EP0232254A1 - Oxazepam enthaltendes arzneimittel - Google Patents
Oxazepam enthaltendes arzneimittelInfo
- Publication number
- EP0232254A1 EP0232254A1 EP85903997A EP85903997A EP0232254A1 EP 0232254 A1 EP0232254 A1 EP 0232254A1 EP 85903997 A EP85903997 A EP 85903997A EP 85903997 A EP85903997 A EP 85903997A EP 0232254 A1 EP0232254 A1 EP 0232254A1
- Authority
- EP
- European Patent Office
- Prior art keywords
- chloro
- phenyl
- hydroxy
- dihydro
- benzodiazepin
- 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- Withdrawn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
- A61K9/00—Medicinal preparations characterised by special physical form
- A61K9/14—Particulate form, e.g. powders, Processes for size reducing of pure drugs or the resulting products, Pure drug nanoparticles
- A61K9/141—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers
- A61K9/146—Intimate drug-carrier mixtures characterised by the carrier, e.g. ordered mixtures, adsorbates, solid solutions, eutectica, co-dried, co-solubilised, co-kneaded, co-milled, co-ground products, co-precipitates, co-evaporates, co-extrudates, co-melts; Drug nanoparticles with adsorbed surface modifiers with organic macromolecular compounds
-
- 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
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/55—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having seven-membered rings, e.g. azelastine, pentylenetetrazole
Definitions
- Oxazepam containing pharmaceutical composition
- the present invention relates to a pharmaceutical composition having improved solubility and improved rate of dissolution for the treatment of sleep disorders and as a tranquiliser containing as an active ingredient 7- chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiaze- pin-2-one associated with a carrier, as well as a process for the preparation of the active ingredient of the pharmaceutical composition and the use thereof.
- compositions for the treatment of sleep disorders should display the following properties:-
- the activity of the medicament should last for a period corresponding to that of the normal period of sleep (8 to 10 hours);
- the compound 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl- 2H- 1,4-benzodiazepin-2-one which has been accorded the international short name oxazepam is a known compound.
- 7-Chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzo- diazepin-2-one is used mainly as the active ingredient in tranquilisers for the alleviation of anxiety states for calming the patient and sometimes for alleviation of sleep disorders.
- tablets or capsules which may for example contain from 15 to 50 mg of 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H- 1,4-benzodiazepin-2-one (Swiss Drug Index 1982).
- a further disadvantage arising out of the low solubility of 7-chloro-1,3-dihydro-3-hydr ⁇ xy-5-phenyl-2H-1,4-benzo- diazepin-2-one is that it is very slowly absorbed in the gastrointestinal tract which results in delayed appearance of hypnotic activity in the body.
- a pharmaceutical composition for the treatment of sleep disorders or for use as a tranquiliser containing as an active ingredient the substance 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzo- diazepin-2-one adsorbed in fine particle form on a pharmaceutial carrier or excipient as a substrate, wherein, the 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl- 2H-1,4-benzodiazepin-2-one has improved solubility and rate of dissolution following administration of the pharmaceutical composition.
- the pharmaceutical carrier or excipient may be one having a large specific surface area on which 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl- 2H-1,4-benzodiazepin-2-one can be deposited from solution in fine particle form, such as a starch or a micro- crystalline cellulose.
- other pharmaceutical carriers may be used such as calcium diphosphate montmorillonite and silicates such as aerosil.
- composition of the present invention is primarily suited to the treatment of sleep disorders since the release pattern of the oxazepam is ideally suited to this indication. However, should the medical picture so dictate, the composition may also be used for other indications calling for oxazepam therapy, including treatment of tension, agitation and anxiety and associated autonomic disorders, i.e. use as a general tranquiliser.
- the said carrier or excipient and also the 7-chloro-1,3-di- hydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one conveniently has a particle size of less than 40 microns, preferably less than 20 microns.
- the particle size will usually lie in the range of from 10 to 40 microns.
- the fine particle size of the 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one is critical to the present invention.
- the 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one should preferably all have a particle size of less than 5 microns and even better solubility and rate of dissolution and hence rapid sleep onset will be achieved if the particle size is less than 1 micron.
- the 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-ben- zodiazepin-2-one and pharmaceutical carrier or excipient may be present in the composition in any desired ratio e.g. 1:1 or 1:2 or more. Larger or smaller ratios may of course be used, eg up to 1:10, but this will simply increase the bulk and expense of the composition. Ratios down to 1:0.5 can also be used, but the problems start to occur with the adsorption of the 7-chloro-1,3-dihy- dro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one.
- the present invention also provides a process for the preparation of the pharmaceutical composition of the instant invention.
- the process according to the invention comprises mixing a solution of 7-chloro-1,3-dihy- dro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one in an organic solvent in which the pharmaceutical carrier or excipient is suspended and which preferably also contains a surfactant, with a non-solvent for 7-chloro- 1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin- 2-one the said organic solvent and the non solvent being mutually miscible under the conditions of mixing so as to precipiate the 7-chloro-1,3-dihydro-3-hydroxy-5-phe- nyl-2H-1,4-benzodiazepin-2-one in fine particle form on the substrate.
- This product serves as the active ingredient component in the pharmaceutical formulation of hypnotics.
- Any suitable organic solvent which is capable of dissolving 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-ben- zodiazepin-2-one at a mildly elevated temeprature can be used in the process of the present invention. It is, however, preferred to use ethanol or acetone as the organic solvent.
- Other organic solvents such as dioxan which are miscible with water in all proportions and conventionally employed in the preparation of pharmaceutical compositions can also be employed.
- the pharmaceutical carrier or diluent may be any pharmaceutically acceptable material which displays the necessary large specific surface area.
- the two materials of choice from the po.ints of view of availability and price are starch and micro crystalline cellulose.
- Direct suspension of the pharmaceutical carrier or excipient in the heated organic solution modifies the pharmaceutical carrier or excipient to such an extent that it results in the association with the active ingredient according to the invention and gives the desired rapid dissolution rate of 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzodiazepin-2-one.
- Suspension of the starch in the organic solution may be effected at any convenient temperature. Such a temperature may conveniently be from 60 to 80°C, preferably about 75°C.
- Starches which may be used include finally milted starches from maize, rice and other cereals as well as potato starch and cassava starch.
- the surfactant or wetting agent which can be used may be any such agent which is convenient.
- One example of such an agent is polyethyleneglycol-sorbitan-monooleate.
- Other surfactants which can be used include polyethyl- eneglycol-sorbitan-monostearate as well as polyhydroxy- ethylene stearate.
- the normal procedure is to first prepare the pharmaceutical composition of the invention (adsorbate) and then to add other conventional pharmaceutical carriers and excipients thereto.
- the other conventional pharmaceutical carriers and excipients can also already be present during the actual precipitation step.
- the oxazepam can be absorbed in fine particle size form by virtue of the use of a pharmaceutical carrier or excipient having a large surface area. It should be noted that in the present invention the pharmaceutical carriers or excipients have no pharmacplogical activity of their own.
- the dosage unit forms of the invention for the treatment of sleep disorders conveniently contain from 10 to 40 mg of 7-chloro-1,3-dihydro-3-hydroxy-5-phenyl-2H-1,4-benzo- diazepin-2-one, preferably from 25 to 35 mg. Other dosages such as 20 or 30 mg may of course be used.
- the dosage unit forms for use as a tranquiliser may vary widely e.g. from 5 to 50 mg. Other dosages which may be similar to those mentioned above for sleep disorders may also be used.
- formulations may conveniently be presented in unit dosage and may be prepared by any of the methods well known in the art of pharmacy.
- Formulations of the present invention suitable for oral administration may be presented as discrete units such as capsules, cachets, tablets or lozenges, each containing a predetermined amount of the pharmaceutical composition of the invention; as a powder or granules; or a suspension in an aqueous liquid or non-aqueous liquid such as a syrup, an elixir, an emulsion or a draught.
- the pharmaceutical composition may also be presented as a bolus, electuary or paste.
- a tablet may be made by compression or moulding, optionally with one or more accessory ingredients.
- Compressed tablets may be prepared by compressing, in a suitable machine, the active compound being in a free-flowing form such as a powder or granules, optionally mixed with a binder, lubricant, inert diluent, surface active or dispersing agent.
- Moulded tablets may be made by moulding in a suitable machine, comprising a mixture of the powdered active compound with any suitable carrier.
- a syrup may be made by adding the active compound to a concentrated, aqueous solution of a sugar, for example, sucrose, to which may also be added any accessory ingredient.
- a sugar for example, sucrose
- Such accessory ingredient (s) may include flavourings, an agent to retard crystallization of the sugar or an agent to increase the solubility of any other ingredient, such as polyhydric alcohol for example glycerol or sorbitol.
- Formulations for rectal administration may be presented as a suppository with a conventional carrier such as cocoa butter.
- the formulations of this invention may further include one or more accessory ingredient (s) selected from diluents, buffers, flavouring agents, binders, surface active agents, thickeners, lubricants, preservatives (including antioxidants) and the like.
- accessory ingredient selected from diluents, buffers, flavouring agents, binders, surface active agents, thickeners, lubricants, preservatives (including antioxidants) and the like.
- oxazepam 100 g was suspended in 5 litres of ethanol (ca 96%) with stirring. 10 g of polyethyleneglycol-sorbitan-monooleate were then added with continued stirring and the mixture warmed to ca 75°C with continued stirring until a clear solution was obtained. To this solution was added 200 g corn starch with stirring until a uniform suspension was obtained. The suspension was then decanted in a thin slow stream into 20 litres of water with continuous rapid stirring. Stirring was continued for a further half hour until a milky white suspension was formed. The ethanol was removed from the suspension by distillation on a rotary evaporator. The aqueous suspension was then passed through a spray-dryer to give a fine flowing white powder which contains 33 to 35% by weight of oxazepam adsorbed on the starch as carrier particles.
- Example 2 The procedure of Example 1 was repeated with the sole difference that acetone was used as the solvent in place of ethanol.
- Example 1 The procedure of Example 1 was followed with the sole difference that microcrystalline cellulose or Montmorillonite was used in place of starch.
- Example 2 a pharmaceutical tablet formulation is given.
- Example 2 The fine powder material obtained in Example 1 was used to prepare a tablet containing 25 or 35 mg oxazepam using the following "direct compression" formula:-
- the oxazepam-starch adsorbate prepared according to Example 1 was formulated as follows to be filled into hard. gelatine capsules Oxazepam-s tarch-adsorbate 100 .00 mg
- the above mixture was f illed into capsules in which 35 mg ox azepam was contained per capsule .
- a comparative in vivo pharmacokinetic study was made in 12 healthy human volunteers using a commercially available oxazepam tablet containing 50 mg oxazepam (Tablet A) and an experimental tablet containing 25 mg oxazepam made according to Example 4 (Tablet B).
- the in vivo study was planned as a cross-over experimental design and blood samples were drawn at various time intervals after the administration of the tablets. The blood samples were then analysed for the oxazepam content, using a gas chromatography method with an electron capture detector.
- Table I shows the time course of average blood concentration of oxazepam for the 12 volunteers, using the two types of tablets for a total period of 48 hours.
- Table II shows a comparison of t max values (the time to reach the maximum blood concentration) in the volunteers individually. It was found that, whereas the commercial tablet A took an average period of about five hours (range 1 - 9 hours), the experimental tablet B reached peak blood concentration within 1 1/2 hours (range 3/4 - 3 hours).
- Table IV shows a comparison of oxazepam blood concentrations reached after 10 minutes and 20 minutes respectively after the administration. It can be observed that after twenty minutes, the blood concentrations of oxazepam reached with tablet B were almost four times higher than those achieved with the commercial tablet A. Evidently it is desirable for the induction of sleep and onset of hypnotic activity that a certain minimum level of drug concentration in the blood is achieved rapidly, which is possible with the tablet B, but not with commercial tablet A.
- Table V shows the comparative oxazepam blood concentrations present after 9 hours and 24 hours respectively.
- the drug concentration level after 9 hours fell back to a very low level, comparable to those reached with tablet A after 24 hours only. This can have an important influence for causing the side effects observed with commercial tablet A.
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Medicinal Chemistry (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Life Sciences & Earth Sciences (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Engineering & Computer Science (AREA)
- Bioinformatics & Cheminformatics (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Medicines Containing Material From Animals Or Micro-Organisms (AREA)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
PCT/EP1985/000408 WO1987000428A1 (en) | 1985-07-24 | 1985-07-24 | Oxazepam containing pharmaceutical composition |
Publications (1)
Publication Number | Publication Date |
---|---|
EP0232254A1 true EP0232254A1 (de) | 1987-08-19 |
Family
ID=8165057
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
EP85903997A Withdrawn EP0232254A1 (de) | 1985-07-24 | 1985-07-24 | Oxazepam enthaltendes arzneimittel |
Country Status (4)
Country | Link |
---|---|
EP (1) | EP0232254A1 (de) |
DK (1) | DK149787D0 (de) |
NO (1) | NO871229D0 (de) |
WO (1) | WO1987000428A1 (de) |
Families Citing this family (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CH673947A5 (de) * | 1986-09-23 | 1990-04-30 | Sandoz Ag | |
SE8803935L (sv) * | 1988-10-31 | 1990-05-01 | Kabivitrum Ab | Laekemedelskomposition |
US6531158B1 (en) | 2000-08-09 | 2003-03-11 | Impax Laboratories, Inc. | Drug delivery system for enhanced bioavailability of hydrophobic active ingredients |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1349158A (en) * | 1971-11-19 | 1974-03-27 | Arpic Sa | Pharmaceutical compositions |
DE2400819C2 (de) * | 1974-01-09 | 1982-04-22 | Bayer Ag, 5090 Leverkusen | Verfahren zur Herstellung fester Zubereitungen von schwerlöslichen Arzneimittelwirkstoffen in feinster Verteilung |
-
1985
- 1985-07-24 WO PCT/EP1985/000408 patent/WO1987000428A1/en not_active Application Discontinuation
- 1985-07-24 EP EP85903997A patent/EP0232254A1/de not_active Withdrawn
-
1987
- 1987-03-24 DK DK149787A patent/DK149787D0/da not_active IP Right Cessation
- 1987-03-24 NO NO1987871229A patent/NO871229D0/no unknown
Non-Patent Citations (1)
Title |
---|
See references of WO8700428A1 * |
Also Published As
Publication number | Publication date |
---|---|
DK149787A (da) | 1987-03-24 |
WO1987000428A1 (en) | 1987-01-29 |
DK149787D0 (da) | 1987-03-24 |
NO871229L (no) | 1987-03-24 |
NO871229D0 (no) | 1987-03-24 |
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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 |
|
17P | Request for examination filed |
Effective date: 19870325 |
|
AK | Designated contracting states |
Kind code of ref document: A1 Designated state(s): AT BE CH DE FR GB IT LI LU NL SE |
|
17Q | First examination report despatched |
Effective date: 19880212 |
|
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: 19890404 |
|
RIN1 | Information on inventor provided before grant (corrected) |
Inventor name: SETH, PAWAN Inventor name: SETH, PYARE |