Classifications

• • 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
  • A61K9/0012—Galenical forms characterised by the site of application
  • A61K9/007—Pulmonary tract; Aromatherapy
  • A61K9/0073—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy
  • A61K9/0075—Sprays or powders for inhalation; Aerolised or nebulised preparations generated by other means than thermal energy for inhalation via a dry powder inhaler [DPI], e.g. comprising micronized drug mixed with lactose carrier particles
• • A—HUMAN NECESSITIES
  • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
  • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
  • A61K31/00—Medicinal preparations containing organic active ingredients
  • A61K31/33—Heterocyclic compounds
  • A61K31/38—Heterocyclic compounds having sulfur as a ring hetero atom
• • 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
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
  • A61K9/5005—Wall or coating material
  • A61K9/5015—Organic compounds, e.g. fats, sugars
• • 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
  • A61K9/48—Preparations in capsules, e.g. of gelatin, of chocolate
  • A61K9/50—Microcapsules having a gas, liquid or semi-solid filling; Solid microparticles or pellets surrounded by a distinct coating layer, e.g. coated microspheres, coated drug crystals
  • A61K9/5005—Wall or coating material
  • A61K9/5021—Organic macromolecular compounds
  • A61K9/5036—Polysaccharides, e.g. gums, alginate; Cyclodextrin
• • 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
  • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00

Definitions

• the present invention relates to new methods for the surface modification of powders. Furthermore the present invention relates to new, improved pharmaceutical dosage forms obtainable by the new methods for surface modification of drugs according to the invention and to the use of these pharmaceutical dosage forms within dry powder inhalation devices (DPI).
• DPI dry powder inhalation devices
• Active substances for dry powder inhalation are often prepared by micronization or by spray drying to have an aerodynamic particle size of approximately 5 ⁇ m or less enabling lung deposition.
• Such powders present difficulties in manufacture and handling as well as in dispensing these powders during application due to particle agglomeration, cohesion and adhesion to manufacturing equipment, inhaler devices and container materials.
• DPI dry powder inhalation device
• a dry powder inhalation device which comprises (a) at least one micronized or microfine solid active ingredient, which is soluble in water, (b) optionally a solid, pharmaceutically acceptable carrier excipient, which dilutes the active ingredient (a), (c) a fatty acid or fatty alcohol derivative or a poloxamer, characterized in that the fatty acid or fatty alcohol derivative or poloxamer (c) coats at least partially the surface of (a), or of the agglomerate formed by (a) and (b).
• DPI dry powder inhalation device
• the micronized or microfine solid active ingredients are drugs for medical or diagnostic use. They are generally selected from those medicaments that are applicable via inhalation. Preferably they may be selected from the group consisting of anti-COPD-agents, anti-asthmatics, anti-migraine agents, anti- infective agents, anti-pain-agents, proteoglycans, therapeutic proteins, peptides and genes.
• Preferred active ingredients according to the invention are selected from the group consisting of beta-agonists such as Fenoterol, Formoterol and Salmeterol, anticholinergic drugs such as Ipratropium, Oxitropium, and Tiotropium, or combinations of beta-agonists and anticholinergics such as Tiotropium + Formoterol or Salmeterol, interferons such as interferon-alpha, interferon-beta, interferon- gamma or interferon-omega, cytokines such as interleukins and their antagonists or receptors, peptide hormones and analogues such as LHRH analogues, growth hormones and analogues, colony stimulating factors, erythropoietin, TNFs, vaccines, blood factors, enzymes, parathyroid hormone, calcitonin, insulin, antibodies such as antibodies to treat immune diseases, virus infections or lung cancer, alpha-1- antitrypsin, proteoglycans such as heparin or low
• the pharmaceutically acceptable acid addition salts are selected from the group consisting of hydrochloride, hydrobromide, sulfate, phosphate, methansulfonate, acetate, fumarate, lactate, citrate, tartrate and maleate.
• Preferred acid addition salts are selected form the group consisting of hydrochloride, hydrobromide, sulfate, phosphate and methansulfonate. More preferred acid addition salts are selected from the group consisting of hydrochloride, hydrobromide and methansulfonate.
• the active ingredient is selected from the group consisting of Ipratropium, Oxitroprium and Tiotropium reference to these ingredients is to be understood as reference to their salts selected from the group consisting of chloride, bromide, iodide, methansulfonate, para-toluenesulfonate or methylsulfate.
• the active ingredients Ipratropium, Oxitroprium and Tiotropium represent kations.
• Preferred salts of Ipratropium, Oxitropium and Tiotropium are selected from the group consisting of chloride, bromide, iodide and methansulfonate, more preferred are methansulfonate and bromide, the latter one being most preferred.
• the active ingredients used for the preparation of the pharmaceutical dosage forms according to the invention can optionally form solvates or hydrates. Accordingly, the term active ingredient not only relates to the salts and acid addition salts as specified hereinbefore, but embraces optionally existing solvates or hydrates thereof. In case of the preferred active ingredient Tiotropiumbromide the monohydrate thereof is of particular interest.
• acceptable carrier or, in the case of spray dried active ingredients encapsulation excipients are selected from the group consisting of monosaccharides (e.g. glucose or arabinose), disaccharides (e.g. lactose, trehalose, sucrose, maltose), oligo- and polysaccharides (e.g. dextranes, hydroxyethyl cellulose), polyalcohols (e.g. sorbit, mannitol, xylit), salts (e.g. sodium chloride, calciumcarbonate), polyesters (e.g. polylactides and their copolymers), polyethers (e.g.
• monosaccharides e.g. glucose or arabinose
• disaccharides e.g. lactose, trehalose, sucrose, maltose
• oligo- and polysaccharides e.g. dextranes, hydroxyethyl cellulose
• polyalcohols e.g.
• PEG polyvinyl derivatives
• Preferred acceptable carrier excipients are selected from mono- or disaccharides, especially lactose and glucose, optionally in the form of their hydrates.
• lactose-monohydrate and anhydrous glucose are lactose-monohydrate and anhydrous glucose.
• encapsulating agents are hydroxyethyl starch, trehalose, mannitol and lactose monohydrate or mixtures of mannitol and sucrose.
• the average geometric particle size of the optionally added acceptable carrier excipients is in the range of 2 - 100 ⁇ m, preferably 4 - 60 ⁇ m, more preferably 6 - 40 ⁇ m, most preferably 8 - 35 ⁇ m.
• carrier excipients Lactose monohydrate 200 mesh, optionally in mixture with micronized lactose, and glucose anhydrous 35 ⁇ m, optionally in mixture with micronized anhydrous glucose .
• the average geometric particle size of the drug substance in line with this patent is 0.5 - 25 ⁇ m, preferably 1 - 20 ⁇ m, more preferably 1 - 15 ⁇ m.
• the average mass median aerodynamic diameter (MMAD) of the drug substance in this patent is targeted to be 0.5 - 15 ⁇ m, preferably 0.5 - 10 ⁇ m, more preferably 0.5 - 8 ⁇ m.
• the term average geometric particle size is defined as the value in ⁇ m at which 50% of the particles as determined from the volume distribution of the particles by laser diffraction (dry suspension method) are smaller than or equal to this value.
• the MMAD in accordance with this patent is measured using appropriate devices such as cascade impactors or impingers as described and defined in the current pharmacopeias (e.g.: European Pharmacopoeia - Supplement 2001, pages 113 - 124 and 1657 - 1661).
• the fatty acid or fatty alcohol derivatives or poloxamers are preferentially sorbitol derivatives, optionally containing polyethylene glycol ether groups, particularly they are selected from the group consisting of sorbitan mono- oleate, sorbitan trioleate, sorbitan monostearate, sorbitan tristearate, sorbitan monolaurate, sorbitan trilaurate, sorbitan monomyristate, sorbitan trimyristate, sorbitan monopalmitate, sorbitan tripalmitate, preferred PEG derivatives are PEG sorbitan monolaurate, PEG sorbitan monopalmitate, PEG sorbitan monostearate, PEG sorbitan tristearate, PEG sorbitan mono-oleate and PEG sorbitan trioleate.
• Preferred sorbitol derivatives are sorbitan mono-oleate , sorbitan trioleate sorbitan monostearate, sorbitan tristearate, PEG sorbitan monolaurate and PEG sorbitan mono-oleate, most preferred being sorbitan mono-oleate, sorbitan monostearate, sorbitan tristearate and PEG sorbitan mono-oleate.
• the term pharmaceutical dosage form is to be regarded as being equivalent to the term powder for inhalation.
• the amounts of fatty acid or fatty alcohol derivative or poloxamer relative to the drug substance or - if carriers or encapsulating agents are present - relative to the drug substance plus excipient complex, i.e. the drug substance-excipient agglomerate or mixture or microcapsule, are in the range of 0.001 - 200% w/w, preferably 0.002 - 100% w/w, more preferably 0.01 - 50% w/w.
• Drug substance and surface modifying component together constitute 0.02 - 100% w/w, preferably 0.05 - 100% w/w, more preferably 0.1 - 100% w/w of the pharmaceutical dosage form.
• the pharmaceutical dosage form according to the invention is obtainable via processes of surface modification, involving the physical adsorption of a fatty acid or alcohol derivative or poloxamer (c) from solution or dispersion onto the surface of a drug (a), present as an insoluble particulate dispersion or by spray drying a solution or dispersion of the drug containing said fatty acid or alcohol derivative or poloxamer or by intensively physically mixing a powder containing the microfine drug with the fatty acid or alcohol derivative or poloxamer.
• Process A comprises the steps of (i) preparation of a solution or dispersion of components (c)in a solvent, in which components (a) and optionally a carrier (b) are insoluble; (ii) adsorption of components (c) to the surface of (a) and optionally (b) until equilibration;
• process B spray drying process
• process B comprises the steps of:
• process C comprises the steps of: (i) intensively mixing a powder containing the microfine drug substance (a), optionally also drug carrier (b), using standard mixing machines such as a Diosna mixer or a Lodige mixer, (ii) either adding before start of the mixing process or, preferentially, during the mixing process components (c) to the powder and
• Another aspect of the invention relates to the processes of preparation of a pharmaceutical dosage form as described hereinbefore. Another aspect of the invention relates to a pharmaceutical dosage form obtainable via to the aforementioned process.
• the active substances are water soluble and thus a non-aqueous solvent, preferably a water-immiscible organic solvent, was required for the adsorbate.
• the solvent for step (i) in the first process (process A) is preferably a C 3 -C-
• the most preferred solvent is n- hexane or cyclohexane.
• the solvent for step (i) in needs not to be a solvent in which for instance component (a) is insoluble.
• the solvent is preferably selected from water, aqueous buffer-solutions like for instance phosphate- buffer solutions, alcohols like for instance methanol, ethanol or isopropanol, C 3 -C- ⁇ 2 alkanes, C 3 -C ⁇ 2 cycloalkanes or mixtures thereof.
• Preferred solvents for step (i) in process B are selected from water, aqueous buffer-solutions like phosphate-buffer solutions, alcohols and mixtures thereof, water and phosphate-buffer solutions being most preferred.
• the concentration of the fatty acid or alcohol derivative or poloxamer in the solvent according to process A can vary from 20 mg / L to 10,000 mg / L, is preferably between 100 mg to 8,000 mg / L, more preferably between 200 mg and 5,000 mg / L, the most preferred concentration being 2000 mg / L.
• the amount of fatty acid or fatty alcohol derivative or poloxamer added relative to the total solids is in the range of 0.001 to 50 % w/w, preferably between 0.005 and 10 % w/w, most preferred between 0.01 and 5 % w/w.
• the drug substance is added in concentrations between 0.001 % and 50%, preferably between 0.1 % and 20%, the most preferred concentration is 2%, i.e. 4 g / 200 ml.
• the pharmaceutical dosage forms display a variety of surprising and unexpected advantages and are therefore superior over conventional micronized and microfine powders for inhalation.
• surface modification of the active substances via adsorption of or coating by or intensive mixing with fatty acid derivatives the following effects proved to be of extraordinary significance:
• the methods according to the invention generally provide for
• a further aspect of the invention generally relates to a method for the reduction of electrostatic charge acquisition by triboelectrification during pharmaceutical processing and during handling/drug administration, characterized in that a surface modification involving the physical adsorption of a fatty acid or alcohol derivative or poloxamer from solution or dispersion onto the surface of a drug present as an insoluble particulate dispersion in the solution or the coating of the dissolved or dispersed drug by a fatty acid or alcohol derivative or poloxamer using spray drying or the intensve mixing of a drug containing powder with a fatty acid or alcohol derivative or poloxamer is conducted.
• Another aspect of the invention generally relates to a method for the reduction of adhesion to contact surfaces, characterized in that a surface modification involving the physical adsorption of a fatty acid or alcohol derivative or poloxamer from solution or dispersion onto the surface of a drug present as an insoluble particulate dispersion in the solution or the coating of the dissolved or dispersed drug by a fatty acid or alcohol derivative or poloxamer using spray drying or the intensive mixing of a drug containing powder with a fatty acid or alcohol or poloxamerderivative is conducted.
• Another aspect of the invention relates to a method for the improvement of powder flow during pneumatic transport, characterized in that a surface modification involving the physical adsorption of a fatty acid or alcohol derivative or poloxamer from solution or dispersion onto the surface of a drug present as an insoluble particulate dispersion in the solution or the coating of the dissolved or dispersed drug by a fatty acid or alcohol derivative or poloxamer using spray drying or the intensve mixing of a drug containing powder with a fatty acid or alcohol derivative or poloxamer is conducted.
• Another aspect of the invention relates to a method for the improvement of drug content uniformity during mixing of actives with excipient carriers in DPI formulations, characterized in that a surface modification involving the physical adsorption of a fatty acid or alcohol derivative or poloxamer from solution or dispersion onto the surface of a drug present as an insoluble particulate dispersion in the solution or the coating of the dissolved or dispersed drug by a fatty acid or alcohol derivative or poloxamer using spray drying or the intensive mixing of a drug containing powder with a fatty acid or alcohol derivative or poloxamer is conducted.
• Another aspect of the invention relates to a method for the improvement of inhalation properties of powders, characterized in that a surface modification involving the physical adsorption of a fatty acid or alcohol derivative or poloxamer from solution or dispersion onto the surface of a drug present as an insoluble particulate dispersion in the solution or the coating of the dissolved or dispersed drug by a fatty acid or alcohol derivative or poloxamer using spray drying or the intensve mixing of a drug containing powder with a fatty acid or alcohol derivative or poloxamer is conducted.
• Figure 1 Mean specific charge of micronized Fenoterol generated during triboelectrification in a stainless steel cyclone with or without sieving and with and without organic solvent / antistatic agent treatment
• Figure 2 Mass of micronized Fenoterol (1 g samples) transported to the Faraday well during triboelectrification in a stainless steel cyclone with or without sieving and with and without organic solvent / antistatic agent treatment;
• Figure 3 Mean specific charge of micronized Tiotropium generated during triboelectrification in a stainless steel cyclone with or without sieving and with and without organic solvent / antistatic agent treatment;
• Figure 4 Mass of micronized Tiotropium (1 g samples) transported to the Faraday well during triboelectrification in a stainless steel cyclone with or without sieving and with and without organic solvent / antistatic agent treatment;
• Figure 5 Mean specific charge after mixing in Turbula mixer (Fenoterol and Ipratropium);
• Figure 6 Mean specific charge after mixing in Turbula mixer (Tiotropium and Oxitropium);
• Figure 1 provides specific charge values of -40 and -92 nC g "1 for unsieved and sieved fenoterol respectively and the charge values in figure 3 for unsieved and sieved tioptropium were +52 and +201 nC g "1 respectively.
• Figures 1 and 3 show that treatment of the active substances with sorbitan trioleate reduces charge acquistion of sieved samples when using the same process of triboelectrification.
• An example from these data in figures 3 and 5 shows the mean charge values for the drugs fenoterol and tiotropium when treated at a concentration of 600mg I "1 of sorbitan trioleate in hexane.
• Sieved samples of the treated fenoterol and tiotropium had mean charge values of -38.4 and +104 nC g "1 respectively, after triboelectrification in the cyclone apparatus. These data show that charge acquisition for sieved samples can be reduced by surface modification. Experimental results show that sieving also adversely affects bulk powder properties of the active substances, including adhesion to contact surfaces and pneumatic flow. Figures 2 and 4 provide mass transfer values of powder through the cyclone apparatus by pneumatic conveyance during triboelectrification experiments. Ideally, 100% w/w of the original sample (1g) should pass through the apparatus and this would indicate good flow and non-adhesion.
• Figures 2 and 4 provide values of mass transfer of 0.083 and 0.025g (8.3 and 2.5 %w/w ) for sieved, untreated fenoterol and tiotropium respectively.
• Treatment of the actives by surface modification with sorbitan trioleate increased the mass transfer values to an extent that was dependent upon treatment concentration.
• Figure 2 shows increases in mass transfer to between 0.45-0.78g (45-78% w/w) for fenoterol and in figure 4 the values increase to between 0.092- 0.29 g (9.2- 29% w/w) for tiotropium.
• Visual inspection of the steel contact surface showed that powder adhesion was considerably less for surface modified actives.
• the adhered treated samples were very easily removed, whereas untreated actives were firmly adhered and very difficult to remove.
• FIGS. 5 and 6 show values for charge acquisition for powder samples of, (a) carrier excipients, (b) untreated and treated actives and (c) DPI formulations of untreated and treated actives.
• the results in these figures show that the treatment by adsorption of sorbitan trioleate reduces charge acquisition of both the unformulated and formulated actives during mixing in a steel mixing vessel of a turbula mixer( for method see experimental part III).
• Untreated fenoterol in a DPI formulation with glucose as carrier had a mean specific charge of -3.2 nC g "1 , whereas the formulation containing treated drug had a value of -0.35 nC g "1 (figure 5).
• Tiotropium (untreated) in DPI formulation with lactose as carrier had a mean charge value of -0.78 nC g "1 and the formulation containing treated drug had a value of 0.15 nC g "1 (figure 6).
• DPI formulations containing untreated and treated actives were prepared by mixing in a steel vessel of a turbula mixer and 20 random samples from each mix were analysed for the active component.
• the methodology applied is outlined in detail below.
• the mean drug content and coefficient of variation (cv) values in table 1 show that the treatment of tiotropium with sorbitan trioleate improves the mixing quality and hence the drug content uniformity.
• Table 1 Mean drug content and coefficient of variation values for DPI formulations prepared in a turbula mixer:
• Sorbitan derivative Mean charge nC g "1 Mean mass transfer %
• Electrostatic charge of powder samples was investigated using a cyclone apparatus linked to a Faraday well and force compensation load cell to measure charge and mass simultaneously. 1 g samples of powder were transported through the apparatus using dry compressed air (rh ⁇ 10%) at 8 m s "1 for triboelectrification against a stainless steel surface.
• the charge Q (nC) and mass M (g) values were used to calculate the specific charge Q/M ( nC g "1 ) at the completion of each experimental run.
• the results are mean values with coefficient of variation values for 5 replicates.
• the mass of material entering the Faraday well was used to quantify the mass transport through the apparatus and this was used to assess the flow and adhesion characteristics of the powder.
• the amount of material adhered to the cyclone wall was estimated visually and rated on a scale from 0 (no adhesion) to 3 (extensive adhesion).
• the electrostatic charge of the drug/carrier powder mixes (5g) was undertaken after mixing in a stainless steel cylindrical vessel, agitated at 100 rpm for 10 minutes on a Turbula mixer under ambient conditions, by pouring the sample into a Faraday well. The mass of powder entering the Faraday well was recorded to determine the specific charge. In addition, the difference between the mass of powder in the mixing vessel and that in the Faraday well was used to quantify the amount of adhesion to the mixer vessel wall. The mean specific charge, and coefficient of variation values for 3 replicates are reported.
• the untreated and treated active substances were mixed with carrier excipient in a ratio selected from the range of drug/carrier compositions used in dry powder inhaler formulations.
• a carrier blend of coarse and micronized carrier was prepared in a turbula mixer for 10 minutes at 100rpm.
• the active substance (treated or untreated drug) was added and mixed for further 10 minutes prior to charging measurements.
• Tiotropiumbromide 15.0 kg Tiotropiumbromide are introduced into 25,7 kg water. Th mixture is heated to
• the crystalline tiotropiumbromide monohydrate thus obtained is micronized according to conventional methods known in the art.
• Example 1 4 g Fenoterol hydrobromide are dispersed in an incubator in 200 ml of n- hexane containing 2000 mg/L sorbitan trioleate and agitated at 220rpm for 3 hours at 25 ⁇ 0.5°C.
• the treated drug is filtered using vacuum and dried in a fume cupboard to constant weight at room temperature, followed by lightly milling using a mortar and a pestle and sieving through a 250 ⁇ m sieve.
• composition of formulation :
• the components are carefully mixed and filled into capsules or blisters for use in commercial inhaler devices
• Tiotropiumbromide monohydrate are dispersed in an incubator in 200 ml of n-hexane containing 3000 mg/L sorbitan trioleate and agitated at 220rpm for 3 hours at 25 ⁇ 0.5°C.
• the treated drug is filtered using vacuum and dried in a fume cupboard to constant weight at room temperature, followed by lightly milling using a mortar and a pestle and sieving through a 250 ⁇ m sieve.
• composition of formulation :
• Example 3 0.2739 g micronized lactose; The components are carefully mixed and filled into capsules or blisters for use in commercial inhaler devices.
• Example 3
• Tiotropiumbromide monohydrate are dispersed in an incubator in 200 ml of n-hexane containing 2000 mg/L sorbitan monostearate and agitated at 220rpm for 3 hours at 25 ⁇ 0.5°C.
• the treated drug is filtered using vacuum and dried in a fume cupboard to constant weight at room temperature, followed by lightly milling using a mortar and a pestle and sieving through a 250 ⁇ m sieve.
• composition of formulation :
• Tiotropiumbromide monohydrate are dispersed in an incubator in 200 ml of n-hexane containing 2000 mg/L sorbitan mono-oleate and agitated at
• composition of formulation :
• the components are carefully mixed and filled into capsules or blisters for use in commercial inhaler devices.
• Oxitropiumbromide 4 g Oxitropiumbromide are dispersed in an incubator in 200 ml of n-hexane containing 2000 mg/L sorbitan trioleate and agitated at 220rpm for 3 hours at 25 + 0.5°C.
• the treated drug is filtered using vacuum and dried in a fume cupboard to constant weight at room temperature, followed by lightly milling using a mortar and a pestle and sieving through a 250 ⁇ m sieve.
• composition of formulation :
• the components are carefully mixed and filled into capsules or blisters for use in commercial inhaler devices.
• Ipratropiumbromide 4 g are dispersed in an incubator in 200 ml of n-hexane containing 2000 mg/L sorbitan trioleate and agitated at 220rpm for 3 hours at 25 ⁇ 0.5°C.
• the treated drug is filtered using vacuum and dried in a fume cupboard to constant weight at room temperature, followed by lightly milling using a mortar and a pestle and sieving through a 250 ⁇ m sieve.
• composition of formulation :
• the components are carefully mixed and filled into capsules or blisters for use in commercial inhaler devices
• Example 7 10 g of trehalose is dissolved in 50 ml of 20 mM phosphate buffer pH 5.5 containing 0.1% Tween 80 (PEG sorbitan mono-oleate). 50 ml of a solution of 55 mg of Interferon-omega in 20 mM phosphate buffer pH 5.5 is slowly added under gentle stirring. The solution is spray dried at 90°C inlet temperature and 60°C outlet temperature. The almost free flowing powder is easily harvested from the cyclon and dried under vacuum for 6 hours at 40°C. The powder is filled into capsules, but may be diluted by carrier 1 :10 prior to filling into the capsules.
• Example 8

Landscapes

• Health & Medical Sciences (AREA)
• Animal Behavior & Ethology (AREA)
• Bioinformatics & Cheminformatics (AREA)
• Chemical & Material Sciences (AREA)
• Engineering & Computer Science (AREA)
• Veterinary Medicine (AREA)
• Medicinal Chemistry (AREA)
• Public Health (AREA)
• General Health & Medical Sciences (AREA)
• Pharmacology & Pharmacy (AREA)
• Life Sciences & Earth Sciences (AREA)
• Epidemiology (AREA)
• Pulmonology (AREA)
• Organic Chemistry (AREA)
• Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
• General Chemical & Material Sciences (AREA)
• Chemical Kinetics & Catalysis (AREA)
• Otolaryngology (AREA)
• Medicinal Preparation (AREA)
• Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
• Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
• Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Priority Applications (6)

Applications Claiming Priority (2)

Publications (2)

Family

ID=9911273

Family Applications (1)

Country Status (10)

Cited By (19)

Families Citing this family (17)

Family Cites Families (15)

• 2001
  • 2001-03-21 GB GBGB0107106.7A patent/GB0107106D0/en not_active Ceased
• 2002
  • 2002-02-28 US US10/085,972 patent/US20030007932A1/en not_active Abandoned
  • 2002-03-16 AT AT02745193T patent/ATE556704T1/de active
  • 2002-03-16 JP JP2002578923A patent/JP2004523594A/ja active Pending
  • 2002-03-16 CA CA2440010A patent/CA2440010C/en not_active Expired - Fee Related
  • 2002-03-16 AU AU2002316820A patent/AU2002316820A1/en not_active Abandoned
  • 2002-03-16 MX MXPA03008398A patent/MXPA03008398A/es active IP Right Grant
  • 2002-03-16 EP EP02745193A patent/EP1372610B1/en not_active Expired - Lifetime
  • 2002-03-16 WO PCT/EP2002/002948 patent/WO2002080884A2/en not_active Ceased
  • 2002-03-20 UY UY27218A patent/UY27218A1/es not_active Application Discontinuation
• 2005
  • 2005-03-30 US US11/093,491 patent/US20050196346A1/en not_active Abandoned
• 2007
  • 2007-01-17 US US11/653,887 patent/US20080057003A1/en not_active Abandoned

Also Published As

Similar Documents

Legal Events