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采用闪式纳米沉淀法制备工程化聚合物负载双正交纳米催化剂。

Engineered Polymer-Supported Biorthogonal Nanocatalysts Using Flash Nanoprecipitation.

机构信息

Department of Chemistry, University of Massachusetts Amherst, 710 North Pleasant Street, Amherst, Massachusetts 01003, United States.

State Key Laboratory of Chemical Engineering, East China University of Science and Technology, Shanghai 200237 P. R. China.

出版信息

ACS Appl Mater Interfaces. 2022 Jul 20;14(28):31594-31600. doi: 10.1021/acsami.2c04496. Epub 2022 Jul 8.

Abstract

Transition-metal catalysts (TMCs) effect bioorthogonal transformations that enable the generation of therapeutic agents , minimizing off-target effects. The encapsulation of insoluble TMCs into polymeric nanoparticles to generate "polyzymes" has vastly expanded their applicability in biological environments by enhancing catalyst solubility and stability. However, commonly used precipitation approaches provide limited encapsulation efficiency in polyzyme fabrication and result in a low catalytic activity. Herein, we report the creation of polyzymes with increased catalyst loading and optimized turnover efficiency using flash nanoprecipitation (FNP). Polyzymes with controlled size and catalyst loading were fabricated by tuning the process conditions of FNP. The biological applicability of polyzymes was demonstrated by efficiently transforming a non-toxic prodrug into the active drug within cancer cells.

摘要

过渡金属催化剂 (TMCs) 可促进生物正交转化,从而生成治疗剂,最大限度地减少脱靶效应。将不溶性 TMC 包封到聚合物纳米颗粒中以生成“多酶”,通过提高催化剂的溶解度和稳定性,极大地扩展了它们在生物环境中的应用。然而,常用的沉淀方法在多酶制备中提供了有限的封装效率,并导致催化活性低。在此,我们报告了使用闪式纳米沉淀 (FNP) 来增加催化剂负载并优化周转效率的多酶的制备。通过调整 FNP 的工艺条件来制备具有可控尺寸和催化剂负载的多酶。通过在癌细胞内将无毒前药有效地转化为活性药物,证明了多酶的生物适用性。

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