小泡
共聚物
对偶(语法数字)
化学
高分子化学
化学工程
自组装
材料科学
纳米技术
聚合物
有机化学
膜
生物化学
哲学
语言学
工程类
作者
April R. Rodriguez,Uh‐Joo Choe,Daniel T. Kamei,Timothy J. Deming
标识
DOI:10.1002/mabi.201200002
摘要
Abstract The design, synthesis, and self‐assembly of the first dual hydrophilic triblock copolypeptide vesicles, ${\rm R}_{m}^{{\rm H}} {\rm E}_{n} {\rm L}_{o} $ and ${\rm K}_{m}^{{\rm P}} {\rm R}_{n}^{{\rm H}} {\rm L}_{o} $ , is reported. Variation of the two distinct hydrophilic domains is used to tune cellular interactions without disrupting the self‐assembled structure. The aqueous self‐assemblies of these triblock copolypeptides in water are characterized using microscopy and DLS. Cell culture studies are used to evaluate cytotoxicity as well as intracellular uptake of the vesicles. The ability of polypeptides to incorporate ordered chain conformations that direct self‐assembly, combined with the facile preparation of functional, multiblock copolypeptide sequences of defined lengths, allow the design of vesicles attractive for development as drug carriers. magnified image
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