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Fluorescence quenching of bioactive molecules by nanodiamonds

机译:纳米金刚石对生物活性分子的荧光猝灭

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In this work, the fluorescence quenching of two types of bioactive molecules – of the protein lysozyme and of the drugdoxorubicin – by carboxylated detonation nanodiamonds in the result of their interaction has been studied. It wasdemonstrated that nanodiamonds effectively quench the fluorescence of lysozyme and doxorubicin but by differentmechanisms. It was found that the fluorescence quenching of lysozyme by nanodiamonds is caused only by a static typeof quenching while the fluorescence quenching of doxorubicin by nanodiamonds is caused by both static and dynamictypes of quenching. We propose a hypothesis that the surface groups of nanodiamonds are the quenchers of thefluorescence and the variety of surface groups with which a fluorescent molecule interacts determines the fluorescencequenching mechanism. The accounting of our results will provide the insight in the nanodiamonds’ visualization as wellas the possible way to track the loading and subsequent unloading of drugs from the nanodiamonds’ surface.
机译:在这项工作中,两种类型的生物活性分子的荧光猝灭–蛋白质溶菌酶和药物 阿霉素–通过羧化引爆纳米金刚石在它们相互作用中的结果得到了研究。它是 证明纳米金刚石有效地抑制了溶菌酶和阿霉素的荧光,但通过 机制。发现纳米金刚石对溶菌酶的荧光猝灭仅是由静态类型引起的。 纳米金刚石对阿霉素的荧光猝灭是由静态和动态引起的 淬火类型。我们提出一个假设,即纳米金刚石的表面基团是纳米金刚石的淬灭剂。 荧光以及与荧光分子相互作用的各种表面基团决定了荧光 淬灭机理。我们对结果的核算也将为纳米金刚石的可视化提供洞察力 作为跟踪从纳米金刚石表面装载和卸载药物的可能方法。

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