发明名称 Crosslinked polysaccharide microparticles and method for their preparation
摘要 The present invention provides long-acting sustained-release formulations of drugs such as proteins or peptides, which are injectable, completely biodegradable and safe, as well as ensuring efficient encapsulation of the drugs such as proteins or peptides without inhibiting their biological activity. It is possible to achieve injectable sustained-release formulations that ensure efficient encapsulation and long-term sustained release of drugs such as proteins or peptides while retaining their biological activity, when a solution containing a drug and a polysaccharide derivative such as hyaluronic acid having a crosslinkable functional group(s) or a salt thereof is dehydrated in microparticulate form starting from a dilute state, where crosslinking proceeds slowly, to reach a concentration which facilitates crosslinking, to thereby cause crosslinking reaction during concentration, so that the drug is encapsulated into the crosslinked polysaccharide to give drug-carrying microparticles.
申请公布号 US8575332(B2) 申请公布日期 2013.11.05
申请号 US20040579032 申请日期 2004.11.15
申请人 HAHN SEI KWANG;SHIMOBOJI TSUYOSHI;CHUGAI SEIYAKU KABUSHIKI KAISHA 发明人 HAHN SEI KWANG;SHIMOBOJI TSUYOSHI
分类号 C08B37/00;A61K9/00;A61K9/16;A61K9/22;A61K9/50;A61K9/62;A61K47/36;C08B37/08;C08J3/12;C08J3/24 主分类号 C08B37/00
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