Fabrication of silica/PVA‑co‑PE nanofiber membrane for oil/water separation

Yuanli Chen,Hui Fan,Xinlin Zha,Wenwen Wang,Yi Wu,Yi Xiong,Kun Yan,Yuedan Wang,Dong Wang 한국의류학회 2021 Fashion and Textiles Vol.8 No.1

High efficiency and anti-pollution oil/water separation membrane has been widely explored and researched. There are a large number of hydroxyl groups on the surface of silica, which has good wettability and can be used for oil-water separation membranes. Hydrophilic silica nanostructures with different morphologies were synthesized by changing templates and contents of trimethylbenzene (TMB). Here, silica nanospheres with radical pores, hollow silica nanospheres and worm-like silica nanotubes were separately sprayed on the PVA-co-PE nanofiber membrane (PM). The abundance of hydroxyl groups and porous structures on PM surfaces enabled the absorption of silica nanospheres through hydrogen bonds. Compared with different silica nanostructures, it was found that the silica/PM exhibited excellent super-hydrophilicity in air and underwater “oil-hating” properties. The PM was mass-produced in our lab through meltextrusion- phase-separation technique. Therefore, the obtained membranes not only have excellent underwater superoleophobicity but also have a low-cost production. The prepared silica/PM composites were used to separate n-hexane/water, silicone oil/ water and peanut oil water mixtures via filtration. As a result, they all exhibited efficient separation of oil/water mixture through gravity-driven filtration.

An Independently Controlled Single-Input-Dual-Output Buck Converter with Coupled Inductor having 1:1 Turns Ratio

Yuwei Liu,Guipeng Chen,Liping Mo,Xinlin Qing 전력전자학회 2019 ICPE(ISPE)논문집 Vol.2019 No.5

Thanks to the favorable advantage of reduced magnetic components, single-inductor multi-output DC-DC converters are attractive in low-cost industrial applications. However, when the converters work in continuous conduction mode (CCM), a severe dynamic cross-regulation problem will occur due to the current multiplex of the same inductor. To solve this problem, an improved single-inputdual-output (SIDO) buck converter is proposed in this paper, which employs one coupled inductor with 1:1 turns ratio as a substitution for the inductor. In the proposed converter, the two output voltages can be controlled independently while the advantage of fewer magnetic cores is retained. Moreover, reduced number of semiconductor components is achieved, leading to a lower cost. Besides, because of the 1:1 turns ratio, the magnetizing current is also effectively decreased to the one output current rather than the sum of two output currents, which will reduce the volume of magnetic core.

Enhanced Selectivity for Oriented Catalyzing Tetracycline by the Functional Inorganic Imprinted ZnFe2O4@Ag3PO4/SiO2 Photocatalyst with Excellent Stability

Ziyang Lu,Zehui Yu,Minshan Song,XINLIN LIU,Yang Liu,Yongsheng Yan,Pengwei Huo,Hongjun Dong,Fei Chen,Song Han 성균관대학교(자연과학캠퍼스) 성균나노과학기술원 2019 NANO Vol.14 No.1

A novel functional inorganic imprinted ZnFe2O4@Ag3PO4/SiO2 photocatalyst was synthesized by a facile sol–gel method combined with the surface imprinting technique, which possessed excellent stability. By optimizing the amount of materials, we determine the preferable addition amounts of tetraethoxysilane (TEOS) and tetracycline to be 0.06 mL and 0.06 g, respectively. This as-prepared functional inorganic imprinted ZnFe2O4@Ag3PO4/SiO2 photocatalyst was proved to not only exhibit high photocatalytic activity (the photodegradation rate was 61.52% under the simulated sunlight irradiation of 60 min), but also possess a strong oriented ability to selectively recognize and photocatalyze tetracycline (the coeficient of selectivity (k selectivity) was 5.14 for ciprofloxacin and 3.63 for gatifloxacin). Moreover, the functional inorganic imprinted ZnFe2O4@Ag3PO4/SiO2 photocatalyst prepared with SiO2 as the inorganic imprinted layer has good stability and can be recycled many times. This work not only puts forward a novel design idea of functional semiconductor materials but also is expected to be widely applied to the oriented catalysis for a target substance according to the practical requirement.

Identification and functional prediction of long non-coding RNAs related to oxidative stress in the jejunum of piglets

Li Jinbao,Zhang Jianmin,Jin Xinlin,Li Shiyin,Du Yingbin,Zeng Yongqing,Wang Jin,Chen Wei 아세아·태평양축산학회 2024 Animal Bioscience Vol.37 No.2

Objective: Oxidative stress (OS) is a pathological process arising from the excessive production of free radicals in the body. It has the potential to alter animal gene expression and cause damage to the jejunum. However, there have been few reports of changes in the expression of long noncoding RNAs (lncRNAs) in the jejunum in piglets under OS. The purpose of this research was to examine how lncRNAs in piglet jejunum change under OS. Methods: The abdominal cavities of piglets were injected with diquat (DQ) to produce OS. Raw reads were downloaded from the SRA database. RNA-seq was utilized to study the expression of lncRNAs in piglets under OS. Additionally, six randomly selected lncRNAs were verified using quantitative real-time polymerase chain reaction (qRT‒PCR) to examine the mechanism of oxidative damage. Results: A total of 79 lncRNAs were differentially expressed (DE) in the treatment group compared to the negative control group. The target genes of DE lncRNAs were enriched in gene ontology (GO) terms and Kyoto encyclopedia of genes and genomes (KEGG) signaling pathways. Chemical carcinogenesis-reactive oxygen species, the Foxo signaling pathway, colorectal cancer, and the AMPK signaling pathway were all linked to OS. Conclusion: Our results demonstrated that DQ-induced OS causes differential expression of lncRNAs, laying the groundwork for future research into the processes involved in the jejunum’s response to OS.

MicroRNA-200a Targets Cannabinoid Receptor 1 and Serotonin Transporter to Increase Visceral Hyperalgesia in Diarrhea-predominant Irritable Bowel Syndrome Rats

( Qiuke Hou ),( Yongquan Huang ),( Changrong Zhang ),( Shuilian Zhu ),( Peiwu Li ),( Xinlin Chen ),( Zhengkun Hou ),( Fengbin Liu ) 대한소화기기능성질환·운동학회(구 대한소화관운동학회) 2018 Journal of Neurogastroenterology and Motility (JNM Vol.24 No.4

Background/Aims MicroRNAs (miRNAs) were reported to be responsible for intestinal permeability in diarrhea-predominant irritable bowel syndrome (IBS-D) rats in our previous study. However, whether and how miRNAs regulate visceral hypersensitivity in IBS-D remains largely unknown. Methods We established the IBS-D rat model and evaluated it using the nociceptive visceral hypersensitivity test, myeloperoxidase activity assay, restraint stress-induced defecation, and electromyographic (EMG) activity. The distal colon was subjected to miRNA microarray analysis followed by isolation and culture of colonic epithelial cells (CECs). Bioinformatic analysis and further experiments, including dual luciferase assays, quantitative real-time polymerase chain reaction, western blot, and enzyme-linked immunosorbent assay, were used to detect the expression of miRNAs and how it regulates visceral hypersensitivity in IBS-D rats. Results The IBS-D rat model was successfully established. A total of 24 miRNAs were differentially expressed in the distal colon of IBS-D rats; 9 were upregulated and 15 were downregulated. Among them, the most significant upregulation was miR-200a, accompanied by downregulation of cannabinoid receptor 1 (CNR1) and serotonin transporter (SERT). MiR-200a mimic markedly inhibited the expression of CNR1/SERT. Bioinformatic analysis and luciferase assay confirmed that CNR1/SERT are direct targets of miR-200a. Rescue experiments that overexpressed CNR1/SERT significantly abolished the inhibitory effect of miR-200a on the IBS-D rats CECs. Conclusions This study suggests that miR-200a could induce visceral hyperalgesia by targeting the downregulation of CNR1 and SERT, aggravating or leading to the development and progression of IBS-D. MiR-200a may be a regulator of visceral hypersensitivity, which provides potential targets for the treatment of IBS-D. (J Neurogastroenterol Motil 2018;24:656-668)

Lactobacillus casei LC01 Regulates Intestinal Epithelial Permeability through miR-144 Targeting of OCLN and ZO1

( Qiuke Hou ),( Yongquan Huang ),( Yan Wang ),( Liu Liao ),( Zhaoyang Zhu ),( Wenjie Zhang ),( Yongshang Liu ),( Peiwu Li ),( Xinlin Chen ),( Fengbin Liu ) 한국미생물 · 생명공학회 2020 Journal of microbiology and biotechnology Vol.30 No.10

Our previous report determined that miR-144 is a key regulator of intestinal epithelial permeability in irritable bowel syndrome with diarrhea (IBS-D) rats. Recent evidence has shown that lactobacilli play an important role in the relief of IBS-D symptoms. However, few studies have addressed the mechanisms by which microRNAs and lactobacilli exert their beneficial effects on intestinal epithelial permeability. Hence, to elucidate whether miRNAs and lactobacilli play roles in intestinal epithelial barrier regulation, we compared miRNA expression levels in intestinal epithelial cells (IECs) under Lactobacillus casei (L. casei LC01) treatment. IECs and L. casei LC01 were co-cultured and then subjected to microRNA microarray assay. qRT-PCR, western blot and ELISA were used to detect the expression of occludin (OCLN) and zonula occludens 1 (ZO1/TJP1). The interaction between miRNAs and L. casei LC01 acting in IECs was investigated through transfection of RNA oligoribonucleotides and pcDNA 3.1 plasmid. The results are as follows: 1) L. casei LC01 decreased the expression of miR-144 and FD4 and promoted OCLN and ZO1 expression in IECs; 2) L. casei LC01 enhanced the barrier function of IECs via downregulation of miR-144 and upregulation of OCLN and ZO1; 3) Under L. casei LC01 treatment, OCLN and ZO1 overexpression could partially eliminate the promoting effect of miR-144 on intestinal permeability in IECs. Our results demonstrate that L. casei LC01 regulates intestinal permeability of IECs through miR-144 targeting of OCLN and ZO1. L. casei LC01 can be a possible therapeutic target for managing dysfunction of the intestinal epithelial barrier.