• 한국수산과학회지
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• 제45권1호
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• pp.1-10
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• 2012

The objective of this study was to investigate the sanitary and nutritional requirements for the industrialization of commercial kwamegi from Pacific herring Clupea pallasii (CK-PH). The proximate composition of CK-PH was 46.4-47.2% moisture, 24.7-25.6% crude protein, 23.6-25.2% crude lipid, and 2.5-2.9% ash, which differed significantly from that of commercial kwamegi from the Pacific saury Cololabis saira. According to the volatile basic nitrogen content, heavy metal content, and viable cell and coliform group counts, products K and F (prepared by a general process) maintained their freshness, whereas product T (treated with green tea extract) did not. Products K and F contained five types of biogenic amine: agmatine sulfate (2,596 and 2,067 mg/kg, respectively), putrescine dihydrochloride (8.5 and 8.0 mg/kg, respectively), cadaverine (3.7 and 3.9 mg/kg, respectively), histamine (17.0 and 12.4 mg/kg, respectively), and spermidine (8.7 and 8.0 mg/kg, respectively). Product T contained six amine types: tyramine (12.5 mg/kg), agmatine sulfate (2,723 mg/kg), putrescine dihydrochloride (29.4 mg/kg), cadaverine (321.6 mg/kg), histamine (45.3 mg/kg), and spermidine (13.6 mg/kg). The total amino acid content of product K (22.16/100g) was 5.8% lower than that of product F. The major amino acids of products K and F were aspartic acid, glutamic acid, leucine, and lysine. No difference was found in the fatty acid composition of products K and F. The major fatty acids in products K and F were 18:1n-9, 20:5n-3, and 22:6n-3. Based on the recommended daily dietary allowances for Koreans, the significant minerals in products K and F were calcium, phosphorus, and magnesium.

• Archives of Pharmacal Research
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• 제25권5호
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• pp.718-723
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• 2002

CKD-602 (7-[2-(N-isopropylamino)ethyl]-(20S)-camptothecin) is a recently-developed synthetic camptothecin analogue and currently under clinical development by Chong Kun Dang Pharm (Seoul, Korea). CKD-602 showed potent topoisomerase inhibitory activity in vitro and broad antitumor activity against various human tumor cells in vitro and in vivo in animal models. This study describes the pharmacodynamics of the immediate and delayed cytotoxicity induced by CKD-602 in a human colorectal adenocarcinoma cell line, HT-29, and its intracellular drug accumulation by HPLC. The present study was designed to address whether the higher activity of CKD-602 with prolonged exposure is due to delayed exhibition of cytotoxicity and/or an accumulation of anti proliferative effect on continuous drug exposure. The drug uptake study was performed to determine whether the delayed cytotoxicity is due to a slow drug accumulation in cells. CKD-602 produced a cytotoxicity that was exhibited immediately after treatment (immediate effect) and after treatment had been terminated (delayed effect). Both the immediate and delayed effects of CKD-602 showed a time dependent decrease in 4IC_{50}$ values. Drug uptake was biphasic and the second equilibrium level was obtained as early as at 24hr, indicating that the cumulative and delayed antitumor effects of CKD-602 were not due to slow drug uptake. On the other hand, CKD-602 treatment was sufficient to induce delayed cytotoxicity after 4hr, however, longer treatment (＞24hr) enhanced its cytotoxicity due to the intracellular accumulation of the drug, which requires 24hr to reach maximum equilibrium concentration. In addition, $C^n$$\times$T=h analysis (n=0.481) indicated that increased exposure times may contribute more to the overall antitumor activity of CKD-602 than drug concentration. Additional studies to determine the details of the intracellular uptake kinetics (e.g., concentration dependency and retention studies) are needed in order to identify the optimal treatment schedules for the successful clinical development of CKD-602.

• 한국재료학회지
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• 제5권6호
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• pp.723-731
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• 1995

x=0.4-0.6이고 작은 $\delta$값을 갖는 P $b_2$S $r_2$( $Y_{1-x}$ C $a_{x}$)C $u_3$ $O_{8+}$$\delta$/초전도체시료를 제조하였다. 시료가 초전도체로 되기 위하여 작은 $\delta$값을 가져야 하는데 이를 위해 소결 후 직접 낮은 산소분압에서 annealing하면 산화성 상분해가 발생하여 과잉의 2차상이 생성된다. 따라서 제조과정중 산화성 상분해의 양을 줄이기 위하여 두 단계의 annealing 과정을 도입하였다. 즉 100% 아르곤 기체 분위기에서의 소결 후 먼저 100% 산소 분위기하에서 시료를 annealing하여 산화시킨 후 0.1~1.0% 산소분압하에서 annealing하여 작은 $\delta$값을 얻는 것이다. 얻어진 시료의 전기저항 측정결과 80K의 초전도 전이온도( $T_{c}$)가 얻어져 지금까지 이 화합물에서 보고된 결과중 가장 높은 $T_{c}$를 나타내었다. 그러나 본 연구에서 도입한 두단계 annealing 과정에 의해서도 작은 $\delta$값을 얻기 위하여는 약간의 산화성 상분해가 발생하여 깨끗한 초전도 전이과정을 블 수 없었다. 수 없었다..

• 한국식품과학회지
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• 제27권5호
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• pp.716-723
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• 1995

갈조류인 한국산 곰피(Ecklonia stolonifera)에서 fucoidan을 추출 정제하여 분자 구조적 특성을 조사하고 항혈액 응고 활성을 측정하였다. 건조곰피 20.0kg을 $100^{\circ}C$에서 2시간동안 2회 열수 추출하고 ethanol로 침전시켜 crude fucoidan 151.1g을 얻었다. Crude fucoidan을 염화칼슘과 cetyl pyridium chloride(CPC)로서 정제하여 Fucoidan-1을 얻었고 수율은 35.2%였다. 이 Fucoidan-1을 여러조건하에서 DEAE-Toyopearl 650 M 이온교환 chromatography법을 이용하여 정제한 결과 cellulose acetate 막 전기영동상에서 하나의 band를 나타내는 순도가 높은 곰피 Fucoidan-5을 얻었으며 dextran을 표준품으로 gel filtration chromatography를 행한 결과 분자량은 21,000∼23,000이었다. 곰피 Fucoidan-5의 구성당은 fucose 35.7%와 galactose 4.3%이였고, fucose와 황산기의 mole 비는 약 1 : 1이었다. 적외선 흡수 spectrum 에서 $1240\;cm^{-1}$와 $850\;cm^{-1}$ 부근에서 흡수가 확인되었으며 비선광도가 $-127.2^{\circ}$인 것으로 보아 황산기는 주로 ${\alpha}-L-fucose$의 4번 위치의 탄소에 결합되어 있는 것으로 추정할 수 있었다. 또한 곰피 Fucoidan-5를 methyl화하여 가수분해하고 methyl alditol acetate를 만든 후 gas chromatography를 행한 결과 Fucoidan-5는 주로 황산기를 C4에 가진 fucose가 ${\alpha}l-2$결합 또는 ${\alpha}l-3$결합으로 이루어진 다당류임을 추정할 수 있었다. 곰피 Fucoidan-5의 항 thrombin 활성은 heparin(140 units/mg)의 약 1.4배이었다. 이상의 결과에서 CPC법과 이온교환 chromatography법을 사용하여 갈조류인 곰피로부터 분리 정제한 곰피 Fucoidan-5는 순도가 높은 fucoidan임을 알 수 있었고 수율은 28.1%였다.