• 제목/요약/키워드: CoV

검색결과 4,126건 처리시간 0.034초

세파클러 250 mg 캅셀의 생물학적 동등성 (Bioequivalence of Cefaclor (250 mg) Capsule)

  • 윤민혁;김호순;최용포;권광일
    • 한국임상약학회지
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    • 제12권2호
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    • pp.71-75
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    • 2002
  • This study was carried out to compare the bioavailability of $Ceclex^{(R)}$ (test drug, cefaclor 250 mg/capsule) with that of $Ceclor^{(R)}$ (reference drug) and to estimate the pharmacokinetic parameters of cefaclor in healthy Korean adult. The bioavailability was examined on 20 healthy volunteers who received a single dose (250 mg) of each drug in the fasting state in a randomized balanced 2-way crossover design. After dosing, blood samples were collected for a period of 6hours. Plasma concentrations of cefaclor were determined using HPLC with UV detection. The pharmacokinetic parameters $(AUC_{0-6hr},\;C_{max},\;T_{max},\;AUC_{int},\;K_e,\;t_{1/2},\;Vd)$ F, and CL/F) were calculated with non-compartmental pharmacokinetic analysis. The ANOVA test was utilized for the statistical analysis of the $T_{max},\;log-transformed\;AUC_{0-6hr}\;log-transformed\;C_{max},\;t_{l/2},\;V_d/F$, and CL/F. The ratios of geometric means of AUC0-6hr and $C_{max}$ between test drug and reference drug were $103.2\%\;(6.74\;{\mu}g{\cdot}hr/ml\;vs\;6.53{\pm}g{\cdot}hr/ml)\;and\;100.4\%\;(4.85\;{\mu}g\ml\;vs\;4.82\;{\mu}g/ml)$, respectively. The $T_{max}$ of test drug and reference drug were $0.9\pm0.38\;hr\;and\;0.83\pm0.34$ hrs, respectively. The $90\%$ confidence intervals of mean difference of logarithmic transformed $AUC_{0-6h},\;and\;C_{max}$ were log $0.98{\sim}log$ 1.08 and log $0.88{\sim}log1.15$, respectively. It shows that the bioavailability of test drug is equivalent with that of reference drug. The estimated half-life of this study was longer $(1.21\pm0.27\;hrs\;vs\;0.5-1\;hr)$, the Vd/F was larger $(68.89\pm25.72L$ vs 24.9L), and the CL/F was higher $(38.62\pm7.09\;L/hr$ vs 24.9 L/hr) than the previously reported values.

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피브리노겐의 수치 및 중요한 아미노산 변형 돌연변이가 뇌중풍에 미치는 영향 (Effects of Fibrinogen Level and Genetic Variation in FGA Gene on Korean Stroke Patients)

  • 양용준;신용철;고성규
    • 대한예방한의학회지
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    • 제14권1호
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    • pp.111-123
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    • 2010
  • Backgrounds : Stroke is characterized by loss of brain functions due to a disturbance in the blood vessels supplying blood to the brain, and classified into hemorrhage and ischemia. Stroke is known to be affected by genetic factors and other diseases such as hypertension and cardiovascular diseases. However, the distinctive association between stroke and genetic variations has not discovered yet. Objectives : This study investigated the effects of fibrinogen level and genetic variations in FGA (Fibrinogen alpha chain) gene on stroke in Korean stroke patients and controls. Methods : DNA samples from 674 stroke patients diagnosed by Oriental medical hospitals and 267 controls were used in this study. Two common single nucleotide polymorphism(SNP) with high minor allele frequency(MAF), rs2070011G/A of promoter region and nonsynonymous rs6050A/G of exon 5 in FGA gene, were targeted for Taqman genotyping. Because the TOAST classification is important to the factors and symptoms of stroke, ischemic patients were further classified into five subtypes using diagnosis and clinical data. One-way ANOVA and chi-square test were used for clinical data and genetic association, respectively. Haploview v4.1 program was used for linkage disequilibrium(LD), haplotype and haplotype block analysis. Results : The levels of red blood cells and fibrinogen from clinical data were shown to be significant factors for the sub-groups of TOAST classification. No significant associations of stroke, hemorrhage, ischemic and subtypes of TOAST with rs2070011 and rs6050 of FGA gene were found(P > 0.05). However, rs2070011 in promoter region and nonsynonymous rs6050 in exon 5 which produce the amino acid change from threonine to alanine showed a haplotype block and three haplotypes of A-G, G-A, A-A, suggesting that rs2070011 and rs6050 might be co-segregated in generic recombination. Although A-A haplotype of stroke patients showed 64-69% low frequency compared to controls, there was no significant association between stroke and haplotype(P > 0.05). Conclusion : This study showed that there was no significant association between stroke and two SNP of rs2070011G/A and nonsynonymous rs6050A/G in FGA gene. However, these two SNP compose a haplotype block and three haplotypes of A-G, G-A, A-A. This finding suggests that rs2070011 and rs6050 are so close as to be positioned as linkage disequilibrium. Nevertheless, no significant association between haplotypes and stroke was found.

주박으로부터 효모포자의 생산 (Producton of Yeast Spores from Rice Wine Cake.)

  • 임용성;배상면;김근
    • 한국미생물·생명공학회지
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    • 제32권2호
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    • pp.184-189
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    • 2004
  • 쌀 양조 후 남은 고체찌꺼기인 주박을 사용하여 Saccharomyces 효모 포자의 대량생산을 위하여 주박의 최적 전 처리과정, 최적 배지조성과 배양조건을 조사하였다. 포자형성을 위하여서는 주박으로 제조한 전포자형성배지(PSM)에서 효모를 배양한 추 1% potassium acetate로 구성된 포자형성배지(SM)에 10%를 재접종한 후 $25^{\circ}C$에서 4일간 포자형성을 시켰다. 주박과 물을 1:2 로 혼합한 후 $51^{\circ}C$에서 24시간 preincubation한 후 그 원심분리 상등액을 PSM으로 사용하여 48시간 배양하고 이를 다시 SM에 접종하여 4일 배양하였을 때 최대 포자 자낭 수 $0.72${\times}$10^{8}$ $m\ell$ 를 얻었다. SM배지에 1.4% 밀기울 국(koji)을 영양원으로 첨가하였을 때 형성된 자낭수는 $1.06${\times}$10^{8}$$m\ell$ 증가하였다 초기 SM pH가 5에서는 포자가 형성되지 않았으며, pH 7∼11에서 포자가 형성되었다. 한편 주박의 전 처리에 소요되는 시간과 노력을 절감하기 위하여, 전 처리 하지 않은 주박을 직접 사용하여 포자형성을 시켜보았는데, 1% 갈색설탕을 함유하는 PSM에 2% 그리고 SM에 0.5%의 전 처리 하지 않은 주박을 각각 첨가하였을 때, 최대 포자 자낭수 $1.27${\times}$10^{ 8}$ $m\ell$를 얻었다.

폴리에스테르 중합 공정에서 발생되는 1,4-dioxane의 분해를 위한 파일럿 규모의 광펜톤산화처리 (Photo-Fenton Oxidation Treatment of Pilot Scale for the Decomposition of 1,4-dioxane Generated in a Polyester Manufacturing Process)

  • 소명호;한지선;한티힙;서장원;김창균
    • 대한환경공학회지
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    • 제31권1호
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    • pp.9-14
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    • 2009
  • 본 연구에서는 폴리에스테르 중합폐수의 배출 원수에 약 600 mg/L의 고농도로 존재하는 1,4-dioxane을 5 mg/L 이하까지 (2011년 규제 시행) 제거할 수 있는 고급산화공정의 현장 적용 기술을 개발하고자 구미지역 폴리에스테르 제조회사 중 K사의 폐수처리 시설을 선정하여 연구를 하였다. 공기의 공급 하에 광펜톤산화반응을 K사에 설치된 pilot에서 운전하였다. 막대형 산기관을 통해 공기를 공급하면서 10개의 UV-C 램프(240 ${\mu}W/cm^2$)의 조사 하에 과산화수소(2,800 ppm)와 철염(1,400 ppm)을 주입하였을 때 1,4-dioxane의 제거 효율이 2시간 만에 90%까지 나타나는 결과를 도출할 수 있었다. 그러나 처리수의 1,4-dioxane 농도는 약 60 mg/L으로 여전히 높았다. 그리하여 후속 처리로 bench-scale의 활성슬러지공정(V=8.9 L)을 이용하여 광펜톤산화 처리수 내의 1,4-dioxane 제거 가능성을 평가하였다. 그 결과로서 활성슬러지공정의 유출수내의 1,4-dioxane의 농도는 약 2~3 mg/L까지 저감되었으며 이를 통해, 광펜톤산화공정과 활성슬러지공정의 연계처리를 통해 1,4-dioxane 배출 허용기준(5 mg/L, 2011년)에 부합될 수 있는 효과적인 처리공정임을 입증하였다.

프로바이오틱스가 생산하는 생리활성 물질의 장내 유해균 억제 효과 (Bioactive Molecules Produced by Probiotics to Control Enteric Pathogens)

  • 임광세;;박동준;오세종
    • Journal of Dairy Science and Biotechnology
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    • 제32권2호
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    • pp.141-145
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    • 2014
  • 시장에는 프로바이오틱스를 포함한 무수히 많은 제품이 판매되고 있는데, 우리에게 어떤 이로운 점을 줄 수 있는지 궁금해 한 적이 있었을 것이다. 프로바이오틱스는 기본적인 영양 측면을 배제하고, 우리가 유효한 양을 섭취하였을 때 건강상의 이점을 주는 살아있는 미생물로 정의된다. 프로바이오틱스는 유용하고 건강에 좋은 미생물로도 불려지고 있으며, 다음과 같은 다섯 가지 측면에서 건강 기능성이 있는 것으로 강조되어 왔는데, 1) 대장암 및 IBS와 같은 다른 대장(결장)관련 질병의 발병율 감소, 2) 면역 시스템의 촉진, 3) 항고혈압 및 항콜레스테롤 작용, 4) 장내세균에 작용하는 항생제의 효과를 경감시키고, 5) 위장관 감염을 예방시키는 점이다. 그러나 이러한 건강기능 작용들에 대한 과학적인 근거가 충분히 구축되어 있지는 않아, 유럽식품 위생위원회(Euroupe Food Safety Authority)는 항생제 투여에 따른 설사증상의 완화와 같은 건강기능 표시를 금지하고 있어, 프로바이오틱스의 작용기전에 대한 연구가 필요한 시점이라 하겠다.

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평면-비구면 2×2 fly-eye 렌즈형태의 2차 렌즈를 사용한 고효율의 좁은 배광각을 갖는 MR-16 램프 시리즈 제작 및 성능평가 (Fabrication and Performance Evaluation of MR-16 Lamp Series with Narrow Angular Distribution of Luminous Intensity Using an Aspherical Planar-convex 2×2 Fly-eye Lens Type)

  • 추경덕;류재명;홍춘강;정연홍;조재흥
    • 한국산학기술학회논문지
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    • 제18권8호
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    • pp.25-33
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    • 2017
  • 본 연구에서는 간편하고 빠른 사출성형을 위하여 한쪽이 평면인 비구면 형상을 갖는 단일 fly-eye 렌즈형태의 2차 렌즈를 사용하는 MR-16 램프 시리즈의 설계를 보고하고자 한다. 인테리어 조명용 할로겐 램프를 대체하기 위해 효율이 높고 좁은 배광각을 갖도록 MR-16 램프용 광학계를 설계하여 이를 제작하고 성능을 확인하였다. 광학설계용 소프트웨어는 ORA사의 CODE V와 LightTools를 사용하였다. 그 결과, 제작된 MR-16 램프의 배광각은 $22.4^{\circ}$, $31.1^{\circ}$, $37.3^{\circ}$, $59.9^{\circ}$였으며, 광효율은 각각 76.5 lm/W, 75.2 lm/W, 72.0 lm/W, 77.8 lm/W 이고, 복사 균제도 81%에서 발산각은 $3^{\circ}$, $15^{\circ}$, $22^{\circ}$, $49^{\circ}$이다. 그리고 제작된 MR-16 램프에 확산시트를 2차 렌즈와 LED사이에 확산 시트를 적용하여 황색 띠를 제거한 후의 배광각은 각각 $20.8^{\circ}$, $31.5^{\circ}$, $37.8^{\circ}$, $68.7^{\circ}$로 측정되었다. 실험적으로 2차 렌즈를 같은 렌즈 4개를 붙이는 형식으로 fly-eye 형태로 함으로써 설계 및 제작이 용이하며 배광각과 균일한 조도 분포를 갖는데 있어서 문제가 없다는 것을 알 수 있었다.

Glass ionomer cement 표면의 산부식 효과에 관한 연구 (THE EFFECT OF ACID ETCHING ON GLASS IONOMER CEMENT SURFACES)

  • 한승원;박상진;민병순;최호영;최기운
    • Restorative Dentistry and Endodontics
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    • 제18권1호
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    • pp.1-26
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    • 1993
  • The purpose of this study was to investigate the effect of acid etching on the surface appearance and fracture toughness of five glass ionomer cements. Five kinds of commercially available glass ionomer cements including chemical curing filling type, chemical curing lining type, chemical curing metal reinforced type, light curing tilling type and light curing lining type were used for this study. The specimens for SEM study were fabricated by treating each glass ionomer cement with either visible light curing or self curing after being inserted into a rubber mold (diameter 4mm, depth 1mm). Some of the specimens were etched with 37% phosphoric acid for 0, 15, 30, 60, go seconds, at 5 minutes, 1 hour and 1 day after mixing of powder and liquid. Unetched ones comprised the control group and the others were the experimental groups. The surface texture was examined by using scanning electron microscope at 20 kV. (S-2300, Hitachi Co., Japan). The specimens for fracture toughness were fabricated by curing of each glass ionomer cement previously inserted into a metal mold for the single edge notch specimen according to the ASTME399. They were subjected to a three-point bend test after etching for 0, 30, 60, and 90 seconds at 5 minutes-, 1 hour-and 1 day-lapse after the fabrication of the specimens. The plane strain fracture toughness ($K_{IC}$) was determined by three-point bend test which was conducted with cross-head speed of 0.5 mm/min using Instron universal testing machine (Model No. 1122) following seven days storage of the etched specimens under $37^{\circ}C$, 100% humidity condition. Following conclusions were drawn. 1. In unetched control group, crack was present, but the surface was generally smooth. 2. Deterioration of the surface appearance such as serious dissolving of gel matrix and loss of glass particles occured as the etching time was increased beyond 15 s following Immediate etching of chemical curing type of glass ionomer cements. 3. Etching after 1 h, and 1 d reduced surface damage, 15 s, and 30s etch gave rough surface appearance without loss of glass particle of chemical curing type of glass ionomer cements. 4. Light curing type glass ionomer cement was etched by acid, but there was no difference in surface appearances according to various waiting periods. 5. It was found that the value of plane stram fracture toughness of glass ionomer cements was highest in the light curing filling type as $1.79\;MNm^{-1.5}$ followed by the light curing lining type, chemical curing metal reinforced type, chemical curing filling type and chemical curing lining type. 6. The value of plane stram fracture toughness of the chemical curing lining type glass ionomer cement etched after 5 minutes was lower than those of the cement etched after 1 hour or day or unetched (P < 0.05). 7. Light curing glass ionomer cement showed Irregular fractured surface and chemical curing cement showed smooth fractured surface.

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Ammonium Thisoulfate 처리가 담수(湛水) 답토양(畓土壤)의 생물활성(生物活性)에 미치는 영향 (Effect of Ammonium Thiosulfate on Biological Activity in a Paddy Soil)

  • 임선욱;서영호
    • 한국토양비료학회지
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    • 제27권1호
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    • pp.40-47
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    • 1994
  • 담수(湛水)된 고유기물(高有機物) 논토양에서의 ammonium thiosulfate(ATS)의 urease 활성(活性) 억제(抑制) 효과(效果)와 토양의 생물학적 활성 및 화학적 성질에 미치는 영향을 조사하고, ATS의 효과를 sodium thiosulfate(STS)와 비교하고 유기물 처리의 영향을 검토한 결과를 요약하면 다음과 같다. 1. Thiosulfate의 urease 활성 저해 효과는 3~5일후부터 나타났다. glucose 첨가구에서는 STS 처리가 ATS보다 효과가 다소 컸고, glucose를 첨가하지 않았을 때에는 처리 효과가 비슷하였다. 2. Thiosulfate 처리구의 pH는 초기에 높아지다가 glucose 무첨가시에는 10일 이후 낮아졌고, glucose 첨가시에는 15일 이후 낮아졌다. Eh는 thiosulfate 처리에 의하여 대체로 낮아졌다. 3. Thiosulfate 처리구에서 acet 산(酸)과 butyr 산(酸)은 소량($10{\mu}g/g$ 이하) 검출되었으므로, thiosulfate 처리에 의해 수도(水稻)의 생육이 저해되지는 않을 것이라 추정된다. 4. Glucose를 첨가하지 않았을 때에는 thiosulfate 처리에 의해 $CO_2$ 발생량이 증가하여 토양 생물의 활성을 높였다고 해석된다.

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Micro-Spot Atmospheric Pressure Plasma Production for the Biomedical Applications

  • Hirata, T.;Tsutsui, C.;Yokoi, Y.;Sakatani, Y.;Mori, A.;Horii, A.;Yamamoto, T.;Taguchi, A.
    • 한국진공학회:학술대회논문집
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    • 한국진공학회 2009년도 제38회 동계학술대회 초록집
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    • pp.44-45
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    • 2010
  • We are currently conducting studies on culturing and biocompatibility assessment of various cells such as neural stem cells and induced pluripotent stem cells(IPS cells) on carbon nanotube (CNT), on nerve regeneration electrodes, and on silicon wafers with a focus on developing nerve integrated CNT based bio devices for interfacing with living organisms, in order to develop brain-machine interfaces (BMI). In addition, we are carried out the chemical modification of carbon nanotube (mainly SWCNTs)-based bio-nanosensors by the plasma ion irradiation (plasma activation) method, and provide a characteristic evaluation of a bio-nanosensor using bovine serum albumin (BSA)/anti-BSA binding and oligonucleotide hybridization. On the other hand, the researches in the case of "novel plasma" have been widely conducted in the fields of chemistry, solid physics, and nanomaterial science. From the above-mentioned background, we are conducting basic experiments on direct irradiation of body tissues and cells using a micro-spot atmospheric pressure plasma source. The device is a coaxial structure having a tungsten wire installed inside a glass capillary, and a grounded ring electrode wrapped on the outside. The conditions of plasma generation are as follows: applied voltage: 5-9 kV, frequency: 1-3 kHz, helium (He) gas flow: 1-1.5 L/min, and plasma irradiation time: 1-300 sec. The experiment was conducted by preparing a culture medium containing mouse fibroblasts (NIH3T3) on a culture dish. A culture dish irradiated with plasma was introduced into a $CO_2$-incubator. The small animals used in the experiment involving plasma irradiation into living tissue were rat, rabbit, and pick and are deeply anesthetized with the gas anesthesia. According to the dependency of cell numbers against the plasma irradiation time, when only He gas was flowed, the growth of cells was inhibited as the floatation of cells caused by gas agitation inside the culture was promoted. On the other hand, there was no floatation of cells and healthy growth was observed when plasma was irradiated. Furthermore, in an experiment testing the effects of plasma irradiation on rats that were artificially given burn wounds, no evidence of electric shock injuries was found in the irradiated areas. In fact, the observed evidence of healing and improvements of the burn wounds suggested the presence of healing effects due to the growth factors in the tissues. Therefore, it appears that the interaction due to ion/radicalcollisions causes a substantial effect on the proliferation of growth factors such as epidermal growth factor (EGF), nerve growth factor (NGF), and transforming growth factor (TGF) that are present in the cells.

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Latex 응집반응을 이용한 동물의 톡소플라즈마병 진단액 개발에 관한 연구 (Development of antigen for the microplate latex agglutination test on toxoplasmosis in animals)

  • 서명득;이응구
    • 대한수의학회지
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    • 제33권4호
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    • pp.623-632
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    • 1993
  • This study was conducted to develop a sensitized latex-antigen for serodiagnosis of toxoplasmosis in animals. Tachyzoites of T gondii(RH-strain) harvested from mouse peritoneal cavity were purified through the filtraton of polycarbonate membrane(pore size, $3.0{{\mu}m}$, Costar Co.) and disrupted by ultrasonicator. The tachyzoite suspension was ultracentrifuged for 30 min at $60,000{\times}g(4{^{\circ}C})$ and the supernatant was used as a water-lysate antigen. Polystyrene latex particles of $0.8{{\mu}m}$ in diameter(Sigma) were used for the preparation of sensitized latex-antigen suspension. The several parameters including the preparation conditions, incubation buffer. serum dilution buffer and stability of agglutination reactions were evaluated and the results obtained were summarized as follows : 1. The antigen consisting of a water-lysate of T gondii tachyzoites was adsorbed onto polystyrene latex particles of $0.8{{\mu}m}$ in diameter by adding a latex suspension to an equal volume of diluted antigen solution and by incubating the mixture at $37{^{\circ}C}$ under different conditions. 2. The optimum incubation buffer used for the antigen sensitization was 0.1M Tris-HCl buffer(pH 8.0). 3. The optimum serum dilution buffer used for the latex agglutination test was 0.1M Tris-HCl-NaCl buffer(pH 7.4) containing 300 mM NaCl. But 0.1M Tris-HCl-NaCl buffer(pH 7.4) containing 300-600 mM NaCl, 0.5% BSA and 0.01% Tween-20 improved the agglutination pattems and cleared the background of microplate well without the effects on L.A titer. 4. The time required for antigen sensitization was 40 and 60 min in incubation buffer(pH 8.0) at $37{^{\circ}C}$. But the optimun time for antigen sensitization was min at $37{^{\circ}C}$. 5. The optimun quantity of antigen absorbed on latex particles for proper agglutination was the range of 20 to $32{\mu}g$ of latex particles. 6. The optimun concentration of the latex-antigen suspension for the proper agglutination reaction was determined as 0.2%(w/v). 7. The specificity, rapidity and simplicity of the latex-particle agglutination test suggested that it might be adaptable to large scale serum screening.

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