• 제목/요약/키워드: Lethal dose 50

검색결과 200건 처리시간 0.028초

연소 독성 기반 우레탄 화재의 위험성 평가 연구 (A Research of Risk Assessment for Urethane Fire Based on Fire Toxicity)

  • 김성수;조남욱;이동호
    • 한국화재소방학회논문지
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    • 제29권2호
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    • pp.73-78
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    • 2015
  • 리스크 관리 대상 중 화재는 대형재해임과 동시에 물적 인적 손실을 동반하는 고위험군 항목에 속한다. 따라서 재난안전관리에서는 실천적 측면에서의 화재예방활동과 발생 가능한 화재위험성 예측, 화재 피해 최소화를 위한 안전관리비용 투자가 요구되며 인적피해 최소화를 위해 가스 유해성 시험(KS F 2271)기반 연소 독성에 대한 위험성 평가를 요구한다. 본 연구에서는 정량적 화재위험성평가 기법의 기초 데이터 확보를 위한 연구로, 두께 5~25 mm의 우레탄 시료를 대상으로 가스 유해성 시험을 실시하였다. 또한 실험동물에 노출되는 연소생성물은 적외선 분광분석기(FT-IR)로 분석하여 ISO 13344의 연소독성지수 Lethal Fractional Effective Dose ($L_{FED}$)를 산출하였다. 또한, $L_{FED}$에 기초하여 시료의 Lethal Concentration 50% ($LC_{50}$)을 산정한 결과, 일정치 이상의 화재하중을 가지는 우레탄 시료의 $LC_{50}$$118{\sim}129g/m^3$임을 확인하였다. 본 연구를 통하여 해당 기법이 우레탄 화재 위험성 분석에 적용 가능함을 확인하였으며, 본 기법의 적용으로부터 유해가스에 의한 인적피해 예측을 기반으로한 건축물 안전 확보 차원의 전략적 투자확대의 자료로 활용 가능케 하였다.

교감신경성 수용체 차단이 Digitalis독성에 미치는 영향 (Effects of Adrenergic Receptor Blockade on Digitalis Intoxication in Mice)

  • 강희룡
    • The Korean Journal of Physiology
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    • 제7권2호
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    • pp.67-70
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    • 1973
  • This experiment was carried out to investigate the influence of adrenergic receptor blockade. on digitalis intoxication. The effects of adrenergic alpha and beta receptor blockade on the lethal dose of digitonin were evaluated. $LD_{50}$ and dose mortality curve of digitonin in mice pretreated with dibenzylin or propranolol hydrochloride (Inderal) were obtained. All drugs were injected subcutaneously. Digitonin toxicity was significantly decreased in mice pretreated with beta·blockade compare with alpha-blockade and control groups.

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선복화 에탄올 추출물의 급성 독성 연구 (Safety Evaluation of Ethanol Extract of Inulae Flos : Single-dose Oral Toxicity Study in Mice)

  • 권다혜;김민영;황보현;지선영;박철;최영현;홍수현
    • 대한한의학방제학회지
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    • 제28권2호
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    • pp.169-177
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    • 2020
  • Objectives : This experiment was designed to assess the single oral toxicity of Ethanol Extract Inulae Flos (IF) ethanol extracts. IF is one of the important herbs to remove phlegmy which is the viscous turbid pathological product that can accumulate in the body, causing a variety of diseases. Nevertheless, there has been a lack of research on the pharmacology toxicity of IF. Methods : In this study, IF was orally administered to 5 weeks ICR mice as an oral dose of 2,000 or 3,000 or 5,000 mg/kg. The condition of the mice was observed for 14 days and their weights were measured every two days. Results : None of the mice died for 14 days. The abnormal clinical symptoms and anatomical signs of toxicity were not found in any treatment groups. The gain of net body weight was observed. There was also no significant difference in the organ weight. The serum biochemistry and hematological analysis showed a decrease in BUN, red blood cells, white blood cells and platelets although within the normal ranges. Conclusions : These results suggest that the 50% lethal dose of IF is more than 5,000 mg/kg. This could be thought that IF is a safe drug without acute toxicity and side effects. However, IF showed some weight loss and change in blood test, so it will need to be careful when using it for high doses.

신경작용제 사린 및 소만 중독에 대한 기니픽에서의 예방패치의 해독 및 뇌보호 효능 (Antidotal and Neuroprotective Efficacies of a Prophylactic Patch against Sarin and Soman Poisonings in Guinea Pigs)

  • 송영조
    • 한국군사과학기술학회지
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    • 제24권1호
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    • pp.144-150
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    • 2021
  • This study was designed to evaluate the prophylactic efficacy of a combinational patch system containing physostigmine and procyclidine against sarin and soman using guinea pig. The median lethal dose values of two nerve agents were calculated by a probit analysis of deaths occurring within 24 h. In this study, the values of median lethal dose of sarin and soman were determined to be 33.0 and 26.7 ㎍/kg in guinea-pigs, respectively. The guinea pigs treated with a prophylactic patch(4×5 ㎠) for 24 h were 100 % protected against a challenge of 1.5 LD50. The combinational KMARK-1(atropine and 2-PAM) and prophylactic patch were more effective than a single KMARK-1, a combination of pyridostigmine and KMARK-1 significantly. Epileptiform seizures in the guinea pigs treated with the combinational antidotes led to neuropathological changes, in comparison with intact feature of brain of the animal treated with the patch.

Evaluation of the sub-lethal toxicity of Cu, Pb, bisphenol A and polychlorinated biphenyl to the marine dinoflagellate Cochlodinium polykrikoides

  • Ebenezer, Vinitha;Ki, Jang-Seu
    • ALGAE
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    • 제27권1호
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    • pp.63-70
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    • 2012
  • Algae are sensitive to a wide range of pollutants, and are effective bioindicators in ecotoxicity assessments. Here, we evaluated the sub-lethal sensitivity of the marine dinoflagellate Cochlodinium polykrikoides upon exposure to copper (Cu), lead (Pb), bisphenol A (BPA), and Aroclor 1016 (polychlorinated biphenyl, PCB). Toxic effects were assessed by observations of the reduction in cell counts and chlorophyll a levels after exposure to each toxicant. C. polykrikoides displayed dose-dependent, sigmoidal responses when exposed to the tested chemicals. $EC_{50}$-72 h values for Cu, Pb, BPA, and PCB were 12.74, 46.70, 68.15, and $1.07mg\;L^{-1}$, respectively. PCB, which is an endocrine-disrupting chemical, was the most sensitive, proving its toxic effect on the dinoflagellate. This study provides baseline data on the toxic effects of commonly used heavy metals and endocrine-disrupting chemicals to a marine dinoflagellate.

흰줄숲모기, Aedes albopictus (Diptera: Culicidae)의 치사농도 및 용화에 대한 구리의 영향 (Effect of Copper on Lethal Dose and Pupation of Aedes albopictus (Diptera: Culicidae))

  • 이수미;윤수진;신병식
    • 환경생물
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    • 제28권2호
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    • pp.64-68
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    • 2010
  • 본 실험은 구리가 흰줄숲모기, Aedes albopictus의 발생에 미치는 생물학적 영향을 조사하기 위하여 수행하였다. 흰줄숲모기 3령, 4령 유충을 각각 다른 농도의 구리 용액(0.0, 2.5, 25.0, 50.0 ppm)에서 24시간, 48시간 처리한 후 치사농도를 결정하고, 사육용액(tap water)으로 옮겨 사육하여, 유충의 용화율, 성충의 날개길이를 측정한 결과는 다음과 같다. 50% 치사농도($LC_{50}$)는 4령 유충 24시간 처리군에서 35.65 ppm으로 나타나 다른 처리군에 비해 가장 저항성을 지닌 것으로 나타났다(Table 1). 유충의 용화율은 고농도 48시간 처리군에서 낮게 나타났으며 특히 3령 유충 48시간 처리 군에서 14% (암컷 9%, 수컷 5%)로 가장 낮았다. 또한 우화 후 성충의 날개 길이는 처리 농도가 증가하고 긴 처리 시간이(48시간) 감소하는 것으로 나타났다. 이러한 실험 결과들은 흰줄 숲모기의 각 발생단계에 구리를 처리한 결과 처리 농도 및 처리 시간에 따라 치사량, 용화율, 날개길이 등에 많은 변화를 나타내었는데 이는 중금속이 곤충의 유충발육과 변태에 영향을 끼치며, 이와 수반되는 물질대사에 도 영향을 미치는 것으로 여겨진다.

한약의 안전성 등급화를 통한 근거중심실용의학적 연구(1) - Aristolochic acid 함유 한약재를 중심으로 - (Introduction of evidence-based practical medicine through safety classification for herbal medicine(1))

  • 박영철;이선동
    • 대한한의학회지
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    • 제35권1호
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    • pp.114-123
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    • 2014
  • Objectives: Evidence-based medicine(EBM) advocates the use of up-to-date "best" scientific evidence from health care research as the basis for making medical decisions. EBM also has been applied to traditional Korean medicine(TKM), especially in the field of safety. Recently, the standard prescription for TKM by Korea Institute of Oriental Medicine was published based on toxic index from various toxicity tests. However, there are some limitations when the results from the study based on EBM are applied in clinics. To overcome these imitations, the term "evidence-based practical medicine" was developed and defined as clinically applicable results from the study based on EBM. And safety classification for TKM was suggested as an example of evidence-based practical medicine. Methods: For safety classification for TKM, the data for $LD_{50}$(50% lethal dose), which was transformed to theoretical $LD_1$(1% lethal dose), was analyzed as one of tools for EMB study and divided by maximum dose used in clinics. Results and Conclusions: As a result, human equivalent dose(HED)-based MOS(margin of safety) for korean traditional medicine was calculated and used for safety classification with 5 categories. These categories would be helpful for oriental medicine clinicians to decide the increase and decrease of dosage according to various factors such as patient's sensitivity, potential toxicity of herbal medicines, clinician's experience for better cure. Thus, this safety classification provides some evidences enough that evidence-based practical medicine should be not the same with EBM and defined differently from EBM.

보중익기탕 및 발효보중익기탕의 단회투여 독성에 대한 연구 (Single Oral Dose Toxicity Test of Bojungikgi-tang (Buzhongyiqi-tang) and Fermented Bojungikgi-tang (Buzhongyiqi-tang) Extracts in Mice)

  • 이지혜;황윤환;곽동훈;김태수;마진열
    • 대한한방내과학회지
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    • 제32권4호
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    • pp.599-609
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    • 2011
  • Objectives : The aim of this study was to evaluate the single oral dose toxicity and safety of Bojungikgi-tang (Buzhongyiqi-tang) and fermented Bojungikgi-tang (Buzhongyiqi-tang) extracts in male and female ICR mice. Methods : In the single oral dose toxicity study, non-fermented and fermented Bojungikgi-tang (Buzhongyiqi-tang) were administered to male and female ICR mice as an oral dose of 1250, 2500 and 5000 mg/kg. Changes of body weights, general behaviors, adverse effects and mortality were determined throughout the experimental period. Hematological parameters, serum chemistry, organ weights and necropsy findings were evaluated at the end of the experiment. Results : There was no mortality or sign of toxicity in the single oral dose toxicity study. There were also no significant differences in body weights, organ weights, and hematological parameters, serum chemistry values between treatment and control groups. Conclusions : The results obtained in this study suggest that the 50% lethal dose of fermented Bojungikgi-tang (Buzhongyiqi -tang) in both female and male mice can be considered as well over 5,000 mg/kg, so these medicines can be safe in clinics.

태음조위탕(太陰調胃湯)의 마우스 단회투여 독성시험 (Single Oral Dose Toxicity Test of Taeumjowi-tang in ICR Mice)

  • 김종대
    • 동의생리병리학회지
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    • 제23권5호
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    • pp.993-1002
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    • 2009
  • The object of this study was to evaluate the single dose toxicity of Taeumjowui-tang(TUJWT), a polyherbal formula have been traditionally used as prevention or treatment agent for obesity, in male and female mice. Aqueous extracts of TUJWT (Yield = 10.5%) was administered to female and male ICR mice as an oral dose of 2000, 1000 and 500 mg/kg (body wt.) according to the recommendation of KFDA Guidelines. Animals were monitored for the mortality and changes in body weight, clinical signs and gross observation during 14 days after dosing, upon necropsy, organ weight and histopathology of 12 principle organs were examined. As results, we could not find any mortality, clinical signs, and changes in the body and organ weight except for diarrhea restricted in TUJWT 2000 mg/kg treated one male mouse at 1 day after administration, and increases of popliteal lymph node weights in all TUJWT administered groups. In addition, no TUJWT-treatment related abnormal gross findings and changes in histopathology of principle organs were detected except for increases of the frequency of hypertrophy and hyperplasia of lymphoid cells in the popliteal lymph nodes in all TUJWT treatment groups with some sporadic accidental findings. These increases of popliteal lymph node weights with hypertrophy and hyperplasia of lymphoid cells were considered that related to the immune modulate effect of TUJWT not toxicological signs. The results obtained in this study suggest that the TUJWT does not cause any toxicological signs. The 50% lethal dose and approximate lethal dose of TUJWT aqueous extracts in both female and male mice were considered as over 2000 mg/kg.

구증황정(九蒸黃精)의 벤조피렌 함량과 마우스 단일투여 독성실험 (Single Toxicity Evaluation of the Polygonati Rhizoma Preparata with Benzo[a]pyrene Contents in ICR Mice)

  • 김용웅;노성수
    • 동의생리병리학회지
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    • 제25권1호
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    • pp.100-108
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    • 2011
  • The object of this study was two. One was if Polygonati Rhizoma preparata had a benzo(a)pyrene, the other was to evaluate the single dose toxicity of 9 repetitive steaming and fermenting processed Polygonati Rhizoma, dried root parts of Polygonati Rhozoma preparata extract, in male and female mice. We measured a content of benzo(a)pyrene in Polygonati Rhozoma preparata using a method with HPLC/FLD. And for single dose toxicity, aqueous extracts of Polygonati Rhozoma preparata (EPP; Yield = 35.4 %) was administered to female and male ICR mice as an oral dose of 2,000, 1,000 and 500 mg/kg (body weight) according to the recommendation of Korea Food and Drug Administration (KFDA) Guidelines. Animals were monitored for the mortality and changes in body weight, clinical signs and gross observation during 14 days after dosing, upon necropsy; organ weight and histopathology of 12 principle organs were examined. As results, we could not find any mortality, clinical signs, and changes in the body and organ weight except for slight soft feces sporadically detected in EPP treated male mice at 1 day after administration. In addition, no EPP-treatment related abnormal gross findings and changes in histopathology of principle organs were detected except for some sporadic accidental findings. The results obtained in this study suggest that benzo(a)pyrene was not existed in Polygonati Rhozoma preparata and the 50% lethal dose and approximate lethal dose of EPP aqueous extracts in both female and male mice were considered as over 2,000 mg/kg, the limited highest dosage recommended by KFDA Guidelines. However, it also observed that the possibilities of digestive disorders, like soft feces when administered over 500 mg/kg of EPP aqueous extracts in the present study.