• Title/Summary/Keyword: Internal Dose

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THE BIDAS-2007: BIOASSAY DATA ANALYSIS SOFTWARE FOR EVALUATING A RADIONUCLIDE INTAKE AND DOSE

  • Lee, Jong-Il;Lee, Tae-Young;Kim, Bong-Whan;Kim, Jang-Lyul
    • Nuclear Engineering and Technology
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    • 제42권1호
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    • pp.109-114
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    • 2010
  • Bioassay data analysis software (BiDAS-2007) has been developed by KAERI, which adds several new functions to its previous version. New functions of the BiDAS-2007 computer code enable the user not only to do a simultaneous analysis by using two or more types of bioassay for the best internal dose evaluation, but also to do a continual internal dose evaluation from a change of the internal exposure conditions such as an intake type (acute, chronic), an intake pathway (inhalation, ingestion), an absorption type (Type F, M, S), and a particle size (AMAD, activity median aerodynamic diameter), and also to estimate the intakes in various conditions of an internal exposure at a time. The values calculated by the BiDAS-2007 code are consistent and in good agreement with those values by IMIE-2004 code by Berkovski and IMBA code by Birchall. The BiDAS-2007 computer code is very useful and user-friendly to estimate the radionuclide intakes and committed effective doses of a radiation worker.

국내 내부피폭방사선량 평가 상호비교 (Intercomparison Exercise on Internal Dose Assessment in Korea)

  • 이종일;김장렬;김봉환
    • Journal of Radiation Protection and Research
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    • 제36권2호
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    • pp.64-70
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    • 2011
  • 국내 최초로 국내 원자력 관련 기관을 대상으로 내부피폭방사선량 상호비교 프로그램을 실시하여 국내 내부선량 평가결과의 조화성을 분석하였다. 이를 위하여 섭취경로, 흡수형태, 방사능 입자크기(AMAD) 및 섭취시점을 모르는 경우에 대한 내부선량 평가문제를 개발하였으며, 세 종류의 문제에 각 세 문항씩 총 9문항을 제시하였다. 이번 상호비교 프로그램에는 원자력의학원, 방사선보건연구원, 원자력발전소(고리, 영광, 울진)의 내부선량평가 담당자 7명이 참가하여 문제에 대한 답안을 제출하였으며, 각 문제별 참가자 답안의 기하평균에 대한 각 참가자 답안의 상대 비 분포는 $5.75{\times}10^{-4}$ ~ 9.81이었고, 평가과정에서 극히 일부의 답안을 제외할 경우 참가자 답안의 기하평균에 대한 각 참가자 답안의 상대 비는 0.216 ~ 3.12의 분포를 보였다.

마황윤폐탕(麻黃潤肺湯) 추출물의 수컷 SD Rats에서 경구 단회투여 독성 평가 (Single Dose Toxicity Test of Mahwangyounpae-tang Extract in Male SD Rats)

  • 조동희;박미연;최해윤;김종대;전귀옥
    • 대한한방내과학회지
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    • 제27권1호
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    • pp.102-113
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    • 2006
  • Objectives & Methods : To obtain the 50% lethal dose(LD50), approximated lethal dose(ALD) and approximated target organs of 'Mahwangyounpae-tang' for further study into such things as repeated dose toxicity, genotoxicity and reproductive toxicity, single dose toxicity was tested in male SD rats according to KFDA Guideline 1999-61[KFDA, 1999] at dosage levels of 2,000, 1,000, 500, 250 and 125 mg/kg/$10m{\ell}$. In this study, mortalities, clinical signs, body weight changes and body weight gains, gross findings and weight of principal organs were detected during and/or after 14 days of single dosing. Results & Conclusions : After 2 or 3 days of dosing, 1 or 2 animals in 2,000 mg/kg-dosing groups died. Excitation and leaping response were observed as test article-treatment related clinical signs. These abnormal signs were restricted to 2,000 and 1,000 mg/kg-dosing groups and survivors recovered to normal within 3 or 4 days after dosing. Significant decrease in body weight were observed in some periods of observation in 2,000 and 1,000 mg/kg-dosing group, from 1 days after dosing compared to those of vehicle control group. Significantly diminished body weight gains were observed in observation periods in 2,000 and 1,000 mg/kg-dosing group compared to those of vehicle control group. Hypertrophy and hemorrhage of heart and decoloration of kidney were observed as test article-treatment related gross findings. These abnormal findings were restricted to 2,000 and 1,000 mg/kg-dosing groups. A significant increase of absolute and relative heart and kidney weight were demonstrated in 2,000 mg/kg-dosing groups. The value for LD50 found in this study was 2,218.57 mg/kg. ALD in this study was 2,000 mg/kg, and the target organs are considered to be the heart and the kidney.

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마황윤폐탕(麻黃潤肺湯) 추출물의 수컷 ICR 마우스에서 경구 단회투여 독성 평가 (Single Dose Toxicity Test of 'Mahwangyounpae-tang' Extract in Male ICR Mouse)

  • 정우식;조동희;서영호;박미연;최해윤;김종대;전귀옥
    • 동의생리병리학회지
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    • 제20권2호
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    • pp.442-448
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    • 2006
  • To obtain the 50% lethal dose (LD50), approximated lethal dose (ALD) and approximated target organs of 'Mahwangyounpae-tang' for further study like repeat dose toxicity, genotoxicity and reproductive toxicity, single dose toxicity was tested in male ICR mouse according to KFDA Guideline 1999-61 [KFDA, 1999] at a dosage level of 2,000, 1,000, 500, 250 and $125\;mg/kg/10m{\ell}$. In this study, mortalities, clinical signs, body weight changes and body weight gains, gross findings and weight of principal organs were detected during and/or after 14 days of single dosing. After 2 or 3 days of dosing, 1 or 2 animals in 2,000 and 1,000 mg/kg-dosing groups were died. Excitation and leaping response were observed as test article-treatment related clinical signs. These abnormal signs were restricted to 2,000 and 1,000 mg/kg-dosing groups and they were recovered to normal within 4 days after dosing in case of survivors. A significant decrease of body weight were observed in some periods of observation in 2,000 and 1,000 mg/kg-dosing group from 1 days after dosing compared to those of vehicle control group. A significant decrease of body weight gains were observed in observation periods in 2,000 and 1,000 mg/kg-dosing group compared to those of vehicle control group. Hypertrophy of heart and decoloration of kidney were observed as test article-treatment related gross findings. These abnormal findings were restricted to 2,000 and 1,000 mg/kg-dosing groups. A significant increase of absolute and relative heart and kidney weight were demonstrated in 2,000 mg/kg-dosing groups. LD50 in this study was detected as 2,242.42 mg/kg. ALD in this study was detected as 1,000 mg/kg and the target organ was considered as the heart and kidney.

갑상선 기능항진증의 $^{131}I$ 치료시 갑상선 조사량에 관한 연구 (A Study on the Radiation Dose of $^{131}I$ in the Thyroid Gland during the Treatment of Hyperthyroidism)

  • 서환조;고창순;이문호
    • 대한핵의학회지
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    • 제9권1호
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    • pp.59-71
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    • 1975
  • 53 patients with hyperthyroidism have been analyzed with special reference to therapeutic response to radioactive iodine ($^{131}I$) treatment. Mean effective half-life, 24 hour uptake rate and radiation dose of $^{131}I$ in hyperthyroid patients included in this study were respectively. 1. Mean effective half-life of $^{131}I\;was\;4.7{\pm}1.5$ days in the tracer dose and $5.0{\pm}1.5$ days in the therapeutic dose. 2. Mean 24 hour uptake rate of $^{131}I\;was\;72.7{\pm}11.1%$ in the tracer dose and $73.4{\pm}12.3%$ in the theapeutic dose. 3. Mean radiation dose of $^{131}I\;was\;5,319{\pm}2,648$ RAD as predicted and $5,692{\pm}2,843$ RAD as actual. A single dose of radioactive iodine treatment was satisfactory in 34 patients (radioiodine sensitive) and multiple doses of radioactive iodine treatments were required in 19 patients (radioiodine resistant). A radioiodine resistant group of patients with hyperthyroidism was distinctively characteristic in the following aspects. 1. Mean thyroid weight calculated in the resistant group ($63.9{\pm}14.0gm$) was significantly (p<0.01) greater than that of the sensitive group ($46.6{\pm}13.3gm$). 2. Mean 24 hour uptake rate of the tracer dose in the resistant group ($67.3{\pm}10.7%$) was significantly (p<0.01) lower than that of the sensitive group ($75.7{\pm}10.5%$). 3. Mean 24 hour uptake rate of the therapeutic dose in the resistant group ($68.5{\pm}13.7%$) was significantly (p<0.05) lower than that of the sensitive group ($76.1{\pm}10.9%$). 4. Mean predicted radiation dose, of $^{131}I$ in the resistant group ($3,684{\pm}1,745$ RAD) was significantly (p<0.01) lower than that of the sensitive group ($6,232{\pm}2,683$ RAD). 5. Mean actual radiation dose of $^{131}I$ in the resistant group ($4,100{\pm}1,691$ RAD) was significantly (p<0.01) lower than that of the sensitive group ($6,582{\pm}3,024$ RAD). 6. No significant difference was detected in terms of effective half-life of $^{131}I$ among the groups (p>0.05). 7. The average mean % difference of effective half-life, uptake rate and radiation dose measured following the tracer and therapeutic dose of $^{131}I$ were not statistically significant (p>0.05). Therefore effective half-life, uptake rate and radiation dose of the therapeutic dose of $^{131}I$ were readily predictable following the tracer dose of $^{131}I$. 8. It is concluded that the possibility of resistance to radioactive iodine treatment may be anticipated in patients with thyroid gland large in size and compromised $^{131}I$ uptake rate.

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Inhibitory Effect of Gamisaenghyeolyunbueum on Mast Cell-Mediated Allergic Inflammatory Reactions

  • Choi Cheol-Ho;Hur Jong-Chan;Kim Hoon;Cho Young-Kee;Moon Mi-Hyun;Baek Dong-Gi;Kim Dong-Woung;Moon Goo;Won Jin-Hee
    • 동의생리병리학회지
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    • 제19권5호
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    • pp.1379-1385
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    • 2005
  • Gamisaenghyeolyunbueum (GSYE) is a traditional Oriental herbal medicine prescription, which has been used for the treatment of various allergic disorders, atopic dermatitis, extravasated bleeding from skin, especially skin related disease. The author investigated the effects of GSYE on mast cell-mediated allergic inflammatory reactions. GSYE dose-dependently (0.01-1 g/kg) inhibited compound 48180-induced systemic anaphylactic shock and ear swelling response. The inhibitory effect of GSYE on the histamine release from rat peritoneal mast cells induced by compound 48f80 reveals significantly (p<0.05) at concentrations ranging from 0.01 to 1 mg/ml in a dose-dependent manner. GSYE also inhibited the passive cutaneous anaphylaxis(PCA) by oral administration at 1 g/kg. In addition, GSYE dose-dependently (0.01-1 g/kg) inhibited the phorbol 12-myristate 13-acetate(PMA) and A23187-induced tumor necrosis $factor-{\alpha}$ secretion from human mast cell line HMC-1 cells. These results indicate that GSYE may be a beneficial applicability in the allergic-related diseases.

Pharmacological Properties of CDBT in Hypoxia-induced Neuronal Cell Injury and Their Underlying Mechanisms

  • Park, Sang-kyu;Jung, Eun-sun;Cha, Ji-yoon;Cho, Hyun-kyoung;Yoo, Ho-ryong;Kim, Yoon-sik;Seol, In-chan
    • 대한한방내과학회지
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    • 제40권3호
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    • pp.425-442
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    • 2019
  • Objectives: This study aimed to reveal the pharmacological properties of the newly prescribed herbal mixture, Chenmadansamgamibokhap-tang(CDBT), against hypoxia-induced neuronal cell injury (especially mouse hippocampal neuronal cell line, HT-22 cells) and their corresponding mechanisms. Methods: A cell-based in vitro experiment, in which a hypoxia condition induced neuronal cell death, was performed. Various concentrations of the CDBT were pre-treated to the HT-22 cells for 4 h before 18 h in the hypoxia chamber. The glial cell BV-2 cells were stimulated with $IFN{\gamma}$ and LSP to produce inflammatory cytokines and reactive oxygen species. When the neuronal HT-22 cells were treated with this culture solution, the drug efficacy against neuronal cell death was examined. Results: CDBT showed cytotoxicity in the normal condition of HT-22 cells at a dose of $125{\mu}g/mL$ and showed a protective effect against hypoxia-induced neuronal cell death at a dose of $31.3{\mu}g/mL$. CDBT prevented hypoxia-induced neuronal cell death in a dose-dependent manner in the HT-22 cells by regulating $HIF1{\alpha}$ and cell death signaling. CDBT prevented neuronal cell death signals and DNA fragmentation due to the hypoxia condition. CDBT significantly reduced cellular oxidation, cell death signals, and caspase-3 activities due to microglial cell activations. Moreover, CDBT significantly ameliorated LPS-induced BV-2 cell activation and evoked cellular oxidation through the recovery of redox homeostasis. Conclusions: CDBT cam be considered as a vital therapeutic agent against neuronal cell deaths. Further studies are required to reveal the other functions of CDBT in vivo or in the clinical field.

유착태반환자의 예방적 내장골동맥 풍선카테터 설치술 시행 시 태아선량 평가 (Evaluation of the Fetal Dose during Prophylactic Placement of Internal Iliac Artery Balloon Occlusion Catheters in Placenta Accreta)

  • 김동식;안성민
    • 대한방사선기술학회지:방사선기술과학
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    • 제39권3호
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    • pp.313-321
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    • 2016
  • 유착태반환자는 분만 시 발생하는 대량의 출혈로 모성 사망률이 높아 수술 중 출혈량 감소를 목적으로 수술 전 예방적 내장골동맥 풍선카테터 설치술(Prophylactic placement of Internal Iliac Artery Balloon Occlusion Catheters;PIIABOCs)을 시행하는데, 시술 중 발생하는 산모와 태아의 방사선 피폭에 대한 연구가 미흡한 실정이다. 본 연구는 PIIABOCs 시술 시 태아가 받는 선량을 측정하여 피폭의 정확한 정보를 제공하고자 본 연구를 시행하였다. MRI영상을 이용하여 선량측정 위치를 설정하고 팬텀과 선량계를 이용하여 실제 시술 시와 같은 환경으로 흡수선량을 측정하였다. 태아의 장기별 평균 흡수선량은 2.38~8.83 mGy로, 중심선속-수정체-위-방광 순으로 높게 측정되었고, 투시시간이 길어질수록, 장기의 위치가 선속의 중심에서 가까울수록, 산모의 복부두께가 두꺼울수록 태아선량이 증가하였다. 조사면적를 각각 25%, 50% 감소시켰을 때 각각 19.0%, 39.4%의 선량 감소, 조사야 전체에 차폐체를 사용하였을 때 약 56.3%의 선량 감소를 보였다. 시술테이블의 높이가 75 cm에서 가장 높게 나타났고 85, 95 cm 순으로 선량 감소를 보였다. 의료행위로 인한 방사선이 태아에게 미치는 영향으로 확률적 영향보다 결정적 영향이 우선 관심사이며 유의한 결정적 영향의 문턱선량은 대략 100 mGy로 알려져 있어, 실험결과 시술 시 태아 장기의 흡수선량은 0.49~18.27 mGy로 문턱선량의 10% 수준임을 확인하였다.

모나자이트 취급공정에서의 라돈 및 토론 노출 특성 (Characteristics of Internal and External Exposure of Radon and Thoron in Process Handling Monazite)

  • 정은교
    • 한국산업보건학회지
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    • 제29권2호
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    • pp.167-175
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    • 2019
  • Objectives: The purpose of this study was to evaluate airborne radon and thoron levels and estimate the effective doses of workers who made household goods and mattresses using monazite. Methods: Airborne radon and thoron concentrations were measured using continuous monitors (Rad7, Durridge Company Inc., USA). Radon and thoron concentrations in the air were converted to radon doses using the dose conversion factor recommended by the Nuclear Safety and Security Commission in Korea. External exposure to gamma rays was measured at the chest height of a worker from the source using real-time radiation instruments, a survey meter (RadiagemTM 2000, Canberra Industries, Inc., USA), and an ion chamber (OD-01 Hx, STEP Co., Germany). Results: When using monazite, the average concentration range of radon was $13.1-97.8Bq/m^3$ and thoron was $210.1-841.4Bq/m^3$. When monazite was not used, the average concentration range of radon was $2.6-10.8Bq/m^3$ and the maximum was $1.7-66.2Bq/m^3$. Since monazite has a higher content of thorium than uranium, the effects of thoron should be considered. The effective doses of radon and thoron as calculated by the dose conversion factor based on ICRP 115 were 0.26 mSv/yr and 0.76 mSv/yr, respectively, at their maximum values. The external radiation dose rate was $6.7{\mu}Sv/hr$ at chest height and the effective dose was 4.3 mSv/yr at the maximum. Conclusions: Regardless of the use of monazite, the total annual effective doses due to internal and external exposure were 0.03-4.42 mSv/yr. Exposures to levels higher than this value are indicated if dose conversion factors based on the recently published ICRP 137 are applied.