Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Tablets – lozenges – or pills
Reexamination Certificate
2002-01-09
2003-05-27
Page, Thurman K. (Department: 1615)
Drug, bio-affecting and body treating compositions
Preparations characterized by special physical form
Tablets, lozenges, or pills
C424S451000, C424S452000, C424S461000, C424S465000, C424S469000, C424S479000, C424S480000
Reexamination Certificate
active
06569455
ABSTRACT:
The present invention relates to stable, fast-release melt extrudates comprising hydroxypropylcellulose of low viscosity and at least one active pharmaceutical ingredient and to a solvent-free process for their production, and to their use in the production of fast-release preparations.
Accurate control of release of active ingredients from preparations is of great pharmaceutical importance. In use besides slow-release preparations and those with controlled release are fast-release preparations which ensure a rapid rise in the level of the active ingredient in the circulation in an acute pathological state.
Extrusion processes are frequently used to produce corresponding preparations. The principle of melt extrusion has been known for a long time (Beckmann 1964). In the extrusion process, active ingredients and polymer are conveyed either simultaneously, without previous mixing, or as mixture, after previous mixing, in an extruder which has been heated so that the mixture becomes extrudable and the active ingredient is not degraded.
In contrast to conventional coprecipitate methods, the use of solvents is unnecessary in this case: this is particularly important because, besides the economic aspects, the use of solvents leads to special technical problems such as prevention of explosions in the premises and equipment.
The production of preparations with rapid release of active ingredient by melt extrusion of hydroxypropylcellulose (HPC) with a molecular weight of from 60 000 to 200 000 is described in the application WO 96/25149. The content of hydroxypropylcellulose in these preparations is from 10 to 30, preferably 20 to 30, % by weight.
Such low contents of polymer are disadvantageous from the pharmaceutical viewpoint because the resulting preparation is, especially on use of high-potency active ingredients, very small and thus difficult for the patient to handle, which considerably reduces patient compliance. Extending the preparation with fillers in turn increases the number of ingredients used and thus complicates the process. This is disadvantageous inter alia in relation to the compatibility of the fillers with the active ingredient in particular at elevated temperature during the extrusion.
A further disadvantage is the difficulty of maintaining content uniformity, i.e. the uniformity of the preparations in relation to the amounts of active ingredient.
One object of the present invention is to be regarded as being to provide fast-release, stable extrudates with good content uniformity and handleability for all types of active ingredients, in particular for slightly soluble active ingredients.
It has now been found, surprisingly, that transparent melt extrudates with the desired fast release and high stability can be obtained in a simple manner with the specifically selected polymer hydroxypropylcellulose of low viscosity with an average molecular weight of from 30 000 to 100 000 and with a molar degree of substitution of at least 3 in an amount of at least 50% by weight, preferably 66% by weight, based on the active ingredient/polymer mixture in conjunction with amorphous active ingredients.
The melt extrudates of the invention comprise hydroxypropylcellulose of low viscosity with an average molecular weight of from 30 000 to 100 000 and with a molar degree of substitution of at least 3 in an amount of at least 50% by weight, preferably 66% by weight, based on the active ingredient/polymer mixture, one or more active ingredients and, where appropriate, excipients.
Preferred melt extrudates comprise hydroxypropylcellulose in an amount of at least 66% by weight based on the active ingredient/polymer mixture.
The hydroxypropylcellulose preferably has an average molecular weight of from 55 000 to 70 000.
The molar degree of substitution refers to the average number of moles of propylene oxide reacted per glucose unit in the cellulose.
The present application also relates to preparations produced with use of the extrudates of the invention. Fast-release extrudates or preparations mean for the purposes of the invention those which release 80% of the active ingredient(s) within 60 min in the USP XXII paddle method. The extrudates or preparations of the invention display very rapid release and show a significant supersaturation. They are therefore particularly well suited for fast reaching of high plasma concentrations of active ingredient. The fast release can be controlled as required by varying the production parameters. The release of active ingredient is influenced, for example, by the concentration of active ingredient in the final product or by extrusion process parameters such as the screw geometry, the extrusion rate, the extrusion temperature, the diameter and surface area of the extrudate etc. The release rate is influenced in particular by the particle size of the extrudate. In single-unit dosage forms such as, for example, tablets, the release is influenced in particular by the content of disintegrant in the finished formulation.
Fast release, but at different times, of the active ingredient on oral administration can be achieved by coating the extrudates or preparations in such a way that they release the active ingredient only in a particular region of the gastrointestinal tract, for example with Eudragit L or S. Coatings of this type are dissolved, for example, specifically at particular pH values and make release possible at the optimal site. It is possible in this way, for example, to protect acid-sensitive active ingredients until the appropriate absorption window is reached (see in this connection Chang, R., Pharmaceutical Technology, October 1990).
It is also possible during the melt extrusion or during further processing, for example tableting, to use other conventional excipients which are conventional in pharmacy in the production of preparations and are known from the literature, such as, for example, magnesium stearate or masking flavors. None of these excipients is, however, necessary in order to achieve essentially the desired fast release of the drug.
In a preferred embodiment, the extrudate or the preparation is administered orally. For this purpose, in one embodiment, the extrudate of the invention is comminuted, for example ground to an average particle diameter of less than 0.5 mm, and packed into gelatin capsules or as sachets.
In a further embodiment, the extrudate of the invention is, where appropriate in comminuted form, mixed with a disintegrant and, where appropriate, further excipients and processed to a single-unit dosage form. Disintegrants are substances which ensure rapid disintegration of the single-unit dosage form in aqueous solution, such as, for example, crosslinked polyvinylpyrrolidone (PVPP). In this case it is preferred to use large amounts of disintegrant, that is to say more than 0.1 part by weight of disintegrant per 1 part of extrudate (active ingredient and HPC).
Single-unit dosage forms mean preparations which are administered as a single dose, for example tablets, coated tablets or capsules.
It is further possible in this way to produce combination products which comprise in a single-unit dosage form contents of different active ingredient-containing extrudates: thus, it is possible to use different active ingredients but also different extrudates differing in release profile in order to control accurately active ingredient contents in the circulation over time.
The active ingredient to be used may be any drugs such as, for example, antiinfectives, cardiovascular agents, antimycotics, antidepressants, antidementia agents, antiepileptics, antiinflammatory agents, analgesics, antiasthmatics, antithrombotics, antitumor agents, antimalarials, non-steroidal antiinflammatory drugs (NSAID), diuretics, antiarrhythmics, hypoglycemic agents, ACE inhibitors, sedatives, decongestants, antihistamines or lipid-lowering agents. Also suitable as active ingredients are crop protection agents or veterinary agents. For the purposes of the present invention, only those drugs which do not decompose under the temperature and processing con
Kanikanti Venkata-Rangarao
Sdebik Jürgen
Page Thurman K.
Pellegrino Susan M.
Tran S.
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