• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2008년도 International Meeting on Information Display
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• pp.450-453
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• 2008

We synthesized a new HIL and HTL materials by using phenothiazinly moiety, 1,4-diphenothiazyl-benzene [DPtzB], 3',7',3",7"-tetrakis(N-phenyl-2-naphthylamine)-1,4-diphenothiazyl-benzene[PNA-DPtzB]. Synthesized materials exhibited high Tg in the range of $175\;-\;202^{\circ}C$. These values are much better than commonly used hole transporting materials (2-TNATA and NPB). The OLED device that used DPtzB as a HIL showed the highest efficiency of 4.31cd/A at $10mA/cm^2$.

• Environmental Analysis Health and Toxicology
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• 제5권1_2호
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• pp.45-50
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• 1990

In order to investigate the phototoxicity of five phenothiazine derivatives and one thioxanthen derivative were examined by using in vitro method based on growth inhibition of Candida albicans and red blood cell hemolysis. Effects of the test compounds on RBCs were monitored with a spectrophotometer and a drug PI in the Candida albicans was calculated on the basis of the lowest concentration giving a yeast-free zone. All phenothiazines phototoxic in the red blood cell hemolysis method were positive in the yeast test except promethazine. It was also observed that toxic photo-products were formed by perphenazine and chlorpromazine in the red blood cell hemolysis.

• 한국식품위생안전성학회지
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• 제7권4호
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• pp.143-147
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• 1992

Phenothiazines류의 약물 중 Chlorpromazine, perhenazine, trifluoperazine, thioridazin의 광독성에 대한 ascorbic acid의 영향을 조사 연구하였다. 각 약물 농도를 $50;\mu\textrm{g}$/ml로하고 UVA(350nm, 2.5mV/cm)로 조사기간은 30분으로 하여 적혈구의 광용혈현상을 Kahn 등의 방법에 의해 spectrophotometer로 측정한 결과 Chlorpromazine, perphenazine, thioridazine에 의한 광용혈도 정도는 ascorbic acid에 의해 유의성 있게 감소되었다. 또한 적혈구를 가하기 전 각 약물을 미리 조사시켜 생성된 물질에 의한 광용혈현상의 광독성 생성물질은 chlorpromazine과 thioridazine에서 보여졌으며, chlorpromazine의 광독성 생성물질에 의한 적혈구 용혈현상만 ascorbic acid에 의해 감소되었다.

• 한국자기공명학회논문지
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• 제4권2호
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• pp.82-90
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• 2000

Photoinduced charge separation of alkylphenothiazines in molecular assemblies such as positively, negatively and neutrally charged micelle interface results in the paramagnetic phenothiazine cation radical. This was studied as a model system for the light energy conversion into chemical energy. The photoproduced phenothaizne cation radical was identified and its amount was quantized with electron spin resonance (ESR). The microenvironment of photoproduced cation radical was studied with pulsed-ESR. Such a charge separation is enhanced by the optimization of various structural factors of the molecular assemblies. The structural factors of molecular assemblies have focused on the interface charge, interface structure with different headgroups and interfacial perturbation by disolving interface active organic additives.

• 약학회지
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• 제38권6호
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• pp.637-645
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• 1994

The effect of various drugs on the stability of the liposomal membrane of phosphatidylcholine and cholesterol was studied, employing the fluorescence self-quenching method. Calcein was entrapped into the phospholipid small unilamellar vesicles and the leakage of the fluorescence probe was monitored on adding the drug to the system. The results of the experiments showed that phenothiazine derivatives, some potent local anesthetics and surface active agents were very effective in inducing the leakage of calcein from the liposome. The leakage-inducing activity of these drug substances has been ascribed to their surface activity and the perturbation of the liposomal membrane by these substances. On the other hand drug substance with low surface activity or without amphiphilic moieties did not show any effect or only small effect on the leakage of calcein from the liposomes. The effect of lipid concentration on the stability of the liposomes was also investigated to show that the higher concentrations of lipid more drug was required to induce the leakage. The effect of surface charges of vesicles was also studied, and the results showed that the charge on the liposomes enhanced the stability of the liposomes against the leakage-inducing activity of these drug substances.

• Journal of Information Display
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• 제7권4호
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• pp.9-12
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• 2006

This paper reports the synthesis and electroluminescent properties of new aromatic compounds as hole-transporting materials based on phenothiazine, such as 1,4-diphenothiazyl-benzene [DPtzB], 1,4-diphenothiazyl-xylene [DPtzX] and 9,10-diphenothiazyl-anthracene [DPtzA]. DPtzB thin film exhibited photoluminescence (PL) maximum emission peak and emission shoulder at 450 and 475 nm, and a maximum emission at 447 nm without emission shoulder was obtained in DPtzX thin film. When DPtzA was excited by incident light of 359 nm, DPtzA showed strong PL emission at 417 nm and weak emission at 600 nm. Luminance efficiency of DPtzB, DPtzX and DPtzA-based electroluminescence (EL) devices was 3.57, 3.46 and 0.47 cd/A, and power efficiency of DPtzB, DPtzX and DPtzA-based EL devices was 1.48, 1.26 and 0.201 m/W.

• 한국정보디스플레이학회:학술대회논문집
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• 한국정보디스플레이학회 2006년도 6th International Meeting on Information Display
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• pp.1054-1058
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• 2006

We report the synthesis and electroluminescent properties of new aromatic compounds as hole-transporting materials based on phenothiazine, such as 1,4-diphenothiazyl-benzene [DPtzB], 1,4-diphenothiazyl-xylene [DPtzX] and 9,10-diphenothiazyl-anthracene [DPtzA]. DPtzB thin film exhibited photoluminescence (PL) maximum emission peak and emission shoulder at 450 and 475nm, and maximum emission at 447nm without emission shoulder was found in DPtzX thin film. When DPtzA was excited by incident light of 359nm, DPtzA showed strong PL emission at 417nm and weak emission at 600nm. Luminance efficiency of DPtzB, DPtzX and DPtzA-based electroluminescence (EL) devices was 3.57, 3.46 and 0.47cd/A, and power efficiency of DPtzB, DPtzX and DPtzA-based EL devices was 1.48, 1.26 and 0.20lm/W.

• 대한약리학회지
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• 제30권3호
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• pp.343-349
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• 1994

정신병치료제들을 장기투여하여 치료를 시도하였을 때에 생기는 여러 부작용은 그 정도 또한 매우 심각하기 때문에 그들의 치료효과와 함께 야기되는 부작용들을 따로 생각할 수가 없게 되었다. 특히 정신병치료는 그 자체에 대한 병인적 원인을 정확히 알 수 없기에 증상에 따른 대중요법이 일괄적으로 사용되므로, 이러한 현재의 치료방법으로는 부작용들이 더 치명적이 될 수 있기 때문에 일차적으로 이들의 공통적약리작용기전들을 연구하는 것은 매우 필요하다. 최근 NO(Nitric oxide)에 대한 많은 연구들에 의하면, 이들이 중추신경계에서 중요한 second messenger 또는 mediator로 신경활동에 영향을 나타내는 것으로 보고되고 있다. 그러므로 저자들은 먼저 이들 약물들과 NO와의 관계를 연구하고자, 중요한 몇종의 정신병치료제들을 택하여 NO생성에 어떤 영향을 미치는 가를 검색하여 다음과 같은 일차 결과를 얻었다 1. 정신병치료제 수종(chlorpromazine, trifluoperazine promazine, pimozide, clozapine, chlorprothixene, haloperidol)을 택하여 쥐의 소내에서 $[^3H]L-arginine$으로부터 $[^3H]L-citrulline$의 생성양을 측정하여 calmodulin antagonist(calmidazolium)와 비교하였다. 2. 이들을 N1E-115 cell에 투여하여 $[^3H]cyclic$ GMP양을 측정하고 그 결과를 calmida-zolium 과 비교하였다. 3. 이들 약물들은 citrulline과 cyclic GMP 모두의 생성양을 의의있게 억제하였으며 그 기전은 calmidazolium과 매우 유사하였다. 위의 일차적 검색결과에 의하면, 정신병치료약물들의 약리작용 기전중에 일부는 중추신경계내의 NO생성 및 cyclic GMP생성에 영향을 나타내는 것으로 사료되며, 이에는 calcium ion이 상당히 중요한 역할을 하는데, 특히 소뇌에서의 NO생성의 감소는 이들 약물들의 치명적 부작용인 tardive dyskinesia와 매우 깊은 관련을 추측할 수 있다. 그러나, 더 많은 약물들의 검색으로 일관적인 기본 결과가 필요 되고 또 각개 약물의 특정적 기전이 연구되기 위하여 현재 실험중이다.

• The Korean Journal of Physiology
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• 제19권1호
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• pp.25-33
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• 1985

Renal arterial infusion of renotropic agents has been a very useful technique in the renal function studies. This type of experiments have usually been conducted in the large animals such as dogs and sheep. In these animals a catheter can be placed in the site without much disturbances of renal blood flow. Rabbits as an experimental model, however, caused a disturbances of renal blood flow by a catheterization of renal artery by its properties. Therefore we have developed a new technique that allows a simple and selective access to one side of renal arteries and the other as a control, without any disturbances of renal function. The distance between the both bifurcations of renal arteries on abdominal aorta is about 7 mm. To locate the tip of catheter on one side renal artery, ascending cannulation performed via femoral artery was done. We did an experiment with the technique to clarify the effect of calmodulin inhibitor on the renal function. One of the phenothiazine derivatives, trifluoperazine known as a powerful calmodulin inhibitor. Trifluoperazine, actual dose ranges of $2.76-5.20\;ug\;{\cdot}\;kg^{-1}\;{\cdot}\;min^{-1}$, increased urine volume and glomerular filtration rate significantly. Significant increases in urinary excretion of sodium, chloride and potassium were found. Fractional excretion of sodium and free water clearance increased significantly. These data suggest that this new technique is very useful in field of renal physiology and that striking effect of trifluoperazine on the renal function may be caused by increasing the renal hemodynamics, and by the inhibition of sodium, chloride and potassium reabsorption in the renal tubules.