• The Journal of Advanced Prosthodontics
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• 제6권2호
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• pp.115-120
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• 2014

PURPOSE. The aim of this in vitro study was to evaluate the effect of aging on the tear strength and cytotoxicity of four soft denture lining materials. MATERIALS AND METHODS. Four commonly used soft denture lining materials, (Coe-Comfort$^{TM}$ GC America Inc., Alsip, IL, USA; Coe-SOFT$^{TM}$ GC America Inc., Alsip, IL, USA; Visco-gel Dentsply Caulk Milford, DE, USA; and Sofreliner Tough M Tokuyama Dental Corporation Tokyo, Japan) were selected. Sixty trouser-leg designed specimens per lining material were fabricated using a stainless steel mold for tear strength testing. The specimens were divided into non-thermocycling and 1000-, and 3000-thermocycling groups. For the cytotoxicity test, twenty-four disk shaped specimens per material were fabricated using a stainless steel mold. The specimens were soaked in normal saline solution for 24 h, 48 h and 72 h. Cytotoxicity was measured by XTT assay in L929 mouse fibroblasts. Data were analyzed by two way analysis of variance and Dunnett's test (P<.05). RESULTS. Before thermocycling, Sofreliner Tough M ($10.36{\pm}1.00N$) had the highest tear strength value while Coe-Comfort$^{TM}$ ($0.46{\pm}0.10N$) had the lowest. After 3000 cycles, Sofreliner Tough M ($9.65{\pm}1.66N$) presented the highest value and Coe-Comfort$^{TM}$ ($0.42{\pm}0.08N$) the lowest. Sofreliner Tough M, in all incubation periods was the least toxic with significant differences compared to all other materials (P<.05). Coe-Comfort$^{TM}$, Coe-$SOFT^{TM}$, and Sofreliner Tough M did not show any significant differences within their material group for all incubation periods. CONCLUSION. This in vitro study revealed that aging can affect both the tear strength and cytotoxicity of soft denture materials depending on the composition.

• Applied Biological Chemistry
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• 제26권1호
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• pp.53-57
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• 1983

이종(二種)의 토양(土壤)을 가지고 논과 유사한 상태(狀態)로 만들어 butachlor를 일정기간(一定其間) 배양시(培養時) 모든 경우 주분해산물(主分解産物)로 2,6-diethyl-N-(butoxymethyl) acetanilide와 신분해산물(新分解産物) C를, 그리고 경우에 따라서는 비교적(比較的) 소량(少量)의 신분해산물(新分解産物) 8-ethyl-2-hydroxy-N-(butoxymethyl) 3,4-dihydroguinoline을 생성(生成)하였다. 토양미산물(土壤微産物)의 작용(作用)으로 추측(推測)되는 이 분해(分解)는 어느 정도 배양기간에 비 해하여 진행(進行)되었다. 전번 연구의 혐기적 배양시에는 2,6-diethyl-N-(butoxymethyl) acetanilide가 주분해산물(主分解産物)인 반면 이번 경우에는 m/z a91의 물질(物質)이 주분해산물(主分解産物)이었다. 그리고 Mass Spectrum의 Fragmentation Pattern에 의(依)하여 이들 신분해산물(新分解産物)의 화학구조(化學構造)를 구명(究明)하고 가능(可能)한 생성경로(生成經路)를 추정(推定)하였다.

• 대한수의학회지
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• 제41권2호
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• pp.133-138
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• 2001

부란 1일부터 부화직후까지의 닭 태자 췌장에서 serotonin 면역반응세포들의 부위별 분포 및 상대적 빈도를 면역조직화학적 방법으로 검색하였다. 췌장은 해부학적으로 배쪽, 등쪽, 제 3엽 및 비장엽의 4개엽으로 구분하였으며, 각 엽은 조직학적으로 외분비 부분, light 및 dark 췌장섬의 3부분으로 세분하였다. 이들의 각 발생단계에 따른 닭 췌장에서 serotonin 면역반응세포들의 분포 및 빈도는 췌장의 엽, 조직학적 부위 및 발생단계에 따라서 매우 다양하게 관찰되었으나, 대체로 원형 또는 난원형의 형태로 모든 엽에서 관찰되었다. 외분비 부분에서 serotonin 면역반응세포들은 비장엽의 경우 부란 13일과 14일에서만 국한되어 관찰되었고, 제 3엽에서는 부란 10일부터 부란 19일 동안 관찰되었다. 또한 배쪽엽에서는 부란 10일부터 부화 직후까지 관찰되었으며, 등쪽엽에서는 부란 11일부터 부화 직후까지 관찰되었다. 췌장섬에서 이들 면역반응세포는 비장엽의 dark 췌장섬에서만 부란 15일과 부란 16일에 국한되어 극소수 관찰되었고 다른 엽 또는 light 췌장섬에서는 관찰되지 않았다. 결론적으로 serotonin 면역반응세포들은 부란 발생 초기에는 다수 관찰된 이후 발생단계에 따라 점차적으로 감소되며 이런 양상은 엽의 종류에 관계없이 나타나는 것으로 관찰되었다.

• Applied Biological Chemistry
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• 제27권2호
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• pp.64-72
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• 1984

담수답 토양중에서 배양된 Alachlor는 그 분해산물로 1-formyl-2, 3-dihydro-7-ethylindole, 2,6-diethylaniline, 2,6-diethylacetanilide, 2,6-diethyl-N-(methoxymethyl) acetanilide, 2-hydroxy-2', 6'-diethyl-N-(methoxymethyl) acetanilide, 그리고 삼종(三種)의 미확인 화합물을 생성하였다. 환(環)-$^{14}C$ 표식(標識) Alachlor의 사용으로 입증된 바와 같이 토양 현탁액중에서 Alachlor의 수용성 분해산물은 배양기간이 증가함에 따라 증가하였고 Rhizoctonia solani의 배양에서도 유사한 결과를 얻었다. Streptomyces lavendulae Ru3340-8은 주요분해산물로 2-hydroxy-2', 6'-diethyl-N-(methoxymethyl) acetanilide를 최고 25%까지 생성하는 반면 Bacillus brevis IFO 3331, Bacillus cruciviae, 그리고 Pseudomonas putida는 그것을 생성하지 않았다.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2003년도 제10차 국제학술회의 및 추계정기 학술발표회
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• pp.20-20
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• 2003

Isolation and culture of leaf protoplasts from two chilli cultivars (Capsicum annuum var. accumnatum and Bird chilli) were developed to enhance selection process in the somatic hybridization programmes. In order to isolate the protoplasts from leaves of these two chilli cultivars different incubation periods (3, 5 and 10 hours) were tested with combinations of enzyme mixtures containing cellulase and macerozyme. Leaves were incubated on three enzyme mixtures (2% cellulase +0.4% macerozyme, 1% cellulase +0.2% macerozyme and 0.5% cellulase +0.1% macerozyme in 13% mannitol) at 251oC in the dark. Three hours of incubation using 2% cellulase and 0.4% macerozyme was the best for the protoplast isolation of both chilli cultivars tested. The yield was 5${\times}$108protoplasts/m1/g leaf tissue in both chilli varieties. It was found that in the mixed nurse method using Nagata and Takebe (NT) medium supplemented with 1.0mg/12,4-D, NAA and BAP with 0.5M mannitol and 1.2% Sea Plaque agarose is the best medium for protoplast culture. Protoplasts of Capsicum annum var. accumnatum were alive for 14 days forming cell walls and initiating cell division.

• 한국패류학회지
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• 제17권2호
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• pp.95-104
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• 2001

To determine optimal conditions for measurement of the clearance rate in feeding experiment of an intertidal bivalve Glauconome chinensis, effects of starvation, extent of mixing at subsampling, and initial prey concentration were assessed. Experiments were conducted separately for each condition with different treatments. Two-way ANOVAs showed that there were significant differences in clearance rates among different starvation periods (p<0.001), extents of mixing (p = 0.005), and prey concentrations (p < 0.001). Starvation for 1 or 2 days gave rise to 2 to 3-fold increase in the clearance rate. After starvation for 5 days, the clearance rate decreased seriously, implying loss of physiological status. It is suggested that animals should be fed during acclimation. The differences of the clearance rates between gentle and vigorous mixings were significant, but the differences were smaller than that among different incubation times. It was found that vigorous mixing is not necessary. The effect of initial prey concentration was great. However, optimal prey concentration could not be determined at any fixed value. Experiments with multiple concentrations of algal prey are recommended. Optimal incubation time for measurement of the clearance rate of G. chinensis was determined to be 2-4 hours.

• 생명과학회지
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• 제6권2호
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• pp.111-119
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• 1996

The production of interleukin-1(IL-1)and nitric oxide(NO) by cultured fibroblast cells of human nasal turbinate was revealed by biological assay respectively. The cells were incubated for various periods of time in the presence of staphyloccocal toxic shock syndrome toxin-1(TSST-1) and house dust mite(Dermatophagoides farinae, HDM), and the culture supernatants were harvested. There was a little difference in the activities of IL-1beta and the amount of NO produced by the cells when stimulated with 0.002-0.1$\mu$g/ml of TSSTO-1 and 0.02-1$\mu$g/ml of HDM. The shapes of the time course curves for the production of IL-1beta and NO by the cells were different. Groups stimulated with TSST-1 or HDM produced more IL-beta in 2 h than no exposure group(Control). A certain mixed group(TSST-1, 10ng+mite, 100 ng) continued to produce IL-1beta highly throughout the entire incubation period. The cells stimulated with TSST-1 or HDM produced more NO in 2 h and 6 h than that produced in the end of incubation(48 h). Also, the mixed groups were generally similar. There results suggest that induction of IL-1beta by a certain mixed condition(TSST-1+mite) in fibroblast cell in vivo may play a role in inflammation.

• 미생물학회지
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• 제23권4호
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• pp.252-258
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• 1985

Aspergillus niger var. macrosporus, Aspergillus fumigatus, Penicillium notatum 및 Penicillium spinulosum의 곰팡이를 배양 온도 및 배양 기간을 달리하여 배양하고 이들 곰팡이가 생산한 지질량과 지질의 지방산 조성을 분석하였다. 이들 곰팡이에 의해 생성된 최대 지질량은 Aspergillus niger var. macrosporus가 17.8%. Aspergillus fumigatus가 31 %. Penicillium notatum이 12.6% 그리고 Pen. spinulosum이 17.5%였다. 이들 균주가 생산한 지질의 주요 지방산은 palmitic acid, stearic acid, oleic acid, linoleic acid였으며 Asp. niger var. macrosporus와 Asp. fumigatus는 전체 배양 기간 동안 oleic acid의 함량이 가장 높았으나 P. nota turn과 P. spinulosum은 linoleic acid의 함량이 가장 높았다. 그리고 지질의 불포화도는 Penicillium속이 Aspergillus속보다 높았다. 한편 지방산 조성은 배양온도에 따라 변화를 보였으나 대부분 일정한 경향을 나타내지 않았는데 Aspergillus fumigatus와 Penicillium notatum에서 저온 일수록 linoleic acid와 불포화도가 높아졌다.

• Parasites, Hosts and Diseases
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• 제39권3호
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• pp.223-226
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• 2001

In South Korea, the north border area has been under vivax malaria epidemic since 1993. However, Jeollabuk-do, which is about 300 kms from the border, has not experienced the same epidemic. 1 investigated a total of 58 notified cases of malaria in Jeollabuk-do in the year 2000. All of the cases had an exposure history in the epidemic area. Among them were 49 ex-soldiers, 3 soldiers who served near the border area and 6 civilians who traveled there. The causal agent of all cases was Plasmodium vivax. Except the civilians, the soldiers and ex-soldiers were aged in their twenty's. In the present study, the incubation period was from 6 to 520 days with a median of 157 days, and the latent onset type (92%) was more prevalent than the early onset type. illness onset of most cases (86%) peaked during the summer season (June to September) despite of variable incubation periods. The time lag for diagnosis ranged from 2 to 42 days with a median of 11 days. Jeollabuk-do has not been an area of epidemic untill now, but incidences have been increasing annually since 1996. In Jeollabuk-do, early diagnosis and treatment can be a feasible disease control measure to prevent spreading from the epidemic area.

• 한국자원식물학회:학술대회논문집
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• 한국자원식물학회 2003년도 심포지엄
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• pp.50-58
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• 2003

Isolation and culture of leaf protoplasts from two chilli cultivars (Capsicum annuum var. accumnatum and Bird chilli) were developed to enhance selection process in the somatic hybridization programmes. In order to isolate the protoplasts from leaves of these two chilli cultivars different incubation periods (3, 5 and 10 hours) were tested with combinations of enzyme mixtures containing cellulase and macerozyme. Leaves were incubated on three enzyme mixtures (2% cellulase + 0.4% macerozyme, 1% cellulase + 0.2% macerozyme and 0.5% cellulase + 0.1 % macerozyme in 13% mannitol) at 251oC in the dark. Three hours of incubation using 2% cellulase and 0.4% macerozyme was the best for the protoplast isolation of both chilli cultivars tested. The yield was 5 ${\times}$ 108protoplasts/ml/ g leaf tissue in both chilli varieties. It was found that in the mixed nurse method using Nagata and Takebe (NT) medium supplemented with 1.0mg/12,4-D, NAA and BAP with 0.5M mannitol and 1.2% Sea Plaque agarose is the best medium for protoplast culture. Protoplasts of Capsicum annum var. accumnatum were alive for 14 days forming cell walls and initiating cell division.