Molecular imaging is an essential tool for disease diagnostics and treatment. Direct imaging of low-abundance nucleic acids in living cells remains challenging because of the relatively low sensitivity and insufficient signal-to-background ratio of conventional molecular imaging probes. Herein, we report a class of DNA-templated gold nanoparticle (GNP)-quantum dot (QD) assembly-based probes for catalytic imaging of cancer-related microRNAs (miRNA) in living cells with signal amplification capacity. We show that a single miRNA molecule could catalyze the disassembly of multiple QDs with the GNP through a DNA-programmed thermodynamically driven entropy gain process, yielding significantly amplified QD photoluminescence (PL) for miRNA imaging. By combining the robust PL of QDs with the catalytic amplification strategy, three orders of magnitude improvement in detection sensitivity is achieved in comparison with non-catalytic imaging probe, which enables facile and accurate differentiation between cancer cells and normal cells by miRNA imaging in living cells.

Triangular voltage waveform was employed to distinguish the contributions of dielectric permittivity, electric conductivity and domain switching in current-electric field curves. At the same time, it is shown how those contributions can affect the shape of the electric displacement — electric field loops (D–E loops). The effects of frequency, temperature and microstructure (point defects, grain size and texture) on the ferroelectric properties of several ferroelectric compositions is reported, including: BaTiO 3; lead zirconate titanate (PZT); lead-free Na 0.5 K 0.5 NbO 3; perovskite-like layer structured A 2 B 2 O 7 with super high Curie point (T c ); Aurivillius phase ferroelectric Bi 3.15 Nd 0.5 Ti 3 O 12; and multiferroic Bi 0.89 La 0.05 Tb 0.06 FeO 3. This systematic study provides an instructive outline in the measurement of ferroelectric properties and the analysis and interpretation of experimental data.

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A facile strategy for the fabrication of novel bouquet-shaped magnetic porous nanocomposite via grafting a covalent organic framework (COF, TpPa-1) onto the surface-modified FeO nanoparticles (FeO NPs) was reported. The magnetic TpPa-1 (a COF synthesized from 1,3,5-triformylphloroglucinol (Tp) and p-phenylenediamine (Pa-1)) contains clusters of core-shell magnetic nanoparticles and interconnected porous TpPa-1 nanofibers. Thus, it possesses larger specific surface area, higher porosity, and supermagnetism, making it an ideal sorbent for enrichment of trace analytes. Its performance was evaluated by the magnetic solid-phase extraction (MSPE) of trace polycyclic aromatic hydrocarbons (PAHs) from environmental samples prior to high-performance liquid chromatographic analysis. The results indicated that the magnetic TpPa-1 possessed superior enrichment capacity of such organic compounds.

A facile, economical, and low-toxicity approach was proposed to coat gold nanoparticles (Au NPs) on the surface of graphene-encapsulated magnetic microspheres. The current method makes it possible to integrate Fe 3 O 4 NPs and metal NPs with graphene without any interference or site competition. Dopamine serves as a reducing agent as well as a coupling agent for the assembly of reduced graphene oxide (RGO) and Au NPs on magnetic cores, so that no additional chemicals and thermal treatments are needed. The X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD), and Fourier transform infrared spectroscopy (FTIR) results demonstrate that GO is successfully deoxygenated by the reduction of the PDA layer, while transmission electron microscopy (TEM), scanning electron microscopy (SEM), and inductively coupled plasma mass spectrometry (ICP-MS) results indicate that plenty of Au NPs (about 7.3 nm in diameter) are homogeneously distributed onto the surface of RGO and the Au content of the composite is 13.58 wt%. The high Au content endows the nanocatalyst with great catalytic performance towards the reduction of o-nitroaniline to benzenediamine by NaBH 4 (completely transformation within 4 min). Furthermore, the as-prepared catalyst can be easily recovered and reused at least ten times due to the high magnetization and stability.

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Polydopamine-coated Fe(3)O(4) nanoparticles (Fe(3)O(4)@PDA NPs) were synthesized and applied as matrix for the detection of pollutants by matrix-assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). The synthesis of Fe(3)O(4)@PDA NPs was accomplished in 30 min by in situ polymerization of dopamine without any toxic reagent. Using Fe(3)O(4)@PDA NPs as matrix of MALDI-TOF, eleven small molecule pollutants (molecular weight from 251.6 to 499.3), including Benzo(a)pyrene (BaP), three perfluorinated compounds (PFCs), and seven antibiotics, were successfully detected in either positive or negative reflection mode without background interference. Furthermore, the Fe(3)O(4)@PDA NPs can also enrich trace amounts of hydrophobic target, such as BaP, from solution to nanoparticles surface. Then the Fe(3)O(4)@PDA-BaP can be isolated through magnetic sedimentation step and directly spotted on the stainless steel plate for MALDI measurement. With Fe(3)O(4)@PDA NPs as adsorbent and matrix, we also realized the analysis of BaP in tap water and lake water samples. Thus, a magnetic solid-phase extraction (MSPE)-MALDI-TOF-MS method was established for the measurement of BaP.