Drug – bio-affecting and body treating compositions – Preparations characterized by special physical form – Particulate form
Reexamination Certificate
1998-12-24
2001-06-05
Page, Thurman K. (Department: 1615)
Drug, bio-affecting and body treating compositions
Preparations characterized by special physical form
Particulate form
C424S464000, C424S451000
Reexamination Certificate
active
06242006
ABSTRACT:
This application is a 371 of PCT/EP97/03877 filed Jul. 15, 1997.
The present invention relates to &bgr;-lactam granules free of organic solvents and a process to prepare the same.
TECHNOLOGICAL BACKGROUND AND FIELD OF INVENTION
For the manufacturing of tablets and capsules containing oral grade penicillins or cephalosporins it is generally found that the crystalline material has no satisfactory flowability so that controlled dosage during tablet and capsule manufacturing-processes is not guaranteed. Therefore it is customary to produce a granulate first by mixing the crystalline powder (1-30 &mgr;m) with a small amount of organic solvent (e.g. alcohol) sometimes diluted with water. It is required then to admix other components as binders (e.g. PVP) and fillers (e.g. lactose) for obtainment of granulates with satisfactory particle size distribution and strength. However, it will not be possible to achieve a high dosage per tablet unless relatively large tablets are made.
The granulation process generally takes place in a high shear mixer granulator by which dense particles of a suitable particle size distribution are produced. After the granulation process the material (particles of approximately 400-500 &mgr;m average diameter) is dried. It is found that while using only water as binding liquid (i.e. no alcohol, no binding agents) wherein Pen VK has been solved which liquid leads to binding into granules during the drying process, the batch-wise operated high shear granulators can not give a satisfactory particle size distribution while excessive fouling of the apparatus occurs.
The use of an organic solvent in this process is a clear disadvantage because of the fact that one has to dry the final product extensively due to the required low levels of solvent in the final dosage form. From a process point of view one would have remarkably less environmental problems if the organic solvent could be circumvented.
Furthermore, the absence of binders could give granulates which can be used in high potency tablets or capsules.
We have found now two granulation methods wherein the organic solvent is not needed for obtaining water soluble penicillins, for instance Pen VK granules. The granulation of Pen VK is carried out using only water as binding solvent while no other additives (like binder materials) are required resulting in &bgr;-lactam granules essentially free of organic solvent, viz. with no more organic solvents than the &bgr;-lactams contain before the formation of granules.
SUMMARY OF THE INVENTION
The present invention provides &bgr;-lactam granules being free of organic solvents, especially granules of the potassium salts of &bgr;-lactams, preferably granules of the potassium salt of penicillin V. Also a process to prepare said &bgr;-lactam granules has been provided for, viz. by applying during the granulation essentially only water as binding solvent. Preferably said process is carried out in a batch-wise operated fluidized bed granulator, more preferably by applying top spray of water. Alternatively said process is carried out in a continuous mixer. Finally, also tablets or capsules comprising said granules do form an aspect of this invention.
DETAILED DESCRIPTION OF THE INVENTION
The two granulation methods, wherein the use of organic solvents have been avoided, consist essentially of the application of a batch-wise operated fluidized bed granulator or a continuous high-shear mixer in combination with a fluidized bed dryer. The application of these two granulation methods results in granules of &bgr;-lactams, for instance the potassium salt of penicillin V with a satisfactory particle size distribution, viz. mainly between 100 and 1400 &mgr;m, bulk and tapped density and particle strength.
The first method comprises the following steps:
A certain amount of crystalline &bgr;-lactam powder, for instance from the potassium salt of penicillin V, is added to a fluidized bed granulator wherein air, conditioned to a certain temperature and humidity, is passed as to move the solids vigorously. After adjustment of the temperature of the bed to the inlet air temperature (typically 0-60° C.), water is added by using spray nozzles (top-spray). Preferably so called two-phase nozzles using compressed air are applied. Within approximately 30-60 minutes 5 to 200%, preferably 10-100 wt % of water is added to the bed mass during which the bed temperature drops, typically to 20-30° C. The exact amount and temperature depend on the air humidity, air flow rate and air temperature. The amount of water can in principle be much larger but this may cause unpracticle long operating times. After reaching a satisfactory particle size (distribution) the water dosage is stopped and the bed mass is dried until the bed temperature reaches a predetermined value (e.g. 50-60° C.).
The bed is emptied while the granulate is passed over a grinder-sieve in which the large (off-spec) particles are broken to a suitable size, viz. between 25 and 2000 &mgr;m, preferably between 100 and 1400 &mgr;m. The process can be carried out in fluid beds of different sizes.
According to the second method, the crystalline material is added on the front end by an adjusted flow rate (e.g. using a screw device) to a continuous high shear mixer granulator such as the Lödige CB type of machine. This consists of a horizontal axis provided with certain types of paddles, rotating at 1000-3000 rpm. Water is admixed (approximately 5-20 wt %, preferably 10-13 wt %) and after only a few seconds (1-30 s) the wet granulate leaves the machine at the rear end. It is subsequently transferred to a continuous type of dryer such as a continuous fluidized bed dryer. After passing this apparatus (typical residence time 1 hr) the material is milled and sieved and ready for use, preferably in a continuous mode. Several batches of the material can be mixed as to achieve one single batch and subsequently filled in a suitable package (e.g. boxes).
REFERENCES:
patent: 4950484 (1990-08-01), Olthoff et al.
patent: 5948422 (1999-09-01), Van Koutrik et al.
patent: 0281200 (1988-09-01), None
patent: 0330284 (1989-08-01), None
patent: 2186230 (1974-01-01), None
patent: WO24337 (1996-08-01), None
Kwant Gerard Jan
Scheffers Nicolaas Henricus
Bierman, Muserlian and Lucas
Ghali Isis
Gist-Brocades B.V.
Page Thurman K.
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