A Surface-Enhanced Raman Spectroscopy-Based Biosensor for the Detection of Biological Macromolecules: The Case of the Lipopolysaccharide Endotoxin Molecules

被引:8
作者
Rusciano, Giulia [1 ]
Capaccio, Angela [1 ,2 ]
Sasso, Antonio [1 ]
Capo, Alessandro [2 ]
Almuzara, Carlos Murillo [2 ]
Staiano, Maria [2 ]
D'Auria, Sabato [3 ]
Varriale, Antonio [4 ]
机构
[1] Univ Naples Federico II, Dept Phys E Pancini, I-80126 Naples, Italy
[2] CNR, Inst Food Sci ISA, I-83100 Avellino, Italy
[3] CNR, Dept Biol Agr & Food Sci, I-00185 Rome, Italy
[4] Univ Naples Federico II, Inst Food Sci, Dept Biol, URT,CNR, I-80126 Naples, Italy
基金
欧盟地平线“2020”;
关键词
LPS; SERS; Raman spectroscopy; antibody; biosensor; Nano immunoassay; SCATTERING; EXPOSURE; ANTIGEN;
D O I
10.3390/ijms241512099
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
The development of sensitive methods for the detection of endotoxin molecules, such as lipopolysaccharides (LPS), is essential for food safety and health control. Conventional analytical methods used for LPS detection are based on the pyrogen test, plating and culture-based methods, and the limulus amoebocyte lysate method (LAL). Alternatively, the development of reliable biosensors for LPS detection would be highly desirable to solve some critical issues, such as high cost and a long turnaround time. In this work, we present a label-free Surface-Enhanced Raman Spectroscopy (SERS)-based method for LPS detection in its free form. The proposed method combines the benefits of plasmonic enhancement with the selectivity provided by a specific anti-lipid A antibody (Ab). A high-enhancing nanostructured silver substrate was coated with Ab. The presence of LPS was quantitatively monitored by analyzing the changes in the Ab spectra obtained in the absence and presence of LPS. A limit of detection (LOD) and quantification (LOQ) of 12 ng/mL and 41 ng/mL were estimated, respectively. Importantly, the proposed technology could be easily expanded for the determination of other biological macromolecules.
引用
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页数:12
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