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      • KCI등재후보

        생물학적 방법에 의한 도시생활폐기물 매립지의 침출수 독성특성 평가

        황인영,류경무 한국환경독성학회 1996 환경독성보건학회지 Vol.11 No.1

        Leachate from municipal solid waste (MSW) landfill, effluent from leachate treatment plant, and ground water sample from a monitoring well near landfill site were tested for an acute toxicity. Microtox toxicity test was used for testing the acute toxicity of leachate and other samples. EG_(50) values which a concentration of pollutant for reducing 50% light output from luminescent bacteria, Phtobacterium phosphoreum were determined to assess the toxicity of pollutants as well as the relative toxicity. In addition, characteristics of leachate were studied and compared to those of phenol and pentachlorophenol(PCP) which are typical aquatic toxic pollutants. For leachate, EC_(50) for 30min incubation was 10.8%, while for phenol and PCP, 46ppm and 1.2 ppm, respectively, the relative toxicity of treated leachate by in 냐셔 aeration with activated sludge was reduced to more than 75% of toxicity the untreated leachate. Microtox toxicity test was failed to figure out EC_(50) values for groundwater from a monitoring well since the relative toxicity of the unconcentrated sample was too low to estimate EC_(50). Addition of activated carbon to leachate was reduced the relative toxicity. The reduction Pattern of the relative toxicity of leachate by mechanical aeration was similar to that of PCP, but different from that of phenol. These findings suggest that the toxicity of leachate may come from PCP-like toxic compounds rather than phenol-like one. In conclusion, the process of aeration with activated sludge might be very important to reduce the environmental toxicity of leachate. And Microtox test could be a reasonable bioassay for screening and monitoring the environmental toxicity of leachate from municipal solid waste landfill as well as for determining the reduction efficiency of the leachate toxicity by various treatment processes in leachate treatment plant.

      • Screening of toxic potential of graphene family nanomaterials using in vitro and alternative in vivo toxicity testing systems

        Chatterjee, Nivedita,Yang, Ji Su,Park, Kwangsik,Oh, Seung Min,Park, Jeonggue,Choi, Jinhee The Korean Society of Environmental Toxicology 2015 환경독성보건학회지 Vol.30 No.-

        Objectives The widely promising applications of graphene nanomaterials raise considerable concerns regarding their environmental and human health risk assessment. The aim of the current study was to evaluate the toxicity profiling of graphene family nanano-materials (GFNs) in alternative in vitro and in vivo toxicity testing models. Methods The GFNs used in this study are graphene nanoplatelets ([GNPs]-pristine, carboxylate [COOH] and amide [$NH_2$]) and graphene oxides (single layer [SLGO] and few layers [FLGO]). The human bronchial epithelial cells (Beas2B cells) as in vitro system and the nematode Caenorhabditis elegans as in vivo system were used to profile the toxicity response of GFNs. Cytotoxicity assays, colony formation assay for cellular toxicity and reproduction potentiality in C. elegans were used as end points to evaluate the GFNs' toxicity. Results In general, GNPs exhibited higher toxicity than GOs in Beas2B cells, and among the GNPs the order of toxicity was pristine > $NH_2$ > COOH. Although the order of toxicity of the GNPs was maintained in C. elegans reproductive toxicity, but GOs were found to be more toxic in the worms than GNPs. In both systems, SLGO exhibited profoundly greater dose dependency than FLGO. The possible reason of their differential toxicity lay in their distinctive physicochemical characteristics and agglomeration behavior in the exposure media. Conclusions The present study revealed that the toxicity of GFNs is dependent on the graphene nanomaterial's physical forms, surface functionalizations, number of layers, dose, time of exposure and obviously, on the alternative model systems used for toxicity assessment.

      • KCI등재

        Hematological and serum biochemical studies in fresh water fish exposed to acute and chronic copper and mercury toxicity

        H.A., Sawsan,H.M., Amira,M.B., Mostafa,AM.M., Nashaat The Korean Society of Fish Pathology 2017 한국어병학회지 Vol.30 No.1

        A total number of 668 apparently healthy fish were obtained from farm to study the effect of two heavy metals in a form of (Copper sulfate and Mercuric chloride) on some hematological and biochemical parameters of blood. The $LC_{50}$ /96 hr. of Cu and Hg were estimated and fish exposed to $\text\tiny{^1/_2}$ $LC_{50}$ for 7 days and for $1/_{10}$ $LC_{50}$ for 8 weeks from each product separately. Results showed decrease in RBCs count, PCV% and Hb in acute and chronic mercury while a significant increase was shown in acute and chronic copper toxicity, total leucocytic count showed decrease in acute mercury toxicity and increase in the chronic case, while in copper toxicity non-significant decrease in acute and significant decrease in chronic toxicity was noticed. Elevated serum urea and creatinine in both acute and chronic mercury and copper toxicity was detected. No changes in total bilirubin in the acute mercury and chronic copper toxicity while significant increase in chronic mercury and acute copper. Elevation of serum AST and ALT in some days of acute toxicity of mercury and copper while in chronic mercury toxicity a significant elevation of both serums AST and ALT were detected .while in chronic copper toxicity serum AST was fluctuated and ALT showed no significant changes. CK study revealed significant decrease in acute mercury with fluctuation in the chronic toxicity while in copper toxicity it showed fluctuation in acute and significant decrease in chronic toxicity. Glucose value decreased in acute and chronic mercury toxicity while in copper toxicity it showed significant increase in the acute and increase followed by significant decrease in the chronic copper toxicity.

      • KCI등재

        Hematological and serum biochemical studies in fresh water fish exposed to acute and chronic copper and mercury toxicity

        ( Sawsan H. A. ),( Amira H. M. ),( Mostafa M. B. ),( Nashaat Am. M. ) 한국어병학회 2017 한국어병학회지 Vol.30 No.1

        A total number of 668 apparently healthy fish were obtained from farm to study the effect of two heavy metals in a form of (Copper sulfate and Mercuric chloride) on some hematological and biochemical parameters of blood. The LC <sub>50</sub> /96 hr. of Cu and Hg were estimated and fish exposed to ½ LC<sub>50</sub> for 7 days and for 1/<sub>10</sub> LC<sub>50</sub> for 8 weeks from each product separately. Results showed decrease in RBCs count, PCV% and Hb in acute and chronic mercury while a significant increase was shown in acute and chronic copper toxicity, total leucocytic count showed decrease in acute mercury toxicity and increase in the chronic case, while in copper toxicity non-significant decrease in acute and significant decrease in chronic toxicity was noticed. Elevated serum urea and creatinine in both acute and chronic mercury and copper toxicity was detected. No changes in total bilirubin in the acute mercury and chronic copper toxicity while significant increase in chronic mercury and acute copper. Elevation of serum AST and ALT in some days of acute toxicity of mercury and copper while in chronic mercury toxicity a significant elevation of both serums AST and ALT were detected .while in chronic copper toxicity serum AST was fluctuated and ALT showed no significant changes. CK study revealed significant decrease in acute mercury with fluctuation in the chronic toxicity while in copper toxicity it showed fluctuation in acute and significant decrease in chronic toxicity. Glucose value decreased in acute and chronic mercury toxicity while in copper toxicity it showed significant increase in the acute and increase followed by significant decrease in the chronic copper toxicity.

      • Screening of toxic potential of graphene family nanomaterials using in vitro and alternative in vivo toxicity testing systems

        Nivedita Chatterjee,Ji Su Yang,Kwangsik Park,Seung Min Oh,Jeonggue Park,Jinhee Choi 환경독성보건학회 2015 환경독성보건학회지 Vol.30 No.-

        Objectives: The widely promising applications of graphene nanomaterials raise considerable concerns regarding their environmental and human health risk assessment. The aim of the current study was to evaluate the toxicity profiling of graphene family nananomaterials (GFNs) in alternative in vitro and in vivo toxicity testing models. Methods: The GFNs used in this study are graphene nanoplatelets ([GNPs]–pristine, carboxylate [COOH] and amide [NH2]) and graphene oxides (single layer [SLGO] and few layers [FLGO]). The human bronchial epithelial cells (Beas2B cells) as in vitro system and the nematode Caenorhabditis elegans as in vivo system were used to profile the toxicity response of GFNs. Cytotoxicity assays, colony formation assay for cellular toxicity and reproduction potentiality in C. elegans were used as end points to evaluate the GFNs’ toxicity. Results: In general, GNPs exhibited higher toxicity than GOs in Beas2B cells, and among the GNPs the order of toxicity was pristine>NH2>COOH. Although the order of toxicity of the GNPs was maintained in C. elegans reproductive toxicity, but GOs were found to be more toxic in the worms than GNPs. In both systems, SLGO exhibited profoundly greater dose dependency than FLGO. The possible reason of their differential toxicity lay in their distinctive physicochemical characteristics and agglomeration behavior in the exposure media. Conclusions: The present study revealed that the toxicity of GFNs is dependent on the graphene nanomaterial’s physical forms, surface functionalizations, number of layers, dose, time of exposure and obviously, on the alternative model systems used for toxicity assessment.

      • KCI등재
      • GSTT1 null and MPO -463G>A Polymorphisms and Carboplatin Toxicity in an Indian Population

        Bag, Arundhati,Pant, Nirdosh Kumar,Jeena, Lalit Mohan,Bag, Niladri,Jyala, Narayan Singh Asian Pacific Journal of Cancer Prevention 2013 Asian Pacific journal of cancer prevention Vol.14 No.8

        Carboplatin, a second generation platinum drug, is widely used to treat different types of cancers. However, myelosuppression remains a major consideration in its use. Genetic polymorphisms of enzymes involved in drug disposition can influence therapeutic outcome. The homozygous null deletion of phase II metabolic gene GSTT1 that abolishes its xenobiotic- detoxifying ability may be associated with carboplatin toxicity. Further, since carboplatin generates oxidative stress, polymorphisms of oxidative stress genes that regulate the cellular level of free radicals may have important roles in generating drug- related adverse effects. We here investigated the null polymorphism of GSTT1, and the -463G>A promoter polymorphism of oxidative stress gene myeloperoxidase (MPO) for carboplatin toxicity in a population of northern India. Cancer patients who were treated with carboplatin, and developed toxicity was considered. The study group comprised of 10 patients who developed therapy- related adverse effects. Peripheral blood was taken from patients for DNA isolation. GSTT1 null genotype was determined by conducting duplex PCR and MPO-463 G>A was determined by PCR followed by RFLP. Hematologic toxicity was experienced by 5 patients, 2 of them had grade 3 and 4 toxicity and 3 others had grade 2 toxicity. They also had gastrointestinal (GI) toxicity. Remaining 5 individuals developed GI toxicity but no hematological toxicity. While GG homozygous of MPO was present in majority of patients having hematologic toxicity (in 4 out of 5 individuals), one A allele (AG genotype) was present in 4 patients who did not have any hematological toxicity. Thus variant A allele of MPO -463G>A may be related to lower hematological toxicity. These preliminary data, however, are required to be confirmed in larger studies along with other relevant polymorphisms.

      • SCISCIESCOPUS

        Sequential assessment via daphnia and zebrafish for systematic toxicity screening of heterogeneous substances

        Jang, Gun Hyuk,Park, Chang-Beom,Kang, Benedict J.,Kim, Young Jun,Lee, Kwan Hyi Elsevier 2016 Environmental pollution Vol.216 No.-

        <P><B>Abstract</B></P> <P>Environment and organisms are persistently exposed by a mixture of various substances. However, the current evaluation method is mostly based on an individual substance’s toxicity. A systematic toxicity evaluation of heterogeneous substances needs to be established. To demonstrate toxicity assessment of mixture, we chose a group of three typical ingredients in cosmetic sunscreen products that frequently enters ecosystems: benzophenone-3 (BP-3), ethylhexyl methoxycinnamate (EHMC), and titanium dioxide nanoparticle (TiO<SUB>2</SUB> NP). We first determined a range of nominal toxic concentration of each ingredient or substance using Daphnia magna, and then for the subsequent organismal level phenotypic assessment, chose the wild-type zebrafish embryos. Any phenotype change, such as body deformation, led to further examinations on the specific organs of transgenic zebrafish embryos. Based on the systematic toxicity assessments of the heterogeneous substances, we offer a sequential environmental toxicity assessment protocol that starts off by utilizing Daphnia magna to determine a nominal concentration range of each substance and finishes by utilizing the zebrafish embryos to detect defects on the embryos caused by the heterogeneous substances. The protocol showed additive toxic effects of the mixtures. We propose a sequential environmental toxicity assessment protocol for the systematic toxicity screening of heterogeneous substances from Daphnia magna to zebrafish embryo in-vivo models.</P> <P><B>Highlights</B></P> <P> <UL> <LI> Contemporary ecological evaluation protocols are mostly based on an individual substance’s toxicity. </LI> <LI> This study proposes a systematic toxicity screening method for heterogeneous substances by demonstrating a proof-of-concept. </LI> <LI> The systematic environmental toxicity assessment protocol used two in-vivo models, Daphnia magna and zebrafish embryo. </LI> <LI> The combined toxicity effects of the mixtures were additive. </LI> </UL> </P> <P><B>Graphical abstract</B></P> <P>[DISPLAY OMISSION]</P>

      • KCI등재

        한국산 복어의 독성: 1. 황복의 부위별 독성

        전중균 ( Joong Kyun Jeon ),유재명 ( Jae Myoung Yoo ) 한국수산학회 1995 한국수산과학회지 Vol.28 No.2

        황복의 독성을 조사하기 위하여 1992년과 1993년에 임진강으로 산란하러 소상한 46 개체를 채집하여 조직별로 나누어 독성을 살펴보았다. 조직중에서는 난소와 간장은 맹독이었으며, 정소, 내장, 담낭과 비장은 강독이었고, 근육과 껍질은 약독이었으나 혈액은 무독이었다. 본 결과는 Tani(1945)의 보고와 정소, 근육, 껍질의 독성에서 차이를 보였으며, 특히 이제까지 무독 또는 약독으로 여겨 식용으로 하여 왔던 근육과 정소의 독성이 본 연구에서는 약독 또는 강독으로 독성을 보이고 있어, 중독 예방을 위해서는 주의할 필요가 있다. The pufferfish Takifugu obscurus (hwang-bok) was examined for toxicity. Forty-six specimens, which had caught at the Imjin River in 1992 and 1993, Korea, were collected and assayed for anatomical distribution of toxicity by the mouse assay method. Ovary and liver showed very strong toxicity, testis, intestine, gall bladder and spleen did moderate toxicity, muscles and skin did weak toxicity, and blood was non-toxic. The results of this study were different from those of Tani, who had examined the toxicity in 19 species of pufferfish, in terms of toxicity in testis, muscle, and skin. The toxicity of testis and muscle had been known to be non-toxic or weakly toxic previously, however, they were known to have weak or moderate toxicity. Therefore, careful attention should be taken to prevent food poisoning by pufferfish ingestion.

      • Identification of toxicity variations in a stream affected by industrial effluents using Daphnia magna and Ulva pertusa

        Yoo, J.,Ahn, B.,Oh, J.J.,Han, T.,Kim, W.K.,Kim, S.,Jung, J. Elsevier Scientific Pub. Co 2013 Journal of hazardous materials Vol.260 No.-

        A comprehensive toxicity monitoring study from August to October 2011 using Daphnia magna and Ulva pertusa was conducted to identify the cause of toxicity in a stream receiving industrial effluents (IEs) from a textile and leather products manufacturing complex. Acute toxicity toward both species was observed consistently in IE, which influenced toxicity of downstream (DS) water. A toxicity identification evaluation (TIE) confirmed that both Cu and Zn were key toxicants in the IE, and that the calculated toxicity based on Cu and Zn concentrations well simulated the variation in the observed toxicity (r<SUP>2</SUP>=0.9216 and 0.7256 for D. magna and U. pertusa, respectively). In particular, U. pertusa was sensitive enough to detect acute toxicity in DS and was useful to identify Zn as a key toxicant. Activities of catalase, superoxide dismutase, glutathione peroxidase, glutathione S-transferase, and malondialdehyde were induced significantly in D. magna, although acute toxicity was not observed. In addition, higher levels of antioxidant enzymes were expressed in DS than upstream waters, likely due to the Cu and Zn from IE. Overall, TIE procedures with a battery of bioassays were effective for identifying the cause of lethal and sub-lethal toxicity in effluent and stream water.

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