AU2002334200A1 - Pharmaceutically acceptable alendronate salts in amorphous form - Google Patents
Pharmaceutically acceptable alendronate salts in amorphous formInfo
- Publication number
- AU2002334200A1 AU2002334200A1 AU2002334200A AU2002334200A AU2002334200A1 AU 2002334200 A1 AU2002334200 A1 AU 2002334200A1 AU 2002334200 A AU2002334200 A AU 2002334200A AU 2002334200 A AU2002334200 A AU 2002334200A AU 2002334200 A1 AU2002334200 A1 AU 2002334200A1
- Authority
- AU
- Australia
- Prior art keywords
- pharmaceutically acceptable
- alendronate
- amoφhous
- salt
- amoφhous form
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Description
PHARMACEUTICALLY ACCEPTABLE
ALENDRONATE SALTS IN AMORPHOUS
FORM
This invention relates to pharmaceutically acceptable salts of 4-amino-l- hydroxybutylidene bisphosphonic acid (alendronate salts) in amorphous form and a process of preparing the same.
Alendronate sodium is an inhibitor of bone resorbtion useful for the treatment of diseases such as Paget's disease and osteoporosis.
Processes used heretofore for the production of alendronate sodium result in a crystalline product. EP 402152 discloses the preparation of alendronate monosodium trihydrate which is crystalline. EP 462663 discloses an improved process for making alendronate and crystalline salts thereof which process avoids the use of a strongly acidic hydrolysis medium. A pharmaceutical composition comprising the anhydrous crystalline form of alendronate sodium is disclosed in WO 96/39149.
In order to facilitate easy formulation into pharmaceutical compositions, high solubility of an alendronate salt, such as alendronate sodium, is desired. High solubility may also be a desirable characteristic in terms of the pharmacological properties of this compound.
The present invention is based on the discovery that pharmaceutically acceptable alendronate salts in an amorphous form are non-hygroscopic and exhibit surprisingly better solubility characteristics as compared to, for example, crystalline alendronate sodium trihydrate. In particular, an alendronate salt in an amoφhous form of the present invention dissolves in water at a faster rate than the crystalline material.
There is provided by the present invention, therefore, a pharmaceutically acceptable alendronate salt in an amoφhous form. In particular, the present invention is concerned with a monovalent pharmaceutically acceptable alendronate salt in an amoφhous form. More particularly, the present invention provides alendronate monosodium in an amoφhous form.
The term "amoφhous" as used herein denotes a physical state which is not crystalline and may be verified by x-ray diffraction and other means including but not limited to observation
with a polarized light microscope and differential scanning calorimetry. More particularly, an amoφhous alendronate salt in accordance with the present invention is preferably essentially free from any crystalline form of alendronate salts.
The present invention provides a pharmaceutically acceptable alendronate salt in an amoφhous form, preferably containing less than about 3%, and most preferably less than about 1%, water. In particular, the present invention is concerned with a monovalent pharmaceutically acceptable alendronate salt in an amoφhous form, preferably containing less than about 3%, and most preferably less than about 1%, water. More particularly, the present invention provides alendronate monosodium in an amoφhous form, preferably containing less than about 3%, and most preferably less than about 1%, water.
The present invention also provides amoφhous alendronate monosodium having an X- ray diffraction pattern as shown in the accompanying Figure.
The invention also includes a pharmaceutical composition comprising a therapeutically effective amount of a pharmaceutically acceptable alendronate salt in an amoφhous form (in particular alendronate monosodium in an amoφhous form), together with a pharmaceutically acceptable carrier, diluent or excipient therefor.
The invention also provides a method of inhibiting bone resoφtion in a patient, which method comprises administering to a patient suffering from or susceptible to bone resoφtion a therapeutically effective amount of a pharmaceutically acceptable alendronate salt in an amoφhous form substantially as herein before described, in particular alendronate monosodium in an amoφhous form substantially as herein before described, or a pharmaceutical composition comprising the same substantially as hereinbefore described.
The term "inhibition of bone resoφtion" as used herein, refers to treatment and prevention of bone loss, especially inhibiting the removal of existing bone, for example through direct or indirect alteration of osteoclast formation or activity. Thus a pharmaceutically acceptable alendronate salt in an amoφhous form according to the present invention can, for example, prevent bone loss by the direct or indirect alteration of osteoclast formation or activity and which may increase bone mass in patient treatment populations.
Such methods of treatment according to the present invention are useful in treating bone fractures, defects and disorders which can result from the pathological conditions of osteoporosis, osteoarthritis, Paget's disease, osteohalisteresis, osteomalacia, bone loss resulting from multiple myeloma and other forms of related cancer, bone loss resulting from side effects of disuse, other
medical treatment (such as steroids), rheumatoid-related and age-related loss of bone mass and the like. Methods according to the present invention may have particular utility for the treatment of female patients who are post-menopausal.
The term "treating" or "inhibiting" as used herein with respect to methods of the present invention shall mean providing a patient with an amount of a pharmaceutically acceptable alendronate salt in an amoφhous form sufficient to act prophylactically with respect to a disease state substantially as herein before described associated with bone resoφtion in the patient, and / or providing a patient with an amount of a pharmaceutically acceptable alendronate salt in an amoφhous form sufficient to alleviate or substantially eliminate a disease state substantially as herein before described associated with bone resoφtion in the patient.
In another aspect, the invention provides a process for the production of a pharmaceutically acceptable alendronate salt in an amoφhous form (in particular alendronate monosodium in an amoφhous form), which process comprises removing solvent from a solution of an alendronate salt, so as to obtain an amoφhous product according to the present invention.
In the process of the invention, solvent is removed from the solution of an alendronate salt therein, to form amoφhous alendronate according to the present invention. The preferred solvent is water since pharmaceutically acceptable alendronate salts in an amoφhous form are not very soluble in other common solvents. In principle, however, any solvent can be used.
The solution of an alendronate salt should be essentially free of any crystalline alendronate salt. The solution can, however, contain some (non-crystalline) suspended alendronate salt so as to form a cloudy solution, although this is not preferred.
The solution of an alendronate salt can be made in any suitable way. For example, it can be prepared by dissolving sodium alendronate, eg trihydrate or anhydrous product, in a solvent. The mixture can be heated to aid in the dissolution: in the case of an aqueous solution, we have found it can be advantageous to heat to about 50°C to 60°C.
Alternatively, an alendronate salt can be formed in situ in the solvent. One example of this is to add sodium hydroxide solution to a suspension of alendronic acid in water to form the alendronate sodium in solution in water. Most preferably, the volume of alendronic acid is suspended in about 30 volumes of water and then the pH is adjusted to about 4.3 to 4.4 with sodium hydroxide.
The solution of an alendronate salt used in the process of the invention will preferably have a volume ratio of an alendronate salt to solvent of about 1:10 to about 1:30 or more,
depending on the solubility in the solvent used. For aqueous solutions, a ratio of about 1:10 is preferred. In general, the less solvent there is present, the less needs to be removed to form the amoφhous product, so lower solvent qualities are preferred for this reason.
The removal of solvent can be effected by any suitable means appropriate to the solvent in question, from simple evaporation to more intensive procedures. In the most usual case of aqueous solutions, we prefer to use spray drying. In spray drying aqueous solutions, the inlet temperature is preferably from 120°C to 250°C, the outlet temperature preferably from 70°C to 120°C and the feed rate preferably from 5 to 25 nri/min. However, other temperatures and rates can be used.
The product can be characterised by powder X-ray crystallography. Amoφhous alendronate sodium is characterised by the absence of a well defined diffiactogram. A typical difrractogram is shown in the accompanying Figure. When observed under a microscope, the amoφhous product of the invention is seen as spherical beads whereas, in contrast, crystalline material exhibits rhombic structure. The moisture content of amoφhous alendronate sodium of the invention is preferably no greater than about 3% by weight, more preferably less than about 1%. At these moisture contents, the amoφhous product is stable.
The following Examples illustrate the process of the invention.
Preparation of Alendronate Soduim Amoφhous Example 1
Alendronate sodium trihydrate 25g in 250ml of water was heated at 60 C to obtain a clear solution. This solution was spray dried in a Lab Plant Spray Drier SD 05 with an inlet temperature of 200 C, outlet temperature of 100 C, compressed air rate of 0.3 m3/hr and a feed rate of 15 ml/min, to obtain 20g of the product.
The amoφhous product was characterised by powder X-ray diffraction.
Moisture content: less than 1%. Example 2
Crystalline alendronate sodium anhydrous 25g in 500ml of water was heated at 50°C to obtain an almost clear solution. This solution was spray dried in a Lab Plant Spray Drier SD 05 with an inlet temperature of 160 C, outlet temperature of 80 C, compressed air rate of 0.3 m3 /hr and a feed rate of 8 ml/min, to obtain 18g of the product.
The amoφhous product was characterised by powder X-ray diffraction. Example 3
To a suspension of alendronic acid 25g in 750ml of water was added a 20% solution of sodium hydroxide and pH adjusted to 4.3 to 4.4 to obtain a clear solution. This solution was spray dried in a Lab Plant Spray Drier SD 05 with an inlet temperature of 180°C, outlet temperature of 90 C, compressed air rate of 0.3 m3 /hr and a feed rate of 10 ml min, to obtain 20g of the product. The amoφhous product was characterised by powder X-ray diffraction.
According to another aspect of the invention, the amoφhous alendronate sodium can be formulated into pharmaceutical compositions, for example in the form of tablets (coated or uncoated) or capsules for oral adrninistration. Suitable carriers include, for example sugars, starch and derivatives, cellulose and derivatives, gums and polyalcohols. The compositions may also contain additional ingredients such as lubricants, compression aids, flavours, sweeteners and preservatives.
Claims (17)
1 A pharmaceutically acceptable alendronate salt in an amoφhous form.
2 A monovalent pharmaceutically acceptable alendronate salt in an amoφhous form.
3 Alendronate monosodium in an amoφhous form.
4 A pharmaceutically acceptable alendronate salt in an amoφhous form, containing less than about 3% water.
5 A monovalent pharmaceutically acceptable alendronate salt in an amoφhous form, αmtaining less than about 3% water.
6 Alendronate monosodium in an amoφhous form, containing less than about 3% water.
7 A pharmaceutically acceptable alendronate salt according to any of claims 1 to 6, containing less than about 1% water.
8 Amoφhous alendronate monosodium having an X-ray diffraction pattern as shown in the accompanying Figure.
9 A process for the production of a pharmaceutically acceptable alendronate salt in an amoφhous form according to any of claims 1 to 8, which process comprises removing solvent from a solution of an alendronate salt, so as to obtain a pharmaceutically acceptable alendronate salt in an amoφhous form according to any of claims 1 to 8.
10 A process according to claim 9, wherein the solvent comprises water.
11 A process according to claim 9, wherein said solution is produced by suspending alendronic acid in water and adjusting the pH using aqueous sodium hydroxide.
12 A process according to any of claims 9 to 11 , in which said solution is spray dried.
13 A process for the production of amoφhous alendronate monosodium substantially as herein described in Example 1, 2 or 3.
14 A pharmaceutical composition comprising a therapeutically effective amount of a pharmaceutically acceptable alendronate salt in an amoφhous form according to any of claims 1 to 8, together with a pharmaceutically acceptable carrier, diluent or excipient therefor.
15 A pharmaceutical composition according to claim 14, in which said pharmaceutically acceptable alendronate salt in an amoφhous form is as claimed in claim 8.
16 A method of inhibiting bone resoφtion in a patient, which method comprises administering to a patient suffering from or susceptible to bone resoφtion a therapeutically effective amount of a pharmaceutically acceptable alendronate salt in an amoφhous form according to any of claims 1 to 8, or a pharmaceutical composition according to claim 14 or 15.
17. A method according to claim 16, for the treatment of fractures, disorders which result from osteoporosis, osteoarthritis, Paget's disease, osteohalisteresis, osteomalacia, bone loss resulting from multiple myeloma and other forms of related cancer, bone loss resulting from side effects of disuse, steroid treatment, rheumatoid-related and age-related loss of bone mass.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB0125081A GB2383042A (en) | 2001-10-18 | 2001-10-18 | Amorphous alendronate sodium |
GB0125081.0 | 2001-10-18 | ||
PCT/GB2002/004730 WO2003033508A1 (en) | 2001-10-18 | 2002-10-18 | Pharmaceutically acceptable alendronate salts in amorphous form |
Publications (2)
Publication Number | Publication Date |
---|---|
AU2002334200A1 true AU2002334200A1 (en) | 2003-07-03 |
AU2002334200B2 AU2002334200B2 (en) | 2008-04-03 |
Family
ID=9924125
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU2002334200A Ceased AU2002334200B2 (en) | 2001-10-18 | 2002-10-18 | Pharmaceutically acceptable alendronate salts in amorphous form |
Country Status (22)
Country | Link |
---|---|
US (1) | US7112577B2 (en) |
EP (1) | EP1436303B1 (en) |
JP (1) | JP4490100B2 (en) |
KR (1) | KR20040053186A (en) |
AT (1) | ATE338761T1 (en) |
AU (1) | AU2002334200B2 (en) |
BR (1) | BR0213398A (en) |
CA (1) | CA2463815C (en) |
CL (1) | CL2004001372A1 (en) |
DE (1) | DE60214576T2 (en) |
EC (1) | ECSP045067A (en) |
ES (1) | ES2271375T3 (en) |
GB (1) | GB2383042A (en) |
HK (1) | HK1066011A1 (en) |
IL (1) | IL161360A0 (en) |
MX (1) | MXPA04003549A (en) |
NZ (1) | NZ532292A (en) |
PT (1) | PT1436303E (en) |
RU (1) | RU2334751C2 (en) |
TN (1) | TNSN04067A1 (en) |
WO (1) | WO2003033508A1 (en) |
ZA (1) | ZA200403024B (en) |
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NZ552514A (en) * | 2001-12-24 | 2008-08-29 | Teva Pharma | Dosage form with a core tablet of active ingredient sheathed in a compressed annular body of powder or granular material, and process and tooling for producing it |
US20040052843A1 (en) * | 2001-12-24 | 2004-03-18 | Lerner E. Itzhak | Controlled release dosage forms |
ITMI20020146A1 (en) * | 2002-01-29 | 2003-07-29 | Lyogen Ltd | AMORPHOUS MONOSODIUM ALENDRONATE AND PROCESS FOR ITS PREPARATION |
DE602005003557D1 (en) † | 2004-02-26 | 2008-01-10 | Zentiva As | AMORPH FORMS OF RISEDRONATE MONONATIUM |
EP1571152B1 (en) * | 2004-03-03 | 2007-08-08 | CHEMI S.p.A. | Amorphous 3-Pyridil-1-Hydroxyethyliden-1,1-Biphosphonic acid monosodium salt and process for the preparation thereof . |
CZ297262B6 (en) * | 2004-12-28 | 2006-10-11 | Zentiva, A. S. | Trisodium salt of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid |
US20090118238A1 (en) * | 2007-09-17 | 2009-05-07 | Protia, Llc | Deuterium-enriched alendronate |
BR112015005404A2 (en) * | 2012-09-11 | 2017-08-22 | Dr Reddys Laboratories Ltd | POLYMORPHIC FORMS OF ENZALUTAMIDE AND THEIR PREPARATION |
EP4169908A1 (en) * | 2012-09-11 | 2023-04-26 | Medivation Prostate Therapeutics LLC | Formulations of enzalutamide |
CN108884111A (en) * | 2016-05-09 | 2018-11-23 | 苏州科睿思制药有限公司 | The crystal form and its preparation method and application of gram vertical boron sieve free form |
US11447506B2 (en) | 2016-05-09 | 2022-09-20 | Anacor Pharmaceuticals, Inc. | Crystal forms of crisaborole in free form and preparation method and use thereof |
CA3026885A1 (en) * | 2016-06-16 | 2017-12-21 | Xenon Pharmaceuticals Inc. | Solid state forms of spiro-oxindole compounds |
US10717715B2 (en) * | 2016-09-06 | 2020-07-21 | Indena S.P.A. | Solid forms of ingenol 3-(3,5-diethylisoxazole-4-carboxylate) and method for preparing the same |
US11369579B2 (en) | 2016-10-24 | 2022-06-28 | Syneurx International (Taiwan) Corp. | Polymorphic forms of sodium benzoate and uses thereof |
US10336679B2 (en) * | 2016-10-24 | 2019-07-02 | Syneurx International (Taiwan) Corp. | Polymorphic forms of sodium benzoate and uses thereof |
CN110248951B (en) * | 2017-02-01 | 2022-10-28 | 阿堤亚制药公司 | Nucleotide hemisulfate salt for treating hepatitis C virus |
EP3601265B1 (en) * | 2017-03-30 | 2023-06-21 | Merck Patent GmbH | Solid form of (s)-[2-chloro-4-fluoro-5-(7-morpholin-4-ylquinazolin-4-yl)phenyl]-(6-methoxy-pyridazin-3-yl)methanol |
RS64592B1 (en) * | 2017-11-22 | 2023-10-31 | Agios Pharmaceuticals Inc | Crystalline forms of n-(4-(4-(cyclopropylmethyl) piperazine-1-carbonyl)phenyl)quinoline-8-sulfonamide |
WO2019200005A1 (en) | 2018-04-10 | 2019-10-17 | Atea Pharmaceuticals, Inc. | Treatment of hcv infected patients with cirrhosis |
US10874687B1 (en) | 2020-02-27 | 2020-12-29 | Atea Pharmaceuticals, Inc. | Highly active compounds against COVID-19 |
WO2022176017A1 (en) * | 2021-02-16 | 2022-08-25 | 大塚製薬株式会社 | Amorphous material and composition containing said amorphous material |
Family Cites Families (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4304734A (en) * | 1980-10-16 | 1981-12-08 | Vysoka Skola Chemicko-Technologicka | 6-Amino-1-hydroxyhexylidene diphosphonic acid, salts and a process for production thereof |
US4922007A (en) * | 1989-06-09 | 1990-05-01 | Merck & Co., Inc. | Process for preparing 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid or salts thereof |
JP3344726B2 (en) * | 1995-06-06 | 2002-11-18 | メルク エンド カンパニー インコーポレーテッド | Anhydrous alendronate monosodium salt preparation |
US5853759A (en) * | 1996-05-17 | 1998-12-29 | Merck & Co.. Inc. | Effervescent alendronate formulation |
YU14701A (en) | 1998-08-27 | 2003-01-31 | Teva Pharmaceutical Industies Ltd. | Novel hydrate forms of alendronate sodium, processes for manufascture thereof and pharmaceutical compositions thereof |
EP1135397B1 (en) * | 1998-12-10 | 2003-04-23 | Aesgen, Inc. | Method for preparation of disodium pamidronate |
US6160165A (en) * | 1998-12-10 | 2000-12-12 | Aesgen, Inc. | Method for preparation of disodium pamidronate |
AU7902800A (en) | 1999-10-26 | 2001-05-08 | A/S Gea Farmaceutisk Fabrik | Novel salts of 4-amino-1-hydroxybutylidene-1,1-bisphosphonic acid, their preparation and use |
-
2001
- 2001-10-18 GB GB0125081A patent/GB2383042A/en not_active Withdrawn
-
2002
- 2002-10-18 AU AU2002334200A patent/AU2002334200B2/en not_active Ceased
- 2002-10-18 PT PT02801429T patent/PT1436303E/en unknown
- 2002-10-18 EP EP02801429A patent/EP1436303B1/en not_active Expired - Lifetime
- 2002-10-18 DE DE60214576T patent/DE60214576T2/en not_active Expired - Lifetime
- 2002-10-18 WO PCT/GB2002/004730 patent/WO2003033508A1/en active IP Right Grant
- 2002-10-18 JP JP2003536247A patent/JP4490100B2/en not_active Expired - Fee Related
- 2002-10-18 IL IL16136002A patent/IL161360A0/en not_active IP Right Cessation
- 2002-10-18 KR KR10-2004-7005768A patent/KR20040053186A/en not_active Application Discontinuation
- 2002-10-18 BR BR0213398-9A patent/BR0213398A/en not_active Withdrawn
- 2002-10-18 NZ NZ532292A patent/NZ532292A/en not_active IP Right Cessation
- 2002-10-18 US US10/492,977 patent/US7112577B2/en not_active Expired - Fee Related
- 2002-10-18 MX MXPA04003549A patent/MXPA04003549A/en active IP Right Grant
- 2002-10-18 RU RU2004113306/04A patent/RU2334751C2/en not_active IP Right Cessation
- 2002-10-18 ES ES02801429T patent/ES2271375T3/en not_active Expired - Lifetime
- 2002-10-18 AT AT02801429T patent/ATE338761T1/en not_active IP Right Cessation
- 2002-10-18 CA CA002463815A patent/CA2463815C/en not_active Expired - Fee Related
-
2004
- 2004-04-16 TN TNP2004000067A patent/TNSN04067A1/en unknown
- 2004-04-16 EC EC2004005067A patent/ECSP045067A/en unknown
- 2004-04-21 ZA ZA200403024A patent/ZA200403024B/en unknown
- 2004-06-04 CL CL200401372A patent/CL2004001372A1/en unknown
- 2004-11-09 HK HK04108787A patent/HK1066011A1/en not_active IP Right Cessation
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