• 대한소아치과학회지
• /
• 제8권1호
• /
• pp.37-46
• /
• 1981

This study was undertaken to evaluate the pulpal responses to the pulp-capping materials such as glutaraldehyde and formocresol in pulpotomy technique, especially in the primary dentition. Mandibular primary canines and molars of 5 dogs (aged about 8-9 weeks)were selected for this study. The intervals of observation for histologic study of pulpotomized primary teeth with 2% glutaraldehyde, formocresol and calcium hydroxide in the usual manner ranged from 2 hours, 1 week, 2 weeks, 3 weeks and 5 weeks after experiments respectively. Each specimens were fixed with 10% formalin and decalcified in 5% nitric acid. All slides were stained with Hematorylin-Eosin and examined histopathologically. The results were as follows; 1. In calcium hydroxide groups, formation of dentin bridge was initiated in 1 week after experiments and completed in 5 weeks after experiments. 2. Formation of dentin bridge was not seen, whereas necrosis of pulp tissue was noted, in formocresol and glutaraldehyde groups. 3. Duration of tissue reactions and tissue changes were similar, in formocresol and glutaraldehyde groups. 4. In formocresol and glutaraldehyde groups, amputation surfaces of the pulp were covered with blood clots, beneath which coagulation necrois was noted, but inflammatory cells were not prominent, in 2 hours and 1 week after experiments. But coagulation necrosis was proceeded to the apical portion, accompanied by infiltration of inflammatory cells, since 2 weeks after experiments. And suppuration or gangrene of the pulp tissue were noted in 3 weeks and 5 weeks groups. 5. Suppuration or gangrene of pulp seemed to provoke the resorption of dentin wall, and inflammatory changes and resorption of roots were noted in the periodontal membrane near the periapical region. 6. As compared with calcium hydroxide groups, resorption of the root was pronounced in form or cresol and glutaraldehyde groups. Effects of medicaments to the succedaneous tooth germ were not seen.

• Journal of Microbiology and Biotechnology
• /
• 제22권5호
• /
• pp.628-636
• /
• 2012

Raw-starch-digesting enzyme (RSDA) was immobilized on Amberlite beads by conjugation of glutaraldehyde/polyglutaraldehyde (PG)-activated beads or by crosslinking. The effect of immobilization on enzyme stability and catalytic efficiency was evaluated. Immobilization conditions greatly influenced the immobilization efficiency. Optimum pH values shifted from pH 5 to 6 for spontaneous crosslinking and sequential crosslinking, to pH 6-8 for RSDA covalently attached on polyglutaraldehyde-activated Amberlite beads, and to pH 7 for RSDA on glutaraldehyde-activated Amberlite. RSDA on glutaraldehyde-activated Amberlite beads had no loss of activity after 2 h storage at pH 9; enzyme on PG-activated beads lost 9%, whereas soluble enzyme lost 65% of its initial activity. Soluble enzyme lost 50% initial activity after 3 h incubation at $60^{\circ}C$, whereas glutaraldehyde-activated derivative lost only 7.7% initial activity. RSDA derivatives retained over 90% activity after 10 batch reuse at $40^{\circ}C$. The apparent $K_m$ of the enzyme reduced from 0.35 mg/ml to 0.32 mg/ml for RSDA on glutaraldehyde-activated RSDA but increased to 0.42 mg/ml for the PG-activated RSDA derivative. Covalent immobilization on glutaraldehyde Amberlite beads was most stable and promises to address the instability and contamination issues that impede the industrial use of RSDAs. Moreover, the cheap, porous, and non-toxic nature of Amberlite, ease of immobilization, and high yield make it more interesting for the immobilization of this enzyme.

• Journal of Microbiology and Biotechnology
• /
• 제23권3호
• /
• pp.289-296
• /
• 2013

Cryptomonads are unicellular, biflagellate algae. Generally, cryptomonad cells cannot be preserved well because of their fragile nature, and an improved methodology should be developed to identify cryptomonads from natural habitats. In this study, we tried using several cytological fixatives, including glutaraldehyde, formaldehyde, and their combinations to preserve field samples collected from various waters, and the currently used fixative, Lugol's solution was tested for comparison. Results showed that among the fixatives tested, glutaraldehyde preserved the samples best, and the optimal concentration of glutaraldehyde was 2%. The cell morphology was well preserved by glutaraldehyde. Cells kept their original color, volume, and shape, and important taxonomic features such as furrow/gullet complex, ejectosomes, as well as flagella could be observed clearly, whereas these organelles frequently disappeared in Lugol's solution preserved samples. The osmotic adjustments and buffers tested could not preserve cell density significantly higher. Statistical calculation showed the cell density in the samples preserved by 2% glutaraldehyde remained stable after 43 days of the fixation procedure. In addition, DNA was extracted from glutaraldehyde preserved samples by grinding with liquid nitrogen and the 18S rDNA sequence was amplified by PCR. The sequence was virtually identical to the reference sequence, and phylogenetic analyses showed very close relationship between it and sequences from the same organism. To sum up, the present study demonstrated that 2% unbuffered glutaraldehyde, without osmotic adjustments, can preserve cryptomonads cells for identification, in terms of both light microscopy and phylogenetic analyses based on DNA sequences.

• 치과방사선
• /
• 제22권2호
• /
• pp.329-335
• /
• 1992

The purpose of the study was to determine whether Sodium hypochlorite and Glutaraldehyde would be effective for the surface disinfection of contaminated radiographic film pockets with saliva The following results were as obtained 1. Proper times for surface disinfection of 2.0% Glutaraldehyde and 3.5% Sodium hypochlorite were 60 seconds. 2. When films were immerged in 2% Glutaraldehyde solution for 1 minute, baterial colonies were present in 24 cases(80%). 3. When films were immerged in 3.5% Sodium hypochlorite solution for 1 minute, bacterial colony was absent in 25 cases(83.3%). 4. Differences of effectiveness on surface disinfection between 2% Glutaraldehyde and 3.5% Sodium hypochlorite were statistically significant.

• 한국잠사곤충학회지
• /
• 제36권2호
• /
• pp.152-156
• /
• 1994

생사에 G.A.(glutaraldehyde)와 formalin을 혼합처리하는 방법으로 세리신정착을 실시한 다음 세리신 정착효과, 정착에 따른 백도의 변화, 물성 변화 등을 검토한 결과를 요약하면 다음과 같다. 1. G.A. 농도에 관계 없이 formalin 1% 용액 이상으로 정착하면 미정착사의 96%까지 백도가 향상된다. 2. Formalin G.A의 혼합처리에 의해 정련에 의한 백도 감소를 방지할 수 있었다. 3. Formalin 0.5% 용액 혼합처리로 완전한 세리신 정착을 얻을 수 있었다. 4. 세리신정착처리는 미정착사에 비해 강·신도의 증가를 가져왔다. 5. 정착사와 미정착사의 표면구조는 큰 차이가 없었다.

• Journal of Microbiology and Biotechnology
• /
• 제18권11호
• /
• pp.1803-1808
• /
• 2008

For practical application, the stability of permeabilized Ochrobactrum anthropi SY509 needs to be increased, as its half-life of enzymatic denitrification is only 90 days. As the cells become viable after permeabilization treatment, this can cause decreased activity in a long-term operation and induce breakage of the immobilization matrix. However, the organic solvent concentration causing zero cell viability was 50%, which is too high for industrial application. Thus, whole-cell immobilization using glutaraldehyde was performed, and 0.1% (v/v) glutaraldehyde was determined as the optimum concentration to maintain activity and increase the half-life. It was also found that 0.1% (v/v) glutaraldehyde reacted with 41.9% of the total amine residues on the surface of the cells during the treatment. As a result, the half-life of the permeabilized cells was increased from 90 to 210 days by glutaraldehyde treatment after permeabilization, and no cell viability was detected.

• Tuberculosis and Respiratory Diseases
• /
• 제40권1호
• /
• pp.29-34
• /
• 1993

연구배경 : Ikeda에 의해 임상에 도입된 굴곡성 기관지경은 각종 폐 질환의 진단과 치료에 광범위하게 이용되고 있으며 시술 증례도 증가하고 있으나 외국에서는 결핵균, 비결핵항산균 및 여러 세균들에 의한 기관지경의 교차오염예가 다수 보고되고 있으므로 기관지경의 세척과 소독방법에 대해 주의를 기울여야 한다. 방법 : 1991년 11월부터 1992년 5월 까지 기관지내시경을 시행한 예중에서 기관지세척액에서 비결핵항산균이 배양된 예들을 분석하고 본원에서 화학살균제로 사용하고 있는 2% alkaline glutaraldehyde의 살균작용을 평가하기 위하여 실험실내에서 2% alkaline glutaraldehyde와 비결핵항산균 및 세균을 접촉시킨후 균의 사멸 여부를 알아 보았다. 결과 : 2% glutaraldehyde 소독제 용액에 비결핵항산균은 2% glutaraldehyde 1:1 용액으로 30분간 접촉한 후 균이 자라지 않았으며 그 밖의 세균들은 접촉 바로 후에 자라지 않았다. 위발생 인지후 철저한 기계적 세척과 함께 세척기내에서 30분이상 2% glutaraldehyde에 담가둔 이후로는 위양성이 발생하지 않았다. 결론 : 기관지경 사용후 기계적 세척을 철저히 하는 것이 중요하며 2% glutaraldehyde 용액으로 소독시 비결핵항산균의 소멸을 기대하려면 적어도 30분 이상 접촉이 필요할 것으로 생각된다. 또한 감염조절 방법을 엄격하게 적용한다 하더라도 오염을 완전히 배제할 수 없으므로, 일반적으로 비병원균으로 알려진 균들이 비통상적으로 갑자가 높은율로 검출되면 위발생을 생각하여야 한다.

• 한국식품과학회지
• /
• 제27권5호
• /
• pp.753-756
• /
• 1995

아스파탐 전구체의 보다 효율적인 효소적 합성 방법을 개발하기 위하여 thermolysin의 고정화 방법을 확립하고자 고정화 담체로서 다공성 수지인 Amberlite XAD-7을, 가교화제로서 glutaraldehyde를 사용하여 최적 고정화 조건을 조사하고자 하였다. Thermolysin이 Amberlite XAD-7에 흡착되는 속도는 초기에 빠른 것으로 나타났으며, $5^{\circ}C$에서 24시간후는 96%가 흡착되었다. Thermolysin에 대한 Amberlite XAD-7의 최대흡착량은 수지 l당 340g 이상이었으며, 투입한 thermolysin 양이 300g일 때까지는 흡착된 양의 증가하는 관계는 직선관계를 보여주었다. thermolysin의 가교화를 위한 효과적인 pH와 glutaraldehyde의 농도, 가교화시간은 각각 $pH\;6.0{\sim}7.0,\;6{\sim}12.5%$ 및 $3{\sim}7$시간이었다. 특히 glutaraldehyde 6%에서는 7시간, 12.5%에서 3시간의 가교화가 효소의 잔존역가와 가교화 정도를 현저히 높였다. 이때의 잔존역가는 30% 이상인 것으로 나타났다.

• 한국양식학회지
• /
• 제21권3호
• /
• pp.172-175
• /
• 2008

본 연구에서는 양식장에서 질병예방용으로 시판되고 있는 hydrogen peroxide, sodium hypochlorite, glutaraldehyde 및 didecyl dimethyl ammonium chloride (DDAC)의 저장 안정을 평가하였다. Hydrogen peroxide와 DDAC는 개봉 후 6개월간 실온저장 및 $4^{\circ}C$ 저장에서 유효 성분의 변화가 없어 안정하였다. 그렇지만, sodium hypochlorite와 glutaraldehyde는 개봉 후 $4^{\circ}C$에서 저장하더라도 각각 15%와 39%의 유효성분이 감소하였다. 이와 같은 결과에 따라 hydrogen peroxide과 DDAC는 개봉 후 6개월까지 보관은 유효하지만, 양식장에서 적용시에는 수질의 유기물 양, pH 등의 조건을 고려해서 사용해야 할 것으로 판단되었다.

• 한국섬유공학회:학술대회논문집
• /
• 한국섬유공학회 1999년도 가을 한국섬유공학회 학술발표회 논문집(Proceedings of the Korean Textile Conference)
• /
• pp.239-242
• /
• 1999