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Lovaplatin crystal, preparation method and drug application

机译:洛伐铂晶体,制备方法和药物应用

摘要

The present invention extends to new crystals A, B and F of lovaplatin and methods for their preparation and drug applications. Among them, the melting point of the donkey platin crystal A is Tm. p. = 220 ± 5 ° C., obtained by adding donkey platin trihydrate to the suspension crystal solvent, melting point of donkey platin B being Tm. p. = 230 ± 5 ° C., and obtained by drying the lobaplatin trihydrate through volatilization of the solvent, volatilizing at room temperature after adding the solvent into the lobaplatin dihydrate, or crystallization of the crystals. The melting point of Lovaplatin crystal form F is Tm. p. = 229 ± 5 ° C., stir until the solid is dissolved at room temperature through addition of methanol or ethanol into the donkey platin dihydrate, remove the insoluble matter, and slowly add the organic solvent, After the crystals are precipitated, the crystals are separated out and obtained after drying. Compared to the existing lovaplatin and lovaplatin trihydrate, these lovaplatin crystals A, B and F have better stability and solubility, and can be used for preparation, storage and use of various types of drug preparations Suitably, it can be used more often for the treatment of cancer diseases such as breast cancer, small cell lung cancer or chronic granulocytic leukemia. [Selection] Figure 2
机译:本发明扩展到新的洛伐铂晶体A,B和F及其制备和药物应用的方法。其中,驴铂晶体A的熔点为Tm。 p。 = 220±5℃,是通过将三水合铂铂加到悬浮晶体溶剂中而得到的,其中,白铂B的熔点为Tm。 p。 = 230±5℃,并且通过使溶剂挥发来干燥三水合铂铂,在将溶剂添加到二水合铂铂中之后在室温下挥发,或者使晶体结晶而获得。洛伐铂晶型F的熔点为Tm。 p。 = 229±5℃,搅拌直到在室温下通过向二水合铂铂中添加甲醇或乙醇使固体溶解,除去不溶物,并缓慢加入有机溶剂,使晶体沉淀后,将晶体分离出来,干燥后得到。与现有的洛伐铂和洛伐铂三水合物相比,这些洛伐铂晶体A,B和F具有更好的稳定性和溶解性,可用于制备,储存和使用各种类型的药物制剂。适当地,它可更常用于治疗癌症疾病,例如乳腺癌,小细胞肺癌或慢性粒细胞性白血病。 [选择]图2

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