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Tropical Medicine and Infectious Disease · 2023 ·Vol. 8 ·期 2 ·105 · IF 2.9

A Rapid and Sensitive Detection of HIV-1 with a One-Pot Two-Stage Reverse Transcription Recombinase Aided Real-Time PCR Assay

Fengyu Tian,Cong Jin,Shangzhi Ji,Yanqing Tie,Guohao Fan,Ruiqing Zhang,Yehuan Zheng,Xinxin Shen,Xuejun Ma,Zhishan Feng

Human immunodeficiency virus 1 (HIV-1) attacks the immune system, making people susceptible to various diseases, thus increasing their risk of death. Comprehensive detection of major HIV-1 strains circulating in China is vital for effective HIV-1 infection prevention and treatment. HIV-1 nucleic acid detection is considered effective for HIV-1 diagnosis since traditional immunological testing may fail to detect HIV-1 infection during the window period. This work demonstrates a one-pot two-stage amplification assay (RT-RAP), a combination of reverse transcription recombinase (RT- RAA), and quantitative real-time polymerase chain reaction (qRT-PCR). The turn-around time of the assay is only 50 min and can be performed with commonly available laboratory equipment, the qPCR devices. The RT-RAP assay could detect approximately 5 and 14 copies/reaction of HIV-1 DNA and RNA using recombinant plasmids and standard reference strains, respectively. Additionally, we found that the clinical performance of RT-RAP (detected 169 samples out of 170 specimens) was consistent with that of qRT-PCR. The sensitivity and specificity of RT-RAP were 100.00% (99/99) and 98.59% (70/71), respectively, while its positive and negative predictive values were 99.00% (99/100) and 100.00% (70/70), respectively. The total coincidence rate of the RT-RAP was 99.41% (169/170), with a kappa value of 0.988 (p< 0.05). We demonstrated that RT-RAP could rapidly detect the common HIV-1 subtypes commonly circulating in China with comparable sensitivity and specificity to qRT-PCR.Keywords:HIV-1;RT-RAA;qRT-PCR;clinical detection

CAS / MDL: 629-97-0
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Theranostics · 2022 · IF 11.6

Sequentially targeting and intervening mutual Polo-like Kinase 1 on CAFs and tumor cells by dual targeting nano-platform for cholangiocarcinoma treatment

Yue Zhou,Lei Xu,Zhangding Wang,Hongwen Liu,Xiang Zhang,Chuanjun Shu,Meng Zhang,Ting Wang,Xinyun Xu,Xiaohong Pu,Jian He,Pin Wang,Yudong Qiu,Guifang Xu,Xiaoping Zou,Yun Zhu,Lei Wang

Rationale : Synergistic treatment strategies for two or more drugs have gradually developed as the main options in clinics for cholangiocarcinoma (CCA) owing to the complicated crosstalk between the tumor and stroma. However, the different synergetic mechanisms pose great challenges to the dosages and order of administration of drugs. Thus, a strategy for exploring and intervening in mutual targets derived from stromal cells and cholangiocarcinoma cells was proposed. Methods : Genes with overexpression patterns in tumors and displaying a significant association with overall survival were identified from RNA-seq data of human CCA patients and CCA mouse models. Western blotting, qRT-PCR, immunofluorescence (IF), colony formation and flow cytometry assays were conducted to determine the biological roles of the key oncogene in cholangiocarcinoma and stromal cells respectively. Additionally, a dual-targeting drug delivery system (AA-HA-ODA) for cancer-associated fibroblasts (CAFs) and tumor cells was constructed to verify the effectiveness of intervening the screened genes in vivo . Results : Polo-like kinase 1 (PLK1) was verified to play vital role in the malignant proliferation of CCA by regulating the cell cycle pathway. PLK1 also decreased stromal production by regulating the CAF phenotype. In addition, a PLK1 inhibitor (Ro3280) loaded dual-targeting drug delivery system (AA-HA-ODA) was prepared and exhibited high affinity for CAFs and cholangiocarcinoma cells. The in vivo distribution pattern and antitumor efficacy of AA-HA-ODA/Ro also verify the effectiveness of inhibiting PLK1 in CCA in vivo . Conclusion : In summary, PLK1 is a mutual target derived from tumor cells and stroma due to its crucial role in the proliferation of tumor cells and stroma regulation in CAFs, which might provide enlightenment for multitarget treatment strategies and guidance for clinical cholangiocarcinoma treatment.

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CHEMICAL ENGINEERING JOURNAL · 2022 · IF 16.744

Hierarchically Z-scheme photocatalyst of {0 1 0}BiVO4/Ag/CdS with enhanced performance in synergistic adsorption-photodegradation of fluoroquinolones in water

Boqiang Gao,Yu Pan,Qianqian Chang,Zhonghua Xi,Hu Yang

In this work, the sheet-like BiVO 4 with a higher exposure ratio of {0   1   0} facets was synthesized by the addition of TiCl 3 , and the ratio of (0   4   0)/(0   1   1) on {0   1   0}BiVO 4 was 2.85 times higher than that of normal decahedral BiVO 4 . Accordingly, the {0   1   0}BiVO 4 /Ag/CdS all-solid-state Z-scheme heterojunction was further constructed by photoreduction of Ag and chemical deposition of CdS on the well prepared {0   1   0}BiVO 4 successively. The performance and mechanism of {0   1   0}BiVO 4 /Ag/CdS in synergistic adsorption-photodegradation of fluoroquinolones (FQs) from water were investigated in detail. The adsorption-photodegradation could be divided into three processes: adsorption, surface degradation, and solution degradation, with the rate constants of 0.118, 0.029, and 0.012 min −1 , respectively. Accordingly, the adsorption was a rapid process due to the combined CdS in this composited photocatalyst had a high affinity to FQs to achieve an adsorption equilibrium on the surfaces<30.0 min. Besides, {0   1   0}BiVO 4 /Ag/CdS had a better separation efficiency of photogenerated electron-hole pairs than BiVO 4 /Ag/CdS, because the enriched {0   1   0} facets of {0   1   0}BiVO 4 caused more BiVO 4 /Ag/CdS ternary structure formed, and>90% photodegradation efficiency for five FQs ( C 0  = 0.062 mmol/L) was thus obtained within 60.0 min. The radical trapping and EPR results showed that holes and superoxide radicals were the main active species for FQs photodegradation. In summary, {0   1   0}BiVO4/Ag/CdS achieved an enhanced performance in synergistic adsorption and photodegradation of organic contaminants from water, and a talented photocatalyst was thus provided in water and wastewater treatment.

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Journal of Environmental Chemical Engineering · 2022 · IF 7.968

Molecularly imprinted polymer capped Au@HKUST−1 nanocapsules-based electrochemical sensing platform for monitoring isoproturon herbicide in water at sub−nanomole level

Xian Liu,Like Chen,Yibo Gao,Jiebin Li,Junyong Sun,Tian Gan

In this context, an innovative design of a molecularly imprinted polymer (MIP) capped Au@HKUST− 1 nanocapsules−based electrode was described for highly sensitive and selective detection of isoproturon herbicide. The Au@HKUST− 1 nanocapsules were constructed by in−situ growth of nanoscaled HKUST− 1 crystals on Cu 2 O core materials and subsequent encapsulation of Au nanoparticles inside the hollow HKUST− 1 walls via galvanic replacement reaction between AuCl 4 − and Cu 2 O. After a further surface imprinting−directing polymerization process in the presence of hydrophobic Au@HKUST− 1, a high−performance electrochemical sensing platform was obtained and used for recognition and quantification of isoproturon. Under the optimal experimental conditions, a linear relationship was observed covering the linear range of 0.0010 − 45 μM with an ultra−low detection limit of 0.45 nM. In addition, the Au@HKUST− 1 @MIP modified electrode had higher sensing specificity for isoproturon in the application of water samples with recoveries in the range of 99.07 − 105.8% and a relative standard deviation of < 4%.

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ORGANIC PROCESS RESEARCH & DEVELOPMENT · 2022 · IF 3.858

Efficient Synthesis of (S)-1-Boc-3-aminopiperidine in a Continuous Flow System Using ω-Transaminase-Immobilized Amino-Ethylenediamine-Modified Epoxide Supports

Xiangxiang Wang,Youyu Xie,Zhicai Wang,Ke Zhang,Hualei Wang,Dongzhi Wei

We developed a continuous flow system using ω-transaminase covalently immobilized on an epoxy resin modified with ethylenediamine (EDA) to synthesize (S)-1-Boc-3-aminopiperidine, which is a key intermediate for several novel inhibitors. A second functional group (−NH3+) was introduced to rapidly adsorb ω-transaminase, which was further rigidified by multipoint covalent attachment to the modified resin with high binding efficiency (>95%) and activity recovery (75%). The resulting immobilized ω-transaminase was stable with 90% residual activity after 15 reuse cycles. We synthesized (S)-1-Boc-3-aminopiperidine using this continuous flow system, and 95% conversion was obtained within 10 min of residence. The system was continuously operated for 24 h and achieved a space–time yield of 930.73 g·L–1·day–1, indicating outstanding reaction efficiency. This efficient continuous bioprocess has potential for large-scale production of (S)-1-Boc-3-aminopiperidine.

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FUEL · 2022 · IF 8.035

Fabrication of Cu (1 0 0) facet-enhanced ionic liquid/copper hybrid catalysis via one-step electro-codeposition for CO2ER toward C2

Lili Gao,Langlang Qin,Haonan Wu,Xuelian Li,Kai Qi,Qun Yi,Jiandong Zhang,Lijuan Shi

Electrochemical reduction of CO 2 (CO 2 ER) to high value-added multicarbon (C 2+ ) is a viable way to promote carbon–neutral cycle. To date, copper (Cu) is reported as the most effective metal catalyst toward C 2+ , but it remains a challenge to achieve high selectivity and large current density. Incorporating ionic liquid in Cu-based catalysis has been proved an effective strategy, however, most reported methods are either involved too much ionic liquid (IL) as electrolyte or too complex & unstable. Herein, an ionic liquid-embedded Cu electrocatalyst (Cu-IL/GDL) was innovatively constructed through one-step electro-codeposition method, in which a kind of amino-ionic liquid, AFIL, was anchored to the gas diffusion layer (GDL) and embedded by the deposited Cu. Under the excellent synergy between Cu and AFIL, Cu-IL/GDL exhibits higher faradaic efficiency toward ethylene (C 2 H 4, 40.67%) and C 2 (C 2 H 4 and C 2 H 5 OH, 61.39%) when directing CO 2 to carbon-fiber side of electrode in H-cell. To be precise, more Cu (1   0   0) facet is stabilized by the capping effect of AFIL, being in favor for C–C coupling; meanwhile more AFIL + is embedded by the deposited Cu, making for the initiation of CO 2 ER. Thus, this paper proposes a facial and effective strategy to reinforce Cu (1   0   0) facet, and couple and heighten the virtues of ionic liquid and Cu during CO 2 ER toward C 2 .

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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

From normal crosslinking to core–shell structure: Improved performance of β-cyclodextrin based adsorbent toward efficient separation of acetophenone and 1-phenylethanol

Dongli Li,Zhaoqiang Zhang,Liqin Zhou,Youquan Zhang,Zhenxia Zhao,Fang Shen,Xingzhen Qin,Kungang Chai,Hongbing Ji

To efficiently separate acetophenone (AP) and 1-phenyethanol (PE) from petrochemical by-product, we herein report a novel feasible strategy to fabricate β-cyclodextrin (β-CD) based core–shell microsphere, which retains the cage-type crystal structure of β-CD and superior affinity to AP over PE. Using triphenylmethane-4,4′,4′'-triisocyanate (TTI) as monomer, the polymeric TTI shell can grow in-situ on the surface of β-CD particles, giving the core–shell structured CD@PTTI. The unique β-CD core and polymeric TTI shell structure was verified by a series of characterization methods. CD@PTTI-3 exhibits both high AP uptake (ca. 2.07 mmol·g −1 ) and AP/PE selectivity (ca. 7.2), outperforming the conventional TTI cross-linked amorphous β-CD polymer (TTI-CDP). The adsorption behavior of CD@PTTI-3 on AP and PE single-component solutions was investigated by batch adsorption experiments. Based on the experimental and theoretical results, a mechanism of competitive adsorption of AP and PE on CD@PTTI-3 involving host–guest inclusion, hydrogen bonding and π-π stacking is proposed. Furthermore, intense competition between AP and PE on CD@PTTI-3 was observed in column breakthrough experiments, and CD@PTTI-3 could purify AP from 77.16% to 93.6% by a single adsorption–desorption process.

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Arabian Journal of Chemistry · 2022 · IF 6.212

Preparation of a novel biodegradable film by co-fermentation of straw and shrimp shell with Aureobasidium pullulans and Photobacterium sp. LYM-1

Xiaohong Yu,Mian Wang,Yiwen Zhang,Xiaochen Liu,Xiaoyang Zhang,Jinbin Liu,Dujun Wang,Wenbin Jin,Yongmei Lyu

The green and high-value recycling of shrimp shell and straw remains a worldwide problem. This study aimed to investigate the potential utilization of a fermentation broth (FB) which contains shrimp shell and straw as a new source for preparation of biodegradable films. Aureobasidium pullulans and Photobacterium sp. LYM-1 were used in the fermentation. The cellulase activity was 115.92 U/mL and chitinase activity was 17.89 U/mL in FB. The polysaccharides concentration in FB was 1.05 mg/mL after 7 days of fermentation. An eco-friendly PVA-reinforced FB biodegradable film (FBBF) was successfully prepared and the effect of different plasticizers and surfactants on the mechanical, structural, and impermeability properties of the film was determined. The formation of new bonds between PVA and FB was proved by FTIR spectroscopy. The FBBF containing 0.25 % ( w/v ) glycerol and 0.01 % ( v/v ) tween-20 showed better strength properties. Elongation and water-swelling properties were highly improved by adding 0.2 % ( m/v ) citric acid. According to FE-SEM images, the smooth and tight surface of citric acid added FBBF was observed. Interestingly, the FBBF film showed good heat/moisture capacity, antifungal, and degradation properties. This report reveals a new green, and high-value recycling of straw and shrimp shell by the co-fermentation with A. pullulans and Photobacterium sp. LYM-1. It is also a novel way for the preparation of biodegradable film.

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Frontiers in Immunology · 2022 · IF 8.786

Baicalin Induces a Potent Innate Immune Response to Inhibit Respiratory Syncytial Virus Replication via Regulating Viral Non-Structural 1 and Matrix RNA

Qin Sheng,Huang Xianzhang,Qu Shaogang

Respiratory syncytial virus (RSV) infection is the most frequent cause of hospitalization in pediatric patients. Current systemic treatment and vaccines are not curative and re-infection is often associated with a more drastic incidence of the disease. Baicalin is a flavonoid isolated from Scutellaria baicalensis with potent anti-viral characteristics, namely against RSV. However, its precise mechanism of action remains unclear. Here, using in vitro methods and an in vivo murine model of RSV infection, we showed that baicalin inhibits RSV replication induces translational upregulation of type I interferons (IFNs), IFN-α and IFN-β, and reverses epithelial thickening in lung tissues. Moreover, baicalin inhibits transcription of the RSV non-structural proteins NS1 and NS2. Molecular docking and surface plasmon resonance-based affinity analysis showed that baicalin also binds to the α3 helix of the NS1 protein with an affinity constant of 1.119 × 10−5 M. Polysome profiling showed that baicalin inhibits translation of the RSV matrix protein (M) RNA. Baicalin mediates increased release of the ribosomal protein L13a from the large ribosomal subunit, where the extra ribosomal subunit L13a inhibits M RNA translation. These results comprehensively establish the multiple mechanisms by which baicalin induces a potent innate immune response against RSV infection.

CAS / MDL: 21967-41-9
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JOURNAL OF CATALYSIS · 2022 · IF 8.047

Selective conversion of 2-methylfuran to 3-acetyl-1-propanol in water over Pd@HZSM-5 catalyst with balanced metal-acid cooperation

Xin-Xin Fu,Jian-Peng Li,Zhuo-Qian Li,Yan Liu,Chen-Xiao Feng,Hai-Yang Wang,Zhi-Peng Zhao,Qiao-Yun Liu,Zhong-Yi Liu,Zhi-Kun Peng

Biomass is a promising renewable carbon resource, and bio-based platform molecules such as furan derivatives play an important role in the green manufacturing of high value-added chemicals. Of these, the conversion of 2-methylfuran (2-MF) to 3-acetyl-1-propanol (3-AP) over a bifunctional catalyst has attracted significant interest. However, bifunctional catalysts prepared by traditional method suffer from poor catalytic performance and limited stability due to the agglomeration of metal NPs. Here, Pd@HZSM-5, in which Pd NPs were encapsulated in HZSM-5 in situ showed improved stability and 3-AP yield. The highest yield of 3-AP (90.6%) to date was obtained with a nearly 100% conversion of 2-MF. The catalytic performance over a series of Pd@Zeolite confirms the superiority of the encapsulation effect, which is ascribed to the optimal adjustment of metal/acid balance. The Pd@HZSM-5 catalyst displayed excellent stability due to the encapsulation structure, which restricts the Pd NPs agglomeration. The highest yield of 3-AP was obtained at a high concentration of 2-MF (60%), which implies a promising strategy for the green industrial manufacture of 3-AP. This work reports a new bifunctional catalytic system for the green synthesis of 3-AP from 2-MF, thus stimulating the downstream biomass market.

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Frontiers in Pharmacology · 2022 · IF 5.988

Therapeutic Effect of Ultrasound Combined With Porous Lipid Clioquinol/PLGA Microbubbles on Ferroptosis in HL-1 Cardiac Cell Induced by Isoproterenol Attack

Nana Li,Lei Dong,Yuanyuan Shen,Yongling Wang,Liansheng Chang,Hongwei Wu,Yuqiao Chang,Menghao Li,Dan Li,Zhaoyi Li,Mei He,Cheng Li,Yao Wei,Haiqin Xie,Feng Wang

In recent years, studies have shown a close relationship between cardiomyocyte death and ferroptosis. Clioquinol (CQ) can inhibit ferroptosis. Porous lipid-poly (lactic-co-glycolic acid) (PLGA) microbubbles (MBs) were prepared by double emulsification (W 1 /O/W 2 ) using 1,2-dioctadecanoyl-sn-glycero-3-phophocholine and PLGA as raw materials. Porous lipid-PLGA MBs were used as carriers to prepare CQ/PLGA MBs containing CQ. CQ/PLGA had the advantages of high drug loading, good biocompatibility, and sustained release. Our results showed that CQ/PLGA improved the effect of CQ and reduced its cytotoxicity. Under low-frequency ultrasound with certain parameters, CQ/PLGA showed steady-state cavitation, which increased the membrane permeability of mouse cardiomyocyte HL-1 to a certain extent and further prevented the process of ferroptosis in mouse cardiomyocyte HL-1.

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JOURNAL OF RADIOANALYTICAL AND NUCLEAR CHEMISTRY · 2022 ·Vol. 332 ·期 7 ·2473-2485 · IF 1.754

Selective extraction of Hf over Zr by a novel extractant (n-octyl)(2,4,4′-trimethylpentyl)phosphinic acid (INET-1) from sulfuric acid media

Wang Junlian,Liu Hui,Zhao Hongru,Wang Huajun

A new Zr/Hf separation system was developed with a novel unsymmetrical dialkylphosphinic acid extractant ( n -octyl)(2,4,4'-trimethylpentyl)phosphinic acid (INET-1). It selectively extracts Hf over Zr, and shows much better Zr/Hf separation efficiency than organophosphorous acid Cyanex 272. The Zr and Hf extraction reactions at acidities of < 2 mol/L H 2 SO 4 and > 5.5 mol/L H 2 SO 4 are revealed, respectively. An organic phase with 10 mmol/L INET-1 can load > 290 mg/L of Hf at 1 mol/L H 2 SO 4 . Acidic H 2 SO 4 solutions with concentration of 3.0–4.5 mol/L is a good Zr scrubbing agent.

CAS / MDL: 13499-05-3 10026-11-6
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