聚合物囊泡
化学
乙二醇
小泡
内体
细胞内
共聚物
PEG比率
生物物理学
药物输送
内吞作用
毒品携带者
纳米载体
两亲性
生物化学
膜
细胞
有机化学
生物
经济
聚合物
财务
作者
Simona Cerritelli,Diana Velluto,Jeffrey A. Hubbell
出处
期刊:Biomacromolecules
[American Chemical Society]
日期:2007-05-12
卷期号:8 (6): 1966-1972
被引量:423
摘要
Under appropriate conditions, block copolymeric macroamphiphiles will self-assemble in water to form vesicles, referred to as polymersomes. We report here polymersomes that can protect biomolecules in the extracellular environment, are taken up by endocytosis, and then suddenly burst within the early endosome, releasing their contents prior to exposure to the harsh conditions encountered after lysosomal fusion. Specifically, block copolymers of the hydrophile poly(ethylene glycol) (PEG) and the hydrophobe poly(propylene sulfide) (PPS) were synthesized with an intervening disulfide, PEG17-SS-PPS30. Polymersomes formed from this block copolymer were demonstrated to disrupt in the presence of intracellular concentrations of cysteine. In cellular experiments, uptake, disruption, and release were observed within 10 min of exposure to cells, well within the time frame of the early endosome of endolysosomal processing. This system may be useful in cytoplasmic delivery of biomolecular drugs such as peptides, proteins, oligonucleotides, and DNA.
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