Modulation of assembly and disassembly of a new tetraphenylethene based nanosensor for highly selective detection of hyaluronidase

•The synthesized tetraphenylethene (TPE)-based derivative exhibited weak emission at 580 nm in water.•Hyaluronic acid (HA) induced the emission recovery due to electrostatic interaction.•Fluorescence quenching has been observed in the presence of hyaluronidase (HAase).•Quantitative evaluation of HAa...

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Published inSensors and actuators. B, Chemical Vol. 276; pp. 95 - 100
Main Authors Li, Xiangqian, Zhou, Zhan, Tang, Yiping, Cheng Zhang, Cheng, Zheng, Yuhui, Gao, Jinwei, Wang, Qianming
Format Journal Article
LanguageEnglish
Published Lausanne Elsevier B.V 10.12.2018
Elsevier Science Ltd
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Summary:•The synthesized tetraphenylethene (TPE)-based derivative exhibited weak emission at 580 nm in water.•Hyaluronic acid (HA) induced the emission recovery due to electrostatic interaction.•Fluorescence quenching has been observed in the presence of hyaluronidase (HAase).•Quantitative evaluation of HAase in human urine samples has been realized. The development of nanoprobes with high sensitivity and specificity for tumor marker detection has gained increasing attention in biological applications. Here, we have designed and synthesized a novel 4,4',4”,4”'-(ethene-1,1,2,2-tetrayltetrakis(benzene-4,1-diyl))tetrakis (1-(4-bromobenzyl)pyridin-1-ium) bromide (TPE-4N+) based aggregation induced emission (AIE) fluorescent sensor and it gives rise to electrostatic adsorption towards hyaluronic acid (HA), resulting in an effective emission recovery in yellow-greenish region. In the presence of hyaluronidase (HAase), the enzymatic digestion between HA and HAase induces the fluorescence quenching and this “on-off” change has been analyzed by two consecutive linear equations. The low detection limit is determined to be 0.02 U/mL by quantitative evaluation and its practical application has been verified by detecting human urine samples. It is promising that this new approach can be utilized to study a wide variety of other depolymerization reactions.
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ISSN:0925-4005
1873-3077
DOI:10.1016/j.snb.2018.08.093