Patent Application
20120058200
Present invention relates to a process for the preparation and pharmaceutical usage of dihydrate form of lanthanum carbonate. Selected Lanthanum carbonate hydrates are used to treat hyperphosphataemia in patients with renal failure. They are administered into the gastrointestinal tract. Shire Pharmaceuticals, under exclusive license from AnorMED, has developed and launched lanthanum carbonate (Fosrenol, formerly Foznol), a phosphate-binding lanthanum salt, for the oral treatment of hyperphosphataemia in dialysis patients. Lanthanum carbonate dihydrate has the formula given below.
La2(CO3)3.xH2O
Wherein x=2.0±0.2
Selected Lanthanum carbonate hydrates of formula La2(CO3)3.xH2O where x has a value from 3-6 are reported in the U.S. Pat. No. 5,968,976 by AnorMED (Canada) for the treatment of hyperphosphataemia by administration into the gastrointestinal tract. A process for the preparation of lanthanum carbonate tetrahydrate was also disclosed in this patent. Phosphate binding studies in this patent showed that samples of lanthanum carbonate with 3.8 to 4.4 moles of hydration are quicker in phosphate removal.
Chemical abstract search shows that the lanthanum carbonate is reported for the first time in 1923 (Z. Anaorg. Allgem. Chem., 131, 275-86, 1923). In the abstract no information regarding its preparation is disclosed. Crystal structure of lanthanum carbonate is reported in Geol. Nauk, #4, 157-95, 1954. No information regarding the preparation or degree of hydration is mentioned in the relevant abstract of this reference.
A process for the preparation of lanthanum carbonate is given in J. Am. Chem. Soc., 72, 3306, 1950. It is mentioned that pure crystalline rare earth compounds are difficult to prepare by the two commonly used methods, namely the precipitation of the compounds by alkali carbonates or bicarbonates from rare earth salt solutions or the conversion, in aqueous suspension, of rare earth hydroxides to carbonates by carbon dioxide. To solve these problems rare earth trichloroacetates were taken in water medium and heated to get pure carbonates. Here, the by-products are water and chloroform.
2La(C2Cl3O2)3+3H2O→3CO2+6CHCl3+La2(CO3)3
A process for the preparation of lanthanum carbonate octahydrate is disclosed in Izv. Akad. Nauk. SSSR, Neorgan. Materialy, 1(7), 1166-70 (1965). According to this process lanthanum nitrate is reacted with ammonium carbonate and the product isolated as octahydrate.
A process for the preparation of rare earth carbonates is discussed in J. Inorg. Nucl. Chem., 27, 1489-1493, 1965. According to this process water solutions of rare earth chlorides are reacted with ammonium trichloroacetate (prepared from ammonia and trichloroacetic acid) to get rare earth carbonates. Lanthanum carbonate prepared according to this process was isolated as octahydrate and its IR spectrum, thermogravimetric curve were given. Product was obtained in 50% yield.
Main drawback in this process is the usage of costly trifluoroacetic acid and low yield.
A process for the preparation of lanthanum carbonate is disclosed in U.S. Pat. No. 5,968,976. According to this reference, lanthanum oxide is converted to lanthanum nitrate using nitric acid. The resultant aqueous solution was reacted with sodium carbonate to get lanthanum carbonate. Alternatively, lanthanum oxide was reacted with hydrochloric acid to get lanthanum chloride. The resultant aqueous solution was reacted with sodium carbonate to get lanthanum carbonate.
Main drawback in this process is the usage of inorganic base, sodium carbonate. Removal of sodium salts from lanthanum carbonate is difficult. Also, lanthanum carbonate formed in the reaction is slimy in nature and filtration/washing of sodium nitrate is tedious.
Keeping in view of the difficulties in commercialization of the above-mentioned processes for the preparation of lanthanum carbonate, we aimed to develop a simple and cost effective process for commercial production of highly pure lanthanum carbonate.
Lanthanum carbonate hydrate is prone to decarboxylation under certain stressful conditions such as high temperature and humidity. The decarboxylation product is lanthanum hydroxycarbonate. Lanthanum hydroxycarbonate is known to exist in two polymorphic forms. An assay method for the quantification of lanthanum hydroxycarbonate in lanthanum carbonate hydrate by powder x-ray analysis is disclosed in EP1852695.
In the preparation of lanthanum carbonate disclosed in U.S. Pat. No. 5,968,976, lanthanum carbonate octahydrate is produced by reacting lanthanum chloride or nitrate with sodium carbonate in water medium. The resultant octahydrate is dried carefully at 80° C. for various durations of time to get the tetrahydrate derivative of lanthanum carbonate. Under these conditions, formation of lanthanum hydroxycarbonate is unavoidable.
We observed that lanthanum carbonate dihydrate exhibit improved performance over standard lanthanum carbonate tetrahydrate in phosphate binding studies.
One aspect of the present invention is the use of lanthanum carbonate dihydrate for the preparation of medicament for the treatment of hyperphasphataemia by administration into the gastrointestinal tract.
The present invention also provides a pharmaceutical composition comprising lanthanum carbonate dihydrate in admixture or association with a pharmaceutically acceptable diluent or a carrier, in a form suitable for administration into the gastrointestinal tract for the treatment of hyperphosphataemia.
We have now observed that lanthanum carbonate hydrate can be prepared by reacting readily available lanthanum chloride with an organic base such as ammonium bicarbonate to get free-flowing and fine crystalline lanthanum carbonate hydrate. Lanthanum carbonate hydrate can be easily isolated from the reaction mass by simple filtration and washing with minimum amount of water to remove the by-product, ammonium chloride. Also, we have now invented that a selected dihydrate of lanthanum carbonate can be obtained readily by drying under azeotropic conditions using a hydrocarbon solvent. Process for the preparation of dihydrate is robust without requiring any special/controlled drying condition as mentioned in U.S. Pat. No. 5,968,976 for similar hydrates.
According to one aspect, the present invention provides a process for the preparation of lanthanum carbonate dihydrate free of lanthanum hydroxycarbonate impurity, which comprises:
The reaction between lanthanum chloride and ammonium bicarbonate is given in the following equation:
2LaCl3+6NH4(HCO3)→La2(CO3)3+6NH4Cl+3CO2+3H2O
Amount of water used in step (i) is selected from 30-70 volumes to the weight of lanthanum chloride, preferably 50-70 volumes. Preferred temperature of reaction in step (i) is 20-40° C., more preferably 25-35° C. Hydrocarbon solvent used in step (v) and (vi) is selected from hexane, heptane, cyclohexane, toluene, xylene, etc., preferably toluene.
Lanthanum carbonate hydrate produced according to the present invention is free flowing in nature and filtration was very fast compared to lanthanum carbonate hydrate produced according to U.S. Pat. No. 5,968,976 process. Also, lanthanum carbonate hydrate produced according to U.S. Pat. No. 5,968,976 is slimy in nature. Lanthanum carbonate dihydrate produced according to the present invention is free of lanthanum hydroxycarbonate impurity. Whereas lanthanum carbonate produced according to U.S. Pat. No. 5,968,976 is always contaminated with about 0.5-1.0% of this impurity. Lanthanum carbonate dihydrate is found to be stable at room temperature.
The details of the invention are given in the Examples given below which are provided to illustrate the invention only and therefore should not be construed to limit the scope of the present invention.
Into a 10 L, three-necked RB flask was charged 7 L of demineralized water. Lanthanum chloride heptahydrate (100 g) was charged into the flask and stirred for 30 min at 25-30° C. The solution was filtered through Bucher funnel and flask under vacuum to get a particle-free solution. Filtrate was transferred into a 10 L, three-necked RB flask.
Ammonium bicarbonate (130 g) was charged into a 2 L, three-necked RB flask and 700 ml of demineralized water was added. The resultant solution was filtered using a funnel and flask to make it particle-free. The filtrate was taken into an addition funnel and added slowly in 3-4 hours into lanthanum chloride solution at 25-30° C. After the completion of addition reaction, the mass was maintained for 1 hour at 25-30° C. The reaction mass was filtered through Buckner funnel and flask under vacuum. The wet cake was washed with 200 ml of demineralized water. The wet material was transferred into a 1 L, three-necked RB flask, 500 ml of demineralized water was added and stirred for 15 min. The mass was filtered though Buckner funnel and flask under vacuum. The chloride content in wet lanthanum carbonate hydrate was checked. The same washing procedure was repeated one more time, if the chloride content is above 500 ppm. The wet material was transferred into a petridish and dried in an oven at 60-65° C. for 4-6 hours.
The above lanthanum carbonate hydrate (69 g) was charged into a 1 L, four-necked RB flask. Particle free toluene (400 ml) was charged into the flask and the reaction mass was heated to reflux. Water was collected azeotropically using a Dean-Stark apparatus. When the water collection stopped (nearly 3-4 hours) the reaction mass was cooled to 30-35° C. The mass was filtered through Buchner funnel and flask under vacuum and finally washed with 100 ml of filtered toluene. The wet material was dried in an oven at 60-65° C. for 4-6 h to get lanthanum carbonate dihydrate (60 g) as white crystalline solid.
The lanthanum carbonate tablets were prepared using the above lanthanum carbonate dihydrate.
Phosphate Binding Studies of Various Lanthanum Carbonate Hydrates
To study the phosphate binding activity of lanthanum carbonate dihdyrate, other hydrates of lanthanum carbonate (monohydrate, tetrahydrate and hexahydrate) were prepared.
The above results are also plotted and shown in
| Filing Document | Filing Date | Country | Kind | 371c Date |
|---|---|---|---|---|
| PCT/IN2009/000288 | 5/15/2009 | WO | 00 | 11/4/2011 |
