Various patterns in dielectric barrier glow discharges simulated by a dynamic model

In this paper, various patterns of dielectric barrier glow discharge simulated by a phenomenological dynamic model are reported.The model is constructed based on the basic dynamic process of dielectric barrier glow discharge and involves the voltage-transfer characteristic as well as the lateral inhibition effect.In simulations, different driving voltage profiles are applied to achieve one or two pulsed discharges in each half-period and the corresponding pattern evolution is investigated.The final stable patterns driven by a rectangular wave voltage organize simply as stationary striations or hexagonal lattices.The patterns driven by a multi-step wave appear to be much more complicated, with complementary striations,concentric rings and square superlattices observed.The evolutions of these patterns from the initial uniform state are described and it is found that the spreading of the inhibition effect plays a key role in these evolutions.The numerical simulations in the present work are in excellent accordance with previous experiments and fluid modeling.This dynamic model proves to be a convenient and promising approach to reproducing different pattern structures and pattern evolutions in dielectric barrier glow discharge systems.

In-situ and one-step preparation of protein film in capillary column for open tubular capillary electrochromatography enantioseparation

In this wo rk,the phase-transitioned BSA(PTB)film using the mild and fast fabrication process adhered to the capillary inner wall uniformly,and the fabricated PTB film-coated capillary column was applied to realize open tubular capillary electrochromatography(OT-CEC)enantioseparation.The enantioseparation ability of PTB film-coated capillary was evaluated with eight pairs of chiral analytes including drugs and neurotransmitters,all achieving good resolution and symmetrical peak shape.For three consecutive runs,the relative standard deviations(RSD)of migration time for intra-day,inter-day,and column-tocolumn repeatability were in the range of 0.3%-3.5%,0.2%-4.9%and 2.1%-7.7%,respectively.Moreover,the PTB film-coated capillary column ran continuously over 300 times with high separation efficiency.Therefore,the coating method based on BSA self-assembly supramolecular film can be extended to the preparation of other proteinaceous capillary columns.

Recent advances in DNA glycosylase assays

Genomic deoxyribonucleic acid(DNA)is selected as the ideal carrier for preserving and transmitting the genetic information over the course of evolution.However,the genomic DNA is constantly exposed to various endogenous and environmental threats,causing a diversity of damaged bases,lesions,mismatches and base-pair modifications in the genome,eventually leading to genomic instability and cancers.Base excision repair(BER)is the most important repair mechanism,repairing a variety of DNA damages arising from oxidation,alkylation,methylation,deamination,and hydrolysis reactions.DNA glycosylases are responsible for initiating the first step of the BER pathway through cleaving the N-glycosidic bond between the damaged base and the DNA backbone.However,abnormal DNA glycosylases are associated with a variety of diseases such as cancer,cardiovascular disease,neurological disease and inflammation,suggesting the important role of DNA glycosylases in cancer diagnosis and treatment.Therefore,it is highly desirable to monitor the activity of DNA glycosylases,gaining a deep understanding of the restoration process of damaged DNA and clinical diagnosis.Recently,a series of novel DNA glycosylases detection methods with excellent performance have been developed.In this minireview,we summarize the recent advances in DNA glycosylase assays including amplification-free assay and amplification-assisted assay.Firstly,a brief introduction of amplification-free assay for DNA glycosylase is given.Then,amplification-assisted assays for DNA glycosylases are discussed in detail.Ultimately,the conclusion and prospects of the directions of DNA glycosylase assays are provided.