聚唾液酸
乙醇酸
乙二醇
免疫原性
药物输送
化学
脂质体
纳米技术
药品
纳米颗粒
体内
药理学
材料科学
生物化学
乳酸
有机化学
医学
免疫系统
生物技术
生物
遗传学
细胞粘附
细胞
细菌
免疫学
神经细胞粘附分子
作者
Dipak S. Pisal,Matthew P. Kosloski,Sathy V. Balu‐Iyer
摘要
The safety and efficacy of protein therapeutics are limited by three interrelated pharmaceutical issues, in vitro and in vivo instability, immunogenicity and shorter half-lives. Novel drug modifications for overcoming these issues are under investigation and include covalent attachment of poly(ethylene glycol) (PEG), polysialic acid, or glycolic acid, as well as developing new formulations containing nanoparticulate or colloidal systems (e.g., liposomes, polymeric microspheres, polymeric nanoparticles). Such strategies have the potential to develop as next generation protein therapeutics. This review includes a general discussion on these delivery approaches.
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