EP1206250A2 - Compositions pharmaceutiques - Google Patents

Compositions pharmaceutiques

Info

Publication number
EP1206250A2
EP1206250A2 EP00954802A EP00954802A EP1206250A2 EP 1206250 A2 EP1206250 A2 EP 1206250A2 EP 00954802 A EP00954802 A EP 00954802A EP 00954802 A EP00954802 A EP 00954802A EP 1206250 A2 EP1206250 A2 EP 1206250A2
Authority
EP
European Patent Office
Prior art keywords
dosage form
release
active agent
form according
formulation
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Withdrawn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
EP00954802A
Other languages
German (de)
English (en)
Inventor
Christian Elan Pharm. Technologies ANDINA
Niall Elan Pharm. Technologies FANNING
Fiona Elan Pharm. Technologies PALMER
Paul Elan Pharm. Technologies STARK
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.)
Elan Corp PLC
Original Assignee
Elan Corp PLC
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 Elan Corp PLC filed Critical Elan Corp PLC
Publication of EP1206250A2 publication Critical patent/EP1206250A2/fr
Withdrawn legal-status Critical Current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
    • A61K31/00—Medicinal preparations containing organic active ingredients
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • 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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/711—Natural deoxyribonucleic acids, i.e. containing only 2'-deoxyriboses attached to adenine, guanine, cytosine or thymine and having 3'-5' phosphodiester links
    • 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
    • A61K31/70—Carbohydrates; Sugars; Derivatives thereof
    • A61K31/7088—Compounds having three or more nucleosides or nucleotides
    • A61K31/7125—Nucleic acids or oligonucleotides having modified internucleoside linkage, i.e. other than 3'-5' phosphodiesters
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K39/39—Medicinal preparations containing antigens or antibodies characterised by the immunostimulating additives, e.g. chemical adjuvants
    • 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
    • A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
    • A61K9/16—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction
    • A61K9/167—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface
    • A61K9/1676—Agglomerates; Granulates; Microbeadlets ; Microspheres; Pellets; Solid products obtained by spray drying, spray freeze drying, spray congealing,(multiple) emulsion solvent evaporation or extraction with an outer layer or coating comprising drug; with chemically bound drugs or non-active substances on their surface having a drug-free core with discrete complete coating layer containing drug
    • 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
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/2004—Excipients; Inactive ingredients
    • A61K9/2022—Organic macromolecular compounds
    • A61K9/205—Polysaccharides, e.g. alginate, gums; Cyclodextrin
    • A61K9/2054—Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
    • 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
    • A61K9/20—Pills, tablets, discs, rods
    • A61K9/28—Dragees; Coated pills or tablets, e.g. with film or compression coating
    • A61K9/2806—Coating materials
    • A61K9/2833—Organic macromolecular compounds
    • A61K9/284—Organic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone
    • A61K9/2846—Poly(meth)acrylates
    • 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
    • A61K9/4808—Preparations in capsules, e.g. of gelatin, of chocolate characterised by the form of the capsule or the structure of the filling; Capsules containing small tablets; Capsules with outer layer for immediate drug release
    • 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
    • A61K9/5084—Mixtures of one or more drugs in different galenical forms, at least one of which being granules, microcapsules or (coated) microparticles according to A61K9/16 or A61K9/50, e.g. for obtaining a specific release pattern or for combining different drugs
    • B—PERFORMING OPERATIONS; TRANSPORTING
    • B82—NANOTECHNOLOGY
    • B82Y—SPECIFIC USES OR APPLICATIONS OF NANOSTRUCTURES; MEASUREMENT OR ANALYSIS OF NANOSTRUCTURES; MANUFACTURE OR TREATMENT OF NANOSTRUCTURES
    • B82Y5/00—Nanobiotechnology or nanomedicine, e.g. protein engineering or drug delivery
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K39/00—Medicinal preparations containing antigens or antibodies
    • A61K2039/555—Medicinal preparations containing antigens or antibodies characterised by a specific combination antigen/adjuvant
    • A61K2039/55511—Organic adjuvants
    • A61K2039/55555—Liposomes; Vesicles, e.g. nanoparticles; Spheres, e.g. nanospheres; Polymers

Definitions

  • the present invention relates to methods of pharmaceutical formulation and administration, and in particular, orally administrable formulations capable of providing a desired pharmacokinetic profile for an active agent .
  • Many pharmaceutically active agents are metabolised by mammalian systems. Any dosing regime must take into account the pharmacokinetic properties of the active ingredient and its interaction with the metabolic system of the subject in order to obtain the required pharmacokinetic profile and bioavailability of the drug. It may be desirable to achieve a slow sustained release rate of a pharmaceutically active agent . This is ideal where a single administration or dose of an active agent is required to act over a long time period, especially where metabolism or degradation of the drug will not significantly reduce its bioavailability.
  • the method of administration must be tailored in order to overcome the problems associated with drug metabolism.
  • the metabolism of some active agents may be saturable. Where this is the case, a pulse of active ingredient sufficient to saturate the relevant metabolic or degradative pathway can enable a therapeutically acceptable quantity of active agent to be delivered to the target tissue or organ.
  • Combination of one or more such dosage forms with immediate release and/or sustained release formulations may enable a single dose formulation to provide multiple, temporally distinct pulses of active agent to a patient. Such a combination would reduce the need for multiple dose administration regimes, and could therefore have significant benefits, for example, in improving patient compliance.
  • One object of the present invention is to provide sustained release formulations, capable of releasing active ingredient over a required time period.
  • a further object of the present invention is to provide delayed release formulations capable of delivering a pulse of active agent, similar to that obtained with an immediate release formulation, after a suitable delay period.
  • a further object of the invention is to provide a dosage form capable of releasing active agent at two different release rates.
  • the dosage form is capable of releasing active agent in two distinct peaks, separated by an appropriate time period. Typically the peaks will be separated by at least two hours, possibly at least five hours, possibly at least 8 hours .
  • the present invention provides a particulate oral dosage form comprising a pharmaceutically active agent, the dosage form also comprising a release modifying layer, the release modifying layer comprising a polymer having solubility properties predetermined to affect the rate of release of the active agent under enteric physiological conditions.
  • the particulate dosage form may be manufactured as a multiparticulate formulation. This may be a granulate, or alternatively a pellet or "non-pareil" type formulation, in which the active agent is applied to an inert support.
  • the particulate dosage form may also be manufactured in a "minitablet” type formulation, in which the active agent is compressed into a minitablet with appropriate excipients .
  • the pharmaceutically active agent is applied to an inert, particulate, pharmaceutically acceptable support.
  • the inert, particulate, pharmaceutically acceptable support comprises carbohydrate beads, such as non-pareil seeds (often referred to as neutral pellets, or sugar spheres) .
  • the active ingredient may be sprayed onto the inert, particulate, pharmaceutically acceptable support from solution, preferably an aqueous solution.
  • the active ingredient may be coated onto the inert, particulate, pharmaceutically acceptable support from suspension, for example, by means of a fluidised bed coating system such as a Wurster system.
  • Trfe active agent may be applied to the inert, particulate, pharmaceutically acceptable support alone or in combination with further pharmaceutically acceptable excipients .
  • the particulate dosage form may be manufactured as a "minitablet" formulation of the pharmaceutically active agent.
  • Minitablets may be formed by the direct compression of active agent with fillers such as microcrystalline cellulose, lactose, dicalcium phosphate, lubricants such as magnesium stearate or stearic acid, disintegrants such as sodium starch glycolate and glidants such as colloidal silicon dioxide.
  • Minitablets may also be formed by wet granulation of the drug with suitable excipients in a fluidised bed.
  • particulate dosage forms will typically initially constitute “immediate release” type formulations, whose release properties may be altered by application of suitable coatings, as will be described below.
  • active agent will constitute 1 to 20%, preferably 3 to 10%, of the total weight of the immediate release particulate dosage form prior to the application of any coating .
  • the particulate dosage form may also comprise a protective sealant or barrier coat, applied to the particulate dosage form.
  • this protective sealant or barrier layer is soluble and does not substantially modify the release of the active drug under physiological conditions, but protects it during processing.
  • the protective coat is composed mainly of hydroxypropyl methylcelltfTose .
  • Other agents can be added to improve the processability of the sealant layer.
  • the protective coat can be applied from solution, such as an aqueous solution, or suspension using a fluidised bed coater (for example, a Wurster system) , or in a pan coating system.
  • Minitablet formulations may include excipients which affect the rate of dissolution of the minitablet, and thus the rate of release of the active agent .
  • Such minitablet formulations may be regarded as "sustained release” type minitablets before any modifying coatings are applied. Their release properties may be further modified by application of release modifying coatings.
  • minitablets providing sustained release of the active agent may be formed by the direct compression or wet granulation of the drug with excipients, as described above, plus the inclusion of rate controlling excipients such as hydroxypropylcellulose, polyethylene glycolate and ethylcellulose, typically in a concentration of 20- 80%.
  • the release profile of the active agent can be modified according to the present invention by applying a modifying coating of material having predetermined dissolution properties to the particulate dosage form.
  • a modifying coating may be used to provide a sustained release profile or a delayed release profile for the active agent, and typically comprise soluble polymers (with solubility being pH independent or pH dependent) that can modify the release of the drug.
  • a "sustained release" type formulation may release between 2.5% and 25% of the active a ' gent in 0.5 hours, between 25% and 70% of the active agent in 1 hour, between 65% and 95% of the active agent in 2 hours, and at least 90% of the active agent in 4 hours, as determined in standard USP method II dissolution assay, in phosphate buffer at pH 6.8 (as described later) .
  • a typical sustained release formulation may provide approximately 10% release of the active agent in 0.5 hours, approximately 50% release of the active agent in 1 hour, approximately 75% release of the active agent in 2 hours, and approximately 95% release of the active agent in 4 hours.
  • the release profile required will vary depending on the active agent employed and the pharmacokinetic profile desired.
  • the modifying coating may comprise soluble or permeable acrylate polymers, e.g. ammonio methacrylate polymers or co-polymers, or methacrylic acid polymers or co-polymers.
  • the polymers can be used alone or in combination with each other. Additionally or alternatively such modifying materials may be blended with active agent as a matrix ingredient.
  • the coatings can also include other agents to improve the processability of the coating.
  • agents include talc, silicon dioxide and glyceryl monostearate .
  • the quantity of such anti-caking agents used for preparing coatings for the dosage form is e.g. from about 2% to about 100% by weight, preferably 30 to 60%, based on the total dry weight of the polymer.
  • the coatings can also include a material that improves the characteristics of the polymer material.
  • materials are generally referred to as “plasrTicisers” and include, for example, dibutyl sebacate (DBS) , diethyl phthalate, citric acid esters, or triethyl citrate (TEC) , stearates, polyethylene glycols and ethylene glycol .
  • DBS dibutyl sebacate
  • TEC triethyl citrate
  • stearates polyethylene glycols and ethylene glycol .
  • Dibutyl sebacate or triethyl citrate are the preferred plasticisers .
  • the amount of plasticiser to be used in the coating is preferably from about 10% to 50%, most preferably about 20%, based on the weight of the dry polymer.
  • the coating solutions can also include an anti-foaming agent.
  • an anti-foaming agent is simethicone emulsion.
  • the amount of anti-foaming agent to be used in the coating is preferably from less than 0.5% of the final coating solution.
  • the amount of coating to be used in preparing the dosage form will be determined by the desired delivery properties, including the amount of drug to be delivered, the time delay desired, and the size of the particles.
  • the coating polymers will typically be coated from 5 to 20% weight gain on the instant release particles, preferably 6-10% polymer weight gain.
  • the polymer layer can be coated by any known method, including spray application. Spraying can be carried out using a fluidised bed coater (preferably using a Wurster system) , or in a pan coating system.
  • the coated particles can be dried and/or cured after application of the polymer layers. "Curing” means that the particles are held at a controlled temperature for a time sufficient to provide stable release rates. Curing can be performed for example in an oven or in a fluid bed drier. Curing can be carried out at temperature within 25° and 50°C, preferably 35° to 45°C.
  • the particulate dosage form may, alternatively or additionally, be coated with a modifying layer able to modify the release of the active agent, to form delayed release particles.
  • a delayed release or sustained release coating comprising a blend of a relatively insoluble or impermeable polymeric material with a more soluble or permeable material, the choice of polymers and the proportions in the blend controlling the release rate.
  • a particularly preferred embodiment uses for the relatively permeable polymer a polymer whose permeability or solubility is pH dependent; in particular being more soluble or permeable in alkaline conditions than in acidic conditions. This enables passage of the coating through the stomach relatively undisrupted, for release of the active agent further along the gut.
  • the pH dependence of polymer solubility or permeability may not be needed.
  • a pH dependent system may be used to provide a delay in initial drug release.
  • It may also be used to provide protection against acid degradation of acid labile drugs in the gut and/or maximise the concentration of drug available to absorption sites in the intestine.
  • Film forming polymers which are swellable or soluble under appropriate conditions and suitable for oral formulation, are available commercially and ' ⁇ no n to the skilled person, e.g. Eudragit polymethacrylate coating systems from Rohm.
  • Eudragit L may be used to provide drug release in the duodenum/jejunum, and Eudragit S for release in the ileum.
  • One particular novel procedure proposed herein is to form a release-delaying coating from a blend of film-forming, swellable acrylate polymers of any suitable kinds as described herein, one of which is in aqueous dispersion (latex) and the other of which is in non-aqueous dispersion (latex) , creating a characteristic and useful difference in film permeability behaviours of the two polymers in the layer.
  • the amount of coating to be used may be determined by the desired delivery properties, including the amount of drug to be delivered, the time delay desired, and the size of the particles.
  • the modifying layer will typically provide 15 to 80% weight gain on the uncoated or sustained release particles, preferably 15 to 40% polymer weight gain on a first layer and possibly 5 to 30% polymer weight gain on a subsequent layer.
  • the first and subsequent layers may have identical or different compositions .
  • Increasing the amount of coating increases the distance the drug has to travel by diffusion through the swelled or permeabilised polymer film to be released into the surrounding medium, and therefore reduces the rate of drug release by diffusion. Decreasing the proportion of permeable component will give less opportunity for the drug to be directly solubilised by the dissolution medium and therefore may provide a longer lag time before drug release begins .
  • the particulate dosage forms will be encapsulated into individual doses.
  • Administration is preferably in a "prophylactically effective amount” or a “therapeutically effective amount", as the case may be (although prophylaxis may be considered therapy) , this being sufficient to show benefit to the individual .
  • the actual amount administered, and rate and time-course of administration will depend on the nature and severity of the condition to be treated. Prescription of treatment, e.g. decisions on dosage etc, is within the responsibility of general practitioners and other medical doctors, and typically takes account of the disorder to be treated, the condition of the individual patient, the site of delivery, the method of administration and other factors known to practitioners. Examples of the techniques and protocols mentioned above can be found in Remington's Pharmaceutical Sciences, 16th edition, Osol , A. (ed) , 1980.
  • any one of the possible component types may contribute to initial, sustained or delayed release elements of the overall pharmacokinetic profile provided.
  • Figure 1 shows dissolution profiles for sustained release multiparticulate formulations.
  • Figure 2 shows dissolution profiles for delayed release multiparticulate formulations.
  • Figure 3 shows dissolution profiles for sustained release minitablet formulations without a modifying coat.
  • Figure 4 shows dissolution profiles for sustained release minitablet formulations coated with Eudragit RS/RL
  • Figure 5 shows dissolution profiles for delayed release minitablet formulations.
  • Figure 6 shows dissolution profiles for co-encapsulated sustained release minitablets and delayed release multiparticulate formulations.
  • dissolution profiles were established by immersion of test formulation for two hours in 0.01M HCl, followed by immersion in pH 6.8 phosphate buffer.
  • the immersion in acid was omitted, and test formulations were immersed in pH 6.8 phosphate buffer for the duration of the assay. Aliquots of the dissolution buffers were removed at intervals and analysed for released rivastigmine by HPLC.
  • 0.01M HCl was prepared by diluting 8.5ml of concentrated HCl 1 litre with de-ionised water to give a solution of 0.1M HCl. This was then diluted to 0.01M HCl with deionised water, and then degassed by sparging with helium at 1.2 litres/min for 20 minutes.
  • phosphate buffer 1 litre of phosphate buffer (pH6.8 ⁇ 0.05) was prepared by adding 250ml of 0.2M potassium phosphate solution (27.22g of monobasic potassium phosphate (KH 2 P0 4 ) per litre distilled water) to 112ml of 0.2M sodium hydroxide solution and diluting to 1000ml with distilled water. Phosphate buffer was degassed as above.
  • Test formulation corresponding to 12.5mg of rivastigmine base was placed into a clean dry dissolution basket assembly (USP Apparatus I, with 40 mesh baskets) .
  • the basket was attached to the apparatus shaft, lowered into a dissolution vessel containing 500ml 0.01M HCl or phosphate buffer at 37.0 + 0.5°C, and rotated at lOOrpm.
  • the 0.01M HCl was neutralised by addition of approximately 50ml 0. IN NaOH to the vessel, with mixing.
  • the basket was then transferred to a second dissolution apparatus containing 500ml phosphate buffer (pH 6.8) .
  • Rivastigmine content of the samples was analysed by HPLC as described below.
  • Mobile phase 1 litre of mobile phase was prepared by adding 670ml of HPLC grade methanol to 330ml of aqueous buffer (3.85g - 3.95g of ammonium carbamate (anhydrous form of carbonate) dissolved in 1 litre of deionised water) . The mobile phase was filtered and degassed for 10 minutes with helium. The pH was adjusted to 9.2 as necessary with cone, ammonia.
  • HPLC HPLC was calibrated with duplicate standards, each prepared by accurately weighing 20mg of rivastigmine tartrate reference standard (equivalent to 12.5mg Rivastigmine base) into a 500ml volumetric flask. This was dissolved and diluted to 500ml with medium, mixed well and an aliquot filtered through a Millipore Millex- HV Hydrophilic PVDF 0.45mm filter into a suitable vial for injection, discarding approximately the first 2ml of filtrate to waste.
  • rivastigmine tartrate reference standard equivalent to 12.5mg Rivastigmine base
  • the coefficient of variation for five injections of a single rivastigmine reference solution was not greater than 2.0%.
  • i Ri Ml + Q ⁇ .5 ⁇ 2
  • R 2 M 2 + Q-. + Q 0 5 ⁇ 4
  • R 4 4 + Q 2 + Q_ + Q 0 . 5
  • a samp . response of sample
  • a std response of standard
  • W std weight of standard (mg)
  • V diss volume of dissolution medium (500ml)
  • V s volume of sample withdrawn at each interval (4ml)
  • R H corrected hourly release (mg)
  • R 6 M 6 + M 4 +Q 2 ⁇ 8
  • R 8 M 8 + Q 6 + M 4 +Q 2 io
  • R 10 Mio + Q 8 + Q-6 + M 4 + Q 2 ⁇ 12
  • R l 2 M_ 2 + M 10 + Q 8 + Q 6 + M 4 + Q 2
  • V s volume of sample withdrawn at each interval (4ml)
  • a solution of hydroxypropyl methylcellulose was prepared by adding 100. Og of hydroxypropyl methylcellulose into 1.900kg of purified water and continuing mixing for 45 minutes .
  • Rivastigmine tartrate was prepared as follows. To 1106.6g of hydroxypropyl methylcellulose solution were added 265.7g of Rivastigmine tartrate. The mixture was stirred for 15 minutes to dissolve the drug. 27.7g of silicon dioxide were added to the solution and the mixture was stirred for 15 minutes.
  • a protective solution was prepared as follows. To 682.9g of hydroxypropyl methylcellulose solution were added 17. Ig of silicon dioxide and the mixture was stirred for 15 minutes.
  • Rivastigmine suspension was sprayed first onto
  • Example 2 Preparation of sustained release (SR) Eudragit RS.RL (98; 2) coated Rivastigmine multiparticulates .
  • Rivastigmine instant release multiparticulates (prepared according to Example 1) were coated with Eudragit RS : Eudragit RL (98:2) aqueous dispersion.
  • a Eudragit RS Eudragit RL (98:2) aqueous dispersion was prepared as follows: 0.5g of Simethicone emulsion USP, to 2.515kg of purified water. The mixture was stirred for 15 minutes in a high shear mixer at 6000 rpm. The suspension was added to 1.960kg of Eudragit RS 30D and 40. Og of Eudragit RL 30D (ammonio methacrylatTe co- polymers in the form of aqueous dispersions from Rohm Pharma, Germany) and stirred for 20 minutes.
  • a polymer weight gain of 12% was coated onto the Rivastigmine coated multiparticulates and in process samples were taken at 6 , 8 and 10% polymer coating.
  • the coated multiparticulates were cured in an oven at 40°C for 40 hours, then screened to remove oversized multiparticulates and fine material.
  • Table 1 shows dissolution rates for sustained release multiparticulates. These profiles are illustrated in Figure 1.
  • Example 3 Preparation of delayed release (PR) Eudragit RS:RL (90:10) coated Rivastigmine multiparticulates.
  • a Eudragit RS Eudragit RL (90:10) aqueous dispersion was prepared as follows: 0.5g of simethicone emulsion USP, 120. Og of triethyl citrate and 360g of talc USP were added with mixing to 2.515kg of purified water. The mixture was stirred for 15 minutes is a high sharer mixer at jSOOO rpm. The suspension was added to 1.800kg of Eudragit RS 30D and 200g of Eudragit RL 30D (ammonio methacrylate co-polymers in the form of aqueous dispersions from Rohm Pharma, Germany) and stirred for 20 minutes .
  • Example 2 The resulting combined dispersion was sprayed onto instant release multiparticulates prepared according to Example 1, using a fluid bed apparatus as used in Example 1. Spray rate was 3.5-15g/min*kg, the inlet temperature was 38-42°C and the cores temperature was 25-30°C. A polymer coating of 40% polymer weight gain was coated onto the instant release multiparticulates and an in process sample was taken at 30% polymer coating. The multiparticulates were cured and screened as described in Example 2.
  • Example 4 Preparation of delayed release (PR) Eudragit RS:RL (98:2) over-coated Rivastigmine multiparticulates.
  • Eudragit RS:RL (90 : 10) coated Rivastigmine multiparticulates prepared according to Example 3 were coated with Eudragit RS : Eudragit RL (98:2) aqueous dispersion (prepared according to Example 2) , using triethyl citrate as plasticiser.
  • a polymer weight gain of 20% was over-coated to the Eudragit RS:RL (90:10) coated Rivastigmine multiparticulates, and an in process sample --"was taken at 10% polymer coating.
  • the multiparticulates were cured and screened as described in Example 2.
  • Example 5 Preparation of delayed release (PR) Eudragit RS:L (75:25) coated Rivastigmine multiparticulates.
  • Eudragit RS Eudragit L (75:25) organic solution was prepared as follows: 4.650kg of isopropyl alcohol were stirred with 125g of triethyl citrate and 3.750kg of
  • Eudragit RS12.5 for 5 minutes. 225g of talc (USP) were added and the mixture stirred for 15 minutes. 1.250kg of Eudragit L12.5 was added to the mixture and stirred for 30 minutes.
  • Example 2 The resulting • solution was sprayed onto instant release multiparticulates prepared according to Example 1, using a fluid bed apparatus as used in Example 1. Spray rate was 5-8.5g/min*kg, and the inlet temperature was 38-40°C. The instant release multiparticulates were maintained at 29-32°C. A polymer coating of 30% polymer weight gain was coated onto the instant release multiparticulates and an in process sample was taken at 20% polymer coating. The multiparticulates were cured and screened as described in Example 2.
  • Table 2 shows dissolution rates for the multiparticulates prepared in Examples 3, 4 and 5. Sample profiles are illustrated in Figure 2
  • Example 6 Manufacture of instant release (IR) Rivastigmine minitablets.
  • the instant release minitablets were produced by direct compression using the following method
  • Figure 3 shows a dissolution profile for instant release minitablets .
  • Example 7 Manufacture of sustained release (SR) Rivastigmine minitablets.
  • Rivastigmine SR minitablets were produced by direct compression using the following method 1. Add a similar quantity of the microcrystalline cellulose to the drug and bag blend for 1 minute .
  • Example 8 Coating of minitablets from Example 6 with the pH independent polymer Eudragit RS:RL (98:2).
  • a Eudragit RS : RL (98:2) aqueous dispersion was prepared as follows:
  • simethicone emulsion USP 12g of triethyl citrate and 36g of talc USP were added with mixing to 251.5g of purified water. The mixture was stirred for 15 minutes using a mixer at 1200rpm. This suspension was then added to 196g of Eudragit RS30D and 4g of Eudragit RL30D (ammonio methacrylate co-polymers in the form of aqueous dispersions from Rohm Pharma, Germany) and stirred for 20 minutes . The resulting dispersion was sprayed onto minitablets as manufactured in step la, using a fluidised bed coater with Wurster column insert.
  • the spray rate was 3.7-5.7g/ min, the inlet temperature was 30-39°C and the bed temperature 28-32 °C.
  • a coating of 20% polymer weight gain was applied and the tablets dried within the fluidised bed coater for 15 minutes and then dried for 40 hours in an oven.
  • Figure 4 shows dissolution profiles for these minitablet formulations .
  • Example 9 Coating of minitablets from Example 6 with the pH dependent polymer Eudragit S 12.5.
  • a Eudragit S 12.5 organic dispersion was prepared as follows :
  • the resulting dispersion was sprayed onto the sustained release minitablets from Example 6 using a fluidised bed coater with a Wurster column insert .
  • the spray rate was 8.4-10.4g/min and the inlet temperature 38-47°C.
  • the minitablets were maintained at approximately 33 °C.
  • a coating of 20% polymer weight gain was coated onto the minitablets with an in-process sample being taken at 15% polymer weight gain, the minitablets were dried for 15 minutes before removal from the fluidised bed coater.
  • Example 10 Coencapsulation of multiparticulates with minitablets .
  • Table 3 shows dissolution profiles for the individual components. These profiles are illustrated in Figure 6
  • Example 11 Coencapsulation of sustained release Rivastigmine multiparticulates and delayed release Rivastigmine multiparticulates.
  • Sustained release Eudragit RS:RL (98:2) coated Rivastigmine multiparticulates were coencapsulated with each of three different delayed release multiparticulates.
  • Instant release multiparticulates were prepared as described in Example 1, and were then coated with Eudragit RS:L (75:25) at 10%, Eudragit RS:L (75:25) at 15%, and Eudragit RS:L (65:35) at 15%.
  • compositions of the three different co-encapsulated formulations are set out below:

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Abstract

L'invention se rapporte à de nouvelles compositions pharmaceutiques conçues pour retarder la libération d'un agent pharmaceutiquement actif. Une formulation médicamenteuse à libération retardée encapsule l'ingrédient actif, qui peut être appliqué sur des microparticules ou se présenter sous forme de comprimés, dans un enrobage retardateur de libération comportant des matières polymères dotées de caractéristiques préétablies de gonflement/perméabilité. Il est en particulier possible d'utiliser des mélanges de polymère d'acide acrylique et/ou d'acrylate, modifiés par des groupes ioniques. Dans une réalisation préférée, un polymère ayant une perméabilité dépendante du pH est utilisé en tant qu'élément plus perméable de l'enrobage. Ces formulations à libération retardée sont administrées sous une seule forme posologique, conjointement à des formulations à libération instantanée ou à libération retenue, de sorte qu'une forme posologique unique, de préférence une forme posologique orale, peut efficacement délivrer deux doses à un patient à des instants différents.
EP00954802A 1999-08-26 2000-08-29 Compositions pharmaceutiques Withdrawn EP1206250A2 (fr)

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US15088099P 1999-08-26 1999-08-26
US15089199P 1999-08-26 1999-08-26
US150880P 1999-08-26
US150891P 1999-08-26
US151221P 1999-08-26
US15121199P 1999-08-27 1999-08-27
PCT/GB2000/003309 WO2001013898A2 (fr) 1999-08-26 2000-08-29 Compositions pharmaceutiques

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US9358214B2 (en) 2001-10-04 2016-06-07 Adare Pharmaceuticals, Inc. Timed, sustained release systems for propranolol
US6663888B2 (en) 2001-12-14 2003-12-16 Eurand Pharmaceuticals Ltd. Pulsatile release histamine H2 antagonist dosage form
AU2003296852A1 (en) * 2002-09-18 2004-05-04 Elan Corporation, Plc Multiparticulate modified release composition comprising beraprost
MY148805A (en) 2002-10-16 2013-05-31 Takeda Pharmaceutical Controlled release preparation
AU2003301762B2 (en) * 2002-10-25 2006-02-09 Collegium Pharmaceutical, Inc. Pulsatile release compositions of milnacipran
US8367111B2 (en) 2002-12-31 2013-02-05 Aptalis Pharmatech, Inc. Extended release dosage forms of propranolol hydrochloride
ES2241478B1 (es) * 2004-02-13 2006-11-16 Lacer S.A. Preparacion farmaceutica para la liberacion sostenida de un principio farmaceuticamente activo.
US8747895B2 (en) 2004-09-13 2014-06-10 Aptalis Pharmatech, Inc. Orally disintegrating tablets of atomoxetine
US9884014B2 (en) 2004-10-12 2018-02-06 Adare Pharmaceuticals, Inc. Taste-masked pharmaceutical compositions
CA2584957C (fr) 2004-10-21 2015-08-25 Eurand Pharmaceuticals Limited Compositions pharmaceutiques a saveur masquee avec substances porogenes gastrosolubles
US9161918B2 (en) 2005-05-02 2015-10-20 Adare Pharmaceuticals, Inc. Timed, pulsatile release systems
US8865197B2 (en) 2005-09-06 2014-10-21 Israel Oceanographic And Limnological Research Ltd. Food formulation for aquatic animals with integrated targeted delivery of bioactive agents
TW200711823A (en) * 2005-09-30 2007-04-01 Primax Electronics Ltd Laminating device and laminating method for use in same
SG10201407965XA (en) 2009-12-02 2015-02-27 Aptalis Pharma Ltd Fexofenadine microcapsules and compositions containing them
KR101990951B1 (ko) 2015-04-27 2019-06-20 주식회사 네비팜 리바스티그민 함유 서방출 의약조성물
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WO2001013898A2 (fr) 2001-03-01

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