A tetracationic aggregation induced emission-based probe for efficient and improved detection of Heparin

肝素 四苯乙烯 化学 鱼精蛋白 荧光 分析物 组合化学 抗凝剂 低分子肝素 生物物理学 聚集诱导发射 生物化学 色谱法 医学 外科 物理 生物 量子力学
作者
Shrishti P. Pandey,Pamela Jha,Dinesh N. Nadimetla,Sheshanath V. Bhosale,Prabhat Kumar Singh
出处
期刊:Sensors and Actuators B-chemical [Elsevier]
卷期号:353: 131016-131016 被引量:18
标识
DOI:10.1016/j.snb.2021.131016
摘要

Designing efficient fluorescent probes with Aggregation Induced Emission (AIE) feature, especially for sensing biologically important analytes, is an intensive area of investigation. Heparin is a well-known blood anticoagulant, and is routinely used as a very important medication in clinical setups. In this contribution, we have utilized a tetraphenylethylene derived AIEgen, named tetrapyridinium-tetraphenylethylene (TPy-TPE), for sensing Heparin. TPy-TPE carries four positive charges and forms aggregates in presence of negatively charged Heparin to generate highly emissive aggregates of TPy-TPE. Most importantly, the tetracationic nature of TPy-TPE provides a stronger binding affinity towards Heparin compared to the previously reported monocationic or dicationic fluorophores. The improved interaction between Heparin and TPy-TPE has proved to be advantageous in terms of improved sensitivity (lower LODs in aqueous and serum samples), higher fluorescence enhancement and better performance in complex matrices. While TPy-TPE is utilized for Heparin determination, its sole U.S. Food and Drug Administration (FDA) authorized antidote, Protamine, and Heparinase, which specifically degrades Heparin to produce clinically important Low Molecular Weight Heparin (LMWH) have also been detected through TPy-TPE molecule. Overall, the photophysical investigation of TPy-TPE for the detection of Heparin is a successful attempt and is expected to enhance Heparin related biosensing research in the biomedical fields.
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