共 44 条
PEG-SS-PPS: Reduction-sensitive disulfide block copolymer vesicles for intracellular drug delivery
被引:368
作者:

Cerritelli, Simona
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1110 Lausanne, Switzerland

Velluto, Diana
论文数: 0 引用数: 0
h-index: 0
机构: Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1110 Lausanne, Switzerland

Hubbell, Jeffrey A.
论文数: 0 引用数: 0
h-index: 0
机构:
Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1110 Lausanne, Switzerland Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1110 Lausanne, Switzerland
机构:
[1] Ecole Polytech Fed Lausanne, Inst Bioengn, CH-1110 Lausanne, Switzerland
[2] Ecole Polytech Fed Lausanne, Inst Chem Sci & Engn, CH-1110 Lausanne, Switzerland
[3] Univ G dAnnunzio, Dipartimento Sci Farmaco, I-66013 Chieti, Italy
关键词:
D O I:
10.1021/bm070085x
中图分类号:
Q5 [生物化学];
Q7 [分子生物学];
学科分类号:
071010 ;
081704 ;
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, PEG(17)-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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页码:1966 / 1972
页数:7
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