Self-Preserved Aqueous Pharmaceutical Compositions
    4.
    发明申请
    Self-Preserved Aqueous Pharmaceutical Compositions 有权
    自保水性药物组合物

    公开(公告)号:US20110195132A1

    公开(公告)日:2011-08-11

    申请号:US13086950

    申请日:2011-04-14

    IPC分类号: A61K33/30 A61P27/02 A61P31/00

    摘要: The present invention is directed to the provision of multi-dose, self-preserved ophthalmic compositions. The compositions possess sufficient antimicrobial activity to satisfy USP preservative efficacy requirements, as well as similar preservative standards (e.g., EP and JP), without requiring the presence of conventional anti-microbial preservative agents, such as benzalkonium chloride. The compositions are effectively preserved by a balanced ionic buffer system containing zinc ions at a concentration of 0.04 to 0.9 mM, preferably 0.04 to 0.4 mM. One aspect of the balanced buffer system is limitation of the amount of buffering anions present to a concentration of 15 mM or less, preferably 5 mM or less. In a preferred embodiment, the compositions also contain borate or, most preferably, one or more borate/polyol complexes. The use of propylene glycol as the polyol in such complexes is strongly preferred. Limiting the amount of divalent metals other than zinc and the amount of ionized salts present has also been determined to be important to maximize the antimicrobial activity of the balanced buffer systems.

    摘要翻译: 本发明涉及提供多剂量,自我保存的眼用组合物。 组合物具有足够的抗微生物活性以满足USP防腐功效要求,以及类似的防腐标准品(例如EP和JP),而不需要存在常规的抗微生物防腐剂,例如苯扎氯铵。 通过含有浓度为0.04至0.9mM,优选0.04至0.4mM的锌离子的平衡离子缓冲系统有效地保护了组合物。 平衡缓冲系统的一个方面是存在的缓冲剂阴离子的量的限制为15mM或更低,优选5mM或更低的浓度。 在优选的实施方案中,组合物还含有硼酸盐或最优选一种或多种硼酸盐/多元醇络合物。 在这种络合物中使用丙二醇作为多元醇是非常优选的。 限制锌以外的二价金属的量和存在的离子盐的量也被确定为使平衡缓冲体系的抗菌活性最大化是重要的。

    Self-preserved aqueous pharmaceutical compositions
    6.
    发明授权
    Self-preserved aqueous pharmaceutical compositions 有权
    自我保护的水性药物组合物

    公开(公告)号:US08323630B2

    公开(公告)日:2012-12-04

    申请号:US13086950

    申请日:2011-04-14

    摘要: The present invention is directed to the provision of multi-dose, self-preserved ophthalmic compositions. The compositions possess sufficient antimicrobial activity to satisfy USP preservative efficacy requirements, as well as similar preservative standards (e.g., EP and JP), without requiring the presence of conventional anti-microbial preservative agents, such as benzalkonium chloride. The compositions are effectively preserved by a balanced ionic buffer system containing zinc ions at a concentration of 0.04 to 0.9 mM, preferably 0.04 to 0.4 mM. One aspect of the balanced buffer system is limitation of the amount of buffering anions present to a concentration of 15 mM or less, preferably 5 mM or less. In a preferred embodiment, the compositions also contain borate or, most preferably, one or more borate/polyol complexes. The use of propylene glycol as the polyol in such complexes is strongly preferred. Limiting the amount of divalent metals other than zinc and the amount of ionized salts present has also been determined to be important to maximize the antimicrobial activity of the balanced buffer systems.

    摘要翻译: 本发明涉及提供多剂量,自我保存的眼用组合物。 组合物具有足够的抗微生物活性以满足USP防腐功效要求,以及类似的防腐标准品(例如EP和JP),而不需要存在常规的抗微生物防腐剂,例如苯扎氯铵。 通过含有浓度为0.04至0.9mM,优选0.04至0.4mM的锌离子的平衡离子缓冲系统有效地保护了组合物。 平衡缓冲系统的一个方面是存在的缓冲剂阴离子的量的限制为15mM或更低,优选5mM或更低的浓度。 在优选的实施方案中,组合物还含有硼酸盐或最优选一种或多种硼酸盐/多元醇络合物。 在这种络合物中使用丙二醇作为多元醇是非常优选的。 限制锌以外的二价金属的量和存在的离子盐的量也被确定为使平衡缓冲体系的抗菌活性最大化是重要的。

    PHARMACEUTICAL COMPOSITION WITH ENHANCED SOLUBILITY CHARACTERISTICS
    10.
    发明申请
    PHARMACEUTICAL COMPOSITION WITH ENHANCED SOLUBILITY CHARACTERISTICS 审中-公开
    具有增强溶解性特征的药物组合物

    公开(公告)号:US20120022149A1

    公开(公告)日:2012-01-26

    申请号:US13186516

    申请日:2011-07-20

    IPC分类号: A61K31/335 A61P27/02

    摘要: There are disclosed pharmaceutical compositions, particularly ophthalmic compositions, that contain relatively high concentrations of solubility enhancing polymer (e.g., polyether polymer, polyvinyl polymer or a combination thereof) for providing enhanced solubility of one or more therapeutic agents. In a preferred embodiment, the composition is a multi-dose topical aqueous ophthalmic composition that contains relatively high concentrations of solubility enhancing polymer (e.g., polyether polymer, polyvinyl polymer or a combination thereof) for providing enhanced solubility of one or more therapeutic agents.

    摘要翻译: 公开了用于提供一种或多种治疗剂的增强的溶解度的药物组合物,特别是眼用组合物,其含有相对高浓度的增溶溶解性聚合物(例如,聚醚聚合物,聚乙烯基聚合物或其组合)。 在优选的实施方案中,组合物是含有相对高浓度的溶解性增强聚合物(例如,聚醚聚合物,聚乙烯基聚合物或其组合)的多剂量局部水性眼用组合物,用于提供一种或多种治疗剂的增强的溶解度。