• 제목/요약/키워드: selenium compounds

검색결과 41건 처리시간 0.019초

손톱과 모발에서의 셀레노 화합물의 화학종 분석 (Speciation Analysis of Seleno-Compounds in Hair and Finger Nails)

  • 지영;금대섭;박용남
    • 대한화학회지
    • /
    • 제64권4호
    • /
    • pp.203-209
    • /
    • 2020
  • 손톱과 모발에서 셀레늄을 추출하고 HPLC-ICP/MS로 셀레늄의 각 화학종을 분리한 뒤 분석하였다. 셀레노 화합물은 주로 SeCys으로 구성되어 있음을 알아내었고 이 들 시료의 분석을 통하여 인체에서의 셀레늄에 농도의 변화에 대한 정보를 얻을 수 있었다. 5명의 참가자들에 대한 손톱을 12개월간 모니터링한 결과, 농도는 평균 858.6 ± 201.2 ng g-1 이었는데 각 개인의 농도는 시간에 따라 변화가 크지 않고 일정하게 유지되었으며 개인간의 평균값차이도 심하지 않았다. 모발의 경우, 평균농도는 205.3 ng g-1으로서 손톱보다는 낮았다. 지원자들에게 셀레늄 보조제 22 ㎍ day-1를 3개월씩 투여하였을 때에 섭취 전후(각 3개월의 기간)의 농도는 크게 변화하지 않았지만 셀레늄보조제의 농도를 300 ㎍ day-1으로 증가시켜 2개월간 투여하였을 때에는 손톱에서의 셀레늄 농도가 1,230 ng g-1으로 현저히 증가하는 것으로 나타났다. 결론적으로 손톱은 인체가 장기간(수 개월 이상)동안 노출되었거나 또는 흡수한 셀레늄에 관한 정보를 반영하여 나타낼 수 있음을 본 연구를 통하여 알아낼 수 있었다.

골다공증 모델의 뼈 재생기에 있어 셀레늄(Selenium)의 방사선 보호작용 (Anti-Ionizing Radiation Effect of Selenium on Osteoporosis Model during Bone Repair Process)

  • 김현;조상래;최창용;성환후
    • 한국수정란이식학회지
    • /
    • 제30권3호
    • /
    • pp.201-206
    • /
    • 2015
  • 본 연구는 방사선 조사 후, 난소 적출을 한 흰쥐에 있어서 골회복과정 중에 셀레늄(Se)에 의한 보호 작용을 평가한 연구이다. 목적 수행을 위해 난소 적출술을 실시한 암컷 Sprague-Dawley계 흰쥐 80마리를 무작위로 ovariectomized(Ov), Ov/Se, Ov/irradiated(Irr) 그리고 Ov/Se/Irr와 같이 4개의 처리군으로 구분하였다. 골 결손은 난소적출(ovariectomy) 후, 40일에 모든 공시동물의 경골(tibia)에서 만들어졌다. 수술 후, 48시간에 Ov/Se군과 Ov/Se/Irr 처리구의 흰쥐에만 0.8 mg Se/kg을 투여하였다. 수술 후, 72시간에 Ov/Irr 군과 Ov/Se/Irr 처리구의 흰쥐에만 10Gy의 X-rays 조사를 사지부위(limb region)에 실시하였다. 수술 후, 모든 공시동물은 7, 15, 22 그리고 29일에 안락사를 시키고, 섬유주골형(trabecular bone)의 개수 분석(Masson Trichrome) 과 복 굴절 분석(Picrosirius)에 의해서 골 회복과정을 평가하였다. 난소적출한 군 및 방사선 조사한 군에서 골 재생 과정이 지연되는 현상을 확인이 가능하였다. 결론적으로, 셀렌산염 (sodium selenite)은 독성 없이 난소 적출을 한 흰쥐의 경골(tibia)의 골 재생과정에서 방사선 보호작용을 할 가능성을 제시하였다.

The protective effects of trace elements against side effects induced by ionizing radiation

  • Hosseinimehr, Seyed Jalal
    • Radiation Oncology Journal
    • /
    • 제33권2호
    • /
    • pp.66-74
    • /
    • 2015
  • Trace elements play crucial role in the maintenance of genome stability in the cells. Many endogenous defense enzymes are containing trace elements such as superoxide dismutase and metalloproteins. These enzymes are contributing in the detoxification of reactive oxidative species (ROS) induced by ionizing radiation in the cells. Zinc, copper, manganese, and selenium are main trace elements that have protective roles against radiation-induced DNA damages. Trace elements in the free salt forms have protective effect against cell toxicity induced by oxidative stress, metal-complex are more active in the attenuation of ROS particularly through superoxide dismutase mimetic activity. Manganese-complexes in protection of normal cell against radiation without any protective effect on cancer cells are more interesting compounds in this topic. The aim of this paper to review the role of trace elements in protection cells against genotoxicity and side effects induced by ionizing radiation.

The Matrix Effect of Biological Concomitant Element on the Signal Intensity of Ge, As, And Se in Inductively Coupled Plasma/Mass Spectrometry

  • Park, Kyung-Su;Kim, Sun-Tae;Kim, Young-Man;Kim, Yun-je;Lee, Won
    • Bulletin of the Korean Chemical Society
    • /
    • 제23권10호
    • /
    • pp.1389-1393
    • /
    • 2002
  • The non-spectroscopic interference effects that occurred in inductively coupled plasma/mass spectrometry were studied for Ge, As and Se in human urine and serum. Many biological samples contain Na, K, Cl and organic compounds, which may cause the enhancement and depression on the analyte signal. The effect of 1% concomitant elements such as N, Cl, S, P, C, Na, and K on a 100 ㎍/L germanium, arsenic and selenium signal has been investigated by ICP/MS. The interference effects were not in the same direction. It appeared that concomitant elements such as Cl, S, and C induce an enhancement effect, whereas N and P did not show any significant effect. And, Na and K caused a depression. We have found a link between the abundance of analytes and the ionization potential of concomitant elements (eV), except carbon and nitrogen.

새로운 1,2-다이아제피노 [3,4-b]퀴녹살린류와 피리다지노 [3,4-b] 퀴녹살린류의 합성 (Synthesis of Novel 1,2-Diazepino[3,4-b] quinoxalines and pyridazino[3,4-b] quinoxalines)

  • 김호식;이성욱;정극;이만길
    • 약학회지
    • /
    • 제44권4호
    • /
    • pp.325-333
    • /
    • 2000
  • The 1,3-dipolar cycloaddition reaction of the quinoxaline 4-oxides 2 with 2-chloroacrylonitrile gave the 2,3-dihydro-1H-1,2-diazepino[3,4-b]quinoxalines 3, which were converted into the 2,3,4,6-tetrahydro-1H-1,2-diazepino[3,4-b]quinoxalines 5-7. The reaction of compounds 3 with selenium dioxide in acetic acid/water resulted in ring transformation to give the 1,4-dihydro-4-oxopyridazino[3,4-b]quinoxalines 8.

  • PDF

Benzofuroxan으로부터 Quinoxaline 유도체의 합성(제1보) (Synthesis of Quinoxaline Derivatives from Benzofuroxan (Part I))

  • 김호식;허재혁
    • 대한화학회지
    • /
    • 제48권4호
    • /
    • pp.385-393
    • /
    • 2004
  • Benzofuroxan과 ethyl acetoacetate를 반응시켜 2-ethoxycarbonyl-3-methylquinoxaline 1,4-dioxide (8)를 합성하고, 이것을 hydrazine hydrate 또는 selenium dioxide와 반응시켜 2-hydrazinocarbonyl-3-methylquinoxaline 1,4-dioxide (9) 또는 2-ethoxycarbonyl-3-formylquinoxaline 1,4-dioxide (10)를 합성하였다. 화합물 9를 alkanoyl chloride류, benzoyl chloride류, heteroacyl chloride류 및 benzenesulfonyl chloride류와 반응시켜 3-methyl-2-(substituted hydrazinocarbonyl)quinoxaline 1,4-dioxide류 (11-14)를 합성하였다. 화합물 9를 sodium nitrite와 반응시켜 2-azidocarbonyl- 3-methylquinoxaline 1,4-dioxide (15)를 합성한 다음, 이것을 디옥산/알코올류 용매하에서 환류시켜 Curtius 자리옮김반응에 의한 N-(3-methyl-1,4-dioxoquinoxalin-2-yl)-alkyl carbamate류 (16)를 합성하였다. 그리고 화합물 15를 치환 아닐린류와 반응시켜 2-(3-substituted phenylureido)-3-methylquinoxaline 1,4-dioxide류 (17)를 합성하였다. 한편 화합물 10을 benzoic hydrazide 또는 치환 아닐린류와 반응시켜 quinoxaline 1,4-dioxide류 (18, 19)를 각각 합성하였다. 그리고 합성한 화합물들에 대한 제초력과 살균력도 조사하였다.

분만전후 젖소의 지방간증에 관한 연구 (A Study on Fatty Liver Syndrome in Periparturient Holstein Cows)

  • 최희인;이준섭;이창우;윤영민
    • 한국임상수의학회지
    • /
    • 제10권2호
    • /
    • pp.147-155
    • /
    • 1993
  • This study was carried out to investigate the Preventive and treatment effects of mixed compound of vitamin E and selenium, and ursodeoxycholic acid on the pre-parturient and post-parturient fatty liver of high. yielding dairy cows. Thirty pregnant dairy cows(2 weeks preparturition) were divided into clinical(13cows) and subclinical(17 cows) groups based upon blood chemical values, blood serum protein levels and clinical symptoms. The clinical group was subdivided into treated clinical group(6 cows) and non-treated clinical group(7 cows). The cows(treated clinical group) with fatty liver diagnosed before parturition were dosed with mixed compound of vitamin I(1head) and selenium(10mg/head) intramuscularly once before and after parturition, respectively. These cows(treated clinical group) were also given ursodeoxycholic acid(50g/head) intramuscularly 3 times before parturition. The cows(treated clinical group) with fatty liver diagnosed after parturition were also given the same compounds as dosed to the above cows at same dose rate once or 3 times, respectively after parturition. Blood samples were collected from the cows on 4th, 7th and 2nd day of preparturition and on 1st, 7th, 14th and 20th day of postparturition. Blood chemical values(non-esterified fatty acid : NEFA) concentration, serum aspartate aminotransferase activity, serum ${\gamma}$-glutamyl transpeptidase activity, bilirubin concentration, glucose level) were checked and clinical symptoms of the cows were also observed. 1. The cows in non-treated clinical group showed severe depression, anorexia and diarrhea from prepartum period, and retained palcenta, endometritis, ketosis, abomasal displacement and mastitis after parturition. Cows in treated clinical group showed moderate depression, anorexia, diarrhea during preparturient period, but they were relieved within a week from parturition. Cows in subclinical group showed mild depression, anorexia and diarrhea after parturition, but these symptoms were not observed in prepartum period. 2. NEFA concentration, serum aspartate aminotransferase activity, serum ${\gamma}$-glutamyl transpeptidase activity and bilirubin concentration observed In the cows of treated clinical group were significantly lower than those of the cows non-treated clinical group. The blood glucose concentration of the cows in treated clinical group were higher than those of the cows in non-treated clinical group. These results indicate that the preparturient and postparturient fatty liver of high-yielding dairy cows could be reduced by dosing the animals with appropriate amounts of mixed compound of vitamin I and selenium, and ursodeoxycholic acid at proper times of the preparturition and postparturition of the dairy cows.

  • PDF

다류원료 식물류 물 추출물의 항산화 효과 (The Antioxidative Effects of the Water-Soluble Extracts of Plants Used as Tea Materials)

  • 김미혜;김명철;박종석;김종욱;이종옥
    • 한국식품과학회지
    • /
    • 제33권1호
    • /
    • pp.12-18
    • /
    • 2001
  • 본 연구는 다류원료 식물류의 물 추출물에 대해 항산화성을 검토하고 그 항산화 물질(페놀성 화합물, 비타민 C, 셀레늄)을 분석하였다. 대두유에 식물류의 물 추출물을 0.02%(추출고형분 함량, w/w) 첨가하여 $55^{\circ}C$ 공기순환식 인큐베이터에서 36일 저장기간 동안 과산화물가 측정과 $110^{\circ}C$에서 Rancimat 방법에 의해 항산화성을 검토하였으며 첨가제가 들어있지 않은 대두유를 대조구에 사용했고 0.02% BHT 첨가한 대두유는 비교구로 사용하였다. 대조구와 BHT 첨가구에 비해 산화 유도기간이 $55^{\circ}C$에서는 구기자, 우롱차, 귤껍질(진피), 유자, 매실 물 추출물 등이 길었으며 $110^{\circ}C$에서는 우롱차, 인스탄트커피, 유자, 구기자, 오미자, 매실 물 추출물 등이 길었다. 추출고형분 g당 총페놀성 물질 함량은 우롱차, 녹차, 홍차, 커피, 계피, 결명자 물 추출물 등에서 높았고 비타민 C 함량은 커피, 두충, 홍차, 영지, 계피, 감잎, 치커리, 녹차, 우롱차 물 추출물 등에서 높았으며 셀레늄은 모든 물 추출물에서 검출되지 않았다. 이들의 항산화성은 단일 항산화성 물질의 효과에 기인하기 보다는 페놀성 화합물, 비타민 C 등 복합적 효과에 의한 것으로 사료된다.

  • PDF

식물성 식품에 존재하는 Flavonoids의 항산화 활성 (Antioxidant Activity of Flavonoids in Plant Origin Food)

  • 김건희;최미희
    • 한국식품저장유통학회지
    • /
    • 제6권1호
    • /
    • pp.121-135
    • /
    • 1999
  • Effective synthetic antioxidants such as butylated hydroxyanisole(BHA) and butylated hydroxytoluene(BHT) have been widely used in the food industry, but they are suspected to be toxic and carcinogenic effects. Therefore, the development of safely available natural antioxidants such as ascorbic acid, ${\alpha}$-tocopherol, ${\beta}$-carotene, flavonoids and selenium is essential. In particular, flavonoids, 2-phenyl-benzo-${\alpha}$-pyrones, are polyphenolic compounds that occur ubiquitously in food of plant origin. flavonoids occur in foods generally as O-glycosides with sugars bound usually at the C\ulcorner position. And variations in their heterocyclic ring gibes rise to flavones, flavonols, flavanones, flavanols, catechins, anthocyanidins, chalcone and isoflavones. Vegetables, fruits, and beverages are the main dietary sources of the flavonols, primarily as quercetin, kaempferol, and myricetin and the corresponding flavones, apigenin and luteolin. These flavonoids have biological activity such as antioxidant, anti-inflammatory, antithrombotic, antimutagenic, anticarcimogenic antiallergic and antimicrobial activity effects in vitro and in vivo. Flavonoids posses strong antioxidant activities acting as oxygen radicals scavenger, metal chelators and enzyme inhibitor. The antioxidant activity of flavonoids is determined by their molecular structure and more specially, by the position and degree of hydroxylation of the ring structure. All flavonoids with the 3`, 4`-dihydroxy(ortho-dihydroxy) posses marked antioxidant activity. And antioxidant activity increases with the number of hydroxyl groups substituted on the A-and B-rings. There is as yet no certainty about the effect of the presence of a double bond between C\ulcorner and C\ulcorner on the antioxidant activity of flavonoids.

  • PDF

Advances in the Field of Thermal Procedures in Direct Combination with Thin-layer Chromatography

  • Stahl, Egon
    • 생약학회지
    • /
    • 제7권1호
    • /
    • pp.3-13
    • /
    • 1976
  • The hitherto existing gap in the field of chromatographic methods has been filled by the direct coupling of a suitable oven (TAS-oven) with TLC. The sample to be examined is heated either isothermally or linearly within the temperature gradient of $50{\sim}450^{\circ}C$. The volatile and/or thermolytically evolved substances are fractionated on the TLC-layer and subsequently chromatographed under standard conditions. Transport mechanisms from the sample to the TLC-layer, applications of the TAS-procedure and further developments are discussed. Thermofractography, developed from the TAS-procedure, is demonstrated on different groups of natural substances such as alkaloids, amino acids, nucleic acids. nucleosides, nucleotides, triglycerides and other lipids, pyrone glycosides and aglycon. Experimental work and results on the thermolysis of macromolecular natural and synthetic substances, natural polyphenols, tanning agents and leather and the possibilities of differentiating various lignins, carbohydrate and synthetic polymers are reported. Further, it is shown that classical reactions in the microgram range, e.g. zinc dust distillation, sulphur-and selenium dehydrogenation and catalytic dehydrogenation, can be coupled directly with TLC. Also described is a method which allows to investigate the gaseous compounds evolved during thermofractography in the range of up to $450^{\circ}C$. Thermal procedures coupled with TLC open up the following new possibilities for chemical microanalysis: fractionated separation of distillable and sublimable components, fractionated thermolysis and carrying out of thermal reactions in the ultra micro range.

  • PDF