Claims Analysis
Total Claims: 34
Claim 1
Independent Claim
57 words
A sustained release, oral pharmaceutical composition in solid unit dosage form, for application to the mucosa of the oral or nasal cavity, comprising compressed granules characterised in that the granules comprise a drug, a higher aliphatic alcohol and a hydrated water soluble hydroxyalkyl cellulose and further in that the granules are coated with a mucosa adhesive cellulose.
Claim 2
Dependent Claim
57 words
A sustained release, oral pharmaceutical composition in solid unit dosage form, for application to the mucosa of the oral or nasal cavity, comprising compressed granules characterised in that the granules comprise a drug, a higher aliphatic alcohol and a hydrated water soluble hydroxyalkyl cellulose and further in that the granules are coated with a mucosa adhesive cellulose.
Claim 3
Dependent Claim
19 words
A composition according to claim 1 characterised in that the granules are coated with a powdered mucosa adhesive cellulose.
Claim 4
Dependent Claim
34 words
A composition according to either claim 1 or claim 2 characterised in that the mucosa adhesive cellulose comprises a carboxyalkyl cellulose or a hydroxyalkyl cellulose, preferably sodium carboxymethyl cellulose, hydroxypropylmethyl cellulose or hydroxypropyl cellulose.
Claim 5
Dependent Claim
16 words
A composition according to claim 3 characterised in that the mucosa adhesive cellulose comprises hydroxypropyl cellulose.
Claim 6
Dependent Claim
38 words
A composition according to any one of claims 1 to 4 characterised in that the mucosa adhesive cellulose coating comprises between 2% and 15% (w/w), especially between 4% and 10% - (w/w), of the total dosage form weight.
Claim 7
Dependent Claim
24 words
A composition according to any one of claims 1 to 5 characterised in that the higher aliphatic alcohol comprises cetyl alcohol or cetostearyl alcohol.
Claim 8
Dependent Claim
37 words
A composition according to any one of claims 1 to 6 characterised in that the higher aliphatic alcohol comprises between 5% and 35% - (w/w), especially between 10% and 30% (w/w), of the total dosage form weight.
Claim 9
Dependent Claim
33 words
A composition according to any one of claims 1 to 7 characterised in that the water soluble hydroxyalkyl cellulose comprises hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose or hydroxypropylmethyl cellulose, . preferably hydroxyethyl cellulose.
Claim 10
Dependent Claim
31 words
A composition according to any one of claims 1 to 8 characterised in that the water soluble hydroxyalkyl cellulose comprises between 2% and 15% (w/w), of the total dosage form weight.
Claim 11
Dependent Claim
25 words
A composition according to any one of claims 1 to 9 characterised in that the drug comprises morphine, nifedipine, phenazocine, verapamil or salbutamol, preferably morphine.
Claim 12
Dependent Claim
49 words
A composition according to any one of claims 1 to 10 characterised in that the granules further comprise between 2% and 15% (w/w), especially between 4% and 10% (w/w), of a binder comprising a carboxyalkyl cellulose or a hydroxyalkyl cellulose, preferably sodium carboxymethyl cellulose, hydroxypropylmethyl cellulose or hydroxypropyl cellulose.
Claim 13
Dependent Claim
14 words
A composition according to claim 11 characterised in that the binder comprises hydroxypropyl cellulose.
Claim 14
Dependent Claim
21 words
A kidney shaped oral vehicle comprising a sustained release, oral pharmaceutical composition according to any one of claims 1 to 12.
Claim 15
Dependent Claim
20 words
14? A buccal tablet comprising a sustained release, oral pharmaceutical composition according to any one of claims 1 to 12.
Claim 16
Dependent Claim
72 words
A process for the preparation of a sustained release, oral pharmaceutical composition in solid unit dosage form, the composition being adapted for application to the mucosa of the oral or nasal cavity, comprising forming granules comprising a drug, a higher aliphatic alcohol and a hydrated water soluble hydroxyalkyl cellulose coating the granules with a mucosa adhesive cellulose, and compressing the mucosa adhesive cellulose coated granules to give a solid unit dosage form.
Claim 17
Dependent Claim
72 words
A process for the preparation of a sustained release, oral pharmaceutical composition in solid unit dosage form, the composition being adapted for application to the mucosa of the oral or nasal cavity, comprising forming granules comprising a drug, a higher aliphatic alcohol and a hydrated water soluble hydroxyalkyl cellulose coating the granules with a mucosa adhesive cellulose, and compressing the mucosa adhesive cellulose coated granules to give a solid unit dosage form.
Claim 18
Dependent Claim
81 words
A process according to claim 15 characterised in that the granules are formed by a process comprising mixing the drug, the water soluble hydroxyalkyl cellulose and, preferably, a binder comprising a carboxyalkyl cellulose or a hydroxyalkyl cellulose to form a drug containing mixture, hydrating the drug containing mixture to form a wet granular mass, drying the wet granular mass to form a dry granular mass, and mixing the dry granular mass with a higher aliphatic alcohol; Claims for contracting state AT
Claim 19
Dependent Claim
72 words
A process for the preparation of a sustained release, oral pharmaceutical composition in solid unit dosage form, the composition being adapted for application to the mucosa of the oral or nasal cavity, comprising forming granules comprising a drug, a higher aliphatic alcohol and a hydrated water soluble hydroxyalkyl cellulose, coating the granules, with a mucosa adhesive cellulose, and compressing the mucosa adhesive cellulose, coated granules to give a solid unit dosage form.
Claim 20
Dependent Claim
72 words
A process for the preparation of a sustained release, oral pharmaceutical composition in solid unit dosage form, the composition being adapted for application to the mucosa of the oral or nasal cavity, comprising forming granules comprising a drug, a higher aliphatic alcohol and a hydrated water soluble hydroxyalkyl cellulose, coating the granules, with a mucosa adhesive cellulose, and compressing the mucosa adhesive cellulose, coated granules to give a solid unit dosage form.
Claim 21
Dependent Claim
19 words
A process according to claim 1 characterised in that the granules are coated with a powdered mucosa adhesive cellulose.
Claim 22
Dependent Claim
34 words
A process according to either claim 1 or claim 2 characterised in that the mucosa adhesive cellulose comprises a carboxyalkyl cellulose or a hydroxyalkyl cellulose, preferably sodium carboxymethyl cellulose, hydroxypropylmethyl cellulose or hydroxypropyl cellulose.
Claim 23
Dependent Claim
16 words
A process according to claim 3 characterised in that the mucosa adhesive cellulose comprises hydroxypropyl cellulose.
Claim 24
Dependent Claim
37 words
A process according to any one of claims 1 to 4 characterised in that the mucosa adhesive cellulose coating comprises between 2% and 15% (wiw), especially between 4% and 10% (w/w), of the total dosage form weight.
Claim 25
Dependent Claim
24 words
A process according to any one of claims 1 to 5 characterised in that the higher aliphatic alcohol comprises cetyl alcohol or cetostearyl alcohol.
Claim 26
Dependent Claim
36 words
A process according to any one of claims 1 to 6 characterised in that the higher aliphatic alcohol comprises between 5% and 35% (w/w), especially between 10% and 30% (w/w), of the total dosage form weight.
Claim 27
Dependent Claim
32 words
A process according to any one of claims 1 to 7 characterised in that the water soluble hydroxyalkyl cellulose comprises hydroxymethyl cellulose, hydroxyethyl cellulose, hydroxypropyl cellulose or hydroxypropylmethyl cellulose, preferably hydroxyethyl cellulose.
Claim 28
Dependent Claim
32 words
A process according to any one of claims 1 to 8 characterised in that the water soluble hydroxyalkyl cellulose comprises between 2% and 15% - (w/w), of the total dosage form weight.
Claim 29
Dependent Claim
25 words
A process according to any one of claims 1 to 9 characterised in that the drug comprises morphine, nifedipine, phenazocine, verapamil or salbutamol, preferably morphine.
Claim 30
Dependent Claim
49 words
A process according to any one of claims 1 to 10 characterised in that the granules further comprise between 2% and 15% (w/w), especially between 4% and 10% (w/w), of a binder comprising a carboxyalkyl cellulose or a hydroxyalkyl cellulose, preferably sodium carboxymethyl cellulose, hydroxypropylmethyl cellulose or hydroxypropyl cellulose.
Claim 31
Dependent Claim
14 words
A process according to claim 11 characterised in that the binder comprises hydroxypropyl cellulose.
Claim 32
Dependent Claim
81 words
A process according to any one of claims 1 to 12 characterised in that the granules are formed by a process comprising mixing the drug, the water soluble hydroxyalkyl cellulose and, preferably, a binder comprising a carboxyalkyl cellulose or a hydroxyalkyl cellulose to form a drug containing mixture, hydrating the drug containing mixture to form a wet granular mass, drying the wet granular mass to form a dry granular mass, and mixing the dry granular mass with a higher aliphatic alcohol.
Claim 33
Dependent Claim
29 words
A process according to any one of claims 1 to 13 characterised in that the mucosa adhesive cellulose, coated granules are compressed to give a kidney shaped oral vehicle.
Claim 34
Dependent Claim
27 words
A process according to any one of claims 1 to 13 characterised in that the mucosa adhesive cellulose, coated granules are compressed to give a buccal tablet.