化学
体内分布
药代动力学
聚乙二醇化
脂质体
PEG比率
乙二醇
体内
药理学
药品
色谱法
聚乙二醇
生物化学
体外
有机化学
经济
生物技术
生物
医学
财务
作者
Tian−Lu Cheng,Kai‐Hsiang Chuang,Bing-Mae Chen,Steve R. Roffler
摘要
Attachment of poly(ethylene glycol) (PEG) to proteins, peptides, liposomes, drugs, and nanoparticles can improve pharmaceutical pharmacokinetic properties and enhance in vivo biological efficacy. Since the first PEGylated product was approved by the Food and Drug Administration in 1990, increasing numbers of PEGylated compounds have entered clinical use. Successful clinical development of PEGylated pharmaceuticals requires accurate methods for the qualitative and quantitative analysis of intact PEG conjugates in biological fluids. In this article, we review assay methods that can be utilized for the detection and measurement of PEGylated pharmaceuticals in complex biological samples for determination of biodistribution and pharmacokinetic properties. In particular, we describe relevant colorimetric, chromatographic, radiolabeled, biological, and enzyme-linked immunosorbent assays for the pharmacokinetic study of PEGylated molecules.
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