PHARMACEUTICAL FORMULATIONS OF ALIPHATIC AMINE POLYMERS AND METHODS FOR THEIR MANUFACTURE
FIELD OF THE INVENTION
The present invention relates to pharmaceutical compositions comprising aliphatic amine polymers, such as for example Sevelamer HCl, as the active pharmaceutical ingredient and methods of preparing pharmaceutical compositions thereof, such as for example Sevelamer HCl Film Coated Tablets employing wet granulation.
BACKGROUND OF THE INVENTION Aliphatic amine polymers are useful as active pharmaceutical ingredients for use in pharmaceutical compositions. A particularly interesting aliphatic amine polymer is Sevelamer, a polymeric phosphate binder intended for oral administration. Sevelamer hydrochloride is a poly(allylamine hydrochloride) crosslinked with epichlorohydrin in which forty percent of the amines are apparently protonated. It is known chemically as poly(allylarnme-co-N,N'-diallyl-1,3-diarnmo-2-hydroxypropane) hydrochloride. Sevelamer hydrochloride is hydrophilic, but insoluble in water. The reported structure of Sevelamer HCl is represented below:
(Figure Removed)
a, b = number of primary amine groups a + b = :
c = number of crosslinking groups c = 1
n = fraction of protonated amines n = 0.4
m = large number to indicate extended polymer network
Sevelamer HC1 is currently being marketed as RENAGEL , for the treatment of patients with Chronic Kidney Disease (CKD) which are on hemodialysis1. According to the prescribing information RENAGEL® is indicated for the control of serum phosphorus in such CKD patients. In. general, commercially available Sevelamer tablets also contain the following inactive ingredients; hypromellose, diacetylatedrnonoglyceride, colloidal silicon dioxide, and stearic acid.
The method of producing a direct compressible composition of a polymer tablet core is described in U.S. Patent No. 6,733,780 Bl and U.S. Patent Application 2005/0260236 Al. These references describe Sevelamer HC1 as a product which compressibility is strongly dependent upon the degree of hydration. Apparently, hydrating the polymer to the desired moisture level is considered by those inventors as an essential first step in manufacturing the finished product.
Further, Sevelamer HC1 is known to be very hygroscopic and swell upon contact with water. Such swelling of the aliphatic amine polymer Sevelamer compUcates formulating the active pharmaceutical ingredient in a pharmaceutical composition. Thus although compressibility is apparently dependant on the degree of hydration, simply adding water to sevelamer results in a swollen material which swollen material is impossible to use to press tablets. The present invention overcomes this problem of swelling of the active pharmaceutical ingredient by providing a more compressible sevelamer formulation within which the water content of sevelamer is not significantly increased compared to the commercially available sevelamer raw material. Even when using a wet granulation method with the present sevelamer formulation, the active pharmaceutical ingredient sevelamer has not swollen significantly. It is noted that commercially available sevelamer raw material is similarly impossible to compress.
SUMMARY OF THE INVENTION
1 Renagel® is sold by Genzyme Corporation. The Prescribing Information is available from www.renagel.com/docs/renagelpipdf which describes the 400mg and 800mg tablets as containing the following inactive ingredients: hypromellose, diacetylated monoglyceride, collodial silicon dioxide and stearic acid.
In one aspect the present invention provides a pharmaceutical composition comprising,
a) aliphatic amine polymers, and b) at least one pharmaceutical excipient, wherein the aliphatic amine polymer in the composition comprises wet granulated aliphatic amine polymers. Preferably, the aliphatic amine polymer is Sevelamer HC1 or another pharmaceutically acceptable salt of Sevelamer, such as for example Sevelamer Carbonate. The granulation liquid for preparing the wet granulation of aliphatic amine polymers is preferably a combination of an organic solvent and water or where the solvent is ethanol, no water may be required.
Further, there is provided a method of preparing a granular composition comprising wet granulated aliphatic amine polymers comprising the following steps of
a) providing aliphatic amine polymers;
b) providing at least one organic solvent preferably together with water to form a granulating solution, which can optionally contain one or more excipients such as a binder;
c) contacting the granulating solution with the aliphatic amine polymers by preferably spraying it onto the aliphatic amine polymers and one or more excipients and forming a wet granulate, more preferably performed in a fluidized bed drier; and
d) mixing the wet granulate with one or more excipients and forming a final blend.
Preferred wet granulation solutions are ethanolic or preferably ethanol/water solutions. Furthermore, the method preferably further comprises the steps of
e) pressing the final blend into tablets.
Alternatively, the method further comprises the step of e) filling capsules with the final blend.
In another aspect, the present invention provides a pharmaceutical composition comprising wet granulated aliphatic amine polymers, preferably manufactured by spray granulation techniques, wherein the pharmaceutical composition has a degree of hydration of less than about 7% as measured by Karl Fischer (KF) analysis and is compressible and suitable for tableting.
In another aspect, the present invention provides a method of treating a patient suffering from chronic kidney disease comprising administering in combination with hemodialysis a therapeutically effective amount of Sevelamer HC1 in a pharmaceutical composition comprising wet granulated Sevelamer HC1.
DETAILED DESCRIPTION OF THE INVENTION
To achieve an adequate protection against swelling upon contact with water of highly hygroscopic active pharmaceutical ingredients such as aliphatic amine polymers in a pharmaceutical composition is an important aspect in formulating a dosage form of aliphatic amine polymers for use in medical treatments. A preferred aliphatic amine polymer composition for use in the formulations of the present invention is Sevelamer HC1. According to the present invention, formulations of aliphatic amine polymers with a low hydration level and which are highly compressible can be achieved when the aliphatic amine polymers are wet granulated with a granulating solution comprising organic solvents preferably mixed with water optionally containing one or more of a binder. In addition, these formulations of ahphatic amine polymers of the present invention have a lower hydration level compared to that of the Renagel® formulations. Moreover, the aliphatic amine polymers in the pharmaceutical composition of the present invention have a similarly low hydration level when compared to the aliphatic amine polymer raw material prior to its use in such pharmaceutical composition. The wet granulation is preferably achieved by techniques of spray granulation. These pharmaceutical compositions according to the present invention are easily prepared and have good storage properties. The present invention thus provides a pharmaceutical composition comprising aliphatic amine polymers wherein the objective of providing a compressible wet granulated formulation of for example sevelamer with a desired protection against the swelling propensity of the active ingredient in such pharmaceutical compositions. This objective is achieved by using a formulation wherein the aliphatic amine polymers are wet granulated with at least one organic solvent preferably mixed with water, most preferably by spray wet granulation.
In a first approach developing a pharmaceutical composition comprising aliphatic amine polymers, tablets were produced using a conventional direct compression method. However, the material of the aliphatic amine polymer formulation was determined to be not compressible. Secondly, a wet granulation method was attempted using a high shear mixer
employing water as the only granulating liquid. Similarly, the method was determined to be not suitable because of swelling of the active material during the granulation process due to the use of water as the only granulating liquid. As a consequence, the material for the aliphatic amine polymer formulation is not compressible. In contrast, it was surprisingly found that using an ethanol/water granulation solution, as for example in a wet granulation method with, such ethanol/water solution, is an appropriate method for producing Sevelamer tablets. The spray granulation technique is particularly favored.
One embodiment of the present invention provides a pharmaceutical composition comprising, a) granulated aliphatic amine polymers, and b) at least one pharmaceutical excipient, wherein the aliphatic amine polymer in the composition comprises preferably wet granulated, more preferably spray wet granulated aliphatic amine polymers. Moreover, granulated aliphatic amine polymers are preferably granulated employing a granulating liquid of an organic solvent/water mixture. Suitable granulation liquids are ethanol, ethanol/water, isopropyl/water, and mixtures thereof. Preferably, the granulation liquid comprises about 82% to about 95% ethanol (95%) and about 5% to about 18% water. More preferably, the granulation liquid comprises 95% ethanol and 5% water. Furthermore, the aliphatic amine polymer is preferably Sevelamer HCl or another pharmaceutical acceptable salt of Sevelamer such as for example Sevelamer Carbonate, more preferably the aliphatic amine polymer is Sevelamer HCL Moreover, the phannaceutical composition comprises preferably from about 60% to about 95% by weight of Sevelamer HCl, more preferably from about 65% to about 85%, most preferably from about 65% to about 80% by weight of Sevelamer HCl. Furthermore, the Sevelamer HCl in the pharmaceutical composition is preferably substantially non-hydrated Sevelamer HCl.
In another embodiment, the present invention provides a pharmaceutical composition comprising spray granulated aliphatic amine polymers, wherein the pharmaceutical composition has a degree of hydration of less than about 7% as measured by Karl Fischer analysis. Preferably, the aliphatic amine polymer is Sevelamer HCl or another phannaceutically acceptable salt of Sevelamer, such as for example Sevelamer Carbonate. More preferably the aliphatic amine polymer used in the process for manufacturing the formulation is a substantially non-hydrated aliphatic amine polymer. Furthermore, in the form of a tablet such pharmaceutical composition preferably has a hardness of at least about 17 Strong Cobb Units (SCU), more preferably from about 17 SCU to about 40 SCU. Further,
such tableted pharmaceutical composition of the present invention preferably has a jfiiability of less than about 1%, more preferably less than 0.1%. Moreover, such tableted pharmaceutical composition of the present invention preferably has a disintegration time in 0.1N HC1 of less than about 5 minutes, more preferably from about 214 to about 3 minutes.
Suitable granulation solutions/liquids for use in the present invention include ethanolic solutions (ethanol), ethanol/water, or isopropyl alcohol/water solutions. More preferably, the granulation solution is an ethanol/water solution. Preferably, the granulation liquid comprises about 82% to about 95% ethanol (95%) and about 5% to about 18% water. More preferably, the granulation liquid comprises 95% ethanol and 5% water.
The pharmaceutical compositions of wet granulated, preferably wet spray granulated, aliphatic amine polymers of the present invention may further contain excipients such as tablet and capsule fillers and diluents (such as microcrystalline cellulose, lactose, starch and tri-basic calcium phosphate), disintegrants (such as starch, croscarmellose sodium, crospovidone and sodium starch glycolate), binders (such as starch, hydroxypropyl methyl cellulose and Povidone), glidant (such as colloidal silicon dioxide), lubricants (such as magnesium stearate, magnesium lauryl sulfate, stearic acid and sodium stearyl fumarate).
More particularly, suitable diluents and fillers for use in the pharmaceutical composition of the present invention include microcrystalline cellulose (e.g. Avicel®), lactose, starch, pregelatinized starch, calcium carbonate, calcium sulfate, sugar, dextrates, dextrin, dextrose, dibasic calcium phosphate dihydrate, tribasic calcium phosphate, kaolin, magnesium carbonate, magnesium oxide, maltodextrin, mannitol, potassium chloride, powdered cellulose, sodium chloride, sorbitol and talc.
Solid pharmaceutical compositions that are compacted into a dosage form, such as a tablet, may include excipients whose functions include helping to bind the active ingredient and other excipients together after compression. Binders for solid pharmaceutical compositions include acacia, alginic acid, carbomer (e.g. carbopol), carboxymethylcellulose sodium, dextrin, ethyl cellulose, gelatin, guar gum, hydroxyethyl cellulose, hydroxypropyl cellulose (e.g. Klucel®), hydroxypropyl methyl cellulose (e.g. Methocel®), liquid glucose, maltodextrin, methylcellulose, polymethacrylates, povidone (e.g. Povidone PVP K-30, Kollidon®, Plasdone®), pregelatinized starch, sodium alginate and starch. Furthermore,
Povidone has been found to be a particularly useful binder. Moreover, this binder is preferably added as a solution in the granulating liquid.
A compacted solid pharmaceutical composition may also include the addition of a disintegrant to the composition. Disintegrants include croscarmellose sodium (e.g. Ac Di Sol®, Primellose®), crospovidone (e.g. Kollidon®, Polyplasdone®), microcrystalline cellulose, polacrilin potassium, powdered cellulose, pregelatinized starch, sodium starch glycolate (e.g. Explotab®, Primoljel®) and starch.
Glidants can be added to improve the flowability of a sohd composition before compaction and to improve the accuracy of dosing especially during compaction and capsule filling. Excipients that may function as glidants include colloidal silicon dioxide, magnesium trisilicate, powdered cellulose, and talc.
A lubricant can be added to the composition to reduce adhesion and/or ease the release of the product from e.g. the dye. Lubricants include magnesium stearate, calcium stearate, glyceryl monostearate, glyceryl palmitostearate, hydrogenated castor oil, hydrogenated vegetable oil, mineral oil, polyethylene glycol, sodium lauryl sulfate, sodium stearyl fumarate, stearic acid, talc and zinc stearate.
Other excipients that may be incorporated into the formulation include preservatives, surfactants, antioxidants, or any other excipient commonly used in the pharmaceutical industry.
The soHd compositions of the present invention include powders, granulates, aggregates and compacted compositions. The dosages include dosages suitable for oral, buccal, and rectal administration. Although the most suitable administration in any given case will depend on the nature and severity of the condition being treated, the most preferred route of the present invention is oral. The dosages may be conveniently presented in unit dosage form and prepared by any of the methods well known in the pharmaceutical arts.
The pharmaceutical composition of the present invention may be prepared in any dosage form such as a compressed granulate in the form of a tablet for example. Also, uncompressed granulates and powder mixes that are obtained by the method of the present
invention in the pre-compression steps can be simply provided in dosage form of a capsule or sachet Therefore, dosage forms of pharmaceutical composition of the present invention include solid dosage forms like tablets, powders, capsules, sachets, troches and losenges. The dosage form of the present invention may also be a capsule containing the composition, preferably a powdered or granulated solid composition of the invention, within either a hard or soft shell. The shell may be made from gelatin and optionally contain a plasticizer such as glycerin and sorbitol, and an opacifying agent or colorant
Once an alphatic amine polymer, preferably Sevelamer HC1, solid composition is prepared in accordance with the present invention, it is preferably formulated into pharmaceutical formulations such as conventional dosage forms, including tablets and capsules. Tablets are preferred dosage forms. In addition, the tablets maybe coated with an optional cosmetic tablet coating.
The present invention also provides a method of preparing pharmaceutical compositions comprising aliphatic amine polymers such as for example Sevelamer HC1. Preferably, the method of the present invention produces compressed solid dosage forms. There are three well known processes for manufacturing such dosage forms; (i) direct compression, (ii) dry granulation and (iii) wet granulation. There are two well known processes for wet granulation. A wet granulate can be prepared using a mixer and subsequently the wet granulate is dried in order to obtain a dry homogenous granulate. In another method a wet granulate is prepared by spray granulation. In a fluid-bed, spray granulation process, particles and granulate are built up in a fluid bed by spraying a liquid onto fluidized particles. Thus in such process materials are fluidized in the fluid bed dryer and subsequently a solution is sprayed through a nozzle. The choice of processing approach depends upon the properties of the drug and chosen excipients, for example particle size, blending compatibility, density and flowability. For preparing Sevelamer HC1 tablets, granulation is preferred, wherein wet granulation being the most preferred with the technique of spray granulation being the method of choice. In addition, the tablets may also be coated to assure ease of swallowing or to provide an elegant appearance.
In one embodiment, the present invention provides a method of preparing a pharmaceutical composition comprising wet granulated aliphatic amine polymers comprising the steps of
a) providing aliphatic amine polymers;
b) wet granulating the aliphatic amine polymers with one or more excipients and forming a pharmaceutical composition. Preferred wet granulation solutions for use in this method of the present invention are ethanolic, ethanol/water, or isopropyl alcohol/water solutions. More preferably, the wet granulation solution is an ethanol/water solution, and most preferably a solution of about 82% to about 95% ethanol (95%) and about 5% to about 18% water. Most preferred is a wet granulation solution of 95% ethanol (95%) and 5% water.
In another embodiment, the present invention provides a method of preparing a granular composition comprising spray granulated aliphatic amine polymers comprising the following steps of
a) providing aliphatic amine polymers;
b) preparing a granulating liquid comprised of at least one organic solvent preferably mixed with water and optionally a binder preferably in the form of a solution;
c) spraying the granulating liquid onto aliphatic amine polymers and one or more excipients and forming a spray granulate; and
d) mixing the spray granulate with one or more excipients and forming a final blend.
Preferably the aliphatic amine polymer is Sevelamer HC1, more preferably the Sevelamer
HCl used in the method is substantially non-hydrated Sevelamer HC1.
Preferably, the method farmer comprises the steps of
e) pressing the final blend into tablets.
Alternatively, the method further comprises the steps of e) filling capsules with the final blend.
Specifically, the preferred method for the production of a pharmaceutical composition of wet granulated aliphatic amine polymers involves spraying of a granulating liquid or solution onto aliphatic amine polymers. The spraying process preferably uses Fluidized bed technology equipment, where the particles are suspended in a vertical column with a rising air stream. While the particles are fluidized, the granulating solution is sprayed into the column. This spraying can be carried out by any one of three methods; top spray, bottom
spray and a "tangential" or powder spray. Preferably the spraying is carried out by a top spray method.
Spray granulation solutions suitable for use in a spray granulated process need to be selected according to requirements some of which are dependent on the physical properties of the active pharmaceutical ingredient. For example the granulation solutions should not alter the physical characteristics of and/or dissolve the active pharmaceutical ingredient. Preferred spray granulation solutions for use in the method of the present invention are ethanolic, ethanol/water, or isopropyl alcohol/water solutions or mixtures thereof. More preferably, the spray granulation solution is an ethanol/water solution, and most preferably a solution of about 82% to about 95% ethanol (95%) and about 5% to about 18% water. Most preferred is a spray granulation solution of 95% ethanol (95%) and 5% water.
The Sevelamer pharmaceutical compositions in the form of film coated tablets prepared by the described method may contain per tablet various amounts of Sevelamer HC1 and preferably contain either about 400 mg or about 800 mg of Sevelamer HC1 as calculated on an anhydrous basis.
In another embodiment, the present invention provides a method of treating a patient suffering from chronic kidney disease comprising administering in combination with hemodialysis a therapeutically effective amount of Sevelamer HC1 in a pharmaceutical composition comprising spray granulated Sevelamer HC1. Patients suffering from chronic kidney disease CKD are frequently treated with hemodialysis. In such patients, which are treated with hemodialysis; it is important to control the phosphorus content in their serum. Sevelamer HC1 binds phosphorus and is therefore used as a phosphorus scavenger in the blood stream of patients to control serum phosphorus content Thus the present invention provides a method of treating a patient suffering from chronic kidney disease and undergoing hemodialysis treatment comprising administering a therapeutically effective amount of Sevelamer HC1 in a pharmaceutical composition comprising wet granulated, preferably wet spray granulated, Sevelamer HC1. Preferably, the method of treating a patient undergoing hemodialysis comprising administering a therapeutically effective amount of Sevelamer HC1 in a pharmaceutical composition comprising wet granulated Sevelamer HC1 controls the serum phosphorus content in such patient.
The scope of the invention should not be limited to the working examples, which are for demonstration purposes. One skilled in the art can practice the invention based on the disclosures in the present patent application.
EXAMPLES Renagel® Tablets and Sevelamer HCl active ingredient
The tablets of the following examples 1 and 2 (tablets A and B respectively) were prepared according to the formulations and methods of the invention. Certain physical properties of these tablets A and B were determined as shown in Table 1 of example 3. Some of these physical properties were also determined for a comparative RENAGEL® tablet as presented in Table 3. In addition to the physical properties of tablets A and B some physical properties of the Sevelamer HCl active ingredient as used in the preparations of Examples 1 and 2 were determined. The active ingredient Sevelamer HCl used in the following examples was manufactured by Shasun Chemicals and Drugs Ltd with the following properties as shown in Table 1. Table 1: Properties of Sevelamer raw material.
(Table Removed)
It is understood that, while the LOD result is indicative of all the material that can be evaporated or removed by heat or drying, it is the Karl Fischer analysis that determines the water content or level of hydration of the material tested.
Example 1: Tablet A of 400 mg spray granulated Sevelamer HCl

(Table Removed)
Batch number
+commeroially available mix of polymer, plasticizer and opacifying agent The Sevelamer HC1 was spray-granulated using a Povidone solution in mixture of
ethanol/ water as a granulating liquid. The granulate was blended with Part II ingredients.
The final blend was compressed into tablet core and coated using Part m material. The
solvents in the granulating liquid were comprised of either a mixture of 95% Ethanol (95%)
and 5% water or a mixture of 82% Ethanol (95%) and 18% water.
Example 2: Tablet B of 800 mg spray granulated Sevelamer HC1
(Table Removed)
+commercially available mix of polymer, plasticizer and opacifying agent The Sevelamer HC1 was spray-granulated using a Povidone solution in mixture of ethanol/ water as a granulating liquid. The obtained granulate was blended with Part II ingredients. The final blend was compressed into tablet core and coated using Part HI material. The solvents in the granulating liquid were comprised of either a mixture of 95% Ethanol (95%) and 5% water or a mixture of 82% Ethanol (95%) and 18% water.
Example 3: Properties of Sevelamer HC1 preparation of Working Examples
The Sevelamer HC1 tablets prepared according to the present invention were subjected to various analyses to determine their physical properties. The following Table 2
shows the results thereof and lists the obtained values for the physical properties of the tablets
according to examples 1 and 2.
Table 2: Physical properties of Sevelamer HC1 preparations.

(Table Removed)
The obtained granulates have very good or excellent flowability. Further, no swelling of the active material was observed to have occurred during the granulation process. Moreover, the compressed tablets have acceptable physical characteristics and disintegration times. The results obtained by Karl Fischer analysis indicate that tablets are produced without a significant change in the water content or Hydration level as evidenced by the KF value. The preferred hydration value as measured by Karl Fischer analysis can therefore be set at not more than 7%. In the following Table 3 some of the physical properties for the commercially available Renagel® tablets are shown. Table 3: Physical properties of Renagel Tablets.

(Table Removed)
It can be seen that the material that can be removed by evaporation from the Renagel tablets consists almost entirely of water. Evidence hereof is the close similarity between the results obtained from the LOD and KF analyses. la contrast, it can be observed that in the tablets of the present invention the water content or hydration level of the sevelamer in the preparations, as evidenced by the Karl Fischer analysis, is very similar to the levels found in the raw active material received from the supplier.

Claims
1. A pharmaceutical composition comprising;
a) wet granulated aliphatic amine polymers; and
b) at least cms pharmaceutical excipient.

2. The pharmaceutical composition according to claim 1, wherein the wet granulated aliphatic amine polymers are granulated using a granulation liquid selected &om the group consistin of ethanol, an ethanol/water solution, an isopropyl alcohol/water solution, txJxtures thereof.
3. The pharmaceutical composition according to claim 2, wherein the ethanol/water solution is a solution of about 82% to about 95% ethanol (95%) and about 5% to about 18% water.
4. The pharmaceutical composition according to claim 3, wherein the ethanol/water solution is a solution of 95% ethanol (95%) and 5% water.
5. The composition according to claim 1, wberein the wet granulated aliphatic amine polymers are spray granulated.
6. The pharmaceutical composition according to claim 1, wharein the alipbatic amine polymer is selected from the group consisting of Sevelamer HCl and Sevelamer Carbonate.
7. The pharmaceutical composition according to claim 6, whOTein tihe aliphatic amine polymer is Sevelamer HCl.
8. The pharmaceutical composition according to claim 6, wherein Sevelamer HCl is substantially non-hydrated and which hydration level is similar in comparison to the hydration level of raw material Sevelamer HCl.
9. The pharmaceutical composition according to claim 6, whereia the amount of Sevelamer HCl is from about 60% to about 95% of the weight of the cornposition.
10. The pharmaceutical composition according to claim 1, wherein the composition is in a pharmaceutical dosags form.
11. The phannacwjtical composition according to claim 10, whorein the dosage form is a tablet.
12. The pharmaceutical composition according to claim 11, wherein the tablet has a water content of less than 7% as measured by Karl Fischer analysis.
13. The pharmaceutical composition according to claim 11, wherein the tablet has a hardness of at least about 17 SCU.
14. The pharmaceutical composition according to claim 11, wherein the tablet has a friability of less than about 1.0%.
15. The pharmaceutical composition according to claim 11, wherein the tablet has a disintegration time in O.IN HCl of less than about 5 minutes.
16. The pharmaceutical composition according to claim 11, wherein the aUphatic amine polymer is selected from the group consisting of Sevelamer HCl and Sevelamer Carbonate.
17. The pharmaceutical composition according to claim 16, wherein the aliphatic amine polymer is Sevelamer HCl.
18. The pharmaceutical composition according to claim 16, wherein the amount of Sevelamer HCl, calculated as anhydrous Sevelamer HCl, is from about 400 mg to about 800 mg in each tablet.
19. The pharmaceutical composition according to claim 10, wherein the dosage form is a capsule.
20. A method of preparing a granular composition comprising wet granulated aliphatic amine polymers comprising the following steps of
a) providing aliphatic amine polymers;
b) preparing a granulating solution or liquid;
c) spraying the granalating liquid or solution onto aliphatic amine polymers and forming a spray granulate; and
d) mixing the spray granulate with one or more excipients forming a final blend.
21. The method according to claim 20, wherein the granulating solution is sdected from the group consisting of an ethanolic solution, an ethanolAvater solution, and an isopropyl/water solution.
22. The method according to claim 21, wherein the granulating solution is an ethanol/water solution.
23. The method according to claim 22, wharein the granulating solution is an ethanol/water solution prepared from about 82% to about 95% of Bfhanol (95%) and about 5% to about 18% water.
24. The method according to claim 23, whacein the granulating solution is an ethanol/water solution prepared from 95% of Ethanol (95%) and 5% water.
25. Tlie method according to claim 20, wherein the granulating solution or liquid fra^er comprises a binder material.
26. Hie method according to claim 23, wherein the binder material is dissolved in the granulating solution or liquid.
27. The method according to claim 26, wherein the binder material comprises povidone.
28. The method according to claim 20, wherein the one or more excipient comprise low-substituted Hydroxypropyl Cellulose, hydrogenated vegetable oil and combinations thOTeof.
29. The method according to claim 20, wherein spraying of the granulation liquid is carried out in a fluidized bed equipment
30. The method according to claim 29, wherein spraying of the granulating liquid is carried ont by using a spraying mefliod sdected from the group consisting of top qnray, bottom spray, and tangential/powder spray.
31. The method according to daim 30, wherein the spraying method is the top spray method.

32. The method according to claim 20, furtiber comprising the steps of e) pressing the final blend into tablets.
33. The method according to daim 32, ftirther comprising the step of e) coating the tablets.
34. The method according to claim 20, fiother comprising the st^s of e) fining capsules with the final blend.

35. Itie method acasrding to claim 20, wh^ein the aliphatic amine polymer is selected from the groitp consisting of Sevelamer HCl and Sevelamer Carbonate.
36. The method according to claim 35, wherein the aUphatica amine polym^ is Sevelamer HCl.
37. A method of treating a patient suffering from chronic kidney disease comprising administering a therapeutically effective amount of sevelamer HCl in a pharmaceutical composition of claim 1 in combiuation with hemodialysis treatment to a patient in need thereof
38. The method according to claim 37, wherein the treatment with Sevahner HCl controls serum phosphate iu a patient suffering from chronic kidney disease which patient is on hemodialysis treatment.