CZ20032984A3 - Tablet containing valsartan produced by direct tabletting - Google Patents

Abstract

In the present invention, there is disclosed a medicinal preparation containing valsartan, optionally a combination of valsartan and hydrochlorothiazide, in the form of a tablet obtained by direct tabletting and containing 40 to 70 percent by weight of valsartan, optionally 3 to 12 percent by weight of hydrochlorothiazide, and microcrystalline cellulose with particle size in the range of 10 to 1000 microns, preferably 90 microns in an amount of 25 to 40 percent by weight based on the medicinal preparation total weight.

Description

A tablet containing valsartan produced by direct tabletting

Technical field

The invention relates to a tablet containing the active ingredient valsartan, optionally valsartan in combination with hydrochlorothiazide, prepared by direct tabletting.

BACKGROUND OF THE INVENTION

Valsartan, with the chemical name N- (1-oxopentyl) -N - [[2 '- (1H-tetrazol-5-yl) [1,1'-biphenyl] -4-yl] methyl] -L-valine, of the formula AND

it belongs to a group of medicines that block angiotensin II receptors, causing a drop in blood pressure. They are used to treat hypertension and to treat chronic heart failure.

Valsartan and related compounds that exhibit affinity for angiotensin II receptors have been described in U.S. Patent No. 5,399,578. The dosage form disclosed in this patent comprises:

Z ..................... ......... ¹ Active substance 100 mg Lactose 100 mg Cornstarch 70 mg Talc 8.5 mg Calcium stearate 1.5 mg Hydroxypropylmethylcellulose 2.36 mg Shellac 0.64 mg

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The mixture of the active ingredient, lactose and corn starch parts was granulated by wet granulation and after drying mixed with the rest of the starch and calcium stearate and talc and then tableted.

International Patent Application WO 95/24901 describes, in Example 1, dosage form A of a capsule having the following composition:

valsartan 80 mg Microcrystalline cellulose 110 mg Polyvidon K30 45.2 mg Sodium lauryl sulfate 1.2 mg Crospovidon 26 mg Magnesium stearate 2.6 mg

The first two components are granulated by wet granulation with a solution of the third and fourth components in water. Components 5 and 6 are added to the dry granulate and the mixture is filled into capsules.

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However, as disclosed in WO 97/49444, these previously published methods were not well reproducible, especially when compressed into tablets. This application applies a dry granulation method for the manufacture of valsartan tablets. A known composition of WO

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95 / 24j901 is slightly modified:

valsartan 80 mg Hydrochloride & thiazide 12.5 mg Colloidal silica AEROSIL 1.5 mg Microcrystalline cellulose 31.5 mg Crospovidon 20 mg Magnesium stearate 4.5 mg

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The 1 to 5 components are mixed and compacted at a pressure of 25 to 65 kN. The compacted material is further passed through a screen. The granulate so formed is mixed with magnesium stearate and tableted.

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A particular advantage of the production method of the present application is that, for each particular formulation, a minimum compaction pressure of 25-65 kN can be found within the range of the compacting latches, resulting in a tablet having about 6 times faster disintegration than in a conventional process ( using higher pressure).

Faster disintegration of the tablets thus obtained leads to a faster release of the active substance and its rapid absorption into the body, and ultimately to improve the bioavailability of _r * y. This has been verified in patent application WO 01/97405, where the bioavailability of tablets and capsules of similar composition was compared.

Surprisingly, however, it has now been found that a small change in the composition of the valsartan-based formulation will make it possible to completely eliminate compacting. This not only reduces the manufacturing effort of the dosage form, but also reliably ensures an adequate tablet disintegration rate without having to seek optimal pressure.

SUMMARY OF THE INVENTION

It is an object of the present invention to provide a tablet containing valsartan, an active ingredient used in the treatment of hypertension, optionally valsartan in combination with hydrochlorothiazide. Hydrochlorbthiazide is a thiazide diuretic, acting diuretically and antihypertensively, and in combination with valsartan, the antihypertensive effect is enhanced. The essence of the production method is to prepare the tablet by dry mixing. The tablet thus prepared may be used to compress cores and / or tablets.

The preparation of the pulp is technologically simple, it is limited to technological and time-saving technological steps. The preparation of the tablet does not include stressful processes such as introducing the wetting agent into the mixture of active ingredient and excipients and dry granulation by compacting the mixture of the active ingredient and excipients for preparing the tablet.

Dry blending of the tablet allows the preparation of cores and / or tablets of satisfactory parameters, and the method of preparation and selection of excipients according to the invention also ensure good stability of the formulation and the desired physical properties of the dosage form.

The direct tableting technique is not only simple, but above all the most environmentally friendly. Thus, it represents a further advance over the previously described dry granulation techniques associated with compacting and the need to apply high pressures, which can then cause drug release problems to the patient. Due to such problems, a substantial part of the drug may not be used at all.

For direct tabletting, however, it is necessary to find such a mixture of the active ingredient and excipients which can be tabletted without any modification, producing a tablet meeting all the requirements. The tablet of the medicinal product must be hard enough to withstand various types of transport burden. Further, however, it must disintegrate sufficiently quickly when in contact with water to release the active ingredient into solution before it passes through the upper part of the patient's digestive tract. The hardness value of the tablet and the release (dissolution) of the active substance are therefore two variables which are more or less opposed and the conditions must always be optimized.

For the direct tabletting technique, excipients having particularly good tabletting properties are selected. It is primarily lactose granulate or microcrystalline cellulose. Such a substance is then mixed with the active substance in a multiple excess so that its positive tableting properties prevail in the mixture. It is not always possible to secure such an excess. In the case of valsartan, where the highest dose is 160 mg, this would produce large, hardly swallowable tablets weighing more than 1 g.

In patent application WO 97a $ ³⁹⁴ highlights the fact that it is possible to produce 300 mg tablets »z"'* containing 160 mg valsartan compaction as surprising possibilities. However, it is much more successful to produce such a tablet without using any granulation.

Thus, the directly tabletable mixture or the tablet produced by this technique preferably comprises 40 to 70% valsartan.

In addition to the active ingredient valsartan, optionally valsartan in combination with hydrochlorothiazide, the tablet described herein contains further excipients such as microcrystalline cellulose as a filler - and flow modifiers, antiadhesive tableting aids and tablet disintegrants.

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The dosage form of the invention is based on the use of microcrystalline cellulose. It has good flow properties. Tablets have satisfactory strength and disintegration because microcrystalline cellulose in the compact ensures the maintenance of capillary openings through which water inhibits the binding force efficiency. They provide the product with very good stability. The quality of the selected microcrystalline cellulose is essential for the X 'formulation of the invention. The particle size of the commercially available cellulose for pharmaceutical purposes ranges from about 1 to 1000 µm. From this range, a size of 90 µm appears to be the most preferred for formulation.

In a particularly preferred embodiment of the invention, the amount of microcrystalline cellulose is in the range of 25 to 40 wt. %.

In another embodiment of the invention, the tablet comprises 3 to 10% disintegrants, of which sodium starch sodium is most preferred. This substance further improves the disintegration of the tablet and makes it possible to achieve an excellent release rate.

In another embodiment, the tabletting composition comprises a substance to improve its flow properties.

The most preferred material for the described composition is silica colloidalis anhydrica, preferably in an amount of 0.1 to 10%, particularly preferably 0.5 to 4%. These substances are important for 4Γ avoiding fluctuations in tablet weight caused by inappropriate flow of solid mixture through the hopper into the high-performance tablet machine.

From these mixtures it is possible to prepare a tablet or a tablet. tablets by dry route, dry blending and direct tabletting.

The tablets thus prepared guarantee reproducibility of the manufacturing process.

The advantage is energy and time saving preparation of the tablet.

Said process for the production of valsartan-containing tablet and solid dosage forms by direct dry-mixing tabletting and the selection of excipients according to the invention make it possible to prepare tablet and solid dosage forms with excellent physical parameters.

Examples of embodiments of the invention

Example 1

Valsartan 160 mg coated tablets

Starting materials weight in g Valsartanum 0.16000 g Cellulosum microcrystallinum, size 90 pm 0,11700 g Carboxymethylamylum natricum 0.01600 g Silicon dioxide colloidale 0.00600 g Magnesii stearas 0.00600 g Total core weight in g 0,30500 g Sepifilm 3084 Orange 0.00150 g Sepifilm 3048 Yellow 0.01350 g Aqua purificata 0,07000 g Total weight packaging. tbl. in g 0,32000 g

Description of the technology of preparation of the pulp (dry way, direct tabletting):

1. Mixing I: The active substance, microcrystalline cellulose and carboxymethylamylum natricum are mixed in a homogenizer for 15 minutes.

2. Stirring II: add finishing - silica colloidale silica and magnesii stearas and mix in a homogenizer for 15 minutes.

3. Tableting

Two important quantities were determined for the tablets thus prepared. This was a fracture resistance that is necessary to keep the tablets whole during transport and the rate of release of the active ingredient into the dissolution medium, the value of which indicates the availability of the drug to the patient. Both quantities were measured by standard procedures.

The tablets thus produced exhibited a fracture resistance of at least 70 µSf, indicating that they would not be damaged during normal transport.

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In the drug release test, at least 75% of the total content was released in 45 minutes. This result was in very good agreement with the Novartis Diovan product already registered and sold.

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Thus, it appears that the tablets produced by this novel process are identical in properties to those obtained by known, standard processes.

Example 2

In the same way, valsartan 80 mg and 40 mg were obtained.

Ingredients:

Valsartan 80 mg coated tablets

Starting materials weight in g Valsartanum 0,08000 g Cellulosum microcrystallinum, size 90 pm 0.05850 g Carboxymethylamylum natricum 0.00800 g Silicon dioxide colloidale 0.00300 g Magnesii stearas 0.00300 g Total core weight in g 0.15250 g Sepifilm 3084 Orange 0.00075 g Sepifilm 3048 Yellow 0.00675 g Aqua purificata 0,03500 g Total weight packaging. tbl. in g: 0.16000 g

Valsartan 40 mg coated tablets

Starting materials weight in g Valsartanum 0,040000 g Cellulosum microcrystallinum, size 90 pm 0.029250 g Carboxymethylamylum natricum 0,004000 g Silicon dioxide colloidale 0.001500 g

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Magnesii stearas 0.001500 g Total core weight in g 0.076250 g Sepifilm 3084 Orange 0.000375 g Sepifilm 3048 Yellow 0.003375 g Aqua purifícata 0.017500 g Total weight packaging. tbl. in g: 0,080000 g

Example 3

Composition with hydrochloride ⁱⁿ thiazide - preparation made in the same way as in Example 1.

Valsartan HCT 80 / 12.5 mg coated tablets

Starting materials weight in g Valsartanum 0,08000 g Hydrochlorothiazidum 0.01250 g Cellulosum microcrastallinum, size 90 pm 0.05850 g Carboxymethylamylum natricum 0.00800 g Silicon dioxide colloidale 0.00300 g Magnesii stearas 0.00300 g Total core weight in g: 0.16500 g Sepifilm 3084 Orange 0.00075 g Sepifilm 3048 Yellow 0.00675 g Aqua purifícata 0,03500 g Total weight packaging. tbl. in g: 0,20750 g

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Claims (10)

PATENT CLAIMS 1 »η A medicament comprising valsartan or a combination of valsartan with hydrochlorothiazide, in the form of a tablet obtained by direct tableting, characterized in that it contains 40 to 70% by weight of valsartan or 3 to 12% of hydrochloride thiazide and microcrystalline cellulose having a particle size of 10 to 1000 µm, preferably 90 µm, in amounts above 25 and up to 40 wt. %, based on the total weight of the preparation. A medicament comprising valsartar according to claim 2, characterized in that it also contains a disintegrant, a flow modifier and a non-sticking agent. Medicament according to any one of the preceding claims, characterized in that it contains 3 to 10% disintegrant, preferably sodium starch carboxymethyl. Medicament according to any one of the preceding claims, characterized in that it contains 0.1 to 10%, preferably 0.5 to 2%, of a flow regulating agent of the tablet, preferably colloidal silica. Medicament according to any one of the preceding claims, characterized in that it contains 0.1 to 10%, preferably 0.5 to 4% of an anti-adhesive substance, preferably magnesium stearate. Medicament according to any one of the preceding claims, characterized in that it contains 160 mg of valsartan, 80 to 140 mg of microcrystalline cellulose and 10 to 20 mg of sodium starch glycolate. Medicament according to any one of the claims, characterized in that it contains 80 mg of valsartan, 40 to 70 mg of microcrystalline cellulose and 5 to 10 mg of sodium starch glycolate. Medicament according to any one of claims 1 to 7, characterized in that it contains 40 mg of valsartan, 20 to 35 mg of microcrystalline cellulose and 2.5 to 5 mg of sodium carboxymethyl starch. -10 Medicament according to any one of claims 1 to 8, characterized in that it contains 80 mg of valsartan, 12.5 mg of hydrochlorothiazide, 58.5 mg of microcrystalline cellulose and 8 mg of sodium starch glycolate. Process for the manufacture of a tablet according to any one of claims 1 to 10, characterized in that the mixture of valsartan, microcrystalline cellulose and disintegrant is mixed in a homogenizer in the apparatus, optionally colloidal silica together with magnesium stearate is added ^{in a} further step. the mixture tablets.