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Yamin Hong,Xiupeng Yue,Yaping Zhang,Kai Shen,Wentao Jiao,Lei Zhao,Beibei Li 대한환경공학회 2023 Environmental Engineering Research Vol.28 No.3
Sulfate radical-based advanced oxidation processes have been applied in the remediation of polycyclic aromatic hydrocarbons (PAHs) contaminated soil, during which sulfate can be activated in different ways. In this work, effects of four different ways (FeSO4, NaOH, H2O2, and Heat) activated sodium persulfate (PS) on PAHs removal and soil physicochemical properties (pH, organic matter, functional groups, surface morphology, and partial heavy metal elements) were compared, and the influencing factors and mechanism of soil PAHs removal by thermally activated PS were also studied. The results showed that at the dosage of 3% of persulfate, the removal efficiency of PAHs followed the sequences of Heat (91.4%) > FeSO4 (86.6%) > H2O2 (86.2%) > NaOH (72.9%). However, thermal activation decreased the soil pH and organic matter content more significantly than other treatments. The reaction tended to reach equilibrium at 6 h when the dosage of persulfate was 3% and the activation temperature was 60 °C, and the reaction obeyed pseudo-first-order kinetics. Through quenching experiments, it was found that the free radicals playing a dominant role in the oxidation process were sulfate radicals. Compared with pH, liquid to soil (L/S ratio) and the temperature had more significant impacts on the degradation efficiency of PAHs.
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Roh, Young Hoon,Lee, Jong Bum,Shopsowitz, Kevin E.,Dreaden, Erik C.,Morton, Stephen W.,Poon, Zhiyong,Hong, Jinkee,Yamin, Inbar,Bonner, Daniel K.,Hammond, Paula T. American Chemical Society 2014 ACS NANO Vol.8 No.10
<P/><P>Antisense oligonucleotides can be employed as a potential approach to effectively treat cancer. However, the inherent instability and inefficient systemic delivery methods for antisense therapeutics remain major challenges to their clinical application. Here, we present a polymerized oligonucleotides (ODNs) that self-assemble during their formation through an enzymatic elongation method (rolling circle replication) to generate a composite nucleic acid/magnesium pyrophosphate sponge-like microstructure, or DNA microsponge, yielding high molecular weight nucleic acid product. In addition, this densely packed ODN microsponge structure can be further condensed to generate polyelectrolyte complexes with a favorable size for cellular uptake by displacing magnesium pyrophosphate crystals from the microsponge structure. Additional layers are applied to generate a blood-stable and multifunctional nanoparticle <I>via</I> the layer-by-layer (LbL) assembly technique. By taking advantage of DNA nanotechnology and LbL assembly, functionalized DNA nanostructures were utilized to provide extremely high numbers of repeated ODN copies for efficient antisense therapy. Moreover, we show that this formulation significantly improves nucleic acid drug/carrier stability during <I>in vivo</I> biodistribution. These polymeric ODN systems can be designed to serve as a potent means of delivering stable and large quantities of ODN therapeutics systemically for cancer treatment to tumor cells at significantly lower toxicity than traditional synthetic vectors, thus enabling a therapeutic window suitable for clinical translation.</P>
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