纳米凝胶
两亲性
肽
透明质酸
化学
药物输送
自愈水凝胶
背景(考古学)
膜
生物物理学
生物化学
聚合物
共聚物
生物
高分子化学
有机化学
古生物学
遗传学
作者
Andrew Simonson,Atip Lawanprasert,Tyler D. P. Goralski,Kenneth C. Keiler,Scott H. Medina
标识
DOI:10.1016/j.nano.2018.10.008
摘要
We report the design, synthesis and efficacy of a new class of gel-like nano-carrier, or ‘nanogel’, prepared via templated electrostatic assembly of anionic hyaluronic acid (HA) polysaccharides with the cationic peptide amphiphile poly-L-lysine (PLL). Small molecules and proteins present during nanogel assembly become directly encapsulated within the carrier and are precisely released by tuning the nanogel HA:PLL ratio to control particle swelling. Remarkably, nanogels exhibit versatile and complimentary mechanisms of cargo delivery depending on the biologic context. For example, in mammalian cells, nanogels are rapidly internalized and escape the endosome to both deliver membrane-impermeable protein cargo into the cytoplasm and improve chemotherapeutic potency in drug resistant cancer cells. In bacteria, nanogels permeabilize microbial membranes to sensitize bacterial pathogens to the action of a loaded antibiotic. Thus, peptide nanogels represent a versatile, readily scalable and bio-responsive carrier capable of augmenting and enhancing the utility of a broad range of biomolecular cargoes.
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