• 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.

• 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.

• 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.

• Journal of Periodontal and Implant Science
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• 제25권2호
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• pp.301-320
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• 1995

The purpose of this study was to evaluate a new biodegradable membrane - atelocollagen as a guided tissue regeneration barrier on the dehiscence defects adjacent to the dental implants. 3 beagle dogs were selected for this study and all the mandibular premolars($P_1,P_2,P_3&P_4$) were extracted. Twelve weeks after the extraction, the edentulous ridges were formed to be placed the titanium plasma-sprayed IMZ implants. Four implant osteotomies were performed on each side of the mandible. The osteotomies were placed facially in the edentulous ridges to approximate an actual dehiscence defect as closely as possible, The standardized dehiscence defects were created 3 mm in width and 4 mm in height by osteotomy. A total 24 implants were placed. e-PTFE, ateloco11agen and $Collatape^{(R)}$ were placed to cover the defects and the one defect served as a control, not covered any membrane. By random selection, three dogs were sacrificed at 2 weeks, 4weeks and 8 weeks after fixation with 3% glutaraldehyde. A week before sacrificing, 8-week dog was infused intravenously with oxy-tetracycline 30mg/kg. The left mandibular blocks were used for full decalcified histologic preparation and the right mandibular blocks were selected for undeca1cified preparation, At 2 weeks, the regenerated bone of e-PTFE and atelocollagen groups appeared to be more dense than other groups and the percentage of bone defect fill was highest for e-PTFE and follwed by ateloco1lagen group. However, the $Collatape^{(R)}$ and control groups showed a little new bone formation. $Collatape^{(R)}$ was almost degraded within 2 weeks. At 4 weeks, the regenerated new bone were much greater and denser than at 2 weeks for e-PTFE and ateloco11agen group. Although a part of atelocollagen bagan to be degraded at the margin and surrounded by foreign body giant cells related to foreign body reaction, it was generally intact and the regenerated new bone was shown much more than at 2 weeks. The amount of new bone in $Collatape^{(R)}$ and control groups at 4 weeks were similar to that of 2 weeks group. At 8 weeks, the regenerated bone was matured and observed along the implant fixture. Direct new bone formation and calcium deposits beneath the e-PTFE were observed. No further bone growth was seen in the $Collatape^{(R)}$ and control groups. In reflected fluoromicrcocopic observation, the osteogenic activity was pronounced between e-PTFE membrane and the old bone. High osteogenic activity was also observed in atelocol1agen group. This study suggested that the ateloco11agen as well as e-PTFE could be used for guided tissue regeneration on dehiscence defects adjacent to the dental implants. But the $Collatape^{(R)}$ was completely resorbed within 2 weeks and was not a suitable membrane for guided bone regeneration.

• 한국수산과학회지
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• 제5권1호
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• pp.29-38
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• 1972

복족류 근육단백질을 다른 연분동물의 그것과 비교생화학적으로 검토하고져 전복을 선정하여 근육단백질의 조성을 측정하고 그 주요 구성단백질인 paramyosin을 정열 단리하여 몇가지 생물물리화학적인 성질에 관하여 실험하였다. 전복근육의 단백조성은 수용성구분 $19\~22\%$, 염용성구분 $27\~39\%$, 알카리 가용성구분 $20\~26\%$, 그리고 stroma $20\~28\%$이었다. 염용성구분은 초원심분석에서 Paramyosin이 약 $65\%$, actomyosin이 약 $30\%$, myosin이 약$5\%$로서 이루어져 있음을 알았다. 그리고 초원심분석상 균질의 단일 표품으로 판명 분리된 본 실험에서의 전복 Paramyosin은 침항정수($S^{\circ}\;_{20,\;{\omega}$) 3.14s, 정전염용 $0.35{\mu}$ 이상, $25^{\circ}C$에서의 고유점도는 3.1이었고, 한편 동 Paramyosin은 염석분석에서 이 단백질의 염석절위가 $18\~30\%$이었다. 그리고 아미노산 분석결과, 구성아미노산은 arginine, aspartic acid, glutamic acid등이 많이 함유되어 있고, proline과 tryptophane이 흠여되어 있는 점 등 2매패류의 아미노산조성과 비슷하였으나, Iysine/arginine의 비는 0.61로서 2매패류보다 낮았다.

• 한국지하수토양환경학회지:지하수토양환경
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• 제17권3호
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• pp.1-9
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• 2012

According to the agreement on WTO/TBT, we are under the situation to adopt international standard (ISO standard) as a national standard if it exists. However, in case of environmental area, it is a domestic legal obligation to use Korean environmental standard method(KESM) for analyzing various contaminants. Therefore it is necessary to assess the comparability between KEM and ISO standard prior to apply ISO standard to soil conservation law in Korea. The main purpose of this study is to assess the comparability of both methods for analyzing heavy metals in soil. We looked over various aspects like pre-treatment, calibration curve range, detection wavelength, soil organic matter content and so on. Apparently, the procedure of both methods is almost same. However in details, both methods are different in stationary time before aqua-regia extraction using reflux system, calibration curve range for Cu, Pb, Ni and measuring wavelength for Pb. According to the results of comparison test, the results were significantly different when the different calibration range was used. In case that all the extracts independent of methods were reanalyzed with the same calibration range of each method, both methods showed statistically same results. Other conditions like different stationary time, measuring wavelength of AAS and soil organic matter content did not have any influence on the analytical result. Therefore, we suggest to extend the calibration curve range to 0~8 mg/L which is used in KS I ISO standard(Korean standard related with environment which is translation version of ISO standard without any technical change). In case of $Cr^{6+}$, the results showed no significant differences between two methods even though the pretreatment, instrumentation and other analysis conditions were different. In addition to UV/Visble spectrometry of KESM for soil contamination, we suggest to adopt ion chromatography of ISO 15192(US EPA method 7199) for analyzing $Cr^{6+}$ with the consideration of laboratory work efficiency.

• Journal of Pharmaceutical Investigation
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• 제36권1호
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• pp.45-51
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• 2006

A rapid, selective and sensitive reversed-phase HPLC method for the determination of dipyridamole in human serum was developed, validated, and applied to the pharmacokinetic study of dipyridamole. Dipyridamole and internal standard, loxapine, were extracted from human serum by liquid-liquid extraction with diethyl ether and analyzed on a Nova Pak $C_{I8}$ column with the mobile phase of 40 mM ammonium acetate:methanol:acetonitrile (35:35:30)(v/v/v, pH 7.8). Detection wavelength of 280 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 dipyridamole concentration (50 ng/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 2-2000 ng/mL with correlation coefficients greater than 0.999. The lower limit of quantification using 0.5 mL of serum was 2 ng/mL, which was sensitive enough for pharmacokinetic studies of dipyridamole. The overall accuracy of the quality control samples ranged from 103.94 to 105.86% for dipyridamole with overall precision (% C.V.) being 4.60-11.49%. The relative mean recovery of dipyridamole for human serum was 97.64%. Stability studies showed that dipyridamole was stable during storage, or during the assay procedure in human serum. The peak area and retention time of dipyridamole 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 dipyridamole in human serum samples for the pharmacokinetic studies of orally administered Dimor tablet (75 mg as dipyridamole) at three different laboratories, demonstrating the suitability of the method.

• Journal of Pharmaceutical Investigation
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• 제36권1호
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• pp.23-29
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• 2006

A rapid, selective and sensitive reversed-phase HPLC method for the determination of promethazine in human serum was developed, validated, and applied to the pharmacokinetic study of promethazine. Promethazine and internal standard, chlorpromazine, were extracted from human serum by liquid-liquid extraction with n-hexane containing 0.8% isopropanol and analyzed on a Capcell Pak CN column with the mobile phase of acetonitrile-0.2 M potassium dihydrogen phosphate (42:58, v/v, adjusted to pH 6.0 with 1 M NaOH). Detection wavelength of 251 nm and flow rate of 0.9 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 promethazine concentration (10 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 1-40 ng/mL with correlation coefficients greater than 0.999. The lower limit of quantification using 1 mL of serum was 1 ng/mL, which was sensitive enough for pharmacokinetic studies. The overall accuracy of the quality control samples ranged from 96.15 to 105.40% for promethazine with overall precision (% C.V.) being 6.70-11.22%. The relative mean recovery of promethazine for human serum was 63.54%. Stability (freeze-thaw and short-term) studies showed that promethazine was stable during storage, or during the assay procedure in human serum. However, the storage at $-80^{\circ}C$ for 4 weeks showed that promethazine was not stable. Extracted serum sample and stock solution were not allowed to stand at ambient temperature for 12 hr prior to injection. The peak area and retention time of promethazine 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 promethazine in human serum samples for the pharmacokinetic studies of orally administered Himazin tablet (25 mg as promethazine hydrochloride) at three different laboratories, demonstrating the suitability of the method.

• 한국지하수토양환경학회:학술대회논문집
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• 한국지하수토양환경학회 2006년도 총회 및 춘계학술발표회
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• pp.247-252
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• 2006

오염 퇴적물내 중금속의 방출과 이에 따른 생이용성(bioavalability)은 기존의 가역 평형관계로써 설명하기에 불충분한 것으로 알려져 있다. 최근 연구결과에 의하면 이러한 탈착 저항성을 설명하기 위한 비가역적 모델에 의해 퇴적물내 중금속의 탈착저항성 부분이 존재함이 밝혀졌다. 탈착저항성에 대해서는 아직 충분한 규명이 이루어지지 않았으나, 오염물질의 노화(aging)에 의해 일단 탈착저항성을 띠게 되면 생이용성(bioavailability)이 감소되는 것으로 알려져 있다. 본 연구에서는 노화(aging)가 연안 퇴적물 내 납과 카드뮴의 흡/탈착 특성에 미치는 영향을 알아보기 위해 연속 탈착실험과 biphasic 탈착모델을 적용함으로써 납과 카드뮴의 탈착저항성을 규명하고자 하였다. 그리고 연속 추출 실험을 통해서 노화(aging)에 따른 퇴적물 내 납과 카드뮴의 흡착 기작을 규명하고자 하였다. 연속탈착 실험 결과 시간이 경과함에 따라 탈착저항성부분의 크기가 증가하였으며, 연속추출 실험 결과 납의 경우 carbonate fraction에서 추출된 납이 가장 많았으며, 노화(aging) 따라 exchangeable fraction에서 추출된 납이 감소하는 반면 reducible, organic material, residual fraction에서 추출된 납의 양이 증가하였다. 카드뮴의 경우 가장 많은 양이 추출된 단계는 exchangeable fraction이였으며, organic material fraction에서는 카드뮴이 추출되지 않았다. 노화(aging) 따라 reducible fraction과 residual fraction에서의 추출량이 증가하는 경향을 보였으나 그 양은 매우 적은 것으로 나타났으며, 노화(aging)에 따른 exchangeable fraction과 carbonate fraction에서의 추출량은 큰 변화가 없었다. 대해서는 북한지역의 분포상황을 밝혔다.것을 알 수 있었으며, 크롬과 비소의 경우는 초기에 많이 용출되고, 구리의 경우는 꾸준히 용출되는 것을 알 수 있었다. 3년 된 통나무집이 8년 된 통나무집보다. 용출양이 더 컸으며, 이는 CCA성분이 초기에 많이 용출된다는 것을 의미한다. 억제 효과를 나타내었고 Hep3B에서는 부탄을 분획물 (1 mg/mL)에서 82%의 비교적 높은 성장억제효과를 나타내었다.as a "front" and "back". Thus, Germany′s private space may face a genuine public space and street, which is rare in the Korean housing. Although the layout of indoor space in the korean housing tends to be open, such an openness may be outstanding in living and dining spaces, kitchen and various accesses to rooms. In the case of Germany, such indoor spaces are usually closed to each other. Thus corridors act to separate these spaces. Such differences are analysed to be due to the different perceptions of interpersonal and socio-cultural attributes as intra-family and inter-neighbor relationships or communications. 알 수 있었다.도 질소와 인산처럼 토양지지대가 있는 경우가 낮은 함량을 유지하였다.pe from the daily life, to fantasize and daydre

• 생명과학회지
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• 제25권12호
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• pp.1370-1376
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• 2015

우슬(牛膝)은 비름과(Amaranthaceae)의 쇠무릎(Achyranthes japonica)의 뿌리를 약용으로 한방에서 사용하고 있다. 1, 1- diphenyl 2-picrylhyorazyl (DPPH)은 잘 알려진 자유 라디칼이다. Hyaluronidase (HAase)은 결합조직의 세포외성 기질에서 히알루론산분해에 관여하는 효소이다. Lipoxygenases (LOX)은 지방산 대사와 면역에 중요한 역할을 수행한다. 본 연구에서는 쇠무릎에서 이 세 작용을 에탄올 추출물을 사용하여 생육 발달 단계(어린 영양기관과 성숙한 영양기관)에 대해 이들 추출물의 활성을 비교 조사하였으며 각 항목에 대해 50% 저해(IC₅₀)의 농도를 산출하였다. 항산화 활성은 잎과 줄기, 뿌리 모두에서 탁월되었다. 특히 히알루로니다아제의 저해작용이 현저하였으며 향후 어떤 화합물인지 심도 있는 연구가 필요하다고 판단되었다. DPPH에 대한 항산화 활성과 LOX에 대한 저해작용은 기존 연구자의 결과와 유사하였다. 어린 식물조직과 성숙한 식물조직에서 추출한 발달 단계에 따른 이들 세 가지 활성에서 어린 뿌리보다 성숙한 뿌리에서 약간 더 우수한 작용을 보였으나 통계적으로 유의한 차이가 없었다.