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公开(公告)号:DK0734249T3
公开(公告)日:1999-12-06
申请号:DK95937397
申请日:1995-10-17
Applicant: PATHOGENESIS CORP , CHILDREN S HOSPITAL AND REGION
Inventor: SMITH ARNOLD L , RAMSEY BONNIE W , MONTGOMERY ALAN B
IPC: A61K9/12 , A61K9/00 , A61K9/72 , A61K31/702 , A61K31/715 , A61P31/04 , A61K31/73
Abstract: An aminoglycoside formulation for delivery by aerosolization. The concentrated aminoglycoside formulation containing an efficacious amount of aminoglycoside able to inhibit 95-100% of susceptible bacteria. Aminoglycoside formulated in 5 ml solution of a quarter normal saline having pH between 5.5 and 6.5. The method for treatment of endobronchial infections by a formulation delivered as an aerosol having mass medium average diameter predominantly between 1 to 5 mu , produced by a jet or ultrasonic nebulizer.
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公开(公告)号:CA2242335A1
公开(公告)日:1998-05-22
申请号:CA2242335
申请日:1997-11-13
Applicant: PATHOGENESIS CORP
Inventor: VANDEVANTER DONALD R , MONTGOMERY ALAN B
IPC: A61K9/12 , A61K9/00 , A61K38/00 , A61K38/12 , A61P11/00 , A61P31/04 , C07K7/50 , C07K7/62 , C07K7/60
Abstract: An anti-Pseudomonas aeruginosa agent which is substantially pure biologically active colistin component, a mixture thereof or a pharmaceutically acceptable salt thereof delivered as an aerosol or dry powder formulation. The figure shows a general structure of a prodrug colimycin (Figure 1A) and a generic formula of a drug colistin and its components substituents (Figure 1B). A formulation and method for preparation of substantially pure biologically active colistin component, a mixture thereof or a pharmaceutically acceptable salt thereof. A method for treatment and prophylaxis of Pseudomonas aeruginosa, Stenotrophomonas maltophilia or other susceptible pulmonary bacterial infections.
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公开(公告)号:AU688166B2
公开(公告)日:1998-03-05
申请号:AU3952295
申请日:1995-10-17
Applicant: PATHOGENESIS CORP , CHILDRENS HOSP MEDICAL CENTER
Inventor: SMITH ARNOLD L , RAMSEY BONNIE W , MONTGOMERY ALAN B
IPC: A61K9/12 , A61K9/00 , A61K9/72 , A61K31/702 , A61K31/715 , A61P31/04 , A61K31/73
Abstract: An aminoglycoside formulation for delivery by aerosolization. The concentrated aminoglycoside formulation containing an efficacious amount of aminoglycoside able to inhibit 95-100% of susceptible bacteria. Aminoglycoside formulated in 5 ml solution of a quarter normal saline having pH between 5.5 and 6.5. The method for treatment of endobronchial infections by a formulation delivered as an aerosol having mass medium average diameter predominantly between 1 to 5 mu , produced by a jet or ultrasonic nebulizer.
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公开(公告)号:CA2179305A1
公开(公告)日:1996-05-02
申请号:CA2179305
申请日:1995-10-17
Applicant: PATHOGENESIS CORP , CHILDRENS HOSP MEDICAL CENTER
Inventor: SMITH ARNOLD L , RAMSEY BONNIE W , MONTGOMERY ALAN B
IPC: A61K9/12 , A61K9/00 , A61K9/72 , A61K31/702 , A61K31/715 , A61P31/04 , A61K31/73
Abstract: An aminoglycoside formulation for delivery by aerosolization. The concentrated aminoglycoside formulation containing an efficacious amount of aminoglycoside able to inhibit 95-100% of susceptible bacteria. Aminoglycoside formulated in 5 ml solution of a quarter normal saline having pH between 5.5 and 6.5. The method for treatment of endobronchial infections by a formulation delivered as an aerosol having mass medium average diameter predominantly between 1 to 5 mu , produced by a jet or ultrasonic nebulizer.
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