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    • 46. 发明公开
    • A method for producing calcium hydroxyapatite nano-crystals of the desired morphology
    • 葛兰素ter ium ium ium ium ium ium ium ie ie ie ie ie ie ie ie ie ie ie ie ie ie ie
    • EP2810917A1
    • 2014-12-10
    • EP14162300.9
    • 2014-03-28
    • UAB Moksliniu Tyrimu Pletros Laboratorija
    • KAREIVA, Aivaras
    • C01B25/32
    • C01B25/324A61K8/025A61K8/0254A61K8/027A61K8/24A61K2800/413A61L27/12A61L2400/12A61L2430/02A61Q11/00C01P2004/10C01P2004/20C01P2004/32C01P2004/61C01P2004/62C01P2004/64
    • The proposed invention is intended to chemical compounds characterised by a porous structure, specifically, to producing calcium hydroxyapatite nano-crystals of the desired morphology intended for the treatment of skeletal disorders.
      The goal of the proposed invention is to obtain calcium hydroxyapatite nano-crystals of the desired morphology and size.
      The goal is achieved by preparing two solutions in the proposed method:
      a) 2.5-5.0wt% of calcium acetate and 1.2-2.4wt% of diammonium hydrogen tetroxo-phosphate is separately dissolved in 80-120 ml of distilled water and stir them at a temperature of 25-65 °C; b) 1.15-2.25wt% of tartaric acid (TA) is dissolved in 90-100 ml of distilled water, and 4.4-8.8wt% of ethylenediaminetetraacetic acid (EDTA), 5.85-11.7wt% of 1,2- diaminocyclohexane-tetra-acetate (DCTA) is dissolved in 100 ml of water and 22 ml of 10% ammonia water solution, and stirred, pouring the solution b) into solution a), stirring for 15-20 hours at 65-75 °C, drying the obtained gel for 20-24 hours at 100 °C and, after it is grounded additionally heating for 5 hours at 900-1200 °C. By changing the molar ratios of the complex-forming reagents (DCTA, EDTA, and TA), it is possible to change the surface morphology of calcium hydroxyapatite.
    • 所提出的发明旨在以特征在于多孔结构的化合物,具体地说,涉及产生用于治疗骨骼疾病的所需形态的羟基磷灰石纳米晶体。 所提出的发明的目的是获得所需形态和尺寸的羟基磷灰石纳米晶体。 目标是通过在所提出的方法中制备两种方案来实现:a)将2.5-5.0重量%的乙酸钙和1.2-2.4重量%的四氢四铵磷酸盐分别溶解在80-120毫升的蒸馏水中,并将其搅拌 温度25-65℃; b)将1.15-2.25重量%的酒石酸(TA)溶于90-100ml蒸馏水中,加入4.4-8.8wt%乙二胺四乙酸(EDTA),5.85-11.7wt%1,2-二氨基环己烷四 乙酸乙酯(DCTA)溶解于100ml水和22ml 10%氨水溶液中,搅拌,将溶液b)倒入溶液a)中,在65-75℃下搅拌15-20小时,干燥 在100℃下获得凝胶20-24小时,并且在900-1200℃下另外加热5小时后再接地。 通过改变络合物形成试剂(DCTA,EDTA和TA)的摩尔比,可以改变钙羟基磷灰石的表面形态。