| Literature DB >> 32213362 |
Fei Ding1, Xihui Gao2, Xiangang Huang1, Huan Ge1, Miao Xie1, Jiwen Qian1, Jie Song3, Yuehua Li4, Xinyuan Zhu1, Chuan Zhang5.
Abstract
Photothermal therapy (PTT) normally requires to maintain the temperature of tumor lesions above 50 °C, which potentially induces local inflammation and tumor metastasis. To avoid these side effects, it is vital to achieve effective antitumor efficacy at relatively low temperature (42-45 °C) during the PTT treatment. Herein, we design a polydopamine (PDA)-coated nucleic acid nanogel as a therapeutic complex for siRNA-mediated low-temperature PTT. First, siRNAs that target the heat-shock-protein 70 (Hsp70) serve as crosslinkers to guide the DNA-grafted polycaprolactone (DNA-g-PCL) assemble into nanosized hydrogel particles through nucleic acid hybridization. Thereafter, the obtained siRNA-embedded nanogels are further coated with a thin layer of polydopamine, which not only protects the nanogels against enzymatic degradation but also endows the nanogels with excellent photothermal conversion capacity under near infrared (NIR) light irradiation. After surface PEGylation, this triple shield siRNA delivery complex shows the capability of effective ablating the tumor under relatively mild condition.Entities:
Keywords: Gene silencing; Low temperature; Photothermal therapy; Polydopamine coating; RNase resistance; siRNA delivery
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Year: 2020 PMID: 32213362 DOI: 10.1016/j.biomaterials.2020.119976
Source DB: PubMed Journal: Biomaterials ISSN: 0142-9612 Impact factor: 12.479