首页> 外国专利> Process of preparation of formulations of the peptide Angiotensin-(1-7) and its analogues, agonists and antagonists using cyclodextrins, liposomes and biodegradable polymers and/or mixtures and products thereof

Process of preparation of formulations of the peptide Angiotensin-(1-7) and its analogues, agonists and antagonists using cyclodextrins, liposomes and biodegradable polymers and/or mixtures and products thereof

机译:使用环糊精,脂质体和可生物降解的聚合物和/或其混合物和产物制备肽血管紧张素-(1-7)及其类似物,激动剂和拮抗剂的制剂的方法

摘要

There is no description in the state of technique of a formulation, application or product of D-Ala7-Angiotensin-(1-7) (A-779) and analogues and derivatives, D-Pro7-Angiotensin-(1-7) and analogues or derivatives or of Ang-(1-7) analogues or derivatives using cyclodextrines, liposomes, biodegradable polymers and its derivatives for the study or treatment of arterial hypertension and other cardiovascular diseases and its complications, wounds, burns, erithema, tumors, diabetes mellitus, sperm mobility, nephropathy, gastrointestinal and gynaecological disorders, angiogenesis, angioplatsy, alopecia and blood diseases in animals of warm blood, or as ligands for de G-protein-coupled receptor MAS. This characterizes the present invention as a more effective option for the study and treatment of pathologies associated or not to this receptor. The present invention is characterized by the combination of two different technologies: the molecular encapsulation of the peptide Angiotensin-(1-7) and its analogues and derivates in cyclodextrin and the microencapsulation in biodegradable polymers and liposomes. It is also characterized by the increase of this peptide and its analogues and derivatives using the formulation of the present invention.
机译:D-Ala 7 -血管紧张素-(1-7)(A-779)及其类似物和衍生物D-Pro <使用环糊精,脂质体,可生物降解的聚合物及其衍生物的Sup> 7 -血管紧张素-(1-7)及其类似物或衍生物或Ang-(1-7)类似物或衍生物,用于研究或治疗高血压和其他心血管疾病及其并发症,伤口,烧伤,风疹,肿瘤,糖尿病,精子活动性,肾病,胃肠道和妇科疾病,血管生成,血管性血小板减少症,脱发和温血动物血液疾病,或作为de G蛋白的配体-偶联受体MAS。这将本发明表征为用于研究和治疗与该受体相关或不相关的病理学的更有效选择。本发明的特征在于两种不同技术的结合:肽血管紧张素-(1-7)及其类似物和衍生物的分子包封在环糊精中以及微囊包封在可生物降解的聚合物和脂质体中。使用本发明的制剂,其特征还在于该肽及其类似物和衍生物的增加。

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