| Literature DB >> 34554623 |
Zhenyu Duan1,2, Qiang Luo1,2, Xinghang Dai1,2, Xiaoling Li1,2, Lei Gu1,2, Hongyan Zhu1, Xiaohe Tian1,3, Hu Zhang4, Qiyong Gong1,2,3, Zhongwei Gu1, Kui Luo1,2,3.
Abstract
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.Entities:
Keywords: bioinspired and biomimetic nanomedicine; branched polymers; glycopolymers; stimuli-responsive drug delivery systems; synergistic therapy; tumor genomic instability
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Year: 2021 PMID: 34554623 DOI: 10.1002/adma.202104594
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849