PAIN REDUCING PARENTERAL LIPOSOME FORMULATION
    1.
    发明公开
    PAIN REDUCING PARENTERAL LIPOSOME FORMULATION 失效
    肠外脂质体配方缓解疼痛

    公开(公告)号:EP0975330A1

    公开(公告)日:2000-02-02

    申请号:EP98903718.9

    申请日:1998-01-26

    CPC classification number: A61K31/7048 A61K9/127

    Abstract: Disclosed is an invention directed towards pain-reducing parenteral formulations comprising a macrolide drug entrapped in a liposome vesicle. The macrolide drug is selected from the group consisting of derivatives of erythromycins A, B, C and D; clarithromycin; azithromycin; dirithromycin; josamycin; midecamycin; kitasamycin; roxithromycin; rokitamycin; oleandomycin; miocamycin; flurithromycin; rosaramicin; 8,9-anhydro-4''-deoxy-3'-N-desmethyl-3'-N-ethylerythromycin B 6,9-hemiacetal; 8,9-anhydro-4''-deoxy-3'-N-desmethyl-3'-N-ethylerythromycin A 6,9-hemiacetal; and 11-amino-11-deoxy-3-oxo-5-O-desosaminyl-6-O-[1'-3'-quinolyl-2'-propenyl]-erythronolide A 11,12-cyclic carbamate. The formulations of the invention are effective in substantially reducing the pain at the injection site typically associated with the injection of macrolide antibiotics.

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