• 제목/요약/키워드: ACUTE TOXICITY

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감마선 처리를 이용한 고무공장 폐수의 생물독성 저감 (Toxicity Reduction of Wastewater from a Rubber Products Manufacturing Factory by Gamma-ray Treatment)

  • 박은주;조훈제;조기종;김정규;정진호
    • 한국물환경학회지
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    • 제22권5호
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    • pp.913-918
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    • 2006
  • Both raw wastewater and effluent from a rubber products manufacturing factory were found to be toxic to Daphnia magna though the effluent satisfied current water quality standards. Thus, in order to reduce toxicity, advanced oxidation processes (AOPs) such as gamma-ray (${\gamma}-ray$) treatment and ozonation ($O_3$) were applied. A combined ${\gamma}-rays/O_3$ treatment at 20 kGy after coagulation significantly reduced toxicity of raw wastewater, changing 48-h toxic unit (TU) value from 201.21 to 23.92. However, toxicity of treated water was higher than that of effluent (TU = 12.15). This shows limitation of gamma-ray treatment to remove toxicity of raw wastewater. In case of effluent, the combined ${\gamma}-rays/O_3$ treatment at 20 kGy efficiently decomposed toxic compounds down to non toxic level. This work strongly supports the necessity of toxicity reduction evaluation as well as toxicity-based effluent management.

식물추출물 마늘 추출액, 잔톡실럼 정유, 레몬그라스 정유 함유 유제 3종의 생태독성평가 (Acute Ecotoxicity Evaluation of 3 Emulsifiable Concentrates Containing Garlic Extract, Zanthoxylum Extract, and Lemon Grass Oil Originated from Plant)

  • 유아선;홍순성;정미혜;박경훈;장희섭;이제봉;박재읍
    • 농약과학회지
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    • 제16권4호
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    • pp.376-382
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    • 2012
  • 식물추출물 함유(마늘추출액, 잔톡실럼오일, 레몬그라스오일 30%) 유제의 물벼룩급성독성 결과 마늘추출액 함유 30% 유제의 $EC_{50}$$3.3mg\;L^{-1}$로 EPA 기준으로 보통독성정도이었고, 레몬그라스오일, 잔톡실럼(Zanthoxylum)오일 함유 30% 유제의 $EC_{50}$$10mg\;L^{-1}$ 이상으로 저독성이었다. 송사리급성독성 시험의 경우, 마늘추출액 함유 30% 유제의 $LC_{50}$ 값이 $3.0mg\;L^{-1}$으로 나타났으며 나머지 두 유제는 모두 $10mg\;L^{-1}$ 이상으로 확인되었다. 꿀벌급성독성시험은 접촉과 섭식 시험으로 나누어서 실시하였고, 접촉독성의 경우 모두 100 a.i ${\mu}g\;bee^{-1}$ 이상으로 확인되었다. 섭식독성의 경우 마늘추출액 함유 30% 유제의 $LD_{50}$ 값이 44.3 a.i ${\mu}g\;bee^{-1}$ 이었으며 잔톡실럼(Zanthoxylum)오일과 레몬그라스오일 함유 30% 유제의 경우 $LD_{50}$ 값이 100 a.i ${\mu}g\;bee^{-1}$ 이상으로 나타나 독성이 낮은 것으로 판단되었다. 지렁이급성독성시험의 경우, 마늘추출액, 잔톡실럼(Zanthoxylum)오일, 레몬그라스오일 함유 30% 유제의 $LC_{50}$ 값이 각각 267, 592, $430mg\;kg^{-1}$ 로 나타났는데 이는 제품살포물량을 확정한 뒤 환경추정농도를 이용한 위해성평가를 통해 안전성을 확보한다면 친환경 농자재로서 활용이 가능할 것으로 판단하였다.

잘피의 광합성에 대한 중금속 및 TBT의 독성 영향과 중금속 흡수에 대한 연구 (Preliminary Study on the Toxicity and Transfer of Heavy Metals and Tributyltin to Seagrass Zostera marina)

  • 최태섭;김광용;이병권;이정석
    • ALGAE
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    • 제20권2호
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    • pp.157-166
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    • 2005
  • Uptake kinetics of Cd and Zn by leaves and rhizome of the seagrass Zostera marina were examined in controlled laboratory radiotracer experiments. Subsequently, acute toxicity of Cd, Cu and TBT on photosynthetic quantum yield (ΔF/Fm’ of Z. marina were determined, and the differential sensitivities of rapid light curve (RLC) to those harmful substances were also compared. All measurements on photosynthetic activity were determined by chlorophyll a fluorescence method using pulse amplitude modulation (PAM). Metal uptake by Z. marina was saturated with increasing exposure time in leaves and rhizomes. Uptake of Zn by Z. marina was faster than that of Cd. Metal uptake rates in Z. marina decreased with the increase of dissolved metal concentrations and also with the increase of biomass. The adverse effect of TBT on effective quantum yield was stronger than other pollutants. Average acute toxicity on the RLC of the seagrass exposed to TBT and two heavy metals (Cd and Cu) was going to decrease as follows: TBT > Cd > Cu. Our preliminary results in this study suggested that Z. marina potentially can be used as a biomonitor of harmful substances contamination in coastal waters.

Acute Dermal Toxicity Study of Bee Venom (Apis mellifera L.) in Rats

  • Han, Sang-Mi;Lee, Gwang-Gill;Park, Kwan-Kyu
    • Toxicological Research
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    • 제28권2호
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    • pp.99-102
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    • 2012
  • Bee venom (Apis mellifera L. BV) has been used as a cosmetic ingredient for anti-ageing, anti-inflammatory and antibacterial functions. The aim of this study was to evaluate the acute toxicity after a single dermal administration of BV, BV was administered to 2 groups of Sprague-Dawley (SD) male and female rats (5 animals/group) at doses of 0 and 1,500 mg/kg body weight (BW). Mortality, clinical signs, body weight changes and gross findings were continually monitored for 15 days following the single dose. There were no unscheduled deaths in any groups during the study period. No BV related clinical signs and body weight changes were observed in any groups during the study period. There were no abnormal gross findings at necropsy on day 15 after the treatment. On the basis of the above results, it was concluded that there were no treatment-related effect on mortality, clinical signs, body weight changes and gross findings in SD rats treated with a single dermal dose of BV at dose of 1,500 mg/kg BW. Therefore, the approximate lethal dose of BV was considered to be over 1,500 mg/kg/day for both sexes of rats. BV may provide a developmental basis for a cosmetic ingredient or external application for topical uses.

A Single Oral Dose Toxicity Study of Bamboo Leaf Water Extract in Sprague-Dawley Rats

  • Shin, Dong-Ho;Jang, Pan-Gu;Oh, Ki-Seok;Kim, Jae-Ha;Chung, Hee-Jong;Kim, Jong-Choon
    • Biomolecules & Therapeutics
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    • 제11권3호
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    • pp.200-203
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    • 2003
  • The present study was carried out to investigate the potential acute toxicity of bamboo leaf water extract by a single oral dose in Sprague-Dawley rats. Twenty male and female rats aged 5 weeks were randomly assigned to four groups of 5 rats each and were administered singly by gavage at dose levels of 0, 1250, 2500, or 5000 mg/kg body weight. Mortalities, clinical findings, and body weight changes were monitored for the l4-day period following the administration. At the end of 14-day observation period, all animals were sacrificed and complete gross postmortem examinations were performed. Throughout the study period, no treatment-related deaths were observed. There were no adverse effects on clinical signs, body weight, and gross finding at any dose tested. The results showed that the single oral administration of bamboo leaf water extract did not induce any toxic effect at a dose level of below 5000 mg/kg in rats and that the minimal lethal dose were considered to be over 5000 mg/kg body weight for both sexes.

황련의 급성독성에 관한 연구 (Acute Toxicity Study on Coptidis Rhizoma in Mice)

  • 마진열;성현제;주혜정;김인락;황금희;정규용
    • Toxicological Research
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    • 제15권1호
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    • pp.103-107
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    • 1999
  • In order to evaluate acute toxicity of Coptidis rhizoma, 6 week- and 13 week-old male ICR mice received Coptidis rhizoma extract (600~4,800 mg/kg body weight) orally, and toxicological responses were observed for consecutive 7 days. In the mice received relatively high concentration of Coptidis rhizoma($\geq$1,200mg/kg), death occurred within 3 hrs after oral administration, and its ratio in 13 week-old mice was conspicuously higher than that in 6 week-old mice. $LD_{50}$ of Coptidis rhizoma were estimated to bi 2,575 mg/kg and 1,490 mg/kg body weight in 6 week and 13 week-old mice, respectively. Coptidis rhizoma-treated animals manifested a variety of abnormal clinical findings such as ptosis, crouching, lethargy, convulsion, bizarre behavior and truning sideway. These abnormalities also ranked highly in the 13 week-old mice compared to those in the 6 week-old mice. In addition to abnormal behaviors, Coptidis rhizoma($\geq$1,200 mg/Kg) significantly elevated the urinary contents of bilirubin, urobilirubin, protein and glucose, and values in 13 week-old mice was higher than those in 6 week-old animals. No toxicological response was observed at concentration less than 600 mg/kg. Our results clearly demonstrate that susceptibility of mice to Coptidis rhizoma may be related with age, indicating that younger age mice is more resistant to the Coptidis rhizoma than the older, and toxicological mechanism of Coptidis rhizoma may be closely associated with its pharmacological mechanism.

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마우스에서 두릅 추출물의 단회경구투여 독성시험 (Single Oval Dose Toxicity Study of the Extract of Aralia elata in Mice)

  • 양희경;진주연;김지민;고문수;홍현주;김상철;이영재
    • Toxicological Research
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    • 제22권4호
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    • pp.439-443
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    • 2006
  • This study was conducted to investigate the potential acute toxicity of Aralia elata by a single oral dose in ICR mice. Thirty mice of each sex were randomly assigned to three groups of 10 mice each. The test articles were administered once by the gavage to mice at dose levels of 0, 2,500 and 5,000 mg/kg body weight. The mortality and changes on body weight and clinical signs of gross observation were monitored for 14 days after dosing. At the end of 14-day observation period, all animals were sacrificed and complete gross postmortem examinations were performed. There were no dead animal and adverse effects on clinical signs, the body weight and the gross finding. As the results, we could not find any toxic effect at the dose levels of 2,500 or 5,000 mg/kg in mice and the minimal lethal dose was considered to be over 5,000 mg/kg body weight in mice.

A Single Oral Dose Toxicity Study of Plant Sterol Ester in Sprague-Dawley Rats

  • Kim, Jong-Choon;Kim, Kab-Sig;Chung, Dae-Won;Chung, Moon-Koo
    • Biomolecules & Therapeutics
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    • 제8권2호
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    • pp.167-170
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    • 2000
  • The present study was conducted to investigate the acute toxicity of plant sterol ester by a single oral dose in Sprague-Dawley rats. Ten males and 10 females aged 5 weeks were randomly assigned to two groups of 5 rats each and were administered by gavage at dose level of 0 or 20 ml/kg body weight. Parameters measured during the 14-day observation period were mortality, clinical signs, body weight changes, and gross findings. No mortality was observed in the present study. Treatment-related clinical signs, such as pasty stool and diarrhea, were observed on the day of treatment and these signs resulted in soiled fur on day 1 after the treatment. However, no clinical signs were observed on days 2-14 after the treatment. There was no significant difference in body weight changes between the control and treatment groups. At necropsy on day 14 after the treatment, no treatment-related gross findings were observed in the treatment group. Based on these results, it was concluded that a single oral dose of plant sterol ester induced pasty stool and diarrhea in Sprague-Dawley rats at dose level of 20 ml/kg and that the lethal doses were considered to be over 20 ml/kg for both sexes.

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랫드에서 죽여(Balbusae caulis in Taeniam)의 단회경구투여 독성시험 (Single Oral Dose Toxicity Study of Balbusae caulis in Taeniam in Rats)

  • 신동호;신진영;김성호;김재하;정희종;김종춘
    • Toxicological Research
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    • 제20권4호
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    • pp.325-328
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    • 2004
  • The present study was carried out to investigate the potential acute toxicity of Balbusae caulis in taeniam by a single oral dose in Sprague-Dawley rats. Twenty rats of each sex were randomly assigned to four groups of 5 rats each and were administered singly by gavage at dose levels of 0, 1250, 2500, and 5000 mg/kg body weight. Mortalities, clinical findings, and body weight changes were monitored for the 14-day period following administration. At the end of 14-day observation period, all animals were sacrificed and complete gross postmortem examinations were per-formed. Throughout the study period, no treatment-related deaths were observed. There were no adverse effects on clinical signs, body weight, and gross finding at any dose tested. The results showed that the single oral administration of Balbusae caulis in taeniam did not cause any toxic effect at the dose levels of 5000 mg/kg or lower in rats and the minimal lethal dose was considered to be over 5000 mg/kg body weight for both sexes.

갈근 다당체 분획의 단회경구투여 독성에 관한 연구 (Single Oral Toxicity Study on the Polysaccharide Fraction of Pueraria lobata in Rats)

  • 장보윤;조형권;전기용;허종문;박현;김성연
    • 생약학회지
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    • 제41권3호
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    • pp.210-215
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    • 2010
  • Acute toxicity on the polysaccharide fraction of Pueraria lobata was examined using male and female Sprague-Dawley rats. The polysaccharide fraction of Pueraria lobata was orally administered at a dose of 5 mg/kg, 50 mg/kg, 500 mg/kg, 2,000 mg/kg and 5,000 mg/kg and observed for two weeks. No mortality and abnormal clinical signs were observed at the doses used. There were not any significant differences in parameters of blood biochemical values and urinalysis by the treatment of test material. All rats were appeared to be healthy and normal throughout the observation period. Also there was no difference in net body weight gain and gross pathological findings among the groups rats treated with different doses of the polysaccharide fraction with Pueraria lobata.