Polydopamine Dots-Based Fluorescent Nanoswitch Assay for Reversible Recognition of Glutamic Acid and Al3+ in Human Serum and Living Cell

被引:38
作者
Ci, Qiaoqiao [1 ]
Liu, Jinhua [1 ,2 ]
Qin, Xiaofei [1 ]
Han, Linqi [1 ]
Li, Hai [1 ]
Yu, Haidong [1 ]
Lim, Kah-Leong [3 ]
Zhang, Cheng-Wu [1 ]
Li, Lin [1 ]
Huang, Wei [1 ,4 ]
机构
[1] Nanjing Tech Univ, NanjingTech, KLOFE, IAM,Jiangsu Natl Synerget Innovat Ctr Adv Mat SIC, 30 South Puzhu Rd, Nanjing 211816, Jiangsu, Peoples R China
[2] Hunan Univ, State Key Lab Chemo Biosensing & Chemometr, Changsha 410082, Hunan, Peoples R China
[3] Natl Univ Singapore, Yong Loo Lin Sch Med, Dept Physiol, Singapore 117593, Singapore
[4] Northwestern Polytech Univ, SIFE, 127 West Youyi Rd, Xian 710072, Shaanxi, Peoples R China
基金
美国国家科学基金会;
关键词
polydopamine dots; nanoswitch assay; reversible recognition; glutamic acid; Al3+; SEMICONDUCTING POLYMER DOTS; SOLUBLE CONJUGATED POLYMERS; INTRACELLULAR DELIVERY; SELF-POLYMERIZATION; SELECTIVE DETECTION; QUANTUM DOTS; NANOPARTICLES; DOPAMINE; EMISSION; SENSOR;
D O I
10.1021/acsami.8b12087
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
We developed a facile and feasible fluorescent nanoswitch assay for reversible recognition of glutamate (Glu) and Al3+ in human serum and living cell. The proposed nanoswitch assay is based on our recently developed method for controlled synthesis of fluorescent polydopamine dots (PDADs) at room temperature with dopamine as the sole precursor. The fluorescence of nanoswitch assay could be quickly and efficiently quenched by Glu (turn-Off), and the addition of Al3+ could recover the fluorescence of the PDADs-Glu system (turn-On). Meanwhile, the reversible recognition of Glu and Al3+ in this nanoswitch system was stable after three cycles. Additionally, the system displayed excellent performance for Glu and Al3+ determination with a low detection limit of 0.12 and 0.2 mu M, respectively. Moreover, PDADs are successfully applied to determine Glu and monitor Al3+ in human serum. Noteworthy, the nanoswitch assay is transported into HepG(2) cells and realized "Off" detection of Glu and "On" sensing Al3+ in the living cells. Therefore, this PDADs-based nanoswitch assay provides a strategy to develop reversible recognition biosensors for intracellular and external molecular analysis.
引用
收藏
页码:35760 / 35769
页数:10
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