Patent US1256936A successfully refreshed from Google Patents.
Patent EP0235986A1 successfully refreshed from Google Patents.
← Back to Patent Explorer
EP0235986A1 Expired / Lapsed EP ⏱️ 0.0 years remaining

Slow release formulation

Assignee: Ethical Pharmaceuticals Ltd
•
Filing: 1987-02-12
•
Granted: —
•
Expires: 2007-02-12
📄 Original PDF 🌐 Google Patents 🔄 Sync Now

Abstract

Abstract A slow release formulation to be administered to humans or animals, comprising primary granules (1) which contain an active ingredient and are in a secondary matrix (2) of a water soluble/ dispersible slow release material, the granules (1) themselves comprising particles (3) containing the active ingredients and in a primary matrix (4) of a water soluble/dispersible slow release material. Optionally the formulation comprises a binder phase (5) of a water insoluble slow release material having embedded therein secondary granules (6) comprising the secondary matrix (2) containing the primary matrix granules (1). The water soluble/dispersible material may be a polysaccharide and acacia and low viscosity methylcellulose are exemplified, as well as alginate and gelatine.

Inventors

  • 👤 Alan Rhodes

Bibliographic Details

Application Number —
Jurisdiction EP
Data Source google_patents
Last Synchronized 2026-11-04 04:41
CPC Classifications
A; A61; A61K; A61K9/00; A61K9/20; A61K9/2072; A61K9/2077

Claims Analysis

Total Claims: 11
Claim 1
Independent Claim 88 words
A method of making a slow release formulation to be administered to humans or animals, comprising mixing particles comprising an active ingredient and a solution or dispersion of a water soluble/dispersible slow release material to form an agglomerate and granulating the agglomerate, drying the resultant primary granules and then mixing them with a solution or dispersion of a water soluble/dispersible slow release material to form an agglomerate and granulating the agglomerate to form secondary granules of a larger size than the primary granules, and drying the secondary granules.
Claim 2
Independent Claim 88 words
A method of making a slow release formulation to be administered to humans or animals, comprising mixing particles comprising an active ingredient and a solution or dispersion of a water soluble/dispersible slow release material to form an agglomerate and granulating the agglomerate, drying the resultant primary granules and then mixing them with a solution or dispersion of a water soluble/dispersible slow release material to form an agglomerate and granulating the agglomerate to form secondary granules of a larger size than the primary granules, and drying the secondary granules.
Claim 3
Dependent Claim 36 words
A method as claimed in claim 1 wherein the liquid vehicle of each solution or dispersion is water or a pharmaceutically acceptable organic liquid, preferably ethanol, methanol, aqueous ethanol, aqueous methanol, chloroform, isopropanol or methylene chloride.
Claim 4
Dependent Claim 26 words
A method as claimed in claim 1 or claim 2, wherein the water soluble/dispersible materials used in the first and second mixing steps are the same.
Claim 5
Dependent Claim 40 words
A method as claimed in claim 1 or claim 2 wherein the water soluble/dispersible material used in the first mixing step, the second mixing step or both the first and second mixing steps is a polysaccharide material, alginate or gelatine.
Claim 6
Dependent Claim 29 words
A method as claimed in claim 4 wherein the polysaccharide material is acacia, a mixture comprising at least 50 wt% acacia and another binder, or is low viscosity methylcellulose.
Claim 7
Independent Claim 60 words
A method as claimed in any one of claims 1 to 5, which has two granulating steps and wherein in the first granulating step the mixture is granulated to a size of 600 um to 250 um mesh aperture and in the second granulating step the mixture is granulated to a size of 2 mm to 1 mm mesh aperture.
Claim 8
Independent Claim 51 words
A method as claimed in any one of claims 1 to 6, wherein the particles containing active ingredient or the primary granules or both are dry blended with a slow release material (e.g. high viscosity methylcellulose) and subsequently admixed with a solution/dispersion of a slow release material (e.g. low viscosity methylcellulose).
Claim 9
Independent Claim 26 words
A method as claimed in any one of claims 1 to 7 which further comprises blending the secondary granules with a water insoluble slow release material.
Claim 10
Dependent Claim 100 words
A method as claimed in claim 8 wherein the water insoluble slow release material is formed of one or more of a mineral, vegetable or animal wax, a C 24 - C 62 ester of a C 12 C 31 fatty acid and a C 12 -C 31 fatty alcohol, a C 10 -C 22 fatty acid, a C 10 - C 22 fatty alcohol, or a mono-, di- or triglyceryl ester formed from a C 10 -C 22 fatty acid, and preferably of one or more of hydrogenated castor oil, glyceryl mono- or distearate, 12-hydroxystearyl alcohol or micro-crystalline wax.
Claim 11
Independent Claim 19 words
A method as claimed in any one of the preceding claims, wherein the formulation is formulated for oral administration.

References Cited (Backward Citations)

US2809916A Cited
GB1033484A Cited
GB1137379A Cited
US3946110A Cited
EP0014514A2 Cited

USPTO Annuity & Maintenance Windows

Maintenance schedule is calculated for granted US utility patents.

Assigned Categories & Tags

No categories assigned to this patent yet.

Assign Category Tag