• 대한공업교육학회지
• /
• 제38권1호
• /
• pp.275-297
• /
• 2013

발명 교사 교육 표준은 발명 내용학 내용 표준과 발명 교육학 내용 표준으로 구분된다. 이 연구는 발명 내용학 내용 표준을 개발하는데 목적이 있다. 연구의 목적을 달성하기 위한 연구의 방법으로 연구팀 회의, 문헌 고찰, 내용 분석, 개발 연구, 조사 연구, 타당성 검증을 이용하였다. 연구의 결과 개발된 발명 내용학 내용 표준 체계는 10가지의 대영역 발명의 개념과 특성, 발명과 사회, 생활 속의 발명, 창의성 계발, 발명과 설계, 발명 문제 해결, 융합 지식과 발명, 발명 프로젝트, 지식 재산과 특허 출원, 발명과 기술 경영로 구성된다. 그리고 10가지의 대영역은 20가지의 핵심내용(중영역), 90가지의 하위요소로 구성된다. 발명 내용학 내용 표준은 추후 교재를 개발하는데 학문적 기반을 마련해 주었을 뿐만 아니라 향후 발명 교육을 전개할 경우 참조적 표준으로 가치가 충분하다.

• 한국의학물리학회:학술대회논문집
• /
• 한국의학물리학회 2004년도 제29회 추계학술대회 발표논문집
• /
• pp.153-156
• /
• 2004

식품의약품안전청은 1978년 12월 방사선 분야의 국가교정검사기관으로 지정되어 현재까지 Co-60선원을 이용 치료준위 방사선측정기에 대한 교정을 수행하고 있다. 식약청의 에어커마와 물 흡수선량 측정값은 국제도량형국(BIPM)과 측정소급성을 유지하고 있으며, 교정계수의 확장불확도는 0.9 %(k=2)이다. 식약청에서는 외부방사선에 대한 선량보증의 일환으로 1999년 전리함을 이용하여 방사선치료기관의 선량측정을 수행하였으며, 2002년부터 열형광선량계(TLD)를 이용한 선량측정체계를 확립 ${\cdot}$ 운영하고 있다. TLD 판독에 대한 측정불확도는 1.6 %(k=1)이며, 측정불확도를 감안하여 선량보증의 허용한계를 ${\pm}$ 5 %로 설정하였다. TLD 판독값을 선량으로 전환하는 과정에서 선질, 비선형성, 홀더사용 등의 영향을 보정하기 위한 보정정수를 사용하였다. 2003년도 치료방사선 선량보증사업에는 53개 기관(71개 선질)이 참여하였다. 선량보증 결과 71개 선질 중63개 선질(89 %)이 1차 측정에서 허용한계를 만족하였다. 허용한계 초과기관에 대해서는 재측정을 수행하였고, 그 결과 모두 허용한계 이내의 값을 나타냄을 확인하였다.

• 한국의학물리학회지:의학물리
• /
• 제21권1호
• /
• pp.99-112
• /
• 2010

국내에서 방사선치료를 위한 선형가속기 품질관리 프로토콜은 많이 개발되어 왔지만 선형가속기를 기반으로 하는 방사선수술장비의 품질관리 프로토콜 개발은 현재까지 거의 이루어져 있지 않고 있다. 이에 본 연구는 선형가속기 기반 일체형 방사선수술장비인 노발리스의 정확도 및 정밀도를 유지하기 위하여 일간, 주간, 월간, 연간에 주기적으로 시행하여야 하는 노발리스 품질관리 프로토콜을 개발 하고 품질관리 상태의 종합적 확인을 할 수 있는 해부학적 팬텀을 제작하였다. 이를 위하여 국내외의 선형가속기를 이용하는 방사선수술 품질관리 프로토콜의 수집 및 분석을 통해 필수적인 품질관리항목과 각 항목의 허용치를 정하였다. 노발리스 품질관리 항목은 기계적 정확도 부분과 방사선 전달 부분의 2가지로 분리하고 기계적 정확도 부분은 방사선발생 장치부, 보조장치부, 그리고 미세다엽 시준기부의 3가지 부분으로 방사선 전달부분은 치료 중심점 평가와 선량학적 평가의 2가지 부분으로 나누어 작성하였다. 최종적으로 노발리스 품질관리 유지를 위하여 시행하여야 하는 일간, 주간, 월간, 연간의 노발리스 품질관리 항목 표를 완성하였다. 완성된 노발리스 품질관리항목 표는 노발리스가 방사선수술에 적합한 정확도 및 정밀도를 유지하는데 필요한 지표로서 기여 할 수 있을 것이라 생각된다.

• 대한교통학회지
• /
• 제27권2호
• /
• pp.107-115
• /
• 2009

교통섬은 차량과 보행자를 안전하고 질서있게 이동시킬 목적으로 설치하며, 상충하는 교통류를 분리하거나 보행자 대피를 위하여 설치한 차로간의 특정구역이다. 기존의 연구문헌이나 설치기준을 살펴보면 설치목적과 설치효과만 언급하고 있을 뿐 교통섬의 설치여부에 따른 안전성 판단기준이 없는 실정이다. 본 연구에서는 도시부 교차로의 도로조건, 교통조건, 교통사고 자료 등을 분석하여 사고발생여부와 관련성이 높은 변수를 선정하고, 그 변수들과 교차로 보행자 교통사고 발생 여부를 이용하여 로짓모형을 통해 보행자 교통사고 확률모형을 구축하였다. 또한 교차로 설계시 교통량과 교차로 크기에 따른 보행자 교통사고 발생확률을 분석하여 교통섬 설치효과를 보행자 안전측면에서 제시하였다. 분석결과 큰 교차로에서 교통량이 많은 경우 교통섬으로 인해 보행자 교통사고가 발생할 확률이 높은 것으로 나타났으며, 큰 교차로에서 교통량이 적은 경우 교통섬으로 인해 보행자 교통사고 발생확률이 적은 것으로 분석되었다. 이는 교통섬 설치로 인해 모든 교차로에서 보행자가 안전성이 향상되는 것은 아니기 때문에, 교통섬 설치시 보행자 안전 측면을 고려한 설계 및 운영이 필요한 것으로 사료된다.

• Environmental Analysis Health and Toxicology
• /
• 제29권
• /
• pp.12.1-12.8
• /
• 2014

Objectives Cohort studies of associations between air pollution and health have used exposure prediction approaches to estimate individual-level concentrations. A common prediction method used in Korean cohort studies is ordinary kriging. In this study, performance of ordinary kriging models for long-term particulate matter less than or equal to $10{\mu}m$ in diameter ($PM_{10}$) concentrations in seven major Korean cities was investigated with a focus on spatial prediction ability. Methods We obtained hourly $PM_{10}$ data for 2010 at 226 urban-ambient monitoring sites in South Korea and computed annual average $PM_{10}$ concentrations at each site. Given the annual averages, we developed ordinary kriging prediction models for each of the seven major cities and for the entire country by using an exponential covariance reference model and a maximum likelihood estimation method. For model evaluation, cross-validation was performed and mean square error and R-squared ($R^2$) statistics were computed. Results Mean annual average $PM_{10}$ concentrations in the seven major cities ranged between 45.5 and $66.0{\mu}g/m^3$ (standard deviation=2.40 and $9.51{\mu}g/m^3$, respectively). Cross-validated $R^2$ values in Seoul and Busan were 0.31 and 0.23, respectively, whereas the other five cities had $R^2$ values of zero. The national model produced a higher cross-validated $R^2$ (0.36) than those for the city-specific models. Conclusions In general, the ordinary kriging models performed poorly for the seven major cities and the entire country of South Korea, but the model performance was better in the national model. To improve model performance, future studies should examine different prediction approaches that incorporate $PM_{10}$ source characteristics.

• Journal of Pharmaceutical Investigation
• /
• 제39권1호
• /
• pp.65-71
• /
• 2009

The aim of the present study was to evaluate the bioequivalence of two domperidone maleate tablets, Motilium-$M^{(R)}$ Tablet (Janssen Korea Ltd., reference product) and $Toriem^{(R)}$ Tablet (Daewon Pharm. Co., Ltd., test product). Domperidone was extracted by liquid-liquid extraction using tert-butyl methyl ether and separated in less than 3 min on $C_{18}$ reverse-phase column using an isocratic elution. A tandem mass spectrometer, as detector, was used for quantitative analysis in positive mode by a multiple reaction monitoring mode to monitor the m/z $426.1{\rightarrow}119.1$ and the m/z $837.4{\rightarrow}158.2$ transitions for domperidone and the internal standard (roxithromycin), respectively. Calibration curves, from $0.05{\sim}50$ ng/mL of domperidone, showed correlation coefficients (r) higher than 0.9941. Intra day and inter day precision (C.V. %) for quality control were ranged from 10.04 to 16.09% and from 10.87 to 18.69%, respectively. The lower limit of quantification (LLOQ) of domperidone was 0.05 ng/mL. The method described is precise and sensitive and has been successfully applied to the study of bioequivalence of domperidone in 24 healthy Korean volunteers. Twenty-four healthy male Korean volunteers received a single dose of each medicine ($2{\times}12.72\;mg$ domperidone maleate) in a $2{\times}2$ crossover study. There was a one-week washout period between the doses. Plasma concentrations of domperidone were monitored for over a period of 24 hr after the administration. $AUC_{0-t}$ (the area under the plasma concentration-time curve) was calculated by the linear trapezoidal rule. $C_{max}$ (maximum plasma drug concentration) and $T_{max}$ (time to reach $C_{max}$) were compiled from the plasma concentration-time data. The 90% confidence intervals for the log transformed data were within acceptable range of log 0.8 to log 1.25 (e.g., $log\;0.92{\sim}log\;1.05$ for $AUC_{0-t}$, $log\;0.81{\sim}log\;1.05$ for $C_{max}$). The major parameters, $AUC_{0-t}$ and $C_{max}$ met the criteria of KFDA for bioequivalence indicating that $Toriem^{(R)}$ tablet is bioequivalent to Motilium-$M^{(R)}$ tablet.

• 분석과학
• /
• 제16권2호
• /
• pp.152-158
• /
• 2003

본 연구는 인체의 골중 납 농도를 측정하는데 필요한 시료 전처리법과 기기 분석법을 평가하기 위하여 수행되었다. 절단한 인간 사체 다리의 뼈를 상온에서의 산 분해법과 마이크로웨이브 분해법 (microwave oven method)을이용하여 납을 추출하였으며, 유도결합 플라즈마 질량분석법 (ICP-MS)과 흑연로 원자 흡수 분광 광도법 (GF-AAS)으로 납 농도를 측정하였다. 표준시료를 이용하여 회수율을 조사한 결과, 산분해 후 ICP-MS로 측정한 경우 높은 회수율을 보였으나, 산분해 후 GF-AAS로 측정한 것은 표준 농도보다 낮은 값을 보였으며, 마이크로웨이브 분해한 경우는 두 측정기기 모두 표준 농도보다 높은 값을 보였다. 뼈 시료의 경우, 산분해 후 ICP-MS로 측정한 납 농도는 GF-AAS의 값과 높은 상관성을 보였으나 (상관계수 = 0.983), GF-AAS가 ICP-MS보다 계통적으로 높은 값을 측정하였다. 마이크로웨이브 분해 역시 두 분석방법이 높은 상관성을 보였으나 (상관계수 = 0.950), 대체로 산분해에 의한 값보다 높은 농도를 보였다. 결론적으로, 상온에서 질산으로 분해 후 ICP-MS를 이용하여 측정한 것이 골중 납 농도를 결정하는데 편이성과 정확성 면에서 가장 효율적인 방법으로 보인다.

• 한국의료질향상학회지
• /
• 제2권1호
• /
• pp.68-84
• /
• 1995

Background: Guideline for practice is useful because it can be the standard for assessment and way to improve quality. We need to take account of expert opinion and consensus as well as scientific evidences to develope practice guideline because it should be practical. Delphi method has been developed to gather opinions from experts fairly. This study was designed to develop practice guideline and apply it to practices as a method to improve quality in primary medical care. Methods: Hypertension(in adults over 18 years old) was selected as a target problem. Self questionnaires about management of hypertensive patients were developed by a researcher with advice of 11 experts. The questionnaires were designed to response as a 5 pont scale. The results of previous questionary were given to respondents in second and third questionnaires. If needed, the questionnaires were changed on the previous responses. The items with medium greater than or equal to 4 point in 1st and 2nd responses were accepted in guideline. The items with medium lesser than or equal to 3 point were questioned again about whether they can be excluded or not. The criteria for assessment was made with reference to guideline and applied to 85 hypertensive patients of 9 family practitioners. At 3 months after practice guideline had been given to family practitioners, performance of same practitioners was assessed with 36 new hypertensive patients. Results: 23 professors in family medicine, 22 family practitioners and 6 cardiologists, responded among 50, 50, 15 respectively. Practice guideline with 33 items was developed as a result of 3 times questionaires. The difference of responses between professors in family medicine, family practitioners and cardiologists was not significant. Performance of practice was improved in diagnosis, history taking about 6 fields, laboratory examination and decision making about time of pharmaceutical prescription. It was not improved in physical examination, life style modification, method of pharmaceutical prescription, choice of initial antihypertensives and history taking about duration of disease and diet habit. It was decreased in history taking about psychosocial factors. The assessment scores were low in history taking, physical examination and life style modification before and after use of practice guideline. Conclusion: Practice guideline for hypertension could be developed by Delphi method. Performance of practice improved partially after use of guideline.

• 대한미생물학회지
• /
• 제22권1호
• /
• pp.35-53
• /
• 1987

Multiply resistant Shigella strains isolated in Taegu area were subjected for the characterization of R plasmids. All strains isolated in 1984 and 1985 were susceptible to gentamicin, amikacin, and cephalothin, and most strains were susceptible to kanamycin (Km) and rifampin by agar dilution antimicrobial susceptibility test. The resistance frequency of S. flexneri against ampicillin (Ap) was higher than that of S. sonnei. The strains resistant to sulfisomidine (Su) and trimethoprim (Tp) were found at higher frequency in S. sonnei than in S. flexneri. The most prevalent resistance pattern of S. flexneri was chloramphenicol (Cm) tetracycline (Tc) streptomycin (Sm) Ap, followed by the pattern of CmTcSmSuApTp, CmTcSmSuApTp nalidixic acid, and CmTcSmSuAp in the decreasing order. The antibiogram of CmTcSmSuTp was found to be the most frequent pattern in S. sonnei. The ratio of conjugal transfer of S. flexneri was 47% and 75% of S. sonnei. The average number of plasmid harboring in Shigella was 4 and the size of plasmid ranged 1.3 to 134 megadalton (Mdal). Most S. flexneri carried plasmids of 2 to 3 Mdal and S. sonnei carried those of 3 to 4 Mdal size. The sizes of conjugative plasmids ranged 40-90 Mdal. The incompatibility group (Inc) F II plasmids (54-59 Mdal) were most frequent and rare Inc B plasmids (60 Mdal) of isolates in 1979 and 1980 and Inc FI (87 Mdal) of 1983 isolates were able to be classified by the colony test with standard reference plasmids. The R plasmids of known Inc group were tested for the restriction endonuclease analysis. The pattern of plasmids digested by EcoRl were apparently different by the Inc group but there was no significant difference between species or by the resistance patterns. Nonconjugative plasmids and their phenotypes were identified by transformation test. The transformants were resistant to less than two drugs. Colicin producing transformants carried the Col plasmid of 3.7 or 3.9 Mdal size. $Ap^r$ plasmids derived from S. sonnei were found to be mobilized by transfer factor RT641 to E. coli #CS100. $Ap^r$ plasm ids of same size shared by S. flexneri, S. sonnei, and E. coli were digested with Pstl. All of them showed two restriction fragments of 2.8 kilobase(kb) and 0.7kb. Other plasmids ($Sm^r\;Su^r$) derived from S. flexneri, S. boydii, and S. sonnei were digested with Pstl and they showed same restriction fragment patterns of 3.1kb and 2.9kb. The plasmid profiles of three strains of S. sonnei producing colicin and showing same resistance pattern of CmTcSmSuApTpKm appeared to be similar. Restriction patterns by EcoRl and the behavior of plasmids in conjugation or transformation process were also similar between those plasmids. The restriction patterns were significantly different between the plasmids of Inc FI group and those of unclassified Inc group.

• 대한두경부종양학회지
• /
• 제27권2호
• /
• pp.204-209
• /
• 2011

Background and Objectives : The usefulness of fine needle aspiration biopsy(FNAB) for diagnosis of parotid gland tumors is controversial, because of the generalized belief requiring surgery for most parotid tumors. The aim of this study was to evaluate the efficacy of FNAB for diagnosis in parotid gland tumors. Material and Methods : FNAB was performed in 91 patients who underwent parotid surgery at Kangbuk Samsung Hospital from January 2007 to December 2010. The result of FNAB, 11 malignancies and 75 benign tumors and 5 non-neoplasms were analyzed and compared with the final histopathologic diagnoses. Sensitivity, specificity, accuracy, positive predictive value(PPV), and negative predictive value(NPV) were calculated using final histopathologic diagnosis of the surgical specimen as the standard diagnostic reference for comparative analysis. Results : 86 specimens(94.5%) were suitable for evaluation. We compared the result of FNAB and the final histopathology in 79(89.4%) cases. The sensitivity, specificity, accuracy, PPV, and NPV of FNAB for detecting pleomorphic adenoma was 95.8%, 88.4%, 92.3%, 90.2%, and 95.0%. In Warthin's tumor, results were 86.4%, 94.2%, 92.3%, 82.6%, and 95.6%. Among 11 patients who were diagnosed with malignancy on final histopathologic report, only 3(30%) patients were diagnosed with the same as on FNAB, the other 8 patients were initially diagnosed incorrectly as benign tumors in FNAB. There were no complications related to FNAB. Conclusion : Diagnostic accuracy for FNAB in benign parotid tumors was high. However, in malignant tumors, FNAB shows low diagnostic usefulness compared with benign tumors. FNAB can be effective and safe diagnostic technique for evaluating the benign parotid glands tumors.