IP Library Granted Patent US 7,871,645
Granted Patent B2
US 7,871,645 · App. 11/674,921 · Granted Jan 18, 2011

Ion exchange resin treated to control swelling

Assignee: Coating Place, Inc.
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Quick Facts
Patent No.
US 7,871,645
App. No.
11/674,921
Granted
Jan 18, 2011
Kind
B2
Abstract

The present invention provides a method and composition for loading one or more drugs in a solution onto one or more ion exchange resin particles to form a drug-loaded resin particle. The drug-loaded resin particle is separated from the solution and dried before recombining the drug-loaded resin particle with the solution to load more drugs onto the drug-loaded resin particle from the solution.

Claims (18)

1. A method of preparing a drug-resin compound comprising the steps of: loading in a solution one or more drugs onto one or more ion exchange resin particles to form drug-loaded resin particle(s); separating the drug-loaded resin particle(s) from the solution and recovering a filtrate containing the drug without washing the drug loaded resin particles; and coating the recovered filtrate back onto the drug-loaded resin particle(s).

2. The method of claim 1 , further comprising the step of drying the drug-loaded resin particle(s) then coating the recovered filtrate back onto the drug-loaded resin particle.

3. The method of claim 1 , wherein the step of separating is selected from the group consisting of filtration, extraction, distillation, precipitation, amalgamation or a combination or series thereof.

4. The method of claim 1 , wherein the drying is accomplished by the use of an oven dryer, flash dryer, spray dryer, a fluid bed dryer or a combination thereof.

5. The method of claim 1 , wherein the step of loading lasts between about 0.1 and 12 hours.

6. The method of claim 1 , further comprising the step of loading one or more sugar alcohols to the drug-loaded resin particle(s).

7. The method of claim 6 , wherein the one or more sugar alcohols is selected from the group consisting of mannitol, sorbitol, xylitol, maltitol, lactitol, 1,3-dihydroxypropane, inositol glucose, sucrose and mixtures or combinations thereof.

8. The method of claim 1 , wherein the ion exchange resin particles comprise sulfonic acid cationic exchange resin particles.

9. The method of claim 1 , wherein the ionic exchange resin is selected from the group consisting of dipropylene glycol diallyl ether, polyglycol diallyl ether, triethylene glycol divinyl ether, hydroquinone diallyl ether, tetraallyloxyethanoyl, vinyl ether, vinyl acetate, vinyl butylbenzoate, crotonic acid, polyfunctional alcohol, tetraethylene glycol diacrylate, triallylamine, trimethylolpropane diallyl ether, methylenebisacrylamide, divinylbenzene, phthalic, sulphonphthalic acid, ethylene glycol, polymethyl siloxane α, γ-hydroxypropyl or combination thereof.

10. The method of claim 1 , wherein the loading solution comprises a second drug selected from narcotic analgesics, sympathomimetics, antitussives, analgesics antiemetics, anticholinergics, muscle relaxants, bronchodilators, antibiotics, antidepressants, antiasthmatics, antineoplastics, antiepileptics, cardiovascular agents, mixtures and combinations thereof.

11. The method of claim 1 , further comprising the step of coating the ion exchange resin particles with a water-permeable diffusion barrier.

12. The method of claim 1 , further comprising the step of drying the drug-loaded resin particle(s) after the separation of the drug-loaded resin particle(s) from the solution.

13. The method of claim 1 , wherein the recovered filtrate is coated back onto the drug-loaded resin particle(s) using a fluid bed coating equipment.

14. The method of claim 1 , wherein the one or more drugs is selected from the group consisting of narcotic analgesics, sympathomimetics, antitussives, analgesics antiemetics, anticholinergics, muscle relaxants, bronchodilators, antibiotics, antidepressants, antiasthmatics, antineoplastics, antiepileptics, cardiovascular agents, mixtures and combinations thereof.

15. The method of claim 1 , wherein the one or more drugs is selected from the group consisting of codeine, dihydrocodeine, hydromorphone, morphine, pentazocine, propoxyphene, norephedrine, pseudoephedrine, dextromethorphan, aspirin, tramadol, metoclopramide, atropine, ipratropium bromide, scopolamine, cyclobenzaprine, papaverine, salbutamol, terbutaline and theophylline, amoxycillin, ampicillin, azlocillin, bacampicillin, cefamandole, cefonicid, cefotaxime, cefotetan, cefoxitin, ceftriaxone, mezlocillin, piperacillin, bupropion, nomifensine, nortriptyline, cromolyn, tamoxifen, valproic acid and phenvtoin, propranolol mixtures and combinations thereof.

16. The method of claim 11 , further comprising suspending the drug-loaded resin particle(s) in a liquid.

17. The method of claim 16 , wherein the liquid is a syrup.

18. The method of claim 1 , wherein the drug-resin compound is a controlled release composition.

Assignments (3)
CHANGE OF NAME Recorded Dec 29, 2025
From: COATING PLACE, INCORPORATED
To: COATING PLACE, LLC
Reel/Frame 074091/0361 →
SECURITY INTEREST Recorded Dec 23, 2025
From: COATING PLACE, LLC
To: APOGEM CAPITAL LLC, AS AGENT
Reel/Frame 073303/0724 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 19, 2007
From: HALL, HARLAN; MADSEN, J. SCOTT
To: COATING PLACE, INC.
Reel/Frame 019031/0538 →
Continuity (2)
Continuation 1122583400 · Sep 13, 2005
Related Publication 20070140983A1 · Jun 21, 2007