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Process for obtenu00c7u00e7o complexes with derivatives of cyclodextrins inclusu00e7o of benznidazole

机译:含苯并硝唑环糊精衍生物的络合物的制备方法

摘要

Process for obtenu00c7u00e7o complexes of inclusu00e7o of benznidazole with derivatives of cyclodextrins.The present invention patent is objective in the process of obtaining complex inclusion of benznidazole (BNZ) (n - benzyl - 2 - (2 - nitroimidazol - 1 - (II) acetamide) and 225 - cyclodextrin (- CD 225) and / or their derivatives (hydroxypropyl 225 - CD., sufobutil 225 CD and 225 CD metilada randomized), Cyclodextrin and cyclodextrin.The solubility of this drug leading to improvement in relation to the drug without complexation and its application in drug formulation of immediate release and / or prolonged the basis of drug for the treatment of Chagas disease.To increase the speed of dissolution of benznidazole by means of its complexation with cyclodextrins in aqueous solution and / or alcoholic in the molar ratio of 1: 1 and / or 1: 2 allows the obtaining of pharmaceutical solids and / or liquid for oral administration, with solubility and / Or dissolution profile modified in relation to the product formulated the basis of the drug not complexed.Giving the medicine greater therapeutic efficacy and lower toxicity.
机译:制备苯并硝唑与环糊精衍生物的络合物的方法。本发明的目的是获得苯并硝唑(BNZ)(n-苄基-2-(2--硝基咪唑-1) -(II)乙酰胺)和<225-环糊精(-CD <225)和/或它们的衍生物(羟丙基<225-CD。,sufobutil <225> CD>和<225 CD甲胺四醇是随机的),环糊精和环糊精。该药物的溶解度导致相对于无络合药物的改善以及其在速释药物制剂中的应用和/或延长了治疗南美锥虫病的药物基础。通过以下方法提高苯并硝唑的溶出速度它与环糊精在水溶液和/或酒精中以1:1和/或1:2的摩尔比络合,从而获得用于口服的药物固体和/或液体,其溶解度和/或溶出度p相对于该产品进行的修饰,配制了不复杂的药物。赋予该药物更大的治疗功效和更低的毒性。

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