A ratiometric Al³⁺ ion probe based on the coumarin-quinoline FRET system

A coumarin-quinoline based fluorescence resonance energy transfer (FRET) system (TCQ) has been synthesized and employed as a ratiometric fluorescence probe. The selective fluorescent response of the probe TCQ toward Al³⁺ was devised by employing a quinoline moiety as a FRET energy donor with a coumarin moiety as an energy acceptor. The quinoline emission at 390 nm decreased and the coumarin emission at 480 nm increased concurrently on addition of Al³⁺ under excitation wavelength at 253 nm. The TCQ probe exhibited high selectivity for Al³⁺ as compared to other tested metal ions and the ratiometric sensing of Al³⁺ was determined by plotting the fluorescence intensity ratio at 480 nm and 390 nm versus Al³⁺ ion concentration. Moreover, test strips based on TCQ were fabricated, which were found to act as a convenient and efficient Al³⁺ ion detection kit. Furthermore, this system has been used for imaging of Al³⁺ in living cells

Characterization of the aggregation-induced enhanced emission of N,N'-bis(4-methoxysalicylide)benzene-1,4-diamine

© 2015 Springer Science+Business Media New York. N,N′-bis(4-methoxysalicylide)benzene-1,4-diamine (S1) was synthesized from 4-methoxysalicylaldehyde and p-phenylenediamine and it was found to exhibit interesting aggregation-induced emission enhancement (AIEE) characteristics. In aprotic solvent, S1 displayed very weak fluorescence, whilst strong emission was observed when in protic solvent. The morphology characteristics and luminescent properties of S1 were determined from the fluorescence and UV absorption spectra, SEM, fluorescence microscope and grading analysis. Analysis of the single crystal diffraction data infers that the intramolecular hydrogen bonding constitutes to a coplanar structure and orderly packing in aggregated state, which in turn hinders intramolecular C-N single bond rotation. Given that the three benzene rings formed a large plane conjugated structure, the fluorescence emission was significantly enhanced. The absolute fluorescence quantum yield and fluorescence lifetime also showed that radiation transition was effectively enhanced in the aggregated state. Moreover, the AIEE behavior of S1 suggests there is a potential application in the fluorescence sensing of some volatile organic solvents

Methyl salicylate 2-O-β-D-lactoside, a novel salicylic acid analogue, acts as an anti-inflammatory agent on microglia and astrocytes

<p>Abstract</p> <p>Background</p> <p>Neuroinflammation has been known to play a critical role in the pathogenesis of Alzheimer's disease (AD). Activation of microglia and astrocytes is a characteristic of brain inflammation. Epidemiological studies have shown that long-term use of non-steroidal anti-inflammatory drugs (NSAIDs) delays the onset of AD and suppresses its progression. Methyl salicylate-2-<it>O</it>-<it>β</it>-<smcaps/><smcaps>D</smcaps>-lactoside (DL0309) is a new molecule chemically related to salicylic acid. The present study aimed to evaluate the anti-inflammatory effects of DL0309.</p> <p>Findings</p> <p>Our studies show that DL0309 significantly inhibits lipopolysaccharide (LPS)-induced release of the pro-inflammatory cytokines IL-6, IL-1β, and TNF-α; and the expression of the inflammation-related proteins iNOS, COX-1, and COX-2 by microglia and astrocytes. At a concentration of 10 μM, DL0309 prominently inhibited LPS-induced activation of NF-κB in glial cells by blocking phosphorylation of IKK and p65, and by blocking IκB degradation.</p> <p>Conclusions</p> <p>We demonstrate here for the first time that DL0309 exerts anti-inflammatory effects in glial cells by suppressing different pro-inflammatory cytokines and iNOS/NO. Furthermore, it also regulates the NF-κB signaling pathway by blocking IKK and p65 activation and IκB degradation. DL0309 also acts as a non-selective COX inhibitor in glial cells. These studies suggest that DL0309 may be effective in the treatment of neuroinflammatory disorders, including AD.</p

Quantum super-cavity with atomic mirrors

We study single-photon transport in an array of coupled microcavities where two two-level atomic systems are embedded in two separate cavities of the array. We find that a single-photon can be totally reflected by a single two-level system. However, two separate two-level systems can also create, between them, single-photon quasi-bound states. Therefore, a single two-level system in the cavity array can act as a mirror while a different type of cavity can be formed by using two two-level systems, acting as tunable "mirrors", inside two separate cavities in the array. In analogy with superlattices in solid state, we call this new "cavity inside a coupled-cavity array" a super-cavity. This supercavity is the quantum analog of Fabry-Perot interferometers. Moreover, we show that the physical properties of this quantum super-cavity can be adjusted by changing the frequencies of these two-level systems.Comment: 13 pages, 9 figure