首页> 外文期刊>Mikrochimica Acta: An International Journal for Physical and Chemical Methods of Analysis >A terbium-based metal-organic framework@gold nanoparticle system as a fluorometric probe for aptamer based determination of adenosine triphosphate
【24h】

A terbium-based metal-organic framework@gold nanoparticle system as a fluorometric probe for aptamer based determination of adenosine triphosphate

机译:基于铽的金属 - 有机框架@金纳米粒子系统作为荧光探针,用于适体的基于腺苷三磷酸腺苷的测定

获取原文
获取原文并翻译 | 示例
获取外文期刊封面目录资料

摘要

This study reports on a method for fluorometric aptasensing of adenosine triphosphate (ATP). It is based on the interaction of dispersed (red) and agglomerated (blue) gold nanoparticles (AuNPs) with a water-dispered terbium(III) based metal-organic framework (Tb-MOF). The dispersed AuNPs quench the emissions of the Tb-MOF, while the aggregated AuNPs have little effect. Under the condition of high salt concentration, the free aptamer against ATP does not stabilize the AuNPs against aggregation. This causes a color change from red to blue and weak quenching of the fluorescence of the Tb-MOF (with peaks at 489 nm and 544 nm after excitation at 290 nm). On addition of ATP, it will be bound by its aptamer to form a complex that is adsorbed on the AuNPs. This protects the AuNPs from salt-induced aggregation and the color (with a peak at 525 nm) remains red. The two fluorescence bands of the Tb-MOF are therefore suppressed by fluorescence resonance energy transfer (FRET) between Tb-MOF and the dispersed AuNPs. Fluorescence drops linearly in the 50 nM to 10 mu M ATP concentration range, and the detection limit is 23 nM. ATP analogs such as guanosine triphosphate, uridine triphosphate, cytidine triphosphate, adenosine monophosphate and cyclic adenosine monophosphate have no obvious interference. The method was successfully applied to the determination of ATP in (spiked) human plasma samples and gave satisfactory recoveries.
机译:该研究报告了腺苷三磷酸腺苷(ATP)的荧光分配方法。基于分散(红色)和附聚(蓝色)金纳米颗粒(AUNP)与水位铽(III)金属 - 有机骨架(TB-MOF)的相互作用。分散的aUnps淬灭TB-MOF的排放,而聚集的aUnps效果不大。在高盐浓度的条件下,对ATP的游离适体不会稳定AUNPS免受聚集。这导致红色从红色变为红色到蓝色和弱淬火TB-MOF的荧光(在290nm的激发后在489nm和544nm处的峰)。在添加ATP时,它将被其适体束缚,以形成吸附在AUNP上的复合物。这保护AUNP免受盐诱导的聚集和颜色(525 nm的峰值)保持红色。因此,TB-MOF的两个荧光带被TB-MOF和分散的AUNP之间的荧光共振能量转移(FRET)抑制。荧光在50nm至10μmatp浓度范围内线性下降,检测限为23nm。 ATP类似物如鸟氨酸三磷酸,尿苷三磷酸,三磷酸三磷酸,腺苷一磷酸盐和环磷酸腺苷无明显干扰。该方法成功地应用于(尖刺)的人血浆样品中的ATP的测定并得到满意的回收率。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号