• 한국생물공학회:학술대회논문집
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• 한국생물공학회 2001년도 추계학술발표대회
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• pp.882-885
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• 2001

The cells of Lactobacillus plantarum MY4 isolated from the human feces were treated for 24 h in artificial bile after incubation for 2 h in artificial gastric juice and final number of the strain was reached to around $3.1{\times}10^8$ CFU/ml. In test of API ZYM kit, ${\beta}$-glucuronidase or ${\beta}$-glucosidase were not produced by L. plantarum MY4. However, ${\beta}$-galactosidase were weakly produced by it, which they would be alleviated the lactose intolerance. L. plantarum MY4 were resistant to antibiotics such as nisin, tetracycline, streptomycin, rifamycin, doxycycline, roxithromycin, chloramphenicol, nystatin, erythromycin, ciprofloxacin and gentamycin. L. plantarum MY4 was affected by alcohol concentration up to 8%, but more than 16%, their growth was not affected significantly. L. plantarum MY4 was shown to inhibit the growth of Listeria monocytogenes ATCC 19111 completely within 24 h of incubation, which indicates its bactericidal nature. Thus, L plantarum MY4 show promise as a probiotic strain because of its characteristics.

• 한국식품과학회지
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• 제27권4호
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• pp.506-515
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• 1995

저온발효된 김치에서 분리되어 Leuconostoc mesenteroides subsp. mesenteroides, Leu. mesenteroides subsp. dextranicum, Leu. paramesenteroides, Leu. lactis, Lactobacillus bavaricus 및 Lac. homohiochii로 각각 동정된 저온성 젖산균 60주에 대하여 여러 조건에서의 배양특성들을 조사하였다. 모든 균주들이 $5^{\circ}C,\;10^{\circ}C$ 및 $37^{\circ}C$에서 증식하였고, $45^{\circ}C$에서는 증식하지 못하였다. 최적 증식 온도는 Leu. mesenteroides의 균주들은 $33{\sim}34^{\circ}C$이었고, Lactobacillus속의 균주들은 $34{\sim}36^{\circ}C$이었다. Leu. mesenteroides와 Lactobacillus속의 균주들은 모두 초기 pH 4.8 및 4.2에서 증식하였으나 4.0에서는 증식하지 못하였다. Glucose broth에서의 최종 pH는 Leu. mesenteroides의 균주들은 $3.85{\sim}4.10$이었고, lactobacillus속 균주들은 $3.82{\sim}3.99$이었다. 60균주 모두 litmus milk에서 우유를 응고시키지 못하였고, litmus를 환원시키지도 못하였다. Leu. mesenteroides와 Lactobacillus속의 균주들은 모두 에탄올 7% 함유배지와 NaCl 6.5% 함유배지에서 증식하였고, 에탄올 15% 함유배지와 NaCl 10% 함유배지에서는 증식하지 못하였다. 모든 균주들이 pH 3.5인 인공위액과 40%의 담즙액에서 내성을 나타내었다. 특히 Leu. mesenteroides의 균주들은 모두 pH 3.0인 인공위액에서도 내성을 나타내었다. 본 젖산균들의 생리적인 특성은 여러 점에서 Bergey's Manual of Systematic Bacteriology에 기재된 내용들과 일치하지 않으므로 더욱 정밀한 조사를 실시하여 분류학상의 위치를 정확히 밝혀 볼 필요가 있을 것으로 생각되었다.

• 한국임상약학회지
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• 제11권1호
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• pp.13-18
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• 2001

Omeprazole is usually administered as encapsulated enteric-coated granules and enteric-coated tablets because of its acid-labile nature. For children and patients who can not swallow, it can be mixed with water or other liquid after a capsule is opened or a tablet is crushed. This study was performed to compare omeprazole liquid formulations of tablet and capsule Omeprazole 20 mg capsule containing enteric coated granules was opened and 20 mg entric-coated tablet was ground to be mixed with sodium bicarbonate solution, orange juice or water. Each liquid formulation was poured into dissolution tester, mixed with first solution (artificial gastric juice; pH 1.2) for two hours, then with second solution (artifical enteric juice; pH 6.8) for thirty minutes. pH was measured periodically for two and half hours. Samples were drawn periodically, mixed with lansoprazole as an internal standard, and injected to HPLC. As results, pH of sodium bicarbonate solution of omeprazole was significantly higher than that of orange juice or water in first solution (6.2-7.4 vs. 1.2, p<0.005). At 150 min, concentrations of omeprazole in three diluents with granules and in sodium bicarbonate solution of tablet powder sustained significantly higher than in other solution of tablet powder (p<0.001). In conclusion, enteric-coated granules from capsule with three diluents and powder from tablet in sodium bicarbonate solution was stable during dissolution test, which would be appropriate and recommended for patient who can not swallow solid preparations.

• 한국식품영양과학회지
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• 제43권7호
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• pp.1009-1016
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• 2014

묵은지 스타터로 개발된 Lb. curvatus ML17의 생균제적 특성 및 기능성 조사를 통하여 기능성 소재로서의 개발 가능성을 검토하였다. Lb. curvatus ML17은 용혈현상을 일으키지 않았으며 ${\beta}$-glucosidase와 ${\beta}$-glucuronidase의 발암효소 활성이 없는 것으로 나타나 균주에 대한 안전성을 확인하였다. 장내 생존성 확인 실험에서는 인공위액에서 2시간 처리한 다음 인공담즙에서 24시간 처리한 결과 초기 균수 대비 12.30%의 생존율을 나타내었다. Caco-2 cell에 대한 부착율은 초기 접종균수가 많을수록 높게 나타났으며, $5.66{\times}10^9$ CFU/mL로 처리 시 17.31%의 부착율을 나타냈는데 20.78%의 부착율을 나타낸 양성 대조군 Lb. rhamnosus GG에 근접하게 높은 부착율을 나타내어 장내환경에서 바람직한 작용을 할 수 있음을 보여주었다. 유해균주에 대한 생육저해 활성 측정에서는 Micrococcus luteus, Bacillus cereus, Salmonella enterica subsp. enterica, Pseudomonas aeruginosa에 대하여 우수한 항균 활성을 나타내었다. DPPH radical 소거능을 이용한 항산화 활성 측정 결과 72.88%로 양성 대조군인 0.1 mg/mL ascorbic acid보다 높은 free radical 소거능을 나타내었다. AGS 위암세포 및 HT-29 결장암세포에 대한 성장 억제 효과에서는 Lb. curvatus ML17의 배양 상등액 $80{\mu}L/mL$ 처리 시 각각 82.91% 및 79.35%의 암세포 성장 억제 효과를 나타내었다. 이와 같은 결과로 Lb. curvatus ML17이 묵은지를 포함한 발효스타터로 사용되었을 경우 식품의 보존성 향상과 품질 유지 및 균주에 의한 건강 기능성을 부여할 수 있으며 식품, 사료, 의약 분야의 다양한 산업적 활용이 기대된다.

• 약학회지
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• 제45권5호
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• pp.536-544
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• 2001

increase the viability of oral typhoid vaccine during the passage through the castro-intes-tidal tract, numerous attempts have been made including the vaccine coating. However problems such as high death rate during the coating process and its instability in the gastric juice still remain to be solved. In this study, the oral vaccine was made as the micro-enteric beads by adding Salmomella typhi Ty21a cells to sodium alginate solution and spraying onto calcium chloride solution (ionotropic relation method). The vaccine showed more than 90% of its original viability after treating it for 1 hour in the artificial gastric juice (37$^{\circ}C$, 300 rpm). The clearance rate of the Ty21a in the liver and spleen of the mice orally administrated with coated Ty21a was similar to that of the mice intraperitoneally administrated with uncoated Ty21a. The peripheral blood lymphocytes (PBL) isolated from the mice orally administered with this vaccine produced 15.5 fold higher specific IgA antibody titer than that from the control mice administerd with saline solution. furthermore, the mice treated with the coated Ty21a had higher survival rates (50~87%) than the control mice treated with saline solution (0~10%) in the intraperitoneal challenge test with wild type S. typhi Ty21a cells. These results suggest that the alginate-based coating technique is effective to protect live Ty21a from acidic environments, and produces better intestinal immune responses thereby providing a potentially excellent oral typhoid vaccine.

• 한국식품과학회지
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• 제33권5호
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• pp.567-573
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• 2001

본 연구에서는 한국인 분변으로 부터 분리, 동정된 Lactobacillus 속 균주의 종별 출현빈도, 산 생성능, 인공 위액 및 인공 담즙에 대한 내성, cholesterol 저하능력 등이 검토되었다. 생후3일부터 37세까지의 총 13명의 남·여의 분변으로부터 총 52균주의 Lactobacilli가 분리되었고 이 중 L. acidophilus가 19주로 가장 많았으며 다음으로 L. plantarum 순이었다. 분리주 중 L. acidophilus로 동정된 17주와 L. casei로 동정된 3주에 대해서 생리적 특성을 검토한 바 각각 다음과 같은 결과가 얻어졌다. 인공위액에 대한 내성 실험결과 L. acidophilus a-4는 pH 2.5에서 3시간 경과 후에도 전혀 사멸하지 않고 100% 생존하는 것으로 나타났으며, L. acidophilus a-2와 L. casei b-3도 75%이상의 높은 생존율을 나타내었다. 나머지 13주는 40%이하의 생존율을 나타내어, 균주 별로 인공위액에 대한 내성은 큰 차이를 나타났다. 내 담즙성을 측정한 결과 L. acidophilus a-3를 포함한 4주는 성장에 지장을 받지 않았으나 대부분의 분리 균주는 생균수가 처리전 보다 $54{\sim}99%$ 정도로 감소되는 것으로 나타나 인공위액 내성과 마찬가지로 균주에 따라 편차가 큰 것으로 나타났다. 환원 탈지유를 이용한 산생성능에 있어서는 두 L. acidophilus 균주 (a-2 및 a-16)가 60시간 경과 후 $2.1{\sim}2.3%$의 적정 산도까지 도달하였고 이때 pH는 $3.5{\sim}3.6%$이었다 60시간 배양 후 적정 산도가 0.8%에 도달하지 못한 것은 총 20주중 10주였다. 한편 cholesterol 저하능을 측정한 결과 공시한 20개 분리주 중에서 L. acidophilus a-2 주와 a-6 주가 70% 이상의 우수한 저하능력을 나타냈고, 12균주가 60% 이상의 저하능을 나타냈다. cholesterol 저하능은 동일 균종이라 하더라도 분리원(사람)은 물론 동일 분리원에서 유래된 균주 간에도 큰 차이가 나타났다. 담즙산에 대한 내성과 cholesterol 저하능력과의 관련성은 상호간의 유의적인 관계가 없는 것으로 나타났다. 결론적으로 본 실험에서 얻은 몇 균주는 인체에 섭취될 경우 사멸하지 않고 소화관 하부까지 도달할 수 있는 잠재성이 있었으며, 따라서 이들 분리주는 정장제로 이용될 수 있다고 생각되었다.

• Journal of Pharmaceutical Investigation
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• 제14권3호
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• pp.105-121
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• 1984

The bioavailability of rifampicin (brand A, B and C) was studied and the dissolution by foamed plastic rotating method and basket rotating method was also investigated. The results were as follows; 1. In the case of foamed plastic rotating method, it was revealed that dissolution rate of brand C was most rapid, but in the case of basket rotating method the results revealed that brand B was most rapid. Also it was observed that the dissolution rate in artificial gastric juice was more rapid than one in artificial intestinal juice, and that Avicel added in capsule increased additively the dissolution rate, particulary brand B. 2. Relative systemic availability by urine data showed that the results from all capsules filled with brand A, B and C were identical but in the case of the ripamficin capsules filled with Avicel, the results showed that Avicel increased the availability of brand A and B. 3. Area under serum concentration curve $(0{\sim}8hrs)$ was in order of $brand\;A{\fallingdotseq}brand\;C$ > brand B, but Avicel increased significantly the AUC of brand B and showed no effect in others. 4. Relative systemic availability calculated with excreted amount of rifampicin in urine was similar in each rifampicin capsules. In rifampicin (A) and rifampicin (B), Avicel which added in capsules appeared increasing tendency in urine excretion of rifampicin, but in rifampicin (C) it did not appeared. 5. Area under serum concentration curve $(0{\sim}8hrs)$ in rifampicin capsules was in order of $rifampicin(A){\fallingdotseq}rifampicin(C)$>rifampicin(B). In rifampicin (B) with Avicel capsules, area under serum concentration curve (0-8hrs.) increased significantly and in others insignificantly.

• 약학회지
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• 제38권2호
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• pp.123-130
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• 1994

Physicochemical properties and hydrolysis kinetics of new some oral cephalosporins were examined in buttered solution and human plasma or rat liver homogenate. The test cephalosporins were 7-[(Z)-2-(2-aminothiazole-4-yl)-2- methoxyiminoacetamido]-3-[4-(2-pyridyl)piperazinyl] thiocarbonylthhiomethyl-3-cephem-4-carboxylic acid (CEN1), 7-[(Z)-2-(2-aminoth iazole-4-yl)-2-methoxyiminoacetamido]-3-[4-(2-pyrimidyl)piperazinyl]th iocarbonylthiomethyl-3-cephem-4-carboxylic acid (CEN2), pivaloyloxymethyl-7-[ (Z)-2-(2-aminothiazole-4-yl)-2-methoxyiminoacetamido]-3-[4-(2-pyridyl)piperazi nyl]thiocarbonylthiomethy1-3-cephem-4-carboxylate (CEN1P), and pivaloyloxymethyl-7-[(Z)-2-(2-aminothiazole-4-yl)-2-methoxyiminoacetamido]-3-[ 4-(2-pyrimidyl)piperazinyl]thiocarbonyl-thiomethyl-3-cephem-4-carboxylate (CEN2P). The partition coefficient(Ko/w) of CEN1P, CEN2P were higher than those of CEN1, CEN2. The calculated pKa values of CEN1, CEN2, CEN1P, and CEN2P were 7.09, 7.75, 4.92, and 5.39, respectively. The hydrolysis of CEN1P and CEN2P were not depend on the composition of pH of the test medium except weak alkaline buffered solution (pH 8.00). CEN1 and CEN2 were very stable in pH 6.80 and 8.00 buffer solutions. CEN1P and CEN2P were rapidly deesterified to CEN1 and CEN2 in human plasma and in rat liver homogenate. Half-lives$(t_{1/2})$ of CEN1 and CEN2 were 3.49 and 4.93 hr in human plasma, 1.47 and 1.26 hr in rat liver homogenate, respectively.

• 약학회지
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• 제37권6호
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• pp.638-646
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• 1993

A cepfialosporin with an aminothiazoiylmethoxyimino-type side chain at the 7 position and bicyclic quinolone dithicarbamate at the 3' position was synthesized. It has broad and potent antivacterial activity in vitro. The antibacterial spectrum reflects contributions of both the cephalosporin moiety and the quinolone moiety. Thus, this compound was named DACD implying a dualaction cephalosporin derivative. In this paper, the physicochemical proper-ties (lipid-water partition, pKa), stability and pharmacokinetics of DACD were determined and compared with cefotaxime 3'-norfloxacin dithiocarbamate (CENO). Stability tests were studied in pH 1.20, 6.80 and 8.00 buffers and in the presence of AB type human plasma, rat liver homogenate and its .betha.-lactamase. The pharmacokinetic parameters of DACD were evaluated in mice after a single intravenous dose of 40 mg/kg. The results are as follows. The lipid-water partition coefficient of DACD was higher than that of CENO. The calculated pKa values of CENO and DACD, were 6.82$\pm$0.03, 7.53$\pm$0.21, respectively. In the hydrolysis test, half-lives (t$^{1/2}$) of CENO and DACD was 66.0 hr and 80.0 hr in pH 6.80 buffer, 190 hr and 91.4 hr in pH 8.00 buffer. CENO and DACD were rapidly hydrolyzed in human plasma and in rat liver hornogenate. Half-lives (t$_{1/2}$ of CENO and DACD were 1.29 hr and 1.15 hr in hyman plasma, 0.62 hr and 0.71 hr rat liver homogenate. In $\beta$-lactamase stability test, CENO and DACD were very stable to the .betha.-lactamases obtained from three different strains. Half-life (t$_{1/2}$) and areas under the curve (AUC) in mice were 2.33 hr and 15.97 (mg.h/1), respectively.

• 한국임상약학회지
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• 제1권1호
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• pp.15-21
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• 1991

This study was attempted to investigate the dissolution rate and bioavailability of commercially available furosemide preparations. A. B. and C. The dissolution test was conducted in an artificial gastric juice using the basket method. and furosemide (40 mg) was administered orally to 8 normal volunteers by cross-over design. The results were as follows: the AUC and dissolution rate in 100 min ($D_{100\;min}$) were higher in order of preparations. A > C > B. But the peak concentration. time to reach peak concentration $(T_{max})$, and mean dissolution time (MDT) were in order of preparations. C > A > B. There were significantly linear correlations between the AUC and the $D_{100\;min}$, and between the $T_{max}$ and the MDT. From the results of this experiment. it can be concluded that commercially available preparations bioavailability of furosemide, which may be predicted from the dissolution rate.