• Macromolecular Research
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• v.11 no.3
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• pp.157-162
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• 2003

6FDA-based polyimides were prepared from the thermal imidization reaction of 6FDA with diamines of BAPAF, DAP, and DABA having a polar group of hydroxyL or carboxyl. Properties of the dense polyimide membranes were characterized and their gas permeation properties for H$_2$, $CO_2$, $O_2$, $N_2$, and CH$_4$ were investigated. Permeabilities, diffusion coefficients and diffusivity selectivities of polar group-containing polyimide membranes including 6FDA-BAPAF, 6FDA-DAP, and 6FDA-DABA polymer for the gases did not change largely. The separation properties of 6FDA-TrMPD polyimide membrane used as a reference polymer were compared with those of the polyimide membranes mentioned above. It was found that the polyimides of 6FDA-BAPAF, 6FDA-DAP, and 6FDA-DABA, which were soluble in alcohol or/and 2-methoxyethanol, could be applicable to the preparation of a dense composite membrane by dip-coating method.

• Proceedings of the Korean Information Science Society Conference
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• 2007.10d
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• pp.317-322
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• 2007

IPv6 이동성 관리를 위한 기존의 호스트 기반 프로토콜인 Mobile IPv6는 오랜 기간 동안 많은 연구에 의해 표준화되어진 안정적인 기술이지만 실제 상용망에서는 잘 사용이 안되고 있다. 그 이유는 단말의 수정 요구, 과도한 유/무선 자원 사용, 느린 핸드오버 지연시간 등이 있다. 이와 같은 Mobile IPv6의 단점을 극복하기 위하여 개발된 네트워크 기반 이동성 관리 프로토콜인 Proxy Mobile IPv6가 최근에 주목받고 있다. Proxy Mobile IPv6는 단말에서의 이동성 지원을 위한 수정이 필요하지 않으며, 유/무선 자원도 효율적으로 사용하며, 핸드오버 지연시간도 단축된다는 장점을 지니고 있다. 본 논문에서는 Proxy Mobile IPv6와 기존 호스트 기반 프로토콜인 Mobile IPv6, Hierarchical Mobile IPv6를 체계적으로 분석하고 핸드오버 지연시간을 비교 분석한다. 비교 분석 결과로서 Proxy Mobile IPv6는 기존 기법들보다 약 $84{\sim}93%$ 정도의 핸드오버 지연시간 단축이 있음을 알 수 있다.

• Proceedings of the Korean Institute of Electrical and Electronic Material Engineers Conference
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• 2007.11a
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• pp.482-483
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• 2007

본 논문에서는 GIS 설계에 있어 기초가 되는 준평등전계 하에서의 가스 절연특성을 검토하기 위하여 순 $SF_6,\;N_2,\;CO_2$ 이들이 혼합된 2종 및 3종 혼합가스에 대해 가스압력 0.6MPa 이하에서 상용교류전압을 인가하여 실험에 의해 그 부분방전특성과 절연특성을 조사하였다. 특히 실용 전력기기의 경우 금속이물질 등의 혼입에 의해 기기 내에서 불평등전계가 형성되어 부분방전을 거쳐 절연파괴에 이르는 가능성이 있으므로 본 연구에서는 불평등전계 하의 절연특성을 검토하였다. 실험 결과 $SF_6/N_2$ 2종 혼합 가스에 비하여 $SF_6/N_2/CO_2$ 3종 혼합 가스의 교류 절연 특성이 향상됨을 확인하였다.

• BMB Reports
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• v.53 no.4
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• pp.223-228
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• 2020

Dysregulation of histone deacetylase 6 (HDAC6) can lead to the pathologic states and result in the development of various diseases including cancers and inflammatory diseases. The objective of this study was to elucidate the regulatory role of microRNA-22 (miR-22) in HDAC6-mediated expression of pro-inflammatory cytokines in lipopolysaccharide (LPS)-stimulated macrophages. LPS stimulation induced HDAC6 expression, but suppressed miR-22 expression in macrophages, suggesting possible correlation between HDAC6 and miR-22. Luciferase reporter assays revealed that 3'UTR of HDAC6 was a bona fide target site of miR-22. Transfection of miR-22 mimic significantly inhibited LPS-induced HDAC6 expression, while miR-22 inhibitor further increased LPS-induced HDAC6 expression. LPS-induced activation of NF-κB and AP-1 was inhibited by miR-22 mimic, but further increased by miR-22 inhibitor. LPS-induced expression of pro-inflammatory cytokines such as TNF-α, IL-1β, and IL-6 was inhibited by miR-22 mimic, but further increased by miR-22 inhibitor. Taken together, these data provide evidence that miR-22 can downregulate LPS-induced expression of pro-inflammatory cytokines via suppression of NF-κB and AP-1 axis by targeting HDAC6 in macrophages.

• Journal of Energy Engineering
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• v.3 no.1
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• pp.70-76
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• 1994

본 연구는 방사성 폐액의 처리를 목적으로 화학처리와 한외여과막(UF)의 결합공정에 의해서 세슘이온의 제거특성을 조사하였다. 이 공정은 대상핵종과 선택성이 크고 한외여과막에 의해서 분리가 가능한 거대분자를 주입하여 핵종을 결합시키고, 이를 한외여과막에 의해서 분리 제거하는 개념이다. 실험은 흡착제로서 K2Cu3(Fe(CN6)2)를 제조하여 주입하였고 회분식 UF stirred cell를 이용하였으며, 용액의 pH, 세슘이온의 농도 및 K2Cu3(Fe(CN6)2)의 농도에 따라 세슘이온의 제거효율을 측정하였다. 세슘의 제거효율은 pH 및 K2Cu3(Fe(CN6)2)의 몰비에 따라 결정되며, pH가 5∼6에서 높은 제거율을 나타내었고 Cs/K2Cu3(Fe(CN6)2)의 몰비가 1.5 이하에서 90% 이상 제거되었다. K2Cu3(Fe(CN6)2)에 대한 Cs의 결합특성은 Langmuir isotherm형태의 식으로 나타내어 평가하였으며, 이때 세슘이온의 최대 흡착용량은 1.72 mM/mM K2Cu3(Fe(CN6)2) 이었다.

• Proceedings of the Korean Information Science Society Conference
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• 2007.10a
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• pp.138-139
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• 2007

기존의 MIPv6는 오랜 시간동안의 핸드오버로 인하여 많은 패킷 손실 및 오랜 세션 단절을 야기시킨다. 이러한 문제점들을 향상시키기 위하여 Fast handover for Mobile IPv6 (FMIPv6) 프로토콜이 개발되었지만 여전히 터널링에 기반한 라우팅 방법은 패킷 순서 어긋남 문제로 인하여 성능이 하락하는 문제를 야기한다. 최근 모바일 단말에서의 이동성 관리 부하를 줄여주기 위하여, 네트워크 이동성 기반인 Proxy Mobile IPv6 (PMIPv6)가 제안되었다. PMIPv6는 모바일 단말에서 수행하던 이동성 관리를 네트워크 에이전트에서 해줌으로서 단말의 부하를 줄이고 이동성 관리 지연 시간을 줄일 수 있다. 하지만 현재 제안된 PMIPv6 또한 터널링 기법에 기반한 비효율적인 라우팅 경로로 인하여 성능이 저하될 수 있다. 본 논문에서는 PMIPv6 에서 안정되고 향상된 최적화 라우팅 기술이 접목된 빠른 핸드오버 방법인 Fast Proxy Mobile IPv6 (EF-PMIPv6) 제안한다.

• Journal of the Korean Chemical Society
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• v.35 no.5
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• pp.575-579
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• 1991

Reaction of 6${\beta}$-bromopenicillanic acid(4a) with p-nitrobenzylbromide, 3-bromophthalide, chloromethylpivalate and 1-chlorodiethylcarbonate afforded 6${\beta}$-bromopenicillanates(4b~4e). New ${\beta}$-lactam compound, 6-(carboxymethylthio)penicillanic acid(5a) and the other esters(5b~5e) were prepared by nucleophilic substitution reaction of 6${\beta}$-bromopenicillanic acid(4a) and the other esters(4b~4e) with thioglycolic acid.

• Proceedings of the KIEE Conference
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• 2003.07c
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• pp.1867-1869
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• 2003

In this paper, chamber(Circuit breaker compartment of C-GIS) made of stainless steel with 4 mm width is used. Artificial defect was made on enclosure or HV conductor of chamber and $SF_6$ gas was injected into it according to pressure. In this experiment, Acoustic emission sensors of different types was used to compare sensitivity to detect acoustic signal occurred by Partial discharge(PD) of according to types and resonance frequency in $SF_6$ gas atmosphere. Sensors used in tests was R6I, R15I and 2/4/6 Pre-Amplifier connected with R6IU without pre. amp. In case of R6IU, gain was adjusted with 40 dB like other sensors and operated by differential mode. Post amplifier(post. amp) and band pass filter(BPF) were developed Gain of post. amp. is 60 dB and BPF has band width of $50{\sim}300$ kHz. Also, envelope circuit developed reduces frequency of AE sensor. As a result, in $SF_6$ atmosphere, R6IU and R6I had resonance frequency of 60 Hz was better than R15I. Also, R6IU was better than R6I because of type property of pre.amp. had differential mode.

• YAKHAK HOEJI
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• v.59 no.2
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• pp.49-54
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• 2015

In the present study we evaluated comparative herb-drug interaction potential of red ginseng total powder, ginsenoside Rg1, and Rb1 by inhibition of CYP isoforms including CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and CYP3A4 using pooled human liver microsomes (HLMs). As measured by liquid chromatography-electrospray ionization tandem mass spectrometry, red ginseng total powder inhibited significantly activities of CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2C19, CYP2D6, CYP2E1 and testosterone 6-beta hydroxylation by CYP3A4, but the $IC_{50}$ values were higher than $556{\mu}g/ml$. Activities of CYP2B6, CYP2C9, CYP2D6 and CYP3A4 were inhibited by ginsenoside Rb1. Also, activities of CYP1A2, CYP2A6, CYP2B6, CYP2C9, CYP2C19, CYP2D6 and testosterone 6-beta hydroxylation by CYP3A4 were inhibited by ginsenoside Rg1. The $IC_{50}$ values of ginsenoside Rb1 and Rg1 were higher than $200{\mu}g/ml$. Based on $IC_{50}$ values against CYP isoforms, ginsenosides-drug interactions by CYP inhibition may be very low in clinical situations.

• Journal of Microbiology and Biotechnology
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• v.6 no.6
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• pp.402-406
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• 1996

Inulin fructotransferase (depolymerizing) (EC 2.4.1.93) was purified 34-fold from the culture broth of Arthrobacter sp. A-6 by using a combination of ammonium sulfate fractionation, DEAE-Sepharose CL-6B chromatography and Sephacryl S-200 gel filtration. The purified enzyme converts inulin into di-D-fructofuranose dianhydride III(DFA III) and small quantities of fructo-oligosaccharides. The temperature and pH optima of the enzyme were $70^{\circ}C$ and 6.0, respectively. Molecular weight of the enzyme was determined to be 49 kDa by 12$%$ SDS-polyacrylamide gel electrophoresis, and 145 kDa by Sephacryl S-200gel filtration. This indicates that the functional inulin fructotransferase of Arthrobacter sp. A-6 has a homomeric trimer structure. The enzyme had an isoelectric point of pH 4.6. The N-terminal amino acid sequence of the purified enzyme subunit was Ala-Asp-Asn-Pro-Asp-Gly(\ulcorner)-Ser-Asn-Met(or Glu)-Tyr-Asp-Val.