• 대한화학회지
• /
• 제6권1호
• /
• pp.10-13
• /
• 1962

Polarograph에 依한 分析方法을 利用하여 Ilmentite 鑛石에서 Titanium을 定量함에 있어서 鑛石을 酸처리하여 그 溶液을 器機에 提供함으로써 長時間 所要되는 在來의 分析方法을 避하여 迅速定量을 試圖하였다. 먼저 各種의 支待電解質에 對하여 檢詩하였으며 그 電解質에 對한 Titanium波의 定量感度와 共存하는 여러 Ion이 Titanium 波에 미치는 영향에 對하여 살폈다. 本實驗에서의 支待電解質로서는 근래에 Chelatometry$^{1)}$에서 많이 쓰이는 EDTA(Disodium etylenediamine tetraacetate)를 擇하였다. 支待電解質로서의 EDTA의 기초액 組成은 0,2M EDTA(pH=6)가 最適임을 알았다. 本支待電解質에서 Titanium의 Polarograph波가 大端히 良好하고 pH 6.3에서 $E_{1/2}$=-0.61V v.s. S.C.E.이면 또한 이 境遇에 濃度의 따라 波高가 比例하여 定量分析의 可能性을 보여 주었다.

• 미생물학회지
• /
• 제45권4호
• /
• pp.377-384
• /
• 2009

전통 메주로부터 plasmin의 혈전용해 활성보다 약 58% 더 높은 활성을 나타내는 MJ-226을 분리하여 동정한 결과, Bacillus subtilis와 유사한 형태학적, 생화학적 및 당 발효능을 나타내었다. B. subtilis MJ-226은 Tryptic Soy Broth (TSB) 배지 상에서 최대의 혈전용해효소 활성을 나타내었고, $37^{\circ}C$에서 24~26시간 배양했을 때 가장 높은 활성을 나타내었고, TSB 배지 내에 glucose와 fructose 2.0%와 peptone 및 yeast extract 1.0% 각각을 첨가한 경우 활성이 증가되었다. 하지만 lactose, sucrose, beef extract, casein 및 tryptophan 등에 의해선 활성이 오히려 감소되었다. B. subtilis MJ-226이 생산하는 혈전용해효소는 pH 6.0~8.0 및 온도 $35\sim40^{\circ}C$에서 매우 안정하였으며, 또한 $MnSO_4$, $CaCl_2$, KCl 및 NaCl 5 mM 농도의 금속이온에 대해서도 비교적 안정함을 유지하였다. 그러나 $CuSO_4$, $MgSO_4$, $ZnSO_4$, $FeSO_4$와 $BaCl_2$에 등의 금속이온과 iodoacetic acid, leupeptin, phenylmethanesulphonyl fluoride (PMSF), sodium dodecyl sulfate (SDS), thiourea, trans-1,2-diaminocyclohexane-N,N,N',N'- tetraacetic acid (CDTA) 및 ethylenediaminetetraacetic acid (EDTA) 등의 저해제들과 반응한 경우에는 매우 불안정한 것으로 나타났다.

• Restorative Dentistry and Endodontics
• /
• 제46권1호
• /
• pp.11.1-11.11
• /
• 2021

Objectives: The aim of this study was to compare smear layer removal by conventional application (CA), passive ultrasonic irrigation (PUI), EasyClean (EC), and XP-Endo Finisher (XPF), using 17% ethylenediaminetetraacetic acid (EDTA) after chemomechanical preparation, as evaluated with scanning electron microscopy (SEM). Materials and Methods: Forty-five single-rooted human mandibular premolars were selected for this study. After chemomechanical preparation, the teeth were randomly divided into 5 groups according to the protocol for smear layer removal, as follows: G1 (control): CA of distilled water; G2 (CA): CA of 17% EDTA; G3 (PUI): 17% EDTA activated by PUI; G4 (EC): 17% EDTA activated by EC; and G5 (XPF): 17% EDTA activated by XPF. SEM images (×1,000) were obtained from each root third and scored by 3 examiners. Data were evaluated using the Kruskal-Wallis and Dunn tests (p < 0.05). Results: In the apical third, there were no statistically significant differences among the groups (p > 0.05). In the cervical and middle thirds, the experimental groups performed better than the control group (p < 0.05); however, G2 presented better results than G3, G4, and G5 (p < 0.05), which showed no differences among one another (p > 0.05). Conclusions: No irrigation method was able to completely remove the smear layer, especially in the apical third. Using CA for the chelating solution performed better than any form of activation.

• Restorative Dentistry and Endodontics
• /
• 제40권3호
• /
• pp.216-222
• /
• 2015

Objectives: To evaluate the effects of copolymer of acrylic acid and maleic acid (Poly[AA-co-MA]) and calcium hypochlorite ($Ca(OCl)_2$) on root canal dentin using scanning electron microscope (SEM). Materials and Methods: Twenty-four single-rooted teeth were instrumented and the apical and coronal thirds of each root were removed, leaving the 5 mm middle thirds, which were then separated into two pieces longitudinally. The specimens were randomly divided into six groups and subjected to each irrigant for 5 min as follows: G1, $Ca(OCl)_2$; G2, Poly(AA-co-MA); G3, $Ca(OCl)_2$ + Poly(AA-co-MA); G4, sodium hypochlorite (NaOCl); G5, ethylenediaminetetraacetic acid (EDTA); G6, NaOCl+EDTA. The specimens were prepared for SEM evaluation. Smear layer, debris and erosion scores were recorded by two blinded examiners. One image from G3 was analyzed with energy dispersive spectroscopy (EDS) on suspicion of precipitate formation. Data were analyzed using the Kruskal-Wallis and Dunn tests. Results: G1 and G4 showed the presence of debris and smear layer and they were statistically different from G2, G3, G5 and G6 where debris and smear layer were totally removed (p < 0.05). In G1 and G4, erosion evaluation could not be done because of debris and smear layer. G2, G3 and G5 showed no erosion, and there was no significant difference between them. G6 showed severe erosion and was statistically different from G2, G3 and G5 (p < 0.05). EDS microanalysis showed the presence of Na, P, and Ca elements on the surface. Conclusions: Poly(AA-co-MA) is effective in removing the smear layer and debris without causing erosion either alone or with $Ca(OCl)_2$.

• Biomolecules & Therapeutics
• /
• 제10권2호
• /
• pp.104-113
• /
• 2002

The effects of enzyme inhibitors and penetration enhancers on the permeation of leucine enkephalin (Leu-Enk) and its synthetic analog, [${D-ala}^2$]-leucine enkephalinamide (YAGFL) across the nasal, rectal and vaginal mucosae were evaluated. Enzyme inhibitors and penetration enhancers employed for Leu-Enk permeation study were amastatin(AM), thimerosal(TM) and ethylenediaminetetraacetic acid disodium salt(EDTA), and sodium taurodihydrofusidate (STDHF). Those for YAGFL permeation study were TM, benzalkonium chloride(BC) and EDTA, and STDHF, sodium deoxycholate(SDC), sodium glycholate(SGC), glycyrrhizic acid ammonium salt (GAA), L-$\alpha$-Iysophosphatidylcholine(LPC) and mixed micelle (MM, STDHF: linoleic acid = 15 mM : 5 mM). The addition of TM alone on the donor and receptor solutions for Leu-Enk permeation study across all the three kinds of mucosae failed to inhibit the degradation; it completely degraded in 6 hrs, and no permeation occurred. However, with addition of three kinds of inhibitors together, the fluxes across nasal, rectal and vaginal mucosae were $\20.7{pm}2.5$>/TEX>,$\0.3{pm}0.05$>/TEX> and $\1.4{pm}0.5$ $\mu$\mid$textrm{m}$/$\textrm{cm}^2$/hr, respectively. Moreover, the addition of STDHF in the presence of the above three inhibitors enhanced permeation across nasal, rectal and vaginal mucosae 1.3, 15 and 1.3 times, respectively. YhGFL also degraded in the donor and receptor solutions rapidly as time went. With mixed inhibitors of TM and EDTA, the percents of YAGFL remaining in the donor solutions facing nasal, rectal and vaginal mucosae were 69.7, 69.8 and 79.8%, respectively; the percent permeated increased to 10, 2.1 and 5.7%, respectively. The addition of STDHF in the presence of either BC/EDTA or TW/EDTA increased the permeation 2.2, 11.0 and 2.9 times, and 2.21, 14.0 and 2.7 times for nasal, rectal and vaginal mucosae, respectively. With SDC, SGC, GAA, LPC ud MM in the presence of TM/EDTA increased permeation; especially, they increased permeation across vaginal mucosae effectively, and the enhancement factors were 12.5, 7.6, 8.7, 5.7 and 5.5, respectively. The degradation extent of YAGFL was correlated with protein concentrations in the epidermal and serosal extracts. The flux of YAGFL across nasal mucosa increased dose-dependently.

• 자원환경지질
• /
• 제43권2호
• /
• pp.123-136
• /
• 2010

사격지로 이용되었던 매향리 농섬 및 곡섬 시료 토양 및 퇴적물의 회분식 반응기 이용 중금속 추출 정화 실험을 수행하였다. 농섬 북쪽방면 사면의 N3 토양은 자갈 12.9%, 모래 47.0%, 실트 35.1%, 점토 5.0%가 함유된 약역머드 사질((g)mS)이었다. 그리고 N3 토양의 중금속 함유량은 Cd $22.5\pm1.9$ ppm, Cu $35.5\pm4.0$ ppm, Pb $1,279.0\pm5.1$ ppm 그리고 Zn $403.4\pm9.8$ppm이였다. 이 N3 토양에 5 종류 추출용매(citric acid, EDTA, phosphoric acid, potassium phosphate and oxalic acid)를 사용하여 추출한 결과 EDTA(ethylenediaminetetraacetic acid, $C_{10}H_{16}N_2O_8$)가 가장 좋은 추출효율을 가져왔다. 이는 N3 토양의 EDTA, oxalic acid 추출전 후 잔류성 fraction 부분이 형태가 파괴됨으로써 상당수가 추출되거나 좀 더 이동이 쉬운 상태로 진화되며 이에 따라 상대적으로 비잔류성 non-fracton 부분인 철/망간 산화물 형태, 유기물/황화물 형태, 이온교환성 형태, 탄산염으로 증가된다는 것을 보였다. 또한 EDTA 추출제를 사용하여 추출제 농섬 1,000 mM, soil:solution 비율 5, 실험 온도 $20^{\circ}C$, shaking 시간 24 hr, pH 2 그리고 200 RPM 조건의 회분식 반응기를 이용한 추출 결과 N3 토양은 Pb과 Zn이 초기농도 대비 각각 92.4%, 94.0% 추출제거되었다. 이러한 결과는 EDTA 추출제가 중금속으로 오염된 농섬 및 곡섬 토양은 회분식 반응기 이용 추출 실험에서 Pb, Zn가 효율적으로 제거 될 수 있음을 의미하나 특정 조건에서만 제거효율이 높은 logarithmic 함수 값을 보였다.

• 생약학회지
• /
• 제47권2호
• /
• pp.122-127
• /
• 2016

Methicillin-Resistant Staphylococcus aureus(MRSA) is a multidrug-resistant(MDR) strain. (+)-Usnic acid(UA) is uniquely found in lichens, and is especially abundant in genera such as Usnea and Cladonia. UA has antimicrobial activity against human and plant pathogens. Therefore, UA may be a good antibacterial drug candidate for clinical development. In search of a natural products capable of inhibiting this multidrug-resistant bacteria, we have investigated the antimicrobial activity of UA against 17 different strains of the bacterium. In this study, the effects of a combination of UA and permeable agents against MRSA were investigated. For the measurement of cell wall permeability, UA with concentration of Ethylenediaminetetraacetic acid(EDTA) was used. In the other hand, Sodium azide($NaN_3$) was used as inhibitors of ATPase. Against the 17 strains, the minimum inhibitory concentrations(MICs) of UA were in the range of $7.81-31.25{\mu}g/ml$. EDTA or $NaN_3$ cooperation against MRSA showed synergistic activity on cell wall. UA and in combination with EDTA and $NaN_3$ could lead to the development of new combination antibiotics against MRSA infection.

• 한국산업보건학회지
• /
• 제4권2호
• /
• pp.189-197
• /
• 1994

Analytic methods for Cr(VI) level in industrial hygienic field were suggested by the National Institute for Occupational Safety and Health(NIOSH method 7600, 7604). There were growing needs for measurement of Cr(III) and Cr(VI) levels simultaneously. Two analytical methods were suggested to determine Cr(III) and Cr(VI) levels simultaneously. The one is method by using reversed phase high peformance liquid chromatography(HPLC) and the other is by using ion exchange HPLC. The purpose of this work was to evaluate the usefulness of these two analytic methods. For the difference of ionic charges of Cr(III)-ethylendiamine tetraacetic acid(EDTA) chelate and $CrO_4{^-2}$, we could detect them simultaneously by ion exchange HPLC. Also, we attempted to determine the levels of Cr(III) and Cr(VI) chelated with sodium diethyldithiocarbamate(NaDDTC) by using reversed phase HPLC. The confirmation of Cr(III) and Cr(VI) were checked by fraction collector and nameless atomic absorption spectrometer. The optimal conditions for the formation of Cr(III)-EDTA chelate were two hours incubation period with pH 5. Cr(III)-EDTA and Cr(VI) in EDTA solution were successfully separated by anion exchange column using $Na_2CO_3/NaOH$ mixture as mobile phase. Peaks of Cr(III)-EDTA and Cr(VI) in EDTA were identified at 5 minutes and 7 minutes of retention time respectively by the ion exchange HPLC. The formation of Cr(III)-NaDDTC and Cr(VI)-NaDDTC chelates were twelve hours incubation period. Cr(III)-NaDDTC and Cr(VI)-NaDDTC chelates were separated by reversed phase column using methanol and water mixture as mobile phase. Peaks of Cr(VI)NaDDTC and Cr(III)-NaDDTC chelates were identified at 13 minutes and 26 minutes of retention time respectively by the reversed phase HPLC. Due to reduction of Cr(VI) to Cr(III), it seems to be not suitable for simultaneous determination of Cr(III)-NaDDTC and Cr(VI)-NaDDTC chelates by reversed phase HPLS. Simultaneos determination of Cr(III) and Cr(VI) by ion exchange HPLC was more accurate and simple method.

• Restorative Dentistry and Endodontics
• /
• 제40권4호
• /
• pp.290-298
• /
• 2015

Objectives: Sodium hypochlorite (NaOCl) is an excellent bactericidal agent, but it is detrimental to stem cell survival, whereas intracanal medicaments such as calcium hydroxide ($Ca[OH]_2$) promote the survival and proliferation of stem cells. This study evaluated the effect of sequential NaOCl and $Ca(OH)_2$ application on the attachment and differentiation of dental pulp stem cells (DPSCs). Materials and Methods: DPSCs were obtained from human third molars. All dentin specimens were treated with 5.25% NaOCl for 30 min. DPSCs were seeded on the dentin specimens and processed with additional 1 mg/mL $Ca(OH)_2$, 17% ethylenediaminetetraacetic acid (EDTA) treatment, file instrumentation, or a combination of these methods. After 7 day of culture, we examined DPSC morphology using scanning electron microscopy and determined the cell survival rate with 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. We measured cell adhesion gene expression levels after 4 day of culture and odontogenic differentiation gene expression levels after 4 wk using quantitative real-time polymerase chain reaction. Results: DPSCs did not attach to the dentin in the NaOCl-treated group. The gene expression levels of fibronectin-1 and secreted phosphoprotein-1 gene in both the $Ca(OH)_2$- and the EDTA-treated groups were significantly higher than those in the other groups. All $Ca(OH)_2$-treated groups showed higher expression levels of dentin matrix protein-1 than that of the control. The dentin sialophosphoprotein level was significantly higher in the groups treated with both $Ca(OH)_2$ and EDTA. Conclusions: The application of $Ca(OH)_2$ and additional treatment such as EDTA or instrumentation promoted the attachment and differentiation of DPSCs after NaOCl treatment.

• Restorative Dentistry and Endodontics
• /
• 제40권2호
• /
• pp.104-112
• /
• 2015

Objectives: This study was performed to investigate the effects of different intracanal medicaments on chemical structure and microhardness of dentin. Materials and Methods: Fifty human dentin discs were obtained from intact third molars and randomly assigned into two control groups and three treatment groups. The first control group received no treatment. The second control group (no medicament group) was irrigated with sodium hypochlorite (NaOCl), stored in humid environment for four weeks and then irrigated with ethylenediaminetetraacetic acid (EDTA). The three treatment groups were irrigated with NaOCl, treated for four weeks with either 1 g/mL triple antibiotic paste (TAP), 1 mg/mL methylcellulose-based triple antibiotic paste (DTAP), or calcium hydroxide [$Ca(OH)_2$] and finally irrigated with EDTA. After treatment, one half of each dentin disc was subjected to Vickers microhardness (n = 10 per group) and the other half was used to evaluate the chemical structure (phosphate/amide I ratio) of treated dentin utilizing attenuated total reflection Fourier transform infrared spectroscopy (n = 5 per group). One-way ANOVA followed by Fisher's least significant difference were used for statistical analyses. Results: Dentin discs treated with different intracanal medicaments and those treated with NaOCl + EDTA showed significant reduction in microhardness (p < 0.0001) and phosphate/amide I ratio (p < 0.05) compared to no treatment control dentin. Furthermore, dentin discs treated with TAP had significantly lower microhardness (p < 0.0001) and phosphate/amide I ratio (p < 0.0001) compared to all other groups. Conclusions: The use of DTAP or $Ca(OH)_2$ medicaments during endodontic regeneration may cause significantly less microhardness reduction and superficial demineralization of dentin compared to the use of TAP.