TIOPRONIN ORAL COMPOSITION

Abstract

The invention relates to an oral tiopronin composition for reducing the dosing frequency in treatment of cysteinuria comprising of therapeutically effective amount of tiopronin and one or more pharmaceutically acceptable excipients.

Claims

1. An oral tiopronin composition for reducing the dosing frequency in treatment of cysteinuria comprising of therapeutically effective amount of tiopronin and one or more pharmaceutically acceptable excipients, wherein the amount of tiopronin is 200 mg.

2. The oral tiopronin composition of claim 1 wherein the pharmaceutically acceptable excipient is selected from the group comprising of fillers, disintegrants, binders, glidants, lubricants or a combination thereof.

3. The oral tiopronin composition of claim 1 wherein the filler is selected from the group consisting of directly compressible starches, hydrolysed starches, Lactose and its derivates dextrose, sorbitol, microcrystalline cellulose, dibasic calcium phosphate dehydrate, Calcium sulphate dehydrate or a combination thereof.

4. The oral tiopronin composition of claim 1 wherein the disintegrant is selected from the group consisting of starches, clays, cellulose and its derivates including hydroxypropyl cellulose, cross linked polymers, modified starches including sodium starch glycolate, magnesium aluminium silicate, crosscarmalose, cross povidone, strach derivatives, alginates, Polyvinylpyrrolidone or a combination thereof.

5. The oral tiopronin composition of claim 1 wherein the binder is selected from the group consisting of acacia, gelatin, starch, pregelatinized starch, polyvinylpyrrolidone, glucose, povidone, cellulose derivatives including methyl cellulose, ethyl cellulose, carboxymethyl cellulose, microcrystallince cellulose, hydroxyethyl cellulose hydroxypropylmethyl cellulose (HPMC), tragacanth, alginate derivatives inclusing sodium alginate, synthetic polymers, shellac or a combination thereof.

6. The oral tiopronin composition of claim 1 wherein the glidant is selected from the group consisting of talc, colloidal silicone dioxide, asbestos free starch, corn starch, maize starch, calcium phosphate, calcium silicate, powdered cellulose, magnesium trisilicate, silicon dioxide, silica derivates including colloidal silica, colloidal silica anhydrous or a combination thereof.

7. The oral tiopronin composition of claim 1 wherein the lubricant is selected from the group consisting of talc, stearic acid, magnesium stearate, calcium stearate, waxes, polyethylene glycol, surfactants or vegetable oil.

8. The oral tiopronin composition of claim 1 is a tablet

9. The oral tiopronin composition of claim 8 wherein the tablet is a sugar coated tablet.

Description

DETAILED DESCRIPTION OF THE INVENTION

[0014] The invention disclosed herein provides a tiopronin oral composition for reducing the dosing frequency and thereby improving the treatment compliance by the patients. The oral tiopronin composition for reducing the dosing frequency in treatment of cysteinuria comprises of therapeutically effective amount of tiopronin and one or more pharmaceutically acceptable excipients. The oral tiopronin composition as disclosed herein comprises of 200 mg of tiopronin or its pharmaceutically acceptable salts.

[0015] According to one embodiment the triopronin is tiopronin hydrochloride. The oral tiopronin composition comprises one or more fillers, one or more disintegrants/disintegrating agents, one or more binders, one or more glidants/gliding agents, one or more lubricants lubricating agents or a combination thereof. According to one embodiment the oral tiopronin composition is a sugar coated tablet.

[0016] The filler is selected from the group consisting of directly compressible starches, hydrolysed starches, Lactose and its derivates dextrose, sorbitol, microcrystalline cellulose, dibasic calcium phosphate dehydrate, Calcium sulphate dehydrate or a combination thereof.

[0017] The disintegrant/disintegrating agent is selected from the group consisting of starches, clays, cellulose and its derivates including hydroxypropyl cellulose, cross linked polymers, modified starches including sodium starch glycolate, magnesium aluminium silicate, crosscarmalose, cross povidone, strach derivatives, alginates, Polyvinylpyrrolidone or a combination thereof.

[0018] The binder is selected from the group consisting of acacia, gelatin, starch, pregelatinized starch, polyvinylpyrrolidone, glucose, povidone, cellulose derivatives including methyl cellulose, ethyl cellulose, carboxymethyl cellulose, microcrystallince cellulose, hydroxyethyl cellulose hydroxypropylmethyl cellulose (HPMC), tragacanth, alginate derivatives inclusing sodium alginate, synthetic polymers, shellac or a combination thereof.

[0019] The glidant/gliding agent is selected from the group consisting of talc, colloidal silicone dioxide, asbestos free starch, corn starch, maize starch, calcium phosphate, calcium silicate, powdered cellulose, magnesium trisilicate, silicon dioxide, silica derivates including colloidal silica, colloidal silica anhydrous or a combination thereof.

[0020] The lubricant/lubricating agent is selected from the group consisting of talc, stearic acid, magnesium stearate, calcium stearate, waxes, polyethylene glycol, surfactants or vegetable oil.

Example 1Compositions of Core Tablet

[0021]

TABLE-US-00001 Amount (mg/Unit) S. No. Name of the Active/Excipient F1 F2 F3 F4 1 Tiopronin 200 200 200 200 2 Lactose anhydrous 40 40 40 40 3 L-Hydroxypropylcellulose 20 20 20 20 4 Polyvinylpyrrolidone 4 4 4 4 5 Isopropyl alcohol q.s. q.s. 6 Ethyl cellulose 13 13 19.50 10.25 7 L-Hydroxypropyl cellulose 20 20 13 6.66 8 Talc 20 20 13 6.66 9 Lactose anhydrous 60 30.70 30.77 10 Magnesium stearate 13 13 20 10.26 Core tablet's weight 390 330 390 390

[0022] Add Polyvinylpyrrolidone to isopropyl alcohol and stir the solution until clear solution observed without any lumps. Tiopronin, Lactose anhydrous Part-1 & L-Hydroxypropylcellulose (LH 21) into RMG and mixed well for 10 minutes with impeller at fast speed. Slowly add Polyvinylpyrrolidone solution into rapid mixer granulator over period of 60-90 seconds at impeller slow speed and rake the material. Knead the wet mass for 30-60 seconds at impeller fast speed and chopper fast speed until get a good granular mass. Unload the wet granular mass into FBD bowl.

[0023] Air-dry the wet granules for 5 minutes to ensure proper fluidization. Dried the wet granular mass in fluid bed drier at an inlet temperature of 55 C.5 C. & outlet temperature 455 C. until get moisture content of NMT 1.5% L achieved.

[0024] Milled the dried granules and sift through 20 ASTM sieve (850). Add the ethyl cellulose, Hydroxypropylcellulose (Part 2), Lactose anhydrous (Part 2) & Talc and blend it for 10 minutes. Finally add magnesium stearate and blend it for 5 min. Compressed the lubricated blend using the BB type, 10.00 mm, Round shape, Deep concave plain punches.

Example 2Coating

[0025]

TABLE-US-00002 Coating Excipients S. No. (7.45% w/w) F5 F6 F7 1 Hydroxypropyl cellulose 5.67 4.8 0 2 Eudragit E1 00 21.27 18 10 3 Triethyl citrate 2.13 1.8 1 4 Isopropyl alcohol q.s. q.s. q.s. 5 Acetone q.s. q.s. q.s.

[0026] Add Eudragit E 100 to the Acetone & IPA mixture under continuous stirring and stir the solution for 1 hr. After dissolving the Eudragit E-100 add Hydroxyl propyl cellulose slowly under continuous stirring and stir the solution for 30-45 minutes. Add triethyl citrate to above solution and stir the solution for 10-15 minutes and filtered the dispersion through #200 (750 nylon cloth. The coated tablets are dried for 120 minutes at 40 C. bed temperature.

Example 3Sub Coating

[0027]

TABLE-US-00003 Coating Excipients S. No. (7.45% w/w) F5 F6 F7 1 Sucrose 118.18 100 80 2 Calcium carbonate 40.99 34.68 50 3 Talc 9.60 8.12 4 4 Purified water q.s. q.s. q.s.

[0028] Heat purified water in steam-jacketed vessel to 80-90 C. Add sucrose to heat water under and Stir the solution without any lumps for 20-30 minutes. After dissolving the sucrose add Calcium Carbonate & Talc and homogenize the solution using homogenizer/colloidal mill for 15-30 minutes. Filtered the coating solution with #100 (1500 nylon cloth in to a clean SS vessel.

[0029] Load Eudragit coated tablets into coating pan and perform the coating using the below mentioned parameters with intermittent spray pattern. After coating tablets to be dried for 30 minutes at 45 C. bed temperature.

Example 4Syrup Coating

[0030]

TABLE-US-00004 S. No. Name of the material F11 F12 F13 1 Sucrose 47.27 40.00 38.00 2 Talc 10.05 3.40 15.00 3 Titanium dioxide 4.02 8.00 14.00 4 Water q.s. q.s. q.s.

[0031] Heat purified water in steam-jacketed vessel to 80-90 C. Add sucrose to heat water and stir the solution without any lumps for 20-30 minutes. After dissolving sucrose add Talc & Titanium dioxide and homogenize the solution using homogenizer/colloidal mill for 15-30 minutes. Filter the suspension with #100 (150) nylon cloth in to a clean SS vessel. Load the sub coated tablets into coating pan and perform the coating using the below mentioned parameters. Spray, pause followed by dry condition has followed during syrup coating. After coating dried the tablets for 30 minutes at 40 C. bed temperature.

Example 5Polishing

[0032]

TABLE-US-00005 S. No. Excipients F14 F15 F16 1 Opagloss 6000P 0.82 1.00 0.60 2 Isopropyl alcohol q.s. q.s. q.s.

[0033] Dispense required quantity of Isopropyl alcohol required to make 5% w/w solution of polishing coating material. Add Opagloss 6000P to the isopropyl alcohol under stirring and continue the stirring for 10-15 minutes until the homogeneous solution observed. Load the syrup coated tablets into pan and perform the process as per given below parameters. After coating tablets are dried for 30 minutes at 40 C. bed temperature.