• Title/Summary/Keyword: Glycolic Acid

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Effects of Ascorbic Acid, Thiols and Organic Acid on Polyphenol Oxidase Activity (아스코르빈산과 티올류 및 유기산이 폴리페놀 화효소 활성에 미치는 영향)

  • 김안근;김유경
    • YAKHAK HOEJI
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    • v.45 no.4
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    • pp.387-396
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    • 2001
  • The effects of ascorbic acid, thiols such as cysteine, n-acetyl-ι-cyteine, glutathione, thiourea, 2-mercaptoethanol and dithiotreithol and organic acids such as magic acid, citric acid, glycolic acid, taurine and kojic acid on polyphenol oxidate (PPO) activity were studied in order to establish if it reacts with oxidized product and/or directly inhibits the enzyme. To investigate the mechanism, the quantification of t-butylcatechol and 4-methylcatechol (phenolic compounds) as substates, their oxidized product and sulphydryl colorless additional compounds were determined by high performance liquid chromatograph (HPLC) method. Chromatographic results indicate that ascorbic acid, organic acids and lower level of cysteine reduced oxidized product of substrates back to their respective positions uf ο-diphenols. On the other hand, other thiols and high level of cysteine reacted with oxidative product of ο-diphenols and then produced sulphydryl colorless compounds. Cysteine apperars to have two types of mechanism of actions in the formation of oxidative products of substrates depending on its concentration; ascorbic acid-type and other thiols-types. The effect of ascorbic acid with thiols on polyphenol oxidase was determined by same method. Chromatographic results indicate that ascorbic acid was more reactive with oxidized product of substrates than thiols.

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Comparison of Acid and Phenol Compounds in Smoke Total Particulate Matter by the Different Tobacco Leaves (잎담배 종류 및 등급에 따른 담배 연기응축물의 Acid 및 Phenol 화합물 함량 비교)

  • 황건중;이문수;나도영;장기철
    • Journal of the Korean Society of Tobacco Science
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    • v.22 no.1
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    • pp.84-90
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    • 2000
  • This study was conducted to determine the acid and phenol compounds in smoke total particulate matter(TPM) by the different tobacco variety, and grade of tobacco leaves. Sixteen kinds of tobacco leaves which were flue-curd, burley, orient, reconstituted tobacco, expanded stem, and expanded cut tobacco, were selected for this study. After collecting a TPM by using smoking machine, the concentration of TPM components was analyzed by GC. Acid components of TPM of mainstream smoke were different from the variety and grade. The order of the highest concentration of acid compounds in TPM was flue-cured > orient> burley> expanded cut tobacco> reconstituted tobacco> expanded stem. Though lactic acid and glycolic acid concentrations in flue-cured tobacco were twice higher than those in burley tobacco, the contents of 2-furoic acid and 3,4-dihydroxy butanoic acid in burley tobacco were higher than those in flue-cured tobacco. The content of phenolic compounds in the high grade and thick leaves was higher than that in other tobacco leaves. Phenol and catechol compounds in burley CD3W-2 revealed the least value in concentration among the samples tested. Pyrocatechol and hydroquinone concentrations in flue-cured tobacco were 2-3 times higher than those in burley and orient tobacco.

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Investigation of Eu(Ⅲ)-Polyfunctional Organic Acid Complexes by Eu(Ⅲ) Luminescence Spectroscopy (Eu(Ⅲ) 발광 분광법을 이용한 Eu(Ⅲ)과 다가 유기산 착물 연구)

  • Lee, Byoung Ho;Shin, Hyun Sang;Moon, HiChung
    • Journal of the Korean Chemical Society
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    • v.40 no.1
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    • pp.59-64
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    • 1996
  • The 7F0→5D0excitation spectra of Eu(Ⅲ) complexed with polyfunctional monocarboxylic acid(glycolic acid, glycine and thioglycolic acid) containing a terminal O, N and S neutral donors and propionic acid were investigated using Eu(Ⅲ) luminescence spectroscopy. In the excitation spectra of Eu(Ⅲ)-propionate system, the stepwise appearance of the peaks was observed at 579.0, 579.2 and 579.5 nm with increasing in the ligand-to-metal ratio, which correspond to the formation of Eu(propionate)2+, Eu(propionate)2+ and Eu(propionate)3 species. Three maximum peaks were also obtained for Eu(Ⅲ)-glycolate, Eu(Ⅲ)-glycinate and Eu(Ⅲ)-thioglycolate systems and were found to be quite similar to those of Eu(Ⅲ)-propionate system. The q values (number of coordinated water molecules of Eu(Ⅲ) ion) obtained from the luminescence decay constants of Eu(Ⅲ)-glycolate and Eu(Ⅲ)-thioglycolate were 7.0 and 7.1, and compare well with 7.3 for Eu(Ⅲ)-propionate: Each ligand units replace around two coordinated water molecules. These results show that the polyfunctional monocarboxylates behaves like the propionate for Eu(Ⅲ) ion coordination.

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Study on Biocompatibility and Morphology with Hydrolysis Degradation of Poly(ester amide) derived from Glycine and/or 4-Aminobutyric acid (Glycine and/or 4-aminobutyric acid로부터 유도된 Poly(ester amide)의 생체 적합성 및 분해에 따른 형태학적 고찰)

  • 한상일;임승순
    • Proceedings of the Korean Fiber Society Conference
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    • 2002.04a
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    • pp.49-52
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    • 2002
  • 합성 고분자의 생분해는 환경 보존이라는 측면에서 중요시 되고 있으며 봉합사나 bone fixation, 그리고 implant와 같은 의학적 응용면에서도 상당한 관심의 대상이 되어오고 있다 glycolic acid, L-lactic acid, $\varepsilon$-caprolactone에 근거하는 지방족 폴리에스터는 생분해성 봉합사로서 응용되고 있으나 여전히 열적, 기계적 가공특성과 같은 적정특성들이 부족하다.$^1$ 한편 폴리아마이드는 유사한 구조를 갖는 폴리에스터와 비교할 때에 상대적으로 높은 유리전이온도와 높은 융점을 가지고 있는 반면 높은 흡습성으로 인한 물성저하가 야기될 수 있다. (중략)

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CORRELATION BETWEEN SKIN IRRITATION AND CYTOTOXICITY OF ANTI-WRINKLE AGENTS

  • Lee, Eun-Hee;Hong, Jin-Tae;Lee, Jong-Kwon;Kim,Yong-Kyu;Park, Ki-Sook;Jung, Kyoung-Mi;Kwan, Jung-Hai;Lee, Sun-Hee;Yang, Ki-Hwa;Chung, Soo-Youn
    • Proceedings of the Korean Society of Toxicology Conference
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    • 2001.05a
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    • pp.110-110
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    • 2001
  • To compare skin irritation and cytotoxicity of anti-wrinkle agents, we examined skin irritation of six anti-wrinkle agents (ascorbic acid, glycolic acid, all trans-retinoic acid, ginseng extract, retinol, EB) in New Zeland white rabbit.(omitted)

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