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CONJUGUÉ D'OLIGOMÈRE D'ACIDE BILIAIRE POUR UN NOUVEAU TRANSPORT VÉSICULAIRE ET UTILISATION CORRESPONDANTE
专利权人:
SNU R&DB FOUNDATION;ST PHARM CO. LTD.;MEDIPLEX CORP.
发明人:
BYUN, YOUNG RO,AHMED, AL-HILAL TASLIM,JEON, OK CHEOL,MOON, HYUN TAE,YUN, YISUK,KIM, KYUNGJIN
申请号:
EP12889309
公开号:
EP2925786A4
申请日:
2012.11.29
申请国别(地区):
EP
年份:
2016
代理人:
摘要:
The present invention relates to a method for preparing an end site-specific macromolecule-bile acid oligomer conjugate, comprising conjugating a bile acid oligomer which is prepared by oligomerization of two or more bile acid monomers to the terminal site of a macromolecule; a method for body absorption of an end site-specific macromolecule-bile acid oligomer conjugate, comprising administering the macromolecule-bile acid oligomer conjugate prepared by the above method to a subject orally; an end site-specific macromolecule-bile acid oligomer conjugate wherein the bile acid oligomer is conjugated to the terminal site of macromolecule; a composition comprising the conjugate; an oral formulation for macromolecule comprising the conjugate, a solubilizer, an excipient, a disintegrant, a binder, and a lubricant; a pharmaceutical composition comprising a heparin-bile acid oligomer conjugate wherein the bile acid oligomer is conjugated to the terminal site of heparin; and a method for treating thrombosis using said composition.
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