| Literature DB >> 28940903 |
Junjie Li1, Anjaneyulu Dirisala2, Zhishen Ge1, Yuheng Wang1, Wei Yin1, Wendong Ke1, Kazuko Toh2, Jinbing Xie2, Yu Matsumoto3, Yasutaka Anraku4, Kensuke Osada4, Kazunori Kataoka2,5.
Abstract
Polymeric nanoreactors (NRs) have distinct advantages to improve chemical reaction efficiency, but the in vivo applications are limited by lack of tissue-specificity. Herein, novel glucose oxidase (GOD)-loaded therapeutic vesicular NRs (theraNR) are constructed based on a diblock copolymer containing poly(ethylene glycol) (PEG) and copolymerized phenylboronic ester or piperidine-functionalized methacrylate (P(PBEM-co-PEM)). Upon systemic injection, theraNR are inactive in normal tissues. At a tumor site, theraNR are specifically activated by the tumor acidity via improved permeability of the membranes. Hydrogen peroxide (H2 O2 ) production by the catalysis of GOD in theraNR increases tumor oxidative stress significantly. Meanwhile, high levels of H2 O2 induce self-destruction of theraNR releasing quinone methide (QM) to deplete glutathione and suppress the antioxidant ability of cancer cells. Finally, theraNR efficiently kill cancer cells and ablate tumors via the synergistic effect.Entities:
Keywords: cancer therapy; enzyme delivery; membrane permeability; nanoreactors; polymersomes
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Year: 2017 PMID: 28940903 DOI: 10.1002/anie.201706964
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336