Molecularly Imprinted Polymer Biosensor Based on Nitrogen-Doped Electrochemically Exfoliated Graphene/Ti3 CNT X MXene Nanocomposite for Metabolites Detection

被引:11
作者
Babamiri, Bahareh [1 ]
Sadri, Rad [2 ]
Farrokhnia, Mohammadreza [1 ]
Hassani, Mohsen [1 ,3 ]
Kaur, Manpreet [2 ]
Roberts, Edward P. L. [2 ]
Ashani, Mehdi Mohammadi [4 ]
Nezhad, Amir Sanati [1 ,3 ]
机构
[1] Univ Calgary, Dept Biomed Engn, BioMEMS & Bioinspired Microfluid Lab, Calgary, AB T2N 1N4, Canada
[2] Univ Calgary, Dept Chem & Petr Engn, Calgary, AB T2N 1N4, Canada
[3] Univ Calgary, Dept Mech & Mfg Engn, Calgary, AB T2N 1N4, Canada
[4] Univ Calgary, Dept Biol Sci, 2500 Univ Dr NW, Calgary, AB T2N 1N4, Canada
基金
加拿大健康研究院; 加拿大自然科学与工程研究理事会;
关键词
molecularly imprintedpolymers; MXene@nitrogen-dopedelectrochemical graphene (MXene@N-EEG); biosensor; microfluidics; Prussian blue nanoparticles; metabolitedetection; PRUSSIAN BLUE; AGMATINE; OXIDE; NANOPARTICLES; FACILE; NANOSHEETS; ARGININE; TI3C2TX; VIRUS;
D O I
10.1021/acsami.4c01973
中图分类号
TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Rapid and accurate quantification of metabolites in different bodily fluids is crucial for a precise health evaluation. However, conventional metabolite sensing methods, confined to centralized laboratory settings, suffer from time-consuming processes, complex procedures, and costly instrumentation. Introducing the MXene/nitrogen-doped electrochemically exfoliated graphene (MXene@N-EEG) nanocomposite as a novel biosensing platform in this work addresses the challenges associated with conventional methods, leveraging the concept of molecularly imprinted polymers (MIP) enables the highly sensitive, specific, and reliable detection of metabolites. To validate our biosensing technology, we utilize agmatine as a significant biologically active metabolite. The MIP biosensor incorporates electrodeposited Prussian blue nanoparticles as a redox probe, facilitating the direct electrical signaling of agmatine binding in the polymeric matrix. The MXene@N-EEG nanocomposite, with excellent metal conductivity and a large electroactive specific surface area, effectively stabilizes the electrodeposited Prussian blue nanoparticles. Furthermore, increasing the content of agmatine-imprinted cavities on the electrode enhances the sensitivity of the MIP biosensor. Evaluation of the designed MIP biosensor in buffer solution and plasma samples reveals a wide linear concentration range of 1.0 nM-100.0 mu M (R-2 = 0.9934) and a detection limit of 0.1 nM. Notably, the developed microfluidic biosensor offers low cost, rapid response time to the target molecule (10 min of sample incubation), good recovery results for detecting agmatine in plasma samples, and acceptable autonomous performance for on-chip detection. Moreover, its high reliability and sensitivity position this MIP-based biosensor as a promising candidate for miniaturized microfluidic devices with the potential for scalable production for point-of-care applications.
引用
收藏
页码:27714 / 27727
页数:14
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