U.S. patent application number 09/789365 was filed with the patent office on 2001-10-04 for anti-inflammatory pharmaceutical formulations.
Invention is credited to McIntyre, Gordon, Sheth, Nitin Vadilal, Woolfe, Austen John.
Application Number | 20010026808 09/789365 |
Document ID | / |
Family ID | 26784516 |
Filed Date | 2001-10-04 |
United States Patent
Application |
20010026808 |
Kind Code |
A1 |
Woolfe, Austen John ; et
al. |
October 4, 2001 |
Anti-inflammatory pharmaceutical formulations
Abstract
A pharmaceutical dosage form comprising a tablet containing a
non-steroidal anti inflammatory drug and misoprostol, wherein the
non-steroidal anti inflammatory drug is in the form of coated
pellets.
Inventors: |
Woolfe, Austen John; (North
Weald, GB) ; McIntyre, Gordon; (Bishops Stortford,
GB) ; Sheth, Nitin Vadilal; (Goshen, NY) |
Correspondence
Address: |
BEYER WEAVER & THOMAS LLP
P.O. BOX 778
BERKELEY
CA
94704-0778
US
|
Family ID: |
26784516 |
Appl. No.: |
09/789365 |
Filed: |
February 20, 2001 |
Related U.S. Patent Documents
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Application
Number |
Filing Date |
Patent Number |
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09789365 |
Feb 20, 2001 |
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09346122 |
Jul 1, 1999 |
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60091960 |
Jul 7, 1998 |
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Current U.S.
Class: |
424/472 ;
514/171 |
Current CPC
Class: |
A61K 31/557 20130101;
A61K 31/557 20130101; A61K 31/557 20130101; A61K 9/209 20130101;
A61K 31/557 20130101; A61K 31/557 20130101; A61K 2300/00 20130101;
A61K 31/19 20130101; A61K 31/54 20130101; A61K 9/2081 20130101;
A61K 31/195 20130101 |
Class at
Publication: |
424/472 ;
514/171 |
International
Class: |
A61K 009/24; A61K
031/56 |
Claims
1. A pharmaceutical dosage form comprising a tablet containing a
non-steroidal anti inflammatory drug and misoprostol, wherein the
non-steroidal anti inflammatory drug is in the form of coated
pellets.
2. A dosage form as claimed in claim 1 containing a uniform mixture
of coated non-steroidal anti inflammatory pellets and
misoprostol.
3. A dosage form as claimed in claim 1 comprising a bilayer tablet
containing coated non-steroidal anti inflammatory pellets in one
layer and misoprostol in a second layer.
4. A dosage form as claimed in claim 1 wherein the pellets include
an overcoating of a barrier layer upon a pellet including a layer
of non-steroidal anti inflammatory drugs sprayed or otherwise
coated on a non-pariel core.
5. A dosage form as claimed in claim 1 wherein the coating is an
enteric coating.
6. A dosage form as claimed in claim 5 wherein the enteric coating
is selected from: a methylmethacrylate copolymer, a
polyvinylacetate phthalate, cellulose acetate phthalate, or
hydroxypropylmethyl cellulose phthalate.
7. A dosage form as claimed in claim 6 wherein the enteric coat
includes a plasticiser.
8. A dosage form as claimed in claim 5 including a barrier inert
coat disposed between the drug core and the enteric coating.
9. A dosage form as claimed in claim 7 wherein the barrier coat is
a cellulose derivative.
10. A dosage form as claimed in claim 1 wherein the pellets are
coated with a barrier coat adapted to delay release of the
non-asteroidal anti inflammatory drug.
11. A dosage form as claimed in claim 1 wherein the pellets are
coated with a delay release coat adapted to release the drug
throughout the gastrointestinal tract.
12. A dosage form as claimed in claim 11 wherein the delay release
coat is formed from a methacrylate polymer or a mixture of a
methacrylate polymer and a cellulose derivative.
13. A dosage form as claimed in claim 1 wherein the pellets have a
diameter of 0.25 to 1.5 mm.
14. A dosage form as claimed in claim 13 wherein the pellets have a
diameter of 0.8 to 1.2 mm.
15. A dosage form as claimed in claim 1 including one or more
excipients selected from binders, lubricants, colorants, bulking
agents and disintegrants.
16. A dosage form as claimed in claim 1 wherein the non-steroidal
anti inflammatory drug is diclofenac.
17. A dosage form as claimed in claim 1 wherein the non-steroidal
anti inflammatory drug is ketoprofen.
18. A dosage form as claimed in claim 1 wherein the non-steroidal
anti inflammatory drug is naproxen.
19. A dosage form as claimed in claim 1 wherein the non-steroidal
anti inflammatory drug is selected from piroxicam and
meloxicam.
20. A dosage form as claimed in claim 1 comprising a tablet
overcoated with a sugar or cellulose film barrier coating.
21. A dosage form as claimed in claim 1 comprising a tablet
overcoated with a barrier or taste masking coating.
22. A dosage form as claimed in claim 1 comprising a tablet wherein
the ratio of diclofenac to excipients either in the whole tablet or
in the diclofenac layer is between 70:30 and 30:70 parts by
weight.
23. A method of manufacture of a pharmaceutical dosage form as
claimed in claim 1 wherein the pellets are formed by extrusion and
spheronisation of a mixture containing a non-steroidal anti
inflammatory drug, followed by coating with a barrier coat.
24. A method of manufacture of a dosage form as claimed in claim 1
wherein the pellets are made by coasservation or precipitation from
solution.
25. A method as claimed in claim 24 wherein an enteric coat is
formed by contacting solutions of an alkali salt of a non-steroidal
anti inflammatory drug, and enteric form forming polymer and an
acid.
26. A method as claimed in claim 24 wherein the misoprostol is
absorbed onto hydroxypropylmethylcellulose or other cellulose
derivative prior to incorporation into a tablet.
27. A method of manufacture of a pharmaceutical tablet comprising
the steps of mixing a coated pellet containing a non-steroidal anti
inflammatory drug together with a powder containing misoprostol
absorbed on a cellulose, polyvinylchloride or other excipient
optionally together with one or more binding agents, bulking
agents, disintegrants and lubricants and compressing the mixture to
form tablets.
28. A method of manufacture of a pharmaceutical bilayer tablet
consisting of mixing coated pellets containing a non-steroidal anti
inflammatory drug with optional excipients selected from binders,
bulking agents, disintegrants and lubricants; compressing the
mixture to form the bottom half of a tablet and superimposing a
mixture of misoprostol absorbed on a cellulose or polyvinylchloride
or other material together with or more optional excipients
selected from binders, bulking agents, disintegrants and
lubricants; to form a tablet suitable for human administration.
Description
[0001] This invention relates to pharmaceutical formulations of
anti-inflammatory drugs, particularly non-steroid and
anti-inflammatory drugs (NSAIDs).
[0002] These NSAIDs are used for the treatment of inflammatory
conditions such as osteoarthritis or rheumatoid arthritis. A side
effect of the oral administration of NSAIDs particularly with long
term usage, is a liability to ulcerogenic effects. NSAID induced
ulcers in the stomach are potentially dangerous because few or no
symptoms may be detected until significant damage has been caused.
Certain prostoglandins, for example misoprostol have been shown to
reduce and even prevent such ulcers.
[0003] It has been found experimentally that it is necessary for
the prostaglandin to be released before the NSAID so as to protect
the stomach from the effects of the NSAID. It is therefore
preferable that the NSAID is coated to delay release. The coating
may be a standard hydroxypropyl methyl cellulose coat of a
thickness sufficient to delay release in the stomach for a short
period, an enteric coat to delay NSAID release until it reaches the
intestine, or a delay release coating to allow drug release over a
period of time to permit less frequent dosing.
[0004] In addition the coating may act as a barrier between the
NSAID and the prostaglandin to prevent decomposition of the
prostaglandin caused by instability in the pressure of the
NSAID.
[0005] EP-527887B discloses a pharmaceutical composition comprising
a core of an NSAID surrounded by a coating containing the
prostaglandin. The core is preferably coated with a barrier of
enteric coat before a mantle coat is added. No experimental details
are given. It appears that this dosage form is made by
press-coating, ie a tablet core containing the drug is made, and
coated before being put in a second tableting operation to cover
the coated core. Such a procedure requires use of specialised
equipment which is not a normal pharmaceutical production tool and
hence would need significant investment.
[0006] According to the present invention an oral pharmaceutical
dosage form comprises a tablet containing a non-asteroidal anti
inflammatory drug and misoprostol, wherein the non-asteroidal anti
inflammatory drug is in the form of coated pellets.
[0007] The NSAID is preferably but not exclusively one of
reasonably low weight per standard dose. That is an NSAID where the
usual dose is 200 mg or below. Examples of such NSAIDs include
indomethacin, piroxicam, meloxicam, flubiprofen, naproxan,
ketoprofen, tenoxicam or similar molecules. Most preferably the
drug is diclofenac sodium.
[0008] Enteric coated or delay release coated pellets have not been
widely used because many workers have found damage or cracking to
the enteric or delay release coating during the tablet compression
stage. The present invention will work most effectively if the
coating remains intact during compression.
[0009] It is possible to produce such pellets by conventional means
although care is needed to ensure coat cracking does not occur.
Techniques which can be used include coating the drug on a
non-pariel core preferably composed of inert sugar or similar
substance and then overcoating with the required coating before
compression.
[0010] A preferred method is to form pellets by co-acervation or
alternatively by precipitation of the pellets from solution as
described by Zaruboru, Fell and Collett, (Int.J.Pharm, 1995, 125,
151-5).
[0011] In another preferred technique the pellets may be formed by
spheronisation, rotogranulation or a similar technique. Preferably
the pellets should be soft enough to deform slightly under
compression to avoid cracking but not too soft so as to deform
significantly which will also cause cracking or rupture of the
coat. A suitable mixture of drug with a suitable amount of an
excipient or several excipients can be found by simple, routine
experiments. Suitable excipients include polyvinyl pyrolidone,
sugars and cellulose derivatives particularly microcrystalline
cellulose. A coating for the pellets may employ cellulose
derivatives eg hydroxypropyl methyl cellulose, methacrylic acid and
derivatives eg methyl methacrylates for example, Eudragrit.RTM.
(Rhom Pharma), especially Eudragrit L or S. Other standard enteric
coating materials for example phthalates, eg cellulose acetate
phthalate or preferably hydroxypropylacetate phthalate or
polyvinylacetate phthalate. Mixtures of these and other materials
may be used to produce delay release coated beads. Normally coating
will include plasticisers eg polyethylene glycol, triacilin or
phthalate esters.
[0012] It has been found in practice that smaller pellets are
better for use in accordance with this invention, preferably
between 0.25 mm to 1.5 mm in diameter. Most preferably pellets
between 0.8 mm to 1.2 mm diameter are employed. Pellets of this
diameter show less tendency to crack under the compression
forces.
[0013] The external compression material will include a
prostaglandin, preferably misoprostol together with inert
excipients. The prostaglandin may be used neat or it may be
preferably diluted on an inert material. A preferred material is
misoprostol diluted on hydroxypropyl methyl cellulose or polyvinyl
pyrolidone. Other diluents may be used. The other materials which
may be employed include inert fillers, binders, lubricants and
colorants as used in normal pharmaceutical tablet making. An
especially useful material for this invention is microcrystalline
cellulose. The dosage of prostaglandin will be chosen to be
suitable to prevent or reduce stomach ulceration caused by the
NSAID. A suitable dose of misoprostol is between 10-200 micrograms
per tablet but this may be increased or decreased depending on the
NSAID used.
[0014] The coated pellets and prostaglandin mixture are then
compressed on conventional tableting equipment. Tablets may have a
break line or break lines to facilitate smaller doses. The tablet
may be film or sugar coated if required.
[0015] Bilayer tablets may be employed. The non-steroidal anti
inflammatory drug and excipients may be compressed into the lower
half of the tablet and the misoprostol together with excipients
superimposed and pressed onto it. A barrier layer may be provided
between the two active ingredient-containing layers. The
misoprostol containing layer may incorporate excipients to
facilitate rapid dissolution of this active ingredient.
[0016] The invention is further described by means of example but
not in any limitative sense.
EXPERIMENT 1
[0017] The following ingredients were employed.
1 Diclofenac Pellets Enteric Coated 40% 123 mg Misoprostol
Dispersion on HPMC (1:100) 20 mg 1) Microcrystaline Cellulose
(Avicel 102) 33 mg 2) Sodium Stored Glycollate 3 mg 3) Hydrogenated
Cottonseed Oil 1 mg
[0018] The excipients 1+2 and misoprostol were sieved through a 250
.mu.m screen. The diclofenac pellets were added and blended for 15
min in a cube blender. The lubricant 3) was added and the mixture
was reblended for 5 min and compressed at 180 mg/tablet.
EXPERIMENT 2
[0019] The mixture from Experiment 1 was blended with the
equivalent of another 100 mg of microcrystalline cellulose and was
then compressed at 280 mg/tablet.
EXPERIMENT 3
[0020] The following ingredients were employed.
2 Mix 1 Diclofenac Pellets Enteric Coated 40% 123 mg
Microcrystalline Cellulose 133 mg Sodium Starch Glycollate 3 mg
Hydrogenated Cottonseed Oil 1 mg Mix 2 Misoprostol dilution (1:100)
20 mg Microcrystalline Cellulose 196 mg Sodium Starch Glycollate 3
mg Hydrogenated Cottonseed Oil 1 mg
[0021] Mixture 1 was prepared with sieved excipients and then
compressed to form a layer, having a weight of 260 mg. Mixture 2
was prepared and compressed on top of the diclofenac layer to atop
weight of 120 mg, ie total 360 mg.
[0022] The resulting bilayer tablets were overcoated with an HPMC
taste masking coat. The bead diameter was 1.05 to 1.16 mm.
[0023] Results
[0024] Experiment 1 using USP baskets
[0025] Dissolution in acid 0.1 MHCL for 2 hrs
[0026] Less than 4% release.
[0027] Dissolution in pH 6.8 buffer
[0028] 98-106% release after 1 hr
[0029] Scanning Electronic Microscopy showed no breakage of the
enteric coating of the pellets after compression.
* * * * *