• 전기의세계
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• 제29권1호
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• pp.21-27
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• 1980

The effect of electric shock on human body is enormousness, which leads to warmth, tingling, and even death. The mean values of perception currents obtained on 91 men and 39 women are about 0.77(mA) for men and 0.57(mA) for women. The mean value for women is approximately seven tenths that of men. An individual can tolerate, with no adverse effects, repeated exposure to the reactions associated with currents of his let-go level, and the mean value of let-go currents obtained from 27 normal men is 6.29(mA). Lethal currents flowing human body is very dangerous even for a short time. So, it is necessary to have recourse to animal experiments ot determine lethal current for human. An analysis of experimental data indicates that body weight and shock duration are important factors in determining the lethal current. It is suggested that the relationship between current and shock duration is given by I=K/.root.T, and lethal current is proportional to body weight, where I is the current in milliampere, and T is the time in seconds.

• 대한수의학회지
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• 제15권1호
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• pp.47-50
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• 1975

Experimental studies were performed to observe the effect of exposure to 100% oxygen in 2 atmospheres on the lung tissue of rats, and to examine the resistant effect of DL-${\alpha}$-tocopherol. The following results were made through this experiment: 1. Half-lethal time by oxygen poisoning was longer in tocopherol treated group than not treated group. 2. Ratio of lung weight to body weight was significantly higher in fatal group within half-lethal time than survival group (p<0.01). 3. Histopathological changes of the lung by oxygen toxicity were vascular congestion, pulmonary edema, hemorrhage and emphysematous change. The degree of changes were rather marked in experimental group than tocopherol untreated group. Those were regard as the changes being occurred during tolerance process by prolonging half-lethal time.

• 한국응용곤충학회지
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• 제62권4호
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• pp.267-275
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• 2023

제충국(Tanacetum cineariaiaefolium), 데리스(Derris elliptica), 고삼(Sophora flavescens) 추출물은 다양한 해충을 방제하는데 사용되고 있다. 하지만, 국내에서 판매되고 있는 식물추춞물 자재는 유효성분의 표기가 없고, 살충농도와 살충시간에 대한 자료가 전무한 상황이다. 본 연구에서는 상용화된 주요 식물추출물의 살충유효성분의 농도를 결정하고 복숭아혹진딧물에 대해 살충농도와 살충시간을 측정하였다. 식물추출물의 살충활성성분인 pyrethrins, rotenone, matrine과 oxymatrine의 농도는 액체 크로마토그래피에서 표준물질을 활용하여 질량분석을 통해 측정하였다. 식물추출물을 농도별로 희석하여 복숭아혹진딧물에 살포하여 살충력을 측정하였다. 표준화합물과 비교한 후 질량분석 및 결정했습니다. Myzus persicae에 대한 lethal concentation과 lethal time을 조사했다. 살포 후 48시간 후 치사 농도(LC50)는 pyrethrins (20.4 ppm), roteone (34.1 ppm), matrine (29.6 ppm)였고, 100 ppm 살포한 LT50은 pyrethrins (13.4시간), rotenone (15.1시간), matrine (14.4시간)로 측정되었다. Kaplan-Meier 생존분석 결과, 100 ppm에서 세 가지 식물 추출물의 LT50은 대조구인 화학 살충제인 Sulfoxaflor를 살포 처리구보다 유의하게 빨랐습니다. 본 결과는 복숭아혹진딧물 방제를 위해 식물추출물의 제형화에 단일 또는 혼합 제제를 개발하는데 기준 살충농도와 살충시간을 제고하는데 의미가 있다.

• 약학회지
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• 제30권3호
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• pp.149-156
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• 1986

Many experiments have showed that the sodium and potassium ion transporting system and the Na, $^+K^+$-ATPase activity of membrane fragments are inhibited by digitalis glycosides and that the pump may be associated with the pharmacological receptor for the drugs. The aim of our investigation is to elucidate the ouabain binding sites occupation in heart following infusion of ouabain to intact animals by the $^3H$-ouabain binding assay. Lethal dose and 26 percent of lethal dose of ouabain were infused to intact rabbit through ear vein. Microsomal fraction was fractionated from ouabain treated rabbit heart. $^3H$-ouabain binding to these fraction in vitro was studied by the Schwartz's method. $^3H$-ouabain binding to heart microsomal fraction was also studied following infusion of ginseng ethanol extract and caffeine to rabbits respectively. 1) The infusion of lethal dose ouabain (113$\mu\textrm{g}$/kg) inhibited the specific $^3H$-ouabain binding to rabbit heart microsomal fraction to the level of 60% (p<0.01) of control group and the infusion of 26% of lethal dose of ouabain led to the level of 79% (p<0.01) of the control group. 2) Time course of binding of 0.4$\mu{M}$ $^3H$-ouabain to microsomal fraction from rabbit heart following infusion of lethal and 26% of lethal dose of ouabain showed dose dependence at various incubation time. 3) Compared with control, only slight change of $K_d$ and $B_{max}$ was detected in in vitro $^3H$-ouabain binding after infusion of ginseng ethanol extract (300mg/kg) to rabbit. 4) In caffeine infusion group, $^3H$-ouabain binding yielded nearly the same results as control group.

• 접착 및 계면
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• 제17권1호
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• pp.21-28
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• 2016

본 연구에서는 불법 조업 어선 제압 및 장비 불용화를 위한 접착형 퇴치제 개발의 일환으로 발포형 생분해성 폴리우레탄 연구를 수행하였다. 발포형 폴리우레탄 접착제는 폴리에스터계 및 폴리에테르 폴리올을 포함하는 주재와 고분자형의 이소시아네이트로 이루어진 경화제를 혼합하여 반응이 완결되는 2액형으로, 단기간의 생분해성을 위해 주재에 starch와 dextrin 및 amylase 등을 첨가하여 4주간 약 34%의 생분해도를 OECD 301C법에 의해 얻을 수 있었다. 주재와 경화제의 온도에 따른 점도를 $0{\sim}50^{\circ}C$의 온도범위에서 측정하여 혼합 시 참고할 수 있도록 하였으며, 또한 신속한 발포 및 접착성능을 위해서 $0{\sim}50^{\circ}C$의 온도 범위에서 발포형 폴리우레탄 접착제의 반응 완결 속도(rising time)를 조절하여 1 min 내외로 제어하였다. 또한 면 직물에 대한 T-peel 시험을 수행한 결과 최대 20.78 N/cm, 평균 11.95 N/cm의 접착력을 얻을 수 있었다.

• Journal of Dental Anesthesia and Pain Medicine
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• 제17권4호
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• pp.323-327
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• 2017

QT prolongation is an electrocardiographic change that can lead to lethal arrhythmia. Acquired QT prolongation is known to be caused by drugs and electrolyte abnormalities. We report three cases in which the prolonged QT interval was improved at the time of operation by briefly discontinuing the drugs suspected to have caused the QT prolongation observed on preoperative electrocardiography. The QTc of cases 1, 2, and 3 improved from 518 to 429 ms, 463 to 441 ms, and 473 to 443 ms on discontinuing the use of a gastrointestinal prokinetic agent, a proton pump inhibitor, and a molecular targeted drug, respectively. These cases were considered to have drug-induced QT prolongation. We reaffirmed that even drugs administered for conditions unrelated to cardiac diseases can have adverse side effect of QT prolongation. In conclusion, our cases indicate that dental surgeons should be aware of the dangerous and even potentially lethal side effects of QT prolongation. For safe oral and maxillofacial surgery, cooperation with medical departments in various fields is important.

• 한국방사선학회논문지
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• 제11권3호
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• pp.147-151
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• 2017

HFL-I 세포를 이용하여 immediate assay를 시행하였다. 발생한 repair의 양이 없기 때문에 $LogSn=-n{\gamma}({\alpha}d+{\beta}d^2$)에서 ${\gamma}$의 값은 1이며 이는 LQ model과 같다. 그리고 세포생존율의 데이터를 바탕으로 ${\alpha}$, ${\beta}$, ${\alpha}/{\beta}$의 값을 얻었다. 또한 12시간, 36시간, 48시간 후 delayed assay를 시행하여 marchese model 통해 ${\gamma}$값을 도출한 후 Pot entially lethal damage repair (PLDR)가 발생한 양을 확인하였다. delay time이 길어질수록 ${\gamma}$값은 감소함으로써 PLDR의 양이 증가함을 확인하였고 이에 따라 세포생존율은 상승됨을 보였다. 탄소빔의 1분할, 2분할, 3분할, 4분할 조사 시 각각의 interval 시간동안 나타나는 ${\gamma}$값 역시 감소하고 있음을 확인하여 PLDR의 발생을 확인할 수 있었지만 ${\gamma}$값만 감안한 marchese model을 surviving fraction값에 적용 시 오류 발생함을 보였다. 이는 탄소빔 분할조사 시 다른 회복의 매커니즘이 존재함을 뜻하여 이를 적용할 수 있는 새로운 파라미터가 고려되어져야 할 것이다.

• 한국환경농학회지
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• 제7권2호
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• pp.124-129
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• 1988

담수산 어류인 송사리(Oryzias latipes)에 대한 6개 농약의 급성독성을 7일동안 시간의 경과에 따라 측정, toxicity curve를 작성하여 각 농약의 시간의 경과에 따른 급성독성 발현의 현상을 평가하고 48시간 및 96시간 LC50값과 lethal threshold 농도와의 관계를 분석하여 얻은 결과는 다음과 같다. 농약의 toxicity curve를 중심으로 시간의 경과에 따른 급성독성값의 변화를 보면 butachlor가 120시간째, fenobucarb가 48시간째, chlorothalonil이 48시간째 lethalthreshold 농도를 나타내어, 각각 120시간, 48시간만에 급성독성현상이 더이상 시간의 경과에 따라 발현되지 않으나, 나머지 3개의 농약인 alachlor, diazinon, iprobenfos는 노출 7일 이후에도 계속 급성독성현상을 나타냄을 알 수 있었다. 이로써 6개의 농약에 대한 lethal threshold 농도는 butachlor 0.53 mg/l(0.49-0.57 mg/1), alfachlor 1.15 mg/1>, fenobucarb 10.3 mg/1(9.3-11.4 mg/1), diazinon 6.70mg/1>, chlorothalonil 0.085 mg/1(0.082-0.087 mg/1), iprobenfos 3.42 mg/1>이었다. 결국 노출시간 96시간이내에 독성현상이 발현되어 더이상 치사율이 증가하지 않은 농약은 6개중 2종류뿐이며 나머지 4개중 3개에서는 노출후 7일이 경과하여도 계속하여 독성이 발현됨을 알 수 있었다.

• 환경생물
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• 제23권4호
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• pp.390-397
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• 2005

The inhibition of cell recovery might be proceeded via either the damage of the mechanism of the recovery itself or via the formation of irreversible damage which could not be repaired at all. Both these processes may take place at the same time. Any of these possibilities would result in a decrease in both the rate and extent of cell recovery. To distinguish them, a quantitative approach describing the process of recovery as a decrease in the effective radiation dose was applied to experimental data on the recovery from potentially lethal damage in Chinese hamster cells exposed to X-rays alone or combined with various chemicals (pyruvate, novobiocin, lactate, nalidixic acid, 3-aminobenzamide). For these particular cases, it is concluded that the recovery process itself is not damaged and the inhibition of the recovery is entirely due to the enhanced yield of the irreversibly damaged cells.

• 한국동물학회지
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• 제8권2호
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• pp.33-36
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• 1965

We have carried out a study on the modification of the frequency of X-ray induced lethal and slow growing mutations by colchincine treatment before and after X-ray irradiation in Paramecium aurelia. 1. Lethal and slow-growing mutation induced by X-ray in Paramecium aurelia were reduced by colchicine treatment. 2. The effects of colchicine on the X-ray induced mutations were remarkable in the radiosensitive stages of cell division. 3. The pre-irradiation treatment with colchicine showed no significant influence on the frequency of mutations. 4. It is believed that the reduction of mutation induced by X-ray after treatment with colchicine was due to the fact that the delay of the cell division allowed more time for the pre-mutational damage to recover.