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METHOD OF PRODUCING ORAL PREPARATION OF PROINSULIN C-PEPTIDE

机译:制备胰岛素原C肽的口服制剂的方法

摘要

FIELD: medicine, pharmaceutics.;SUBSTANCE: invention refers to pharmacology and medicine, and represents a method of producing an oral preparation of proinsulin C-peptide of activated polyethylene glycol differing by the fact that polyethylene glycol is activated by ionising radiation in an acidic medium with calcium and/or zinc cations added to final concentration 5-10 mM, and then mixed with proinsulin C-peptide, polyethylene glycol is characterised by molar mass 0.4-40 kDa and concentration 1.0-50.0%, in relation of proinsulin C-peptide: polyethylene glycol equal to 1:(1-500) to final concentration of proinsulin C-peptide in mixture 1-10 mg/ml.;EFFECT: invention provides higher therapeutic activity in oral administration with respect to diabetic complications.;4 cl, 3 ex,1 tbl, 2 dwg
机译:领域:本发明涉及药理学和医学,并且代表一种生产活化的聚乙二醇的胰岛素原C肽的口服制剂的方法,其不同之处在于聚乙二醇通过在酸性介质中电离辐射而被活化加入钙和/或锌阳离子至终浓度5-10 mM,然后与胰岛素原C肽混合,聚乙二醇的特征在于摩尔质量为0.4-40 kDa,浓度为1.0-50.0%(相对于胰岛素原C肽) :等于1:(1-500)的聚乙二醇与混合物中胰岛素原C肽的终浓度为1-10 mg / ml 。;效果:本发明在糖尿病糖尿病并发症口服方面具有更高的治疗活性; 4 cl, 3 ex,1 tbl,2 dwg

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