Glucose and Ethanol Detection with an Affinity-Switchable Lateral Flow Assay.

The lateral flow assay (LFA) is one of the most successful analytical platforms for rapid on-site detection of target substances. This type of assay has been used in many rapid diagnoses, for example, pregnancy tests and infectious disease prevention. However, applications of LFAs for very small molecules remain a demanding challenge due to the problem of obtaining the corresponding binding partners to form sandwich complexes. In this paper, we report an affinity-switchable (AS) LFA (ASLFA) for the rapid and selective detection of hydrogen peroxide (H2O2), glucose, and ethanol in blood serum and urine samples. Unlike classical LFAs, which rely on the "always on" interaction between the antigen and the antibody, the working principle of ASLFA is based on the gold nanoparticle-conjugated AS biotin probe Au@H2O2-ASB, which can be activated by H2O2 for binding with the streptavidin (SA) protein. In the presence of glucose and ethanol, glucose oxidase and alcohol oxidase can react with the substrate to generate H2O2 and thereby activate Au@H2O2-ASB for binding with SA. Therefore, this ASLFA approach can be an alternative for classical glucose and ethanol detection methods in a wide variety of samples, where simple and rapid on-site detection is essential.

Affinity-Switchable Lateral Flow Assay.

Lateral flow assay (LFA) has been a valuable diagnostic tool in many important fields where rapid, simple, and on-site detection is required, for applications such as pregnancy tests and infectious disease prevention. Currently, two types of LFAs are available: lateral flow immunoassay (LFIA) and nucleic acid lateral flow assay (NALFA). Both are generally used for the testing of proteins and nucleic acids. However, enzyme activities and small molecules without the corresponding binding partner cannot be detected by the existing LFAs. In this paper, we introduce a LFA approach termed affinity-switchable lateral flow assay (ASLFA) to overcome the limitations. The detection principle is based on the switchable binding between the affinity-switchable biotin (ASB) probe and avidin protein. In the presence of the target molecule, the activated ASB probe would be captured by the avidin, thereby leaving a distinct test line on the membrane. The ASLFA concept was demonstrated by testing the F ion, NADH cofactor, and nitroreductase activity. Thus, this general ASLFA can be used for the rapid detection of molecules that cannot be accessed by the classical LFAs.

Thermally pressure-induced partial structural phase transitions in core-shell InSb-SiO2 nanoballs/microballs: characterization, size and interface effect.

Core-shell InSb-SiO(2) nanoballs/microballs were synthesized on a Si substrate by carbonthermal reactions at a temperature of 900 °C. High-resolution transmission microscopy (HRTEM) images revealed that the surfaces of the InSb nanoballs/microballs were covered by amorphous SiO(2) layers. On the basis of our theoretical calculation, the thermal expansion coefficient (TEC) of the InSb crystals is ten times higher than that of the SiO(2) shell. Therefore, the SiO(2) serves as a constraining shell for the InSb core so that the compressive stress of ∼-94 MPa can accumulate in the InSb core while a tensile stress of 196 MPa forms in the SiO(2) shell. The thermal excitation accumulated compressive stress in the InSb core, causing a partial structural phase transition from a cubic zinc-blende structure to a hexagonal wurtzite structure. Many lattice defects, such as stacking faults and Moiré fringes, have been observed on the surface of the InSb core. In situ temperature-dependent XRD patterns showed that a reversible InSb hexagonal (002) peak appeared and disappeared as the temperature increased and decreased at a transit point of 200 °C, respectively. As the temperature increased, the XRD diffraction peaks of the InSb wurtzite phase shifted significantly to lower angles because of the formation of compressive stress in the InSb nanoballs. The pressure-induced partial structural phase transitions of the nanostructured InSb occurred at -94 MPa of the compressive stress. This is the first report of this value, which is the lowest value in the pressure-induced phase transition of the nanostructure InSb from the cubic zinc-blende structure to the hexagonal wurtzite structure.