Enteric Coated Azithromycin Multiparticulates

• US 20080199527A1
• Filed: 12/09/2005
• Published: 08/21/2008
• Est. Priority Date: 12/21/2004
• Status: Abandoned Application

• Current Assignee: Pfizer Inc.
• Original Assignee: Pfizer Inc.
• Inventors: Lo, Julian B., Lyon, David K., Appel, Leah E., Friesen, Dwayne T., Herbig, Scott M., McCray, Scott B., Curatolo, William J., West, James B., LeMott, Steven R.
• Application Number:
  US11/722,364
• Publication Number:
  US 20080199527A1
• Time in Patent Office: Days
• US Class Current: 424/494
• CPC Class Codes: A61K 9/0095 Drinks; Beverages; Syrups; Compositions for reconstitution thereof, e.g. powders or tablets to be dispersed in a glass of water; Veterinary drenches A61K9/0007 takes precedence; eatable gels or foams A61K9/0056; oral mucosa adhesive forms A61K9/006
• CPC Class Codes: A61K 9/1617 Organic compounds, e.g. phospholipids, fats
• CPC Class Codes: A61K 9/5026 obtained by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyvinyl pyrrolidone, poly(meth)acrylates
• CPC Class Codes: A61K 9/5042 Cellulose; Cellulose derivatives, e.g. phthalate or acetate succinate esters of hydroxypropyl methylcellulose
• CPC Class Codes: A61K 9/5073 having two or more different coatings optionally including drug-containing subcoatings
• CPC Class Codes: A61P 31/04 Antibacterial agents

Abstract

A pharmaceutical composition is disclosed which comprises multiparticulates wherein said multiparticulates further comprise an azithromycin core and an enteric coating disposed upon said azithromycin core.

Claims

1. A pharmaceutical composition comprising multiparticulates, wherein said multiparticulates comprise an azithromycin core and an enteric coating disposed upon said azithromycin core.

2. The pharmaceutical composition of claim 1 wherein said enteric coating has a thickness of between about 3 μ

m to about 3 mm.

3. The pharmaceutical composition of claim 1 wherein there is a concentration of azithromycin esters in said composition is less than about 5 wt % relative to the total weight of azithromycin originally present in the composition.

4. The pharmaceutical composition of claim 1 wherein said azithromycin is substantially in the form of the crystalline dihydrate.

5. The pharmaceutical composition of any of claims 1-4 wherein said enteric coating comprises at least one material selected from the group consisting of polyacrylamides, acid phthalates of carbohydrates, amylose acetate phthalate, cellulose acetate phthalate, cellulose ester phthalates, cellulose ether phthalates, hydroxypropylcellulose phthalate, hydroxypropylethylcellulose phthalate, hydroxypropylmethylcellulose phthalate, methylcellulose phthalate, polyvinyl acetate phthalate, polyvinyl acetate hydrogen phthalate, sodium cellulose acetate phthalate, starch acid phthalate, styrene-maleic acid dibutyl phthalate copolymer, styrene-maleic acid polyvinylacetate phthalate copolymer, cellulose acetate trimellitate, hydroxypropyl methylcellulose acetate succinate, cellulose acetate succinate, carboxymethyl cellulose, carboxyethyl cellulose, carboxymethyl ethyl cellulose, styrene and maleic acid copolymers, polyacrylic acid derivative, polymethacrylic acid and esters thereof, poly acrylic methacrylic acid copolymers, shellac, vinyl acetate and crotonic acid copolymers, and mixtures thereof.

6. The pharmaceutical composition of any of claims 1-4 wherein said enteric coating comprises at least one material selected from the group consisting of carboxymethyl cellulose, carboxyethyl cellulose, carboxymethyl ethyl cellulose, styrene and maleic acid copolymers, polyacrylic acid, polymethacrylic acid, polyacrylic and methacrylic acid copolymers, crotonic acid copolymers, hydroxypropylmethyl cellulose acetate succinate, and mixtures thereof.

7. The pharmaceutical composition of any of claims 1-4 wherein said enteric coating comprises a mixture of (i) a copolymer of methacrylic acid and ethyl acrylate and (ii) triethyl citrate.

8. The pharmaceutical composition of any of claims 1-4 wherein said azithromycin core comprises an azithromycin-containing particle coated with a sustained release coating.

9. A pharmaceutical composition of claim 3 wherein said enteric coating is selected so that the rate of azithromycin ester formation R_e in wt %/day at temperature T in °

C. of said pharmaceutical composition is less than or equal to

1.8×

10⁸·

e^7070/(T+273), and

wherein T ranges from 20°

C. to 50°

C.

10. The pharmaceutical composition of claim 3 wherein said enteric coating is selected so that the rate of azithromycin ester formation R_e in wt %/day at temperature T in °

C. of said pharmaceutical composition is less than or equal to

3.6×

10⁷·

e<sup>−

7070/(T+273)</sup>, and

wherein T ranges from 20°

C. to 50°

C.

11. The pharmaceutical composition of claim 3 wherein said enteric coating is selected so that the rate of azithromycin ester formation R_e in wt %/day at temperature T in °

C. of said pharmaceutical composition is less than or equal to

1.8×

10⁷·

e<sup>−

7070/(T+273)</sup>, and

wherein T ranges from 20°

C. to 50°

C.

12. The pharmaceutical composition of claim 1 wherein said core comprises about 35 to about 55 wt % azithromycin;

about 40 to about 65 wt % of a carrier selected from the group consisting of waxes, glycerides, and mixtures thereof; and

about 0.1 to about 15 wt % of a dissolution enhancer.

13. The pharmaceutical composition of claim 12 wherein said core comprises about 45 to about 55 wt % azithromycin;

about 40 to about 55 wt % of a glyceride, and about 0.1 to about 5 wt % of a poloxamer.

14. The pharmaceutical composition of any of claims 1-4 wherein said multiparticulates further comprise a barrier coat located between said core and said enteric coating;

wherein said barrier coat is selected from the group consisting of long-chain alcohols, poloxamers, ethers, ether-substituted cellulosics, sugars, salts, and mixtures thereof.

15. The pharmaceutical composition of claim 20 wherein said enteric coating is a trimellitate-containing coating or a phthalate-containing coating selected from the group consisting of acid phthalates of carbohydrates, amylose acetate phthalate, cellulose acetate phthalate, cellulose ester phthalates, cellulose ether phthalates, hydroxypropylcellulose phthalate, hydroxypropylethylcellulose phthalate, hydroxypropylmethylcellulose phthalate, methylcellulose phthalate, polyvinyl acetate phthalate, polyvinyl acetate hydrogen phthalate, sodium cellulose acetate phthalate, starch acid phthalate, styrene-maleic acid dibutyl phthalate copolymer, styrene-maleic acid polyvinylacetate phthalate copolymer, cellulose acetate trimellitate, and mixtures thereof.