglicher Salze und Derivate der Steroide können sein: Alkalisalze, wie beispielsweise Natrium- oder Kaliumsalze, Sulfobenzoate, Phosphate, Isonicotinate, Acetate, Dichloroacetate, Propionate, Dihydrogenphosphate, Palmitate, Pivalate oder auch Furoate.6α, 9α-difluoro-LLβ-hydroxy-16α-methyl-3-oxo-17α- (2,2,3,3-tertamethylcyclopropylcarbonyl) oxy-androsta-1,4-diene-17β-carboxylic acid cyanomethyl ester, optionally in Form of their racemates, enantiomers or diastereomers and optionally in the form of their salts and derivatives, their solvates and / or hydrates. Any reference to steroids includes reference to their optional salts or derivatives, hydrates or solvates. Examples of possible salts and derivatives of steroids may be: alkali metal salts, such as, for example, sodium or potassium salts, sulfobenzoates, phosphates, isonicotinates, acetates, dichloroacetates, propionates, dihydrogen phosphates, palmitates, pivalates or even furoates.
Als PDE4-Inhibitoren gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Enprofyllin, Theophyllin, Roflumilast,Preferred PDE4 inhibitors here are compounds which are selected from the group consisting of enprofylline, theophylline, roflumilast,
Ariflo (Cilomilast), Tofimilast, Pumafentrin, Lirimilast, Arofyllin, Atizoram, D-4418, Bay- 198004, BY343, CP-325,366, D-4396 (Sch-351591), AWD-12-281 (GW-842470), NCS- 613, CDP-840, D-4418, PD-168787, T-440, T-2585, V-11294A, Cl-1018, CDC-801, CDC-3052, D-22888, YM-58997, Z-15370 und - N-(3,5-Dichloro-l-oxo-pyridin-4-yl)-4-difluormethoxy-3- cyclopropylmethoxybenzamid - (-)p-[(4αR*,10bS*)-9-Ethoxy-l,2,3,4,4a,10b-hexahydro-8-methoxy-2- methylbenzo[s][l,6]naphthyridin-6-yl]-N,N-diisopropylbenzamid (R)-(+)-l-(4-Brombenzyl)-4-[(3-cyclopentyloxy)-4-methoxyphenyl]-2-pyrrolidon 3-(Cyclopentyloxy-4-methoxyphenyl)-l-(4-N'-[N-2-cyano-S-methyl- isothioureido]benzyl)-2-pyrrolidon cis[4-Cyano-4-(3-cyclopentyloxy-4-methoxyphenyl)cyclohexan-l-carbonsäure] 2-carbomethoxy-4-cyano-4-(3-cyclopropylmethoxy-4-difluoromethoxy- phenyl)cyclohexan- 1 -on cis[4-Cyano-4-(3-cyclopropylmethoxy-4-difluormethoxyphenyl)cyclohexan-l-ol] - (R)-(+)-Ethyl[4-(3-cyclopentyloxy-4-methoxyphenyl)pyrrolidin-2-yliden]acetat (S)-(-)-Ethyl[4-(3-cyclopentyloxy-4-methoxyphenyl)pyrrolidin-2-yliden]acetatAriflo (cilomilast), tofimilast, pumafentrin, lirimilast, arofylline, atizoram, D-4418, bay 198004, BY343, CP-325,366, D-4396 (Sch-351591), AWD-12-281 (GW-842470), NCS - 613, CDP-840, D-4418, PD-168787, T-440, T-2585, V-11294A, CI-1018, CDC-801, CDC-3052, D-22888, YM-58997, Z-15370 and - N- (3,5-dichloro-1-oxo-pyridin-4-yl) -4-difluoromethoxy-3-cyclopropylmethoxybenzamide - (-) p - [(4αR *, 10bS *) - 9-ethoxy-1,2,3,4,4a, 10b-hexahydro-8-methoxy-2-methylbenzo [s] [l, 6] naphthyridine 6-yl] -N, N-diisopropylbenzamide (R) - (+) - 1- (4-bromobenzyl) -4 - [(3-cyclopentyloxy) -4-methoxyphenyl] -2-pyrrolidone 3- (cyclopentyloxy-4- methoxyphenyl) -1- (4-N '- [N-2-cyano-S-methylisothioureido] benzyl) -2-pyrrolidone cis [4-cyano-4- (3-cyclopentyloxy-4-methoxyphenyl) cyclohexane-1 -carboxylic acid] 2-carbomethoxy-4-cyano-4- (3-cyclopropylmethoxy-4-difluoromethoxyphenyl) cyclohexane-1-one cis [4-cyano-4- (3-cyclopropylmethoxy-4-difluoromethoxyphenyl) cyclohexane-1-one ol] - (R) - (+) - ethyl [4- (3-cyclopentyloxy-4-methoxyphenyl) pyrrolidin-2-ylidene] acetate (S) - (-) - ethyl [4- (3-cyclopentyloxy-4- methoxyphenyl) pyrrolidin-2-ylidene] acetate
- 9-Cyclopentyl-5,6-dihydro-7-ethyl-3-(2-thienyl)-9H-pyrazolo[3,4-c]-l,2,4-triazolo[4,3- a]pyridin9-cyclopentyl-5,6-dihydro-7-ethyl-3- (2-thienyl) -9H-pyrazolo [3,4-c] -1,4,4-triazolo [4,3-a] pyridine
- 9-Cyclopentyl-5,6-dihydro-7-ethyl-3-(tert-butyl)-9H-pyrazolo[3,4-c]-l,2,4- triazolo[4,3-a]pyridin gegebenenfalls in Form ihrer Racemate, Enantiomere, Diastereomere und gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, Solvate oder Hydrate. Erfindungsgemäß bevorzugt sind die Säureadditionssalze der PDE4-Inhibitoren ausgewählt aus der Gruppe bestehend aus Hydrochlorid, Hydrobromid, Hydroiodid, Hydrosulfat, Hydrophosphat, Hydromethansulfonat, Hydronitrat, Hydromaleat,9-cyclopentyl-5,6-dihydro-7-ethyl-3- (tert -butyl) -9H-pyrazolo [3,4-c] -1,4,4-triazolo [4,3-a] pyridine, optionally in the form of their racemates, enantiomers, diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates. According to the invention, the acid addition salts of the PDE4 inhibitors are preferably selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate,
Hydroacetat, Hydrocitrat, Hydrofumarat, Hydrotartrat, Hydrooxalat, Hydro succinat, Hydrobenzoat und Hydro-p-toluolsulfonat.Hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydrooxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
Als LTD4- Antagonisten gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Montelukast, Pranlukast, Zafirlukast, MCC-847 (ZD-3523), MN-001, MEN-91507 (LM-1507), VUF-5078, VUF-K-8707, L- 733321 undPreferred LTD4 antagonists here are compounds selected from the group consisting of montelukast, pranlukast, zafirlukast, MCC-847 (ZD-3523), MN-001, MEN-91507 (LM-1507), VUF-5078 , VUF-K-8707, L-733321 and
- l-(((R)-(3-(2-(6,7-Difluor-2-quinolinyl)ethenyl)phenyl)-3-(2-(2-hydroxy-2- propyl)phenyl)thio)methylcyclopropan-essigsäure, - l-(((l(R)-3(3-(2-(2,3-Dichlorthieno[3,2-b]pyridin-5-yI)-(E)-ethenyl)phenyl)-3-(2-(l- hydroxy-l-methylethyl)phenyl)propyl)thio)methyl)cyclopropanessigsäure [2-[[2-(4-tert-Butyl-2-thiazolyl)-5-benzofuranyl]oxymethyl]phenyl]essigsäure gegebenenfalls in Form ihrer Racemate, Enantiomere, Diastereomere und gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, Solvate oder Hydrate. Erfindungsgemäß bevorzugt sind diese Säureadditionssalze ausgewählt aus der Gruppe bestehend aus Hydrochlorid, Hydrobromid, Hydroiodid, Hydrosulfat, Hydrophosphat, Hydromethansulfonat, Hydronitrat, Hydromaleat, Hydroacetat, Hydrocitrat, Hydrofumarat, Hydrotartrat, Hydrooxalat, Hydro succinat, Hydrobenzoat und Hydro-p-toluolsulfonat. Unter Salzen oder Derivaten zu deren Bildung die LTD4- Antagonisten gegebenenfalls in der Lage sind, werden beispielsweise verstanden: Alkalisalze, wie beispielsweise Natriumoder Kaliumsalze, Erdalkalisalze, Sulfobenzoate, Phosphate, Isonicotinate, Acetate, Propionate, Dihydrogenphosphate, Palmitate, Pivalate oder auch Furoate.- l - (((R) - (3- (2- (6,7-Difluoro-2-quinolinyl) ethenyl) phenyl) -3- (2- (2-hydroxy-2-propyl) phenyl) thio) methylcyclopropane -acetic acid, - l - (((l (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) cyclopropaneacetic acid [2 - [[2- (4-tert-butyl-2-thiazolyl) -5-benzofuranyl] oxymethyl] phenyl] acetic acid, if appropriate in the form of their racemates, enantiomers, diastereomers and, if appropriate, in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates, these acid addition salts are preferably selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, Hydroacetate, hydrocitrate, hydrofumarate, Hydrotartrate, hydrooxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate. Examples of salts or derivatives whose formation the LTD4 antagonists are capable of are understood to be: alkali metal salts, such as, for example, sodium or potassium salts, alkaline earth salts, sulfobenzoates, phosphates, isonicotinates, acetates, propionates, dihydrogen phosphates, palmitates, pivalates or furoates.
Als EGFR-Hemmer gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Cetuximab, Trastuzumab, ABX-EGF, Mab ICR-62 und - 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(morpholin-4-yl)-l-oxo-2-buten-l-yl]amino}- 7-cyclopropylmethoxy-chinazolinThe EGFR inhibitors used are preferably compounds selected from the group consisting of cetuximab, trastuzumab, ABX-EGF, Mab ICR-62 and - 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (morpholin-4-yl) -1-oxo-2-buten-1-yl] amino} -7-cyclopropylmethoxyquinazoline
- 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-diethylamino)-l-oxo-2-buten-l-yl]- amino } -7-cyclopropylmethoxy-chinazolin 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-l- yl] amino } -7-cyclopropylmethoxy-chinazolin- 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N, N-diethylamino) -l-oxo-2-buten-1-yl] -amino} -7-cyclopropylmethoxy quinazoline 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N, N-dimethylamino) -1-oxo-2-buten-1-yl] amino} -7-cyclopropylmethoxyquinazoline
4-[(R)-(l-Phenyl-ethyl)amino]-6-{ [4-(morpholin-4-yl)-l-oxo-2-buten-l-yl]amino}-7- cyclopentyloxy-chinazolin4 - [(R) - (1-phenylethyl) amino] -6- {[4- (morpholin-4-yl) -1-oxo-2-buten-1-yl] amino} -7-cyclopentyloxy- quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ [4-((R)-6-methyl-2-oxo-morpholin-4-yl)-l-oxo-4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {[4 - ((R) -6-methyl-2-oxo-morpholin-4-yl) -l-oxo]
2-buten- 1 -yl] amino } -7-cyclopropylmethoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ [4-((R)-6-methyl-2-oxo-morpholin-4-yl)-l-oxo-2-butene-1-yl] amino} -7-cyclopropylmethoxy-quinazoline - 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- [4 - ((R) -6-methyl-2 oxo-morpholin-4-yl) -l-oxo-
2-buten-l-yl]amino}-7-[(S)-(tetrahydrofuran-3-yl)oxy]-chinazolin2-buten-l-yl] amino} -7 - [(S) - (tetrahydrofuran-3-yl) oxy] -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ [4-((R)-2-methoxymethyl-6-oxo-morpholin-4- yl)- 1 -oxo-2-buten- 1 -yl]amino } -7-cyclopropylmethoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- {[4 - ((R) -2-methoxymethyl-6-oxo-morpholin-4-yl) -1-oxo-2-butene - 1 -yl] amino} -7-cyclopropylmethoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[2-((S)-6-methyl-2-oxo-morpholin-4-yl)-ethoxy]- 7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [2 - ((S) -6-methyl-2-oxo-morpholin-4-yl) -ethoxy] -7-methoxy-quinazoline
4-[(3-Chlor-4-fluorphenyl)amino]-6-({4-[N-(2-methoxy-ethyl)-N-methyl-amino]-l- oxo-2-buten- 1 -yl } amino)-7-cyclopropylmethoxy-chinazolin4 - [(3-Chloro-4-fluorophenyl) amino] -6 - ({4- [N- (2-methoxyethyl) -N-methyl-amino] -l-oxo-2-butene-1-yl } amino) -7-cyclopropylmethoxy-quinazoline
4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-l- yl] amino } -7-cyclopentyloxy-chinazolin - 4-[(R)-(l-Phenyl-ethyl)amino]-6-{ [4-(N,N-bis-(2-methoxy-ethyl)-amino)-l-oxo-2- buten- 1 -yl] amino } -7-cyclopropylmethoxy-chinazolin4 - [(3-Chloro-4-fluorophenyl) amino] -6- {[4- (N, N-dimethylamino) -l-oxo-2-buten-1-yl] amino} -7-cyclopentyloxy-quinazoline - 4 - [(R) - (1-Phenyl-ethyl) -amino] -6- {[4- (N, N-bis (2-methoxy-ethyl) -amino] -l-oxo-2-butene-1 -yl] amino} -7-cyclopropylmethoxy-quinazoline
- 4-[(R)-(l-Phenyl-ethyl)amino]-6-({4-[N-(2-methoxy-ethyl)-N-ethyl-amino]-l-oxo-2- buten- 1 -yl } amino)-7-cyclopropylmethoxy-chinazolin- 4 - [(R) - (1-Phenyl-ethyl) -amino] -6 - ({4- [N- (2-methoxyethyl) -N-ethyl-amino] -l-oxo-2-butene 1 -yl} amino) -7-cyclopropylmethoxy-quinazoline
- 4-[(R)-(l-Phenyl-ethyl)amino]-6-({4-[N-(2-methoxy-ethyl)-N-methyl-amino]-l-oxo-2- buten- 1 -yl } amino)-7-cyclopropylmethoxy-chinazolin- 4 - [(R) - (1-Phenyl-ethyl) -amino] -6 - ({4- [N- (2-methoxyethyl) -N-methyl-amino] -l-oxo-2-butene 1 -yl} amino) -7-cyclopropylmethoxy-quinazoline
- 4-[(R)-(l-Phenyl-ethyl)amino]-6-({4-[N-(tetrahydropyran-4-yl)-N-methyl-amino]-l- oxo-2-buten- 1 -yl } amino)-7-cyclopropylmethoxy-chinazolin - 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-l- yl]amino}-7-((R)-tetrahydrofuran-3-yloxy)-chinazolin- 4 - [(R) - (1-phenylethyl) amino] -6 - ({4- [N- (tetrahydropyran-4-yl) -N-methylamino] -l-oxo-2-butene 1 -yl} amino) -7-cyclopropylmethoxy-quinazoline - 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N, N-dimethylamino) -1-oxo-2-buten-1-yl] amino} -7 - ((R ) -tetrahydrofuran-3-yloxy) -quinazoline
- 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-l- yl]amino}-7-((S)-tetrahydrofuran-3-yloxy)-chinazolin- 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N, N-dimethylamino) -1-oxo-2-buten-1-yl] amino} -7 - ((S. ) -tetrahydrofuran-3-yloxy) -quinazoline
5 - 4-[(3-Chlor-4-fluorphenyl)amino]-6-({4-[N-(2-methoxy-ethyl)-N-methyl-amino]-l- oxo-2-buten- 1 -yl } amino)-7-cyclopentyloxy-chinazolin5 - 4 - [(3-Chloro-4-fluorophenyl) amino] -6 - ({4- [N- (2-methoxyethyl) -N-methyl-amino] -l-oxo-2-butene-1 -yl} amino) -7-cyclopentyloxy-quinazoline
4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N-cyclopropyl-N-methyl-amino)- l-oxo-2- buten- 1 -yl] amino } -V-cyclopentyloxy-chinazolin4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N-cyclopropyl-N-methylamino) -1-oxo-2-butene-1-yl] amino} -V- cyclopentyloxy-quinazoline
- 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-l- o yl] amino } -7-[(R)-(tetrahydrofuran-2-yl)methoxy] -chinazolin- 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N, N-dimethylamino) -l-oxo-2-buten-1-yl] amino} -7 - [( R) - (tetrahydrofuran-2-yl) methoxy] quinazoline
- 4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-l- yl] amino } -7- [(S)-(tetrahydrofuran-2-yl)methoxy] -chinazolin 4-[(3-Ethinyl-phenyl)amino]-6,7-bis-(2-methoxy-ethoxy)-chinazolin 4-[(3-Chlor-4-fluorphenyl)amino]-7-[3-(morpholin-4-yl)-propyloxy]-6-[(vinyl-5 carbonyl)amino] -chinazolin- 4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (N, N-dimethylamino) -1-oxo-2-buten-1-yl] amino} -7- [(S. ) - (tetrahydrofuran-2-yl) methoxy] quinazoline 4 - [(3-ethynylphenyl) amino] -6,7-bis (2-methoxyethoxy) quinazoline 4 - [(3-chloro-4 -fluorophenyl) amino] -7- [3- (morpholin-4-yl) -propyloxy] -6 - [(vinyl-5-carbonyl) amino] quinazoline
4-[(R)-(l-Phenyl-ethyl)amino]-6-(4-hydroxy-phenyl)-7H-pyrrolo[2,3-d]pyrimidin4 - [(R) - (l-Phenyl-ethyl) amino] -6- (4-hydroxy-phenyl) -7H-pyrrolo [2,3-d] pyrimidine
3-Cyano-4-[(3-chlor-4-fluorphenyl)amino]-6-{ [4-(N,N-dimethylamino)-l-oxo-2-buten-3-cyano-4 - [(3-chloro-4-fluorophenyl) amino] -6- [4- (N, N-dimethylamino) -l-oxo-2-butene
1 -yl] amino } -7-ethoxy-chinolin1 -yl] amino} -7-ethoxy-quinoline
4-{ [3-Chlor-4-(3-fluor-benzyloxy)-phenyl]amino}-6-(5-{ [(2-methansulfonyl- o ethyl)amino]methyl}-furan-2-yl)chinazolin4- {[3-Chloro-4- (3-fluoro-benzyloxy) -phenyl] -amino} -6- (5- {[(2-methanesulfonyl-o-ethyl) -amino] -methyl} -furan-2-yl) -quinazoline
- 4-[(R)-(I -Phenyl-ethyl)amino] -6- { [4-((R)-6-methyl-2-oxo-morpholin-4-yl)- 1 -oxo-2- buten- 1 -yl] amino } -7-methoxy-chinazolin- 4 - [(R) - (1-phenylethyl) amino] -6- {[4- ((R) -6-methyl-2-oxo-morpholin-4-yl) -1-oxo-2-ol butene-1-yl] amino} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluorphenyl)amino]-6-{ [4-(morpholin-4-yl)-l-oxo-2-buten-l-yl]amino}- 7-[(tetrahydrofuran-2-yl)methoxy]-chinazolin 5 - 4-[(3-Chlor-4-fluorphenyl)amino]-6-({4-[N,N-bis-(2-methoxy-ethyl)-amino]-l-oxo-2- buten-l-yl}amino)-7-[(tetrahydrofuran-2-yl)methoxy]-chinazolin4 - [(3-chloro-4-fluorophenyl) amino] -6- {[4- (morpholin-4-yl) -1-oxo-2-buten-1-yl] amino} - 7 - [(tetrahydrofuran 2-yl) methoxy] quinazoline 5 - 4 - [(3-chloro-4-fluorophenyl) amino] -6 - ({4- [N, N-bis (2-methoxy-ethyl) -amino] -l -oxo-2-buten-1-yl} amino) -7 - [(tetrahydrofuran-2-yl) methoxy] quinazoline
4-[(3-Ethinyl-phenyl)amino]-6-{ [4-(5,5-dimethyl-2-oxo-morpholin-4-yl)-l-oxo-2- buten- 1 -yl] amino } -chinazolin4 - [(3-ethynyl-phenyl) -amino] -6- {4- (5,5-dimethyl-2-oxomorpholin-4-yl) -l-oxo-2-but-1-yl] -amino } -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[2-(2,2-dimethyl-6-oxo-morpholin-4-yl)-ethoxy]-0 7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [2- (2,2-dimethyl-6-oxomorpholin-4-yl) -ethoxy] -O-7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[2-(2,2-dimethyl-6-oxo-morpholin-4-yl)-ethoxy]-4 - [(3-chloro-4-fluoro-phenyl) amino] -6- [2- (2,2-dimethyl-6-oxo-morpholin-4-yl) -ethoxy] -
7-[(R)-(tetrahydrofuran-2-yl)methoxy]-chinazolin7 - [(R) - (tetrahydrofuran-2-yl) methoxy] -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-7-[2-(2,2-dimethyl-6-oxo-morpholin-4-yl)-ethoxy]-4 - [(3-chloro-4-fluoro-phenyl) amino] -7- [2- (2,2-dimethyl-6-oxo-morpholin-4-yl) -ethoxy] -
6-[(S)-(tetrahydrofuran-2-yl)methoxy]-chinazolin 5 - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{2-[4-(2-oxo-morpholin-4-yl)-piperidin-l-yl]- ethoxy } -7-methoxy-chinazolin 4-[(3-Chlor-4-fluor-phenyl)amino]-6-[l-(tert.-butyloxycarbonyl)-piperidin-4-yloxy]-7- methoxy-chinazolin6 - [(S) - (tetrahydrofuran-2-yl) methoxy] quinazoline 5 - 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {2- [4- (2-oxo-4-yl) morpholin-4-yl) -piperidin-1-yl] -ethoxy} -7-methoxy-quinazoline 4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [1- (tert-butyloxycarbonyl) -piperidin-4-yloxy] -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(trans-4-amino-cyclohexan-l-yloxy)-7-methoxy- chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(trans-4-methansulfonylamino-cyclohexan-l- yloxy) -7 -methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (trans-4-amino-cyclohexan-1-yloxy) -7-methoxy-quinazoline-4 - [(3-chloro-4-fluoro -phenyl) amino] -6- (trans-4-methanesulfonylamino-cyclohexan-1-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(tetrahydropyran-3-yloxy)-7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) amino] -6- (tetrahydropyran-3-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-methyl-piperidin-4-yloxy)-7-methoxy- chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(morpholin-4-yl)carbonyl]-piperidin-4-yl- oxy } -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (1-methyl-piperidin-4-yloxy) -7-methoxy-quinazoline-4 - [(3-chloro-4-fluoro-phenyl ) amino] -6- {1- (morpholin-4-yl) carbonyl] -piperidin-4-yl-oxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(methoxymethyl)carbonyl]-piperidin-4-yl- oxy } -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- {1 - [(methoxymethyl) -carbonyl] -piperidin-4-yl-oxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(piperidin-3-yloxy)-7-methoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-[l-(2-acetylamino-ethyl)-piperidin-4-yloxy]-7- methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (piperidin-3-yloxy) -7-methoxyquinazoline-4 - [(3-chloro-4-fluoro-phenyl) -amino] - 6- [1- (2-acetylamino-ethyl) -piperidin-4-yloxy] -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(tetrahydropyran-4-yloxy)-7-ethoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) amino] -6- (tetrahydropyran-4-yloxy) -7-ethoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-((S)-tetrahydrofuran-3-yloxy)-7-hydroxy- chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(tetrahydropyran-4-yloxy)-7-(2-methoxy- ethoxy)-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6 - ((S) -tetrahydrofuran-3-yloxy) -7-hydroxy-quinazolin-4 - [(3-chloro-4-fluoro-phenyl ) amino] -6- (tetrahydropyran-4-yloxy) -7- (2-methoxyethoxy) quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{trans-4-[(dimethylamino)sulfonylamino]- cyclohexan- 1 -yloxy } -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- {trans-4 - [(dimethylamino) -sulfonyl-amino] -cyclohexane-1-yloxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{trans-4-[(morpholin-4-yl)carbonylamino]- cyclohexan- 1 -yloxy } -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- {trans-4 - [(morpholin-4-yl) carbonylamino] -cyclohexane-1-yloxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{trans-4-[(morpholin-4-yl)sulfonylamino]- cyclohexan- 1 -yloxy } -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- {trans-4 - [(morpholin-4-yl) -sulfonyl-amino] -cyclohexane-1-yloxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(tetrahydropyran-4-yloxy)-7-(2-acetylamino- ethoxy)-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(tetrahydropyran-4-yloxy)-7-(2- methansulfonylamino-ethoxy)-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (tetrahydropyran-4-yloxy) -7- (2-acetylamino-ethoxy) -quinazoline-4 - [(3-chloro-4-fluoro -phenyl) amino] -6- (tetrahydropyran-4-yloxy) -7- (2-methanesulfonylamino-ethoxy) quinazoline
4- [(3 -Chlor-4-fluor-phenyl)amino] -6- { 1 - [(piperidin- 1 -yl)carbonyl] -piperidin-4-yloxy } -4- [(3-Chloro-4-fluoro-phenyl) -amino] -6- {1 - [(piperidine-1-yl) -carbonyl] -piperidin-4-yloxy} -
7-methoxy-chinazolin7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-aminocarbonylmethyl-piperidin-4-yloxy)-7- methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (1-aminocarbonylmethyl-piperidin-4-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-{N-[(tetrahydropyran-4-yl)carbonyl]-N- methyl-amino} -cyclohexan- l-yloxy)-7-methoxy-chinazolin 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-{N-[(morpholin-4-yl)carbonyl]-N-methyl- amino } -cyclohexan- 1 -yloxy)-7-methoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-{N-[(morpholin-4-yl)sulfonyl]-N-methyl- amino } -cyclohexan- 1 -yloxy)-7-methoxy- chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(trans-4-ethansulfonylamino-cyclohexan-l- yloxy ) -7 -methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (cis-4- {N - [(tetrahydropyran-4-yl) -carbonyl] -N-methyl-amino} -cyclohexan-1-yloxy ) -7-methoxy-quinazoline 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (cis-4- {N - [(morpholin-4-yl) -carbonyl] -N-methyl-amino} -cyclohexane-1-yloxy ) -7-methoxy-quinazoline - 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (cis-4- {N - [(morpholin-4-yl) -sulfonyl] -N-methyl- amino} -cyclohexan-1-ylxy) -7-methoxy-quinazoline-4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (trans-4-ethanesulfonylamino-cyclohexan-1-yloxy) -7 methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-methansulfonyl-piperidin-4-yloxy)-7-ethoxy- chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (1-methanesulfonyl-piperidin-4-yloxy) -7-ethoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-methansulfonyl-piperidin-4-yloxy)-7-(2- methoxy-ethoxy)-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (1-methanesulfonyl-piperidin-4-yloxy) -7- (2-methoxy-ethoxy) -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[l-(2-methoxy-acetyl)-piperidin-4-yloxy]-7-(2- methoxy-ethoxy)-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [1- (2-methoxy-acetyl) -piperidin-4-yloxy] -7- (2-methoxyethoxy) -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-acetylamino-cyclohexan-l-yloxy)-7- methoxy-chinazolin - 4-[(3-Ethinyl-phenyl)amino]-6-[l-(tert.-butyloxycarbonyl)-piperidin-4-yloxy]-7- methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (cis-4-acetylamino-cyclohexan-1-yloxy) -7-methoxy-quinazolin-4 - [(3-ethynyl-phenyl) -amino ] -6- [1- (tert-butyloxycarbonyl) -piperidin-4-yloxy] -7-methoxy-quinazoline
4-[(3-Ethinyl-phenyl)amino]-6-(tetrahydropyran-4-yloxy]-7-methoxy-chinazolin4 - [(3-ethynyl-phenyl) amino] -6- (tetrahydropyran-4-yloxy] -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-{N-[(piperidin-l-yl)carbonyl]-N-methyl- amino } -cyclohexan- 1 -yloxy)-7-methoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-{N-[(4-methyl-piperazin-l-yl)carbonyl]-N- methyl- amino } -cyclohexan- 1 -yloxy)-7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (cis-4- {N - [(piperidin-1-yl) -carbonyl] -N-methyl-amino} -cyclohexan-1-yloxy ) -7-methoxyquinazoline - 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (cis-4- {N - [(4-methylpiperazin-1-yl) carbonyl] - N-methylamino} -cyclohexan-1-ylxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{cis-4-[(morpholin-4-yl)carbonylamino]- cyclohexan- 1 -yloxy } -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- {cis-4 - [(morpholin-4-yl) carbonylamino] -cyclohexane-1-yloxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[2-(2-oxopyrrolidin-l-yl)ethyl]-piperidin-4- yloxy} -7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {1- [2- (2-oxopyrrolidin-1-yl) -ethyl] -piperidin-4-yloxy} -7-methoxy-quinazoline
4- [(3 -Chlor-4-fluor-phenyl)amino] -6- { 1 - [(morpholin-4-yl)carbonyl] -piperidin-4- yloxy}-7-(2-methoxy-ethoxy)-chinazolin4- [(3-Chloro-4-fluoro-phenyl) -amino] -6- {1 - [(morpholin-4-yl) -carbonyl] -piperidin-4-yloxy} -7- (2-methoxy-ethoxy) - quinazoline
4-[(3-Ethinyl-phenyl)amino]-6-(l-acetyl-piperidin-4-yloxy)-7 -methoxy-chinazolin4 - [(3-Ethynylphenyl) amino] -6- (1-acetyl-piperidin-4-yloxy) -7-methoxy-quinazoline
4-[(3-Ethinyl-phenyl)amino]-6-(l-methyl-piperidin-4-yloxy)-7-methoxy-chinazolin - 4-[(3-Ethinyl-phenyl)amino]-6-(l-methansulfonyl-piperidin-4-yloxy)-7-methoxy- chinazolin4 - [(3-Ethynylphenyl) amino] -6- (1-methylpiperidin-4-yloxy) -7-methoxyquinazoline-4 - [(3-ethynylphenyl) amino] -6- (1 -methanesulfonyl-piperidin-4-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-methyl-piperidin-4-yloxy)-7(2-methoxy- ethoxy)-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (1-methyl-piperidin-4-yloxy) -7 (2-methoxy-ethoxy) -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-isopropyloxycarbonyl-piperidin-4-yloxy)-7- methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (1-isopropyloxycarbonyl-piperidin-4-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(cis-4-methylamino-cyclohexan-l-yloxy)-7- methoxy-chinazolin 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{cis-4-[N-(2-methoxy-acetyl)-N-methyl-amino]- cyclohexan- 1 -yloxy } -7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (cis-4-methylamino-cyclohexan-1-yloxy) -7-methoxy-quinazoline 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {cis-4- [N- (2-methoxy-acetyl) -N-methyl-amino] -cyclohexane-1-yloxy} -7 methoxy-quinazoline
4-[(3-Ethinyl-phenyl)amino]-6-(piperidin-4-yloxy)-7-methoxy-chinazolin 4-[(3-Ethinyl-phenyl)amino]-6-[l-(2-methoxy-acetyl)-piperidin-4-yloxy]-7-methoxy- chinazolin4 - [(3-Ethynylphenyl) amino] -6- (piperidin-4-yloxy) -7-methoxy-quinazoline 4 - [(3-ethynylphenyl) amino] -6- [1- (2-methoxy -acetyl) -piperidin-4-yloxy] -7-methoxy-quinazoline
4-[(3-Ethinyl-phenyl)amino]-6-{ l-[(morpholin-4-yl)carbonyl]-piperidin-4-yloxy}-7- methoxy-chinazolin4 - [(3-ethynylphenyl) amino] -6- {1- (morpholin-4-yl) carbonyl] -piperidin-4-yloxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(cis-2,6-dimethyl-morpholin-4-yl)carbonyl]- piperidin-4-yloxy} -7-methoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(2-methyl-morpholin-4-yl)carbonyl]- piperidin-4-yloxy} -7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {1 - [(cis-2,6-dimethyl-morpholin-4-yl) -carbonyl] -piperidin-4-yloxy} -7- methoxy-quinazoline - 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {1 - [(2-methyl-morpholin-4-yl) carbonyl] -piperidin-4-yloxy} -7- methoxy-quinazoline
- 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(S,S)-(2-oxa-5-aza-bicyclo[2.2.1]hept-5- yl)carbonyl]-piperidin-4-yloxy}-7-methoxy-chinazolin- 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {1 - [(S, S) - (2-oxa-5-aza-bicyclo [2.2.1] hept-5-yl ) carbonyl] piperidin-4-yloxy} -7-methoxy-quinazoline
- 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(N-methyl-N-2-methoxyethyl- amino)carbonyl] -piperidin-4-yloxy } -7-methoxy-chinazolin- 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {1 - [(N-methyl-N-2-methoxyethyl-amino) -carbonyl] -piperidin-4-yloxy} -7-methoxy -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-ethyl-piperidin-4-yloxy)-7-methoxy- chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (1-ethyl-piperidin-4-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(2-methoxyethyl)carbonyl]-piperidin-4- yloxy} -7-methoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-{ l-[(3-methoxypropyl-amino)-carbonyl]- piperidin-4-yloxy} -7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- {1- (2-methoxyethyl) -carbonyl] -piperidin-4-yloxy} -7-methoxy-quinazoline-4 - [(3 Chloro-4-fluoro-phenyl) amino] -6- {1 - [(3-methoxy-propyl-amino) -carbonyl] -piperidin-4-yloxy} -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[cis-4-(N-methansulfonyl-N-methyl-amino)- cyclohexan-l-yloxy]-7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [cis-4- (N-methanesulfonyl-N-methyl-amino) -cyclohexan-1-yloxy] -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[cis-4-(N-acetyl-N-methyl-amino)-cyclohexan-l- yloxy] -7-methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [cis-4- (N-acetyl-N-methyl-amino) -cyclohexan-1-yloxy] -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(trans-4-methylamino-cyclohexan-l-yloxy)-7- methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (trans-4-methylamino-cyclohexan-1-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[trans-4-(N-methansulfonyl-N-methyl-amino)- cyclohexan-l-yloxy]-7-methoxy-chinazolin - 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(trans-4-dimethylamino-cyclohexan-l-yloxy)-7- methoxy-chinazolin4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- [trans-4- (N-methanesulfonyl-N-methyl-amino) -cyclohexan-1-yloxy] -7-methoxy-quinazoline - 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (trans-4-dimethylamino-cyclohexan-1-yloxy) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(trans-4-{N-[(morpholin-4-yl)carbonyl]-N- methyl-amino} -cyclohexan- l-yloxy)-7-methoxy-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (trans-4- {N - [(morpholin-4-yl) -carbonyl] -N-methyl-amino} -cyclohexan-1-yloxy ) -7-methoxy-quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-[2-(2,2-dimethyl-6-oxo-morpholin-4-yl)-ethoxy]- 7-[(S)-(tetrahydrofuran-2-yl)methoxy]-chinazolin4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- [2- (2,2-dimethyl-6-oxomorpholin-4-yl) -ethoxy] - 7 - [(S) - (tetrahydrofuran-2-yl) methoxy] -quinazoline
4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-methansulfonyl-piperidin-4-yloxy)-7- methoxy-chinazolin 4-[(3-Chlor-4-fluor-phenyl)amino]-6-(l-cyano-piperidin-4-yloxy)-7-methoxy- chinazolin gegebenenfalls in Form ihrer Racemate, Enantiomere, Diastereomere und gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, Solvate oder Hydrate. Erfindungsgemäß bevorzugt sind diese Säureadditionssalze ausgewählt aus der Gruppe bestehend aus Hydrochlorid, Hydrobromid, Hydroiodid, Hydrosulfat, Hydrophosphat, Hydromethansulfonat, Hydronitrat, Hydromaleat, Hydroacetat, Hydrocitrat, Hydrofumarat, Hydrotartrat, Hydrooxalat, Hydro succinat, Hydrobenzoat und Hydro-p-toluolsulfonat.4 - [(3-Chloro-4-fluoro-phenyl) -amino] -6- (1-methanesulfonyl-piperidin-4-yloxy) -7-methoxy-quinazoline 4 - [(3-chloro-4-fluoro-phenyl) -amino] -6- (1-cyano-piperidin-4-yloxy) -7-methoxy-quinazoline, optionally in the form of their racemates, enantiomers, diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates. According to the invention, these acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
Als Dopamin- Agonisten gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Bromocriptin, Cabergolin, Alpha- Dihydroergocryptin, Lisurid, Pergolid, Pramipexol, Roxindol, Ropinirol, Talipexol, Tergurid und Viozan, gegebenenfalls in Form ihrer Racemate, Enantiomere, Diastereomere und gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, Solvate oder Hydrate. Erfindungsgemäß bevorzugt sind diese Säureadditionssalze ausgewählt aus der Gruppe bestehend aus Hydrochlorid, Hydrobromid, Hydroiodid, Hydrosulfat, Hydrophosphat, Hydromethansulfonat, Hydronitrat, Hydromaleat, Hydroacetat, Hydrocitrat, Hydrofumarat, Hydrotartrat, Hydrooxalat, Hydro succinat, Hydrobenzoat und Hydro-p-toluolsulfonat.Preferred dopamine agonists are compounds selected from the group consisting of bromocriptine, cabergoline, alpha-dihydroergocryptine, lisuride, pergolide, pramipexole, roxindole, ropinirole, talipexole, terguride and viozan, optionally in the form of their racemates, enantiomers , Diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates. According to the invention, these acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
Als Hl -Antihistaminika gelangen hierbei vorzugsweise Verbindungen zur Anwendung, die ausgewählt sind aus der Gruppe bestehend aus Epinastin, Cetirizin, Azelastin, Fexofenadin, Levocabastin, Loratadin, Mizolastin, Ketotifen, Emedastin, Dimetinden, Clemastin, Bamipin, Cexchlorpheniramin, Pheniramin, Doxylamin, Chlorphenoxamin, Dimenhydrinat, Diphenhydramin, Promethazin, Ebastin, Desloratidin und Meclozin, gegebenenfalls in Form ihrer Racemate, Enantiomere, Diastereomere und gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, Solvate oder Hydrate. Erfindungsgemäß bevorzugt sind diese Säureadditionssalze ausgewählt aus der Gruppe bestehend aus Hydrochlorid, Hydrobromid, Hydroiodid, Hydrosulfat, Hydrophosphat, Hydromethansulfonat, Hydronitrat, Hydromaleat, Hydroacetat, Hydrocitrat, Hydrofumarat, Hydrotartrat, Hydrooxalat, Hydro succinat, Hydrobenzoat und Hydro-p-toluolsulfonat.As Hl antihistamines here preferably compounds are used, which are selected from the group consisting of epinastine, cetirizine, azelastine, fexofenadine, levocabastine, loratadine, mizolastine, ketotifen, emedastine, dimetindene, clemastine, bamipine, Cexchlorpheniramin, pheniramine, doxylamine, chlorphenoxamine , Dimenhydrinate, diphenhydramine, promethazine, ebastine, desloratidine and meclocine, optionally in the form of their racemates, enantiomers, diastereomers and optionally in the form of their pharmacologically acceptable acid addition salts, solvates or hydrates. According to the invention, these acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, hydroiodide, hydrosulfate, hydrophosphate, hydromethanesulfonate, hydronitrate, hydromaleate, hydroacetate, hydrocitrate, hydrofumarate, hydrotartrate, hydroxalate, hydrosuccinate, hydrobenzoate and hydro-p-toluenesulfonate.
Als pharmazeutisch wirksame Substanzen, Substanzformulierungen oder Substanzmischungen werden alle inhalierbaren Verbindungen eingesetzt, wie z.B. auch inhalierbare Makromoleküle, wie in EP 1 003 478 offenbart. Vorzugsweise werden Substanzen, Substanzformulierungen oder Substanzmischungen zur Behandlung von Atemwegserkrankungen eingesetzt, die im inhalativen Bereich Verwendung finden. Weiterhin kann die Verbindung aus der Gruppe der Derivate von Mutterkornalkaloiden, der Triptane, der CGRP-Hemmern, der Phosphodiesterase-V-Hemmer stammen, gegebenenfalls in Form ihrer Racemate, Enantiomere oder Diastereomere, gegebenenfalls in Form ihrer pharmakologisch verträglichen Säureadditionssalze, ihrer Solvate und/oder Hydrate.As pharmaceutically active substances, substance formulations or substance mixtures all inhalable compounds are used, such as, for example, inhalable macromolecules, as disclosed in EP 1 003 478. Preferably, substances, substance formulations or substance mixtures are used for the treatment of respiratory diseases, which are used in the inhalation area. Furthermore, the compound may be derived from the group of derivatives of ergot alkaloids, triptans, CGRP inhibitors, phosphodiesterase V inhibitors, optionally in the form of their racemates, enantiomers or diastereomers, optionally in the form of their pharmacologically acceptable acid addition salts, their solvates and / or or hydrates.
Als Derivate der Mutterkornalkaloide: Dihydroergotamin, Ergotamin.As derivatives of ergot alkaloids: dihydroergotamine, ergotamine.
Experimenteller TeilExperimental part
(7) Messverfahren zur Bestimmung des hydrodynamischen Durchmessers(7) Measuring method for determining the hydrodynamic diameter
Photonenkorrelationsspektroskopie (Zetasizer, Malvern) Messgerät: Zetasizer, Malvern, Typ Zetasizer Nano ZSPhoton correlation spectroscopy (Zetasizer, Malvern) Measuring instrument: Zetasizer, Malvern, type Zetasizer Nano ZS
Software: Dispersion Technology Software Version 4.10 (Malvern) Messbedingungen / Messparameter Durchführung:Software: Dispersion Technology Software Version 4.10 (Malvern) Measurement Conditions / Measurement Parameters Execution:
Messverfahren gemäß Angaben des Geräteherstellers. Das Messgerät berechnet den hydrodynamischen Durchmesser (Dh) einer Suspension und gibt die Größenverteilung wieder (Volumenbezogener Bestimmungsmodus).Measuring procedure according to the device manufacturer. The meter calculates the hydrodynamic diameter (Dh) of a suspension and gives the size distribution (volume-related determination mode).
Die nachfolgend aufgeführten Messergebnisse entsprechen den jeweiligen Hauptpeaks der ermittelten Größenverteilungen (im Sinne dieser Erfindung entspricht die Tröpfchengröße des Hauptpeaks dem hydrodynamischen Durchmesser).The measurement results listed below correspond to the respective main peaks of the determined size distributions (for the purposes of this invention, the droplet size of the main peak corresponds to the hydrodynamic diameter).
(2) Beispiele(2) Examples
Die Herstellung der Emulsionslösungen in den folgenden Beispielen 1 bis 4 erfolgte derart, dass die Wirkstoffe bzw. Polymere in einer Konzentration von 0,75 % (Gewicht pro Volumen in Gramm pro 100 milli-Liter) in ihrer jeweiligen Phase gelöst vorlagen. Die Phasen wurden zusammengeführt und mittels eines Ultraschallfingers 2 min bei 30% Leistung behandelt. Dabei wird die Spitze 0.5 - 2 cm in die Lösung eingetaucht und die Ultraschall-Apparatur (Hersteller: Sonics & Materials Inc. (Darbury, CT, USA), Typ: „Vibra Cell", Modell: VC 50) bei 30 % der Maximalkraft 5 Minuten betrieben. Einfhiss der Ionenstärke auf die Stabilität der erfindungsgemäßen W/O (Wasser in Ql)- EmulsionenThe preparation of the emulsion solutions in the following Examples 1 to 4 was carried out such that the active ingredients or polymers were dissolved in a concentration of 0.75% (weight per volume in grams per 100 milli liters) in their respective phase. The phases were combined and treated by means of an ultrasonic finger for 2 min at 30% power. The tip is immersed 0.5 - 2 cm in the solution and the ultrasonic apparatus (manufacturer: Sonics & Materials Inc. (Darbury, CT, USA), type: "Vibra Cell", model: VC 50) at 30% of the maximum force Operated for 5 minutes. Influence of the ionic strength on the stability of the W / O (water in Q1) emulsions according to the invention
Beispiel 1 : Stabilität von W/O (Wasser in Öl) Emulsionen mit unterschiedlichen Salzen in Abhängigkeit der ZeitExample 1: Stability of W / O (water in oil) emulsions with different salts as a function of time
Es wurde der Einfluss von unterschiedlichen Salzen, die in der wässrigen Phase in gleicher Ionenstärke (20 mM) in den W/O (Wasser in Öl)-Emulsionen enthalten waren, auf den hydrodynamischen Durchmesser in Abhängigkeit der Zeit getestet. In Abbildung 1 sind erfindungsgemäße W/O (Wasser in Öl) -Emulsionen dargestellt, die als Emulgator das Polymer des Resomer®-Typs LGPt8546 enthalten (siehe Legende der Abbildung und Angaben gemäß Tabelle 1). Im Rahmen der Herstellung dieser W/O (Wasser in 01)- Emulsionen wurde Budesonid und das Polymer in Dichlormethan (DCM), welches die organische Phase darstellt, gelöst. Die organische Phase wurde dann mit einer wässrigen Phase im Verhältnis 1:4 (Volumen: Volumen, d.h. ein Volumenanteil wässrige Phase zu vier Volumenanteile organische Phase) zu einer Emulsion mittels Ultraschallbehandlung verarbeitet. Dabei enthielt die jeweilige wässrige Phase ein unterschiedliches Salz in einer Ionenstärke von 20 mM. Die erhaltenen Emulsionen stellen somit erfindungsgemäße (W/O) Wasser-in-Öl-Emulsionen dar (Wasser/DCM-Emulsionen).The influence of different salts contained in the aqueous phase in the same ionic strength (20 mM) in the W / O (water in oil) emulsions on the hydrodynamic diameter as a function of time was tested. FIG. 1 shows W / O (water-in-oil) emulsions according to the invention which contain, as emulsifier, the polymer of the Resomer® type LGPt8546 (see legend of the figure and details according to Table 1). As part of the preparation of these W / O (water in 01) emulsions, budesonide and the polymer were dissolved in dichloromethane (DCM), which is the organic phase. The organic phase was then processed with an aqueous phase in a ratio of 1: 4 (volume: volume, i.e. one volume of aqueous phase to four volumes of organic phase) to form an emulsion by sonication. The respective aqueous phase contained a different salt in an ionic strength of 20 mM. The emulsions obtained are thus (W / O) water-in-oil emulsions (water / DCM emulsions).
Wie in Abbildung 1 (x- Achse: Messzeitpunkt der Bestimmung des hydrodynamischen Durchmessers, wobei der Nullwert den Zeitpunkt der Herstellung der Emulsion angibt; y- Achse: hydrodynamischer Durchmesser Dh) zu sehen ist, lassen sich mit allen getesteten Salzen stabile Emulsionen herstellen, da die Emulsionströpfchengröße (hydrodynamischer Durchmesser der Emulsion) in einem geeignetem Bereich zwischen 300nm und 3000 nm liegt (K2SO4 = Kaliumsulfat, Sbs = Salbutamolsulfatsalz (Additionssalz aus der Wirkstoffbase Salbutamol und Schwefelsäure), NaCl = Natriumchlorid, Na2HPO4 = Natriumhydrogenphosphat, di-Na-Tartrat = Di-Natriumtartrat; Bud = Budesonid). Darüber hinaus bleibt die Emulsionströpfchengröße mindestens innerhalb der Messdauer von ca.l Stunde stabil innerhalb dieses für die Tröpfchengröße geeigneten Bereiches. Beispiel 2:As can be seen in Figure 1 (x-axis: measurement time of determination of hydrodynamic diameter, the zero value indicates the time of emulsion preparation, y-axis: hydrodynamic diameter Dh), stable emulsions can be prepared with all the salts tested, since the emulsion droplet size (hydrodynamic diameter of the emulsion) is in a suitable range between 300 nm and 3000 nm (K 2 SO 4 = potassium sulfate, Sbs = salbutamol sulphate salt (addition salt from the active substance base salbutamol and sulfuric acid), NaCl = sodium chloride, Na 2 HPO 4 = sodium hydrogen phosphate, di-Na tartrate logo CNRS logo INIST Di-sodium tartrate, Bud = budesonide). In addition, the emulsion droplet size remains stable at least within the measurement period of about 1 hour within this range suitable for the droplet size. Example 2:
Stabilität der W/O (Wasser in Öl) Emulsion in Abhängigkeit der SalzkonzentrationStability of W / O (water in oil) emulsion depending on the salt concentration
Es wurden W/O (Wasser in Öl)-Emulsionen hergestellt, die 4 verschiedene Emulgatoren (siehe Angaben Abbildung 2 und Angaben gemäß Tabelle 1, (Res = Resomer®)) und vergleichbar zu Beispiel 1 den Wirkstoff Budesonid in der organischen Phase enthielten. In Abbildung 2 (x- Achse: Konzentration des in der wässrigen Phase gelösten Salzes NaCl in mmol/Liter; y- Achse: hydrodynamischer Durchmesser Dh zum Zeitpunkt 30 Minuten nach Herstellung der Suspension) ist die Tröpfchengröße (hydrodynamischer Durchmesser) in Abhängigkeit der Salzkonzentration dieser W/O (Wasser in Öl)-Emulsionen dargestellt. In der anorganische Phase, die im Rahmen der Herstellung dieser erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen verwendet wurden, wurde jeweils Natriumchlorid gelöst. Die Konzentrationen betrugen dabei im Minimum eine Ionenstärke von 10 mM. Bei dem Versuch vergleichbare Emulsionen unter Weglassens des Natriumschlorids herzustellen wurde beobachtet, dass spontan nach Mischen der Phasen innerhalb von weniger als 10 Minuten eine Phasentrennung eintrat, so dass die Bestimmung eines hydrodynamischen Durchmessers nicht möglich war / keine stabile Emulsion vorlag (nicht dargestellt, da aufgrund der Instabilität keine Messwerte erhältlich sind).There were prepared W / O (water in oil) emulsions containing 4 different emulsifiers (see Figure 2 and data according to Table 1, (Res = Resomer ® )) and comparable to Example 1, the active ingredient budesonide in the organic phase. In Figure 2 (x-axis: concentration of the salt dissolved in the aqueous phase NaCl in mmol / liter; y-axis: hydrodynamic diameter Dh at the time 30 minutes after preparation of the suspension) is the droplet size (hydrodynamic diameter) depending on the salt concentration of this W / O (water in oil) emulsions shown. In the inorganic phase used in the preparation of these W / O (water in oil) emulsions of the invention, sodium chloride was dissolved in each case. The concentrations were at least an ionic strength of 10 mM. In an attempt to prepare comparable emulsions with the sodium chloride being omitted, it was observed that spontaneous phase mixing occurred within less than 10 minutes after mixing the phases so that determination of a hydrodynamic diameter was not possible / no stable emulsion was present (not shown because of instability no measurements are available).
Stabilität der Emulsionströpfchengröße der erfindungsgemäßen W/O (Wasser in Ql)- EmulsionenStability of the emulsion droplet size of the W / O (water in QI) emulsions according to the invention
Beispiel 3: Stabilität der W/O (Wasser in Öl) Emulsion mit unterschiedlichen Emulgatoren (Polymeren) in Abhängigkeit derZeitExample 3: Stability of W / O (water in oil) Emulsion with different emulsifiers (polymers) as a function of time
Es wurde der Einfluss von unterschiedlichen erfindungsgemäßen Emulgatoren (Block-Co- Polymere des Resomer®-Typs - siehe Legende der Abbildung und Angaben gemäß Tabelle 1), die in den W/O (Wasser in Öl)-Emulsionen enthalten waren, auf den hydrodynamischen Durchmesser in Abhängigkeit der Zeit getestet. Die W/O (Wasser in Öl)-Emulsionen enthielten ein Säureadditionssalz eines Wirkstoffes, welches gelöst in der wässrigen Phase vorlag. In Abbildung 3 (x-Achse: Messzeitpunkt der Bestimmung des hydrodynamischen Durchmessers, wobei der Nullwert den Zeitpunkt der Herstellung der Emulsion angibt; y- Achse: hydrodynamischer Durchmesser Dh) ist die Tröpfchengröße der erfindungsgemäße W/O (Wasser in Öl)-Emulsionen in Abhängigkeit der Zeit dargestellt. Die erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen der in Abbildung 3 dargestellten Ergebnisse wurden dadurch erhalten, dass als Emulgatoren verschiedene Polymere des Resomer®-Typs (in der organischen Phase (DCM) gelöst wurden. In der anorganischen (wässrigen) Phase wurde Salbutamolsulfatsalz gelöst. Aus diesen Phasen wurden W/O 5 (Wasser/DCM)-Emulsionen, wobei die Menge der wässrigen Phase zur organischen Phase 1:4 betrug (Volumen: Volumen, d.h. ein Volumenanteil wässrige Phase zu vier Volumenanteile organische Phase), durch Ultraschallbehandlung hergestellt.The influence of different emulsifiers according to the invention (block co-polymers of the Resomer® type - see legend of the figure and data according to Table 1), which were contained in the W / O (water in oil) emulsions, on the hydrodynamic Diameter tested as a function of time. The W / O (water in oil) emulsions contained an acid addition salt of an active ingredient which was dissolved in the aqueous phase. In Figure 3 (x-axis: measurement time of determining the hydrodynamic diameter, the zero value indicating the time of preparation of the emulsion, y-axis: hydrodynamic diameter Dh) is the droplet size of the W / O (water in oil) emulsions according to the invention in Dependence of time shown. The W / O (water-in-oil) emulsions according to the invention of the results shown in Figure 3 were obtained by dissolving as emulsifiers various Resomer® type polymers (in the organic phase (DCM)) in the inorganic (aqueous) phase Salbutamol sulphate salt was dissolved from these phases W / O 5 (water / DCM) emulsions, the amount of aqueous phase to the organic phase being 1: 4 (volume: volume, ie one volume of aqueous phase to four volumes of organic phase), produced by ultrasonic treatment.
Wie in Abbildung 3 zu sehen ist, zeigen alle erfindungsgemäßen W/O (Wasser/DCM)- l o Emulsionen stabiles Verhalten auf. Die Emulsionströpfchengröße (hydrodynamischer Durchmesser der Emulsion) liegt in einem geeignetem Bereich zwischen 300nm und 3000 nm. Darüber hinaus bleibt die Emulsionströpfchengröße mindestens innerhalb der Messdauer von ca. 1 Stunde stabil innerhalb dieses für die Tröpfchengröße geeigneten Bereiches.As can be seen in FIG. 3, all W / O (water / DCM) -10 emulsions according to the invention exhibit stable behavior. The emulsion droplet size (hydrodynamic diameter of the emulsion) is in a suitable range between 300 nm and 3000 nm. In addition, the emulsion droplet size remains stable at least within the measurement period of about 1 hour within this range suitable for the droplet size.
1515
Beispiel 4:Example 4:
Stabilität von W/O (Wasser in Öl) Emulsionen mit unterschiedlichen Salzen inStability of W / O (water in oil) emulsions with different salts in
Abhängigkeit der ZeitDependence of time
2020
Weitere Beispiele für das Stabilitätsverhalten von erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen sind in Abbildung 4 dargestellt (x- Achse: Messzeitpunkt der Bestimmung des hydrodynamischen Durchmessers, wobei der Nullwert den Zeitpunkt der Herstellung der Emulsion angibt; y-Achse: hydrodynamischer Durchmesser Dh). Die in Abb. 4 25 dargestellten erfindungsgemäßen W/O (Wasser in Öl)-Emulsionen können in vergleichbarer Art und Weise zu Beispiel 1 bis 3 erhalten werden. Dabei wurde die Zusammensetzung derart gewählt, dassFurther examples of the stability behavior of W / O (water-in-oil) emulsions according to the invention are shown in Figure 4 (x-axis: measurement time of determining the hydrodynamic diameter, the zero value indicating the time of preparation of the emulsion, y-axis: hydrodynamic Diameter ie). The W / O (water in oil) emulsions of the invention shown in FIG. 4 can be obtained in a comparable manner to Examples 1 to 3. The composition was chosen such that
(a) [siehe Datenpunkte „gefüllte Quadrate"] als Salzkomponente in der wässrigen Phase Kaliumsulfat (Angabe in Abb.4: K2SO4 ) in einer Konzentration gelöst war,(a) [see data points "filled squares"] as a salt component in the aqueous phase potassium sulfate (in Figure 4: K2SO4) was dissolved in a concentration,
30 so dass die Ionenstärke / = 20 mM betrug, und in der organischen Phase unabhängig davon Budesonid (Angabe in Abb.4: Bud) gelöst war, desweiteren,30 so that the ionic strength / = 20 mM, and in the organic phase, regardless budesonide (indicated in Figure 4: Bud) was solved, furthermore,
(b) [siehe Datenpunkte „gefüllte Dreiecke"] als Salzkomponete der wässrigen Phase Salbutamolsulfatsalz (Angabe in Abb.4: Sbs) in einer Konzentration von 0,75%(b) [see data points "filled triangles"] as salt component of the aqueous phase salbutamol sulphate salt (data in Fig. 4: Sbs) in a concentration of 0.75%
35 (w/v) Verwendung fand (ohne Budesonid in der organischen Phase) sowie wiederum (c) [siehe Datenpunkte „gefüllte Kreise"] als Salzkomponete der wässrigen Phase Salbutamolsulfatsalz in einer Konzentration von 0,75% (w/v, Masse pro Volumen in Gramm pro 100 milli-Liter) Verwendung fand, jedoch zusätzlich Budesonid in der organischen Phase gelöst war.35 (w / v) was used (without budesonide in the organic phase) and again (c) [see data points "filled circles"] as salt component of the aqueous phase salbutamol sulphate salt in a concentration of 0.75% (w / v, mass per volume in grams per 100 milli liters) was used, but in addition budesonide in the organic Phase was solved.
5 Als Emulgator war jeweils LGPt8546 (siehe Legende der Abbildung und Angaben gemäß Tabelle 1) verwendet worden.5 The emulsifier used was LGPt8546 (see legend of the figure and data according to Table 1).
Wie in Abbildung 4 zu sehen ist, zeigen alle erfindungsgemäßen W/O (Wasser/DCM)- Emulsionen stabiles Verhalten auf. Die Emulsionströpfchengröße (hydrodynamischer l o Durchmesser der Emulsion) liegt in einem geeignetem Bereich zwischen 300nm und 3000 nm. Darüber hinaus bleibt die Emulsionströpfchengröße mindestens innerhalb der Messdauer von ca. 1 Stunde stabil innerhalb dieses für die Tröpfchengröße geeigneten Bereiches. As can be seen in FIG. 4, all W / O (water / DCM) emulsions according to the invention exhibit stable behavior. The emulsion droplet size (hydrodynamic oil diameter of the emulsion) is in a suitable range between 300 nm and 3000 nm. In addition, the emulsion droplet size remains stable at least within the measurement period of about 1 hour within this range suitable for the droplet size.
Tabelle 2: Zusammensetzung der gemäß Beispiel 1 bis 4 hergestellten Emulsionen (%-Angaben entsprechen Masse pro Volumen (w/v) in Gramm pro 100 milli-Liter).Table 2: Composition of the emulsions prepared according to Examples 1 to 4 (% data corresponds to mass per volume (w / v) in grams per 100 milli liters).

Claims

Patentansprüche claims
1. W/O (Wasser in Öl)-Emulsion, die einen pharmakologisch aktiven Wirkstoff enthält, gekennzeichnet dadurch, dass die Emulsionströpfchen einen hydrodynamischen Durchmesser zwischen 200 nm und 3000 nm aufweisen und die wässrige Phase, die zur Herstellung dieser Emulsion verwendet wird, dadurch charakterisiert ist, dass in ihr ein Salz gelöst ist und die wässrige Phase eine Ionenstärke von mehr als 10 mM aufweist.1. W / O (water in oil) emulsion containing a pharmacologically active ingredient characterized in that the emulsion droplets have a hydrodynamic diameter between 200 nm and 3000 nm and the aqueous phase used to prepare this emulsion is characterized characterized in that a salt is dissolved in it and the aqueous phase has an ionic strength of more than 10 mM.
2. W/O (Wasser in Öl)-Emulsion gemäß Anspruch 1, dadurch gekennzeichnet, dass das in der wässrigen Phase gelöste Salz ausgewählt ist aus der Gruppe bestehend aus einem Alkalisalz, einem Erdalkalisalz, einem Säureadditionssalzes eines Wirkstoffes oder einer Kombination derselben.2. W / O (water in oil) emulsion according to claim 1, characterized in that the salt dissolved in the aqueous phase is selected from the group consisting of an alkali metal salt, an alkaline earth metal salt, an acid addition salt of an active ingredient or a combination thereof.
3. W/O (Wasser in Öl)-Emulsion gemäß Anspruch 2, dadurch gekennzeichnet, dass in der wässrigen Phase neben einem pharmakologisch aktiven Wirkstoff ein Alkalisalz oder Erdalkalisalz, bevorzugt NaCl vorliegt.3. W / O (water in oil) emulsion according to claim 2, characterized in that in the aqueous phase in addition to a pharmacologically active ingredient is an alkali salt or alkaline earth metal salt, preferably NaCl.
4. W/O (Wasser in Öl)-Emulsion nach einem der Anspruch 1 bis 3, dadurch gekennzeichnet, dass diese als Emulgator eine Substanz aus der Klasse der Block-Co-4. W / O (water in oil) emulsion according to one of claims 1 to 3, characterized in that it contains as emulsifier a substance from the class of the block co
Polymere enthalten.Contain polymers.
5. W/O (Wasser in Öl)-Emulsion nach einem der Anspruch 1 bis 4, dadurch gekennzeichnet, dass diese als Emulgator eine Substanz aus Gruppe, ausgewählt aus der Klasse der PEG-[Poly-(Laktid-co-Glykolide)] und der PEG-[Poly-Laktide] enthalten.5. W / O (water in oil) emulsion according to one of claims 1 to 4, characterized in that it contains as emulsifier a substance selected from the class of PEG [poly (lactide-co-glycolides)] and the PEG [poly-lactides].
6. W/O (Wasser in Öl)-Emulsion gemäß Anspruch 5, dadurch gekennzeichnet, dass der Emulgator einen PEG- Anteil zwischen 1 bis 15% (Massen- % bezogen auf die Gesamtmolekularmasse des Block-Co-Polymers), eine Molekularmasse von 37.5 bis6. W / O (water in oil) emulsion according to claim 5, characterized in that the emulsifier has a PEG content between 1 to 15% (% by mass based on the total molecular weight of the block co-polymer), a molecular mass of 37.5 to
600 kD, eine Diblock- oder Triblockstruktur aufweist, der Glykolid- Anteil zwischen 0-50 % (Massen-% bezogen auf das Poly-(Laktid-co-Glykolides) bzw. des PoIy- Laktides) liegt und der Laktid-Anteil zwischen 50 - 100 % (Massen-% bezogen auf das Poly-(Laktid-co-Glykolides) bzw. des Poly-Laktides) liegt. 600 kD, has a diblock or triblock structure, the glycolide proportion between 0-50% (mass% based on the poly (lactide-co-glycolide) or the poly-lactide) and the lactide content is between 50 - 100% (mass% based on the poly (lactide-co-glycolide) or the poly-lactide) is.
7. W/O (Wasser in Öl)-Emulsion nach einem der Anspruch 1 bis 6, dadurch gekennzeichnet, dass in der organischen Phase ein pharmakologisch aktiver Wirkstoff gelöst ist.7. W / O (water in oil) emulsion according to any one of claims 1 to 6, characterized in that in the organic phase, a pharmacologically active ingredient is dissolved.
5 8. Verfahren zur Herstellung von W/O (Wasser in Öl)-Emulsionen nach einem der Anspruch 1 bis 7, dadurch gekennzeichnet, dass5 8. A process for the preparation of W / O (water in oil) emulsions according to one of claims 1 to 7, characterized in that
a. einer organischen Phase, die einen Emulgator, der eine Substanz ausgewählt aus der Gruppe bestehend aus der Klasse der PEG- [PoIy- (Laktid-co-0 Glykolide)] und der Klasse der PEG-[Poly-Laktide] darstellt, enthält, b. einer wässrigen Phase, die ein Salz enthält, welches ausgewählt ist aus der Gruppe bestehend aus einem Alkalisalz, einem Erdalkalisalz, einem Säureadditionssalzes eines pharmakologisch aktiven Wirkstoffes oder einer Kombination derselben, 5 durch intensives Mischen beigemengt wird.a. an organic phase containing an emulsifier which is a substance selected from the group consisting of the class of PEG- [poly (lactide-co-0 glycolides)] and the class of PEG- [poly-lactides], b , an aqueous phase containing a salt selected from the group consisting of an alkali salt, an alkaline earth salt, an acid addition salt of a pharmacologically active agent, or a combination thereof, mixed by intensive mixing.
9. Arzneimittel gekennzeichnet dadurch, dass dieses eine W/O (Wasser in Öl)-Emulsion o nach einem der Ansprüche 1 bis 7 enthält. 9. Medicament characterized in that it contains a W / O (water in oil) emulsion o according to one of claims 1 to 7.
EP09761683A 2008-06-09 2009-06-08 New emulsions for producing medicinal products Withdrawn EP2296624A1 (en)

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