• Title/Summary/Keyword: 1H-NMR spectroscopy

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Evaluation of Hydration Effect on Human Skin by $^1H$ MRS at 14.1T

  • Choi Chi-Bong;Hong Sung-Tak;Choe Bo-Young;Woo Dong-Chul;Yoon Seong-Ik;Cho Ji-Hyun;Lee Chul-Hyun;Cheong Chae-Joon;Park Sang-Yong;Oh Chil-Hwan
    • Journal of the Korean Magnetic Resonance Society
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    • v.10 no.1
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    • pp.105-114
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    • 2006
  • Purpose: We achieved high resolution MR imaging and spectra of human skin in vitro with using a 14.1 T MRI/MRS system, and evaluated the hydration effect of various cosmetic products by measuring the skin's. moisture concentration. Materials and Methods: We used the Bruker 14.1 T MRI/MRS system with a vertical standard bore that was equipped with a DMX spectrometer gradient system (200 G/cm at a maximum 40 A), RF resonators (2, 5 and 10 mm) and Para Vision software. Spin echo and fast spin echo pulse sequences were employed for obtaining the high resolution MR images. The 3D-localized point resolved spectroscopy (PRESS) method was used to acquire the MR spectra. Results: The high resolution MR images and spectra of human skin in vitro were successfully obtained on a 14.1 T system. The water concentration of human skin after applying a moisturizer was higher than that before applying a moisturizer. Conclusions: The present study demonstrated that the high-resolution MR images and spectra of human skin from a high field NMR instrument could be applicable to evaluating the hydration state of the stratum corneum.

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Trisoxazole Macrolide from a Marine Sponge Sarcotragus Species

  • Liu, Yong-Hong;Shinde, Pramod B.;Hong, Jong-Ki;Lee, Chong-O.;Im, Kwang-Sik;Jung, Jee-H.
    • Natural Product Sciences
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    • v.11 no.1
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    • pp.50-53
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    • 2005
  • Bioassay-directed fractionation of the lipophilic extract of a marine sponge Sarcotragus sp. led to the isolation of a known trisoxazole containing macrolide, mycalolide B (1). Its structure was identified by NMR and MS analyses. This is the first report on the isolation of macrolide from a sponge of the genus Sarcotragus (Order: Dictyoceratida).

Synthesis and characterization of ABA types tri-block copolymers derived from p-dioxanone, ${\varepsilon}-caprolactone$ and poly(ethylene glycol)

  • Remant Bahadur K.C.;Bhattarai Shanta Raj;Aryal Santosh;Khil, Myung-Seob;Kim, Hak-Yong;Lee, Douk-Rae
    • Proceedings of the Polymer Society of Korea Conference
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    • 2006.10a
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    • pp.255-255
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    • 2006
  • Polymeric nanoparticles are recognized as promising drug carriers [1]. Here, novel tri-block copolymers based on poly PPDO, PCL and PEG were synthesized and employed for the formulation of reproducible polymeric nanoparticles [2]. To estimate the feasibility of the polymer to form polymeric nanoparticles, nanoparticles were prepared by co-solvent evaporation technique. Polymerization and structural features of the polymer were analyzed by different physico-chemical techniques. Existence of hydrophobic domains as a core of nanoparticles was characterized by $^{1}H-NMR$ spectroscopy, and further confirmed by fluorescence technique using pyrene as probe.

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A Study on the Preparation of New Functionalized Aminosilanes as a promising coupling agent(I) (결합제로서 가능성 있는 새로운 작용기를 갖는 Aminosilane 제조에 관한 연구(I))

  • 한정식;서태석
    • Proceedings of the Korean Society of Propulsion Engineers Conference
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    • 1998.10a
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    • pp.23-23
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    • 1998
  • Michael Reaction을 이용하여 상업적으로 이용 가능한 APS(3-aminopropyltrime thoxysilane)과 AEAPS(N-[3-(trimethoxysilyl)propy1] ethylenediamine)을 다수의 Michael acceptor(ethyl acrylate, acrylonitrile, acrylamide, 2-cyanoethyl acrylate, 2-hydroxyethyl acrylate 그리고 3-(trimethoxysilyl)propylmethacrylate)와 반응시켜 10종류의 aminosilane ([3-{N-2-carboethoxyethyl)aminopropyl]triethoxysilane, [3-(N-2-cyanoethyl)aminopropyl] triethoxysilane, [3-(N-di-2-carboethoxyethyl) aminopropyl]triethoxysilane, [3-(N-di-2-cyanoethyl)aminopropyl]triethoxysilane, [3-(N-2-cyanoethoxypropionyl)aminopropyl] triethoxysilane, [3-(N-di-2-cyanoethoxypropionyl)aminopropyl] triethoxysilane, [3-(N-di-2-hydroxyethoxypropionyl) aminopropyl]-triethoxysilane, [3-(N-2-amidoethyl aminopropyl]triethoxysilane, {3-[N-(N-di-2-cyanoethyl)ethyl]aminopropyl)triethoxysilane, {3-[N-(3-trimethoxy-silylpropyl)-2-methylpropionyl]aminopropyl)triethoxysilane 등을 35-70% 수율로 제조하였으며, 이들의 구조는 $^1$H-NMR과 FT-IR spectroscopy를 이용하여 확인하였다.

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Chemical Investigation of the Sea Cucumber Stichopus japonicus

  • Shinde, Pramod B.;Dang, Hung The;Li, Huayue;Hong, Jong-Ki;Shin, Sook;Jung, Jee-H.
    • Natural Product Sciences
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    • v.14 no.1
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    • pp.12-15
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    • 2008
  • A chemical investigation of the polar extract of the sea cucumber Stichopus japonicus, collected from Jeju Island, Korea, has led to isolation of five new fatty acid derivatives (1, 4 - 7) along with known compounds (2 - 3, 8 - 14). Their structures were elucidated by a combination of MS and NMR spectroscopy.

Chemical Analyses of Coniferous Flavonoids in Korea - The Flavonoids of Red Pine Bark(Pinus densiflora) - (침엽수(針葉樹) 수피(樹皮)의 Flavonoid에 관한 성분분석(成分分析) (I) - 소나무 수피(樹皮)의 Flavonoids -)

  • Kim, Hoon;Song, Hong-Keun;Chung, Dae-Kyo
    • Journal of the Korean Wood Science and Technology
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    • v.19 no.4
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    • pp.73-79
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    • 1991
  • The flavonoids from plants is very widly used as natural dye for food and medicine etc. In this study, red pine which is widespread in Korea was studied to find new chemicals which may use as raw material for the special purpose. The fIavonoids of red pine bark were separated with Sephadex LH-20 and Toyo pearl HW-40F as packed materials and the structure of separated f1avonoids was determined by $^1H$-and $^{13}C$-NMR spectroscopy. The (+) catechin which is widespread in nature and dihydroquercetin-3'-0-${\beta}$-galactoside were found in red pine bark. The dihydroquercetin-3'-0-${\beta}$-galactoside is newly found in this species.

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Synthesis of Hole Transport Materials for Organic Light Emitting Device (유기발광디바이스용 정공수송재료의 합성)

  • Chung, Pyung-Jin;Cho, Min-Ju
    • Korean Journal of Materials Research
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    • v.15 no.7
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    • pp.448-452
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    • 2005
  • This study was based on organic electroluminescence display. Especially, TPD and $\alpha-NPD$ for the hole transport materials were synthesized by Ullmann reaction. This reaction was conducted between 3­methylphenylamine, 1-naphthylamine and 4,4'-diiodobiphenyl in toluene containing CuCl catalyst and KOH base. The structural property of reaction products were analyzed by FT-IR, $^1H-NMR$ spectroscopy, and thermal stability, reactivity and PL property were analyzed by melting point, yield and emission spectrum, respectively. The photoluminescence spectra of a pure TPD and $\alpha-NPD$ were observed at approximately 416nm and 438nm respectively. In this study, it was known that the melting point, yield, PL properties of TPD and $\alpha-NPD$ were changed by substituent group of amines.

Synthesis of (Diamine)platinum(II) and (Diamine)platinum(IV) Complexes of Isopropylidenmalonate Ligand and Their Interaction with Guanosine-$5^{\prime}$-Monophosphate

  • 이은주;전무진;손윤수
    • Bulletin of the Korean Chemical Society
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    • v.19 no.10
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    • pp.1099-1105
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    • 1998
  • A series of (diamine)isopropylidenmalonatoplatinum(Ⅱ) complexes and the oxidation products, (diamine)Pt (OOC)2C=C(CH3)2(X)2, (diamine=ethylenediamine(en), 1,2-diaminopropan(dap), N-methylethylenediamine(men); X=OH, OCOCH3, OCOCF3), have been prepared, and their interaction with guanosine-5'-monophosphate (5'-GMP) have been examined by means of 1H NMR spectroscopy. The present platinum(Ⅱ) complexes have shown to interact with 5'-GMP through N7 coordination in two concecutive steps in a similar way as with cisplatin, but no interaction between the present platinum(Ⅳ) complexes and 5'-GMP was observed. However, in the presence of ascorbic acid, the platinum(Ⅳ) complexes have been found to interact with 5'-GMP with the reaction rate depending on their reduction rate.

Analysis of Medicinal Plants in Cosmetics(II) The HPLC Separation and Quantitation of Artemisia Extract in Cosmetic SOAP (화장품중 생약성분의 분석(II) 화장비누중의 쑥추출액의 함량분석)

  • Im, Ho-Bin;Choe, Sang-Won;Kim, Jin-U
    • Journal of the Society of Cosmetic Scientists of Korea
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    • v.16 no.1
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    • pp.40-46
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    • 1990
  • A method was described for the analysis of Artemisia extract in cosmetic soap. Esculetin-6-methylether was used as indicator ingredient for analysis of Artemisia extract. It was isolated from the plant and purified with silicagel column. The structure was conformed with IR, NMR and MASS spectroscopy. The Artemisia extract in sample was isolated with chloroform and interfering com- pounds were eliminated with silicagel column. The Artemisia extract was determined by reverse phase high- performance liquid chromatography with a fluorescence detector and a solvent system of H2O/THF/MeOH. The recorveries of Artemisia extract were 93.9-106.1% in the cosmetic soap.

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Isolation and Purification of an Antitumor Metabolite from Alternaria brassicicola SW-3, the Cause of Brassica Black Leaf Spot Disease. (Phytopathogenic fungus Alternaria brassicicola SW-3가 생산하는 항암활성 물질의 분리 정제)

  • 나여정;이방숙;남궁성건;정동선
    • Microbiology and Biotechnology Letters
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    • v.30 no.1
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    • pp.51-56
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    • 2002
  • An antitumor substance was purified from the culture filtrate of phytopathogenic fungus Alternaria brassicicola SW-3 isolated from soil of a chinese cabbage patch, and its characteristics were investigated. Antitumor activity of A. brassicicola SW-3 was measured by MTT assay. The cytotoxic activity against human cancer cell line was detected in the culture filtrate of A. brassicicola SW-3, but no activity found in mycelium. Antitumor substance was isolated from the culture broth by ethyl acetate extraction and purified by silica gel column chromatography. Structure of the purified compound was analyzed by the instrumental analysis such as $^1$H-NMR, $^{13}$ C-NMR and IR spectroscopy. The purified fungal metabolite of an A. brassicicola SW-3, consists of 11 carbon chain with two hydroxyl groups and two epoxides which is identical to depudecin. The $IC_{50}$/ values of the active compound identified as depudecin were $69\mu$g/mL and $57\mu$g/mL against mouse melanoma B16BL6 cell line, and human hepatoma SK-HEP1 cell line, respectively.