• Journal of Pharmaceutical Investigation
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• v.1 no.1
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• pp.101-108
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• 1971

The stability and toxicity test for p.p'-DDT, DDVP and dipterex that put to used sample in this study effects is follows A. about p.p'-DDT (1) In elevating the stability of p.p'-DDT, best stabilizing solvent was benzene. (2) The stability-agent has no difficulty as long as it not contain metal ion for instance $Z_n^{2+}$,$C_r^{3+}$,$Al^{3+}$,and $Fe^{2+or3+}$ but in case of contain $F_e^{3+}$, the combination of salicylaminoguanidine is best effective. (3) Using this product for water-suspension, We must use span 40 for stability agent and adding it at the same time. (4) We must use container which does not week alkali and metal ion but it is to preserved in tight light-resistant container. (5) The stopper of container is adapted with above-mentioned condition of container, but it is better not to use metal material. (6) This product needs opening ventilation more than 30 minutes after diffusion or spray and in the room we remove cause of remained poison by cleaning the bottom. B. about DDVP and Dipterex (1) Benzene or toluene in best solvent to preserve stability of DDVP and Dipterex. (2) Span 40 is superior for stability agent of this product and second is span 80. (3) The pH of solution is very stable in pH 5-6 and comparative stable in alkali more than p,p'-DDT. (4) Container is to preserved in tight, lightresistant container and especially be careful of outflow and inflow of water. (5) Because this product is centeral stimulant poison, we must pay attention to prevent cause of contact diadermic toxicity after use.

• Environmental Analysis Health and Toxicology
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• v.14 no.3
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• pp.113-120
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• 1999

Fluorination of drinking water has been used world widely to reduce the incidence of caries. Recently, contradictory results on the cytotoxicity of fluoride compounds are reported. In addition, there are attempts to use fluorosilicate for fluorination of drinking water in Korea, therefore, we tried to analyze the cytotoxicity of fluoride compounds on oral epidermoid carcinoma (KB and A253) and osteosarcoma (HOS and MG-63) cells in this study. We treated cells with 0, 10, 50 and 250 ppm of fluorosilicic acid (domestic or from Fluka, F$\_$6/H$_2$Si), sodium fluorosilicate (F$\_$6/Na$_2$Si), sodium fluoroacetate (FCH$_2$CO$_2$Na), sodium fluoride (NaF) or potassium fluoride(KF) and measured the relative cell survival by MTT assay. At the concentration of < 10ppm, no significant cytotoxicity was observed. At 50 ppm, each cells revealed different response to fluoride treatment. Among cells used in this study, MG-63 was the most resistant to fluoride treatment. Comparable toxicity data from domestic and imported fluorosilicic acids were obtained. When we compared the relative cytotoxicity of fluoride compounds against their fluoride contents, the differences in relative cell survival were smaller. Most of cells showed < 20% of survival at 250 ppm. In order to analyze the pH dependence of the cytotoxicity of fluorosilicates, the pH of cell culture media containing fluorosilicate was adjusted to 7.4 or 6.5 and the relative cytotoxicity was measured. At lower pH, about 10% higher cytotoxicity was obtained. Thus, our data suggested that the toxicity of domestic fluorosilicic acid was similar to that of fluorosilicic acid from Fluka, and the cytotoxicity of fluoride compounds was dependent on the relative content of fluoride and pH.

• Journal of the Korean Institute of Gas
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• v.19 no.1
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• pp.38-44
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• 2015

FDS (Fire Dynamics Simulator) is the most widely used computational fluid dynamics software in the fire safety engineering community, and it is applicable to various evaluations of fire growth and its effects. This study made use of a range of outputs from FDS simulation to predict FED (Fractional Effective Concentration) and FEC (Fractional Effective Concentration) levels which are often adopted to evaluate toxicity of fire smoke. As it is not possible to calculate these values directly from outputs of FDS, it was necessary to produce them by means of additional calculation procedures incorporating results of evacuation simulation. In this study, the latest version of FDS, which was recently updated in November 2013, was utilized for the purpose of quantitative comparison with the old version of FDS. As a result, it was found that they make about 10 percent difference on average in predicting FED and FEC levels for the cable fire case study.

• Restorative Dentistry and Endodontics
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• v.38 no.4
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• pp.204-209
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• 2013

Objectives: The objective of this in vitro study was to evaluate and compare the cytotoxicity of four different root canal sealers i.e. Apexit Plus (Ivoclar Vivadent), Endomethasone N (Septodont), AH-26 (Dentsply) and Pulpdent Root Canal Sealer (Pulpdent), on a mouse fibroblast cell line (L929). Materials and Methods: Thirty two discs for each sealer (5 mm in diameter and 2 mm in height) were fabricated in Teflon mould. The sealer extraction was made in cell culture medium (Dulbecco's Modified Eagle's Medium, DMEM) using the ratio 1.25 $cm^2/mL$ between the surface of the sealer samples and the volume of medium in a shaker incubator. Extraction of each sealer was obtained at 24 hr, 7th day, 14th day, and one month of interval. These extracts were incubated with L929 cell line and 3-(4,5-dimethylthiazol-2yl)-2,5-diphenyltetrazolium bromide (MTT) assay was done. Two-way ANOVA for interaction effects between sealer and time and Post-hoc multiple comparison using Tukey's test across all the 16 different groups were used for statistical analysis. Results: Apexit Plus root canal sealer was significantly less toxic than other sealers (p < 0.05) and showed higher cellular growth than control. Endomethasone N showed mild cytotoxicity. AH-26 showed severe toxicity which became mild after one month while Pulpdent Root Canal Sealer showed severe to moderate toxicity. Conclusions: Apexit Plus was relatively biocompatible sealer as compared to other three sealers which were cytotoxic at their initial stages, however, they became biocompatible with time.

• The Korea Journal of Herbology
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• v.34 no.4
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• pp.9-18
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• 2019

Objectives : It has been known to be correlated between phlegm and dementia from the perspective of oriental medicine, but it is unexplored whether herbal medicines to treat phlegm have pharmacological actions on Alzheimer's disease (AD). The aim of this study was to evaluate and to compare effects of herbal medicines to treat phlegm against AD in vitro. Methods : We selected 11 herbal medicines which treat phlegm and obtained each extract by boiling in 10-fold distilled water for 2 h. And we performed the assay of acetylcholinesterase (AChE) inhibitory effects of 11 herbal extracts. Next, we evaluated neuroprotective effects of them against amyloid $beta_{25-35}$ ($A{\beta}_{25-35}$) plaque-induced toxicity in HT22 mouse hippocampal neuronal cells using 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazolium bromide assay. To investigate whether they show the anti-inflammatory effects against lipopolysaccharide (LPS), we also measured the levels of nitric oxide (NO) in BV2 microglia cells using griess reagent assay. Results : We found that Gamiyeongsin-hwan (GYH) and Cheonghunhwadam-tang (CHT) exhibited remarkable AChE inhibitory effects. In HT22 cells, Arisaematis Rhizoma, Trichosanthis Semen and Fritillariae Thunbergii Bulbus suppressed $A{\beta}_{25-35}$ plaque-induced neuronal cell death. In BV2 cells, Cheongung-hwan significantly inhibited the increase of NO contents induced by LPS and GYH and CHT showed a tendency to inhibit LPS-induced NO generation. Conclusions : These results suggest that several herbal medicines to treat phlegm showed the significant effects on AChE inhibition, neuroprotection against $A{\beta}_{25-35}$ plaque-induced toxicity, and inhibition of NO generation. Therefore, we demonstrate the possibility that herbal medicines with treating phlegm has effects against AD.

• Korean journal of applied entomology
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• v.32 no.2
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• pp.123-128
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• 1993

The comparative toxicities of selected acaricides against the twospotted spider mite, Tetranychus urticae, were investigated. The ovicidal and adulticidal activities of selected acaricides were examined under different developmental stages. Fenpyroximate showed high activity throughout all developmental stages of mites. The oviposition inhibition effect of fenpyroximate was more highly effective than that of cyhexatin. At 100 ppm concentration, the effect of fenpyroximate on the residual oviposition inhibition was persistant during 25 days with 85% level, while the effect of cyhexatin gradually decreased, and then decreased to 40% at 25 days after treatment. Fenpyroximate at 100 ppm showed 100% knockdown activity within 3 hour while cyhexatin showed only 91% knockdown activity within 24 hours after treatment. Most of selected acaricides had no systemic activity, but metasystox at 800 ppm had 100% of the systemic activity at 24 hours after treatment. For the influence of temperature on the activity, fenpyroximate showed stable activity and no temperature-dependent in comparison with other selected adaricides.

• Journal of Korean Society of Environmental Engineers
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• v.38 no.7
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• pp.395-401
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• 2016

Nano-saftey has become an emerging issue recently, because of the broad use of nanomaterials in nano-industries and commercial areas. For a sustainable development in the nano-industry, active studies on nano-safety should be executed, especially on the potential risks in engineered nanomaterials (ENMs). Although acute and chronic assessments of nanomaterials have been extensively studied in many studies, multigenerational studies are very scarce. Overall, multigenerational studies have progressed as two different trends, studying post-generational effects or trans-generation effects. This study intended to suggest further nano-safety studies based on the trends and limitations of current ones. Through a comparative analysis, we investigated peer-reviewed multigenerational studies that used nanomaterials. Thirteen studies on post-generation effects confirmed generational nano-toxicity via several bioassays, such as mortality, fertility, and behavioral assays. Seven studies on trans-generation effects demonstrated nanomaterial pathways to next generations, using imaging techniques. Until now, mechanisms for post-generational nano-toxicity has been rarely proposed. Thus, we propose that complementary studies on such mechanisms are imperative for future studies.

• The Korean Journal of Pesticide Science
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• v.12 no.3
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• pp.249-255
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• 2008

The comparative toxicity of recommended rates of three acaricides, fluacrypyrim, cyflumetofen and spiromesifen to the predatory mite, Neoseiulus womersleyi and its prey, Tetranychus urticae was bioassayed in the laboratory. Fluacrypyrim and cyflumetofen were much less toxic to adult females of N. womersleyi than to those of T. urticae. Adult female predators treated with these two acaricides produced $88{\sim}93%$ as many eggs as did control females. Fluacrypyrim and cyflumetofen did not affect the hatch of N. womersleyi eggs or the development of surviving immature predators, and $92{\sim}96%$ of immature predators reached adulthood. Spiromesifen at its treated concentration did not significantly affect the survival and reproduction of adult female predators but caused 100% mortality in larvae of N. womersleyi. Adult female predators survived on a diet of spider mites treated with fluacrypyrim and cyflumetofen, and their fecundity was not significantly affected. Moreover, immature predators developed normally on prey treated with these two acaricides. The results indicate that fluacrypyrim and cyflumetofen are promising candidates for use in integrated mite management programs where N womersleyi is the major natural enemy.

• Asian Pacific Journal of Cancer Prevention
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• v.16 no.6
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• pp.2355-2359
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• 2015

Background: Combination chemotherapy of 5 fluorouracil (5-FU) and leucovorin (LV) with oxaliplatin, mainly FOLFOX regimens, has shown considerable antitumor activity and a tolerable toxicity profile in gastric cancer. The goal of this study was to retrospectively compare the efficacy and toxicity of modified FOLFOX-6 (mFOLFOX6) regimen in advanced gastric cancer (AGC) patients with good and poor performance status (PS). Materials and Methods: AGC patients receiving the mFOLFOX6 regimen including oxaliplatin $85mg/m^2$, bolus of 5-FU $400mg/m^2$ and LV $400mg/m^2$ on the first day, followed by $2400mg/m^2$ of 5- FU as a continious infusion over 46 hour for first-line treatment were eligible for the study. Results: A total 58 patients with a median age of 59.5 (32-81) were included. The median follow up of the study was 9.2 months. Thirty patients (51.7%) with an ECOG PS 0-1 were assigned to the good PS arm, while 28 patients (48.3%) with ECOG PS 2 were in the poor PS arm. Overall response rates were 36.6 and 28.8%, respectively (p=0.91). Median PFS was 6.7 and 6.3 months in good PS and poor PS arms (p=0.50) and median OS was 9.6 and 10.4 months (p=0.55). As compared with good PS arm, poor PS arm was associated with more grade 3-4 neutropenia and anemia. Dose reduction and dose delays were also significantly higher. Conclusions: In this study, mFOLFOX6 was similarly effective in both arms. Although hematologic toxicity was significantly higher in patients with poor PS, it remained manageable. Our results suggest that this regimen may be an effective treatment option for AGC patients with poor PS.

• Korean journal of applied entomology
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• v.35 no.3
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• pp.232-237
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• 1996

Toxicity of 5 acaricides, 4 insecticides. and 6 fungicides to the twospotted spider mite, Tetranychus urticae Koch, and its predator Amblyseius womersleyi Schicha was assessed in a laboratory using a leaf disk bioassay. Dicofol was equally very toxic to aduly females of T. urticae and A. womersleyi, and caused 46% and 40% mortality of eggs of those two species, respectively. Adult females of A. womersleyi dipped in Abamectin solution showed low mortality(16.6%), while all T. urticae females died within 24 hours after dipping. Three ovicidal acaricides (Tetradifon, Clofentezine, and Hexythiazox) showed no mortality of predator eggs, but more than 90% mortality of T. urticae eggs. Four insecticides (Teflubenzuron, Triflumuron, Diflubenzuron, and Imidacloprid) and three fungicides (Propineb, Fenarimol, and Polyoxin-B captan) were non toxic to the A. womersleyi adult females. The other fungicides (Chlorothalonil, Nuarimol.Mancozeb, and Folpet) were a little toxic to adult females of the predator, showing$\leq$23.3% mortality, It may be suggested from these results that 4 insecticides, 4 acaricides, and 6 fungicides described could be incorporated into the integrated pest management system with A. womersleyi in apple orchard.