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Gold Nanocluster-Molybdenum Disulfide Nanosheet Couple-Based Immunoassay Probe for the Selective Detection of Glial Fibrillary Acidic Protein (GFAP)-A Biomarker for Ischemic Stroke
被引:1
|作者:
Varghese, Susan
[1
]
Madanan, Anju S.
[1
]
Abraham, Merin K.
[1
]
Shkhair, Ali Ibrahim
[1
,2
]
Indongo, Geneva
[1
]
Rajeevan, Greeshma
[1
]
Kala, Arathy B. K.
[1
]
George, Sony
[1
,3
]
机构:
[1] Univ Kerala, Sch Phys & Math Sci, Dept Chem, Thiruvananthapuram 695581, Kerala, India
[2] Al Qasim Green Univ, Coll Food Sci, Babylon 51013, Iraq
[3] Univ Kerala, Int Inter Univ Ctr Sensing & Imaging IIUCSI, Thiruvananthapuram 695581, Kerala, India
关键词:
glial fibrillary acidic protein;
ischemicstroke;
fluorescent immunoassay;
gold nanoclusters;
molybdenum disulfide nanosheet;
FLUORESCENT;
DIFFERENTIATION;
D O I:
10.1021/acsanm.4c05607
中图分类号:
TB3 [工程材料学];
学科分类号:
0805 ;
080502 ;
摘要:
Stroke, an incapacitating cerebrovascular catastrophe, imposes significant socio-economic burdens by affecting individuals, families, and society at large. Ischemic stroke (IS) particularly disrupts the cerebral blood flow, causing vascular compromise and neurological impairment. The present study introduces a fluorescence immunoassay platform for detecting glial fibrillary acidic protein (GFAP), a critical marker responsive to IS. Employing molybdenum disulfide nanosheet (MoS2 NS) as a quencher upon GFAP antibody-conjugated bovine serum albumin-capped fluorescent gold nanoclusters (MoS2@Ab@AuNCs), the developed assay demonstrates robust detection capabilities. The platform exhibits a linear detection range from 31.15 to 447.76 pg/mL with a detection limit of 1.30 pg/mL. Selectivity and sensitivity assessments against coexisting biomolecules and ions validate the reliability of the probe. Furthermore, feasibility studies using real serum samples confirm its applicability in clinical settings. Additionally, a paper strip-based, cost-effective platform is introduced for rapid GFAP detection, facilitating broader accessibility and utility.
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