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Chitosan functionalisation of gold nanoparticles encourages particle uptake and induces cytotoxicity and pro-inflammatory conditions in phagocytic cells as well as enhancing particle interactions with serum components

机译:金纳米颗粒的壳聚糖功能化可促进颗粒摄取并诱导吞噬细胞中的细胞毒性和促炎条件并增强颗粒与血清成分的相互作用

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摘要

Background Gold nanoparticles (AuNPs) are a popular choice for use in medical and biomedical research applications. With suitable functionalisation AuNPs can be applied in drug delivery systems, or can aid in disease diagnosis. One such functionalisation is with chitosan, which enables efficient interaction and permeation of cellular membranes, providing an effective adjuvant. As both AuNPs and chitosan have been shown to have low toxicity and high biocompatibility their proposed use in nanomedicine, either individually or combined, is expanding. However, further toxicological and immunological assessments of AuNP-chitosan conjugates are still needed. Therefore, we have evaluated how AuNP functionalisation with chitosan can affect uptake, cytotoxicity, and immunological responses within mononuclear cells, and influence the interaction of AuNPs with biomolecules within a complex biofluid. The AuNPs used were negatively charged through citrate-coating, or presented either low or high positive charge through chitosan-functionalisation. Uptake by THP-1 cells was assessed via transmission electron microscopy and electron energy loss spectroscopy, pro-inflammatory responses by ELISA and qRT-PCR, and cell death and viability via lactate dehydrogenase release and mitochondrial activity, respectively. Interactions of AuNPs with protein components of a frequently used in vitro cell culture medium supplement, foetal calf serum, were investigated using mass spectrometry.
机译:背景技术金纳米颗粒(AuNPs)是用于医学和生物医学研究应用的流行选择。通过适当的功能化,AuNP可以应用于药物输送系统,或有助于疾病诊断。一种这样的功能化是用壳聚糖,其能够有效地相互作用和渗透细胞膜,从而提供有效的佐剂。由于已经证明AuNP和壳聚糖都具有低毒性和高生物相容性,因此它们在纳米药物中的建议用途,无论是单独使用还是组合使用,都在不断扩大。但是,仍然需要对AuNP-壳聚糖结合物进行进一步的毒理学和免疫学评估。因此,我们评估了壳聚糖的AuNP功能化如何影响单核细胞内的摄取,细胞毒性和免疫反应,以及如何影响AuNP与复杂生物流体中生物分子的相互作用。所用的AuNPs通过柠檬酸盐涂层带负电,或通过壳聚糖功能化呈现低或高正电荷。通过透射电子显微镜和电子能量损失光谱,通过ELISA和qRT-PCR的促炎反应以及通过乳酸脱氢酶释放和线粒体活性的细胞死亡和生存力来评估THP-1细胞的摄取。使用质谱法研究了AuNPs与经常使用的体外细胞培养基补充剂,胎牛血清中蛋白质成分的相互作用。

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