WO1985003436A1

WO1985003436A1 - Diffusion coated multiple-units dosage form

Info

Publication number: WO1985003436A1
Application number: PCT/DK1985/000005
Authority: WO
Inventors: Kim KJO^/RNA^ES; Finn Norring Christensen; Jens Rasmus Jensen
Original assignee: A/S Alfred Benzon
Priority date: 1984-02-10
Filing date: 1985-02-08
Publication date: 1985-08-15
Also published as: AU571312B2; HK1000201A1; DE3586600D1; EP0153105A2; AU3935985A; CA1247009A; IE59287B1; DK462685D0; US4716041A; EP0153105B1; EP0153105A3; DK462685A; JPH0759499B2; DK158032C; DK158032B; DE3586600T2; JPS61501150A; IE850307L

Abstract

In an oral pharmaceutical controlled release multiple-units formulation, individual units containing an active substance are coated with a substantially water-insoluble, but water-diffusible controlled release coating which includes 1) an inner film layer which causes adhesion between the units at elevated temperatures, comprising a water-dispersible film-forming agent, and 2) an outer film layer comprising a water-based film-forming agent which prevents adhesion between the units at elevated temperatures and imparts flowability to the units. The inner film layer may additionally comprise a substance which is capable of forming a continuous phase. By subjecting the thus coated units to heating to accelerate the formation of a continuous phase of the film-forming agent of the inner layer and optionally also of the additional substance, a coating is formed which substantially does not change its diffusion characteristics in the course of time.

Description

DI FFUS ION COATED MULTI PLE-UN ITS DOSAGE FORM

The present invention relates to an oral pharmaceutical controlled release multiple-units dosage form in which individual units containing an active substance are coated with a water-based diffusion coating .

TECHNICAL BACKGROUND

Many physiological factors influence both the gastrointestinal transit time and the release of a drug from a controlled release dosage form and thus the uptake of the drug into the systemic circulation . Dosage forms should therefore be designed so that such variable factors do not compromise the efficacy and safety of the product.

In humans, a reproducible gastrointestinal transit time of a depot formulation can be achieved only by a controlled release multiple-units dosage form.

The term "controlled release multiple-units formulation" (Bechgaard & Hegermann Nielsen, 1978) indicates a pharmaceutical formulation com¬ prising a multiplicity (typically at least 100) of individual coated (or "microencapsulated") units contained in the formulation in such a form that the individual units will be made available from the formulation upon disintegration of the formulation in the stomach of animals, including humans, who have ingested the formulation . Typically, the multiple-units formulation may be a capsule which disintegrates in the stomach to make available a multiplicity of individual coated units con¬ tained in the capsule, or a tablet which disintegrates in the stomach to make available a multiplicity of coated units originally combined in the tablet.

Drug release from a controlled release dosage form is generally con¬ trolled either by diffusion through a coating or by erosion of a coat¬ ing by a process dependent on, e. g. , enzymes or pH . The importance of a pH independent diffusion with respect to obtaining a reproducible rate of availability and to minimizing intra- and intersubject variations is known (GB Patent No. 1 468 172 and Bechgaard & Baggesen, 1980) . It is also known that controlled drug release in vivo can be achieved through an erodable process by enteric coating of a mul¬ tiple-units dosage form (Green, 1966; McDonald et al. , 1977; Bogen- toft et al., 1978) .

Both above-mentioned types of controlled release multiple-units formu¬ lation techniques aim at a controlled release of active substance in a predetermined pattern to reduce and delay the peak plasma concen¬ tration without affecting the extent of drug availability. Due to a lower peak plasma concentration, the frequency of undesirable side- effects may be reduced, and due to the delay in the time it takes to obtain the peak plasma concentration and the prolongation of the time at the therapeutically active plasma concentration, the dosage fre¬ quency may be reduced to a dosage taken only twice or once a day, in order to improve patient compliance.

A further advantage of the controlled release multiple-units dosage form is that high local concentrations of the active substance in the gastrointestinal system is avoided, due to the units being distributed freely throughout the gastrointestinal tract, independent of gastric emptying. If the mucosa of the stomach is more sensitive to the active substance than the intestinal mucosa, controlled release formulations avoiding release of active substance in the gastric area will be pre¬ ferred; formulations of this type are controlled release multiple-units formulations in which the coatings are substantially resistant to gastric conditions .

The present invention deals with multiple-units dosage forms which are diffusion coated.

In the known art preparation of diffusion coated controlled release multiple-units formulations, diffusion film-coating mixtures have been used which contain synthetic film-forming agents dissolved or dis¬ persed in organic solvents, e.g. isopropanol, ethanol, acetone, or mixtures thereof. However, although these mixtures show advantages in that the film-forming agents are diffusion controlling per se, that is, without any modification or addition, and the film formed is non- tacky, they suffer from serious disadvantages from an environmental and process -economic point of view:

The use of organic solvents gives rise to environmental pollution, danger of explosion, and health hazards unless costly recycling procedures are used, such as recycling in scrubber towers, and the fact that the film coating mixtures have a low dry matter content (normally less than 15% by weight) , incurs long processing periods resulting in a low process efficiency.

From an environmental and process-economic point of view, water-ba¬ sed film-coating mixtures are more desirable; the present invention concerns developments relating to water-based film coatings.

DISCLOSURE OF THE INVENTION

A number of coatings employed in connection with pharmaceutical controlled release multiple-units formulations and based on water-dis- persible film-forming agents have been observed to suffer from the disadvantage that they change their release characteristics in the course of time due to the fact that a coagulation and consequently formation of a continuous phase proper of the film-forming agent only occurs over a longer period of time. This means that it is not possi¬ ble to maintain a reproducible release rate of an active substance contained in the multiple-units formulation as a decreasing release rate has been observed for such coatings . In accordance with the present invention, it has. surprisingly been found that by heating units coated with such coatings, the formation of a continuous phase of the film-forming agent and the relaxation of the long, intertangled polymer chains of the film-forming agent, that is, the chains are relaxed to their lowest possible energy level, is accelerated so that the resulting coating will be a diffusion coating which substantially does not change its diffusion characteristics in the course of time, whereby storage stability is imparted to the pharmaceutical composi¬ tion comprising the coated units. Thus, an aspect of the present invention relates to a method of preparing an oral pharmaceutical controlled release multiple-units formulation in which

a) individual units containing an active substance are coated with a coating composition comprising an aqueous dispersion of a film- forming agent to form an inner film layer which causes adhesion between the units at elevated temperatures,

b) the thus coated units are provided with an outer film layer of a water-based film-forming agent which prevents adhesion between the units at elevated temperatures and imparts flowability to the coated units, and

c) the coated units are subsequently heated to a temperature at which the inner film layer is tacky, and at which the formation of a continuous phase of the film-forming agent is accelerated, and subsequently cooled, whereby a coating which substantially does not change its diffusion characteristics in the course of time is formed.

The inner film layer may additionally comprise a substance which is capable of forming a continuous phase, the presence of which sub- stance imparts specific desirable characteristics to the final coating, especially with respect to the formation of a coating which delays and controls the diffusion through the inner film layer in a useful and reproducible manner to confer desirable controlled release characteris¬ tics to the coated units . When used in connection with this additional substance, the term "capable of forming a continuous phase" is inten¬ ded to indicate that the substance is capable, in itself, that is, without admixture with other components, of forming a continuous phase (that is, either by being molten or by being dissolved and subjected to removal of the solvent) , and that it forms a homogeneous lattice-like structure in the inner layer. The term "homogeneous" is intended to indicate that, throughout the inner layer, the two compo¬ nents are present in the same proportions and uniformly distributed in each other. In the present context, the term "diffusion coating" indicates a coating which does not disintegrate or dissolve in water, but which gradually lets the active substance in the units pass through . The term is intended to include the so-called enteric coat¬ ings which at an acid pH have properties similar to those of the conventional diffusion coatings.

When an additional substance is incorporated in the inner layer, the coated units are also subjected to elevated temperatures, either to cause formation of a continuous phase of the substance in question in the film-forming agent concurrently with accelerating the formation of a continuous phase of the film-forming agent as described above or solely to accelerate the formation of a continuous phase of the film- forming agent, which may be further impeded by the presence of the substance which may constitute a steric hindrance to the coagulation of the film-forming agent to further prolong the period needed for the film-forming agent to form a continuous phase.

An example of a substance which needs heating to form a continuous phase in the inner film layer is a hydrophobic substance which con¬ tributes to delaying and controlling diffusion through the inner layer. It has in fact surprisingly been found that by incorporating a hydro- phobic substance in the inner layer, it may be possible to use film- forming substances which are not in themselves diffusion-controlling as diffusion-controlling coatings, and water-dispersible film-forming substances which in themselves are diffusion-controlling are improved to obtain a more efficient diffusion control, both combining the inhe- rent advantages of the diffusion controlled release multiple-units formulations and the easy, economic, and hazard-free application of water-based coating mixtures. I n order to contribute to the sustained release effect, however, the hydrophobic substance should be present in the form of a film which is homogeneously mixed with the film of the film-forming substance. Therefore, the units coated according to steps a) and b) in the method outlined above, after which steps the hydrophobic substance is present in the inner film layer as a disperse phase, are suitably heated to a temperature above the melting point of the hydrophobic substance which, on melting and subsequent cooling, forms a continuous phase in the inner film layer in homoge- neous admixture with the film-forming agent. The hydrophobic sub¬ stance is preferably present in the coating composition in the form of a suspension of particles thereof.

An example of a substance which delays the coagulation of the film- forming agent in the inner film layer is a polymeric substance which prevents adhesion between the units during coating and which, in the final coating, is homogeneously admixed with the continuous phase of the film-forming agent in the inner layer imparting compressibility to the coating. In the present context, the term "compressibility" when used to describe a property of the coating refers to a coating pos¬ sessing a sufficient plastic deformability to result in no significant changes in the release characteristics of compressed coated units relative to non-compressed coated units. It has surprisingly been found that such compressibility may be provided by homogeneously mixing the film-forming agent with a polymeric substance which func¬ tions as a reinforcing agent by imparting greater hardness as well as plastic deformability to the layer. When units coated according to steps a) and b) above are heated, coagulation of the film-forming agent is accelerated, and the film-forming agent forms a continuous phase in homogeneous admixture with the polymeric substance so that a reproducible release rate of the active substance in the units is obtained.

The water-dispersible film-forming agents contemplated for the pur¬ pose of the present invention are pharmaceutically acceptable film- forming polymers which are substantially water-insoluble, but which permit water diffusion . Examples of such substances are cellulose derivatives, silicone polymers and copolymers, vinyl polymers and copolymers, acrylic polymers and copolymers and biodegradable poly¬ mers such as polyamino acids, polylactic acid and copolymers and derivatives thereof, or mixtures thereof. More specifically, the film- forming substance is selected from ethylcellulose and a copolymerisate of anionic or non-ionic poly (meth) acrylic acid esters, hydroxypropyl- methylcellulosephthalate, celluloseacetatephthalate, polyvinylacetate- phthalate and vinylacetate-crotonic acid copolymerisates. When a hydrophobic substance is incorporated in the inner film layer according to the invention, it may be any pharmaceutically acceptable hydrophobic substance which will result in the desired retardation of the diffusion (in the present context, the term "hydrophobic" indica- tes substances which, relative to water, have a contact angle of more than 90°) . All such hydrophobic substances are substances which in themselves are capable of forming a continuous phase. The amount of the hydrophobic substance incorporated will depend on the properties of the hydrophobic substance, in particular its hydrophobicity, with respect to retarding the water diffusion of the polymeric film.

Typical examples of such hydrophobic substances are substances se¬ lected from hydrocarbons and hydrocarbon derivatives, waxes, oils and fats, and mixtures thereof.

One class of hydrophobic substances which are interesting for the purposes of the present invention are waxy substances, examples of which are

natural waxes such as paraffin wax, microcrystalline wax, other mineral waxes, e. g. montan wax or ceresin wax, vegetable waxes, e. g . candelilla wax, carnauba wax or cocoa butter, or animal waxes, e. g . beeswax, spermaceti or wool wax,

synthetic waxes such as fatty alcohols and acids, e. g . cetyl alco¬ hol, stearyl alcohol, stearic acid, palmitic acid or myristic acid, fatty esters and glycerides, e. g . glyceryl stearates, hydrogena- ted oils, e. g . hydrogenated castor oil, higher ketones, amines or amides, e. g . stearone or lau rone, synthetic hydrocarbon waxes, synthetic animal waxes and other synthetic waxes,

- and mixtures thereof.

The hydrophobic substances will often have a melting temperature be¬ low 200°C, more often below 150°C and usually below 100°C. ^ The hydrophobic substance, e.g. a waxy substance such as paraffin wax, will normally be present in the inner film layer in an amount of between about 0.1 and 50%, in particular between 1 and 40%, especi¬ ally between about 10 and 30%, by weight of the inner film layer.

When a polymeric substance is incorporated in the inner film layer according to the invention, it may be any pharmaceutically acceptable polymeric substance which will bring about the desired compressibility of the coating. As is the case with the hydrophobic substances, the polymeric substances to be employed according to the invention are substances which, in themselves, are capable of forming a continuous phase. The amount of the polymeric substance incorporated will de¬ pend on the properties of the polymeric substance, in particular its film-forming properties and its hardness and plasticity. Apart from this, it is important that the polymeric substance is one which con- tributes to imparting anti-adhesive properties to the inner film layer during coating.

The polymeric substance is preferably a water-soluble polymeric substance as substances which are precipitated from an aqueous solution during the coating process are more easily homogeneously admixed with the film-forming agent in the inner film layer. Typical examples of such polymeric substances are polyvinylpyrrolidone, poly- alkylene glycols such as polyethylene glycol, and cellulose derivatives such as hydroxypropylcellulose, carboxymethylcellulose, methylcellulo- se, propylcellulose, hydroxyethylcellulose, carboxyethylcellulose, carboxymethylhydroxyethylcellulose, hydroxymethylcellulose, carboxy- methylethylcellulose, methylhydroxypropylcellulose or hydroxypropyl- methylcellulose.

The polymeric substance will normally be present in the inner film layer in an amount of between about 1 and 10%, in particular between about 2 and 8%, especially about 4%, by weight relative to the amount of film-forming agent in the inner film layer. If the substance is a waϊer-soluble substance, such as one of those mentioned above, it is important not to incorporate it in amounts which would significantly reduce or even destroy the sustained release effect. It may be . advantageous to incorporate an anti-adhesive in the inner film layer in order to avoid agglomeration of the units during the coating step a) above. However, when the inner layer comprises a polymeric substance with an inherently anti-adhesive effect, it may only be necessary to add small amounts of this anti-adhesive (if any) , which is desirable as the anti-adhesives usually employed for the present purpose do not contribute to the desired sustained release and often necessitate the use of larger amounts of coating material which, in turn, prolongs the coating process. The anti-adhesive is preferably a finely divided, substantially insoluble, pharmaceutically acceptable non-wetting powder having anti-adhesive properties in the coating. Examples of anti-adhesives are metallic stearates such as magnesium stearate or calcium stearate, microcrystalline cellulose, or mineral substances such as calcite, substantially water-insoluble calcium phosphates or substantially water-insoluble calcium sulphates, colloidal silica, titanium dioxide, barium sulphates, hydrogenated aluminium silicates, hydrous aluminium potassium silicates and talc. The preferred anti-adhesive is talc. The anti-adhesive, e.g. talc, is preferably incorporated in the coating in an amount of between about 0.1 and 50%, preferably between 1 and 40%, especially about 10-30%, such as about 15%, by weight of the inner film layer. The particle size of the anti-adhesive should normally be below about 40 μm, as by selecting a small particle size a larger surface area is obtained; the consequent higher anti-adhesive effect makes it possible to incorpora- te smaller amounts of anti-adhesive. The particle size should also be adapted so as to prevent sedimentation of the anti-adhesive in the coating mixture or blocking of jets and tubes in the coating equip¬ ment.

In most cases, it has been found that, when subjected to the elevated temperatures necessary to obtain the effect described above, the in¬ ner film layer tends to become tacky (adhesive) causing an undesira¬ ble agglomeration of the units . The tackiness on heating may either be due to an inherent property of the film-forming agent and is, in fact, a common characteristic of many water-dispersible film-forming agents, or it may be due to the presence of the additional substance described above. This latter, for instance, is the case with film layers containing a hydrophobic substance, as the formation of the continuous phase of the hydrophobic substance in homogeneous admixture with the film- forming substance necessary to provide the aimed-at additional sus- tained release is most conveniently performed by heating the units to a temperature above the melting point of the hydrophobic substance. This treatment, however, is not possible with coatings of this compo¬ sition as the hydrophobic substance tends to become sticky or tacky with heating causing the units to agglomerate.

In both instances, i . e. both when the substance incorporated in the coating and when the film-forming agent itself causes adhesion, it is therefore necessary to provide the units with an additional, protective layer which is composed of a substance or a mixture of substances which is anti-adhesive at elevated temperatures and, preferably, also imparts flowability to the coated units . In cases where a hydrophobic substance is incorporated in the inner layer, the outer layer should furthermore be one which, at temperatures above the melting point of the hydrophobic substance, is impermeable to the molten hydrophobic substance.

As a general rule, the film-forming agent in the outer film layer is one which is anti-adhesive at temperatures above about 40°C, especi¬ ally temperatures above about 50°C, such as a temperature between about 60°C and about 120°C. The choice of a specific film-forming agent of the outer film layer may depend on the melting temperature of a particular hydrophobic substance employed. However, additional criteria may also be applied to select a film-forming agent with the desired properties. For instance, it may in some cases be advantage¬ ous to provide a further sustained release effect, so the outer layer may also function as an additional diffusion barrier throughout the gastrointestinal tract or be one which is dissolved in intestinal fluids only (an enteric coating) . Furthermore, the outer layer may addition¬ ally contain an active substance which may either be the same sub¬ stance as the one contained in the units, and which may for instance be designed for instant release, or which may be another drug ad- vantageously administered simultaneously therewith . These additional characteristics are not vital, however, and suitable film-forming agents for this purpose are found within most categories of film- forming agents. The film-forming agent of the outer layer is most preferably water-based, which means that the film-forming material is one which is either water-dispersible or water-soluble.

Examples of such agents are diffusion coating materials such as ethyl- cellulose or enteric coating materials such as anionic poly(meth)acrylic acid esters, hydroxypropyimethylcellulosephthalate, ceiluloseacetate- phthalate, polyvinylacetatephthalate, polyvinylacetatephthalate-crotonic acid copolymerisates, or mixtures thereof, or water-soluble coating materials such as water-soluble cellulose derivatives, e. g. hydroxy- propylcellulose, carboxymethylcellulose, methylcellulose, p ropy lcel I u lo¬ se, hydroxyethylcellulose, carboxyethylcellulose, carboxymethylhydro- xyethylcellulose, hydroxymethylcellulose, carboxymethylethylcellulose, methylhydroxypropylcellulose and hydroxypropylmethylcellulose. The currently favoured film-forming agent for the outer layer is in fact hydroxypropylmethylcellulose although, as indicated above, it is water-soluble and thus does not contribute to delaying release. The layer of the protective film-forming agent need not be particularly thick, and is usually applied in an amount of about 0.1 -10%, espe¬ cially about 0.5-5%, in particular about 1% by weight of the uncoated units .

According to the invention, it has been found that the properties of the outer layer with respect to imparting improved flowability to the powder of the coated units may be considerably improved if a lubri¬ cant is incorporated therein in admixture with the film-forming agent. The lubricant is preferably present in the form of a finely divided, pharmaceutically acceptable powder, such as a metallic stearate, e.g. magnesium stearate or calcium stearate, microcrystalline cellulose, or a mineral substance such as titanium dioxide, calcite, calcium phospha¬ te, calcium sulphate, colloidal silica, barium sulphates, hydrogenated aluminium silicates, or hydrous aluminium potassium silicates . Most preferably, the lubricant is talc. The individual units of the multiple-units formulations according to the invention will normally be either coated crystals or pellets (coated cores) . In the pellets, the core is constituted by a combination of active substance and excipients . A type of core which is widely used in the known art (vide, e.g. , European Patent Application, Publica¬ tion No. 0 013 262) is a substantially spherical particle of a size of about 0.5 - 1 mm consisting of excipient(s) with active substance applied to its surface. Typical cores of this type are the so-called "non-pareil" cores where the excipients are in the form of spherical particles of saccharose. It is also known, e.g. , from GB Patent Speci¬ fication No. 1 468 172, to prepare cores which are cross-sectionally substantially homogeneous . In the present context, the term "cores which are cross-sectionally substantially homogeneous" designates cores in which the active substance is not confined to an exterior layer on the core body, in other words normally cores which, through the cross-section of the core body, contain substantially the same type of composition comprising microparticles containing active sub¬ stance, in contrast to the non-pareil type of cores which each consist of an excipient body with active substance applied to its surface, and in contrast to coated crystal units which are substantially monolithic crystals. From this definition, it will be understood that the cores which are cross-sectionally substantially homogeneous will normally consist of a mixture of active substance with excipient(s) , (and in spite of the term "homogeneous", this mixture will not necessarily be qualitatively or quantitatively homogeneous through the cross-section of the particle but may show, e.g. , a concentration gradient of one or more of its constituents) or they may consist substantially solely of active substance in a non-monolithic form, e.g. as a sintered mass of crystalline or amorphous particles of active substance. In the follow- ing specification and claims, such cores which are cross-sectionally substantially homogeneous will, for the sake of brevity, often simply be designated "cores" .

The oral pharmaceutical controlled release multiple-units formulation according to the invention will typically be a capsule containing a multiplicity of the units, typically more than 100, a sachet containing a multiplicity of the units, typically more than 1000, or a tablet made from a multiplicity of the units, typically more than 100, in such a manner that the tablet will disintegrate substantially immediately upon ingestion in the stomach into a multiplicity of individual units which are distributed freely throughout the gastro-intestinal tract.

The pharmaceutical formulation of the invention may also be one in which units of the type described above, that is, diffusion coated units are combined with uncoated units which comprise the same or another active substance for instant release thereof, and/or with non-diffusion coated units which have been provided with a coating selected from hydrophilic coatings, hydrophobic coatings, water-based coatings and organic coatings imparting desired properties to the unit such as acid or alkali resistance, storage stability, taste masking, light stability, colouring, improved processability, etc. The ratio between diffusion coated and uncoated or non-diffusion coated units in the composition may be adjusted according to, for instance, the desired release characteristics of the compositon , but is preferably in the range of about 10:90 - 90: 10 of diffusion coated units to uncoated or non-diffusion coated units .

The formulations mentioned above may be prepared by conventional methods known in the pharmaceutical industry. One particularly interesting shape of a tablet according to the invention, in particular when the tablet is to contain a rather large amount of active sub¬ stance and is to be easy to swallow, is a shape substantially corres¬ ponding to a cylinder with rounded ends, a raised area circumscrib- ing the periphery of the cylinder in the form of a flat belt and a score dividing the cylinder, but not the peripheral belt, into two parts, substantially as shown in the drawing. As an example of such tablets may be mentioned tablets in which the active substance is potassium chloride crystals, e. g . in tablet sizes comprising 600 mg and 750 mg of potassium chloride, respectively, for use as potassium supplement for patients in diuretic treatment.

In another aspect, the present invention relates to an oral pharma¬ ceutical controlled release multiple-units formulation with the charac¬ teristics specified above which may be summarized as follows : indivi- dual units containing an active substance which are coated with a substantially water-insoluble, but water-diffusible controlled release coating which includes

1 ) an inner film layer which causes adhesion between the units at > elevated temperatures, comprising a water-dispersible film-forming agent, and

2) an outer film layer comprising a water-based film-forming agent which prevents adhesion between the units at elevated temperatu¬ res and imparts flowability to the units .

DETAI LED DESCRI PTION OF THE INVENTION

Crystals

When the units coated according to the invention are crystals, they normally have a size between about 0.1 and 1 .5 mm, preferably be¬ tween about 0.4 and 1 .0 mm. As an important example of an active substance which is suitably used in the form of crystals, potassium chloride may be mentioned.

Cores

According to the invention, the cores are preferably cross-sectionally substantially homogeneous cores.

The cores are typically made by granulating particles of the active substance together with excipients, including bulk agents such as carbohydrates and derivatives thereof such as starch and starch derivatives, including microcrystalline cellulose, binders such as cellulose derivatives, including methylcellulose or hydroxypropylme- 5 thylcellulose, polyethylene glycol, polyvinylpyrrolϊdone, agar, or gelatin, for instance by treatment in a high speed mixer (to directly obtain compact-shaped cores) , or by treatment in a planet mixer with subsequent extrusion of the mixture into strings of a predetermined diameter approaching the desired final cross-sectional dimension of the cores and treatment of the strings in a marumerizer or similar equip¬ ment to obtain compact-shaped cores . The diameter of the cores is normally adapted so that the diameter of the coated core is about 0.1 -1 .5 mm, in particular about 0.4-1 .0 mm, e. g . about 0.4-0.7 or 0.7-1 .0 mm.

Active Substance

The active substance in the formulations according to the invention may be any active substance which is advantageously administered in a controlled release multiple-units formulation . Examples of suitable active substances are found among almost all therapeutic groups, including diuretics, antiepileptics, sedatives, antiarrhytmics, anti- rheumatics, fi-blockers, vasodilators, analgesics, bronchodilators, hormones, vitamins, oral antidiabetics, antibiotics, antihypertensives, anti inflammatory drugs, antimicrobial agents and antidepressants, polypeptides (enkephalines and endorphines) , enzymes and mucopoly- saccha rides.

As examples of active substances may be mentioned pindolol, quinidine salts, lithium carbonate, acemetacin, vincamine, dipyridamol, theophyl- line, dextropropoxyphene, amitriptyline, hydralazine, digoxin, furo- semide, propranolol, ibuprofen, lidocaine, mepyramine, nitroglycerin, clonidine, disopyramide, verapamil, captopril, prazocin, nifedipine, paracetamol and indomethacin .

Among these substances, some are characterized as having a pH- dependent solubility, others as having a pH-independent solubility. Active substances having a pH-dependent solubility (that is, a solu¬ bility which differs corresponding to a ratio of 10: 10³ over the phy¬ siological pH range of 1 -7.5) are preferably incorporated in cores in combination with buffer substances such as discussed above, in order to obtain a dissolution of active substance which is substantially independent of the gastrointestinal pH variations through which the units pass . Especially important formulations according to the invention are for¬ mulations in which the active substance, apart from being a substance about which it is known or indicated from a pharmacokinetic and/or clinical point of view that it is advantageously administered in a controlled release multiple-units formulation, is a substance which exerts an irritating effect on the gastrointestinal mucosa such as acetylsalicylic acid, potassium chloride, lithium salts, propionic acid derivatives, iron salts and magnesium salts.

In utilizing the principle of the invention, the units are freely distri- buted throughout the gastrointestinal tract, independent of gastric emptying, as the units are small enough to pass the pylorus even when the sphincter is closed. This makes it possible to obtain a low concentration at the mucosa and thus to minimize the risk of local irritation .

Coating

The diffusion coating (i .e. usually the inner film layer) applied on the units according to the invention is a diffusion coating which is applied from a dispersion in water. The application of the coating is typically performed in a fluidized bed or by pan coating.

Examples of diffusion coating materials which may be used for the purpose of the present invention are coatings selected from the group consisting of acrylic polymers and copolymers, e.g . , a polymerisate of acrylic acid ethylesters and methacrylic acid methylester such as Eudragit® E 30 D or ethylcellulose such as Aquacoat® ECD-30. Enteric coating materials such as hydroxypropylmethylcellulosephthalate, e.g. HP 50 or HP 55, polyvinylacetatephthalate, e.g. Coateric®, cellulose- acetatephthalate and the like may also be employed^* according to the same principles.

Coating compositions containing a hydrophobic substance are prefe- rably applied in the form of a suspension of particles of the hydro¬ phobic substance at a temperature below the melting or softening temperature of the hydrophobic substance. Normally, it is preferred to disperse the hydrophobic substance in water, optionally together with the anti-adhesive (which preferably forms agglomerates with the hydrophobic substance) , by heating to about the melting or softening point of the hydrophobic substance, dispersing, and subsequently cooling. The dispersion is then added to the aqueous dispersion of the film-forming substance.

Coating compositions containing a polymeric substance such as a water-soluble polymer as the reinforcing agent, e. g. hydroxypropyl¬ methylcellulose which in fact is the preferred substance, are suitably prepared by heating water to a temperature at which the hydroxypro¬ pylmethylcellulose is not soluble in water (i . e. a temperature above about 60°C) , the anti-adhesive such as talc is dispersed in the hot water, which is an advantage as, at the higher temperature, there is less surface tension, and the hydroxypropylmethylcellulose is disper- sed in the mixture in the form of discrete particles . After dispersion, the mixture is slowly cooled to below about 60°C with stirring so that the hydroxypropylmethylcellulose is dissolved. The film-forming agent is then added to the resulting cooled mixture with stirring until a homogeneous mixture is obtained .

The coating material may be admixed with various excipients such as plasticizers, inert fillers, and pigments, in a manner known per se.

Examples of plasticizers include triacetin , Myvacet™ 9-40T (acetylated monoglyceride) , rape oil, olive oil, sesame oil, acetyltributylcitrate, acetyltriethylcitrate, glycerin, sorbitol, diethyloxalate, diethylmalate, diethylfumarate, diethylsuccinate, diethylmalonate, diethyltartrate, tri-n-butylcitrate, dibutylphthalate, diethylphthalate, dioctylphthalate, dibutylsebacate, triethylcitrate, tributylcitrate, glyceroltributyrate, polyethyleneglycol, propyleneglycol, and mixtures thereof . The plas- ticizer is normally incorporated in an amount of 1 -30%, calculated on the dry matter content of the coating mixture.

However, according to the invention , it has been found that for certain polymers, in particular an acrylic polymer such as a copoly- merisate of acrylic acid ethylester and methacrylic acid methylester, a plasticizer may not be necessary, and hence, a particular aspect of the invention provides units coated with a plasticizer-free coating, in particular a coating based on a copolymerisate of acrylic acid ethyl- ester and methacrylic acid methylester as the film-forming polymer, of the type according to the invention .

The amount of inner film layer applied is adapted so as to obtain a predetermined dissolution characteristic of the coated units. Normally, the amount of the inner film layer will be about 1 -30% by weight, especially about 5-25%, particularly about 15%, by weight of the uncoated units depending on the predetermined dissolution charac¬ teristics of the active substance and the desired release profile.

The amount of dry matter in the film-coating mixture will normally be about 1-50%, especially 5-30%, and typically about 20%. It is advan¬ tageous to have a high dry matter content in the film-coating mixture as this reduces the coating time necessary to obtain an adequate coating of the units.

As mentioned above, hydroxypropylmethylcellulose is a preferred film-forming agent for the outer film layer. Apart from being anti- adhesive at elevated temperatures, the currently preferred hydroxy- propylmethylcellulose, e. g. Methocel® E5 premium or Pharmacoat® 606, has a low viscosity in an aqueous solution so that it is possible to obtain as high a dry matter content as 6-8%. This means that a re¬ duction of the coating time is obtained for the outer film layer as well . When using hydroxypropylmethylcellulose, it may be advantage- ous to incorporate a plasticizer such as one of the plasticizers men¬ tioned above. Similarly, surfactants, pigments and other conventional additives may be incorporated in a manner known per se.

Dosage forms

The units prepared according to the invention may be incorporated in normal pharmaceutical dosage forms or formulations such as capsules containing a multiplicity of the units, sachets containing a multiplicity of the units, or tablets which will disintegrate substantially immedia- tely upon ingestion in the stomach to form a multiplicity of individual units.

A favoured tablet according to the invention is one in which the mul¬ tiplicity of units are coated crystals or coated cores of the type defined above which are compressed together with about 25-40% of conventional tabletting excipients to a tablet hardness of at least about 4 kp (as measured by means of a Schleuniger apparatus as described below) without any significant change in release charac¬ teristics relative to non -compressed units of the same composition .

The adjuvants and excipients used in the preparation of disintegrata- ble tablets are of the same kind as conventionally used in the phar¬ maceutical industry for this purpose. Examples of filler or diluents useful for preparing tablets according to the invention are lactose, sucrose, dextrose, mannitol, calcium sulphate, dicalcium phosphate, tricalcium phosphate, starches such as rice starch and microcrystal- line cellulose. Useful binders are acacia, tragacanth, gelatine, su¬ crose, pregelatinized starch, starch, sodium alginate, ammonium calcium alginate, methylcellulose, sodium carboxymethylcellulose, ethy (cellulose, hydroxypropylmethylcellulose, polyvinylpyrrolidone, magnesium aluminium silicate, and polyacrylamides . As examples of disintegrants may be mentioned cross-linked polyvinylpyrrolidone, starch derivatives such as sodium carboxymethylcellulose, and cellulo¬ se derivatives. As lubricants, "gliders" and "anti-adhesives" may be mentioned metallic stearates, talc, high melting point waxes, and colloidal silica.

When it is desired to use excipients or adjuvants for the preparation of sachets or capsules, such as fillers and lubricants, these may be of the same type as described above.

The filling of capsules and sachets and the compression of tablets are performed in a manner known per se. MATERIALS AND METHODS

In the examples, the following materials were used:

Sodium dihydrogen phosphate: Anhydrous. Analyzed according to BP 80.

Sucrose powder: Ph . Eur.

Microcrystalline cellulose: BPC 79. Avicel® supplied by FMC, Philadel¬ phia.

Talc: Ph. Eur. and additionally comply¬ ing with the following require¬ ments:

About 0.002 g of talc is distribu¬ ted in 1 drop of cyclohexanoi and investigated under microscope. 45 particles out of 50 may not be above 40 ym.

Potassium chloride: Ph . Eur.

Hydroxypropylmethylcellulose: USP 20. Methocel® E5 premium. Supplied by Dow Chemicals, Michigan, USA. Abbreviated to HPMC.

Propranolol hydrochloride: BP 80.

Sodium carboxymethylcellulose: USP 20. Bianose® 7 LFD. Sup¬ plied by Hercules through Scan- dibutor, Copenhagen, Denmark. Purified water: Ph . Eur.

Eudragit® E 30 D: A neutral acrylic acid ethylester/ methacrylic acid methylester copolymerisate in the ratio 70:30, molecular weight above 800,000, as a 30% aqueous dispersion, supplied by Rohm Pharma GmbH, Darmstadt, Germany.

Rice starch : Ph . Eur. /USP 20.

Magnesium stearate: Ph . Eur./USP 20.

Determination of in vitro dissolution characteristics:

In vitro dissolution rates were determined according to Baggesen . et al . (1981) . The rotation speed was 30±1 r. p. m. , and the dissolution medium was 25 ml of 0.1 M hydrochloric acid (pH 1 .2) , maintained at 37±0.1 °C.

Release of propranolol into the dissolution medium was determined by means of UV spectrometry at 290 nm.

Release of potassium chloride into the dissolution medium was deter¬ mined by means of a potassium-selective electrode.

Disintegration time of tablets was measured according to Ph . Eur. 2nd Ed . I , V.5.1 .1 .

Tablet hardness was determined in a Schleuniger-2E apparatus avail¬ able from Dr. K. Schleuniger & Co. , Switzerland, in kp.

The tabletting machine employed was an excenter press single-punch machine TM 20. Calculation of the Dissolution Index

In the range of 20-80% drug released, an estimation was performed for at least four pairs of figures, e.g . , t«_Q, -.,-, t_ςg, tgc/ of correspond¬ ing times for the two profiles so as to release the same amount of drug.

The correlated values were plotted in a time-time coordinate system, with the abscissa as time for the dissolution profile in simulated gastric fluid and the ordinate as the time in the simulated intestinal fluid.

A linear regression analysis was performed (at least four points, excluding 0.0) . Provided that the shape of the two profiles are simi¬ lar a straight line through the origin is achieved.

The dissolution index is calculated as :

Dl = (b-D-100

where b is the slope.

When the formulation dissolves faster in simulated intestinal fluid than in simulated gastric juice the calculated Dl value will be negative.

The limit of pH-independency is a Dl of <25.

EXAMPLE 1

Preparation of Film-Coated Potassium Chloride Crystals

Preparation of inner Film-Coating Composition Containing a Polymeric Substance

An inner film-coating composition was prepared from the following ingredients: Eudragit® E 30 D 43.3%

Methocel® E5 0.65%

Talc 1 .35%

Purified Water to 100% (-= 15% dry matter)

Water was heated to 80°C and talc was dispersed therein by means of a disperser. To the heated mixture was added Methocel® E5 premium which was dispersed in the form of discrete particles . This dispersion was slowly cooled to room temperature with stirring causing the HPMC to dissolve. The Eudragit® E 30 D was added with stirring.

Application of Inner Film-Coating Composition on Potassium Chloride Crystals

The film-coating composition prepared as described above at ambient temperature was sprayed onto the potassium chloride crystals in a fluidized bed using an outlet air temperature of max . 40°C.

Preparation of Outer Film-Coating Composition

A film-coating composition was prepared from the following ingre¬ dients :

Methocel® E5 premium 6%

Talc 6%

Purified water 92^Q xt

100 o%, ( (-= 12% dry matter) Water was heated to 80°C and talc was dispersed therein by means of a disperser. To the heated mixture was added Methocel® E5 premium which was dispersed in the form of discrete particles. This dispersion was slowly cooled to room temperature with stirring causing the HPMC to dissolve.

Application of Outer Film- Coating Composition on Potassium Cloride Crystals

The outer film-coating composition prepared as described above was sprayed onto the potassium chloride crystals already coated with the inner film layer in a fluidized bed using an outlet air temperature of max. 40°C. The outlet air temperature was then raised to 70°C for 1 hour followed by cooling. The presence of the outer film layer makes this heat treatment possible without causing agglomeration of the coated crystals, which would have occurred if the crystals had been coated with the inner film layer only.

The amount of inner film layer applied was 13% and the amount of outer film layer was 1%, by weight of the uncoated crystals.

The release of potassium was measured as described in MATERIALS AND METHODS .

It appears from Table 1 that a prolonged dissolution profile has been obtained.

TABLE 1

Percentage of Potassium Released at pH = 1 .2 (n=3) after

1 h 2 h 6 h

23.40 (s=0.96) 52.97 (s=2.09) 90.86 (s=2.39)

EXAMPLE 2

The Effect of Heating with Respect to the Dissolution Characteristics of the Film-Coated Crystals

Inner and outer film-coating compositions were prepared and applied as described in Example 1 with the exception that, in one experiment, no heating of the coated units took place.

The release of potassium was determined as described in MATERIALS AND METHODS .

TABLE 2

Percentage of Potassium Released at pH = 1 .2 after 1 hour (n=3)

Time 0 2 weeks

No heating 41 .85 37.14

(s=1 .52) (s=2.73)

Heating at 70°C for 1 h 22.89 23.40

(s=0.87) (s=0.96)

It appears from Table 2 that the release of potassium from the unhea- ted units has decreased after a week, while remaining constant from the heat-treated units.

EXAMPLE 3

Preparation of Film-Coated Potassium Chloride Crystals

Preparation of Inner Film-Coating Composition Containing a Hydro¬ phobic Substance

A film-coating composition was prepared from the following ingre- dients:

Eudragit® E 30 D 47.6%

Paraffin 2.9%

Talc 2.9% Purified Water 46.6%

100% (equals 20% dry matter) The paraffin was heated in purified water (14% of the 47.3% of puri¬ fied water as stated above) to a temperature well above the melting point of paraffin, i . e. between 70 and 80°C. The heated mixture was treated with a disperser under addition of talc. The mixture was cooled to about 30°C under continued dispersion, and Eudragit® E 30 D was added with stirring. This film-coating composition was sieved and finally diluted to a dry matter content of 20% using 33.3% of water.

The film-coating composition prepared as described above was applied on potassium chloride crystals as described in Example 1 .

The outer film-forming composition was prepared and applied as described in Example 1 .

The amount of inner film layer applied was 14% and the amount of outer film layer was 1%, by weight of the uncoated crystals .

The release of potassium was measured as described in MATERIALS AND METHODS.

It appears from Table 3 that a prolonged dissolution profile has been obtained .

TABLE 3

Percentage of Potassium Released at pH = 1 .2 (n=3) after

1 h 2 h 6 h

24.21 (s=0.62) 51 .04 (s=2.69) 92. 13 (s=0.16) Preparation of a Pharmaceutical Dosage Form

The film-coated crystals prepared as described above may be filled into a capsule size No. 1 and No. 00. Each capsule comprises 300 mg and 600 mg of potassium chloride, respectively. The same film-coated crystals may be filled into sachets to comprise a pharmaceutical dosa¬ ge form of 1000 mg or more of potassium chloride. The film-coated crystals may also be granulated and compressed into tablets of diffe¬ rent shapes, each comprising 600 mg or 750 mg of potassium chloride, respectively, e.g. a tablet substantially as shown in the appended drawing.

EXAMPLE 4

The Effect of Different Amounts of Dry Matter on the Release of Potassium from Film-Coated Crystals

Inner and outer film-coating compositions were prepared as described in Example 1 and 3. The inner film coating composition was applied in varying amounts as shown in Table 4a and 4b below. The outer film- coating composition was applied as described in Example 1 .

The release of potassium was measured as described in MATERIALS AND METHODS.

TABLE 4a

Percentage of Potassium Released at pH = 1 .2 after 1 hour (n=3)

Dry matter¹ 8% 10% 13% 15 »'%t_>

95.19 72.76 22.89 12.57 (8=1 .13) (s=1 .64) (s=0.87) (s=0.62)

¹ by weight of coating solids, calculated on the weight of the uncoat- ed crystals. I nner film layer according to Example 1 .

TABLE 4b

Percentage of Potassium Released at pH = 1 .2 after 1 hour (n=3)

Dry matter¹ 10.0% 12.0% 14.0%

30.44 25.79 23.64

(s=1. !2) (s=1 .06) (s=0.78)

¹ by weight of coating solids, calculated on the weight of the uncoated crystals. Inner film layer according to Example 3.

It appears from Table 4a and 4b that the release of potassium is cor¬ related to the amount of inner film applied so that a reduction in re¬ lease may be obtained by increasing the amount of dry matter in the inner film layer.

EXAMPLE 5

The Effect of Paraffin Added to the Film-Coating Composition with Respect to the Dissolution Characteristics of the Film-Coated Crystals. Hydrophobic Effect before and after Heat Treatment

Preparation of Inner Film-Coating Composition

Inner film-coating compositions were prepared from the following ingredients:

A B C

Eudragit® E 30 D 47.6% 41 .7% 37.6%

Paraffin 2.9% 3.8% 4.4%

Talc 2.9% 3.8% 4.4%

Purified water 46.6% 50.7% 54.2%

100.0% 100.0% 100.0%

(=20% dry (=20% dry (=20% dry matter) matter) matter)

as described in Example 3.

Application of the Inner Film-Coating Composition on Crystals

Film-coating mixtures A, B and C were all applied on potassium chlo¬ ride crystals in an amount corresponding to 10% of the Eudragit® E 30 D (dry matter) .

The outer film-coating composition was applied as described in Exam- pie 1 in an amount of 1% (dry matter) .

The release of potassium was measured as described in MATERIALS AND METHODS . TABLE 5

Percentage of Potassium Released at pH = 1 .2 after 1 hour (n=3)

Film-coating mixture A B C

Percent of paraffin 2 3 4

No heat treatment 18.21 19.88 20.83

(s=2.67) (s=1 .33) (s=0.55)

Heat treatment for 14.91 14.80 12.30

1 hour at 70°C (s=0.07) (s=0.24) (s=0.40)

Reduction in release (%) 3.30 5.08 8.53

It appears from Table 5 that, prior to heating, paraffin has no sus- tained-release effect. After heating, a notable reduction in release is observed which increases with increasing amounts of paraffin .

EXAMPLE 6

The Effect of Hydroxypropylmethylcellulose on the Release of Potas¬ sium from the Coated Crystals

Preparation of Inner Film-Coating Composition

Inner film-coating compositions were prepared from the following ingredients : A B C

Eudragit® E 30 D 44.3% 43.2% 41.5%

Methocel® E5 prem. 0.3% 0.7% 1 .2%

Talc 1 .4% 1 .4% 1 .3%

Purified Water to 100% to 100% to 100%

(= 15% dry (= 15% dry (= 15% dry matter) matter) matter)

The inner film-coating compositions were prepared and applied as described in Example 1 in an amount corresponding to 10% of the Eudragit® E 30 D (dry matter) .

The outer film-coating composition was prepared and applied as de- scribed in Example 1 .

The release of potassium chloride was measured as described in . MA¬ TERIALS AND METHODS.

TABLE 6

Percentage of Potassium Released at pH = 1 .2 after 1 hour (n=3)

Film-coating mixture B

Percent of HPMC¹ 2.5 10

20.05 25.49 37.34 (s=0.31) (s=1.74) (s=1.04)

Calculated as dry matter on the amount of Eudragit® and Methocel®. It appears from Table 6 that the release of potassium increases with the amount of HPMC added to the film-coating composition . This means that HPMC should be incorporated in amounts which are sufficient to impart compressibility to the coating, but not sufficient to impair the release characteristics of the inner film layer.

EXAMPLE 7

Tabletting of Coated Potassium Chloride Crystals

Coated potassium chloride crystals prepared as described in Example 1 and 3 were compressed to tablets with 27.3% of excipients in an ex- center press single-punch tabletting machine TM 20 to a hardness of 7.6 kp and 11 .0 kp (n=6) , respectively. The resulting tablets had a gross weight of about 1200 mg, corresponding to 750 mg of KCI . The disintegration time of the tablets was 3 and 2 minutes, respectively.

The release of potassium was measured as described in MATERIALS AND METHODS.

TABLE 7a

Coated Crystals According to Example 1

Percentage of Potassium Released at pH = 1 .2 (n=3) after

1 h 2 h 6 h

Crystals 23.40 52.97 90.86

(s=0.96) (s=2.09) (s=2.39) Tablets 22.89 54.42 94.30

(s=0.98) (s=1 .45) (s=1 .18) TABLE 7b

Coated Crystals According to Example 3

Percentage of Potassium Released at pH = 1 .2 (n=3) after

1 h 2 h 6 h

Crystals 24.21 51.04 92.13

(s=0.62) (s=2.69) (s=0.16) Tablets 23.62 50.07 88.92

(s=0.67) (s=0.94) (s=2.03)

It appears from Table 7a and 7b that there is correlation between the results obtained for compressed coated crystals and non -compressed coated crystals.

EXAMPLE 8

Preparation and Tabletting of Coated Cores

Preparation of Cores

Cores were prepared from the following ingredients :

Propranolol hydrochloride 60%

Microcrystalline cellulose 22%

Sodiumdihydrogenphosphate 15% Sodiumcarboxymethylcellulose 1%

Eudragit® E 30 D 2% (dry matter) 100% A mixture . of the above ingredients was moistened with purified water and mixed until the mixture was a little grainy.

The moist mixture was extruded through a 0.75 mm sieve. The result¬ ing extrudate consisted of strings breaking off in lengths of a few cm.

The extruded strings were formed into compact-shaped cores in a marumerizer. The resulting compact-shaped cores had a size of about 0.7-1 .0 mm.

Inner and outer film-coating compositions were prepared and applied as described in Example 1 .

The coated cores were compressed into tablets with 40% of convention¬ al excipients on the tabletting machine specified in MATERIALS AND METHODS.

The tablets had a weight of 500 mg, corresponding to 162.2 mg of propranolol hydrochloride per tablet.

Tablet hardness was 6.3 kp when measured as described in MATERI ¬ ALS AND METHODS .

The disintegration time was <1 minute.

The propranolol released was measured as described in MATERIALS AND METHODS .

TABLE 8

Percentage of propranolol released at pH = 1 .2 (n=3) after

1 h 2 h 6 h

Cores 23.26 40.86 77.54

(s=0.25) (s=0.64) (s=0.14) Tablets 27.28 45.79 79.74

(s=0.92) (s=0.47) (s=1.46)

Percentage of propranolol released at pH = 7.5 (n=3) after

1 h 2 h 6 h

Cores 28.75 51.30 82.00

(s=0.1l) (s=0.80) (s=0.56) Tablets 31.96 55.16 82.46

(s=0.32) (s=0.35) (s=1.10)

It appears from Table 8 that there is no significant difference in the release of propranolol from cores and tablets, respectively. The dis¬ solution index is 4 determined as described in MATERIALS AND ME¬ THODS which means that the release is pH-independent.

EXAMPLE 9

Preparation of Film-Coated Cores

Preparation of Cores

Cores were prepared from the following ingredients : Caffeine 20%

Sodium dihydrogen phosphate 20%

Microcrystalline cellulose 29%

Talc 19%

Sucrose powder 7%

Methocel® E5 premium 3%

Methocel® El 5 premium 2%

100%

as described in Example 8.

Inner and outer film-coating compositions were prepared and applied as described in Example 3.

The caffeine released into, the dissolution medium was measured as described in MATERIALS AND METHODS .

TABLE 9

Percentage of Caffeine Released at pH = 1 .2 (n=3) ^** after

1 h 2 h 6 h

19.13 30.25 65.67

(s=0.98) (s=1 .31 ) (s=1 .38)

¹ The amount of inner film layer is 5% by weight of the uncoated cores .

It appears from Table 9 that a prolonged dissolution profile has been obtained. Preparation of Pharmaceutical Dosage Form

The film-coated cores prepared as above may be filled into capsules or sachets .

EXAMPLE 10

The Effect of the Amount of Dry Matter Applied to Cores with Re¬ spect to the Dissolution Characteristics of the Coated Cores

The caffeine released into the dissolution medium was measured as described in MATERIALS AND METHODS.

TABLE 10

Percentage of Caffeine Released at pH = 1 .2 (n=3) after 1 hour

Dry matter¹ 3% 5% 8% 50.79 19.13 10.75 (s=1 .38) (s=0.98) (s=1 .36)

¹ Dry matter by weight of coating solids, calculated on the weight of the uncoated cores.

It appears from Table 10 that the release of caffeine is correlated to the amount of dry matter applied to the cores, i .e. by increasing the amount of dry matter the dissolution of caffeine is diminished. EXAMPLE 11

The Effect of the Dry Matter Content in the I nner Film-Coating Com¬ position

Inner and outer film-coating compositions were prepared and applied as described in Example 1 with the exception that the dry matter content of the inner film-coating composition was 15%, 20%, 25% and 30%, respectively, in different experiments.

All crystals were coated with 15% of dry matter relative to the weight of the uncoated crystals.

The release of potassium was measured as described in MATERIALS AND METHODS .

TABLE 11

Percentage of Potassium Released at pH = 1 .2 (n=3) after

% of dry matter 15 20 25 30

23. 13 21 .58 29.06 27.57

(s=0.82) (s=0.14) (s=0.53) (s=1 .11 )

It appears from Table 11 that it is possible to use film-coating compo¬ sitions with as high a dry matter content as 30% without any signifi¬ cant change in release. This is important as a high dry matter con¬ tent will lead to a shorter coating period. LITERATURE

GB Patent 1 468 172

European Patent Application 79 850 110, Publication No. 0 013 262

US Patent 4 193 985

Baggensen S, Bechgaard H, & Schmidt K, "Content and dissolution uniformity testing of controlled- release products: The Repro-Dose® quality control procedure", Pharm. Ada Helv 56, 1981 , pp. 85-92.

Bechgaard, H & Hegermann Nielsen, G, "Controlled release multiple- units and single-units doses. A literature review". Drug Develop Ind Pharm . , 1978, pp. 53-67.

Bechgaard, H & Ladefoged, K, "Distribution of pellets in the gastro¬ intestinal tract. The influence on transit time exerted by the density or diameter of pellets", J Pharm Pharmacol 30, 1978, pp. 690-692.

Bechgaard, H & Baggesen, S, "Propoxyphene and norprppoxyphene: Influence of type of controlled release formulation on intra- and intersubject variations", J Pharm Sci 69, 1980, pp. 1327-1330.

Bogentoft, C, Carlsson, I , Ekenved, G & Magnusson, A, "Influence of food on the absorption of acetylsalicylic acid from enteric-coated dosage forms", Eur J Clin Pharmacol . , 1978, pp. 351 -355.

Green, DM, "Tablets of coated aspirin microspherules - A new dosage form", J New Drugs 6, 1966, pp. 294-303.

McDonald, PJ, Mather, LE & Story, MJ, "Studies on absorption of a newly developed enteric-coated erythromycin base", J Clin Phar¬ macol 17, 1977, pp. 601 -606.

Snedecor, GW & Cochran, WG, Statistical Methods. Iowa State Univer¬ sity Press, Iowa, 1967, pp. 271 -275.

Claims

1 . An oral pharmaceutical controlled release multiple-units formulation in which individual units containing an active substance are coated with a substantially water-insoluble, but water-diffusible controlled release coating which includes

1 ) an inner film layer which causes adhesion between the units at elevated temperatures, comprising a water-dispersible film-forming agent, and

2) an outer film layer comprising a water-based film-forming agent which prevents adhesion between the units at elevated tempera¬ tures and imparts flowability to the units .

2. A formulation according to claim 1 , in which the inner film layer additionally comprises a substance which, in itself, is capable of forming a continuous phase.

3. A formulation according to claim 2, in which the substance is a hydrophobic substance, and the outer film layer is impermeable, at temperatures above the melting point of the hydrophobic substance, to the molten hydrophobic substance.

4. A formulation according to claim 2, in which the substance is a polymeric substance which imparts compressibility to the coating .

5. A formulation according to any of claims 1 -4, in which the film- forming agent of the inner film layer is selected from cellulose deriva¬ tives, silicone polymers and copolymers, vinyl polymers and copoly¬ mers, biodegradable polymers such as polyamino acids, polylactic acid and copolymers and derivatives thereof, and acrylic polymers and co¬ polymers, or mixtures thereof.

6. A formulation according to claim 5, in which the film-forming agent is selected from ethyl cellulose and a copolymerisate of poly(meth) - acrylic acid esters, hydroxypropylmethylcellulosephthalate, cellulose- acetatephthalate, polyvinylacetatephthalate and vinylacetate-crotonic acid copolymerisates.

7. A formulation according to claim 3, in which the hydrophobic sub- stance of the inner film layer is selected from hydrocarbons and hy¬ drocarbon derivatives, waxes, oils and fats, and mixtures thereof, especially a waxy substance such as paraffin wax .

8. A formulation according to claims 3 or 7, in which the hydrophobic substance is present in an amount of between about 0.1 and 50%, in particular between 1 and 40%, especially between about 10 and 30%, by weight of the inner film layer.

9. A formulation according to claim 4, in which the polymeric sub¬ stance in the inner film coating is selected from polyvinylpyrrolidone, polyalkylene glycols such as polyethylene glycol, and cellulose deriva- tives such as hydroxypropylcellulose, carboxymethylcellulose, methyl- cellulose, propylcellulose, hydroxyethylcellulose, carboxyethylcellulo- se, carboxymethylhydroxyethylcellulose, hydroxymethylcellulose, carboxymεthylethylcellulose, methylhydroxypropylcellulose or hydro¬ xypropylmethylcellulose.

10. A formulation according to claim 9, in which the polymeric sub¬ stance is present in an amount between 1 and 10%, such as an amount between 2% and 8%, especially an amount of about 4% by weight rela¬ tive to the amount of film-forming agent in the inner film layer.

11 . A formulation according to any of the preceding claims, in which the inner film layer comprises an anti-adhesive which is a finely divided, substantially water-insoluble, pharmaceutically acceptable, non -wetting powder.

12. A formulation according to claim 11 , in which the anti-adhesive is present in an amount of between about 0.1 and 50%, preferably be- tween about 1 and 40%, especially about 10-30% such as about 15% by weight of the inner film layer.

13. A formulation according to any of claims 1 -12, in which the inner film layer is present in an amount of about 1 -30%, especially about 5-25%, in particular about 15%, by weight of the uncoated units .

14. A formulation according to any of claims 1 -13, in which the film- forming agent of the outer film layer is one which is anti-adhesive at temperatures above about 40°C, especially temperatures above about 50°C, such as a temperature between about 60°C and about 120°C.

15. A formulation according to claim 14, in which the film-forming agent of the outer film layer is selected from diffusion coating mate- rials such as ethylcellulose or enteric coating materials such as an- ionic poly (meth) acrylic acid esters, hydroxypropylmethylcellulose- phthalate, celluloseacetatephthalate, polyvinylacetatephthalate, polyvi- nylacetatephthalate-crotonic acid copolymerisates, or mixtures thereof, or water-soluble coating materials such as water-soluble cellulose derivatives, e.g. hydroxypropylcellulose, carboxymethylcellulose, methylcellulose, propylcellulose, hydroxyethylcellulose, carboxyethyl- cellulose, carboxymethylhydroxyethylcellulose, hydroxymethylcellulose, carboxymethylethylcellulose, methylhydroxypropylcellulose „ or hydro¬ xypropylmethylcellulose.

16. A formulation according to claim 14 or 15, in which the film- forming agent of the outer film layer is present in an amount of about 0.1 -10%, especially 0.5-5%, in particular about 1% by weight of the uncoated unit.

17. A formulation according to any of claims 14-16, in which the outer. film coating additionally comprises a lubricant which is a finely divi¬ ded pharmaceutically acceptable powder.

18. A formulation according to any of the preceding claims, in which the units are crystals of a size between 0.1 and 1 .5 mm.

19. A formulation according to any of claims 1 -17, in which the units are cross-sectionally substantially homogeneous cores of a size of about 0.1 -1 .5 mm, in particular about 0.4-1 .0 mm, such as about 0.4-0.7 mm or 0.7-1 .0 mm.

20. A method of preparing an oral pharmaceutical controlled release multiple-units formulation as claimed in any of claims 1 -19, in which

c) the coated units are subsequently heated to a temperature at which the inner film layer is tacky, and at which the formation of a continuous phase of the film-forming agent is accelerated, and subsequently cooled, whereby a coating which substantially does not change its diffusion characteristics in the course of time is formed .

21. A method according to claim 20, in which the coating composition additionally comprises a substance which, in itself, is capable of form¬ ing a continuous phase.

22. A method according to claim 21 , in which the substance is a hy¬ drophobic substance, and the units coated according to steps a) and b) in the method of claim 20, after which steps the hydrophobic substance is present in the inner film layer as a disperse phase, are heated to a temperature above the melting point of the hydrophobic substance which, on melting and subsequent cooling, forms a continu¬ ous phase in the inner film layer in homogeneous admixture with the film-forming agent, the outer film layer being one which is imperme¬ able, at temperatures above the melting point of the hydrophobic substance, to the molten hydrophobic substance.

23. A method according to claim 21 , in which the substance is a polymeric substance which, in step a) of the method of claim 20, prevents adhesion between the units and which imparts compressibility to the inner film layer, and the units coated according to steps a) and b) in the method of claim 20 are heated to a temperature at which the film-forming agent forms a continuous phase in homogeneous admixture with the polymeric substance.

24. A method according to any of claims 20-23, in which the coated units are heated to a temperature above about 40°C, especially a temperature above about 50°C, such as a temperature between about 60°C and about 120°C.

25. An oral pharmaceutical controlled release composition which com¬ prises a multiplicity of units as specified in any of claims 1 -19 ad¬ mixed with one or more pharmaceutically acceptable fillers, diluents, binders, lubricants or disintegrants .

26. A pharmaceutical composition according to claim 25 which is a tablet which disintegrates substantially immediately upon ingestion in the stomach into a multiplicity of individual units.