• 제목/요약/키워드: Quantitative analytical method

검색결과 461건 처리시간 0.025초

폐콘덴서의 절록유 중에 함유된 PCB 분석에 관한 연구 (A Study on PCB Analysis of Insulating Oil in Waste Condenser)

  • 김귀자;박재주
    • Environmental Analysis Health and Toxicology
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    • 제4권1_2호
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    • pp.11-17
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    • 1989
  • A quantitative analytical method of highly concentrated PCB is established in the research. With the quantitative analytical method PCB of insulating oil was examined. The following conclusions are derived from this research. 1. The recovery ratio was 95.7% with the quantitative analytical method, which indicates it can be used for the analysis of PCB. 2. PCB concentration of insulation oil in waste condenser was found to be 21.2% thru 13.85% , which was highly concentrated. 3. PCB insulation oil in waste condenser was same as PCB-42.

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Quantitative analysis and validation of naproxen tablets by using transmission raman spectroscopy

  • Jaejin Kim;Janghee Han;Young-Chul Lee;Young-Ah Woo
    • 분석과학
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    • 제37권2호
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    • pp.114-122
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    • 2024
  • A transmission Raman spectroscopy-based quantitative model, which can analyze the content of a drug product containing naproxen sodium as its active pharmaceutical ingredient (API), was developed. Compared with the existing analytical method, i.e., high-performance liquid chromatography (HPLC), Raman spectroscopy exhibits high test efficiency owing to its shorter sample pre-treatment and measurement time. Raman spectroscopy is environmentally friendly since samples can be tested rapidly via a nondestructive method without sample preparation using solvent. Through this analysis method, rapid on-site analysis was possible and it could prevent the production of defective tablets with potency problems. The developed method was applied to the assays of the naproxen sodium of coated tablets that were manufactured in commercial scale and the content of naproxen sodium was accurately predicted by Raman spectroscopy and compared with the reference analytical method such as HPLC. The method validation of the new approach was also performed. Further, the specificity, linearity, accuracy, precision, and robustness tests were conducted, and all the results were within the criteria. The standard error of cross-validation and standard error of prediction values were determined as 0.949 % and 0.724 %, respectively.

육두구(Myristica fragrans Houttuyn) 내의 myristicin의 분리 및 HPLC를 이용한 함량분석 방법 밸리데이션 (Isolation and Quantitative Determination Method Validation of myristicin from Myristica fragrans Houttuyn)

  • 김수환;이동호;권수한;임병호;이상훈;민범찬
    • 생약학회지
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    • 제38권1호
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    • pp.19-21
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    • 2007
  • Myristica fragrans has been used for the treatment of stomachache in East Asia. It is very important to determine the amount of myristicin in Myristica fragrans, because excess myristicin causes side effects. In this study, we developed and validated the method for determination contents of myristicin in Myristica fragrans which was purchased from various regions of Korea. The average content of myristicin in Myristica fragrans was 2.10% with the validated HPLC analysis method.

Quantitative Analytical Method for Eighteen Marker Compounds in Ongyeong-tang, a Traditional Herbal Formula, Using High-Performance Liquid Chromatography for Quality Assessment

  • Kim, Jung-Hoon;Shin, Hyeun-Kyoo;Seo, Chang-Seob
    • 대한본초학회지
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    • 제30권4호
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    • pp.11-20
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    • 2015
  • Objectives : Ongyeong-tang (OGT) is a traditional herbal formula used to cure gynaecological disorders. OGT consists of 12 herbal medicines containing various bioactive components. Therefore, the development of suitable analytical method for the marker compounds is necessary for the quality control of OGT. Methods : Determination of the 18 marker compounds in OGT preparations was quantitatively performed by high-performance liquid chromatography-photodiode array detection analysis. The marker compounds were separated on a reversed-phase C 18 column and the analytical method was successfully validated, which was applied to compare OGT extracts from laboratory preparation and commercial OGT granules. Results : Limit of detection and limit of quantification values were in the ranges of $0.001-0.016{\mu}g/mL$ and $0.003-0.047{\mu}g/mL$, respectively. Precision was 0.03-3.71 % within a day and 0.03-3.81 % over four consecutive days. Recovery of marker compounds ranged from 90.63-108.26 %, with relative standard deviation (RSD) values < 4.0 %. Reproducibility was < 2.5 % of the RSD value. The 18 marker compounds were stable within 16 h at $10^{\circ}C$, with the RSD value < 3.5 %. Quantitative analysis results showed that the quantities of the 18 marker compounds varied among OGT samples. Pearson coefficient evaluation and principal component analysis demonstrated that an OGT water extract produced by a laboratory method clearly differed from commercial OGT granules. Conclusions : The developed analytical method was simple, precise, and reliable. Therefore, it can be used for the quality assessment of OGT preparations.

실험실 GC-MS를 이용한 사고대비물질 분석방법 연구 (Study on the analytical method using GC-MS for the accident preparedness substances)

  • 김기준;이진선;이수영;황승률;김영희;석광설
    • 분석과학
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    • 제26권1호
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    • pp.80-85
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    • 2013
  • 본 연구는 유해화학물질관리법에 지정되어 있는 사고대비물질에 대한 실험실적 분석방법을 정립하기 위한 것으로, GC/MS 분석이 가능한 25종 사고대비물질을 대상으로 정량분석을 수행하였다. GC/MS 정량분석결과 69종 사고대비물질 중 산화프로필렌(propylene oxide) 등 21개 물질에 대한 결정계수($r^2$)는 0.998 이상을 보였고, 포스겐(phosgene)의 결정계수는 0.994, 노말-부틸아민(n-butyl amine) 외 1종은 0.987, 에틸렌디아민(ethylene diamine)은 0.958의 결정계수를 보였다. 동일한 GC/MS 분석 조건으로 표준물질을 분석한 결과 총 25종에 대한 검량선이 작성되었다. 현재 사고대비물질에 대한 분석 연구가 필요한 상황에서, 본 연구결과는 화학사고 사후 환경 영향 조사를 위한 정량분석에 도움이 될 것으로 판단된다.

QbD6시그마 프로세스를 통한 D-항원 정량 시험법의 유효성과 동등성에 관한 연구 (A Study on the Efficacy and Equivalence of D-antigen Quantitative Analysis through QbD6sigma Process)

  • 김강희;김현정
    • 품질경영학회지
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    • 제50권4호
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    • pp.831-842
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    • 2022
  • Purpose: This study carried out the Quality by Design (QbD)6σ process to verify the effectiveness and equivalence of the finished D-antigen quantitative test method, and compared the OFAT-based method validation and test result acceptance criteria with the Analytical Quality by Design (AQbD)-based method validation and test method. This is a study on how to reduce the risk of delay in permit change by increasing the reliability of permit data in the existing method by statistically analyzing the results. Methods: With the QbD6σ process, the effectiveness and equivalence of the D-antigen quantitative test method were verified with the data of the existing test method and the new test method. Results: Method validation tests are performed based on AQbD. Critical Method Parameters are identified through risk assessment, and single/combined actions are verified by designing and performing tests for Critical Method Parameters (analysis of variance, full factorial design method). Method validation can be effectively accomplished with the QbD6σ process. Conclusion: The use of QbD6σ can be used to achieve satisfactory results for both pharmaceutical companies and regulators by using appropriate statistical analytical methods for method validation as required by regulatory agencies.

A preliminary study of semi-quantitative, comparative evaluation of split or half fingerprints using Densitometric Image Analysis (DIA) - Inter-analyst differences for split or half fingerprints -

  • Song, Minkyu;Kim, Seung-chan;Choi, Sung-Woon
    • 분석과학
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    • 제34권2호
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    • pp.56-67
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    • 2021
  • Due to the difficulty of grading visualized fingerprints with previously known evaluation methods for the comparison of split fingerprints, a preliminary study was performed with the densitometric image analysis (DIA) method as a potential quantitative and supplementary evaluation method. Each image of inked split fingerprints was divided into 4 zones for analysis. Weekly intra- and inter- analysis by two analysts with three whole fingerprints that were constructed by combining inked split fingerprints showed that the average area values and the ranges of difference fluctuation were not significantly different between strong fingerprints and strong-weak pairs, while they were different in weak fingerprints and weak-weak pairs. In the case of weak fingerprints, the exact acquisition of ridges was difficult and this seemed to influence the results. An additional study is needed for the improved reliability using DIA method with weak fingerprints such as 8 zones division rather than 4 zones. In addition, the analysis results performed by several analysts at different times should be used to improve the reliability of the analysis method further. Based on the above result, it can be judged that utilizing the DIA method as a secondary evaluation method of the existing scoring system would be effective with the additional studies especially on weak fingerprints.

유처리제의 방향족 탄화수소 정량방법에 대한 표준화 (Standardization for Quantitative Analysis of Aromatic Hydrocarbon in Oil Spill Dispersant)

  • 조종희;임윤택;김우석;윤영자;김신종
    • 한국응용과학기술학회지
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    • 제19권4호
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    • pp.302-310
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    • 2002
  • Demand for organic analysis increase as industries are growing and many products are spreaded in the daily life. One of many products is oil spill dispersant. It was used for oil accident in the ocean. When oil spill dispersant spread at the ocean, the petroleum in the ocean is dispersed. The oil spill dispersant is made of non ionic surfactant and petroleum oil. The non ionic surfactant disperse petroleum from oil accident. The other part is petroleum oil which has aromatic hydrocarbon. Because the aromatic hydrocarbon is cancerogenic material, it directly injure animals in the ocean. This cause the second pollution in the human body. Many oil accidents still are controlled by oil spill dispersant. Therefore quality control of the oil spill dispersant become important and this also demand for the exact quantitative analysis of aromatic hydrocarbon. Hereupon the first we develop separate petroleum oil from surfactant. The second standardize analytical method of aromatic hydrocarbon in the separated petroleum oil.

남조류 독소 정량을 위한 스트립분석법과 HPLC 분석법의 비교 (Comparison of strip analysis and HPLC analysis for the quantitative analysis of cyanobacterial toxin)

  • 표동진;임미연
    • 분석과학
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    • 제28권3호
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    • pp.168-174
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    • 2015
  • 남조류 독소인 마이크로시스틴은 여름철 우리나라 여러 호수들에 존재하여 물고기와 가축 그리고 인간에게 강한 독성을 나타내는 독소이다. 본 논문에서는 이러한 수중 남조류 독소, 마이크로시스틴을 정량분석하는 두가지 방법, 즉 고성능 액체크로마토그래피(HPLC) 분석법과 최근 우리 실험실에서 개발한 스트립분석법의 비교를 시도하였다. 두 분석법의 측정가능농도범위가 많이 달라 HPLC 법으로 먼저 측정한 후 시료를 물로 희석시켜 스트립분석법에 적용하였다. 서로 다른 농도의 마이크로시스틴을 함유한 7가지 물시료들을 사용하여 HPLC분석법과 스트립 분석법으로 남조류 독소 총량을 측정하였다. 그 결과 두 분석법의 정량측정결과가 매우 잘 일치하는 것을 볼 수 있었다. 두 분석법의 상관분석 결과 r 값은 0.99998 이었으며 통계적인 유의성을 나타내는 p 값은 0.00001 이었다.

지역규모의 지형경관 보전을 위한 상대고도 분석 방법론 제안 : 분석범위 설정을 중심으로 (Suggestion of the Relative Elevation Analysis Methods for Conservation of Local Topography : Focused on Analysis Range)

  • 송원경
    • 한국환경복원기술학회지
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    • 제17권5호
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    • pp.19-28
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    • 2014
  • Given the structure of Korean mountains, it is more appropriate to apply the relative elevation method than the absolute elevation method. However, so far there were not suitable quantitative methodologies to analyze relative elevation, these analytical concepts were difficult to be utilized in urban environmental planning. This study suggested three methods for analyzing relative elevation, and one method for setting the analytical scope of relative elevation by calculating terrain relief. The results showed that the procedure considering 500m radius of each point and standardizing to 30% of the 7th height ridge was the most effective method to extract the local topography. This methodology is the quantitative tool to be able to conserve local important hills and ridges, and apply to fields of urban environmental planning and ecological restoration, especially urban ecological network.