Pharmaceutical composition containing 6-dimethylaminomethyl-1-(3-methoxyphenyl)-cyclohexane-1,3-diol with delayed active ingredient release
    32.
    发明申请
    Pharmaceutical composition containing 6-dimethylaminomethyl-1-(3-methoxyphenyl)-cyclohexane-1,3-diol with delayed active ingredient release 审中-公开
    含有6-二甲基氨基甲基-1-(3-甲氧基苯基) - 环己烷-1,3-二醇的药物组合物,具有延迟的活性成分释放

    公开(公告)号:US20060121113A1

    公开(公告)日:2006-06-08

    申请号:US11334344

    申请日:2006-01-19

    IPC分类号: A61K31/137 A61K9/22

    CPC分类号: A61K9/2054

    摘要: Pharmaceutical compositions with delayed release which contains 6-dimethylaminomethyl-1-(3-methoxyphenyl)-cyclohexane-1,3-diol or a pharmaceutically acceptable salt thereof in a matrix with delayed active ingredient release, wherein the matrix contains 1 to 80 wt. % of one or more hydrophilic or hydrophobic polymers as pharmaceutically acceptable matrix formers and exhibits the following in vitro release rate: 3-35 wt. % (relative to 100 wt. % of active ingredient) of 6-dimethylaminomethyl-1-(3-methoxyphenyl)-cyclohexane-1,3-diol released after 0.5 hours, 5-50 wt. % after 1 hour, 10-75 wt. % after 2 hours, 15-82 wt. % after 3 hours, 30-97 wt. % after 6 hours, more than 50 wt. % after 12 hours, more than 70 wt. % after 18 hours, and more than 80 wt. % after 24 hours.

    摘要翻译: 在具有延迟活性成分释放的基质中含有6-二甲基氨基甲基-1-(3-甲氧基苯基) - 环己烷-1,3-二醇或其药学上可接受的盐的具有延迟释放的药物组合物,其中所述基质含有1至80wt。 %的一种或多种亲水或疏水聚合物作为药学上可接受的基质形成剂并且具有以下体外释放速率:3-35wt。 0.5小时后释放的6-二甲基氨基甲基-1-(3-甲氧基苯基) - 环己烷-1,3-二醇的%(相对于100重量%的活性成分)为5-50重量% 1小时后,10-75重量% 2小时后,15-82重量% 3小时后,30-97重量% 6小时后,超过50重量% 12小时后,超过70重量% 18小时后,超过80重量% 24小时后。

    Abuse-safeguarded dosage form
    33.
    发明申请
    Abuse-safeguarded dosage form 审中-公开
    滥用安全剂型

    公开(公告)号:US20050214223A1

    公开(公告)日:2005-09-29

    申请号:US11113118

    申请日:2005-04-25

    摘要: A pharmaceutical dosage form that is safeguarded against abuse containing at least one active substance that is susceptible to abuse and at least two of the following constituents (a) through (d): (a) at least one substance that irritates the nasal and/or pharyngeal region; (b) at least one viscosity increasing agent that together with a required minimum quantity of an aqueous liquid forms a gel in an extract obtained from the dosage form, which gel can still be discerned after being introduced into an additional quantity of aqueous liquid; (c) at least one antagonist for the at least one active substance that is susceptible to abuse; and (d) at least one emetic.

    摘要翻译: 防止滥用的药物剂型,其含有至少一种易于滥用的活性物质和至少两种以下成分(a)至(d):(a)至少一种刺激鼻和/或 咽部区域 (b)至少一种增粘剂,其与所需最小量的水性液体一起在从剂型获得的提取物中形成凝胶,该凝胶在引入额外量的含水液体之后仍然可以被辨别出来; (c)至少一种易受滥用的活性物质的拮抗剂; 和(d)至少一种催吐剂。