Autor: |
Mugo SM; Physical Sciences Department, MacEwan University, 10700-104 Avenue, Edmonton, AB, T5J 4S2, Canada. mugos@macewan.ca., Alberkant J; Physical Sciences Department, MacEwan University, 10700-104 Avenue, Edmonton, AB, T5J 4S2, Canada. |
Jazyk: |
angličtina |
Zdroj: |
Analytical and bioanalytical chemistry [Anal Bioanal Chem] 2020 Mar; Vol. 412 (8), pp. 1825-1833. Date of Electronic Publication: 2020 Jan 30. |
DOI: |
10.1007/s00216-020-02430-0 |
Abstrakt: |
A selective cortisol sensor based on molecularly imprinted poly(glycidylmethacrylate-co ethylene glycol dimethacrylate) (poly(GMA-co-EGDMA)) has been demonstrated for detection of cortisol in human sweat. The non-enzymatic biomimetric flexible sweat sensor was fabricated inexpensively by layer by layer (LbL) assembly. The sensor layers comprised a stretchable polydimethylsiloxane (PDMS) base with carbon nanotubes-cellulose nanocrystals (CNC/CNT) conductive nanoporous nanofilms. The imprinted (MIP) poly(GMA-co-EGDMA) deposited on the CNC/CNT was the cortisol biomimetric receptor. Rapid in analyte response (3 min), the cortisol MIP sensor demonstrated excellent performance. The sensor has a limit of detection (LOD) of 2.0 ng/mL ± 0.4 ng/mL, dynamic range of 10-66 ng/mL, and a sensor reproducibility of 2.6% relative standard deviation (RSD). The MIP sensor also had high cortisol specificity and was inherently blind to selected interfering species including glucose, epinephrine, β-estradiol, and methoxyprogestrone. The MIP was four orders of magnitude more sensitive than its non-imprinted (NIP) counterpart. The MIP sensor remains stable over time, responding proportionately to doses of cortisol in human sweat. Graphical abstract. |
Databáze: |
MEDLINE |
Externí odkaz: |
|
Nepřihlášeným uživatelům se plný text nezobrazuje |
K zobrazení výsledku je třeba se přihlásit.
|