• 제목/요약/키워드: Mg extraction

검색결과 1,570건 처리시간 0.025초

포도부산물인 과피로부터 항산화 물질 최적 추출방법 확립 (Optimal Extract Methods of Antioxidant Compounds from Coat of Grape Dreg)

  • 유미애;정혜경;강명화
    • 한국식품과학회지
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    • 제36권1호
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    • pp.134-140
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    • 2004
  • Anthocyanin색소의 추출은 일반적으로 산을 첨가하면 그 추출효율이 증가한다고 보고되어진 바가 있다. 따라서 본 실험에서는 campbell early 포도의 부산물인 과피로부터 항산화 물질을 추출하기 위한 최적추출조건을 확립하기 위하여 ethanol 용매에 산의 종류를 달리하여 추출한 후 anthocyanin, resveratrol, quercetin함량을 측정하고, 이들의 항산화 효과를 분석하였다. 그 결과, anthocyanin색소 중 peonidin-3-glucoside는 0.1% HCl을 첨가한 추출물에서 가장 효과적이었으며, cyanidin-3-glucoside는 오히려 산을 첨가하지 않은 ethanol 용매에서 추출한 campbell early 과피 추출물이 가장 효과적이었다. 또한 항산화 활성을 가지고 있는 페놀성 화합물인 resveratrol과 quercetin의 함량은 0.1% HCl을 첨가한 campbell early 과피 추출물에서 각각 8.1 mg/100g coats로 다른 종류의 산을 처리한 것보다 더 많은 양이 함유되어 있는 것으로 나타났다. DPPH에 의한 항산화 효과 측정에서는 산을 첨가한 추출물 모두 15분 이내에 모든 반응이 정지되었으며, 대조군에 비해 높은 전자공여능을 보였다. Lecithin을 이용한 TBARS는 citric acid와 phosphoric acid, formic acid를 첨가한 경우 각각 59.3, 60.5, 56.8%로 유의적으로 높은 수준을 보였다. 이러한 결과로부터 campbell early 과피에 0.1% HCl가 첨가된 ethanol용매로 추출시 항산화 활성이 높은 추출물을 제조할 수 있었다.

테르페나딘 체내동태 연구를 위한 혈청 중 펙소페나딘의 HPLC 정량법 개발 및 검증 (Development and Validation of an HPLC Method for the Pharmacokinetic Study of Fexofenadine in Human)

  • 조혜영;강현아;김윤균;최후균;이용복
    • Journal of Pharmaceutical Investigation
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    • 제35권6호
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    • pp.437-443
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    • 2005
  • A rapid, selective and sensitive reversed-phase HPLC method for the determination of a major metabolite of terfenadine, fexofenadine, in human serum was developed, validated, and applied to the pharmacokinetic study of terfenadine. Fexofenadine and internal standard, haloperidol were extracted from human serum by liquid-liquid extraction with acetonitrile and analyzed on a $Symmetry^{TM}$ C8 column with the mobile phase of 1% triethylamine phosphate (pH 3.7)-acetonitrile (67:33, v/v, adjusted to pH 5.6 with triethylamine). Detection wavelength of 230 nm for excitation, 280 nm for emission and flow rate of 1.0 mL/min were fixed for the study. The assay robustness for the changes of mobile phase pH, organic solvent content, and flow rate was confirmed by $3^{3}$ factorial design using a fixed fexofenadine concentration (50 ng/mL) with respect to its peak area and retention time. In addition, the ruggedness of this method was investigated at three different laboratories using same quality control (QC) samples. This method showed linear response over the concentration range of 10-500 ng/mL with correlation coefficients greater than 0.999. The lower limit of quantification using 0.5 mL of serum was 10 ng/mL, which was sensitive enough for the pharmacokinetic studies of terfenadine. The overall accuracy of the quality control samples ranged from 95.70 to 114.58% for fexofenadine with overall precision (% C.V.) being 3.53-14.39%. The relative mean recovery of fexofenadine for human serum was 90.17%. Stability studies (freeze-thaw, short-term, extracted serum sample and stock solution) showed that fexofenadine was stable during storage, or during the assay procedure in human serum. However, the storage at $-70^{\circ}C$ for 4 weeks showed that fexofenadine was not stable. The peak area and retention time of fexofenadine were not significantly affected by the changes of mobile phase pH, organic solvent content, and flow rate under the conditions studied. This method showed good ruggedness (within 15% C.V.) and was successfully used for the analysis of fexofenadine in human serum samples for the pharmacokinetic studies of orally administered Tafedine tablet (60 mg as terfenadine) at three different laboratories, demonstrating the suitability of the method.

에토돌락 체내동태 연구를 위한 혈청 중 에토돌락의 HPLC 정량법 개발 및 검증 (Development and Validation of an HPLC Method for the Pharmacokinetic Study of Etodolac in Human)

  • 조혜영;강현아;문재동;최후균;이용복
    • Journal of Pharmaceutical Investigation
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    • 제35권4호
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    • pp.265-271
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    • 2005
  • A rapid, selective and sensitive reversed-phase HPLC method for the determination of etodolac in human serum was developed, validated, and applied to the pharmacokinetic study of etodolac. Etodolac and internal standard, ibuprofen were extracted from human serum by liquid-liquid extraction with hexane/isopropanol (95:5, v/v) and analyzed on a Luna C18(2) column with the mobile phase of 1% aqueous acetic acid-acetonitrile (4:6, v/v). Detection wavelength of 227 nm and flow rate of 1.0 mL/min were fixed for the study. The assay robustness for the changes of mobile phase pH, organic solvent content, and flow rate was confirmed by $3^3$ factorial design using a fixed etodolac concentration $(1\;{\mu}g/mL)$ with respect to its peak area and retention time. And also, the ruggedness of this method was investigated at three different laboratories using same quality control (QC) samples. This method showed linear response over the concentration range of $0.05-40\;{\mu}g/mL$ with correlation coefficients greater than 0.999. The lower limit of quantification using 0.5 mL of serum was 0.05 ${\mu}g/mL$, which was sensitive enough for pharmacokinetic studies. The overall accuracy of the quality control samples ranged from 92.00 to 110.00% for etodolac with overall precision (% C.V.) being 1.08-10.11%. The percent recovery for human serum was in the range of 76.73-115.30%. Stability studies showed that etodolac was stable during storage, or during the assay procedure in human serum. The peak area and retention time of etodolac were not significantly affected by the changes of mobile phase pH, organic solvent content, and flow rate under the conditions studied. This method showed good ruggedness (within 15% C.V.) and was successfully used for the analysis of etodolac in human serum samples for the pharmacokinetic studies of orally administered Lodin XL tablet (400 mg as etodolac) at three different laboratories, demonstrating the suitability of the method.

페노프로펜 체내동태 연구를 위한 혈청 중 페노프로펜의 HPLC 정량법 개발 및 검증 (Development and Validation of an HPLC Method for the Pharmacokinetic Study of Fenoprofen in Human)

  • 조혜영;강현아;김윤균;사홍기;이용복
    • Journal of Pharmaceutical Investigation
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    • 제35권6호
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    • pp.423-429
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    • 2005
  • A selective and sensitive reversed-phase HPLC method for the determination of fenoprofen in human serum was developed, validated, and applied to the pharmacokinetic study of fenoprofen calcium. Fenoprofen and internal standard, ketoprofen, were extracted from human serum by liquid-liquid extraction with diethyl ether and analyzed on a Luna C18(2) column with the mobile phase of acetonitrile-3 mM potassium dihydrogen phosphate (32:68, v/v, adjusted to pH 6.6 with phosphoric acid). Detection wavelength of 272 nm and flow rate of 0.25 mL/min were fixed for the study. The assay robustness for the changes of mobile phase pH, organic solvent content, and flow rate was confirmed by $3^{3}$ factorial design using a fixed fenoprofen concentration $(2\;{\mu}g/mL)$ with respect to its peak area and retention time. And also, the ruggedness of this method was investigated at three different laboratories using same quality control (QC) samples. This method showed linear response over the concentration range of $0.05-100\;{\mu}g/mL$ with correlation coefficients greater than 0.999. The lower limit of quantification using 1 mL of serum was $0.05\;{\mu}g/mL$, which was sensitive enough for pharmacokinetic studies. The overall accuracy of the quality control samples ranged from 92.27 to 109.20% for fenoprofen with overall precision (% C.V.) being 5.51-11.71 %. The relative mean recovery of fenoprofen for human serum was 81.7%. Stability (freeze-thaw, short and long-term) studies showed that fenoprofen was not stable during storage. But, extracted serum sample and stock solution were allowed to stand at ambient temperature for 12 hr prior to injection without affecting the quantification. The peak area and retention time of fenoprofen were not significantly affected by the changes of mobile phase pH, organic solvent content, and flow rate under the conditions studied. This method showed good ruggedness (within 15% C.V.) and was successfully used for the analysis of fenoprofen in human serum samples for the pharmacokinetic studies of orally administered Fenopron tablet (600 mg as fenoprofen) at three different laboratories, demonstrating the suitability of the method.

양송이 버섯의 생물활성 다당류에 관한 연구 (Studies on Bioactive Polysaccharide Isolated from Agaricus bisporus)

  • 임은정;성하진;권미향
    • Applied Biological Chemistry
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    • 제41권1호
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    • pp.60-66
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    • 1998
  • 10종의 식용 버섯 자실체에 대한 항보체 활성 검색에서 가장 높은 활성을 나타낸 양송이버섯 자실체를 대상으로 항보체 활성물질의 추출조건을 조사하였다. 최적조건으로서 5% urea가 함유된 0.1 N NaOH 용액으로 $65^{\circ}C$에서 2시간동안 양송이버섯 자실체를 추출한 후 methanol 가용획분이 제거된 조다당 획분 AB-0를 얻었다. AB-0는 1 mg/ml에서 90% 이상의 높은 항보체활성을 나타내었으며 마우스에 이식된 sarcoma-180에 대하여 74%의 저지효과를 보였다. AB-0를 acetone 농도에 따른 침전 분획을 실시하여 AB-20, AB-40, AB-60, AB-80, AB-A의 5개의 획분을 얻었다. 이중 가장 높은 항보체활성과 수율을 나타낸 AB-20 획분은 탄수화물 39%, 단백질 46%를 함유하였으며, 구성당은 glucose, arabinose, xylose, galactose, mannose가 6.49 : 1.98 : 1.24 : 1.00 : 0.71의 비율로 존재하였고 구성아미노산은 isoleucine(12.60%), glutamic acid+glutamine(12.45%), valine(11.79%), alanine(11.46%), leucine(10.19%)와 aspartic acid, asparagine(10.56%) 등 이었다. Pronase 처리한 AB-20에서는 78.5%의 항보체활성을 나타내고 대조군에 비해 14.5% 감소하였으나, AB-20의 periodate 산화물에서는 활성이 42.6%로 50% 이상 크게 감소하였다. 따라서 양송이 버섯의 알칼리 추출물중 가장 강한 활성을 보인 AB-20의 주요 활성부위는 다당류이며 단백질도 일부 관여하는 것으로 생각되었다.

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체내동태 연구를 위한 혈청 중 펜톡시필린의 HPLC 정량법 개발 및 검증 (Development and Validation of an HPLC Method for the Pharmacokinetic Study of Pentoxifylline in Human Serum)

  • 조혜영;강현아;류희두;이화정;문재동;이용복
    • Journal of Pharmaceutical Investigation
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    • 제36권2호
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    • pp.89-95
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    • 2006
  • A selective and sensitive reversed-phase HPLC method for the determination of pentoxifylline in human serum was developed, validated, and applied to the pharmacokinetic study of pentoxifylline. Pentoxifylline and internal standard, chloramphenicol, were extracted from the serum by liquid-liquid extraction with dichloromethane and analyzed on a Luna CI8(2) column with the mobile phase of acetonitrile-0.034 M phosphoric acid (25:75, v/v, adjusted to pH 4.0 with 10 M NaOH). Detection wavelength of 273 nm and flow rate of 0.8 mL/min were used. This method showed linear response over the concentration range of 10-500 ng/mL with correlation coefficients greater than 0.999. The lower limit of quantification using 0.5 mL of the serum was 10 ng/mL, which was sensitive enough for pharmacokinetic studies of pentoxifylline. The overall accuracy of the quality control samples ranged from 89.3 to 92.7% for pentoxifylline with overall precision (% C.V.) being 4.1-9.2%. The relative mean recovery of pentoxifylline for human serum was 105.8%. Stability (stock solution, short and long-term) studies showed that pentoxifylline was not stable during storage. But three freeze-thaw cycles and extracted serum samples were stable. This method showed good ruggedness (within 15% C.V.) and was successfully applied for the analysis of pentoxifylline in human serum samples for the pharmacokinetic studies of orally administered $Trental^{\circledR}$ tablet (400 mg pentoxifylline), demonstrating the suitability of the method.

정상산란계(正常産卵鷄)에 있어서 탄수화물(炭水化物)과 지질대사(脂質代謝)의 생동역학(生動力學) -제2보(第二報) 방사능(放射能)$(C^{14})$포도당 주사후(注射後) 혈장(血漿) 지질(脂質)로의 방사능(放射能)의 병합(倂合)- (Biokinetics of Carbohydrate and Lipid Metabolism in Normal Laying Hen -II. Incorporation of Activity in Plasma Lipid After Injection of Glucose-U-$C^{14}$-)

  • 장윤환;피엠리스
    • Applied Biological Chemistry
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    • 제21권1호
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    • pp.63-67
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    • 1978
  • 균일(均一)하게 표식(漂識)된 $C^{14}$-포도당을 산란계(産卵鷄)에 주사후(注射後) 혈장(血漿) 지질(脂質)로 방사능(放射能)이 병합(倂合)되는 상태(狀態)를 조사(調査)하였다. 혈장(血漿)에서 전지질(全脂質)을 추출(抽出)하는 방법(方法)은 Folch등(等)의 방법(方法)을 조금 변형(變型)하여 적용(適用)하였으며 방사능(放射能)의 측정(測定)은 액체(液體)신치레숀카운터에 의(依)하여 실시(實施)하였다. 공시(供試)한 산란계(産卵鷄)의 혈장(血漿) 지질(脂質)의 농도(濃度)는 추적자량(追跡子豊)의 $C^{14}$-포도당을 정맥(靜脈)에 주사(注射)한 후(後) 5분(分)에 채취(採取)한 시료(試料)에서 100m1당(當) 3.07g을 나타내었다. 포도당의 비방사능(比放射能)은 대수적(對數的)으로 급속(急速)하게 감소(減少)하는 반면(反面) kg체중당(體重當), 주사단위량당(注射單位量當), 그리고 혈장(血漿) 지질(脂質)의 그람 탄소원자량(炭素原子當) 비방사능(比放射能)은 주사후(注射後) 120분(分)까지 시간(時間)에 따라서 매우 서서(徐徐)히 증가(增加)하였다. 포도당의 방사능(放射能)으로부터 혈장(血漿) 지질(脂質)의 방사능(放射能)으로 병합(倂合)되는 율(率)은 주사후(注射後) 120분(分)까지 0.73%이었다.

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크릴을 이용한 키토산 제조 및 품질 특성 (Study on the Manufacturing of Chitosan Using Krill(Euphausia superba Dana) and Quality Characteristics)

  • 도정룡;박인성;이성갑;김동수
    • Applied Biological Chemistry
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    • 제43권4호
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    • pp.309-313
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    • 2000
  • 무한한 잠재 자원량으로 미래의 식량자원으로서의 주목받고 있는 크릴에서 단백질을 추출하고 난후 생기는 부산물인 키틴 키토산의 특성을 조사하였다. raw krill과 krill powder의 일반성분은 수분 79.1, 5.6%, 단백질 13.1, 56.1%, 지방 4.0, 18.8%, 회분 2.7, 11.4%, 기타 1.1%, 8.1%로 나타났고 크릴로부터 추출된 키틴의 수율은 3.7%로 나타났고 일반성분 분석 결과 수분 7.1%, 회분 0.4%, 질소함량 3.5%,지방 3.1%로 나타났다. 추출된 키틴은 50% NaOH, $121^{\circ}C$에서 2시간 반응시켰을 때 가장 높은 탈아세틸화도인 82%의 수치를 나타냈다. 키토산 제조시 알칼리 농도와 반응온도가 일정할 때 반응 시간이 경과할수록 탈아세틸화도는 감소하였다. 키토산의 농도가 1%이고 shear rate 700 $S^{-1}$ 일때의 겉보기 점도는 0.09241 pa s로 나타났다. 크릴로부터 추출된 키토산은 Sigma사의 chitosan보다 탈아세틸화도와 점도가 낮게 나타났다.

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해산복족류(海産腹足類)의 Paramyosin의 분리(分離) 및 그 특성(特性)에 관(關)한 연구(硏究) (Isolation and Characterization of Paramyosins of Marine Gastropods)

  • 변재형
    • 한국식품영양과학회지
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    • 제2권1호
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    • pp.1-21
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    • 1973
  • The muscle of abalone, Notohaliotis discus (REEVE), and top-shell, Turbo cornutus Solander, were examined for protein composition. Then paramyosins which are known as one of the important structural protein of the muscle fibrils were isolated from the both muscle and their physico-chemical properties such as solubility, salting-out behaviour, intrinsic viscosity, ATPase activity, etc. involving amino acid composition and N-terminal amino acid residues were investigated to elucidate phylogenie characteristics more intensively from the viewpoint of comparative biochemistry. The analysis of protein composition resulted in the following estimations: abalone muscle; water-soluble protein of 22 %, salt-soluble protein, 34%, alkali-soluble protein, 20%, and stroma protein, 24%, and top-shell muscle; water-soluble protein of 16%, salt-soluble protein, 30%, alkali-soluble protein, 29%, and stroma protein, 25%, respectively. It is demonstrated in sedimentation analysis that paramyosin and myosin-actomyosin account for approximately 65% and 35% of the salt-soluble protein of abalone, and that the composition of both sediments in top-shell was approximately 70% and 30%, respectively. The ultracentrifugally homogenous paramyosins isolated essentially according to Bailey's ethanol-dried method from both of the muscle showed a $S^{\circ}_{20,w}$ of 3. 14s for abalone and a $S^{\circ}_{20,w}$ of 3.50s for top-shell. The both paramyosins were commonly rich in arginine, aspartic acid, and glutamic acid, while scarcely contained proline and tryptophan, in rough accord with the other paramyosins thus far reported. It is clear that these gastropod paramyosins showed of having the characteristic N-terminal amino acid residues such as N-aspartic acid, N-valine, N-serine, and N-threonine in common. The abalone paramyosin completely salted in with KCl beyond $0.35{\mu}$ and the top-shell paramyosin beyond $0.30{\mu}$. The abalone paramyosin was salted-out between 18% and 30% saturation of ammonium sulphate and the top-shell paramyosin between 22% and 29% saturation. The intrinsic viscosities at abalone and top-shell paramyosins at $25^{\circ}C$ were estimated respectively to be 3.1 dl/g and 2.6 dl/g showing somewhat higher than the values for some other paramyosins from lamellibranchs. In regard with the ATPase activity, the para myosin specimens did not exhibit any significant activity over through the pH conditions of 5 to 9.5. irrespective of the presence of $Ca^{++}$ or $Mg^{++}$. So was the case with the abalone paramyosin prepared by a slightly modified Bailey's wet-extraction method.

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꾸지뽕나무 부위별 추출물의 생리활성 탐색 (Physiological Activities of Extracts from Different Parts of Cudrania tricuspidata)

  • 이혜진;도정룡;권중호;김현구
    • 한국식품영양과학회지
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    • 제40권7호
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    • pp.942-948
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    • 2011
  • 꾸지뽕나무를 잎, 줄기, 열매로 부위별 추출조건에 따른 추출물의 생리활성을 알아보고자 전자공여작용, 총 폴리페놀 함량, SOD 유사활성, tyrosinase 저해 효과, 아질산염 소거작용 및 ACE 저해 활성을 측정하였다. 전자공여능의 경우 추출용매에 따라 70% 에탄올>70% 메탄올>물 추출물순으로 활성을 나타냈으며, 특히 줄기의 70% 에탄올 추출물이 90.20%로 가장 높았다(p<0.05). 이는 비교물질인 Lascorbate의 활성보다 높은 수치였다. 총 폴리페놀 함량 측정 결과 모든 추출조건에서 잎 추출물이 가장 많은 폴리페놀을 함유하고 있었다(p<0.05). 또한 추출용매에 따라 70% 메탄올 추출물들이 폴리페놀을 많이 포함하고 있음을 알 수 있었다. SOD 유사활성은 잎의 물 추출물이 64.54%로 가장 높은 활성을 나타냈다(p<0.05). Tyrosinase 저해효과에서는 열매 추출물이 가장 높은 저해능을 보였다. 아질산염 소거능은 모든 추출물이 산성조건에서 소거능이 높게 나타났고, 추출조건과 상관없이 잎 추출물의 소거능이 가장 높은 것으로 분석되었다. ACE 저해 활성은 열매 물 추출물에서 85.14%의 활성을 가장 높은 경향을 보였다. 꾸지뽕 나무의 부위 및 용매에 따라 각각 활성이 다르게 나타났다. 이러한 결과를 토대로 활성이 다소 뛰어난 잎의 경우, 일상에서도 쉽게 구할 수 있어 일반인들이 식용으로 이용하기 용이하므로 차와 음료 등의 건강 음료개발을 통해 소비를 활성화할 수 있다. 그 외 줄기, 열매 등도 잎과 함께 이를 이용한 환, 캡슐 등의 다양한 기능성식품으로의 개발 가능성을 확인하였다.