4.8 Article

Preparation of Conjugated Polymer Grafted with H2O2-Sensitive Prodrug for Cell Imaging and Tumor Cell Killing

Journal

ACS APPLIED MATERIALS & INTERFACES
Volume 8, Issue 1, Pages 42-46

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsami.5b11846

Keywords

conjugated polymer; prodrug; cell imaging; tumor cell killing; nitrogen mustard

Funding

  1. National Natural Science Foundation of China [21473220, 21473221]
  2. Major Research Plan of China [2013CB932800, 2012CB932600]

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In this work, a new conjugated polymer poly(fluorene-co-phenylene) derivative containing pendent quaternized chlormethine (PFP-Chl) was synthesized by covalent linking small molecular prodrug groups onto conjugated polymer side chains. H2O2-sensitive prodrug with an eight-member-cyclic boronate ester structure could suffer from H2O2-triggered nitrogen mustard release and further DNA cross-linking and alkylation. PFP-Chl combines therapeutic characteristic with excellent optical property of conjugated polymers. It is found that PFP-Chl could enter into cells by endocytosis to simultaneously exhibit abilities of fluorescent imaging and tumor cell inhibition.

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