利索-全球专利检索

  1. 登录
  2. 注册

搜索结果

5 条记录 (耗时 0.014 秒)

    NEW CRYSTALLINE FORM OF CEFAMANDOLE SODIUM COMPOUND, FORMULATION AND PREPARATION METHOD THEREOF
    2.
    发明申请
    NEW CRYSTALLINE FORM OF CEFAMANDOLE SODIUM COMPOUND, FORMULATION AND PREPARATION METHOD THEREOF 审中-公开
    CEFAMANDOLE SODIUM化合物的新型结晶形式，其制备方法及其制备方法

    公开(公告)号：US20170050982A1

    公开(公告)日：2017-02-23

    申请号：US15305661

    申请日：2015-11-20

    申请人： TIANJIN UNIVERSITY ,  HAINAN LINGKANG PHARMACEUTICAL CO., LTD

    发明人： Hongxun HAO ,  Linggang TAO ,  Fang He ,  Baohong HOU ,  Jingkang WANG ,  Jun LV ,  Qiuxiang YIN ,  Yongli WANG ,  Junbo GONG ,  Chuang XIE ,  Ying Bao

    IPC分类号： C07D501/36 ,  C07D501/12

    CPC分类号： C07D501/36 ,  C07B2200/13 ,  C07D501/12

    摘要： A novel crystalline form is defined by diffraction angle 2θ° of X-ray powder diffraction pattern and characteristic peak of differential scanning calorimetry (DSC). The novel crystalline form of Cefamandole Nafate is prepared as follows: adding Cefamandole Nafate in solid state to an organic solvent to form a suspension with a concentration of 0.04˜0.3 g/ml, stirring the suspension at 40˜50° C. for a period of time, and then cooling to 5˜15° C. at certain cooling rate, continuing to stir for a period of time, then suction filtrating the obtained suspension, the resulting filer cake is Cefamandole Nafate as wet product, which is dried to constant weight to provide the novel crystalline form of Cefamandole Nafate as final product.

    摘要翻译： 新型结晶形式由X射线粉末衍射图的衍射角2θ°和差示扫描量热法（DSC）的特征峰定义。 头孢丹多奈非糖酸盐的新型结晶形式如下制备：将固体状态的头孢马替奈啡钠加入到有机溶剂中，形成浓度为0.04〜0.3g / ml的悬浮液，在40〜50℃下搅拌悬浮液一段时间 的时间，然后以一定的冷却速度冷却至5〜15℃，继续搅拌一段时间，然后抽滤所得悬浮液，得到的滤饼为头孢丹多，作为湿产品干燥至恒定 重量，以提供新颖的头孢曼陀螺Nafate的结晶形式作为最终产品。

    NEW CRYSTAL FORM OF CEFATHIAMIDINE COMPOUND AND PREPARATION METHOD THEREFOR
    3.
    发明申请
    NEW CRYSTAL FORM OF CEFATHIAMIDINE COMPOUND AND PREPARATION METHOD THEREFOR 有权
    新戊酰胺化合物的新晶体形式及其制备方法

    公开(公告)号：US20170044184A1

    公开(公告)日：2017-02-16

    申请号：US15304824

    申请日：2015-11-20

    申请人： TIANJIN UNIVERSITY ,  HAINAN LINGKANG PHARMACEUTICAL CO., LTD

    发明人： Hongxun HAO ,  Linggang TAO ,  Zhihong SUN ,  Baohong HOU ,  Jun LV ,  Qiuxiang YIN ,  Yongli WANG ,  Junbo GONG ,  Chuang XIE ,  Ying BAO

    IPC分类号： C07D501/60

    CPC分类号： C07D501/60 ,  C07B2200/13 ,  C07D501/12 ,  C07D501/28

    摘要： A novel crystalline form of Cefathiamidine compound and its preparation method, characterizing in its X-ray powder diffraction pattern and differential scanning calorimetry thermogram. Dissolving Cefathiamidine compound with a purity of 98% or higher in a solvent at a temperature of 30˜45° C. to form a solution, whose concentration is controlled within 0.05˜0.2 g/mL, and then adding a solventing-out agent to the solution, wherein the amount of the solventing-out agent is 3˜5 times (in volume) of that of the solvent; followed by cooling the solution down to 0˜10° C. at a rate of 0.2˜1° C./min; continuing to stir for 1˜3 hours, and separating the obtained solid-liquid suspension to provide a novel crystalline form of Cefathiamidine compound after drying.

    摘要翻译： 尖晶石化合物的新型结晶形式及其制备方法，其X射线粉末衍射图和差示扫描量热法热分析图表征。 在溶剂中在30〜45℃的温度下溶解纯度为98％以上的头孢硫脒化合物，形成浓度为0.05〜0.2g / mL的溶液，然后加入溶剂 溶剂，其中溶剂量为溶剂量的3〜5倍（体积）; 然后以0.2〜1℃/分钟的速度将溶液冷却至0〜10℃; 继续搅拌1〜3小时，分离得到的固液悬浮液，干燥后提供新型的头孢噻肟化合物结晶形式。

    METHODS FOR PREDICTING CRITICAL CAKING CYCLE OF CRYSTAL PARTICLE
    4.
    发明公开
    METHODS FOR PREDICTING CRITICAL CAKING CYCLE OF CRYSTAL PARTICLE 审中-公开

    公开(公告)号：US20240344954A1

    公开(公告)日：2024-10-17

    申请号：US18657771

    申请日：2024-05-07

    申请人： TIANJIN UNIVERSITY ,  ZHEJIANG HUAKANG PHARMACEUTICAL CO., LTD. ,  ZHEJIANG INSTITUTE OF TIANJIN UNIVERSITY (SHAOXING)

    发明人： Junbo GONG ,  Mian LI ,  Mingyang CHEN ,  Wulong YANG ,  Jiahui LI ,  Mingxuan LI ,  Qiang WU ,  Baohong HOU ,  Qiuxiang YIN

    IPC分类号： G01N15/06

    CPC分类号： G01N15/06

    摘要： The present disclosure provides a technology field of caking of crystal particles, and in particular relates to a method for predicting a critical caking cycle of crystal particle. The method includes: establishing a CHS crystal bridge growth model database of a crystal particle with a same type of crystal particle to be predicted firstly, selecting existed data in the corresponding CHS crystal bridge growth model database based on an equivalent particle radius, a stored ambient temperature, and an environmental high and low humidity cycle condition of the crystal particle to be predicted, respectively, and calculating the critical caking cycle according to experience calculation equations, wherein a result obtained by calculation is a predicted critical caking cycle of the crystal particle to be predicted. The present disclosure has characteristics of time-saving, convenience, good universality, and high prediction accuracy, which can quickly predict the critical caking cycle of multi-particle crystal particle products under different humidity storage conditions within a week, resulting in greatly reducing time costs and providing guidance for storage of industrial crystal particle products.