• 지구물리와물리탐사
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• 제5권1호
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• pp.23-32
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• 2002

비접지식 전기비저항 탐사는 땅에 접지전극을 설치하기 어려운 곳에서 전기비저항 탐사를 수행할 수 있는 방법으로 국내에서도 관심이 높아지고 있는 방법이다. 이 방법의 기본원리는 땅과 송수신 안테나의 용량결합(capacitive coupling)에 의하여 지하로 전류를 주입하고 이에 의한 전위차를 측정하여 자료를 획득하는 것이다. 본 연구에서는 쌍극자 및 단극 형태의 송수신 안테나를 일렬로 배치하는 방사 배열(radial array)에 대한 기하학적 상수를 유도하였다. 또한, 기존의 접지식 전기비저항 해석 알고리듬을 이용하여 비접지식 전기비저항 자료를 해석하기 위한 자료 전처리 및 변환 과정을 제시하였다. 즉, 획득된 탐사 자료를 기하학적 상수를 이용하여 일단 겉보기 비저항으로 변환한 후 쌍극자 배열이나 변형된 쌍극자 배열 자료로 보간 혹은 재샘플링함으로써 기존의 접지식 전기비저항 역산 알고리듬을 이용하여 해석하였는데, 동일 측선에서 수행한 접지식 및 비접지식 탐사 자료와 비교하여 그 타당성을 검증하였다. 비접지식 전기비저항 탐사법은 전류를 많이 주입할 수 없는 기기 상의 단점을 갖고 있음을 알 수 있었는데, 특히 전기비저항이 낮은 곳이나, 전기적 잡음이 심한 곳, 그리고 송수신 안테나의 접촉이 좋지 않은 지역에 적용함에 있어 세심한 주의가 요구된다. 그러나, 송수신 안테나를 일렬로 배열하여 견인함으로써 연속적으로 탐사 자료를 획득할 수 있고 전극 설치가 불가능한 지역에서 전기비저항 탐사를 수행할 수 있으므로, 신속하게 지하 천부에 대한 전기비저항 분포를 알고자 할 때 유용하게 쓰일 것으로 생각된다.

• Archives of Pharmacal Research
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• 제18권6호
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• pp.449-453
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• 1995

The search for patinum (II)-based compounds with improved therapeutic properties was prompted to design and synthesize a new family of water-soluble, third generation cis-diamminedichlorplatinum (II) complexes linked to uracil and uridine. Six heretofore undescribed uracil and uridine-platinum (II) complexes are ; [N-(2-aminoethyl)uracil-5-carboxamide]dichloroplatinum (II)(3a), [N-2(2-aminoethyl)uracil-6-carboxmide]dichloroplatinum (II) (3b),[5-(2-aminorthyl)carbamoyl-2',3',5',-tri-O-acetyluridine] dichloroplatinum (II) (6b), [5-(2-aminoethyl)-carbamoyl]-2',3',5',-tri-O-acetyluridine] dichloroplatinum (II) (6b), [5-(2-aminoethyl)carbamoylu-ridine]dihloroplatinum (II) (7a), [6-(2-aminoethyl)carbamoyluridine]dichloroplatinum (II) (7b). These analogues were prepared from the key starting materials, 5-carboxyuracil (1a) and 6-carboxyuracil (1b) which were reacted with ethylenediamine to afford the respective N-(2-aminoethyl)uracil-5-carboxmide (2a) land N-(2-aminoethyl)uracil-6-carboxamide (2b). The cisplatin complexes 3a and 3b were obtained through the reaction of the respective 2a and 2b ficiently introduced on the .betha.-D-ribose ring via a Vorbruggen-type nucleoside coupling procedure with hexamethyldisilazane, trimethylchlorosilane and stannicchloride under anhydrous acetonitfile to yield the sterospecific .betha.-anomeric 5-carboxy-2',3',5'-tri-O-acetyluridine (4a) and 6-carboxy-2',3',5'-tri-O-acetyluridine (4b), respective 5-(2-aminoethyl)carbamoyl-2',3',5'-tri-O-acetyluridine (5a) and 6-(2-aminoethyl)carbamoyl-2',3',5'-tri-O-acetyluridine (5b). The diamino-uridines 5a and 5b were reacted with potassium tetrachloroplatinate (II) to give the novel nucleoside complexes, 6a and 6b respectively which were deacetylated into the free nucleosides, 7a and 7b by the treatment with CH/sub 3/ONa. The antitumor activities were evaluated against three cell lines (K-562, FM-3A and P-388).

• Archives of Pharmacal Research
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• 제20권3호
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• pp.253-258
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• 1997

Ten, heretofore unreported, $ 5^I-methyl-5^I-[2-(5-substituted uracil-1-yl)ethyl)]-2^I-oxo-3^I$-methylenetetrahydrofurans (H, F, Cl, Br, I, $ CH_3$,$CF_3$,$CH_2CH_3$,$ CH=CH2$, SePh) (7a-j) were synthesized and evaluated against four cell lines (K-562, FM-3A, P-388 and U-937). For the preparation of ${\alpha}$-methylene-${\gamma}$-butyrolactone-linked to 5-substituted uracils (7a-j), the convenient Reformasky type reaction was employed which involves the treatment of ethyl ${\alpha}$-(bromomethyl)acrylate and zinc with the respective 1-(5-substituted uracil-1-yl)-3-butanone (6a-j). The 5-substituted uracil ketones (6a-j) were directly obtained by the respective Michael type reaction of vinyl methyl ketone with the $K_2CO_3$(or NaH)-treated 5-substituted uracils (5a-j) in the presence of acetic acid in the DMF solvent. The .alpha.-methylene-.gamma.-butyrolactone compounds showing the most significant antitumor activity are 7e, 7f, 7h and 7j (inhibitory concentration $(IC_50)$ ranging from 0.69 to $2.9 {\mu}g/ml$), while 7b, 7g and 7i have shown moderate to significant activity. The compounds 7a, 7c and 7d were found to be inactive. The synthetic intermediate compounds 6a-j were also screened and found marginal to moderate activity where compounds 6b and 6g showed significant activity $(IC_50:0.4~2.8 {\mu}g/ml)$.

• Archives of Pharmacal Research
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• 제21권4호
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• pp.465-469
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• 1998

The search for platinum (II)-based compounds with improved therapeutic properties was prompted to design and synthesize a new family of water-soluble, third generation cis-diaminedichloroplatinum (II) complexes linked to uracil and uridine. Six heretofore unreported uracil and uridine-platinum (II) complexes are; [N-(uracil-5-yl-methyl)ethane-1,2-di-amine]dichloroplatinum (II) (3a), [N-(uracil-6-yl-methyl)ethane-1,2-diaminel dichloroplatinum (II) (3b), t[N-($2^1$, $3^1$,$5^1$-tri-O-acetyl)uridine-5-yl-methyl] ethane-1,2-diamineldichloroplatinum (II) (6a), {[N-($2^1$,$3^1$, $5^1$-tri-O-acetyl) uridine-6-yl-methyl]ethane-1,2-diamine)dichloroplatinum (II) (6b),[N-(uridine- 5-yl-methyl)ethane-1,2-diamine]dichloroplatinum (II) (7a), [N-(uridine-6-yl- methyl)ethane-1,2-diamine]dichloroplatinum (II) (7b). These analogues were prepared from the key starting materials, 5-chloromethyluracil (1a) and 6-chloromethyluracil (1b) which were reacted with ethylenediamine to afford the respective 5-[(2-aminoethyl)aminol methyluracil (2a) and 6-[(2-aminoethyl)amino]methyluracil (2b). The cis-platin complexes 3a and 3b were obtained through the reaction of the respective 2a and 2b with potassium tetrachloroplatinate (II). The heterocyclic nucleic acid bases 1a and 1b were efficiently introduced on the .betha.-D-ribose ring via a Vorbruggen-type nucleoside coupling procedure with hexamethyldisilazane, trimethylchlorosilane and stannic chloride under anhydrous acetonitrile to yield the stereospecific .betha.-anomeric 5-chloromethyl- $2^1$,$3^1$,$5^1$-tri-O-acetyluridine (4a) and 6-chloromethyl-$2^1$,$3^1$,$5^1$-tri-O-acetyluridine (4b), respectively. The nucleosides 4a and 4b were coupled with ethylenediamine to provide the respective 5-[(amino-ethyl)aminolmethyl-$2^1$,$3^1$,$5^1$-tri-O-acetyluridine (5a) and 6-[(aminoethyl)amino] methyl-$2^1$,$3^1$,$5^1$-tri-O-acetyluridine (5b). The diamino-uridines 5a and 5b were reacted with potassium tetrachloroplatinate (II) to give the novel nucleoside complexes, 6a and 6b, respectively which were deacetylated into the free nucleosides, 7a and 7b by the treatment with CH$_{3}$ONa. The cytotoxic activities were evaluated against three cell lines (FM-3A, P-388 and J-82) and none of the synthesized compounds showed any significant activity.

• KIEE International Transactions on Electrophysics and Applications
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• 제5C권3호
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• pp.102-110
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• 2005

Piezoelectric transformers(PT) are expected to be small, thin and highly efficient, and which are attractive as a transformer with high power density for step down voltage. For these reasons, we have attempted to develop a step-down PT for the miniaturized adaptor. We propose a PT, operating in thickness extensional vibration mode for step-down voltage. This PT consists of a multi-layered construction in the thickness direction. In order to develop the step-down PT of 10 W class and turn ratio of 0.1 with high efficiency and miniaturization, the piezoelectric ceramics and PT designs are estimated with a variety of characteristics. The basic composition of piezoelectric ceramics consists of ternary yPb(Zr$_{x}$Ti$_{1-x}$)O$_{3}$-(1-y)Pb(Mn$_{1/3}$Nb1$_{1/3}$Sb$_{1/3}$)O$_{3}$. In the piezoelectric characteristics evaluations, at y=0.95 and x=0.505, the electromechanical coupling factor(K$_{p}$) is 58$\%$, piezoelectric strain constant(d$_{33}$) is 270 pC/N, mechanical quality factor(Qr$_{m}$) is 1520, permittivity($\varepsilon$/ 0) is 1500, and Curie temperature is 350 $^{\circ}C$. At y = 0.90 and x = 0.500, kp is 56$\%$, d33 is 250 pC/N, Q$_{m}$ is 1820, $\varepsilon$$_{33}$$^{T}$/$\varepsilon$$_{0}$ is 1120, and Curie temperature is 290 $^{\circ}C$. It shows the excellent properties at morphotropic phase boundary regions. PZT-PMNS ceramic may be available for high power piezoelectric devices such as PTs. The design of step-down PTs for adaptor proposes a multi-layer structure to overcome some structural defects of conventional PTs. In order to design PTs and analyze their performances, the finite element analysis and equivalent circuit analysis method are applied. The maximum peak of gain G as a first mode for thickness extensional vibration occurs near 0.85 MHz at load resistance of 10 .The peak of second mode at 1.7 MHz is 0.12 and the efficiency is 92$\%$.

• 폴리머
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• 제24권3호
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• pp.389-398
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• 2000

폴리카보네이트 표면에 spin-coating한 유/무기 복합 코팅막을 자외선 경화와 가열(12$0^{\circ}C$, 12시간)처리함으로써 약 4~13 $\mu\textrm{m}$ 두께의 투명한 내마모성 유/무기 복합코팅막을 제조하였다. 코팅용액은 무기상과 유기상을 각각 0 : 100, 20 : 80, 30 : 70, 50 : 50, 80 : 20 중량비로 혼합한 다음 광개시제, 증감제 및 계면활성제를 첨가하여 제조하였다. 무기상은 TEOS와 실란커플링제 MPTMS을 1 : 2 혹은 2 : 1몰비로 흔합하여 졸ㆍ겔 반응으로 제조하였으며, 유기상은 2관능형 urethane acrylate 올리고머, 다관능형 TMPTA와 HDDA를 4:3:3 wt% 비율로 흔합하여 제조하였다. 유/무기복합상의 화학적 변화는 FT-IR, $^{29}$ Si-NMR로 분석하였으며, 열분석과 코팅층 표면 형상은 TGA/DSC, SEM, AFM으로 분석하였다. 무기물의 함량과 실란커플링제의 첨가량이 증가 할수록 분자수준의 흔화도가 개선되고 표면 평활도와 내마모성도 향상되었다. 즉 약 10 $\AA$ 이하의 표면 거칠기와 약 15$0^{\circ}C$의 T$_{g}$를 나타내는 시료는 500회 마모시험 전후 단지 16%의 광투과도 감소만을 보인 반면에, 무코팅 폴리카보네이트를 46%의 광투과율 감소를 나타내었다..

• Molecules and Cells
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• 제37권3호
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• pp.213-219
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• 2014

MicroRNAs (miRNAs) represent a class of small non-coding regulatory RNAs that play important roles in normal hematopoiesis, including erythropoiesis. Although studies have identified several miRNAs that regulate erythroid commitment and differentiation, we do not understand the mechanism by which the crucial erythroid transcription factors, GATA-1and NF-E2 directly regulate and control differentiation via miRNA pathways. In this study, we identified miR-199b-5p as a key regulator of human erythropoiesis, and its expression was up-regulated during the erythroid differentiation of K562 cells. Furthermore, the increase of miR-199b-5p in erythroid cells occurred in a GATA-1- and NF-E2-dependent manner during erythrocyte maturation. Both GATA-1 and NF-E2 bound upstream of the miR-199b gene locus and activated its transcription. Forced expression of miRNA-199b-5p in K562 cells affected erythroid cell proliferation and maturation. Moreover, we identified c-Kit as a direct target of miR-199b-5p in erythroid cells. Taken together, our results establish a functional link among the erythroid transcription factors GATA-1/NF-E2, miR-199b-5p and c-Kit, and provide new insights into the coupling of transcription and post-transcription regulation in erythroid differentiation.

• 공업화학
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• 제25권3호
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• pp.254-261
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• 2014

변압기 내부에서 발생한 열의 냉각과 절연의 목적으로 채워지는 전기절연유는 광유가 널리 이용되고 있지만, 유출 시야기되는 환경오염 문제와 열적 불안정성 등의 문제가 있다. 친환경적이고 넓은 온도 범위에서 사용 가능한 전기절연유를 합성하기 위해, 디글리세롤과 두 종류의 지방산을 반응시켜 diglycerol ester를 합성하였다. 서로 다른 특성을 가진 올레산과 카프릴산의 몰비에 따른 절연특성을 분석한 결과, 지방산의 몰비가 Oleic acid:Caprylic acid = 1:3일 때 유동점은 $-50^{\circ}C$, 인화점은 $306^{\circ}C$로 가장 우수한 절연특성을 보였다. 또한, 합성물은 지방산의 전환율이 상승할수록 인화점은 상승하고 유동점은 감소하였다. $SO_4{^{2-}}/ZrO_2$의 소성온도에 따른 촉매특성 및 전환율을 살펴본 결과, $600^{\circ}C$에서 소성한 $SO_4{^{2-}}/ZrO_2$가 결정성을 가지면서 비표면적 당 산점의 밀도가 높아 가장 높은 전환율을 보였다. 합성한 diglycerol ester는 식물성 절연유와 비교했을 때 전반적으로 식물성 절연유보다 우수한 특성을 보였다.

• 폴리머
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• 제36권1호
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• pp.98-103
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• 2012

구리 계열의 $Cu(NO_2)_2{\cdot}3H_2O$와 CuCl을 중합촉매로 사용하고 다양한 용매, 리간드와 염기의 함량을 변화시켜 poly(2,6-dimethyl-1,4-phenylene ether)(PPE) 중합반응을 고찰하였다. 이 가운데 CuCl/1-methylimidazole/ammonium hydroxide 시스템에서 가장 높은 중합 수율을 나타내었다. 한편, 몇 가지 다른 유기용매와 메탄올의 혼합용매 시스템에서 용매의 성분비율을 변화시켜 용매의 조성이 중합반응에 미치는 영향을 조사하였으며 2,4,6-trimethylphenol (TMP)를 사용하여 TMP 함량에 따른 분자량 조절 효과를 조사하였다. 클로로포름/메탄올 9/1(v/v) 혼합용매를 사용했을 때 가장 높은 중합 수율과 높은 분자량을 갖는 중합체($\overline{M_n}$ : 55 K; $\overline{M_w}$ : 92 K; PDI: 1.7)를 얻었다. 구리 일가 촉매인 CuCl 과 CuI를 사용하여 서로다른 짝이온, 즉 $Ci^-$와 $I^-$ 이온이 중합결과에 미치는 영향을 조사하였다. 촉매의 활성 비교를 위하여 산소 흡수량(oxygen-uptake)을 측정하였으며, 중합반응의 부산물인 5,5'-tetramethyl-4,4'-diphenoquinone (DPQ)의 함량을 자외선 분광기(ultraviolet spectroscopy)를 통하여 분석하였다.

• Experimental and Molecular Medicine
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• 제50권11호
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• pp.3.1-3.11
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• 2018

This study aimed to verify the effects of estrogen on the onset and development of adolescent idiopathic scoliosis and the mechanisms associated with these effects by constructing a pubescent bipedal rat model. Experiments were conducted to investigate whether scoliosis progression was prevented by a Triptorelin treatment. One hundred twenty bipedal rats were divided into female, OVX (ovariectomy), OVX + E2, Triptorelin, sham, and male groups. According to a spinal radiographic analysis, the scoliosis rates and curve severity of the female and OVX + E2 groups were higher than those in the OVX, Triptorelin, and male groups. The measurements obtained from the sagittal plane of thoracic vertebrae CT confirmed a relatively slower growth of the anterior elements and a faster growth of the posterior elements between T11 and T13 in the female and OVX + E2 groups than in the OVX and Triptorelin groups. Histomorphometry and immunohistochemistry revealed a significantly longer hypertrophic zone of the vertebral cartilage growth plates that expressed more type X collagen and less type II collagen in the OVX and Triptorelin groups than in the female and OVX + E2 groups. Ki67 immunostaining confirmed an increase in the proliferation of vertebral growth plate chondrocytes in the OVX group compared with the female and OVX + E2 groups. In conclusion, estrogen obviously increased the incidence of scoliosis and curve severity in pubescent bipedal rats. The underlying mechanism may be a loss of coupling of the endochondral ossification between the anterior and posterior columns. Triptorelin decreased the incidence of scoliosis and curve magnitudes in bipedal female rats.