首页> 外国专利> A process for preparing Drug formulations and antichagasicas molecules derived from 2 - nitroimidazoles micro or nano Encapsulated in phospholipid vesicles

A process for preparing Drug formulations and antichagasicas molecules derived from 2 - nitroimidazoles micro or nano Encapsulated in phospholipid vesicles

机译:一种制备自2-硝基咪唑的微型或纳米封装在磷脂囊泡中的药物制剂和抗chagasicas分子的方法

摘要

Claim 1: a method for preparing Drug formulations and antichagu00e1sicas molecules derived from 2 - nitroimidazoles as active Principles) in micro or nano vesicles, are characterized by being composed of phospholipids and cholesterol, oligo or multilamellar and possess A size between 100 nm and 2 microns; the amount of active principle, minimum is 0.5 grams / 100 grams lt. claim 2: a method according to claim 1, characterized by antichagu00e1sicas Drugs effective in vivo with widespread Clinical application as active principles derived from 2 - nitroimidazoles: benznidazole and nifurtimox.Claim 3: a method according to claim 1, characterized by the use of Drugs derived from 2 - nitroimidazoles as active Principles misonidazole, etanidazole.Claim 4, a method according to claim 1, characterized by antichagu00e1sicas Drugs effective in vivo without widespread Clinical application as active Principles: ketoconazole, itraconazole, allopurinol, pyrazole - pyrimidines, amphotericin B.Claim 5: a method according to claim 1, characterized by the use of Drugs antichagu00e1sicas effective in Experimental models with predictable Clinical Utility as the active Principles: Peptide inhibitors of cysteine protease of Trypanosoma cruzi (cruzipau00edna, Cruceu00edna); phenothiazines.
机译:权利要求1:一种在微或纳米囊泡中制备以2-硝基咪唑为活性成分的药物制剂和抗chachasicas分子的方法,其特征在于由磷脂和胆固醇,寡聚体或多层分子组成,其大小在100nm至100nm之间。 2微米;有效成分的量,最小为0.5克/ 100克lt。权利要求2:根据权利要求1的方法,其特征在于,作为自2-硝基咪唑类的活性成分的活性成分,在体内具有广泛临床应用的抗effective药。3.根据权利要求1的方法,其特征在于: 2.根据权利要求1的方法,其特征在于,抗2-硝基咪唑衍生的药物为有效成分的咪唑并咪唑,乙苯咪唑。4,根据权利要求1的方法,其特征在于抗cha药在体内有效而没有广泛应用的药物作为活性成分。 ,两性霉素B.权利要求5的方法,其特征在于使用在可预测的临床效用的实验模型中有效的药物抗anti药作为活性成分:克鲁氏锥虫(cruzipa u00edna,Cruce)的半胱氨酸蛋白酶的肽抑制剂 u00edna);吩噻嗪。

著录项

  • 公开/公告号AR037807A1

    专利类型

  • 公开/公告日2004-12-09

    原文格式PDF

  • 申请/专利权人 UNIVERSIDAD NACIONAL DE QUILMES;

    申请/专利号AR2001P105534

  • 发明设计人 ROMERO EDER LILIA;MORILLA MARIA JOSE;

    申请日2001-11-28

  • 分类号A61K9/127;A61K31/351;A61K31/4164;A61K31/4168;A61K31/496;A61K31/519;A61K31/541;A61P33/02;

  • 国家 AR

  • 入库时间 2022-08-21 22:18:56

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