Pharmaceutical compositions of amorphous dispersions of drugs and lipophilic microphase-forming materials

• US 9,486,410 B2
• Filed: 10/26/2007
• Issued: 11/08/2016
• Est. Priority Date: 02/01/2002
• Status: Active Grant

• Current Assignee: Lonza Bend Incorporated (Lonza Group AG)
• Original Assignee: Bend Research Inc. (Lonza Group AG)
• Inventors: Smithey, Dan Tod, Perlman, Michael E., Shanker, Ravi M., Babcock, Walter C., Friesen, Dwayne Thomas, Rabenstein, Mark D.
• Primary Examiner(s): Wax, Robert A
• Assistant Examiner(s): AL-AWADI, DANAH J
• Application Number:
  US11/924,988
• Publication Number:
  US 20080063708A1
• Time in Patent Office: 3,301 Days
• Field of Search: None
• US Class Current: 1/1
• CPC Class Codes: A61K 31/40 having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
• CPC Class Codes: A61K 31/44 Non condensed pyridines; Hydrogenated derivatives thereof
• CPC Class Codes: A61K 31/4706 4-Aminoquinolines; 8-Aminoquinolines, e.g. chloroquine, primaquine
• CPC Class Codes: A61K 31/496 Non-condensed piperazines containing further heterocyclic rings, e.g. rifampin, thiothixene or sparfloxacin
• CPC Class Codes: A61K 9/10 Dispersions; Emulsions A61K9/06 takes precedence; composition of dispersions, emulsions A61K47/00
• CPC Class Codes: A61K 9/145 with organic compounds
• CPC Class Codes: A61K 9/146 with organic macromolecular compounds
• CPC Class Codes: A61K 9/1617 Organic compounds, e.g. phospholipids, fats
• CPC Class Codes: A61K 9/1652 Polysaccharides, e.g. alginate, cellulose derivatives; Cyclodextrin homeopathic globules A61K9/1623
• CPC Class Codes: A61K 9/2013 Organic compounds, e.g. phospholipids, fats
• CPC Class Codes: A61K 9/2031 obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds, e.g. polyethylene glycol, polyethylene oxide, poloxamers
• CPC Class Codes: A61K 9/2054 Cellulose; Cellulose derivatives, e.g. hydroxypropyl methylcellulose
• CPC Class Codes: A61K 9/4858 Organic compounds
• CPC Class Codes: A61K 9/4866 Organic macromolecular compounds

Abstract

A pharmaceutical composition comprises a solid amorphous dispersion comprising a low-solubility drug and a concentration-enhancing polymer and a lipophilic microphase-forming material. Alternatively, a solid amorphous dispersion comprising a low-solubility drug and a concentration-enhancing polymer is co-administered with a lipophilic microphase-forming material to an in vivo use environment.

Claims

1. A composition, comprising:

(a) a first solid amorphous dispersion comprising a low-solubility drug and a concentration-enhancing polymer, wherein said low-solubility drug is dispersed in said concentration-enhancing polymer, wherein said concentration-enhancing polymer is selected from the group consisting of hydroxypropyl methyl cellulose acetate succinate, hydroxypropyl methyl cellulose phthalate, cellulose acetate phthalate, cellulose acetate trimellitate, carboxymethyl ethyl cellulose, hydroxypropyl methyl cellulose, poloxamers, polyvinylpyrrolidone, polyvinyl alcohols that have at least a portion of their repeat units in hydrolyzed-form, and mixtures thereof; and

(b) a second solid adsorbate blended with the first solid amorphous dispersion, the solid adsorbate comprising a water immiscible lipophilic microphase-forming material adsorbed onto a porous substrate, the water immiscible lipophilic microphase forming material comprising a mixture of a hydrophobic material selected from medium-chain glycerol mono-, di-, and tri-alkylates, sorbitan esters, sorbitan fatty acid esters, or a mixture thereof, and an amphiphilic material selected from polyoxyethylene sorbitan fatty acid esters, alpha tocopheryl polyethylene glycol 1000 succinate, or mixtures thereof, said lipophilic microphase-forming material being capable of forming a separate phase within an in vitro or in vivo aqueous use environment; and

wherein said composition has a mass ratio of said lipophilic microphase-forming material to said low solubility drug of from 0.1 to 100; and

wherein said lipophilic microphase-forming material is present in a sufficient amount so that said composition provides concentration enhancement of said drug in said aqueous use environment of at least 1.25-fold relative to both a first control composition and a second control composition, wherein (i) said first control composition consists essentially of an equivalent amount of said solid amorphous dispersion with no lipophilic microphase-forming a material present; and

(ii) said second control composition consists essentially of an equivalent amount of said low-solubility drug in undispersed form with an equivalent amount of said lipophilic, microphase-forming material but with no concentration-enhancing polymer.

2. The composition of claim 1 wherein said lipophilic microphase-forming material forms lipophilic microphases in said use environment having a characteristic diameter of less than 10 μ

m.

3. The composition of claim 1 wherein said low-solubility drug has a solubility in said use environment of less than 10 μ

g/ml.

4. The composition of claim 1 wherein said lipophilic microphase forming material is selected from the group consisting of mixtures of medium-chain glyceryl mono-, di-, and/or tri-alkylates and alpha tocopheryl polyethylene glycol 1000 succinate, and mixtures of polyoxyethylene sorbitan fatty acid esters and medium-chain glyceryl mono-, di-, and/or tri-alkylates.

5. The composition of claim 1 wherein said lipophilic, microphase-forming material is dispersed in a water soluble or water dispersible matrix.

6. The composition of claim 1 wherein said lipophilic, microphase-forming material comprises from 10 wt % to 80 wt % of the composition.

7. The composition of claim 1 wherein said drug is a cholesterol ester transfer protein inhibitor.

8. The composition of claim 1 where said mass ratio of said lipophilic microphase-forming material to said low solubility drug is at least 1.

9. The composition of claim 1 wherein said composition provides a dissolution area under the curve in a use environment for any 90-minute period between the time of introduction to the use environment and 270 minutes following introduction to the use environment that is at least 1.25-fold that provided by at least one of said first control composition and said second control composition.

10. The composition of claim 1 wherein said composition provides a fed/fasted relative bioavailability ratio of from 0.5 to 2.0.

11. The composition of claim 1 wherein said drug is selected from the group consisting of antihypertensives, antianxiety agents, anticlotting agents, anticonvulsants, blood glucose-lowering agents, decongestants, antihistamines, antitussives, antineoplastics, beta blockers, anti-inflammatories, antipsychotic agents, cognitive enhancers, anti-atherosclerotic agents, cholesterol-reducing agents, antiobesity agents, autoimmune disorder agents, anti-impotence agents, antibacterial and antifungal agents, hypnotic agents, anti-Parkinsonism agents, anti-Alzheimer'"'"'s disease agents, antibiotics, anti-depressants, and antiviral agents, glycogen phosphorylase inhibitors, and cholesterol ester transfer protein inhibitors.

12. A composition, comprising:

a first solid amorphous dispersion comprising a low-solubility drug dispersed in a concentration-enhancing polymer, the low-solubility drug having a solubility in an in vitro or in vivo aqueous use environment of less than 10 μ

g/ml, the low-solubility drug being selected from antihypertensives, antianxiety agents, anticlotting agents, anticonvulsants, blood glucose-lowering agents, decongestants, antihistamines, antitussives, antineoplastics, beta blockers, anti-inflammatories, antipsychotic agents, cognitive enhancers, anti-atherosclerotic agents, cholesterol-reducing agents, antiobesity agents, autoimmune disorder agents, anti-impotence agents, antibacterial and antifungal agents, hypnotic agents, anti-Parkinsonism agents, anti-Alzheimer'"'"'s disease agents, antibiotics, anti-depressants, antiviral agents, glycogen phosphorylase inhibitors, and cholesterol ester transfer protein inhibitors, the concentration-enhancing polymer being selected from the group consisting of hydroxypropyl methyl cellulose acetate succinate, hydroxypropyl methyl cellulose phthalate, cellulose acetate phthalate, cellulose acetate trimellitate, carboxymethyl ethyl cellulose, hydroxypropyl methyl cellulose, poloxamers, polyvinylpyrrolidone, polyvinyl alcohols that have at least a portion of their repeat units in hydrolyzed-form, and mixtures thereof; and

a second solid adsorbate comprising a water immiscible lipophilic microphase-forming material adsorbed onto a porous substrate, the water immiscible lipophilic microphase forming material comprising a mixture of a hydrophobic material and an amphiphilic material, the lipophilic microphase-forming material being capable of forming a separate phase within the in vitro or in vivo aqueous use environment, the composition having a mass ratio of the lipophilic microphase-forming material to the low solubility drug of from 0.1 to 100, the lipophilic microphase-forming material being present in an amount sufficient to provide concentration enhancement of the drug in the aqueous use environment of at least 1.25-fold relative to both a first control composition and a second control composition, wherein (i) the first control composition consists essentially of an equivalent amount of the solid amorphous dispersion with no lipophilic microphase-forming a material present, and (ii) the second control composition consists essentially of an equivalent amount of the low-solubility drug in undispersed form with an equivalent amount of the lipophilic, microphase-forming material but with no concentration-enhancing polymer.

13. A method, comprising:

forming a first solid amorphous dispersion comprising a low-solubility drug homogeneously dispersed in a concentration-enhancing polymer selected from the group consisting of hydroxypropyl methyl cellulose acetate succinate, hydroxypropyl methyl cellulose phthalate, cellulose acetate phthalate, cellulose acetate trimellitate, carboxymethyl ethyl cellulose, hydroxypropyl methyl cellulose, poloxamers, polyvinylpyrrolidone, polyvinyl alcohols that have at least a portion of their repeat units in hydrolyzed-form, and mixtures thereof;

forming a second solid adsorbate by adsorbing a water immiscible lipophilic microphase-forming material capable of forming a separate phase within an in vitro or in vivo aqueous use environment onto a porous substrate; and

forming a composition comprising the first solid amorphous dispersion and the second solid adsorbate, the composition having a mass ratio of the lipophilic microphase-forming material to the low solubility drug of from 0.1 to 100, the lipophilic microphase-forming material being present in a sufficient amount so that the composition provides concentration enhancement of the drug in the aqueous use environment of at least 1.25-fold relative to both a first control composition and a second control composition, wherein (i) the first control composition consists essentially of an equivalent amount of the solid amorphous dispersion with no lipophilic microphase-forming a material present; and

(ii) the second control composition consists essentially of an equivalent amount of the low-solubility drug in undispersed form with an equivalent amount of the lipophilic, microphase-forming material but with no concentration-enhancing polymer.

14. The method according to claim 13 where the first solid amorphous dispersion comprising a low-solubility drug homogeneously dispersed in a concentration-enhancing polymer is formed by spray drying.