An electrochemical biosensor based on multi-wall carbon nanotube-modified screen-printed electrode immobilized by uricase for the detection of salivary uric acid.

The amounts of uric acid (UA) in non-invasive biological samples, such as saliva, are critical for diagnosis and therapy of gout, hyperuricemia, Lesch-Nyhan syndrome, and several other diseases. Here, disposable UA biosensors were fabricated with the screen printing technique on the substrate of flexible PET. The working electrode was modified with carbon nanotubes followed by uricase for UA detection with excellent selectivity. The biosensor showed good electrocatalytic activity toward UA with high sensitivity, low detection limit, and wide linear range, which covers the full range of UA levels in human saliva. We demonstrate that UA can be directly detected in human saliva with the biosensor and the experimental data were consistent with the clinical analysis. This study indicated that the non-invasive biosensor is an attractive and possible approach for the monitoring of salivary UA. Graphical abstract A disposable uric acid biosensor modified with carbon nanotubes followed by uricase was fabricated on flexible PET and applied for the monitoring of salivary uric acid in human saliva.

Preparation of nanostructured PDMS film as flexible immunosensor for cortisol analysis in human sweat.

This work proposed a novel and flexible immunosensor for highly selective and sensitive determination of cortisol in sweat. The flexible electrode was developed by transferring multi-walled carbon nanotubes (MWCNTs) film on polydimethylsiloxane (PDMS) substrate and subsequent electrochemical deposition of Au nanoparticles (AuNPs) on the MWCNTs surface. The obtained AuNPs/MWCNTs/PDMS electrode was then covalently immobilized with anti-cortisol monoclonal antibody (Anti-Cmab) and blocked with BSA. Scanning electron microscope confirmed that MWCNTs have been firmly combined with PDMS and AuNPs distributed uniformly on the surface of MWCNTs. The PDMS-based sensor possesses a good mechanical stability against stretching, bending and twisting, displaying stable electrochemical performance under deformation. After optimizing the analytical parameters, the developed immunosensor allowed a facile quantification of cortisol in the range of 1 fg/mL-1 µg/mL with a detection limit of 0.3 fg/mL. The cortisol immunosensor was further used to evaluate cortisol levels in human sweat, and the results corresponded closely with commercially available chemiluminescence immunoassay (CLIA) method. Results indicated that the new cortisol immunosensor could provide an effective tool for the noninvasive, point of care measurement of sweat cortisol levels and is promise to be a wearable biosensor for the healthy monitoring.

Determination of salivary uric acid by using poly(3,4-ethylenedioxythipohene) and graphene oxide in a disposable paper-based analytical device.

We developed a paper-based analytical device based on the electropolymerization of poly (3,4-ethylenedioxythipohene) (PEDOT) and graphene oxide (GO) composites on the ITO substrate for the detection of uric acid (UA) in authentic human saliva. Scanning electron microscopy, UV-vis spectrum and X-ray diffraction confirmed the formation of porous PEDOT combined with GO film during the electropolymerization process. The nanocomposite based sensor showed an enhanced electrocatalytic activity toward UA with high sensitivity and stability. We demonstrate that UA can be directly detected in undiluted saliva using the paper-based electroanalytical device with no interference from ascorbic acid and dopamine that are normally present in biological fluids. The results indicated that the developed device is promising for non-invasive monitoring of salivary UA in human body.