• Environmental Analysis Health and Toxicology
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• 제14권1_2호
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• pp.13-19
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• 1999

Cisplatin is an inorganic complex formed by a central atom of platinum surrounded by chlorine and ammonia atoms in the cis position in the horizontal plane, Cisplatin is one of the most effective anticancer drug, widely used against various tumor such as testicular tumor, brain tumor, ovary tumor, bladder carcinoma, colon cancer etc. However its clinical use has been limited by nephrotoxicity, ototoxicity , gastrointestinal disturbances, myeloscrppression and allergic reactions. In these toxicities, dose related and cumulative nephrotoxicity is the major dose limit factor. So, to evaluate the protective effect of aspalactone on cisplatin nephrotoxicity in rats, both compounds were given intraperitoneally, Protective effects of aspalactone against nephrotoxicity of cisplatin were observed when aspalactone was administered to rats 1hr beforecisplatin injection. Hepatotoxicity induced by combination treatment of cisplatin and aspalactone was not observed. The present results indicate that aspalactone may provide protection against cisplatin nephrotoxicity, when it is given 1hr before cisplatin injection.

• 한방안이비인후피부과학회지
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• 제21권2호
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• pp.19-27
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• 2008

Objective : The side effect of prolonged use of topical corticosteroids to skin is well-known. Moreover, resent studies have shown that prolonged use of systemic corticosteroids also negatively impacts skin barrier function. Corticosteroids have a major role in the practical management of many variable conditions. So, it is important to find the drug or the method which could protect the skin from the damage caused by corticosteroids. At former study, we investigated that Insamyangyoung-tang has some effect on skin barrier function of DNCB induced contact dermatitis hairless mice. So, this study was performed to research the effect of Insamyangyoung-tang on the TEWL with high dose steroid injected hairless mice. Method : Hairless mice were divided into 4 groups ; Control group, Group A, Group B and Group C. All groups were injected triamcinolone O.4mg for 10 times. Control group was medicated distilled water during the experimental period. Group A was medicated distilled water for 5 days before the $1^{st}$ injection day, and then medicated Insamyangyoung-tang extract during the experimental period. Group B was medicated Insamyangyoung-tang extract for 5 days before the $1^{st}$ injection day, and then medicated distilled water during the experimental period. Group C was medicated Insamyangyoung-tang extract for 5 days before the $1^{st}$ injection day, and then medicated Insamyangyoung-tang extract during the experimental period. TEWL of each group was measured for 5 times. After the $10^{th}$ injection, the tissue sample was made and the damage of epithelial cell was examined. Statistical significance was set at p<0.05 by using non parametric methods and repeated-anova.. Results : Group C showed significant effect on TEWL change of hairless mice evoked by triamcinolone injection. Group A and Group B also showed some effect, but there was no statistical significance.

• Toxicological Research
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• 제19권2호
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• pp.105-114
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• 2003

TO evaluate an effect of cyclohexane treatment on the degree of liver damage, rats were induced liver damage with 10 or 17 times $CCl_4$ injection (0.1 m1/100 g body wt., 50% $CCl_4$ dis-solved in olive oil) at intervals of every other day. Cyclohexane (1.56 g/kg body wt., i.p.) was administrated to the animals at 48 hours after the last pretreatment of $CCl_4$ . Rats were sacrificed at 4 hours after injection of cyclohexane. On the basis of histopathological findings, liver weight/body weight (LW/ BW, %), activities of serum alanine aminotransferase (ALT), xanthine oxidase (XO) and akaline phosphatase (ALP), and contents of liver protein and manlondialdehyde (MDA), $CCl_4$ -pretreatment induced liver damage. And $CCl_4$ 17 times treated group showed more severe liver damage than $CCl_4$ 10 times treated group. Administration of one dose of cyclohexane to $CCl_4$ 10 times treated animals resulted in the enhanced liver damage; liver necrosis with proliferation of fibroblast and bile duct abnormality, and increase in hepatic MDA content and the activities of serum ALP and ALT, But the enhanced liver damage was not found in $CCl_4$ 17 times treated animals. Serum cyclohexanone concentrations at 4 or 8 hours after injection of cyclohexane were higher in all liver damaged groups than normal group and were somewhat higher In $CCl_4$ 17 times treated animals than $CCl_4$ 10 times treated ones. Among the oxygen free radical metabolizing enzymes, hepatic cytochrome P45O dependent aniline hydroxylase (CYPdAH) activity in cyclohexane metabolizing enzyme system was meaningfully increased by the injection of cyclohexane to the liver damaged rats, with increased Vmax and high affinity to aniline. LW/BW (%) and activities of serum XO and ALT were more significantly increased in liver damaged groups than normal group by administration of cyclohexanone. In conclusion, it is assumed that an enhancement of liver damage by injection of one dose of cyclohexane to liver damaged animals might be caused by oxygen free radicals and cyclohexanone.

• Journal of Yeungnam Medical Science
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• 제29권2호
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• pp.129-131
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• 2012

A 70-year-old male came to the emergency room of the authors' hospital because of sudden cardiac arrest due to inferior wall ST elevation myocardial infarction. His coronary angiography revealed multiple severe coronary spasms in his very long left anterior descending artery. After an injection of intracoronary nitroglycerine, his stenosis improved. The cardiac arrest relapsed, however, accompanied by ST elevation of the inferior leads, while the patient was on diltiazem and nitrate medication to prevent coronary spasm. Recovery was not achieved even with cardiac massage, intravenous injection of epinephrine and atropine, and intravenous infusion of nitroglycerine. The patient eventually recovered through high-dose nicorandil intravenous infusion without ST elevation of his inferior leads. Therefore, intravenous infusion of a high dose of nicorandil must be considered a treatment option for cardiac arrest caused by refractory coronary vasospasm.

• 대한방사선기술학회지:방사선기술과학
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• 제25권1호
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• pp.73-76
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• 2002

In order to evaluate the exposure to the radiologic technologists from patients who had been administrated with radiopharmaceuticals, we measured the spatial dose rates at 5 cm, 50 cm, and 100 cm from skin surface of patients using an proportional digital surveymeter, both 5 min after injection and right before the studies. In results, the exposure to the technologists in each procedure was small, compared nth the dose limits of the medical workers. However, the dose-response relationships in cancer and hereditary effects, referred to as the stochastic effects, have been assumed linear and no threshold models ; therefore, the exposure should be minimized. For this purpose, the measurements of spatial dose rate distributions were thought to be useful.

• 대한방사선기술학회지:방사선기술과학
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• 제34권4호
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• pp.351-357
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• 2011

PET/CT 검사에서 $^{18}F$-FDG가 가장 널리 이용되며, 장비의 물리적 특성에 따라 환자 주입 $^{18}F$-FDF량이 다르게 권고되고 있다. 또한 검사 특성상 방사선종사자와 환자의 접촉으로 인하여 방사선의 피폭이 불가피하기에 본 연구에서는 각기 다른 PET/CT 장비를 대상으로 환자에게 주입되는 $^{18}F$-FDG가 방사선종사자에게 미치는 피폭선량과의 관계를 분석하였다. 총 3대의 각각 다른 PET/CT(Scanner1(S1): 0.15 mCi/kg, Scanner2(S2): 0.17 mCi/kg, Scanner3(S3): 0.12 mCi/kg)를 대상으로 각 장비에 숙련도를 고려하여 총 6명의 방사선종사자를 5개월간 순환근무하였고, 하루에 검사하는 환자수를 일정하게 유지하였다. 또한 검사진행 방법을 유사하게 유지하고, 방사선종사자의 개인피폭선량계인 열형광유리선량계(TLD)를 매월 판독하여 분석하였다. 개인의 월별 평균 피폭선량은 방비에 따라 S1은 0.76 mSv, S2는 0.93 mSv, S3는 0.47 mSv였다. 피폭선량은 개인 최대 1.12 mSv, 최저 0.42 mSv로 숙련도와 경험에 따라 유의한 차이를 보였고, 또한 각 주입량에 따른 PET/CT의 종류에 따라 피폭선량은 유의한 상관관계를 나타냈다. 본 연구를 통하여 주입 $^{18}F$-FDG가 적을수록 방사선종사자의 피폭선량이 낮았다. 또한 개인 숙련도에 따라 피폭선량이 감소하였으나, 장비의 특성에 따라 적은 방사선의약품 주입량의 영향이 방사선종사자의 피폭선량을 현저하게 감소할 수 있기에 이에 대한 연구가 보다 활성화 되어야 할 것이다.

• 대한약침학회지
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• 제17권3호
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• pp.25-30
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• 2014

Objectives: This study was performed to evaluate the single-dose intravenous toxicity of Guseonwangdo-go glucose 20% pharmacopuncture. Methods: Forty Sprague-Dawley rats were divided into four groups of five males and five females per group: an intravenous (IV) injection of 1.0 mL of normal saline solution per animal was administered to group 1 (G1, control group); an IV injections of 0.1, 0.5, and 1.0 mL of Guseonwangdo-go glucose pharmacopuncture per animal were administered to experimental groups 2, 3, and 4 (G2, G3, and G4), respectively. General symptoms, body weights, hematological and biochemical test results, and necropsy histopathological observation were recorded in all groups. In the statistical analyses, significance was determined by using the one-way analysis of variance (ANOVA). The significance level was 0.05 in all comparisons. Results: For 14 days, no deaths or abnormalities were observed in any of the 4 groups. The body weights of all groups continuously increased during the observation period. In the hematological test, the WBC count was significantly increased in female rats of G4 compared to the control group, but this difference was considered not to be statistically meaningful. No significant biochemical changes were observed. On necropsy, crust formation was observed in one rat of the control group, and granulation tissues were observed around the injection site in one rat of G4; these changes were concluded to have been caused by injection of the needle into a vein. Conclusion: The findings suggest that the lethal dose of Guseonwangdo-go glucose pharmacopuncture is more than 1.0 mL per animal in both male and female rats. Thus, we can conclude that Guseonwangdo-go glucose pharmacopuncture injection is relatively safe to use in acute toxicity tests. Further studies are needed to establish more detailed evidences of its toxicity.

• 한국원자력학회:학술대회논문집
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• 한국원자력학회 1999년도 추계학술발표회요약집
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• pp.326.2-326
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• 1999

• Journal of Radiation Protection and Research
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• 제37권2호
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• pp.103-107
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• 2012

PET-CT 검사 환자의 피폭선량 감소를 위한 기초자료 제공의 일환으로 PET-CT 검사 환자의 방사선량률의 변화를 분석하고자 하였다. PET-CT 검사 환자의 방사선량률을 측정한 결과 이론과 같이 방사성의약품이 투여된 환자로부터 거리가 멀수록, 시간이 지날수록 방사선량률은 감소되는 것을 볼 수 있었다. 특히 신체부위에 따라서는 방사성의약품 정맥 주사 즉시인 약 4.17분에서는 흉부, PET-CT 검사 전 배뇨 후인 약 77.47분 이후부터는 두부가 가장 높게 나타났다. 일반화되어 있는 정보와 같이 PET-CT 검사 환자로부터 받는 방사선 피폭량을 감소시키기 위해서는 보호자나 방사선작업종사자가 환자로부터 거리를 멀리하거나 방사능이 감소된 이후의 시간부터 접촉하는 것이 바람직하다. 불가피한 접촉이 필요하다면 가능한 거리는 200 cm이상을 확보하는 것이 바람직하다. 또한 초기에는 흉부, 방사성의약품 투여 후 약 77분 이후부터는 두부에 방사선량률이 높기 때문에 환자 신체적 특징을 고려한 접촉도 함께 이루어진다면 최적화 달성에 도움이 될 것이라고 보여 진다. 본 연구에서 도출된 PET-CT 검사 환자의 거리, 시간, 신체부위에 따른 방사선량률 변화를 알 수 있다는 점에서 연구에 의의가 있다고 본다. 향후 연구에서는 본 연구에서 도출된 결과를 바탕으로 환자 개인특성에 따른 방사선량률의 변화 차이를 분석하여 환자, 보호자, 종사자의 피폭선량 감소에 활용할 수 있도록 지속적인 연구가 수행되는 것이 필요하다고 본다.

• 대한약침학회지
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• 제18권2호
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• pp.42-50
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• 2015

Objectives: The aims of the study were to test the single- dose intravenous toxicity of Daebohwalryeok pharmacopuncture (DHRP) in Sprague-Dawley (SD) rats and to estimate the crude lethal dose. Methods: The experiments were conducted at Biotoxtech Co., a Good Laboratory Practice (GLP) laboratory, according to the GLP regulation and were approved by the Institutional Animal Care and Use Committee of Biotoxtech Co. (Approval no: 110156). The rats were divided into three groups: DHRP was injected into the rats in the two test groups at doses of 10 mL/kg and 20 mL/kg, respectively, and normal saline solution was injected into the rats in the control group. Single doses of DHRP were injected intravenously into 6 week old SD rats (5 male and 5 female rats per group). General symptoms were observed and weights were measured during the 14 day observation period after the injection. After the observation period, necropsies were done. Then, histopathological tests were performed. Weight data were analyzed with a one-way analysis of variance (ANOVA) by using statistical analysis system (SAS, version 9.2). Results: No deaths and no statistical significant weight changes were observed for either male or female SD rats in either the control or the test groups during the observation period. In addition, no treatment related general symptoms or necropsy abnormalities were observed. Histopathological results showed no DHRP related effects in the 20 mL/kg DHRP group for either male or female rats. Conclusion: Under the conditions of this study, the results from single-dose intravenous injections of DHRP showed that estimated lethal doses for both male and female rats were above 20 mL/kg.