首页> 外国专利> Method for obtaining conjugate of paclitaxel, trastuzumab and dendrimer PAMAM of 4th generation that has 64 amino groups on its surface and application of paclitaxel, trastuzumab and dendrimer PAMAM of 4th generation that has 64 amino groups on its surface for production of a drug intended for therapy of breast cancer

Method for obtaining conjugate of paclitaxel, trastuzumab and dendrimer PAMAM of 4th generation that has 64 amino groups on its surface and application of paclitaxel, trastuzumab and dendrimer PAMAM of 4th generation that has 64 amino groups on its surface for production of a drug intended for therapy of breast cancer

机译:获得表面具有64个氨基的第四代紫杉醇,曲妥珠单抗和树枝状聚合物PAMAM的结合物的方法和表面具有64个氨基的第四代紫杉醇,曲妥珠单抗和树枝状聚合物PAMAM的应用以生产用于治疗的药物乳腺癌

摘要

the object of the application is the way to receive trastuzumab and paclitaxel conjugate, dendrymeru pamam generation 4 having surface amino groups and the use of paclitaxel 64,trastuzumab and dendrymeru pamam generation 4 having surface amino groups to produce 64 your medicine for therapy of breast cancer.process to obtain a conjugate of paclitaxel and trastuzumab, dendrymeru pamam generation 4 having amino group on the surface 64, is thatin the first stage of succinic acid molecules undergo modification of hydroxyl groups of paclitaxel.next, in the presence of edc (ethyl n - (3-dimethylamino) propyl - n '- etylokarbodiimidu) is formed between the surface dendrymeru binding amide linkages, with the previously modified substrate.the reaction results in dmso at room temperature.in the later stage of reaction, in order to connect to dendrymeru trastuzumab pamam uses adapter molecule n - sukcynoimidylo - 4 - (nmaleimidometylo) cykloheksylokarboksylan - (smcc) holding onits end functional group forming reaction with both tiolami and amines.in addition to the surface dendrymeru is tiolową - sh group, using trauta reagent (ethyl 2 - iminotiolanu).the modified dendrymerów pamam accompanied by monoclonal antibody previously sprzęgnięte hyphenated smcc.
机译:本申请的目的是接受曲妥珠单抗和紫杉醇共轭物,具有表面氨基的第4代登德里莫鲁pamam的方法,以及使用具有表面氨基的紫杉醇64,曲妥珠单抗和第4代dendrymeru pamam产生第64种乳腺癌药物获得紫杉醇和曲妥珠单抗的缀合物的方法,即在表面64上具有氨基的dendrymeru pamam第4代,是在琥珀酸分子的第一阶段中,在edc(乙基n -(3-二甲基氨基)丙基-n'-乙炔基二酰胺基)与表面改性的底物之间形成酰胺,并与之前修饰的底物形成反应。在室温下,该反应在dmso中进行。 dendrymeru trastuzumab pamam使用衔接子分子n-sukcynoimidylo-4-(nmaleimidometylo)cykloheksylokarboksylan-(smcc)保持其末端功能正常除表面dendrymeru外,还使用trauta试剂(乙基2-亚氨基tiolanu)将tiolową-sh基团与基团形成反应。

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