• Title/Summary/Keyword: $\mu$ synthesis

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Preparation of $Pb(Sc_{1/2}Nb_{1/2})O_3$ Powders by the molten salt synthesis method (솔-젤법에 의한 $Pb(Sc_{1/2}Nb_{1/2})O_3$ 분말의 제조)

  • ;;D. A. Payne
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.7 no.4
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    • pp.555-559
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    • 1997
  • Lead scandium niobate $Pb(Sc_{1/2}Nb_{1/2})O_3$ powders were prepared by the sol-gel method using lead acetate, scandium acetate, and niobium isopropoxide as precursors. Crystallization behavior and phase formation were investigated for gel-derived powders. After the calcination at $700^{\circ}C$ for 1 hr, $Pb(Sc_{1/2}Nb_{1/2})O_3$ powder with the purity of 97% was formed and the average particle size of powder was below 0.2 $\mu \textrm{m}$.

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Bioenvironmental Interaction of Toxic Peptide Hornet Venom with Phospholipid (Hornet 독액의 독성 Peptide와 Phospholipid 간의 생체환경적 상호작용)

  • 김광호;이봉헌
    • Journal of Environmental Science International
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    • v.6 no.2
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    • pp.189-194
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    • 1997
  • Toxic peptides from hornet venom, mastoparan and mastoparan-B were synthesized us- ing the solid phase peptide synthesis method and investigated the interaction of them with phospholipid bilayer, antibacterial activity, and hemolytic activity. Both toxic peptides could induce dye release at a low concentration in neutral liposome. The binding affinity of mastoparan-B for neutral liposome was smaller than that for acidic one. Mastoparan and mastoparan-B had strong antibacterial activity for gram-positive bacteria, but weak or potent activity for gram-negative ones, respectively. Mastoparan and mastoparan-B lysed erythrocyte very little up to 5 $\mu$M.

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Synthesis of Tetracyclic Pyrido[2,3-b]azepine Derivatives as Analogues of Mirtazapine via N-Acyliminium Ion Cyclization

  • Lee, Jae-Yeol;Bang, Sung-Hun;Lee, Sook-Ja;Song, Yun-Seon;Jin, Chang-Bae;Park, Ho-Koon;Lee, Yong-Sup
    • Bulletin of the Korean Chemical Society
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    • v.23 no.11
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    • pp.1623-1628
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    • 2002
  • Tetracyclic pyrido[2,3-b]azepine derivatives 4a-d and 4f as analogues of mirtazapine were synthesized via N-acyliminium ion cyclization by using aromatic rings such as benzene and thiophene ring as a ${\pi}-nucleophile$, and evaluated for the binding affinity for ${\alpha}2-adrenoceptor$. Among tested compounds, 2,3,9,13b-tetrahydro-1H-benzo[f]pyrrolo[2,1-a]pyrido[2,3-c]azepine (4a) was the most potent (Ki = 0.26 ${\mu}M)$ but showed about 3-fold less binding affinity than mirtazapine (Ki = 0.08 ${\mu}M)$ for a2-adrenoceptor.

The Effects of NOG-YONG Aqua-Aqupuncture Solution on Cytotoxicities in Primary Culture of Adult Rat Hepatocytes

  • Byun, Boo-Hyeong;Jeong, Hye-Kwang
    • Proceedings of the Korean Society of Food Hygiene and Safety Conference
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    • 2002.05a
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    • pp.147-147
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    • 2002
  • This experimental study was carried out to investigate on the safety of Nog-yong aqua-acupuncture solution in primary culture of adult rat hepatocytes. Primary culture of adult rat hepatocytes has been considered as a ideal model for toxicological studies because cultured hepatocytes maintained many liver-specific functions. In this research, we investigated the effects of Nog-yong aqua-aqupunture(1-10$\mu\textrm{g}$/ml) on cytotoxicites in primary culture of adult rat hepatocytes using LDH release assays. Hepatic glutathione level. glutathione-S-transferase activity, and albumin synthesis were not affected by treatment with Nog-yong aqua-aqupuntur alone. Nog-yong aqua-aqupuncoure solution(0.5-$10{\mu}\textrm{g}$/ml) on cytotoxicites in primary culture of adult rat hepatocytes using LDH release not significantly affected normal functional charaterists.

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Chemical Modification of Rupestonic Acid and Preliminarily In Vitro Antiviral Activity Against Influenza A3 and B Viruses

  • Yong, Jian-Ping;Aisa, Haji Akber
    • Bulletin of the Korean Chemical Society
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    • v.32 no.4
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    • pp.1293-1297
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    • 2011
  • To improve the biological activities of rupestonic acid, 21 new rupestonic acid fatty ester derivatives (2a-2h) and aromatic ester derivatives (2i-2u) were synthesized and preliminarily evaluated for their anti-influenza activity in vitro by the national center for drug screening of China, using the Oseltamivir and Ribavirin as reference drugs. The results showed that 2l ($IC_{50}=0.5{\mu}mol/L$) exhibited potent anti-influenza $A_3$ viral activity among the synthesized compounds and was 10-fold more potent than that of the reference drug Oseltamivir ($IC_{50}=5.1{\mu}mol/L$).

RF (Radio-Frequency) Thermal Plasma Synthesis of Ni-Based Nano Powders

  • Seo, Jun-Ho;Nam, Jun-Seok;Lee, Mi-Yeon;Kim, Jeong-Su
    • Proceedings of the Korean Vacuum Society Conference
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    • 2013.02a
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    • pp.138-138
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    • 2013
  • Ni-CeO2 및 Ni-MgO와 같이 Ni이 포함된 나노복합물질을 고주파 유도결합 플라즈마를 이용하여 합성하였다. 이를 위해, 먼저, 1~100 ${\mu}m$ 크기의 가상 Ni 입자와 고융점 세라믹 입자가 플라즈마 유동 내에서 겪는 열전달 과정을 수치해석을 통해 묘사하였다. 묘사 결과로부터, 완전 기화한 Ni 증기가, 채 기화하지 못하고 고체 형태로 남은 세라믹 입자 위에서 균일하게 응축된 형태를 갖는 Ni-세라믹 나노입자 합성을 예측하고, 실제 합성 실험을 25 kW 급 고주파 유도결합 플라즈마에 0.1~10 ${\mu}m$ 크기의 Ni, CeO2 및 MgO 분말을 주입하여 수행하였다. 마지막으로, 실험을 통해 합성된 Ni 계 복합나노물질에 대해, FE-SEM 및 TEM 사진 분석과 EDS 및 ICP-AES 성분 분석을 진행하고, 수치해석을 통해 예측된 결과와 비교 검토하였다.

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Synthesis and Absorption Spectra of 1,4-Diketo-3,6-Diphenyl-Pyrrolo-[3,4c]-Pyrrole (1,4-Diketo-3,6-Diphenyl-Pyrrolo-[3,4c]-Pyrrole(DPP)계 유기안료의 합성 및 흡수스펙트라)

  • 김성훈
    • Journal of the Korean Graphic Arts Communication Society
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    • v.14 no.1
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    • pp.1-15
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    • 1996
  • In this paper, the preparation of lead zirconium titanate(PZT) thin film by sol-gel processing was descried. Thin film coated with thickness of 4${\mu}{\textrm}{m}$ on the stainless steel substrates using the multiple spin-coating process. The crystalline phases of PZT powder and film were investigated by X-ray diffraction pattern and PZT thin film has perovskite structure over 600 C annealing temperature. Corona charging characteristics of the ferroelectric PZT thin film at 600 C were investigated by electrophotographic measurement. A difference in the charging characteristics between positive and negative corona charging was found. The charge acceptance depended in the polarity of corona and the poling of film. According to the D-E hysteresis measurment, PZT thin film can be poled by corona charging without use of top electrode. The remnant polarization in the PZT thin film is generally in the order of 48$\mu$C/$\textrm{cm}^2$. From this results, the ferroelectric PZT thin film will be possible to apply for the add-on type imaging formation.

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Preparation of Oriented MFI Zeolite Membranes (배향된 MFI 제올라이트 박막의 제조)

  • Song, Kyeong-Keun;Ha, Kwang
    • Korean Chemical Engineering Research
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    • v.44 no.3
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    • pp.243-247
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    • 2006
  • MFI zeolite membranes were prepared on anodic alumina (Anodisc) as support. First, silicalite-1(${\approx}1.2{\mu}m$) seed crystals were attached to the surface of the support via chemical bonding, and the a- and b-axis oriented zeolite membranes could be synthesized on the support coated with the monolayer of the seed crystals by secondary growth hydrothermal synthesis. The zeolite membranes prepared were characterized using scanning electron microscope and analyzed by X-ray diffraction.

Studies on hydrothermal synthetic conditions for preparation of PZT powders (PZT 분말 제조를 위한 수열합성 조건에 관한 연구)

  • 정성택;이기정;서경원
    • Journal of the Korean Crystal Growth and Crystal Technology
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    • v.6 no.2
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    • pp.254-262
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    • 1996
  • $Pb(Zr_{0.52}Ti_{0.48})O_{3}$ (PZT) ceramics were prepared with uniform particle size of $1~3\;\mu\textrm{m}$ by hydrothermal synthesis at various conditions, such as hydrothermal reaction temperature, concentration of mineralizer and reaction time. PZT ceramics were formed above $180^{\circ}C$ for 2 hrs reaction using 10 M KOH solution as a mineralizer, but reaction condition was slightly different by starting materials. Morphology and characterization of PZT powders were investigated by XRD and SEM. By increasing the reaction temperature, KOH concentration and reaction time, the composition of the PZT phase tended to be homogeneous phase.

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Anti-inflammatory Effects of Asiaticoside on Inducible Nitric Oxide Synthase and Cyclooxygenase-2 in RAW 264.7 Cell Line (Asiaticoside가 RAW 264,7 세포에서 Inducible nitric oxide synthase와 Cyclooxygenase-2에 미치는 항염증 작용에 관한 연구)

  • 주상섭;배옥남;정진호
    • Toxicological Research
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    • v.19 no.1
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    • pp.33-37
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    • 2003
  • Asiaticoside has been tested for the ability as an anti-inflammatory drug using lipopolysaccharide (LPS)-stimulated macrophage cell line (RAW 264.7 cell). LPS treatment induced dramatically inducible nitric oxide synthase (iNOS) in RAW cells. However, asiaticoside inhibited LPS-stimulated iNOS induction in a concentration-dependent manner. Especially, higher concentrations (>50 $\mu\textrm{M}$) of asiaticoside completely blocked iNOS induction. In addition, LPS-stimulated expression of inducible cyclooxygenase (COX-2) and interleukin-1 $\alpha$ (IL-1 $\alpha$) was inhibited by asiaticoside treatment. Asiaticoside up to 50 $\mu\textrm{M}$ still required to inhibit COX-2 and IL-1 $\alpha$ induced by LPS. Consistent with these findings, treatment with asiaticoside suppressed do novo synthesis and cellular accumulation of prostaglandin $E_2$ to a lesser extent, suggesting that asiaticoside blocked the induction as well as the activity of COX-2 These results suggest the possibility that asiaticoside may be effective therapeutic agents for septic shock and other inflammatory diseases.