脂质体
体内
药代动力学
药理学
PEG比率
间隙
化学
药品
毒品携带者
医学
生物物理学
生物化学
生物
泌尿科
生物技术
经济
财务
作者
Peter Laverman,Otto C. Boerman,Wim J.G. Oyen,Frans H.M. Corstens,Gert Storm
出处
期刊:Critical Reviews in Therapeutic Drug Carrier Systems
[Begell House]
日期:2001-01-01
卷期号:18 (6): 16-16
被引量:69
标识
DOI:10.1615/critrevtherdrugcarriersyst.v18.i6.40
摘要
Recent studies with PEG liposomes in patients have consistently shown that liposomes can induce side effects (flushing, tightness of the chest). Furthermore, the blood clearance of PEG liposomes was shown to be dose-dependent: at lipid doses lower than 1 micromol/kg, PEG liposomes do not show the long-circulation property but instead are cleared relatively rapidly from the bloodstream. Another remarkable observation was that repeated injections of PEG liposomes led to significant pharmacokinetic changes: the circulatory half-life of a second dose of radiolabeled PEG liposomes dramatically decreased when given from 5 days to up to 4 weeks after a first injection. In these three unexpected phenomena, proteins of the complement system seem to play a key role. Therefore, one has to consider that PEG liposomes are not inert drug-carrying vehicles in vivo. Pharmacological effects can occur, induced solely by using liposomal particles irrespective of the drug content.
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