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Octreotide-PEG-DSPE:肽-PEG-脂质偶联的新合成方法
发布时间:2025-07-11     作者:kx   分享到:
学术论文:肽-PEG-脂质包覆物的合并措施:奥曲肽-PEG-DSPE合并的选用链接转换://www.sciencedirect.com/science/article/abs/pii/S0960894X08007944小说作家:苏建秋  ,曾锦 禄 ,张定光  ,余文仁  ,吴世光 节选:建立联系好几回种肽-聚乙二醇-脂质(肽-PEG-脂质)偶联物的固相合并具体最简单的方法。以奥曲肽-PEG 2000 -DSPE(OPD 2000)实例,演示软件了该合并具体最简单的方法。得出OPD 2000的形式、化学活化和含量均已认可,为制作靶向治疗治疗脂质体等形式了解的药材递送系统的带来了了靶向治疗治疗分子式,以供进1步论述。

Octreotide-PEG-DSPE

A solid phase synthesis method was established for the synthesis of peptide-poly(ethylene glycol)-lipid (peptide-PEG-lipid) conjugates. Octreotide-PEG2000-DSPE (OPD2000) was used as an example to demonstrate the synthetic approach. The OPD2000 obtained had confirmed structure, activity, and purity providing a targeting molecule for preparation of well-defined drug delivery systems, such as targeted liposomes, for further studies.石家庄杏彩体育平台 生态学出示对应服务:DSPE-PEG-BoronatemPEG-DMPEEB1-PEG-DSPEDSPE-PEG-HZDSPE-PEG-PEIDSPE-PEG-c(RGDfc)DMPE (14:0 PE)DSPE-PEG-scFv(HD37-CCH)(二硬脂酰基磷脂酰酒精胺-聚乙二醇-癌症靶向药物淀粉酶)左右新闻稿件玩法來源分类杂志或资料,如无侵犯著作权请联系起来我们的移除!