• 한국한의학연구원논문집
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• 제16권1호
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• pp.135-140
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• 2010

This study was carried out to investigate the acute toxicity and safety of Ssanghwa-tang extract fermented with Ganoderma lucidum. To evaluate the acute toxity and safety, 0(control group), 1250, 2500 and 5000 mg/kg of Ssanghwa-tang and fermented Ssanghwa-tang extracts were orally administered to 20 male and 20 female ICR mice. After single administration, we observed survival rates, general toxicity, changes of body weight, and autopsy. Compared with the control group, we could not find any toxic alteration in all treated groups (1250, 2500 and 5000 mg/kg). $LD_{50}$ of Ssanghwa-tang and fermented Ssanghwa-tang extracts might be over 5000 mg/kg and it is very safe to ICR mice.

• 한국한의학연구원논문집
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• 제15권3호
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• pp.93-98
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• 2009

In this research, the acute toxicity of fermented Yukmijihwangtang extract was examined using male and female ICR mice, To evaluate the acute toxity and safety, 0(control group), 1250, 2500 and 5000 mg/kg of fermented Yukmijihwangtang extract were orally administered to male and female ICR mice. After single administration, we observed survival rates, general toxicity, changes of body weight for the 14 days and autopsy at 1 day following the administration according to the Regulation of Korean Food and Drug Administration. Compared with the control group, we could not find any toxic alteration in all treated groups (1250, 2500 and 5000 mg/kg). $LD_{50}$ of fermented Yukmijihwangtang extract might be over 5000 mg/kg and it is very safe to ICR mice.

• 생약학회지
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• 제42권3호
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• pp.265-270
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• 2011

Acute toxicity of a combined preparation of the standardized extracts Scutellaria baicalensis GEORGI and Salvia miltiorrhiza BUNGE in a ratio of 3:1 was examined in male and female ICR mice. Mice were treated with the test substance intragastrically at a dose of 0 mg/kg, 5 mg/kg, 50 mg/kg, 500 mg/kg or 2,000 mg/kg and observed for two weeks. No death or abnormal clinical sign was shown during the observation period. Also there were no difference in net body weight gain, organ weight, and gross pathological findings at the terminal sacrifice. The results suggested that acute oral toxicity of a combined preparation of the standardized extracts is very low at the conditions employed in this study.

• 대한한방부인과학회지
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• 제22권4호
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• pp.19-27
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• 2009

Purpose: This study was carried out to investigate the acute toxicity and safety of fermented Ojeok-san(Wuji-san) extract. Methods: To evaluate the acute toxity and safety, 0(control group), 1250, 2500 and 5000 mg/kg of fermented Ojeok-san(Wuji-san) extract were orally administered to 20 male and 20 female ICR mice. After single administration, we observed survival rates, general toxicity, changes of body weight, and autopsy. Results: Compared with the control group, we could not find any toxic alteration in all treated groups (1250, 2500 and 5000 mg/kg). Conclusions: $LD_{50}$ of fermented Ojeok-san(Wuji-san) extract might be over 5000 mg/kg and it is very safe to ICR mice.

• 환경생물
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• 제23권2호
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• pp.146-151
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• 2005

본 연구를 통한 결론은 다음과 같다. 5개의 염색폐수배출업소에서 각각 3회씩 채취한 최종 방류수를 대상으로 한 생물독성시험 결과 미생물독성시험에서는 B시료와 E시료에서 독성이 관찰되었고 급성 물벼룩시험에서는 반수치사농도가 C시료에서만 관찰되어 염색폐수의 독성이 시험 생물종별로 다르게 나타날 수 있음을 제시하였다. 동일 생물종을 대상으로 실시한 급성 및 만성시험에서는 급성반수치사가 5개 방류수 중 C시료에서만 비교적 낮은 농도에서 관찰이 된 것에 비해 만성반수치사는 3개 방류수에서 나타났고 $EC_{50}$도 급성영향의 $1/2\~1/5$ 수준에서 결정되었다. 특히 만성노출에 의한 생식 및 성장에 미치는 영향은 치사에 미치는 영향농도보다 더 낮은 농도에서 나타나는 경향을 보이고 있다 따라서 방류수가 연속적으로 수계에 배출되는 특성을 고려하면 만성노출에 의한 영향을 평가하는 것이 중요한 의미를 갖는다. 한편 염색폐수의 경우 동일업종 또는 동일한 시료에서도 독성평가방법에 따라 서로 다른 정도의 독성이 관찰되는 등 독성발현이 매우 다양하게 나타났다. 그러므로 염색폐수가 수중생태계에 미치는 영향을 정확하게 파악하고 제어하기 위해서는 물고기나 조류 등 다른 영양단계에 있는 생물종에 미치는 영향 등의 연구가 요구된다.

• 대한환경공학회지
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• 제27권2호
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• pp.191-197
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• 2005

Ceriodaphnia dubia를 이용한 새로운 독성시험법인 온도증가 단기독성평가법(ToxTemp, ToxCity test based on TEMPerature control)을 이용하여 농약성분에 대한 민감도를 조사하였다. BPMC, Diazinon, Fenitrothion등 하수의 생물학적 처리에 독성을 나타낼 수 있는 물질들에 대하여 기존의 실험방법인 표준 48시간 독성시험법과 비교했을 때 온도증가법은 $1{\sim}1.5$시간의 짧은 접촉시간에도 농약의 독성을 잘 감지할 수 있음을 알 수 있었다. 또한 중금속, 독성 유기화합물 그리고 농약성분을 비교, 평가했을 때 온도증가법은 1.25시간의 짱은 접촉시간 내에 48시간독성법의 결과와 높은 상관관계를 유지하며 독성을 감지하였다. 염색공단 폐수와 하수 등 실폐수에서의 독성평가능을 검토하기 위하여 활성슬러지를 이용한 질산화율, 산소이용율(OUR)과 C. dubia를 이용한 표준 48시간 독성시험법, 온도증가법을 비교하였다. 그 결과 OUR을 이용한 평가에서는 비교적 높은 질산화율 저해도를 보인 원수에 대해서도 독성민감도가 낮아 현장적용에 한계를 나타낸 반면 C. dubia를 이용한 표준 48시간 독성시험법과 온도증가법은 각기 다른 수준의 독성에 대해 민감하게 차이를 보였으며, 이 두 방법은 질산화율 저해도와 좋은 상관관계를 보였다. 온도증가법은 표준 48시간 독성시험법에 비해 1.5% 정도 민감도가 떨어지지만 현장에서의 신속한 감지가 가능하다는 점에서 현장에서의 질산화 독성진단에 대한 적용가능성이 높음을 보여주었다.

• Asian Pacific Journal of Cancer Prevention
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• 제16권16호
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• pp.7331-7335
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• 2015

Background: Concurrent chemoradiation with three weekly high dose cisplatin is the non-surgical standard of care for the treatment of locally advanced head and neck cancers. Although this treatment regime is efficacious, it has high acute toxicity, which leads not only to increased treatment cost, but also to increased overall treatment time. Hence, the current study was undertaken to evaluate the acute toxicity and tumor response in head and neck cancer patients treated with concurrent chemoradiation using $40mg/m^2$ weekly cisplatin, which has been our institutional practice. Materials and Methods: This single institution retrospective study included data for 287 head and neck cancer patients treated with concurrent chemoradiation from 2012 to 2014. Results: The mean age of the patients was 48.8 years. The most common site of involvement was oral cavity. Most of the study patients presented with advanced stage disease. The mean overall treatment time was 56.9 days. Some 67.2% had overall complete response to treatment as documented till 90 days from the start of treatment. According to the Radiation Therapy Oncology Group (RTOG) acute radiation morbidity scoring criteria, mucositis was seen in 95.1% of the patients. Dermatitis and emesis were observed in 81.9% and 98.6%, respectively. Regarding haematological toxicity, 48.8% and 29.6% suffered from anaemia and leukopenia, respectively, during treatment. Acute kidney injury was assessed using the Common Terminology Criteria for Adverse Events (CTCAE), and was found in 18.8% of the patients. Conclusions: Concurrent chemoradiotherapy with weekly cisplatin is an effective treatment regime for head and neck cancers with reasonable toxicity which can be used in developing countries, where cost of treatment is so important.

• Toxicological Research
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• 제13권4호
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• pp.435-447
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• 1997

l-Muscone is synthesized for use as substitutive material of musk which is the active ingredient of woohwangchungsimwon. The objective of this investigation was to evaluate the acute and subacute toxicity of l-muscone in rats. In oral acute toxicity test, SPF Sprague-Dawley male and female rats were gayaged with l-muscone of two doses(0, 5.0 g/kg). No dead animal and abnormal autopsy findings were found in control and treated group. Body weights were slightly decreased in both sexes of rats treated with 5.0 g/kg. Therefore, oral $LD_{50}$ of l-muscone was consider to be higher than 5.0 g/kg in male and female rats. In intraperitoneal acute toxicity test, rats were injected intraperitoneally with dosages of 0, 1,000, 1,316, 1,732, 2,279 and 3.000 mg/kg. Decreased body weights and motor activities were observed at high dose group. Intraperitoneal $LD_{50}$ of l-muscone were 1,920 mg/kg in male and female rats. In the subacute study, l-muscone was administrated orally to both sexes of rats for 4 weeks as several doses(0, 10, 100 and 1,000 mg/kg). There were neither dead animals nor significant changes of body weights during the experimental period. In addition, no differences were found between control and treated groups in clinical signs, urinalysis, hematology, serum biochemical analysist and other findings. Above data suggest that no observed adverse effect level of l-muscone in rats might be over 1,000 mg/kg/day in this study.

• 대한임상검사과학회지
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• 제44권2호
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• pp.59-65
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• 2012

Previous studies have shown that modified Je-Ho-Tang (MJHT) has anti-platelet effects. Je-Ho-Tang (JHT), a Korean court beverage, is a traditional Korean herbal medicine that has been used for the treatment of a disease attended by great thirst, and for prevention of illness in hot summers. We made MJHT from JHT by excluding honey. The present study was performed to determine the acute oral toxicity of crude extract of MJHT in male and female ICR mice. We investigated the in vivo single dose acute toxicity of MJHT hot-water extraction. This test was orally administered once by gavage to 20 mice of each sex received doses of 0 (control group), 1250, 2500 and 5000 mg/kg body weight. Mortalities, clinical findings, autopsy findings and body weight changes were monitored daily for 14 days following the administration. We observed survival rates, general toxicities, changes of body weight, and autopsy. No significant lethality was observed after single oral administration of MJHT at the different dosages. Autopsies on the animals revealed no gross abnormalities. Therefore, the LD50 value of MJHT for ICR mice was estimated more than 5000 mg/kg by the oral route. These results suggest that no toxic dose level of MJHT in mice is considered to be more than 5000 mg/kg. Consequently, it was concluded that MJHT have no effect on acute toxicity and side effect in ICR mice.

• 대한한의학방제학회지
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• 제30권4호
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• pp.281-291
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• 2022

Objectives : In this study, acute oral toxicity test of pomace Schisandra chinensis extracts was conducted in order to up-cycling to a high value-added industry using by-products discarded in the production process of Schisandra chinensis products and active ingredients such as dibenzocyclooctadiene lignans in Schisandra chinensis. Methods : Pomace Schisandra chinensis extracts were orally administered to SD-rats(female, n=3) without a control group according to the 'OECD guidelines'. After, mortality and clinical signs were observed, and the deceased animals were subjected to an autopsy. In addition, acute oral toxicity test was sequentially performed in step I (300 mg/kg), step II(300 mg/kg), step III(2,000 mg/kg), and step IV(2,000 mg/kg) according to the mortality. Results : There were no abnormalities caused by pomace Schisandra chinensis extracts in step I and step II. However, one animal each died in step III and step IV. In addition, clinical signs(salivation, decrease in food intake, prone position, decrease of locomotor activity, loss of locomotor activity, convulsion, hypothermia, lacrimation, staining around mouth, soiled perineal region, reddish urine, chromaturia, decrease of fecal volume, lying on side, blackish stool, no stool, compound-colored stool, refusal to feed, excitement, hypersensitivity, rigidity, dorsal position, etc.) were observed. But, no clinical signs were observed from 5th day, and experiment animals recovered completely. Conclusions : As a result of this study, pomace Schisandra chinensis extracts may exhibit acute toxicity at concentrations of 2,000 to 5,000 mg/kg, and the GHS classification was designated as 'Category 5'.