AU1871302A - Rapidly disintegrating methylcellulose tablets - Google Patents

Description

AUSTRALIA

PATENTS ACT 1990 DIVISIONAL APPLICATION NAME OF APPLICANT: SmithKline Beecham Corporation ADDRESS FOR SERVICE: DAVIES COLLISON CAVE Patent Attorneys 1 Little Collins Street Melbourne, 3000.

INVENTION TITLE: "Rapidly disintegrating methylcellulose tablets" The following statement is a full description of this invention, including the best method of performing it known to us: -1- RAPIDLY DISINTEGRATING METHYLCELLULOSE

TABLETS

This application is a divisional of Australian Patent Application No. 92022/98, the entire contents of which are incorporated herein by reference.

FIELD OF THE INVENTION The present invention relates to an improved process for preparing compressed methylcellulose containing tablets which meet USP disintegration standards.

BACKGROUND OF THE INVENTION The history of cellulose ethers, such as methylcellulose and carboxymethylcellulose suggests that these agents are effective as bulk laxatives.

1 5 Their mechanism of action involves increasing both the water content of, and the bulk content of the stool, as well as lubricating the stool; thereby relieving constipation.

Cellulose ethers have been administered as bulk laxatives in dosage forms comprising of tablets, suspensions, and bulk powders; the latter as sugar-free or in compositions containing high amounts of sugar.

Cellulose ethers administered as suspensions in water may contain high concentrations of sucrose or other sugars and flavors. In such formulations, the 25 sugar competes with the cellulose ether for available water, thereby preventing the cellulose ether from hydrating sufficiently to form a gel. The advantages of using a suspension formulation is that the cellulose ether is dispersed sufficiently to avoid any significant lumping in the digestive tract. However, these suspensions are viscous, semi-gelatinous, and visually unappealing to the consumer. Another disadvantage is the unpalatability of the suspensions due to the slimy mouth feel and extreme sweetness of such suspensions. Hence, these dosage forms have not gained significant consumer acceptance.

Bulk powders of cellulose ethers often exhibit lumping of individual particles and gelation and thus, remain undissolved as they pass through the digestive tract. Additionally, administration of bulk powders has caused cramping, nausea, and vomiting in some patients. Therefore, bulk powders are not the preferred dosage form for cellulose ethers.

Palatable and visually appealing bulk powders have, however, been accomplished by addition of water or another aqueous liquid to a dry powder mix of a water-soluble cellulose ether and a dispersing agent/sweetening component, typically sugar. This technology is disclosed in South African patent No. 84, 1044.

published Sept. 26, 1984. The pitfall with these compositions is that they contain about 400 calories of nutritive value per dose. primarily due to the high sugar content. This high caloric value is not acceptable to the average consumers or to .users suffering from blood sugar disorders, including diabetics. Elderly people are normally, the common strata of the population that suffers from constipation and the more frequent users of laxatives, and are also commonly suffering with blood sugar disorders. The consumption of large quantities of sugar could aggravate blood sugar 15 disorders.

Sugar encrusted cellulose ethers have been proposed as alternatives to the .i .bulk powders containing high amounts of sugar. Such formulations have 1) less sugar such as natural sugar or combination of sugars such as sucrose, glucose, fructose or corn syrup solids; 2) lower caloric value; and 3) are readily dispersed in S. cold aqueous liquids.

oo Citrucel® Orange Flavor, a bulk forming laxative containing methylcellulose as its active ingredient, was first introduced into the market in 1986. This product 25 contains 15 g of sucrose in a 19 g adult dose, which corresponds to a 2 g dose of methylcellulose. To decrease the sugar content of this product, a natural flavored formula lower in caloric value, and containing only 1 g sucrose, was developed and introduced in 1988. Additional patent protection for this product has focused on producing a sugar-free and virtually calorie-free powder. The product has a sugarfree sweetener, a dispersing agent, other excipients, and flavoring and was marketed in 1991 as Sugar Free Citrucel® Orange Flavor.

There still remains a need in the art to develop a rapidly disintegrating solid dosage form of a bulk agent, preferably methylcellulose, which is convenient to take and transport, sugar free, and easily administered to the consumer having blood sugar disorders or diabetics, for instance.

-2- SUMMARY OF THE INVENTION The present invention relates to an improved process for preparing methylcellulose tablets which are readily dispersible and meet United States Pharmacopoeia standards for disintegration. The methylcellulose is compressed into tablets which contain an edible calcium salt, in preferred w/w ratios. Preferably the tablets rapidly disintegrate, in-vitro in 0.1N hydrochloric acid and water at 37 '0.5 "C.

DETAILED DESCRIPTION OF THE INVENTION There is a common belief that tabletted cellulose ethers do not readily dissolve in the digestive tract because these cellulose ethers are highly hygroscopic.

The outer portion of the tablet is said to form a gel-like hydrate that prevents the tablet from breaking up and greatly retards the hydration of the inner portion of the tablet. The present invention overcomes this art recognized problem and involves preparation of a novel composition and process of making, by which a rapidly i 15 disintegrating tablet of methylcellulose is prepared.

The tablets are prepared by a novel process involving a high-shear wet granulation method, followed by fluidized bed drying, milling, mixing with the other ingredients, and compression.

The present invention is to a methylcellulose tablet which comprises omethylcellulose having a viscosity of 1000 centipoise, and at least one excipient selected from an edible calcium salt. It is recognized that the formulation will also include diluents and fillers well known to the skilled artisan.

The tablet formulations of the present invention are advantageous over other dosage forms of methylcellulose because of their convenience of administration and rapid disintegration. This is in contrast to tablets of methylcellulose, formulated as 100% w/w methylcellulose in a 0.5 gm caplet which have been found not to disintegrate in 0. 1N HCI solution, using a conventional dissolution apparatus even after two hours. The present tablets should disintegrate in 0. IN HCI from about to about 30 minutes, preferably from about 10 to about 19 minutes, and more preferably less than 10 minutes; and in water, the tablets should disintegrate from about 25 to about 30 minutes, preferably from about 15 to about 24 minutes, and more preferably less than 15 minutes.

-3- It has been found that low molecular weight (mw) methylcellulose is less effective for use as a laxative, and therefore is less desirable for use in a rapidly disintegrating tablet formulation. Higher molecular weight methylcellulose is therefore both desirable and necessary in the present invention. The fibers must have a sufficient viscosity to gel and retain water in the gut to provide the stool bulking and softening for laxation use.

By using the testing methods for methylcellulose under standard conditions, such as those found in the USP XXII, p. 894, Apparent Viscosity method for Methylcellulose, or as discussed in Handbook of Pharmaceutical Excipients. APhA, a preferred methylcellulose for use herein should have a viscosity of 1000 centipoises (cps), preferably 2000 centipoises, more preferably 3000 centipoises, and most preferably >4000 centipoise. Higher molecular weight methylcellulose than those described is also desirable, however, the commercially availability of this 15 grade of methylcellulose being the limiting feature. At present the upper limit commercially available is about 6000 cps, which is encompassed within the scope of this invention. One presently available methylcellulose product for use herein is Methocel A4M. made by Dow Chemical Company, Midland Michigan as Dow Methocel A4M, having a viscosity of about 3000 to about 5,600 cps, which is within 75 to 140% of the desired target viscosity herein.

Some of the additional diluents or fillers for use in this formulation are Spreferably swellable agents, and may include, but are not limited to, various grades of microcrystalline cellulose, such as Avicel PHIO1, Avicel PH102, Avicel 25 PH200; Corn starch; or Starch 1500.

The edible calcium salts suitable for use herein include but are not limited to, dibasic calcium phosphate dihydrate, calcium phosphate anhydrous, and tribasic calcium phosphate; or mixtures thereof. A preferred edible calcium salt is the dibasic calcium phosphate dihydrate salt, which salt also provides good compressibility.

If microcrystalline cellulose is added, it is preferably from about 50 to 180 microns in size, more preferably about 50. Avicel PH 101 has a mean particle size of about 50; Avicel PH 102 has a mean particle size of about 100; and Avicel PH 200 has a mean particle size of about 190 microns. Preferably the preferred microcrystalline cellulose is Avicel PH 101.

-4- It is noted that the ratio of methylcellulose to edible calcium salt, and additional diluents will depend upon the diluent chosen, and is within the skill of the art to determine with preciseness the necessary ratios.

Suitable ratios for particular diluents however, are described below: For Methylcellulose:Dibasic calcium phosphate, dihydrate, from about 2 to about 4:1, preferably from about 2.6-3.1:1; For Methylcellulose:Calcium phosphate, anhydrous from about 2 to about 4:1, preferably from about 3.1:1 Methylcellulose:Tribasic calcium phosphate, WG® from about 2 to about 4:1, preferably from about 3.1:1 For Methylcellulose: microcrystalline cellulose, from about 2:1 to about 14:1.

Preferably for Avicel PH 101 from about 2.2-13.5:1; for Avicel PH 102 from about 2.4- 8.3:1; and for Avicel PH 200 from about 2.4-4:1.

For Methylcellulose:Com starch from about 7.5 to about 15, preferably from about 13.5:1; For Methylcellulose:Starch 1500 from about 2.0 to about 5.0:1, preferably from about 2.4:1; For Methylcellulose:Explotab, from about 5 to about 25:1, preferably from about 8.1 to about 21.3:1.

It is recognized that with the edible calcium salt, the formulation must also have an ingredient which keeps the granules together, i.e. a binding agent. A preferred binding agent is PVP, or the alternative agents noted below.

In addition to the above noted edible calcium salt(s), optional diluents or fillers, and binding agent(s), the formulation may also include additional components such as, but are not limited to, a wetting agent, (super)disintegrant(s), a second binding agent(s), dye(s) or colouring agents, and lubricants, which are preferably used to prepare a tablet that is wetted readily, and is rapidly disintegrated in 0.1N hydrochloric acid and water, the USP test standard test for methylcellulose.

A preferred wetting agent is sodium lauryl sulfate.

A preferred lubricant is magnesium stearate.

A preferred binding agent is polyvinylpyrrolidone, or PVP, such as Povidone 29K/32. Preferably, the PVP is present in an amount of about 4 to about 6.5 w/w.

A preferred disintegrating agent is sodium starch glycolate, such as Explotab®. Preferably, the sodium starch glycolate is present in an amount of about 3 to about 8% w/w.

15 As various excipents and diluents will be formulated together, and used in combination herein, suggested w/w ratios for various formulations are presented below. While not all of these ratios include the edible calcium salts, these are merely illustrative of the invention and the skilled artisan will readily recognize how to formulate the product of this invention with the addition of the edible calcium salts.

o. Sodium lauryl sulfate:Explotab:Dibasic calcium phosphate, dihydrate:Povidone 2 9K/32:Magnesium stearate include: 0.38-0.40:3.5-7.9:20.6-24.8:4.0-6.5:0.5-1.0 25 Sodium lauryl sulfate:Explotab:Tribasic calcium phosphate WG®: Povidone 29K/32:Magnesium stearate include: 0.40:3.5:21.6:6.4:1.0 Sodium lauryl sulfate:Explotab:Calcium phosphate, anhydrous: Povidone 29K/32:Magnesium stearate include: 0.40:3.5:21.6:6.4:1.0 Methylcellulose:sodium lauryl sulfate (SLS), from about 60 to about 170:1, preferably from about 155:1-170:1; Methylcellulose:Povidone, preferably PVP 29K/32, from about 8 to about 22:1, preferably from about 10.4:1-16.7:1; Methylcel lulose: Magnesiu staaefo bu 0t bot101rfrbyfo about 58-132: 1; lm taaefo bu 0t bu 5;1 rfrbyfo Sodium lauryl sulfate: Ex plotab: Avicel PH 101lk: Povidone 2 9

KI

3 2 :Magnesium stearate include: 0.35-0.46:3.05-6.17:4.38-27.13:4.38-6.66:0.76-1.14 Sodium lauryl sulfate: Explotab: Avicel PH 1020: Povidone 29

K

13 2 :Magriesiurn stearate include: 0.35-0.46:4.9-6.17:9.21-25.53:4.38-6.66:0.76-1 .14 Sodium lauryl sulfate:Avicel PH 200@: Povidone 29K132:Magnesium stearate include: 0.38-0.42:19.27-2-5.53:5.99-6.66:0.94-1 .04 Sodium lauryl sulfate: Expl otab: Corn starch: Povidone 2 9K/32: Magnesium stearate include: 0.36-0.38:3.66-7.07:4.35-4.68:4.35-4.68:0.88-0.95 Sodium lauryl sulfate: Explotab: Starch 15000: Povidone 2 9K/32:Magnesium stearate include: 0.36-0.38:3.66-7.07:24.05-25.89:4.35-..468 :0.88-0.95 Not wishing to be limited to the explicit excipients noted above, the following alternative agents may also be used herein.

lteraties lbricntsto mgneium stearate include, but are not limited to, calcium stearate, sodium stearate, Cab-O-Sil, Syloid, stearic acid and talc.

Alternatives binding agents to PVP include but are not limited to, hydroxypropylIcellujlose, hydroxypropy] methylcellulose, acacia, gelatin, tragacan th, pregelatinized starch and starch.

Alternatives disintegrants to Explotab® include but are not limited to, sodium carboxymethylcel lu lose, Ac-di-sol®, carboxymethylcellu lose, veegum, alginates, agar, guar, tragacanth, locust bean, karaya, pectin, and crospovidone.

Alternative wetting agents to sodium lauryl sulfate, include but are not limited to, magnesium lauryl sulfate.

All of these formulations can be prepared with and without sugar. A sugarfree formulation has the advantage that it can be administered easily to consumers with blood sugar disorders or to diabetics in need of such preparations.

-7- Another advantageous property of the present invention is that the formulations contain calcium, such as dibasic calcium phosphate dihydrate. These formulations, for instance, will contain approximately an 80 mg/dose, anticipating formulating a 0.5gm/tablet X 2 tablets/dose of methylcellulose. If desired the amount of calcium can be increased in these tablets to provide increased therapeutic value to the consumer.

The amount of methylcellulose present in each dose, as well as the number of doses of laxative taken per day, will depend somewhat on the age, sex, size of the patient, severity of the patient's particular problem, the advice of the treating physician, if any, and the particular taste and habits of the patient. Accordingly, the tablets of this invention are advantageously administered in a single dose which may contain as much as 500 to 1000 mg of methyl cellulose tablet, or in a plurality of 15 smaller doses containing as little as 250mg per tablet. Most preferably, for laxative effect, each tablet will contain about 500mg methylcellulose and the patient may take 1 to 2 tablets per dose. This dosage, of 1000mg should adequately provide optimal laxative efficacy. Therefore, a preferred range of methylcellulose per tablet is optimally from about 450 to 550 mg, preferably about 500mg; or alternatively from about 200 to about 300mg for a smaller tablet, preferably about 250mg; or i even in increments of about 125mg tablet, i.e. 75 to 175mg per tablet.

While preferably the compressed tablets are uncoated, they may, if desired, be coated with any suitable coating agent well known in the art. Suitably the coating 25 agents are those used for immediate release purposes and will dissolve in the gastric juices. Such coating agents are well known to those skilled in the art and include, but are not limited to hydroxypropyl methylcellulose, or methyl cellulose, or w/w Opadry II, orange in water.

As will readily be seen by the working examples, there are various combinations of intra and extragranular mixing which are possible using the ingredients herein. All are encompassed within the scope of this invention. Penerally, the high viscosity methylcellulose, such as Methocel A4M, will first be granulated with a binder, such as povidone, a wetting agent, such as sodium lauryl sulfate, and a suitable colouring agent to form the intragranular mixture which is then granulated. These granular components are then admixed with additional wetting agents, and disintegrating agents and finally -8blended with lubricant. This final granular mixture is then blended and compressed into the tablets of the present invention.

Therefore, an aspect of the present invention is a process for preparing a tablet formulation which comprises a) blending together to form an intragranular mixture high viscosity methylcellulose of 3000cps, a wetting agent, povidone or sodium starch glycolate, and an edible calcium salt; and b) adding to the mixture of step a PVP aqueous solution, or alternatively spraying the mixture of step with a PVP aqueous solution; and preparing granulates: and c) blending together an extragranular mixture of an edible calcium salt, a wetting agent; a lubricating agent; povidone or sodium starch glycolate or a mixture thereof; and d) compacting the granulates of step with the extragranular mixture of step Another aspect of the present invention is a process for the manufacture of a pharmaceutical tablet, which process comprises mixing a) granulates comprising high viscosity methylcellulose of 3000cps, a wetting agent, povidone or sodium starch glycolate, an edible calcium salt; and b) blending together an extragranular mixture of an edible calcium salt, a wetting agent; a lubricating agent; povidone or sodium starch glycolate or a mixture thereof; and c) compacting the granulates of step with the granular mixture of step and d) compressing into a tablet.

Another aspect of the present invention is the method of relieving constipation by increasing the water content of the stool, or by providing a lubricating effect on the stool in a mammal in need thereof, which method comprises administering to said mammal, an effective amount of a high viscosity methylcellulose compressed into a tablet with a suitable diluent.

METHODS OF PREPARATION The following examples illustrates the invention but is not intended to limit the scope thereof. All parts and percentages are by weight unless otherwise indicated.

The disintegration time of the formulations described in the Tables below were obtained by using a conventional disintegration apparatus.

-9- EXAMPLE 1 TABLE I Swallowable Methvlcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 67.27 Dibasic Calcium phosphate, dihydrate 0.0370 4.98 10 Sodium lauryl sulfate 0.0015 0.20 o Dye/Colouring agent 0.0010 0.13 Povidone 29K/32 0.0480 6.46 DI water q.s. q.s.

L|.A q.s.

Phase B Phase A 0.5875 79.04 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0260 3.50 Dibasic Calcium phosphate, dihydrate 0.1245 16.75 Magnesium stearate 0.0038 0.51 TOTAL 0.7433 100.00 The process of preparing the rapidly disintegrating tablet of methylcellulose is carried out using specified quantities of ingredients, such as those mentioned in TABLE I above, using the following steps: 1. Preparation of Povidone K29/32 (PVP) Solution The specified amount of PVP was weighed and added to the weighed quantity of water and stirred till all the PVP was dissolved completely.

2. Preparation of Phase A Accurately weighed amounts of Methocel A4M, calcium phosphate, dibasic dihydrate, sodium lauryl sulfate, and colouring agent, such as any suitable FD&C Aluminium lake, were transferred to a Key Hi-shear granulator and mixed for about 10 minutes with impellor speed at 135 rpm and chopper speed at 10%. The PVP solution was sprayed onto the mixture in the granulator at a rate of approx. >200 mL/min. Once addition of PVP solution was complete, the chopper was stopped.

The mixing was continued in the granulator till resistance reads about 130-135 watts and the time noted to reach that wattage. A sample was withdrawn from the wet 10 granulation to record loss on drying LOD). The moist granules were dried in the *Aeromatic Fluid bed dryer in portions till the LOD reading approximated The temperature of the air in the fluid bed dryer was maintained at approx.

90-95 "C and the sample was found to be dry at an outlet air temperature of approx.

32-52 The dried granules were milled through a 12# screen in the Fitz Mill at a high speed. The granules were weighed and percent yield calculated. The moisture content was measured for the dry granules. A sample from the granules was withdrawn and analyzed for particle size distribution, bulk and tap density, flow index, and moisture studies. The granules were weighed and ingredients of Phase B were calculated based on the weight of remaining granules.

3. Preparation of the Final Blend To the weighed milled granules produced in Phase A above, specified amounts of sodium lauryl sulfate, sodium starch glycolate (Explotab®), and dibasic calcium phosphate, dihydrate were added into the V-blender and mixed about minutes. Magnesium stearate was then added to the blend and mixed for an additional 3 minutes or so. Samples from different sections of the V-blender were drawn and submitted for analyzing blend uniformity. A sample from the final blend was analyzed for particle size distribution, bulk and tap density, flow index, and moisture studies. The granules were then weighed.

11-- 4. Compression of methylcellulose tablets The final blend was charged into the hopper of a Stokes single punch 'F' tablet press and compressed into caplets with a suitable tooling. Target hardness desired is between 10 and 25, preferably 8-12 SCU. a preferred target weight of each tablet of less than 750 mg; an estimated friability of less than more preferably less than and target disintegration times below 30 minutes in water and acid (shorter disintegration times, less than 10 minutes, more preferably less than 8 minutes, in 0.1N HCI and less than 15 minutes in water, more preferably about 8 minutes, are preferred). The tablets were packaged in Ziplock bags. The tablets 10 were tested for weight variation, hardness, disintegration in acid and water, friability, moisture LOD), thickness, viscosity, and content uniformity.

of S o S500 The formulation in TABLE I exhibited a disintegration time of less than minutes in 0.1N HC1 and less than 9 minutes in water by the conventional

USP

method using Disintegration Apparatus with disks.

The disintegration time for the formulation of Table 1, Example 1, was less

*S

than 5 minutes in 0.1N HCI was less than 9 minutes in water.

S.

o. It is noted that Examples 2 to 6, and 11 to 15 are Avicel based formulations, and Examples 7 tolO are strach based formulations which do not contain an edible calcium salt excipients. These are merely for illustration purposes, and may be formulated to include the edible calcium salts as desired using the teachings of this invention and working examples 1, and 16 to 23.

12f.

EXAMPLE'2 A formulation containing both Avicel PH 1010 and Explotab®, intra and extragranularly as shown in TABLE 11 below, exhibited an average disintegration time of less than 1 minute in 0. 1iN HCl at 37V 0.5"C using the automated disintegration apparatus.

TABLE 11 Swallowable Methvlcellulose Tablets 0 Formula g/tablet wiw) Ingredient Phase A Methocel A4M 0.5000 60.31 Avicel PH 101@ 0.0370 4.46 Sodium lauryl sulfate 0.0015 0.18 Povidone29K132 0.0370 4.46 Explotab® 0.0300 3.62 DI water q.s. q.s.

Phase B Phase A 0.6055 73.03 Sodium lauryl sulfate 0.0017 0.21 Sodium starch glycolate 0.0253 3.05 Avicel PH 101@ 0.1880 22.67 Magnesium stearate 0.0086 1.04 TOTAL 0.8291 100.00 13- EXAMWPLE 3 A formulation containing Avicel PHiOI® intragranularly, extragranular Avicel PH 1020 and Explotab®, intra and extragranularly, as shown below in TABLE

III

exhibited an average disintegration time of less than 3 minutes in 0. IN HCI at 37 50.5 'C using the automated disintegration apparatus.

TABLE

III

Swallowable Methvlcellulose Tablets Formula g/tablet w/w) .Ingredient Ph as e A Metliocel A4M 0.5000 59.24 Avicel PH 101® 0.0370 4.38 Sodium lauryl sulfate 0.0015 0.18 *Povidone 29K/32 0.0370 4.38 Explotab® 0.0300 3.56 .:Dye/colouring agent 0.0040 0.47 *20 DI water q.s. q.s.

Phase B Phase A 0.6095 72.21 .Sodium lauryl sulfate 0.0015 0.18 Sodium starch glycolate 0.0220 2.61 Avicel PH 102@ 0.2035 24.11 Magnesium stearate 0.0075 0.89 TOTAL 0.8440 100.00 14 EXAMPLE 4 A formulation containing Avicel PH1010 intragranularly, extragranular Avicel PH 102@ and Explotab® intra and extragranularly as shown in TABLE IV below exhibited an average disintegration time of less than 2 minutes in 0. IN HCI at 37 0.5 "C using the automated disintegration apparatus.

TABLE IV Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 59.52 Avicel PH 101® 0.0370 4.41 Sodium lauryl sulfate 0.0015 0.18 Povidone 29K/32 0.0370 4.41 Explotab® 0.0300 3.57 DI water q.s. q.s.

Phase B Phase A 0.6055 72.08 Sodium lauryl sulfate 0.0015 0.18 Sodium starch glycolate 0.0220 2.62 Avicel PH 102® 0.2035 24.23 Magnesium stearate 0.0075 0.89 TOTAL 0.8400 100.00 In an alternative embodiment of Example 4 a coated version of the formulation shown in TABLE IV was tested for disintegration time. The coating solution used was w/w Opadry II, Orange in water. The average disintegration time of coated tablets was less than one minute in 0.1N HCI at 37 0.5 "C using the automated disintegration apparatus.

EXAMPLE A formulation containing Avicel PHI10l1 intragranularly, extragranular Avicel PH 1020 and Explotab®D intra and extragranularly as shown in TABLE V exhibited an average disintegration time of less than one minute in 0. IN HCI at 37 0.5 using, the automated disintegration apparatus.

TABLE V Swallowable Methvlcellulose Tablets Formula g/ablet (170 w/w) Ingredient Phase A Methocel A4M 0.5000 60.24 Avicel PH 10l@ 0.0370 4.46 Sodium lauryl sulfate 0.0015 0.18 :Povidone 29K/32 0.0370 4.46 Explotab® 0.0300 3.62 .:DI water q.s. q.s.

Phase B Phase A 0.6055 72.95 **.Sodium lauryl sulfate 0.0015 0.18 Sodium starch glycolate 0.0110 1.33 Avicel PH 102® 0.2045 24.64 Magnesium stearate 0.0075 0.90 TOTAL 0.8300 100.00 -16- EXAMPLE 6 A formulation containing Avicel PH101® intragranularly, extragranular Avicel PH102® and no Explotab® as shown in TABLE VI below, exhibited an average disintegration time of less than 3 minutes in 0. 1N HCI and less than 2 minutes at 37 0.5 "C using the automated disintegration apparatus. The disintegration times using the conventional apparatus were about 1 minute in acid and less than 2 minutes in water.

TABLE VI Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 67.94 Avicel PH 101® 0.0370 5.03 Sodium lauryl sulfate 0.0015 0.20 Povidone 29K/32 0.0370 5.03 20 Dye/Colouring Agent 0.0010 0.14 DI water q.s. q.s.

Phase B Phase A 0.5765 78.34 Sodium lauryl sulfate 0.0011 0.15 Avicel PH 102® 0.1527 20.75 Magnesium stearate 0.0056 0.76 TOTAL 0.7359 100.00 -17- EXAMPLE 7 A formulation containing corn starch intragranularly, extragranular Starch 1500 and no Explotab® as shown in TABLE VII exhibited an average disintegration time of less than 16 minutes in 0. IN HCI at 37 0.5 °C using the automated disintegration apparatus.

TABLE VII Swallowable Methvlcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 63.29 Corn starch 0.0370 4.68 Sodium lauryl sulfate 0.0015 0.19 S. Povidone 29K/32 0.0370 4.68 Dye/Colouring Agent 0.0010 0.13 DI water q.s. q.s.

20 Phase B Phase A 0.5765 72.97 Sodium lauryl sulfate 0.0015 0.19 Starch 1500® 0.2045 25.89 Magnesium stearate 0.0075 0.95 TOTAL 0.7900 100.00 18- EXAMPLE 8 A formulation containing corn starch intragranularly, extragranular Starch 1500 and intragranular Explotab®D as shown in TABLE V111 exhibited an average disintegration time of less than 14 minutes in 0. IN HCJ at 37 0.5 "C using the automated disintegration apparatus.

TABLE V1I1 Swallowable Methvlcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 61.00 Corn starch 0.0370 4.51 Sodium lauryl sulfate 0.0015 0.18 Povidone 29K/3.) 0.0370 4.51 Explotab® 0.0300 3.66 :Dye/Colouring Agent 0.0010 0.12 DI water q.s. q.s.

Phase B Phase A 0.6065 73.98 Sodium lauryl sulfate 0.0015 0.18 Starch 1500@ 0.2045 24.93 Magnesium stearate 0.0075 0.91 TOTAL 0.8200 100.00 19- EXAMPLE 9 A formnulation containing corn starch intragranularly, extragranular Starch 1500 and intra as well as extragranular Explotab® as shown in TABLE IX exhibited an average disintegration time of less than 13 minutes in 0. IN HCI at 37 ±0.5 "C using, the automated disintegration apparatus.

TABLE IX Swallowable Methvlcellulose Tablets Foml /tablet w/w) Ingredient Phase A Methocel A4M 0.5000 59.88 Corn starch 0.0370 4.43 Sodium lauryl sulfate 0.0015 0.18 Povidone 29K/32 0.0370 4.43 .:Explotab®D 0.0300 3.59 Dye/Colouring Agent 0.0010 0.12 DI water q.s. q.s.

Phase B *Phase A 0.6065 72.63 Sodium lauryl sulfate 0.00 15 0.18 Starch 15000 0.2045 24.49 Explotab®D 0.0150 1.80 Magnesium stearate 0.0075 0.90 TOTAL 0.8350 100.00 EXAMPLE A formulation containing corn starch intragranularly, extragranular Starch 1500 and intra as well as extragranular Explotab® (in higher amounts than shown above in Example 9, TABLE IX) as shown in TABLE X exhibited an average disintegration time of less than 11 minutes in 0.1N HCI and less than 18 minutes in water at 37 0.5 "C using the automated disintegration apparatus.

TABLE X Swallowable Methvlcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 58.82 Corn starch 0.0370 4.35 Sodium lauryl sulfate 0.0015 0.18 Povidone 29K/32 0.0370 4.35 Explotab® 0.0300 3.53 20 Dye/Colouring Agent 0.0010 0.12 DI water q.s. q.s.

Phase B Phase A 0.6065 71.35 Sodium lauryl sulfate 0.0015 0.18 Starch 1500@ 0.2045 24.05 Explotab® 0.0300 3.54 Magnesium stearate 0.0075 0.88 TOTAL 0.8500 100.00 -21 EXAMPLE 11 Various formulation containing Avicel PH101® intragranularly and different levels of extragranular Avicel PHI 02® (as shown in Examples 6, 7, and 8 above) were made to observe their effect on disintegration time of the tablets.

The formulation in TABLE XI, below, exhibited an average disintegration time of less than one minute in 0. IN HCI and less than 2 minutes in water at 37 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 1 minute in both acid and water.

TABLE XI *Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 62.42 Avicel PH 101® 0.0370 4.62 Sodium lauryl sulfate 0.0015 0.19 20 Povidone 29K/32 0.0480 5.99 Dye/Colouring Agent 0.0010 0.12 DI water DI water q.s. q.s.

Phase B Phase A 0.5875 73.34 Sodium lauryl sulfate 0.0015 0.19 Avicel PH 102® 0.2045 25.53 Magnesium stearate 0.0075 0.94 TOTAL 0.8010 100.00 -22- EXAMPLE 12 The formulation in TABLE XII exhibited an average disintegration time of less than 5 minutes in 0.1N HCI and less than 7 minutes in water at 37 0.5 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 5 minutes in acid and less than 8 minutes in water.

TABLE XII Swallowable Methvlcellulose Tablets 0 Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 69.35 Avicel PH 101® 0.0370 5.13 Sodium lauryl sulfate 0.0015 0.21 Povidone 29K/32 0.0480 6.66 Dye/Colouring Agent 0.0010 0.14 DI water q.s. q.s.

Phase B Phase A 0.5875 81.48 Sodium lauryl sulfate 0.0015 0.21 Avicel PH 102® 0.1245 17.27 Magnesium stearate 0.0075 1.04 STOTAL 0.7210 100.00 4 4 4* -23- *i *i EXAMPLE 13 The formulation in TABLE XIII exhibited an average disintegration time of less than 10 minutes in 0.1N HCI and less than 14 minutes in water at 37 0.5 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 14 minutes in acid and less than 22 minutes in water.

TABLE XIII Swallowable Methylcellulose Tablets 0 Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 76.10 Avicel PH 101® 0.0370 5.63 Sodium lauryl sulfate 0.0015 0.23 Povidone 29K/32 0.0480 7.31 Dye/coloring agent 0.0010 0.15 DI water q.s. q.s.

Phase B Phase A 0.5875 89.42 Sodium lauryl sulfate 0.0015 0.23 Avicel PH 102® 0.0605 9.21 Magnesium stearate 0.0075 1.14 STOTAL 0.6570 100.00 *i a.

24-

C.

C

C*CC

CC

C

C

EXAMPLE 14 Two formulations containing Avicel PHI01® intragranularly with different levels of extragranular Avicel PH 200® shown in TABLE XIV and XV below) were made to observe the effect on disintegration time of tablets.

The formulation in TABLE XIV exhibited an average disintegration time of less than 7 minutes in 0. IN HCI and less than 9 minutes in water at 37 0.5 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 8 minutes in acid and less than 13 minutes in water.

TABLE XIV Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 62.42 Avicel PH 101 0.0370 4.62 Sodium lauryl sulfate 0.0015 0.19 Povidone 29K/32 0.0480 5.99 Dye/Coloring Agent 0.0010 0.12 DI water q.s. q.s.

Phase B Phase A 0.5875 73.34 Sodium lauryl sulfate 0.0015 0.19 Avicel PH200® 0.2045 25.53 Magnesium stearate 0.0075 0.94 TOTAL 0.8010 100.00 C C

CC

C a S o C C go

C

CC..

CC*

C. C

CC..

CC

0

S

eq EXAMPLE The formulation in TABLE XV exhibited an average disintegration time of less than 4 minutes in 0.1N HCI and less than 7 minutes in water at 37 0.5 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 5 minutes in acid and less than 9 minutes in water.

TABLE XV Swallowable Methvlcellulose Tablets 0 Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 69.35 Avicel PHl01® 0.0370 5.13 Sodium lauryl sulfate 0.0015 0.21 Povidone 29K/32 0.0480 6.66 Dye/Coloring Agent 0.0010 0.14 DI water q.s. q.s.

Phase B Phase A 0.5875 81.48 Sodium lauryl sulfate 0.0015 0.21 Avicel PH200® 0.1245 17.27 Magnesium stearate 0.0075 1.04 TOTAL 0.7210 100.00 5

S'S.

5 5 5 0065 @5 5 0S -26- EXAMPLE 16 A formulation containing a calcium source from the intragranular and extragranular excipient. dibasic calcium phosphate, dihydrate with extragranular Explotab® is shown in TABLE XVI.

The formulation in TABLE XVI exhibited an average disintegration time of less than 6 minutes in 0. IN HCI and less than 9 minutes in water at 37 0.5 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 5 minutes in acid and less than 12 minutes in water.

TABLE XVI Swallowable Methvlcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 66.93 Dibasic Calcium phosphate, dihydrate 0.0370 4.95 Sodium lauryl sulfate 0.0015 0.20 20 F, D, and C Yellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.43 DI water q.s. q.s.

Phase B Phase A 0.5875 78.65 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0260 3.48 Dibasic Calcium phosphate, dihydrate 0.1245 16.67 Magnesium stearate 0.0075 1.00 TOTAL 0.7470 100.00 00 0 1.

-27- EXAMPLE 17 A formulation containing a calcium source from the intra and extragranular excipient, dibasic calcium phosphate, dihydrate with a higher amount of extragranular Explotab® than in Example 17, is shown below in TABLE XVII.

The formulation in TABLE XVII exhibited an average disintegration time of less than 9 minutes in 0.1N HCI and less than 14 minutes in water at 37 0.5 "C using the automated disintegration apparatus. The conventional disintegration apparatus yielded less than 6 minutes in acid and less than 12 minutes in water.

TABLE XVII Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 65.19 Dibasic Calcium phosphate, dihydrate 0.0370 4.82 Sodium lauryl sulfate 0.0015 0.20 20 F, D, and C Yellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.26 DI water q.s. q.s.

Phase B Phase A 0.6105 79.60 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0230 3.00 Dibasic Calcium phosphate, dihydrate 0.1245 16.23 Magnesium stearate 0.0075 0.97 TOTAL 0.7670 100.00 -28- EXAMPLE 18 Formulations containing a calcium source from the intra and extragranular excipient, dibasic calcium phosphate, dihydrate with different levels of extragranular Explotab®, in combination with similar amount of intragranular Explotab®, are shown below in TABLE XVIII and XIX (Example 19).

The formulation in TABLE XVIII exhibited an average disintegration time of less than 6 minutes in 0. IN HCI and less than 11 minutes in water at 37 0.5 "C using the automated disintegration apparatus.

TABLE XVIII Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 65.19 Dibasic Calcium phosphate, dihydrate 0.0370 4.82 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0230 3.00 F, D, and C Yellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.26 DI water q.s. q.s.

Phase B Phase A 0.6105 79.60 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0230 3.00 Dibasic Calcium phosphate, dihydrate 0.1245 16.23 Magnesium stearate 0.0075 0.97 TOTAL 0.7670 100.00 -29- EXAMPLE 19 The formulation in TABLE XIX exhibited an average disintegration time of less than 9 minutes in 0. IN HCI and less than 14 minutes in water at 37 10.5 "'C using the automated disintegration apparatus.

TABLE XIX Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 63.86 Dibasic Calcium phosphate, dihydrate 0.0370 4.73 Sodium lauryl sulfate 0.00 15 0.19 Sodium starch glycolate 0.0230 2.94 F, D, and CYellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.13 DI water q.s. q.s.

Phase B Phase A 0.6105 77.97 Sodium lauryl sulfate 0.0015 0.19 Sodium starch glycolate 0.0390 4.98 Dibasic Calcium phosphate, dihydrate 0.1245 15.90 Magnesium stearate 0.0075 0.96 TOTAL 0.7830 100.00 30 EXAMPLE Formulations containing a calcium source from the intra and extragranular excipient, dibasic calcium phosphate, dihydrate with extragranular Explotab® are shown in TABLE XX and XXI (Example 21) below.

The formulation in TABLE XX exhibited an average disintegration time of less than 5 minutes in 0.1N HCI and less than 13 minutes in water at 37 0.5 "C using the automated disintegration apparatus.

TABLE XX 0 Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 66.89 Dibasic Calcium phosphate, dihydrate 0.0370 4.95 Sodium lauryl sulfate 0.0015 0.20 F, D, and C Yellow #6 0.0010 0.13 SPovidone 29K/32 0.0300 4.01 DI water q.s. q.s.

Phase B Phase A 0.5695 76.19 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0445 5.95 Dibasic Calcium phosphate, dihydrate 0.1245 16.66 Magnesium stearate 0.0075 1.00 TOTAL 0.7475 100.00 -31 EXAMPLE 21 The formulation in TABLE XXI exhibited an average disintegration time of less than 7 minutes in 0. IN HCI and less than 9 minutes in water at 37 :t 0.5 -C using the conventional disintegration method.

TABLE XXI Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 64.52 Dibasic Calcium phosphate, dihydrate 0.0370 4.77 Sodium lauryl sulfate 0.0015 0.19 F, D,and CYellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.19 DI water q.s. q.s.

Phase B Phase A 0.5875 75.81 Sodium lauryl sulfate 0.0015 0.19 Sodium starch glycolate 0.0235 3.03 Dibasic Calcium phosphate, dihydrate 0.1550 20.00 Magnesium stearate 0.0075 0.97 TOTAL 0.7750 100.00

C

C.

C C C C

C.

32 EXAMPLE 22 A formulation containing a calcium source from the intra and extragranular excipient, calcium phosphate. anhydrous with extragranular Explotab® is indicated in TABLE XXII.

The formulation in TABLE XXII exhibited an average disintegration time of less than 11 minutes in 0.1N HCI and less than 19 minutes in water at 37 0.5 "C using the conventional disintegration apparatus.

TABLE XXII Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 66.93 Calcium phosphate, Anhydrous 0.0370 4.95 Sodium lauryl sulfate 0.0015 0.20 F. D, and C Yellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.43 DI water q.s. q.s.

Phase B Phase A 0.5875 78.65 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0260 3.48 Calcium phosphate, Anhydrous 0.1245 0.67 Magnesium stearate 0.0075 1.00 TOTAL 0.7470 100.00 -33- EXAMPLE 23 A formulation containing a calcium source from the intra and extragranular excipient, tribasic cahcium phosphate WG® with extragranular Explotab® is indicated in TABLE XXIII.

The formulation in TABLE XXIII exhibited an average disintegration time of less than 13 minutes in 0.IN HCI and less than 24 minutes in water at 37 0.5 'C using the conventional disintegration apparatus.

TABLE XXIII Swallowable Methylcellulose Tablets Formula g/tablet w/w) Ingredient Phase A Methocel A4M 0.5000 66.93 Tribasic Calcium phosphate, WG® 0.0370 4.95 Sodium lauryl sulfate 0.0015 0.20 F. D, and C Yellow #6 0.0010 0.13 Povidone 29K/32 0.0480 6.43 DI water q.s. q.s.

Phase B Phase A 0.5875 78.65 Sodium lauryl sulfate 0.0015 0.20 Sodium starch glycolate 0.0260 3.48 Tribasic Calcium phosphate, WG® 0.1245 16.67 Magnesium stearate 0.0075 1.00 TOTAL 0.7470 100.00 -34- All publications, including but not limited to patents and patent applications, cited in this specification are herein incorporated by reference as if each individual publication were specifically and individually indicated to be incorporated by reference herein as though fully set forth.

The above description fully discloses the invention including preferred embodiments thereof. Modifications and improvements of the embodiments specifically disclosed herein are within the scope of the following claims. Without further elaboration, it is believed that one skilled in the art can, using the preceding description, utilize the present invention to its fullest extent. Therefore the Examples herein are to be construed 10 as merely illustrative and not a limitation of the scope of the present invention in any way.

The embodiments of the invention in which an exclusive property or privilege is claimed are defined as follows.

Throughout this specification and the claims which follow, unless the context requires otherwise, the word "comprise", and variations such as "comprises" and 15 "comprising", will be understood to imply the inclusion of a stated integer or step or group of integers or steps but not the exclusion of any other integer or step or group of integers or :steps.

The reference to any prior art in this specification is not, and should not be taken as, an acknowledgment or any form of suggestion that that prior art forms part of the 20 common general knowledge in Australia.

Claims (45)

1. A method of relieving constipation in a mammal in need thereof, comprising administering to said mammal a rapidly disintegrating tablet comprising a compacted mixture of methylcellulose having a viscosity of 1000 centipoise; and an edible calcium salt selected from the group consisting of dibasic calcium phosphate dihydrate, calcium phosphate anhydrous, and tribasic calcium phosphate; or mixtures thereof.

2. The method according to Claim 1 wherein the tablet further comprises a binding agent.

3. The method according to Claim 2 wherein the binding agent is selected from the group consisting of PVP, hydroxypropylcellulose, hydroxypropyl methylcellulose, acacia, gelatin, tragacanth, pregelatinized starch and starch.

4. The method according to Claim 3 wherein the binding agent is PVP. The method according to Claim 1 wherein the tablet further comprises a *20 disintegrating agent.

6. The method according to Claim 5 wherein the disintegrating agent is selected from the group consisting of sodium starch glycolate, sodium carboxymethylcellulose, sodium crosscarmellose, carboxymethylcellulose, veegum, an alginate, agar, guar, tragacanth, locust bean, karaya, pectin, and crospovidone.

7. The method according to Claim 6 wherein the disintegrating agent is sodium starch glycolate.

8. The method according to Claim 7 wherein the sodium starch glycolate P\OPERVWA400292022-98 dir vp .doc-20A)2/2 -37- is present in an amount of about 3 to about 8% w/w.

9. The method according to Claim 1 wherein the tablet further comprises a wetting agent. The method according to Claim 9 wherein the wetting agent is sodium lauryl sulfate.

11. The method according to Claim 1 wherein the tablet further comprises a S• 10 lubricating agent.

12. The method according to Claim 11 wherein the lubricating agent is magnesium stearate. 15 13. The method according to Claim 1 wherein the methylcellulose has a viscosity of >2000 centipoises. o.

14. The method according to Claim 13 wherein the methylcellulose has a viscosity of >3000 centipoises.

15. The method according to Claim 14 wherein the methylcellulose has a viscosity of>4000 centipoises.

16. The method according to Claim 1 wherein the edible calcium salt is Dibasic calcium phosphate dihydrate and is present in a ratio of methylcellulose to calcium from about 2 to about 4:1.

17. The method according to Claim 1 wherein the edible calcium salt is Calcium phosphate anhydrous and is present in a ratio of methylcellulose to calcium from about 2 to about 4:1. PAOPERIaI\10O2\92022-99 div spc.doc-2O/O2/O2 -38-

18. The method according to Claim 1 wherein the edible calcium salt is Tribasic calcium phosphate and is present in a ratio of methylcellulose to Tribasic calcium phosphate, from about 2 to about 4:1.

19. The method according to Claim 1 wherein the tablet further comprises additional excipients and diluents in the ratio of: Sodium lauryl sulfate:Explotab:Tribasic calcium phosphate:Povidone 29K/32:Magnesium stearate include: 0.40:3.5:21.6:6.4:1.0; or Sodium lauryl sulfate:Explotab:Calcium phosphate, anhydrous: Povidone 29K/32:Magnesium stearate include: 0.40:3.5:21.6:6.4:1.0.

20. The method according to Claim 1 wherein the methylcellulose is present in an amount of about 450 to about 550mg. 15 21. The method according to Claim 1 wherein the methylcellulose is present in an amount of about 200 to about 300mg.

22. A method of relieving constipation in a mammal in need thereof, comprising administering to said mammal a rapidly disintegrating tablet 20 comprising methylcellulose having a viscosity of 3000 centipoise; dibasic calcium phosphate, sodium lauryl sulfate, povidone; sodium starch glycolate, and magnesium stearate.

23. The method according to Claim 5 wherein the PVP is present in an amount of about 4 to about 6.5 w/w.

24. A method of relieving constipation in a mammal in need thereof, comprising administering to said mammal a rapidly disintegrating tablet comprising a compacted mixture of methylcellulose having a viscosity of 1000 centipoise; and an edible calcium salt wherein the ratio of methylcellulose to calcium salt is from about 2:1 to about 4:1. P.XOPER\Mal1\0J292022-98 div Sp.doc-2/02/O -39- The method according to Claim 24 wherein the ratio of methylcellulose to calcium salt is from about 2:6 to 3.1:1.

26. The method according to Claim 24 wherein the edible calcium salt is dibasic calcium phosphate dihydrate, calcium phosphate anhydrous, tribasic calcium phosphate; or mixtures thereof. S* 27. The method according to Claim 24 wherein the tablet further comprises 10 a binding agent.

28. The method according to Claim 27 wherein the binding agent is selected from the group consisting of PVP, hydroxypropylcellulose, hydroxypropyl methylcellulose, acacia, gelatin, tragacanth, pregelatinized 15 starch and starch.

29. The method according to Claim 24 wherein the tablet further comprises a disintegrating agent. 20 30. The method according to Claim 29 wherein the disintegrating agent is selected from the group consisting of sodium starch glycolate, sodium carboxymethylcellulose, sodium crosscarmellose, carboxymethylcellulose, veegum, an alginate, agar, guar, tragacanth, locust bean, karaya, pectin, and crospovidone.

31. The method according to Claim 30 wherein the disintegrating agent is sodium starch glycolate.

32. The method according to Claim 31 wherein the sodium starch glycolate is present in an amount of about 3 to about 8% w/w. P:\OPERVIA0202\92O22-9 dN spcdom-20/02M2

33. The method according to Claim 24 wherein the tablet further comprises a wetting agent.

34. The method according to Claim 33 wherein the wetting agent is sodium lauryl sulfate. The method according to Claim 24 wherein the tablet further comprises a lubricating agent. 9 9*9*9*

36. The method according to Claim 35 wherein the lubricating agent is magnesium stearate.

37. The method according to Claim 24 wherein the methylcellulose has a viscosity of>2000 centipoises.

38. The method according to Claim 37 wherein the methylcellulose has a viscosity of >3000 centipoises. 9*

39. The method according to Claim 38 wherein the methylcellulose has a 20 viscosity of >4000 centipoises. The method according to Claim 28 wherein the PVP is present in an amount of about 4 to about 6.5 w/w.

41. A method of lubricating the stool in a mammal in need thereof, comprising administering to said mammal a rapidly disintegrating tablet comprising a compacted mixture of methylcellulose having a viscosity of 1000 centipoise; and an edible calcium salt wherein the ratio of methylcellulose to calcium salt is from about 2:1 to about 4:1.

42. The method according to Claim 41 wherein the ratio of methylcellulose P:AOPERMal\002\92022-98 div spe.doc-2002/02 -41 to calcium salt is from about 2:6 to 3.1:1.

43. The method according to Claim 41 or 42 wherein the edible calcium salt is dibasic calcium phosphate dihydrate, calcium phosphate anhydrous, tribasic calcium phosphate; or mixtures thereof.

44. The method according to Claim 41 wherein the tablet further comprises a binding agent.

45. The method according to Claim 44 wherein the binding agent is selected from the group consisting of PVP, hydroxypropylcellulose, hydroxypropyl methylcellulose, acacia, gelatin, tragacanth, pregelatinized starch and starch. 15 46. The method according to Claim 45 wherein the PVP is present in an amount of about 4 to about 6.5 w/w.

47. The method according to Claim 48 wherein the tablet further comprises a disintegrating agent.

48. The method according to Claim 47 wherein the disintegrating agent is selected from the group consisting of sodium starch glycolate, sodium carboxymethylcellulose, sodium crosscarmellose, carboxymethylcellulose, veegum, an alginate, agar, guar, tragacanth, locust bean, karaya, pectin, and crospovidone.

49. The method according to Claim 48 wherein the disintegrating agent is sodium starch glycolate.

50. The method according to Claim 49 wherein the sodium starch glycolate is present in an amount of about 3 to about 8% w/w. PRUPERVdAzfM20M920-98 div q.do-25M2/2 -42-

51. The method according to Claim 41 wherein the tablet further comprises a wetting agent.

52. The method according to Claim 51 wherein the wetting agent is sodium lauryl sulfate.

53. The method according to Claim 41 wherein the tablet further comprises a lubricating agent.

54. The method according to Claim 53 wherein the lubricating agent is magnesium stearate. The method according to Claim 41 wherein the methylcellulose has a viscosity of >2000 centipoises.

56. The method according to Claim 55 wherein the methylcellulose has a viscosity of>3000 centipoises. 20 57. The method according to Claim 56 wherein the methylcellulose has a viscosity of >4000 centipoises. DATED this 26th day of February, 2002 SmithKline Beecham Corporation By DAVIES COLLISON CAVE Patent Attorneys for the Applicants