• 제목/요약/키워드: MS analysis

검색결과 3,904건 처리시간 0.029초

경락시스템의 층차적 모형에 관한 고찰 (A Study on the dimensional model of the meridian system)

  • 최환수
    • Journal of Acupuncture Research
    • /
    • 제20권2호
    • /
    • pp.1-10
    • /
    • 2003
  • Objective : It is limited to verify existence and a part of characteristic of MS(Meridian system) in modern MS hypothesis. Because it is that an object of scientific approach is to prove a structure of MS. Then according to DMMS, we will research on a subject of MSs rules. This is a paper on the investigation of DMMS in aspects of propriety and supplement. Results : DMMS is composed of organizational anatomy system, MS, signal system. This means that the contents of classic MS theory divide into three dimensions. It includes classic MS theory and explains modern MS hypothesis with DMMS. But is has two problems that one is the difference between the right side and the left in the same meridian and the other is a lack of dynamic idea(動態觀念). After apply this ti analysis system, it will be reasonable to DMMS. It indicates to use various ways of a science, especially, mathematics, system theory, information theory, control theory to supplement the DMMS. Conclusions : Although the scientific study of MS is stagnant, the approach of this DMMS will provide us with a new result of MS.

  • PDF

Analysis and Detection of Malicious Data Hidden in Slack Space on OOXML-based Corrupted MS-Office Digital Files

  • Sangwon Na;Hyung-Woo Lee
    • International journal of advanced smart convergence
    • /
    • 제12권1호
    • /
    • pp.149-156
    • /
    • 2023
  • OOXML-based MS-Office digital files are extensively utilized by businesses and organizations worldwide. However, OOXML-based MS-Office digital files are vulnerable to forgery and corruption attack by including hidden suspicious information, which can lead to activating malware or shell code being hidden in the file. Such malicious code can cause a computer system to malfunction or become infected with ransomware. To prevent such attacks, it is necessary to analyze and detect the corruption of OOXML-based MS-Office files. In this paper, we examine the weaknesses of the existing OOXML-based MS-Office file structure and analyzes how concealment and forgery are performed on MS-Office digital files. As a result, we propose a system to detect hidden data effectively and proactively respond to ransomware attacks exploiting MS-Office security vulnerabilities. Proposed system is designed to provide reliable and efficient detection of hidden data in OOXML-based MS-Office files, which can help organizations protect against potential security threats.

Comparative Investigation of Flavors in Cigarettes by Electronic Nose and GC/MS

  • Lee, Yelin;Park, Jin-Won;Lee, Hwan-Woo;Lee, Seung-Yong;Lee, Hyung-Suk
    • 한국연초학회지
    • /
    • 제35권1호
    • /
    • pp.20-27
    • /
    • 2013
  • An Electronic Nose(E-Nose) and Gas Chromatography/Mass Spectroscopy (GC/MS) are meanwhile conventional technique to analyze volatile materials in many industries (e.g., food, medicine, environment) and have broad acceptance in the analysis of tobacco products. In this study, an experiment where tin oxide gas sensor array responses and GC/MS profiles are used to characterize the volatile compounds of different cigarettes at the same time is performed and the measurements of two instruments are compared for cigarette samples with a known chemical information. E-Nose and GC/MS were employed to differentiate and match flavored cigarettes with commercial tobacco flavoring agents (lavender, vanilla, peppermint, orange, star anise). For verifying reliability of two systems, the analyses were conducted in terms of amount of flavors in each cigarettes using partial least squares (PLS) and with the principal components analysis (PCA). Various chemical sensors and GC/MS data was reduced into two principal factors (PC1, PC2) for being distinguished with visualized regions. Both systems provided adequate results for odor characteristics of cigarettes in this study with each instrument having its own advantages and disadvantages.

Maternal 3-methylcrotonyl-coenzyme A carboxylase deficiency with elevated 3-hydroxyisovalerylcarnitine in breast milk

  • Cho, Kyung Lae;Kim, Yeo Jin;Yang, Song Hyun;Kim, Gu-Hwan;Lee, Jun Hwa
    • Clinical and Experimental Pediatrics
    • /
    • 제59권sup1호
    • /
    • pp.41-44
    • /
    • 2016
  • We report here a case of maternal 3-methylcrotonyl-coenzyme A carboxylase (3-MCC) deficiency in a Korean woman. Her 2 infants had elevated 3-hydroxyisovalerylcarnitine (C5-OH) on a neonatal screening test by liquid chromatography-tandem mass spectrometry (LC-MS/MS), but normal results were found on urine organic acid analysis. The patient was subjected to serial testing and we confirmed a maternal 3-MCC deficiency by blood spot and breast milk spot test by LC-MS/MS, serum amino acid analysis, urine organic acid and molecular genetic analysis that found c.838G>T (p.Asp280Tyr) homozygous mutation within exon 9 of the MCCB gene. Especially, we confirmed marked higher levels of C5-OH on breast milk spot by LC-MS/MS, in the case of maternal 3-MCC deficiency vs. controls.

NEAR INFRARED TRANSFLECTANCE SPECTROSCOPY (NIRS) IN PHYTOCHEMISTRY

  • Huck, C.W.;W.Guggenbichler;Bonn, G.K.
    • 한국근적외분광분석학회:학술대회논문집
    • /
    • 한국근적외분광분석학회 2001년도 NIR-2001
    • /
    • pp.3114-3114
    • /
    • 2001
  • During the last years phytochemistry and phytopharmaceutical applications have developed rapidly and so there exists a high demand for faster and more efficient analysis techniques. Therefore we have established a near infrared transflectance spectroscopy (NIRS) method that allows a qualitative and quantitative determination of new polyphenolic pharmacological active leading compounds within a few seconds. As the NIR spectrometer has to be calibrated the compound of interest has at first to be characterized by using one or other a combination of chromatographic or electrophoretic separation techniques such as thin layer chromatography (TLC), high performance liquid chromatography (HPLC), capillary electrophoresis (CE), gas chromatography (GC) and capillary electrochromatography (CEC). Both structural elucidation and quantitative analysis of the phenolic compound is possible by direct coupling of the mentioned separation methods with a mass spectrometer (GC-MS, LC-MS/MS, CE-MS, CEC-MS) and a NMR spectrometer (LC-NMR). Furthermore the compound has to be isolated (NPLC, MPLC, prep. TLC, prep. HPLC) and its structure elucidated by spectroscopic techniques (UV, IR, HR-MS, NMR) and chemical synthesis. After that HPLC can be used to provide the reference data for the calibration step of the near infrared spectrometer. The NIRS calibration step is time consuming, which is compensated by short analysis times. After validation of the established NIRS method it is possible to determine the polyphenolic compound within seconds which allows to raise the efficiency in quality control and to reduce costs especially in the phytopharmaceutical industry.

  • PDF

생체시료 중 멜라민 화합물의 미량분석법 개발연구 (Establishment of Analytical Methods for Melamine Related Compounds in Biological Samples)

  • 한경문;김진호;조수열;심선보;이진희;이지현;황의선;김성일;조양하;채갑용;권순재;이준호
    • 한국식품위생안전성학회지
    • /
    • 제26권2호
    • /
    • pp.125-141
    • /
    • 2011
  • 본 연구에서는 비료나 수지의 원료물질로 알려진 멜라민이 최근 수입식품 및 가공식품 등에서 검출되어 국제적으로 문제가 되어 생체시료 중 멜라민의 분석법을 확립하고 벨리데이션을 실시하여 신뢰성을 확보하고자 하였다. 생체시료(뇨 및 혈액) 중 멜라민 및 시아누르산 분석을 위해 단백질 침전법, 액체상 추출법으로 불순물을 제거하였고 LC/MS를 이용한 멜라민 최적분석법의 벨리데이션 결과에서 검출한계는 0.2 ng/mL(멜라민), 2.0 ng/mL(시아누르산)이었으며 각 정량범위내의 직선성은 0.9990이상을 가졌다. 뇨및 혈 중 멜라민의 quality control 시료는 0.5 ng/mL, 0.8 ng/mL, 2.0 ng/mL, 3.0 ng/mL으로서 뇨 중 멜라민 및 시아누르산의 정확성은 91.6%-107.6%범위를 나타내었고 정밀성은 2.0%-11.8%으로 나타났다. 혈 중 멜라민 및 시아누르산의 정확성은 94.9%-119.0%범위를 나타내었고 정밀성은 3.7%-13.5%으로 나타났다. 또한, GC/MS를 이용한 멜라민 분석의 검출한계는 5.0 ng/mL(멜라민), 5.0 ng/mL(시아누르산)이었고, 뇨 및 혈중 멜라민의 quality control 시료는 10.0~40.0 ng/mL이었으며, 뇨 및 혈 중 멜라민 및 시아누르산의 정확성은 83.7%~ 10.7% 범위를 나타내었고, 정밀성은 3.5%-13.8% 으로 나타났다.

ICP-MS에 의한 지하수 중의 Germanium 분석에 관한 연구 (Determination of Germanium in Spring Waters by Inductively Coupled Plasma Mass Spectrometry)

  • 박경수;송승연;심의섭;김선태
    • 분석과학
    • /
    • 제11권2호
    • /
    • pp.120-124
    • /
    • 1998
  • 지하수 중의 극미량 germanium을 ICP-MS로 신속, 정확하게 분석할 수 있었으며 질량수 74를 분석하는 것이 가장 방해영향이 적음을 알 수 있었다. 지하수 중의 약 30%만이 $0.1{\mu}g/L$ 이상의 germanium을 함유하였고, 유기 germanium을 포함하는 지하수의 존재도 확인하였다.

  • PDF

LC/ESI-MS를 이용한 아미트롤의 정성확인 및 정량분석 (Quantitative Analysis and Qualification of Amitrole Using LC/ESI-MS)

  • 박찬구;어수미;김민영;손종열;모세영
    • 분석과학
    • /
    • 제17권2호
    • /
    • pp.117-129
    • /
    • 2004
  • 본 연구에서는 극성이 높고, 휘발성이 낮아 GC나 GC/MS로 분석이 곤란한 환경매체 중의 아미트롤을 LC/ESI/MS를 사용하여 분석한 결과 다음과 같은 결론을 얻었다. 분자량이 84인 아미트롤은 LC/ESI/MS 방식에서는 m/z 85인$(M+H)^+$형태로 나타났으며, 피크강도는 30V에서 (SIR mode) 최대를 나타내었다. 질량 스펙트럼 비를 정성확인에 적용하기 위하여 실험한 결과 아미트롤은 m/z 85 와 m/z 58 이온으로 나타났으며, 50V에서 이 비는 1 : 7.03~7.58 로 나타났다. 동위원소 비를 이용한 정성확인은 isotope MS나 HR/MS가 주로 사용되나, 본 연구에서는 정성확인을 위한 보조수단으로 이용하고자 실험한 결과 아미트롤의 동위원소는 $86([M+H])^+$ 형태로 나타났으며, 시료에서(30V) m/z 85와 m/z 86의 질량 스펙트럼 비는 27.1~28.6 : 1(이론적 비 26.6 : 1)로 나타났다. 단계별 표준액을 시료의 전 처리 방법과 동일하게 처리하여 분석한 검량선의 직선성은 $y=1.09354e^6X+26947.2$이었으며, $r^2=0.99$로 나타났다. 분석의 정도관리를 위한 회수율검정과 반복 재현성을 알아보기 위한 실험에서 수질시료의 회수율은 77.64~83.44%, 토양시료에서는71.11~79.44%로 나타났으며, 각 농도 단계별 반복(5회)실험결과 상대표준편차 값은 10%이하를 나타내었다.

황칠나무(Dendropanax morbiferus) 잎 추출물의 LC-MS/MS 분석 및 항산화 효과 (LC-MS/MS analysis and antioxidant activity of Dendropanax morbiferus extract.)

  • 김민정;손재동;양예진;허지웅;이후장;박광일
    • 대한한의학방제학회지
    • /
    • 제32권3호
    • /
    • pp.235-245
    • /
    • 2024
  • Objective : The study's objective is to assess the components of Dendropanax morbifera (DM) utilizing UPLC-MS/MS and assess their antioxidant properties in order to establish fundamental information for quality control of herbal formulations. Methods : The DM leaves were ground into powder and extracted with water at 80℃. The extract was subsequently concentrated and subjected to freeze-drying for subsequent analysis. The LC-MS/MS analysis was performed using a 1260 series HPLC system and a 3200 QTrap tandem mass system in positive ion mode, with detection conducted at 280 nm. The Folin-Ciocalteu method was employed to measure the phenolic content, while a colorimetric method using aluminum chloride was used to determine the flavonoid content, with gallic acid and quercetin as standards, respectively. The evaluation of antioxidant activity was conducted through the measurement of DPPH radical scavenging activity, by adding the DPPH solution to the extract and recording the absorbance at 517 nm. Results : The UPLC-MS/MS analysis identified five polyphenolic compounds in the DM extract, specifically syringin, 6-hydroxyluteolin 7-O-laminaribioside, shaftoside, rutin, and kaempferol-3-O-rutinoside. The extract was found to contain a total phenolic content of 83.106 ± 0.21 mg GAE/g and a total flavonoid content of 87.963 ± 1.014 mg QE/g. The DM extract demonstrated substantial antioxidant properties, resulting in a reduction of DPPH radicals that was evident at concentrations as low as 40 ㎍/㎖. Conclusions : The study determined important polyphenolic compounds in DM and established its considerable antioxidant efficacy. These findings provide evidence for the efficacy of DM in disease prevention related to oxidative stress and establish a foundation for ensuring quality control in herbal preparations.

Direct Analysis in Real Time Mass Spectrometry (DART-MS) Analysis of Skin Metabolome Changes in the Ultraviolet B-Induced Mice

  • Park, Hye Min;Kim, Hye Jin;Jang, Young Pyo;Kim, Sun Yeou
    • Biomolecules & Therapeutics
    • /
    • 제21권6호
    • /
    • pp.470-475
    • /
    • 2013
  • Ultraviolet (UV) radiation is a major environmental factor that leads to acute and chronic reactions in the human skin. UV exposure induces wrinkle formation, DNA damage, and generation of reactive oxygen species (ROS). Most mechanistic studies of skin physiology and pharmacology related with UV-irradiated skin have focused on proteins and their related gene expression or single-targeted small molecules. The present study identified and analyzed the alteration of skin metabolites following UVB irradiation and topical retinyl palmitate (RP, 5%) treatment in hairless mice using direct analysis in real time (DART) time-of-flight mass spectrometry (TOF-MS) with multivariate analysis. Under the negative ion mode, the DART ion source successfully ionized various fatty acids including palmitoleic and linolenic acid. From DART-TOF-MS fingerprints measured in positive mode, the prominent dehydrated ion peak (m/z: 369, M+H-$H_2O$) of cholesterol was characterized in all three groups. In positive mode, the discrimination among three groups was much clearer than that in negative mode by using multivariate analysis of orthogonal partial-least squares-discriminant analysis (OPLS-DA). DART-TOF-MS can ionize various small organic molecules in living tissues and is an efficient alternative analytical tool for acquiring full chemical fingerprints from living tissues without requiring sample preparation. DART-MS measurement of skin tissue with multivariate analysis proved to be a powerful method to discriminate between experimental groups and to find biomarkers for various experiment models in skin dermatological research.