4.8 Article

Synergistic Therapy of a Naturally Inspired Glycopolymer-Based Biomimetic Nanomedicine Harnessing Tumor Genomic Instability

Journal

ADVANCED MATERIALS
Volume 33, Issue 45, Pages -

Publisher

WILEY-V C H VERLAG GMBH
DOI: 10.1002/adma.202104594

Keywords

bioinspired and biomimetic nanomedicine; branched polymers; glycopolymers; stimuli-responsive drug delivery systems; synergistic therapy; tumor genomic instability

Funding

  1. National Natural Science Foundation of China [52073193, 51873120, 81621003]
  2. 1.3.5 Project for Disciplines of Excellence, West China Hospital, Sichuan University [ZYJC21013, ZYGD18028, ZYGD20007, ZYJC18011]
  3. Research Funds in West China Hospital of Sichuan University [2020HXBH072]
  4. China Postdoctoral Science Foundation [2019TQ0220]

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Inspired by natural saccharide-protein complexes, a stimuli-responsive biodegradable and branched glycopolymer-pyropheophorbide-a conjugate for cancer therapy was constructed. Through structure-activity relationship studies, the conjugate forms stable nanostructures and regulates the stacking state of Ppa to improve the photodynamic therapy effect. The biomimetic nanomedicine showed highly efficient tumor targeting and cellular internalization properties, resulting in a prominent antitumor effect when combined with laser irradiation.
Inspired by natural saccharide-protein complexes, a stimuli-responsive biodegradable and branched glycopolymer-pyropheophorbide-a (Ppa) conjugate (BSP) with saccharide units for cancer therapy is constructed. A linear glycopolymeric conjugate (LSP), a branched glycopolymeric conjugate (BShP) from Ppa with long carbon chains, and a branched conjugate (BHSP) based on poly[N-(2-hydroxypropyl) methacrylamide] (polyHPMA) without saccharide units are prepared as controls. Through structure-activity relationship studies, BSP with a 3D network structure forms stable nanostructures via weak intermolecular interactions, regulating the stacking state of Ppa to improve the singlet oxygen quantum yield and the corresponding photodynamic therapy (PDT) effect. BSP shows high loading of olaparib, and are further coated with tumor cell membranes, resulting in a biomimetic nanomedicine (CM-BSPO). CM-BSPO shows highly efficient tumor targeting and cellular internalization properties. The engulfment of CM-BSPO accompanied with laser irradiation results in a prominent antitumor effect, evidenced by disruption of cell cycles in tumor cells, increased apoptosis and DNA damage, and subsequent inhibition of repair for damaged DNA. The mechanism for the synergistic effect from PDT and olaparib is unveiled at the genetic and protein level through transcriptome analysis. Overall, this biodegradable and branched glycopolymer-drug conjugate could be effectively optimized as a biomimetic nanomedicine for cancer therapy.

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