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首页> 外文期刊>Analytical and bioanalytical chemistry >Determination of ATP using a double-receptor sandwich method based on molecularly imprinted membrane and fluorescence-labeled uranyl-salophen complex
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Determination of ATP using a double-receptor sandwich method based on molecularly imprinted membrane and fluorescence-labeled uranyl-salophen complex

机译:基于分子印迹膜和荧光标记的铀酰-salophen复合物的双受体夹心法测定ATP

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摘要

A double-receptor sandwich method for the fluorescence determination of adenosine triphosphate (ATP) is proposed in this paper. The solid phase receptor on the surface of glass slides is a molecularly imprinted membrane (MIM) containing an artificial nanocavity. It is constructed by a molecular imprinting technique using adenosine monophosphate (AMP) as a template molecule. The labeled receptor is a uranyl-salophen complex containing a fluorescent group or uranyl-salophen-fluorescein (USF). It is synthesized with salophen, 5-aminofluorescein, and uranyl. In a procedure of determining ATP, ATP in sample solution is first adsorbed on the surface of the glass slide through the combination of the AMP group in ATP with the nanocavity in MIM. Then, the adsorbed ATP binds USF through the coordination reaction of the phosphate group in ATP with uranyl in USF to form a sandwich-type structure of MIM-ATP-USF. The amount of ATP is detected through the fluorescence determination of USF bound on the slide. Under optimal conditions, the linear range for the determination of ATP is 0.3 to 4.8 nmol/mL with a detection limit of 0.041 nmol/mL. The proposed method has been successfully employed for the determination of ATP in real samples with the recoveries of 98.5 to 102.5 %.
机译:提出了一种双受体夹心法测定三磷酸腺苷(ATP)的荧光。载玻片表面上的固相受体是包含人工纳米腔的分子印迹膜(MIM)。它是通过分子印迹技术使用单磷酸腺苷(AMP)作为模板分子构建的。标记的受体是含有荧光基团的铀酰-salophen复合物或铀酰-salophen-荧光素(USF)。它与salophen,5-氨基荧光素和铀酰合成。在确定ATP的过程中,样品溶液中的ATP首先通过ATP中的AMP基团与MIM中的纳米腔相结合而吸附在载玻片的表面上。然后,吸附的ATP通过ATP中的磷酸基与USF中的铀酰的配位反应与USF结合,形成MIM-ATP-USF的夹心型结构。 ATP的量通过载玻片上USF的荧光测定来检测。在最佳条件下,用于测定ATP的线性范围为0.3至4.8 nmol / mL,检测极限为0.041 nmol / mL。该方法已成功用于实际样品中ATP的测定,回收率为98.5%至102.5%。

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