Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Tablets – lozenges – or pills
Reexamination Certificate
2000-05-31
2002-02-26
Spear, James M. (Department: 1615)
Drug, bio-affecting and body treating compositions
Preparations characterized by special physical form
Tablets, lozenges, or pills
C424S468000, C424S482000, C514S772300, C514S781000, C514S770000, C514S772200, C514S777000, C514S784000
Reexamination Certificate
active
06350471
ABSTRACT:
BACKGROUND OF THE INVENTION
Numerous drugs require a delayed release dosage form. However, current technology for manufacturing such dosage forms usually involves matrix technology or the use of pore-forming agents. In some instances, these routes cannot be followed.
There is a need to obtain new release dosage form, which can be applied to numerous drugs, especially oxybutynin hydrochloride, propranolol hydrochloride, buspiron hydrochloride, niacin, cetirizin hydrochloride, cerivastin sodium, metoprolol fumarate, and alendronate sodium.
SUMMARY OF THE INVENTION
The invention provides a controlled release tablet comprising:
(i) a core comprising the active ingredient and conventional excipients; and
(ii) a coating consisting essentially of a water-insoluble, water-permeable film-forming polymer, a plasticizer and a water-soluble polymer.
The invention thus provides a new drug controlled release composition under the form of a tablet, the core of which comprising the active ingredient. Also, the controlled release is obtained thanks to a semi-permeable release coating, free of (monomeric) pore-forming agent. The tablets of the invention exhibit specific dissolution profiles.
DETAILED DESCRIPTION OF THE INVENTION
The invention consists in a tablet comprising a core and a coating.
The core includes the active ingredient, and conventional excipients, notably a lubricant, and a binder and/or a filler, and optionally a glidant as well as other excipients.
Examples of lubricants include stearic acid, magnesium stearate, glyceryl behenate, stearyl behenate, talc, mineral oil (in PEG), sodium stearyl fumarate, etc.. Stearyl behenate is one preferred lubricant. Examples of binders include water-soluble polymer, such as modified starch, gelatin, polyvinylpyrrolidone, polyvinylalcohol (PVA), etc.. The preferred binder is polyvinylalcohol. Examples of fillers include lactose, microcristalline cellulose, etc, the latter being preferred. An example of glidant is silicon dioxide (Aerosil® of Degussa). A further pharmaceutical aid that can be used with advantage in the invention is fumaric acid. The above binders, lubricants, fillers, glidants, and any other excipient that may be present can further be found in the relevant literature, for example in the Handbook of Pharmaceutical Excipients. An acidifying or alkanizing agent can be present. The relative amounts of ingredients in the core are preferably as follows. The proportion of active ingredient in the core may vary between broad limits, as will recognize the skilled man. The proportion of lubricant and/or glidant, of binder, filler or any other excipients may also vary between broad limits, as will recognize the skilled man in the pharmaceutical field.
The active ingredient is preferably selected from the group consisting of oxybutynin hydrochloride, propranolol hydrochloride, buspiron hydrochloride, niacin, cetirizin hydrochloride, cerivastin sodium, metoprolol fumarate, and alendronate sodium.
The manufacturing process of the core can be as follows. The active ingredient and optionally other ingredients is first granulated with a binder, in a granulator, preferably but not necessarily a fluidized bed granulator. The binder is first dissolved or dispersed in a suitable solvent, preferably water. The solution or suspension of binder is then sprayed onto the drug in a granulator, e.g. fluidized bed granulator. For example, fluidized bed granulators manufactured by Glatt (Germany) or Aeromatic (Switzerland) can be used for this operation. An alternative process can be to use a conventional or high shear mixer to proceed granulation. If necessary, the drug can be mixed with a filler, prior to the granulation step. Granules once dried can be mixed with the other excipients, especially with the lubricant, but also with glidants and any other excipient suitable to improve processing. The mixture of granules (preferably with lubricant), and optionally glidant is pressed into tablets. Alternatively, the active ingredient and lubricant and/or glidant can be mixed in a granulator, e.g. a fluidized bed granulator, and heated to the melting point of the lubricant to form granules. This mixture can then be mixed with a suitable filler and compressed into tablets. Also, it is possible to mix the active ingredient and the lubricant in a granulator, e.g. a fluidized bed granulator, and then to press the resulting granules into tablets. Tablets can be obtained by standard techniques, e.g. on a (rotary) press (for example Manesty Betapress®) fitted with suitable punches. The resulting tablets are hereinafter referred as tablet cores.
These tablet cores are then coated with the semi-permeable coating designed to achieve a controlled release of metformin.
The coating comprises a water-insoluble, water-permeable film-forming polymer, together with a plasticizer and a water-soluble polymer.
The water-insoluble, water-permeable film-forming polymer can be a cellulose ether, such as ethylcellulose, a cellulose ester, such as cellulose acetate, etc. The preferred film-forming polymer is ethylcellulose (available from Dow Chemical under the trade name Ethocel®). The plasticizer can be an ester such as a citrate ester or dibutyl sebacate, an oil such as castor oil, a polyalkyleneglycol such as polyethyleneglycol of various MWs, a fatty acid such as stearic acid. The preferred plasticizer is stearic acid. The water-soluble polymer is preferably polyvinylpyrrolidone (PVP) or a cellulose ether such as hydroxypropylcellulose (HPC). Some other excipients can be used in the coating, as for example acrylic acid derivatives (available from Roehm Pharma under the trade name “Eudragit®”), pigments, etc.. The relative amounts of ingredients in the coating are preferably as follows. The proportion of water-insoluble, water-permeable polymer (e.g. ethylcellulose) in the coating may vary between 20 and 85% of the coating dry weight. The proportion of water-soluble polymer (e.g. polyvinylpyrrolidone or HPC) in the coating may vary between 10 and 75% of the coating dry weight. The proportion of plasticizer (e.g. stearic acid) in the coating may vary between 5 and 30% of the coating dry weight. The relative proportions of ingredients, notably the ratio water-insoluble, water-permeable film-forming polymer to water-soluble polymer, can be varied depending on the release profile to be obtained (where a more delayed release is generally obtained with a higher amount of water-insoluble, water-permeable film-forming polymer).
The coating process can be as follows. Ethylcellulose, stearic acid and polyvinylpyrrolidone or HPC are dissolved in a solvent such as ethanol. The resulting solution is sprayed onto the tablet cores, using a coating pan or a fluidized bed apparatus.
The weight ratio coating/tablet core is comprised e.g. between 1/50 and 5/10.
The tablet comprises an amount of active ingredient that can be from 0.1 to 1500 mg per tablet, depending on the specific active ingredient selected.
Surprisingly, it was discovered that the above formulation did not lead to any degradation of the active ingredient though no stabilizer was present in the formulation. Stability studies were conducted in oven, under the storage test conditions described in the US pharmacopoeia 23
rd
edition page 1961. Under these conditions no significant change in drug potency could be seen.
Surprisingly, it was also discovered that the above formulation did provide a controlled (sustained) release though no pore-forming agent was present in the coating.
The invention thus provides a controlled release tablet free of stabilizer and free of pore-forming agent, exhibiting a dissolution profile such that after 2 hours, from 5 to 40% of the active ingredient is released, after 4 hours, from 10 to 60% of the active ingredient is released, after 12 hours, from 50 to 98% of the active ingredient is released, after 24 hours, more than 80% of the active ingredient is released.
BEST MODES FORE CARRYING THE INVENTION
A preferred tablet composition comprises:
(i) a core comprising the active ingredient, optionally sili
Alston & Bird LLP
Pharma Pass LLC
Spear James M.
LandOfFree
Tablet comprising a delayed release coating does not yet have a rating. At this time, there are no reviews or comments for this patent.
If you have personal experience with Tablet comprising a delayed release coating, we encourage you to share that experience with our LandOfFree.com community. Your opinion is very important and Tablet comprising a delayed release coating will most certainly appreciate the feedback.
Profile ID: LFUS-PAI-O-2977819