Coated drug delivery formulations

Abstract

The invention relates generally to methods of making formulations for delivering biological agents to a patient. In one aspect, proliposomal drug-delivery systems for medicaments are provided. In another aspect, coated proliposomal formulations for poorly water soluble drugs, and methods for making the same, are provided. Certain embodiments of the present invention provide enhanced stability and bioavailability for pharmaceutical formulations.

What is claimed is: 
     
         1 . A dosage form comprising:
 a proliposomal powder comprised of a dispersion of glyburide and phospholipid, and   an enteric coating.   
     
     
         2 . A dosage form of  claim 1 , further comprising a capsule and wherein the proliposomal powder is contained within the capsule. 
     
     
         3 . A dosage form of  claim 2 , wherein the capsule is coated with an enteric coating. 
     
     
         4 . A dosage form of  claim 1 , wherein the phospholipid is selected from the group consisting of one or more of the following: distearoyl phosphatidylcholine, dipalmitoyl phosphatidylcholine, dimyristoyl phosphatidylcholine, egg PC, soy PC, DMPG, DMPA, DPPG, DPPA, DSPG, DSPA, phosphatidylserine and sphigomyelin. 
     
     
         5 . A dosage form of  claim 4 , further comprising a surfactant. 
     
     
         6 . A dosage form of  claim 4 , wherein the enteric coating is at least one of, cellulose acetate phthalate, alginates, alkali-soluble acrylic resins, hydroxypropyl methylcellulose phthalate, methacrylate-methacrylic acid copolymers, polyvinyl acetate phthalate, styrol maleic acid copolymers, shellac, and cellulose acetate. 
     
     
         7 . A dosage form of  claim 4  wherein the phospholipid is distearoyl phosphatidylcholine. 
     
     
         8 . A dosage form of  claim 4  further comprising an additional ingredient selected from a carrier, a diluent, a lubricant and mixtures thereof. 
     
     
         9 . A dosage form of  claim 8 , further comprising a plasticizer selected from the group consisting of phthalate esters, citrate esters and triacetin. 
     
     
         10 . A dosage form of  claim 8 , wherein the additional ingredient is selected from at least one of microcrystalline cellulose, starch, lactose, talc, mannitol, polyethylene glycol, polyvinylpyrrolidone, hydroxypropylmethyl cellulose, ethyl cellulose, fatty acids, fatty acid salts, glyceryl behenate, dextrose, dicalcium phosphate. 
     
     
         11 . A dosage form of  claim 1 , wherein the dosage form is a tablet or capsule. 
     
     
         12 . A proliposomal powder comprised of a dispersion of glyburide and phospholipid. 
     
     
         13 . A proliposomal powder of  claim 12 , wherein the phospholipid is selected from the group consisting of one or more of the following: distearoyl phosphatidylcholine, dipalmitoyl phosphatidylcholine, dimyristoyl phosphatidylcholine, egg PC, soy PC, DMPG, DMPA, DPPG, DPPA, DSPG, DSPA, phosphatidylserine and sphigomyelin. 
     
     
         14 . A proliposomal powder of  claim 13 , further comprising a surfactant. 
     
     
         15 . A proliposomal powder of  claim 12  coated with an enteric coating selected from cellulose acetate phthalate, alginates, alkali-soluble acrylic resins, hydroxypropyl methylcellulose phthalate, methacrylate-methacrylic acid copolymers, polyvinyl acetate phthalate, styrol maleic acid copolymers, shellac, cellulose acetate, and mixtures thereof. 
     
     
         16 . A proliposomal powder of  claim 13 , wherein the phospholipid is distearoyl phosphatidylcholine. 
     
     
         17 . A method of treating a patient in need of glyburide comprising the step of:
 administering a dosage form of  claim 1 .   
     
     
         18 . A method of treating a patient in need of glyburide comprising the step of:
 administering a dosage form of  claim 4 .   
     
     
         19 . A method of making a proliposomal dispersion of glyburide and a phospholipid, comprising the steps of:
 dissolving glyburide and at least one phospholipid in a non-aqueous solvent without exposure to an aqueous phase to form a solution, and   removing the non-aqueous solvent to form a dry powder dispersion comprising the glyburide and at least one phospholipid.   
     
     
         20 . A method of  claim 19 , wherein the phospholipid is selected from the group consisting of one or more of the following: distearoyl phosphatidylcholine, dipalmitoyl phosphatidylcholine, dimyristoyl phosphatidylcholine, egg PC, soy PC, DMPG, DMPA, DPPG, DPPA, DSPG, DSPA, phosphatidylserine and sphigomyelin.