Ti3C2Tx-Au hybrid composites-based electrochemical biosensors for calreticulin biomarker detection

被引:4
|
作者
Naz, Gul [1 ]
Salem, Mohamed A. [2 ]
Sharma, Bharat Prasad [3 ,4 ]
Mekkey, Saleh D. [5 ]
Soomro, Razium Ali [6 ]
Karakus, Selcan [7 ]
El-Bahy, Zeinhom M. [5 ]
机构
[1] Tsinghua Univ, Dept Chem, Beijing Key Lab Microanalyt Methods & Instrumentat, Key Lab Bioorgan Phosphorus Chem & Chem Biol, Beijing 100084, Peoples R China
[2] King Khalid Univ, Fac Sci & Arts, Dept Chem, Mohail 61421, Assir, Saudi Arabia
[3] Beijing Univ Chem Technol, Beijing Key Lab Electrochem Proc & Technol Mat, Beijing 100029, Peoples R China
[4] Chinese Acad Sci, Inst Proc Engn, Beijing 100190, Peoples R China
[5] Al Azhar Univ, Fac Sci, Dept Chem, Cairo 11884, Egypt
[6] Beijing Adv Innovat Ctr Soft Matter Sci & Engn, Sch Chem, State Key Lab Chem Resource Engn, Beijing 100029, Peoples R China
[7] Istanbul Univ Cerrahpasa, Fac Engn, Dept Chem, TR-34320 Istanbul, Turkiye
关键词
Breast cancer biomarker; Calreticulin; Immunosensor; MXenes nanosheets; GOLD NANOPARTICLES; BREAST-CANCER; MXENE; SURFACE; PLATFORM;
D O I
10.1016/j.microc.2023.109307
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
A sensitive biosensor is critical for early breast cancer treatment and prognosis. Herein, a label-free electrochemical immunosensor is proposed for the sensitive detection of calreticulin (CALR), a new breast cancer biomarker. The biosensor relied upon an electroactive hybrid of ultra-thin Ti3C2Tx nanosheets preadsorbed with Au NPs and methylene blue (MB)(MB-Ti3C2Tx-Au), which served as redox-active centers and an electroactive probe to detect CALR biomarkers respectively. The detection mechanism followed a simple inhibition strategy, where the optimal differential pulse voltammetry (DPV) response of preadsorbed MB over the Ti3C2Tx-Au electrode decreased in proportion to the concentration of CALR biomarkers owing to the formation of the antibody-antigen immunocomplex. The biosensor could detect CALR-biomarker in the concentration range of 0.0015 to 0.94 ng mL-1 with a limit of detection (LOD) of 0.28 pg mL-1 and showed excellent antifouling properties against commonly encountered biomolecules such as hemoglobin (Ig), immunoglobulin G (IgG), neuron-specific enolase (NSE), and tumor necrosis factor-alpha (TNF). The proposed strategy provides an efficient method for utilizing MXene nanosheets to construct advanced biosensors with promising clinical applications.
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页数:9
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