CONTROLLED RELEASE BUPROPION FORMULATION
    1.
    发明公开
    CONTROLLED RELEASE BUPROPION FORMULATION 有权
    安非他酮控释制剂

    公开(公告)号:EP1162951A1

    公开(公告)日:2001-12-19

    申请号:EP00908780.0

    申请日:2000-02-24

    IPC分类号: A61K9/14 A61K9/52 A61K9/58

    摘要: A controlled release dosage form of bupropion hydrochloride which comprises: (a) a first pellet having a core of bupropion hydrochloride and hydroxypropyl methylcellulose at a weight ratio of 10:1 to 30:1 and a coating of a mixture of an acrylic resin which is soluble in acidic media and ethyl cellulose; (b) a second pellet having a core of bupropion hydrochloride and hydroxypropyl methylcellulose at a ratio of 10:1 to 30:1; an inner coating of a mixture of an acrylic resin which is soluble in acidic media and a water insoluble polymer and an outer coating which comprises an enteric coating polymer.

    CONTROLLED RELEASE FORMULATION FOR WATER SOLUBLE DRUGS
    2.
    发明公开
    CONTROLLED RELEASE FORMULATION FOR WATER SOLUBLE DRUGS 审中-公开
    控释制剂水溶性药物

    公开(公告)号:EP1124543A1

    公开(公告)日:2001-08-22

    申请号:EP99957493.2

    申请日:1999-11-01

    IPC分类号: A61K9/58 A61K9/60 A61K9/62

    摘要: A once-a-day controlled release diltiazem formulation comprises: (a) 20-50 wt.% of enteric polymeric membrane coated pellets comprising a polymer membrane coated core which comprises a biologically inert core which is coated with a first layer consisting essentially of diltiazem and polymeric binder; and a second layer which comprises a membrane comprising a pH dependent polymeric material; and (b) 50-80 wt.% of delayed pulse polymeric membrane coated pellets comprising a polymeric membrane coated core comprising a biologically inert core which is coated with a first layer which consists essentially of diltaziem and a polymeric binder and a second layer which comprises a polymeric membrane and a akaline a alkaline earth metal stearate which will substantially maintain its integrity in the varying pH conditions of the gastrointestinal tract but is permeable to diltiazem, and (c) a unit dose containment system.

    CONTROLLED RELEASE FORMULATION FOR WATER SOLUBLE DRUGS IN WHICH A PASSAGEWAY IS FORMED IN SITU
    5.
    发明公开
    CONTROLLED RELEASE FORMULATION FOR WATER SOLUBLE DRUGS IN WHICH A PASSAGEWAY IS FORMED IN SITU 失效
    FORWASSERLÖSLISCHE原料药控释制剂原位出口开口冷弯

    公开(公告)号:EP0822809A1

    公开(公告)日:1998-02-11

    申请号:EP96908796.0

    申请日:1996-03-13

    IPC分类号: A61K9 A61K31

    摘要: A controlled release pharmaceutical tablet is disclosed which is based on: (a) a compressed core which contains: i) a medicament; ii) from 5 to 20 % by weight of a water soluble osmotic agent based on the total weight of the compressed core; iii) a water soluble pharmaceutically acceptable polymeric binder; iv) a conventional pharmaceutical excipient; and (b) a dual layer membrane coating around said core which consists essentially of: i) a first inner coating layer for sustained release of the medicament, said inner coating layer consisting essentially of a plasticized water insoluble pharmaceutically acceptable polymer and a pharmaceutically acceptable water soluble polymer, and; ii) a second outer coating layer for immediate release of a medicament, said outer coating layer consisting essentially of an effective amount of a medicament and a water soluble polymer. The controlled release formulation is suitable for the once-a-day administration of medicaments.

    CONTROLLED RELEASE FORMULATION FOR WATER SOLUBLE DRUGS IN WHICH A PASSAGEWAY IS FORMED IN SITU
    6.
    发明授权
    CONTROLLED RELEASE FORMULATION FOR WATER SOLUBLE DRUGS IN WHICH A PASSAGEWAY IS FORMED IN SITU 失效
    FORWASSERLÖSLISCHE原料药控释制剂原位出口开口冷弯

    公开(公告)号:EP0822809B1

    公开(公告)日:2006-06-07

    申请号:EP96908796.4

    申请日:1996-03-13

    IPC分类号: A61K9/22 A61K9/36

    摘要: A controlled release pharmaceutical tablet is disclosed which is based on: (a) a compressed core which contains: i) a medicament; ii) from 5 to 20 % by weight of a water soluble osmotic agent based on the total weight of the compressed core; iii) a water soluble pharmaceutically acceptable polymeric binder; iv) a conventional pharmaceutical excipient; and (b) a dual layer membrane coating around said core which consists essentially of: i) a first inner coating layer for sustained release of the medicament, said inner coating layer consisting essentially of a plasticized water insoluble pharmaceutically acceptable polymer and a pharmaceutically acceptable water soluble polymer, and; ii) a second outer coating layer for immediate release of a medicament, said outer coating layer consisting essentially of an effective amount of a medicament and a water soluble polymer. The controlled release formulation is suitable for the once-a-day administration of medicaments.

    CONTROLLED RELEASE FORMULATION HAVING A PREFORMED PASSAGEWAY
    7.
    发明授权
    CONTROLLED RELEASE FORMULATION HAVING A PREFORMED PASSAGEWAY 失效
    与控释开口预制配方

    公开(公告)号:EP0835102B1

    公开(公告)日:2005-01-19

    申请号:EP96918078.5

    申请日:1996-06-05

    IPC分类号: A61K9/36

    CPC分类号: A61K9/0004

    摘要: A controlled release pharmaceutical tablet having at least one passageway, said tablet having: (a) a compressed core which comprises: (i) a medicament; (ii) an amount of a water soluble osmotic agent which is effective to cause the medicament to be delivered from said passageway in the presence of aqueous media; (iii) a water-swellable pharmaceutically acceptable polymer; and (b) a membrane coating around said core tablet which comprises a water insoluble pharmaceutically acceptable polymer.

    DILTIAZEM CONTROLLED RELEASE FORMULATION
    8.
    发明授权
    DILTIAZEM CONTROLLED RELEASE FORMULATION 失效
    地尔硫制剂具有控释

    公开(公告)号:EP0814780B1

    公开(公告)日:2003-10-01

    申请号:EP96910439.7

    申请日:1996-03-13

    发明人: CHEN, Chih-Ming

    摘要: A once-a-day controlled release diltiazem formulation is described which includes: (a) from 20 to 50 % by weight of enteric polymeric membrane coated pellets comprising a polymer membrane coated core which comprises a biologically inert core which is coated with a first layer which consists essentially of diltiazem and a polymeric binder; and a second layer which comprises a membrane comprising a pH dependent polymeric material; and (b) from 50 % to 80 % by weight of delayed pulse polymeric membrane coated pellets comprising a polymeric membrane coated core which comprises a biologically inert core which is coated with a first layer which consists essentially of diltiazem and a polymeric binder and a second layer which comprises a polymeric membrane which will substantially maintain its integrity in the varying pH conditions of the gastrointestinal tract but is permeable to diltiazem; and (c) a unit dose containment system.