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publicationDate 2005-12-22-04:00^^<http://www.w3.org/2001/XMLSchema#date>
publicationNumber PE-20050960-A1
titleOfInvention PANTOPRAZOLE MULTIPARTICLE FORMULATIONS
abstract REFERS TO A FORMULATION OF STABLE MULTIPARTICLES OF PANTOPRAZOLE SODIUM CHARACTERIZED BY HAVING A REDUCED RELEASE UNDER GASTRIC CONDITIONS AND RAPID RELEASE TO NEUTRAL PH, EACH MULTIPATICLE IS UNDERSTOOD AT LEAST A SODIUM PANTOPRAZOLE PROVIDED IN 5 SODIUM ESOPLE BY: 50% P / P, AND A SURFACTANT SUCH AS POLYSORBATE 80, IN ADDITION SUCH A NUCLEUS MAY CONTAIN A DISINTEGRANT, A pH REGULATOR AND HYPROMELLOSE; b) AN ENTERIC LAYER IN THE NUCLEUS CONSTITUTED BY A COPOLYMER OF METHACRYLIC ACID AND METHACRYLATES IN A RANGE OF 15 TO 45% P / P OF THE MULTIPARTICLES, SUCH MICROPARTICLES HAVE AN AVERAGE SIZE OF 1mm IN DIAMETER, AND ALSO UNDERTAKE INITIAL SEALING IN THE NUCLEUS AND A FINAL SEALING IN THE FINAL ENTERIC LAYER CONSTITUTED BY HYDROXYPROPYLMETILCELLULOSE (HYPROMELLOSE) AND WATER. IT ALSO REFERS TO A PRODUCTION METHOD OF SUCH FORMULATION. THIS FORMULATION IS LESS PRONE TO ADHERENCE TO THE INTESTINAL WALLS SO IT ALLOWS AN APPROPRIATE ADMINISTRATION OF THE DRUG THROUGH NASOGASTRIC TUBES AND GASTROSTOMY
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