An in-tube aptamer/gold nanoparticles coated capillary solid-phase microextraction for separation of adenosine in serum and urine samples

被引:23
作者
Ma, Yanxia [1 ]
Hao, Lixian [1 ]
Lin, Xiangjun [1 ]
Liu, Xiaofei [1 ]
Qiu, Xinni [1 ]
Zhang, Xiaoting [1 ]
Hu, Xiaogang [1 ]
机构
[1] South China Normal Univ, Guangzhou Key Lab Analyt Chem Biomed, Key Lab Theoret Chem Environm, Minist Educ,Sch Chem, Guangzhou, Peoples R China
基金
中国国家自然科学基金;
关键词
Aptamer; AuNPs; In-tube solid-phase microextraction; Adenosine; HPLC; PERFORMANCE LIQUID-CHROMATOGRAPHY; MOLECULARLY IMPRINTED POLYMERS; MASS-SPECTROMETRY; GOLD NANOPARTICLES; NUCLEOSIDES; RECOGNITION; EXTRACTION; FIBER; ASSAY; ELECTROPHORESIS;
D O I
10.1016/j.chroma.2019.460617
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
As an endogenous nucleoside, adenosine was significant for the diagnosis and treatment of some diseases, such as schizophrenia. However, due to the complicated matrix interference, it was difficult to monitor trace or ultra-trace adenosine directly in bio-samples. In this contribution, a novel in-tube SPME technique based on aptamer/Au nanoparticles coated open tubular fused-silica capillary was established to separate and enrich adenosine in bio-samples with high affinity. Therefore, a uniform and dense AuNPs layer was coated on the inner surface of the open tubular capillary, and then adenosine aptamer was immobilized on AuNPs with a high capacity of 2.44 mu g per 27-cm capillary. As a result, the capillary shown high selectivity to adenosine with a selectivity factor of 14.4 when compared with the scrambled aptamer/AuNPs coated capillary. Also, the extraction amount of adenosine was 2.8-24.8 times higher than those of its structural analogs and contrast, such as guanosine, uridine, cytidine, thymidine, and toluic acid. After the optimization of extraction conditions, the aptamer/AuNPs coated in-tube SPME-HPLC method was developed for the adenosine assay with the linear range of 0.002-0.100 mu g mL(-1) and the detection limit of 0.45 ng mL(-1). Subsequently, the approach was applied for trace adenosine monitoring in human serum and urine samples. It showed a strong performance of reducing matrix interference and improving sensitivity, and the spiking recoveries of 89.9-92.6% and 91.1-94.5% were achieved respectively. (C) 2019 Elsevier B.V. All rights reserved.
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页数:10
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