化学
共聚物
两亲性
紫杉醇
乙二醇
黏膜黏附
生物粘附
药物输送
高分子化学
纳米颗粒
组合化学
聚合物
有机化学
纳米技术
材料科学
医学
外科
化疗
作者
Robert C. Sabatelle,Abraham D. Geller,Siyuan Li,Audrey Van Heest,Uma M. Sachdeva,Eric M. Bressler,Jenny T. Korunes-Miller,Bassel Tfayli,Aya Tal-Mason,Hussein Kharroubi,Yolonda L. Colson,Mark W. Grinstaff
标识
DOI:10.1021/acs.bioconjchem.4c00325
摘要
Drug delivery to the esophagus through systemic administration remains challenging, as minimal drug reaches the desired target. Local delivery offers the potential for improved efficacy while minimizing off-target toxicities but necessitates bioadhesive properties for mucosal delivery. Herein, we describe the synthesis of two new mucoadhesive amphiphilic copolymers prepared by sequential ring-opening copolymerization or postpolymerization click conjugation. Both strategies yield block copolymers containing a hydrophilic amine-functionalized poly-amido-saccharide and either a hydrophobic alkyl derivatized poly-amido-saccharide or poly(lactic acid), respectively. The latter resulting copolymers readily self-assemble into spherical, ≈200 nm diameter, positively charged mucoadhesive nanoparticles. The NPs entrap ultrahigh levels of paclitaxel via encapsulation of free paclitaxel and paclitaxel conjugated to a biodegradable, biocompatible poly(1,2-glycerol carbonate). Paclitaxel-loaded NPs rapidly enter cells, release paclitaxel, are cytotoxic to esophageal OE33 and OE19 tumor cells in vitro, and, importantly, demonstrate improved mucoadhesion compared to conventional poly(ethylene glycol)-poly(lactic acid) nanoparticles to ex vivo esophageal tissue.
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