| Literature DB >> 32830477 |
Dongdong Wang1,2,3, Conghui Liu2,4, Shiquan You3, Kai Zhang2, Meng Li3, Yu Cao2, Changtao Wang3, Haifeng Dong1,2,4, Xueji Zhang2,4.
Abstract
Cell membrane camouflaged nanoparticles (NPs) have been increasingly explored to leverage natural cellular functions and adapt to various biomedical applications. Herein, we report an OMV-CC hybrid membrane, which consists of a bacterial outer membrane vesicle (OMV) and B16-F10 cancer cell (CC) membrane, and successfully coat it onto hollow polydopamine (HPDA) NPs. We harness the advantage of OMV immunotherapy together with HPDA-mediated photothermal therapy (PTT) to improve the antitumor efficacy toward melanoma. When injected intravenously via the tail vein, HPDA@[OMV-CC] NPs homogeneously target melanoma and activate the immune response by rapidly stimulating dendritic cell (DC) maturation in lymph nodes in the vaccinated mice. Our results show that the antitumor immune response and PTT reciprocally potentiate the therapeutic ability and fully eradicate melanoma without notable adverse effects. The homogeneous-target and immune activation hybrid biomimetic membrane provides the adaptability to various synergistic therapeutic and imaging applications by incorporating payload with application-specific functions.Entities:
Keywords: antitumor immune response; hollow polydopamine nanoparticles; homogeneous target; hybrid biomimetic membrane; photothermal therapy
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Year: 2020 PMID: 32830477 DOI: 10.1021/acsami.0c13169
Source DB: PubMed Journal: ACS Appl Mater Interfaces ISSN: 1944-8244 Impact factor: 9.229