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首页> 外文期刊>Nanoscale >Chitosan derived nitrogen-doped carbon dots suppress osteoclastic osteolysisviadownregulating ROS
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Chitosan derived nitrogen-doped carbon dots suppress osteoclastic osteolysisviadownregulating ROS

机译:壳聚糖衍生nitrogen-doped碳点抑制监测osteolysisviadownregulating凯皮

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Osteoclasts are the main cells involved in normal bone remodeling and pathological bone destructionin vivo. Overactivation of osteoclasts can lead to osteolytic diseases, including breast cancer, bone tumors, arthritis, the aseptic loosening of orthopedic implants, and Paget's disease. Excessive reactive oxygen species are the main cause of osteoclast overactivation. We have synthesized chitosan derived nitrogen-doped carbon dots (N-CDs) with a high synthetic yield and the ability to scavenge reactive oxygen species (ROS). N-CDs effectively abrogated RANKL-induced elevation in ROS generation and therefore impaired the activation of NF-kappa B and MAPK pathways. Osteoclastogenesis and bone resorption was effectively attenuatedin vitro. Furthermore, thein vivoadministration of N-CDs in mice protected them against lipopolysaccharide (LPS)-induced calvarial bone destruction and breast cancer cell-induced tibial bone loss. Based on the good biocompatibility of N-CDs and the ability to efficiently remove ROS, a nanomaterial treatment scheme was provided for the first time for the clinical treatment of osteolytic diseases.
机译:破骨细胞是主要的细胞参与正常骨重建和病理骨头destructionin体内。会导致溶骨的疾病,包括乳腺癌癌症、骨肿瘤、关节炎、无菌骨科植入物松动,佩吉特氏疾病。破骨细胞的主要原因overactivation。合成壳聚糖衍生nitrogen-doped吗碳点(N-CDs)合成高的收益率和清除活性氧的能力物种(ROS)。RANKL-induced ROS生成和海拔因此受损nf -κB的激活和MAPK通路。吸收是有效attenuatedin体外。此外,登vivoadministration N-CDs老鼠对脂多糖保护他们(有限合伙人)全身的颅顶的骨破坏和乳腺癌cell-induced胫骨骨质流失。基于N-CDs和良好的生物相容性有效地清除活性氧的能力,纳米材料提供了处理方案第一次的临床治疗溶骨的疾病。

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