Bacterial cellulose composite hydrogel for pre-concentration and mass spectrometric detection of thiol-containing biomarker.

Simple soaking of bacterial cellulose (BC) membrane in carboxymethyl cellulose (CMC) solution yielded BC/CMC hydrogel having re-swellable property. Then, gold nanoparticles (AuNPs) were embedded in the BC/CMC hydrogel via in situ chemical reduction to form BC/CMC/AuNPs composite hydrogel. It was found that the composite hydrogel exhibited physical/chemical characteristics similar to those of BC.

Microfluidic Paper-based Device for Medicinal Diagnosis.

Background: The demand for point-of-care testing (POCT) devices has rapidly grown since they offer immediate test results with ease of use, makingthem suitable for home self-testing patients and caretakers. However, the POCT development has faced the challenges of increased cost and limited resources. Therefore, the paper substrate as a low-cost material has been employed to develop a cost-effective POCT device, known as "Microfluidic paper-based analytical devices (μPADs)".

Non-invasive electrochemical immunosensor for sweat cortisol based on L-cys/AuNPs/ MXene modified thread electrode.

Thread-based electrochemical immunosensor is fabricated for non-invasive detection of cortisol in sweat by immobilization of anti-cortisol on L-cys/AuNPs/MXene modified conductive thread electrode. MXene and AuNPs increase the surface area of conductive thread electrode and facilitate anti-cortisol immobilization leading to enhanced sensor sensitivity. Anti-cortisol is immobilized on L-cys/AuNPs/MXene modified electrode by using 1-ethyl-3-(3-dimethylaminopropyl) carbodiimide and N-hydroxysulfosuccinimide coupling agents.

Enhanced and Selective MALDI-MS Detection of Peptides via the Nanomaterial-Dependent Coffee Ring Effect.

Nanomaterials have been explored as alternative matrices in MALDI-MS to overcome some of the limitations of conventional matrices. Recently, we demonstrated a new means by which nanomaterials can improve peptide ionization and detection in MALDI-MS analyses by exploiting the tendency of nanomaterials to form "coffee rings" upon drying from liquids. In the current work, we investigate how nanomaterial size and composition affect the signal enhancement of peptides through the coffee-ring effect.

Label-free anti-Müllerian hormone sensor based on polyaniline micellar modified electrode.

A label-free electrochemical immunosensor based on polyaniline (PANI) micellar electrode was firstly fabricated for direct AMH detection. To control the size regularity of PANI, a micelle-based method using ammonium peroxydisulfate (APS) as a reducing agent was employed in the polymerization process. The Anti-AMH antibodies were readily immobilized onto PANI via peptide bond to enhance the sensor specificity and sensitivity.

3D paper-based microfluidic device: a novel dual-detection platform of bisphenol A.

A novel platform of microfluidic paper-based analytical devices (μPADs) for dual detection of bisphenol A (BPA), a model analyte, was fabricated using an electronic digital plotter to create the stacked layer of μPADs and generate the lateral-flow channel without using an external pump. Two detection techniques, including electrochemical detection and laser desorption ionization mass spectrometric detection (LDI-MS), were used complementarily to improve the precision in the detection of BPA. The fluid sample was delivered to both detection zones by the capillary action, automatically generated from the fabricated microfluidic device.

Label-free immunosensor based on graphene/polyaniline nanocomposite for neutrophil gelatinase-associated lipocalin detection.

A novel label-free electrochemical immunosensor for neutrophil gelatinase-associated lipocalin (NGAL) detection has been developed. The immunosensor has been constructed by immobilization of NGAL capture antibodies to electropolymerized aniline deposited on top of an electrosprayed graphene/polyaniline (G/PANI) modified screen printed carbon electrode. Electrospraying of G/PANI increases the electrode surface area while electropolymerization of aniline increases the number of amino groups (-NH) for antibody immobilization.