• Title/Summary/Keyword: Aniline

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Effect of the Combination of Ethanol with Toluene Treatment for a Short Time Period on the Toluene Metabolizing Enzyme Activity (흰쥐에 Toluene과 Alcohol의 병행투여가 Toluene 대사 효소활성에 미치는 영향)

  • 윤종국;전재현;신중규
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.25 no.6
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    • pp.976-980
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    • 1996
  • To elucidate the effect of acute ethanol pretreatment on some toluene metabolizing enzyme activities, rats were divided into 4groups: control, alcohol-treated, toluene-treated, rat's and toluene-treated rats pretreated with ethanol. The alcohol or toluene-treated rats showed the significantly increased activities of hepatic aniline hydroxylase(AH) and aminopyrine demethylase(AD) compared to the control group. And the toluene-treated rats pretreated with ethanol showed somewhat decreased tendency of these enzyme activities compared to only toluene-treated rats. Liver benzylalcohol or aldehyde dehydrogenase activities were higher in alcohol or toluene-treated rats than those of the control group. The toluene-treated rats showed the decreased tendency of benzylalcohol dehydrogenase activities by the pretreatment of alcohol. Furthermore, toluene treated-rats showed the markedly decreased activity of benzaldehyde dehydrogenase by the ethanol pretreat-ment. On the other hand, hepatic xanthine oxidase activity in toluene-treated animals pretreated with ethanol was significantly higher than those of the toluene alone-treated rats. These results indicate that the combination of ethanol with toluene treatment for a short period of time possibly results in decreased activity of some toluene metabolizing enzymes in rats.

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Opto-Physical Properties of Ophthalmic Lens Polymer Containing σ, m, p-Substituted Difluoroaniline as Additives (σ, m, p-위치로 치환된 Difluoroaniline을 첨가제로 사용한 안의료용 렌즈 고분자의 물리·광학적 특성)

  • No, Jung-Won;Sung, A-Young
    • Journal of Korean Ophthalmic Optics Society
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    • v.19 no.1
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    • pp.69-77
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    • 2014
  • Purpose: The functional ophthalmic lenses containing fluorine-substituted aniline group (2,4-difluoroaniline, 2,6-difluoroaniline, 3,4-difluoroaniline) were manufactured and the physical and optical characteristics of copolymerized ophthalmic lens were investigated. Methods: HEMA (2-hydroxyethylmethacrylate), NVP (N-vinyl pyrrolidone), MA (methacrylic acid), the cross-linker EGDMA (ethylene glycol dimethacrylate) and the initiator AIBN (azobisisobutyronitrile) were used as a basic combination and fluorine-substituted aniline group (2,4-difluoroaniline, 2,6-difluoroaniline, 3,4-difluoroaniline) were used as additives for preparing the hydrogel soft contact lenses. The hydrogel ophthalmic lens was manufactured by cast mould method and the ophthalmic lenses were stored in a 0.9% NaCl normal saline for 24 hrs. Results: The optical transmittance of the sample with addition 2,4-difluoroaniline showed that the UV-B(9.8~51.4%), UV-A(58.8~79.2%) and visible transmittance(87.0~90.4%). In the case of 2,6-difluoroaniline were measured the UV-B(80.2~83.2%), UV-A(85.8~86.4%), and visible transmittance(90.8~91.4%). Also, the optical transmittance of ophthalmic lens containing 3,4-difluoroaniline were measured the UV-B transmittance of 3.8~30.4%, UV-A transmittance of 47.8%~74.4% and the visible transmittance of 86.2~91.0% respectively. Conclusions: Based on the results of this study, 2,4-difluoroaniline and 3,4-difluoroaniline can be used effectively as additive for UV-blocking ophthalmic contact lenses.

Studies on the Preparation of Organic Compounds Labelled by $^{38}Cl$.(I) - Inorganic Yields of $^{38}$ Cl in Szilard Chalmer Reaction of Aromatic Chloro Derivatives

  • Kim, You-Sun
    • Nuclear Engineering and Technology
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    • v.5 no.1
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    • pp.44-54
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    • 1973
  • In order to clarify an effective procedure of labelling organic chloro compounds by $^{38}$ Cl, phenyl chloro derivatives(7 kinds), chloro nitrobenzenes(6 kinds), chloro anisoles(2 kinds), chloro anilines(3 kinds), chloro toluenes(3 kinds), benzyl cholorides(4 kinds), and other comparing samples(3 kinds) were irradiated in the TRIGA Mark-II research reactor and the inorganic $^{38}$ Cl yields were compared with the irradiation times after extracting the inorganic portion with an aqueous solution of alkali. It was found that the relative change between the inorganic $^{38}$ Cl yield and the irradiadiation time depends a great deal on the state of the sample, and a solid sample gave a lower and steady inorganic yield. The inorganic $^{38}$ Cl yield was decreased in the order of phenyl chloro derivatives < chloro tol uene$^{38}$ Cl yield of homo functional compounds and the number of chlorine atoms on the benzene ring. Generally, poly chloro substituted derivatives could give a higher yield than those of less chloro substituted. The results were discussed and the feasibility of these results for labelling purpose was criticized.

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Kinetics of the Reaction of Phenacyl Bromide with Anilines in Methanol and Dimethylformamide (Phenacyl Bromide와 置換아닐린類와의 反應에 關한 反應速度論的 硏究)

  • Soo-Dong Yoh;Doo-Jung Kim
    • Journal of the Korean Chemical Society
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    • v.25 no.6
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    • pp.376-382
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    • 1981
  • The rates and the activation parameters for the reaction of phenacyl bromide with substituted anilines in methanol and dimethylformamide were measured. The effects of substituted anilines were discussed. The rate of the reaction was increased with the electron donating power of substituent and showed larger value in DMF than in MeOH. The isokinetic relationship was shown between ${\delta}H^{\neq}$ and ${\delta}S^{\neq}$, isokinetic temperature was 539 and $400^{\circ}C$ in MeOH and DMF respectively, but p-nitro aniline was deviated from linearity in both solvents caused by solvent effects. The excellent linear relationship between log k and p$K_a$ of substituted anilines was observed by following equation. log k = 0.57p$K_a$-1.28 (r = 0.996) in MeOH at $45^{\circ}C$, log k = 0.65p$K_a$-0.88 (r = 0.970) in DMF at $45^{\circ}C$. From the Hammett plot, this reaction was a nucleophilic displacement of aniline to phenacyl bromide and the following equation was obtained at $45^{\circ}C$. log k/$k_0$ = -2.00${\sigma}$ + 0.06 (r = 0.985) in MeOH; log k/$k_0$ = -2.22${\sigma}$ + 0.08 (r = 0.995) in DMF. Large deviation of p-nitro aniline in DMF is resulted from solvent effects too. From above results, the substituent effect of this reaction can be described as $S_N2$ mechanism and bond formation more proceeds in DMF relative to MeOH.

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Effect of Aging on the Liver Damage in Bromobenzene-pretreated Rats (연령이 다른 흰쥐에 Bromobenzene 미치는 영향)

  • 한선일;윤형원;윤종국
    • Biomedical Science Letters
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    • v.5 no.2
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    • pp.201-208
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    • 1999
  • To evaluate an effect of growth periods on the bromobenzene-induced liver damage, bromobenzene was administrated to 5-week-old rats and 10-week-old rats pretreated with bromobenzene 5 times every other day for 10 days and then the animals were sacrificed. The results were obtained as follows; The increasing rate of serum levels of alanine aminotransferase, xanthine oxidase activity, hepatic lipid peroxide contents, liver weight per body weight (%) and decreasing rate of hepatic contents of protein to each control group were higher in 10-week-old rats than 5-week-old rats by the pretreatment of bromobenzene. According to the above results, 10-week-old rats indicated more severe liver injury than 5-week-old those in case of bromobenzene pretreatment. On the other hand, hepatic aniline hydroxylase activity was more increased in 10-week-old rats than 5-week-old rats both in control and bromobnezene pretreated rats where as the reverse in hepatic glutathione S-transferase. In case of hepatic GSH determination at the intervals of 2, 4, 8, 24 hours throughout 24 hr after administration of single dose of bromobenzene to 5-week-old and 10-week-old rats both in control and bromobnezene pretreated, the rate of GSH utilization was lower in 10-week-old rats than 5-week-old rats. In conclusion, from the above experimental, it is deduce that the 10-week-old rats showed more severe liver injury than 5-week-old rats by the bromobenzene treatment because the disposal ability of bromobenzene in liver was lower in 10-week-old rats than 5-week-old rats.

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Effect of Dietary Monascus Koji on the Liver Damage Induced by Bromobenzene in Rats (식이성 홍국이 Bromobenzene에 의한 간 손상의 해독에 미치는 영향)

  • 오정대;윤종국;유대식
    • Journal of the Korean Society of Food Science and Nutrition
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    • v.33 no.6
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    • pp.965-972
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    • 2004
  • In the present study, it is observed that Monascus diet may have a hepatoprotective effect on the liver damage induced by bromobenzene in rats. By treatment with bromobenzene (400 mg/kg, i.p.) once a day for 3 consecutive days, the liver damage was reduced in rats fed 2% Monascus diet, based on the liver functional and histopathological findings. Furthermore, retreatment of bromobenzene to the animals with damaged liver showed higher decreasing rate of hepatic glutathione content and increasing rate of cytochrome P450 dependent aniline hydroxylase activity at 4 h in rats fed 2% Monascus diet than those fed STD diet, and V$_{max}$ in glutathione S-transferase was higher in liver of rats fed 2% Monascus diet than those fed STD diet. On the other hand, activities of antioxidant enzymes such as hepatic glutathione S-transferase, catalase and superoxide dismutase were generally higher both in bromobenzene and 2% Monascus diet treated group than those fed STD diet. In conclusion, the rats fed 2% Monascus diet showed lower liver damage than those fed STD diet, which may be due to the acceleration of bromobenzene metabolism and detoxication of oxygen free radicals.s.

Development of 500 Kgf Thrust Liquid Propellant Rocket Engine (추력 500 Kgf 액체추진제 로켓엔진 개발)

  • 정동호;조용재;정규상
    • Proceedings of the Korean Society of Propulsion Engineers Conference
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    • 1997.04a
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    • pp.3-10
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    • 1997
  • 본 연구에서는 추력 500 Kgf의 액체 추진기관을 설계, 제작 및 연소시험을 수행하여 연소 특성을 살펴보았다. 추진제로는 우주발사체 Booster용으로 폭넓게 사용되는 탄화수소계 연료인 kerosene과 산화제로 취급이 용이하고 저장 특성을 지닌 98 % White Fuming Nitric Acid(WFNA)를 사용하였고, 엔진 점화를 위해 WFNA와 접촉 발화성 (Hypergolic)을 갖는 Furfuryl Alcohol/Aniline 혼합액을 사용하였다. 로켓엔진은 20 Kgf/$cm^2$의 연소실 압력으로 500 Kgf의 평균 추력을 내도록 설계되었고, 연소실벽을 고온 연소가스로 부터 보호하기 위해 Film Cooling 방식을 적용하였다.

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Structural Properties of Polyaniline Blended with PNIPAM

  • Neupane, Kosh-Prasad;Ha, Jin-Wook
    • Journal of the Korea Academia-Industrial cooperation Society
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    • v.4 no.3
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    • pp.209-213
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    • 2003
  • Polyaniline (PANi) composite particles were synthesized by chemical oxidation polymerization of aniline in presence of poly-n-isopropyl acryl amide (PNIPAM). The PANi particles formed in the reaction medium deposited onto non-conducting PNIPAM template to produce PANi-coated composite particles. The formation of composite was confirmed by FT-IR spectroscopy, and UV-VIS spectroscopy, and their morphological structures were examined by scanning electron microscopy (SEM). From the experimental results, it was determined that PANi was successfully coated onto non-conducting PNIPAM.

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