Title
SERS-based immunoassay for monitoring cortisol-related disorders
Date Issued
01 October 2020
Access level
open access
Resource Type
journal article
Author(s)
Villa J.E.L.
Garcia I.
Jimenez de Aberasturi D.
Pavlov V.
Liz-Marzán L.M.
Universidade Estadual Paulista (UNESP)
Publisher(s)
Elsevier Ltd
Abstract
As a natural response to a stressful situation, the human body produces cortisol. For this reason, cortisol is also called “the stress hormone” and is considered to be the principal stress biomarker. Although cortisol response to stress is essential for survival, abnormal levels in biological fluids may represent serious health risks. In this work, we present a cortisol biosensor which relies on a highly sensitive technique (surface-enhanced Raman spectroscopy, SERS) and a specific recognition (immunoassay). Gold nanostars were used as SERS nanotags, since they provided a better response than nanorods or nanospheres. Using the same concept, two different immunoassay modalities were evaluated, using either magnetic beads or gold-coated glass slides decorated with cortisol antibodies as the capture substrates. The magnetically-assisted SERS immunoassay presented a better performance and was therefore selected to quantify cortisol content in biological fluids (urine and serum). Significant advantages of this assay were found over standard methods such as Ultra Performance Liquid Chromatography-Mass Spectrometry (UPLC-MS) and Enzyme-Linked Immunosorbent Assay (ELISA), including higher sensitivity and repeatability, minimum sample preparation, simplicity, and portability. Therefore, the proposed SERS immunoassay might be implemented as a highly efficient tool for in situ monitoring of human stress levels and cortisol-related disorders (e.g. Cushing's syndrome and Addison's disease).
Volume
165
Language
English
OCDE Knowledge area
Biotecnología médica Inmunología
Scopus EID
2-s2.0-85088114338
PubMed ID
Source
Biosensors and Bioelectronics
ISSN of the container
09565663
Sponsor(s)
The authors would like to thank the Fundação de Amparo à Pesquisa do Estado de São Paulo ( FAPESP – Grant No. 2018/24202-5 and 2014/50945-4 ) for the financial support. Funding by the European Research Council ( ERC-AdG 4D-bioSERS, 787510 ) and the Spanish State Research Agency (Grants MAT2017-86659-R and BIO2017-88030-R ) are gratefully acknowledged. This work was performed under the Maria de Maeztu Units of Excellence Program from the Spanish State Research Agency – Grant No. MDM-2017-0720 . The authors thank Dr. Ana Sánchez Iglesias and Dr. Christian Kuttner for valuable advice regarding colloidal synthesis.
Sources of information: Directorio de Producción Científica Scopus