EP0276288A1 - Pharmaceutical compositions containing a bisphosphonate and their use for nasal administration - Google Patents
Pharmaceutical compositions containing a bisphosphonate and their use for nasal administrationInfo
- Publication number
- EP0276288A1 EP0276288A1 EP87905191A EP87905191A EP0276288A1 EP 0276288 A1 EP0276288 A1 EP 0276288A1 EP 87905191 A EP87905191 A EP 87905191A EP 87905191 A EP87905191 A EP 87905191A EP 0276288 A1 EP0276288 A1 EP 0276288A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- acid
- hydroxy
- bisphosphonic acid
- nasal
- bisphosphonate
- 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.)
- Withdrawn
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K47/00—Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
- A61K47/06—Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
- A61K47/28—Steroids, e.g. cholesterol, bile acids or glycyrrhetinic acid
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/66—Phosphorus compounds
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/0012—Galenical forms characterised by the site of application
- A61K9/0043—Nose
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P29/00—Non-central analgesic, antipyretic or antiinflammatory agents, e.g. antirheumatic agents; Non-steroidal antiinflammatory drugs [NSAID]
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
- A61P3/00—Drugs for disorders of the metabolism
Definitions
- compositions containing a bisphosphonate and their use for nasal administration are provided.
- the present invention relates to new pharmaceutical compositions containing a bisphosphonate and their use for the nasal administration to patients suffering from diseases where treatment with a bisphosphonate is indicated.
- Bisphosphonates are drugs which can be used in certain diseases involving calcium metabolism, such as Paget's disease, hypercalcaemia due to malignancy, osteoporosis and rheumatoid arthritis.
- Bisphosphonates have hitherto been administered either orally or intravenously to patients.
- the oral absorption is poor and often accompanied by gastro ⁇ intestinal side effects.
- the degree of absorption shows substantial individual variations. Consequently, intravenous administration has up till now had to be used whenever a rapid and reliable delivery of bisphosphonates was needed.
- penetration enhancers can be used to improve the nasal absorption of compounds of higher molecular weight, such as insulin, glucagon and calcitonin, but it was not to be expected that such enhancers would be able to improve the absorption of compounds of relatively low molecular weight like bisphosphonates.
- Any bisphosphonic acid or salt thereof suitable for treatment of patients can form part of the pharmaceutical compositions according to the present invention.
- bisphosphonic acids mention may be made of l-hydroxy-alkylidene-l,l-bisphosphonic acids, e.g.
- the bisphosphonic acids are tetrabasic acids which can form mono-, di-, tri- and tetra-salts with bases.
- the bisphosphonic acids are preferably being used in the form of neutral salts with pharmaceutically acceptable bases.
- Suitable enhancers for the nasal absorption of bisphosphonates include, but are not limited to, compounds of the general formula I:
- X in the o- or ⁇ -position
- Y in the o- or ⁇ -position
- Y in the o- or ⁇ -position
- R stands for -OH or -NHZ, and in which the dotted lines indicate the possibility of double bond(s); when R represents -NHZ, then Z stands for alkyl or aryl, substituted with carboxyl, sulfonic acid groups, and/or quaternary ammonium groups; or compounds of the general formula II:
- R , R , and R in the o- or ⁇ -position, which can be the same or different, each stands for hydrogen or -OH, and in which R has the same meaning as in formula I, provided that not all R , R , R can be hydrogen at
- the pharmaceutical composition of the present invention is formed into a nasal preparation.
- the physiologically active bisphosphonate is contained as the drug, optionally together with an absorption enhancer.
- the nasal preparation according to the present invention can be produced by conventional processes. For example, small amounts of a pH adjusting agent, preservative, thickening agent (natural gums, cellulose derivatives, acrylic acid polymers, vinyl polymers etc.) and/or excipients are incorporated.
- the nasal preparation of the present invention may take a solid, liquid or semi-liquid form.
- a solid form the above components may be simply blended or be freeze-dried to provide a powdery composition, the preferred particle size in either case being about 20 to 250 ⁇ .
- a liquid preparation it is preferably an aqueous solution, an aqueous suspension or an oil suspension.
- the semi-solid preparation is preferably an aqueous or oleaginous gel or ointment.
- the content of bisphosphonate in the final preparation is about 0.005 to 50 w/v% and preferably about 0.01 to 30 w/v% and the optional content of absorption 5 enhancer is from 0 to 5 w/v%, preferably from 0 to 1 w/v%.
- the amount of bisphosphonate in the preparation is about 0.001 to 50 w/v% and preferably about 0.05 to 40 w/v%, and the optional content of absorption enhancer is from 0 to 5 ° w/v%, preferably from 0 to 1 w/v%.
- the excipient is exemplified by glucose, mannitol, inositol, sucrose, lactose, fructose, starch, corn starch, microcrystalline cellulose, hydroxypropylcellulose, hydroxy- propylmethyl cellulose, polyvinylpyrrolidone, etc.
- the liquid preparation can be produced by known procedure.
- an aqueous preparation for nasal administration can be produced by dissolving, suspending or emulsifying the active components in water, a buffer solution or an aqueous medium.
- the oil suspension for nasal use can be produced by suspending or emulsifying the active components in an oleaginous base.
- the above mentioned oleaginous basis is examplified by various oils and fats such as sesame oil, olive oil, corn oil, soybean oil, cotton seed oil, peanut oil, lanoline, vaseline, paraffin, coparaffinate, silicone oil, glycerol fatty acid having 6 to 30 carbon atoms or its glycerol ester or its alcoholic ester, or a mixture thereof.
- oils and fats such as sesame oil, olive oil, corn oil, soybean oil, cotton seed oil, peanut oil, lanoline, vaseline, paraffin, coparaffinate, silicone oil, glycerol fatty acid having 6 to 30 carbon atoms or its glycerol ester or its alcoholic ester, or a mixture thereof.
- an aqueous or oleaginous gel or ointment can be produced by the per se conventional procedure.
- an aqueous gel for nasal administration can be produced in the following manner. First, an aqueous solution or suspension of the active components is prepared and, if required, a pH adjusting agent, a preservative and/or the like are added. The solution is divided into halves and an aqueous gel base is dissolved or dispersed in one of the halves and heated or cooled to give a stable gel. The two halves are combined and evenly mixed to give an aqueous gel preparation.
- Adjustment of the pH of the preparation can be effected by adding an acid, a base, a buffer solution or the like in the course of the production of the preparation.
- the acid there may be mentioned inorganic acids (like hydrochloric acid, boric acid, phosphoric acid, carbonic acid, etc), amino acids and organic acids (e.g. monocarboxylic acids, oxycarboxylic acids, polycarboxylic acids).
- the base is exemplified by sodium hydroxide, potassium hydroxide, sodium hydrogen carbonate, sodium carbonate etc.
- aqueous gel basis examples include natural gums (e.g. gum tragacanth, gum acasia, gum karaya, Irish moss, gum guaiac, gum xanthane, locust bean gum etc) , cellulose derivati es (e.g. methylcellulose, carboxymethylcellulose etc), acrylic acid polymers (e.g. polyacrylic acid, polymethacrylic acid etc) , vinyl polymers (e.g. polyvinyl pyrrolidone, polyvinyl alcohol, polyvinyl methyl ether, carboxypolymethylene etc) , synthetic polysaccharides (e.g. polysucrose, polyglucose, polylactose etc), starch, dextrin, pectin, sodium alginate etc. These bases may be used in the form of appropriate mixtures of two or more species.
- natural gums e.g. gum tragacanth, gum acasia, gum karaya, Irish mos
- the oleaginous ointment for nasal administration can be produced by dispersing the active components evenly in a hot melt of an oleaginous base and cooling the same under stirring.
- the oleaginous- base may be one of those mentioned hereinbefore.
- Preservatives may be incorporated in nasal preparations.
- preservatives include phenolic compounds such as phenol, cresol etc; alcohols such as chlorobutanol, phenylethyl alcohol, propylene glycol etc; invert soaps such as benzalkoniu chloride, benzethonium chloride etc; benzoic acid, sorbic acid, dehydroacetic acid and sulfurous acid and salts thereof; acids and their salts such as sodium hydrogen sulfite.
- the nasal preparation of the invention is in solid form, it can be administered in the following exemplary way.
- a capsule containing the powdery preparation is set in an exclusive dust applicator equipped with needles to pierce the capsule at the top and bottom thereof and an air balloon is used to drive the powdery contents into the nasal cavity.
- a liquid preparation In the case of a liquid preparation, it is put into a nasal douche, an atomizer or a spray-mist applicator suited for nasal application of liquids and dripped or sprayed into the nasal cavity.
- the semi-solid preparation can be administered, for example by filling a tube with the preparation and sending the preparation directly into the nasal cavity through an applicator attached to the mouth of the tube or by administering the indicated dose of the preparation by means of a nasal insertion device.
- the proper amount of the solid preparation per dose is about 5 mg to 100 mg, that of the liquid preparation is about 0.05 to 0.5 ml, and that of the semi-solid preparation is about 50 mg to 500 mg.
- the nasal preparation may be administered from one to about four times per day.
- the invention also relates to a method for treating patients suffering from a disease where treatment with a bisphosphonate is indicated, such as Paget's disease, hyper- calcaemia due to malignancy, osteoporosis and rheumatoid arthritis, said treatment consisting of administering to the patient in need of treatment an effective amount of the present composition.
- the final solution was diluted with water to a total volume of 100 ml.
- Preparation II was sprayed into the nasal cavity of 2 dogs. Preparation I was given either orally, intravenously or nasally (as a spray) to the same two dogs. Urine (0 - 24 hours) was collected in all four experiments and the urinary excretion of EB 899 was determined analytically.
- Example 2 The following preparation may be used for the nasal administration of the disodium salt of 3-amino-l-hydroxy- propylidene-1,1-bisphosphonic acid (APD) either as drops or as a spray:
- APD 3-amino-l-hydroxy- propylidene-1,1-bisphosphonic acid
- Example 3 For the nasal administration of 3-(N,N-dimethylamino)- -l-hydroxy-propylidene-l,l-bisphosphonic acid, the following preparation may be used:
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Life Sciences & Earth Sciences (AREA)
- Veterinary Medicine (AREA)
- Animal Behavior & Ethology (AREA)
- Epidemiology (AREA)
- General Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Diabetes (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Rheumatology (AREA)
- Hematology (AREA)
- Obesity (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Otolaryngology (AREA)
- Pain & Pain Management (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicinal Preparation (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
GB8618259 | 1986-07-25 | ||
GB868618259A GB8618259D0 (en) | 1986-07-25 | 1986-07-25 | Pharmaceutical compositions |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0276288A1 true EP0276288A1 (en) | 1988-08-03 |
Family
ID=10601726
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP87905191A Withdrawn EP0276288A1 (en) | 1986-07-25 | 1987-07-03 | Pharmaceutical compositions containing a bisphosphonate and their use for nasal administration |
Country Status (5)
Country | Link |
---|---|
EP (1) | EP0276288A1 (ja) |
JP (1) | JPH01500754A (ja) |
DK (1) | DK153988A (ja) |
GB (1) | GB8618259D0 (ja) |
WO (1) | WO1988000829A1 (ja) |
Families Citing this family (19)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4994439A (en) * | 1989-01-19 | 1991-02-19 | California Biotechnology Inc. | Transmembrane formulations for drug administration |
US5011678A (en) * | 1989-02-01 | 1991-04-30 | California Biotechnology Inc. | Composition and method for administration of pharmaceutically active substances |
PH26923A (en) * | 1989-03-08 | 1992-12-03 | Ciba Geigy | N-substituted amino alkanediphosphonic acids |
MX21452A (es) * | 1989-07-07 | 1994-01-31 | Ciba Geigy Ag | Preparaciones farmaceuticas que se administran en forma topica. |
MX21453A (es) * | 1989-07-07 | 1994-01-31 | Ciba Geigy Ag | Preparaciones farmaceuticas que se administran en forma topica. |
US5139786A (en) * | 1989-07-07 | 1992-08-18 | Ciba-Geigy Corporation | Topical formulations |
US5283057A (en) * | 1992-04-24 | 1994-02-01 | The Procter & Gamble Company | Risedronate in oral compositions |
US6406714B1 (en) | 1992-12-02 | 2002-06-18 | Merck & Co., Inc. | Dry mix formulation for bisphosphonic acids |
US5462932A (en) * | 1994-05-17 | 1995-10-31 | Merck & Co., Inc. | Oral liquid alendronate formulations |
SE9703691D0 (sv) * | 1997-10-10 | 1997-10-10 | Astra Ab | Pharmaceutical compositions |
US8586781B2 (en) | 1998-04-02 | 2013-11-19 | Mbc Pharma, Inc. | Bone targeted therapeutics and methods of making and using the same |
US7598246B2 (en) | 1998-04-02 | 2009-10-06 | Mbc Pharma, Inc. | Bisphosphonate conjugates and methods of making and using the same |
US6750340B2 (en) | 1998-04-02 | 2004-06-15 | Mbc Research, Inc. | Bisphosphonate conjugates and methods of making and using the same |
US6896871B2 (en) | 1998-04-02 | 2005-05-24 | Mbc Research, Inc. | Biphosphonate conjugates and methods of making and using the same |
US6214812B1 (en) * | 1998-04-02 | 2001-04-10 | Mbc Research, Inc. | Bisphosphonate conjugates and methods of making and using the same |
US6160165A (en) * | 1998-12-10 | 2000-12-12 | Aesgen, Inc. | Method for preparation of disodium pamidronate |
SE9901272D0 (sv) * | 1999-04-09 | 1999-04-09 | Astra Ab | New improved formulation |
IL146520A0 (en) * | 1999-05-21 | 2002-07-25 | Novartis Ag | Use of bisphosphonic acids for treating angiogenesis |
CA2843885C (en) | 2011-08-01 | 2020-03-10 | Mbc Pharma, Inc. | Vitamin b6 derivatives of nucleotides, acyclonucleotides and acyclonucleoside phosphonates |
Family Cites Families (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4067971A (en) * | 1976-05-13 | 1978-01-10 | The Procter & Gamble Company | Therapeutic composition |
DE2813121A1 (de) * | 1977-03-29 | 1978-10-12 | Procter & Gamble | Verwendung von dichlormethan-diphosphonatverbindungen bei der bekaempfung von collagen-erkrankungen und zur wundheilung |
JPS6034925B2 (ja) * | 1979-07-31 | 1985-08-12 | 帝人株式会社 | 持続性鼻腔用製剤およびその製造法 |
IT1194748B (it) * | 1981-02-12 | 1988-09-28 | Gentili Ist Spa | Composizioni farmaceutiche per il trattamento di osteopatie |
US4746508A (en) * | 1983-06-06 | 1988-05-24 | Beth Israel Hospital Assn. | Drug administration |
US4537776A (en) * | 1983-06-21 | 1985-08-27 | The Procter & Gamble Company | Penetrating topical pharmaceutical compositions containing N-(2-hydroxyethyl) pyrrolidone |
US4687768A (en) * | 1984-12-21 | 1987-08-18 | The Procter & Gamble Company | Certain hexahydroindan-2,2-diphosphonic acids useful in treating diseases associated with abnormal calcium and phosphate metabolism |
-
1986
- 1986-07-25 GB GB868618259A patent/GB8618259D0/en active Pending
-
1987
- 1987-07-03 JP JP62504730A patent/JPH01500754A/ja active Pending
- 1987-07-03 WO PCT/DK1987/000084 patent/WO1988000829A1/en not_active Application Discontinuation
- 1987-07-03 EP EP87905191A patent/EP0276288A1/en not_active Withdrawn
-
1988
- 1988-03-22 DK DK153988A patent/DK153988A/da not_active IP Right Cessation
Non-Patent Citations (1)
Title |
---|
See references of WO8800829A1 * |
Also Published As
Publication number | Publication date |
---|---|
DK153988D0 (da) | 1988-03-22 |
JPH01500754A (ja) | 1989-03-16 |
DK153988A (da) | 1988-03-22 |
WO1988000829A1 (en) | 1988-02-11 |
GB8618259D0 (en) | 1986-09-03 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
EP0276288A1 (en) | Pharmaceutical compositions containing a bisphosphonate and their use for nasal administration | |
US7390793B2 (en) | Micelles | |
JP3962429B2 (ja) | 静脈内注入用アレンドロナート組成物 | |
US20070077286A1 (en) | Drug-containing nanoparticle, process for producing the same and parenterally administered preparation from the nanoparticle | |
JP2007516269A (ja) | ビスホスホネートの医薬製剤 | |
US5283067A (en) | Parenteral suspensions | |
EP0573604B1 (en) | Methods for the treatment of osteoporosis | |
US6235724B1 (en) | Injections containing lipid a analogues and process for the preparation thereof | |
KR20010104389A (ko) | 비스포스포네이트 및 비스포스포네이트의 흡수를향상시키는 첨가제를 포함하는 제약 제제 | |
ES2254410T3 (es) | Composicion farmaceutica como gel para administracion subcutanea que comprende acidos bisfosfonicos o sus sales. | |
JPH026409A (ja) | ジホスホン酸誘導体経口医薬組成物 | |
EP0449405B1 (en) | Use of bisphosphonic acids for the treatment of calcium metabolism disorders | |
JP2002501015A (ja) | リーシュマニア症の治療における経口投与のためのミルテフォシンを含有する固形医薬品 | |
IE60453B1 (en) | Parenteral suspensions of diclofenac | |
KR890000907B1 (ko) | 안정한 현탁액 제조용 고체 약물 제형의 제조방법 | |
CA2356262A1 (en) | Use of bisphosphonates for the prevention and treatment of infectious processes | |
EP1016409A1 (en) | Freeze-dried composition containing glycosphingolipid and process for producing the same | |
EP2668952B1 (en) | Aqueous formulations of bisphosphonates, vitamin D and benzyl alcohol suitable for subcutaneous or intramuscular use | |
JP2004504346A (ja) | 骨転移の治療におけるリン酸エストラムスチンの使用 | |
EP0338081A1 (en) | Oily rectal instillation | |
EP1136069A1 (en) | Pharmaceutical compositions containing clodronates for high local tolerance intramuscular administration | |
KR100552593B1 (ko) | 리피드a유사체함유주사용제제및그제조방법 | |
JP2002332235A (ja) | 骨疾患治療用液体医薬組成物 | |
US20040014729A1 (en) | Use of estramustine phosphate in the treatment of bone metastasis | |
JPH1171284A (ja) | リピッドa類縁体含有注射用製剤及びその製造方法 |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PUAI | Public reference made under article 153(3) epc to a published international application that has entered the european phase |
Free format text: ORIGINAL CODE: 0009012 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): BE DE FR GB IT LU NL SE |
|
17P | Request for examination filed |
Effective date: 19880803 |
|
STAA | Information on the status of an ep patent application or granted ep patent |
Free format text: STATUS: THE APPLICATION IS DEEMED TO BE WITHDRAWN |
|
18D | Application deemed to be withdrawn |
Effective date: 19900201 |