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The hemocompatibility of oxidized diamond nanocrystals for biomedical applications

机译:氧化金刚石纳米晶体在生物医学中的血液相容性

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摘要

Low-dimensional carbon-based nanomaterials have recently received enormous attention for biomedical applications. However, increasing evidence indicates that they are cytotoxic and can cause inflammatory responses in the body. Here, we show that monocrystalline nanodiamonds (NDs) synthesized by high-pressure-high-temperature (HPHT) methods and purified by air oxidation and strong oxidative acid treatments have excellent hemocompatibility with negligible hemolytic and thrombogenic activities. Cell viability assays with human primary endothelial cells suggested that the oxidized HPHT-NDs (dimensions of 35–500 nm) are non-cytotoxic. No significant elevation of the inflammatory cytokine levels of IL-1β and IL-6 was detected in mice after intravenous injection of the nanocrystals in vivo. Using a hindlimb-ischemia mouse model, we demonstrated that 35-nm NDs after covalent conjugation with polyarginine are useful as a drug delivery vehicle of heparin for prolonged anticoagulation treatment. The present study lays a solid foundation for further therapeutic applications of NDs in biomedicine.
机译:低维碳基纳米材料最近在生物医学应用中受到了极大的关注。但是,越来越多的证据表明它们具有细胞毒性,并且可以在体内引起炎症反应。在这里,我们表明通过高压高温(HPHT)方法合成并通过空气氧化和强氧化酸处理纯化的单晶纳米金刚石(NDs)具有优异的血液相容性,溶血和血栓形成活性可忽略不计。用人类原代内皮细胞进行的细胞活力分析表明,氧化的HPHT-ND(尺寸为35-500nm)是无细胞毒性的。在体内静脉内注射纳米晶体后,在小鼠中未检测到IL-1β和IL-6的炎性细胞因子水平的显着升高。使用后肢缺血小鼠模型,我们证明了与聚精氨酸共价缀合后的35 nm NDs可作为肝素的药物递送载体用于延长抗凝治疗。本研究为ND在生物医学中的进一步治疗应用奠定了坚实的基础。

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