Near-infrared fluorescent probe for sensitive detection and imaging of DNA G4s in living cells.

G-quadruplexs (G4s), four-stranded nucleic acid secondary structures, which formed by guanine-rich sequences play a vital role in human biological systems. Studies have shown that the formation of G4s is closely related to tumor development and apoptosis, which is considered as a new target for the development of anti-tumor drugs. Therefore, it is important to develop novel probes for G4s imaging. In this article, we engineered a near-infrared fluorescent probe (TOH) which can be activated by DNA G4s in living cells and tumor. TOH exhibits high selectivity to the structure of DNA G4s with the limit of detection for DNA G4s (Mito-0.5-2) is calculated to be 0.43 nM. Imaging studies of different cell lines revealed that the brighter fluorescence in cancer cell lines than in normal, indicating that DNA G4s maybe highly express in tumor cell lines. Simultaneously, TOH is also introduced into live tumor tissue imaging and found that the fluorescence intensity of tumor is the brightest relative to normal tissue, further validating the high expression of DNA G4s structures in tumor tissue. These features demonstrate TOH not only have the ability to image DNA G4 structures in real time, but also may have tumor diagnostic capabilities.

Decomplexation of Cu(II)-EDTA by synergistic activation of persulfate with alkali and CuO: Kinetics and activation mechanism.

Heavy metals usually coexist with a variety of chelating agents to form heavy metal complexes in industrial wastewater. The decomplexation of heavy metal complexes is the crucial step before the removal of heavy metals via alkaline precipitation process. An efficient synergistic activation of persulfate (PS) with alkali and CuO was used for the simultaneous decomplexation of Cu-ethylenediamine tetraacetic acid (Cu(II)-EDTA) (3.14 mM) and the Cu(II) precipitation. The experimental results demonstrated that nearly complete removal of Cu(II) could be achieved by synergistic activation of PS with alkali and CuO at pH 11 after 2 h of decomplexation reaction. However, sole PS could not effectively decomplex Cu(II)-EDTA (13.5%), while the alkaline activation of PS could accomplish 57.0% removal of Cu(II). Radical scavenger tests indicated that reactive oxygen species (ROS) including SO4•-, •OH and O2•- were responsible for the decomplexation of Cu(II)-EDTA in the synergistic activation of PS with alkali and CuO. As a heterogeneous activator, CuO possessed excellent reusability and long-lasting catalytic activity and the rate constant value (k) of Cu(II) removal showed an increase (from 0.0326 min-1 in the first cycle to 0.0491 min-1 in the 24th cycle) with 24 cycles experiments. Furthermore, the biotoxicity evaluation of treated solution revealed that the biotoxicity of Cu(II)-EDTA contaminated wastewater could be effectively mitigated by the synergistic activation of PS with alkali and CuO because of the efficient precipitation of Cu(II) and oxidative degradation of EDTA organic ligands, which was favorable for the subsequent biochemical treatment.

The treatment of electroplating wastewater using an integrated approach of interior microelectrolysis and Fenton combined with recycle ferrite.

Heavy metal ions in chelated forms have aroused great concerns because of their high solubility, poor biodegradation and extreme stability. In this research, an efficient strategy, interior microelectrolysis-Fenton-recycle ferrite (IM-Fenton-RF), was developed to treat simulated electroplating wastewater containing chelated copper at room temperature. The decomplexation of chelated copper was carried out by both interior microelectrolysis and Fenton reactions. IM process can not only partly degrade the complexes of chelated copper via the microelectrolysis reaction but also it produces Fe2+ ions for the Fenton reaction. After decomplexation, the IM-Fenton effluent directly flowed into the RF reactor for copper ions removal. Under optimum reaction conditions (reflux ratio = 0.37, Fe2+ concentration = 9.20 g/L at pH 10.18), 99.9% copper was removed by the IM-Fenton-RF system. The produced IM-Fenton-RF sludge is based on ferrite precipitate and has several advantages over metal hydroxides sludge. Ferrite sludge is stable owing to the stability of ferrite's crystal structure, while the toxicity characteristic leaching procedure (TCLP) test meets relevant standards. The sedimentation rate and volume of ferrite sludge were 3.86 times faster and 11.0 times lower than those of metal hydroxides sludge. Furthermore, the yielding sludge of ferrite can be recovered and utilized for the synthesis of Fe-C metallic species, the main compound of IM packing for interior microelectrolysis reaction. All these results show that a combination of IM-Fenton and RF is an effective approach to treat wastewater containing chelated copper, showing great potential for industrial applications.

Remediation of phenanthrene contaminated soil by ferrous oxalate and its phytotoxicity evaluation.

Phenanthrene contaminated soil was remediated by the photochemical process of ferrous oxalate. Without using H2O2 and adjusting soil pH, phenanthrene in contaminated soil was degraded effectively by the ferrous oxalate under visible light irradiation. Ferrous oxalate possesses excellent visible light absorption ability which benefits the degradation of phenanthrene in soil under visible light irradiation. Via the Fe(II)/Fe(III) catalytic cycle of ferrous oxalate, H2O2 and Fe(II) could be produced continuously and H2O2 was further catalyzed by Fe(II) and released hydroxyl radicals (•OH) to degrade the phenanthrene in soil. The dosage of ferrous oxalate, moisture content of soil, and soil thickness were most important factors for degradation of phenanthrene in soil. In addition, a good mixing of ferrous oxalate and soil was vital for enhancing the degradation ratio of phenanthrene. After phenanthrene contaminated soil was treated by ferrous oxalate, the toxicity of treated soil was evaluated via the lettuce cultivation experiments. It was demonstrated the toxicity of phenanthrene contaminated soil was significantly reduced by ferrous oxalate according to the growth indexes of lettuces, including root length, leaf length, and fresh weight. This environment-friendly soil remediation method based on ferrous oxalate has huge potential in the remediation of organic pollutant contaminated soil.

Selective visualization of endogenous hypochlorous acid in zebrafish during lipopolysaccharide-induced acute liver injury using a polymer micelles-based ratiometric fluorescent probe.

The development of effective method for monitoring of endogenous hypochlorous acid (HClO) in vivo is of great significance for early diagnosis of lipopolysaccharide (LPS) induced acute liver injury. Herein, we report a polymer micelles-based ratiometric fluorescent probe (PM) based on the combination of intramolecular charge transfer (ICT) mechanism and fluorescence resonance energy transfer (FRET) principle for selective visualization of endogenous HClO in vivo. Upon the reaction of PM with HClO, the electron-donating thiourea moiety is oxidized and transformed into imidazoline moiety (electron-withdrawing group), resulting in a dramatic blue shift (˃100nm) in the fluorescence emission. The as-prepared PM shows good water dispersibility (100% aqueous media), fast response (<40s), high sensitivity (a detection limit of 1.75nM), and outstanding selectivity toward HClO over other ROS/RNS (50 equiv.). In addition, the vivo imaging experiments demonstrate that PM facilitates the visualization of endogenous HClO generation with LPS induced acute liver injury in zebrafish model.

Fabrication of Water-soluble Fluorescent Polymeric Micelles for Selective Detection of Hg2+ in Blood Serum.

In this study, amphiphilic diblock copolymers were designed and synthesized via the incorporation of reversible addition-fragmentation chain transfer radical polymerization (RAFT) and a subsequent grafting technique. Subsequently, Hg2+-sensitive water-soluble fluorescent polymeric micelles (FNs) were prepared by a reprecipitation strategy. The spectroscopic characteristics demonstrate that the fluorescein isothiocyanate (FITC) was successfully linked into the polymer. Due to the promoted reaction of desulfurization cyclization by Hg2+, the fluorescence of fluorescein in FNs was obviously quenched. The as-prepared FNs showed admirable Hg2+-sensitivity (detection limit: 54 nM), excellent water-solubility and high selectivity. In addition, FNs were successfully used to determine Hg2+ in blood serum. We expected that the as-prepared FNs could perform potential applications in imaging, sensing, and bioanalytic chemistry.

Isolation of a thermostable trypsin inhibitor with exploitable potential.

A novel trypsin inhibitor with considerable thermal and pH stability, designated Glytine, was isolated from seeds of the Chinese black soybean Glycine max (L.) Merr. The purification procedure involved ammonium sulfate precipitation, ion-exchange chromatography on CM-Sephadex C-50, gel filtration chromatography on Sephacryl S-200HR, and gel filtration chromatography on POROS HS-20. The 20 N-terminal amino acid sequences were determined to be DEYSKPCCDLCMCTRRCPPQ, demonstrating close homology with the sequences of leguminous trypsin inhibitors. The molecular mass and isoelectric point of the inhibitor were estimated by SDS-PAGE and isoelectric focusing to be 19.9 kDa and 6.2, respectively. Trypsin could be completely inhibited by Glytine when the weight ratio was 1.5. The inhibitory activity of Glytine was unaffected by exposure to temperatures up to 100 °C, or within the pH range 2-12. Besides trypsin-chymotrypsin inhibition activity, Glytine demonstrated other biological activities including antiproliferative activity against tumor cells including human liver hepatoma cells Bel-7402 and neuroblastoma cells SHSY5Y. In addition, the inhibitor showed antifungal activity against Pythium aphanidermatum, Fusarium oxysporum, Alternaria alternata (Fr.) Keiss, Fusarium solani, and Botrytis cinerea. This study extended research on leguminous trypsin-chymotrypsin inhibitor and suggested exploitable potential.