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Tran Dang Thanh,Phan, T. L.,Nguyen Van Chien,Do Hung Manh,Yu, S. C. IEEE 2014 IEEE transactions on magnetics Vol.50 No.4
<P>In this paper, we present a detailed study of the magnetocaloric effect and critical properties around the ferromagnetic-paramagnetic (FM-PM) phase transition of La<SUB>0.7</SUB>Ca<SUB>0.3-x</SUB>Sr<SUB>x</SUB>MnO<SUB>3</SUB> nanoparticles with x = 0.10, 0.11, and 0.12. The samples were synthesized by a combination of reactive milling and thermal processing. The average crystallite size of nanoparticles estimated from the linewidth of X-ray diffraction peaks by using the Williamson-Hall method is about 50 nm. Under a magnetic field change of 10 kOe, the maximum magnetic entropy change (|ΔS<SUB>max</SUB>|) reaches values of 1.47, 1.42, and 1.38 J·kg<SUP>-1</SUP>·K<SUP>-1</SUP> for x = 0.10, 0.11, and 0.12, respectively, at around 300 K. The refrigerant capacity is thus in between 44 and 54 J·kg<SUP>-1</SUP>. Particularly, the M<SUP>2</SUP> versus H/M curves prove that all the samples exhibit a second-order magnetic phase transition. Based on Landau's phase-transition theory and careful analyses of the magnetic data around the FM-PM transition region, we have determined the critical exponents β, y, δ, and T<SUB>C</SUB>. Here, the β values obtained are 0.397, 0.453, and 0.456 for x = 0.10, 0.11, and 0.12, respectively, which are in between those expected on the basis of the mean-field theory (β = 0.5) and value of the 3-D Heisenberg model (β = 0.365). The result proves the coexistence of shortand long-range FM interactions in La<SUB>0.7</SUB>Ca<SUB>0.3-x</SUB>Sr<SUB>x</SUB>MnO<SUB>3</SUB> nanoparticles. The nature of this phenomenon is discussed thoroughly.</P>
Van Tran, Thuan,Nguyen, Duyen Thi Cam,Le, Hanh T.N.,Bach, Long Giang,Vo, Dai-Viet N.,Dao, To-Uyen T.,Lim, Kwon Taek,Nguyen, Trinh Duy Elsevier 2019 Journal of environmental chemical engineering Vol.7 No.5
<P><B>Abstract</B></P> <P>Discharge of nonsteroidal anti-inflammatory drugs (NSAIDs) from wastewater has been increasingly alarmed, led to the advent of the treatment techniques. Among these methods, adsorption is regarded as a tunable and green approach with the utilization of mesoporous carbon (MC) as an efficient and recyclable adsorbent. Herein, we described the strategy for the synthesis of novel MC from Fe-MIL-88B as a self-sacrificial template. Three thermolysis temperatures (550, 750, and 950 °C) were investigated to compare the structural characteristics and absorbability towards selected NSAIDs compounds including diclofenac sodium (DCF), aspirin (APR), and ibuprofen (IBU). Effect of contact time (0–480 min), concentration (10–40 mg/L), pH (2–10), and MC dosage (0.1–0.5 g/L) was systematically studied. Kinetic and isotherm models were also used to find out the adsorption mechanism and behavior of NSAIDs pharmaceutical over MC materials. Proposed mechanism and recyclability test were rigorously studied to gain more insight into how the NSAIDs molecules adsorb on the MC materials and their potential towards drug treatment.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Effect of thermolysis temperature on characteristics and absorbability towards anti-inflammatory drugs was conducted. </LI> <LI> Kinetic, isotherm, and recyclability experiments were systematically studied. </LI> <LI> Adsorption mechanisms including H-bond, π–π interaction, metal–oxygen bridging, and electrostatic attraction were rigorously proposed. </LI> <LI> Outstanding adsorption capacity (∼144 mg/g), and excellent reusability were monitored with Fe-MIL-88B-derived mesoporous carbon. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Ngo, Van T.H.,Hoang, Van-Hai,Tran, Phuong-Thao,Van Manh, Nguyen,Ann, Jihyae,Kim, Eunhye,Cui, Minghua,Choi, Sun,Lee, Jiyoun,Kim, Hee,Ha, Hee-Jin,Choi, Kwanghyun,Kim, Young-Ho,Lee, Jeewoo Elsevier 2018 Bioorganic & medicinal chemistry Vol.26 No.12
<P><B>Abstract</B></P> <P>Glutamyl cyclase (QC) is a promising therapeutic target because of its involvement in the pathogenesis of Alzheimer’s disease. In this study, we developed novel QC inhibitors that contain 3-aminoalkyloxy-4-methoxyphenyl and 4-aminoalkyloxyphenyl groups to replace the previously developed pharmacophore. Several potent inhibitors were identified, showing IC<SUB>50</SUB> values in a low nanomolar range, and were further studied for <I>in vitro</I> toxicity and <I>in vivo</I> activity. Among these, inhibitors <B>51</B> and <B>53</B> displayed the most potent Aβ<SUB>N3pE−40</SUB>-lowering effects in <I>in vivo</I> acute model with reasonable BBB penetration, without showing cytotoxicity and <I>h</I>ERG inhibition. The molecular modeling analysis of <B>53</B> indicated that the salt bridge interaction and the hydrogen bonding in the active site provided a high potency. Given the potent activity and favorable BBB penetration with low cytotoxicity, we believe that compound <B>53</B> may serve as a potential candidate for anti-Alzheimer’s agents.</P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Ngo, Van T.H.,Hoang, Van-Hai,Tran, Phuong-Thao,Ann, Jihyae,Cui, Minghua,Park, Gyungseo,Choi, Sun,Lee, Jiyoun,Kim, Hee,Ha, Hee-Jin,Choi, Kwanghyun,Kim, Young-Ho,Lee, Jeewoo Elsevier 2018 Bioorganic & medicinal chemistry Vol.26 No.5
<P><B>Abstract</B></P> <P>Pyroglutamate-modified amyloid β peptides (pGlu-Aβ) are highly neurotoxic and promote the formation of amyloid plaques. The pGlu-Aβ peptides are generated by glutaminyl cyclase (QC), and recent clinical studies indicate that QC represents an alternative therapeutic target to treat Alzheimer’s disease (AD). We have previously developed a series of QC inhibitors with an extended pharmacophoric scaffold, termed the Arg-mimetic D-region. In the present study, we focused on the structure activity relationship (SAR) of analogues with modifications in the D-region and evaluated their biological activity. Most compounds in this series exhibited potent activity in vitro, and our SAR analysis and the molecular docking studies identified compound <B>202</B> as a potential candidate because it forms an additional hydrophobic interaction in the <I>h</I>QC active site. Overall, our study provides valuable insights into the Arg-mimetic pharmacophore that will guide the design of novel QC inhibitors as potential treatments for AD.</P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>
Hoang, Van-Hai,Ngo, Van T. H.,Cui, Minghua,Manh, Nguyen Van,Tran, Phuong-Thao,Ann, Jihyae,Ha, Hee-Jin,Kim, Hee,Choi, Kwanghyun,Kim, Young-Ho,Chang, Hyerim,Macalino, Stephani Joy Y.,Lee, Jiyoun,Choi, S American Chemical Society 2019 Journal of medicinal chemistry Vol.62 No.17
<P>Alzheimer’s disease (AD) is an incurable, progressive neurodegenerative disease whose pathogenesis cannot be defined by one single element but consists of various factors; thus, there is a call for alternative approaches to tackle the multifaceted aspects of AD. Among the potential alternative targets, we aim to focus on glutaminyl cyclase (QC), which reduces the toxic pyroform of β-amyloid in the brains of AD patients. On the basis of a putative active conformation of the prototype inhibitor <B>1</B>, a series of N-substituted thiourea, urea, and α-substituted amide derivatives were developed. The structure-activity relationship analyses indicated that conformationally restrained inhibitors demonstrated much improved QC inhibition in vitro compared to nonrestricted analogues, and several selected compounds demonstrated desirable therapeutic activity in an AD mouse model. The conformational analysis of a representative inhibitor indicated that the inhibitor appeared to maintain the Z-E conformation at the active site, as it is critical for its potent activity.</P> [FIG OMISSION]</BR>
Ngoc Thuy Nguyen,Nhat Thong Tran,Tan Phat Phan,Anh Thu Nguyen,My Xuyen T. Nguyen,Nguyen Ngan Nguyen,Young Ho Ko,Dai Hai Nguyen,Tran T.T. Van,DongQuy Hoang 한국공업화학회 2022 Journal of Industrial and Engineering Chemistry Vol.108 No.-
While the efficient usage of biomass waste can significantly help in addressing environmental issues,there are only a few reports that discuss about processing such waste effectively at a low-cost. Such challengearises from the strong association between the components biomass. In this study, an abundantagricultural byproduct, rice husk (RH), was used as the starting resource. A simple biorefining processof alkaline peroxide treatment followed by acid precipitation and ethanol extraction was performed onRH to obtain cellulose, hemicellulose, lignin, and silica. The chemical structures, morphologies, andphysic-chemical properties of the separated components were identified through a wide range of characterizationapproaches. The final products obtained from of this process were (i) bundles of fiber-likecellulose with a fiber width of 6 mm and (ii) small particles of hemicellulose and lignin with nonuniformshapes. The lignocelluloses products had over 90 wt% carbon with 52.28% crystalline ratio. Meanwhile, the other products comprising hemicelluloses, lignin, and silica were amorphous. The outcomeof this study contributes to expanding and developing the simple and efficient conversion processof biomass waste into sustainable value-added materials. It is crucial to reduce the environmental impactby using renewable materials as the new building block resources for synthetic chemicals.
Tran Dang Thanh,Phan, T. L.,Le Mai Oanh,Nguyen Van Minh,Jong Suk Lee,Yu, S. C. IEEE 2014 IEEE transactions on magnetics Vol.50 No.6
<P>This paper presents the influence of Mn doping on the structural characterization, and optical and magnetic properties of SrTi<SUB>1-x</SUB>Mn<SUB>x</SUB>O<SUB>3</SUB>(x = 0.0-0.1) materials prepared by a solid-state reaction method. The detailed analyses of X-ray diffraction patterns indicate an incorporation of Mn dopants into Ti sites of the SrTiO<SUB>3</SUB> host lattice. There is a cubic to tetragonal transformation, which takes place at a threshold concentration x ≈ 0.04. The optical absorption spectra show a rapid increase in the absorption coefficient. The bandgap energy (Eg) related to the direct electron transition decreases with increasing Mn concentration: Eg decreases from 3.15 eV for x = 0 to 1.28 eV for x = 0.10. From this point of view, the SrTi<SUB>1-x</SUB>Mn<SUB>x</SUB>O<SUB>3</SUB> materials are considered as promising materials for photocatalytic applications. Interestingly, while the samples with x = 0.0-0.02 are diamagnetic, the others with x = 0.04-0.10 exhibit weak ferromagnetism. The ferromagnetic order increases with increasing Mn concentration. Based on the results of structural and optical analyses, the nature of magnetism in the samples is explained thoroughly.</P>
Endemic Severe Fever with Thrombocytopenia Syndrome, Vietnam
Tran, Xuan Chuong,Yun, Yeojun,Van An, Le,Kim, So-Hee,Thao, Nguyen T. Phuong,Man, Phan Kim C.,Yoo, Jeong Rae,Heo, Sang Taek,Cho, Nam-Hyuk,Lee, Keun Hwa U.S. Department of Health and Human Services * Cen 2019 Emerging Infectious Diseases Vol.25 No.5
Van-Anh Nguyen,Huy L. Nguyen,Dzung T. Nguyen,Quan P. Do,Lam D. Tran 한국물리학회 2017 Current Applied Physics Vol.17 No.11
In this paper, an electrosynthesized bilayer film of polypyrrole nanowire and poly(1,5- diaminonaphthalene) on a disposable screen-printing carbon ink electrode is presented. The inner polypyrrole nanowire layer had a large surface-to-volume ratio and high conductivity in the neutral medium, whereas the outer layer of poly(1,5diaminonaphthalene) had functional amino groups on the polymer chains. The combination of polypyrrole nanowire and poly(1,5diaminonaphthalene) showed a promising material for electrochemical biosensing. Here we reported an electrochemical immunosensor based on this approach for the purpose of detecting breast cancer biomarkers. The bilayer could enhance the surface coverage of antibody anti-CA 15-3 and consequently improve the sensitivity and stability of the immunosensors. The magnetic beads were used as carriers of labeled antibody anti-CA15-3 and HRP (horseradish peroxidase) in order to achieve an amplification of the signal. Under optimized conditions, the linear range of the immunoassay was 0.05e20 U mL1 with a detection limit of 0.02 U mL1 CA 15-3 antigen.