• Communications for Statistical Applications and Methods
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• 제29권2호
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• pp.151-160
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• 2022

The total system is composed of the main system (MS) and the failure detection equipment (FDE) which detects failures of MS. The analysis of system reliability is performed when the failure of FDE is possible. Several repair policies are considered to determine the order of repair of failed systems, which are sequential repair (SQ), priority repair (PR), independent repair (ID), and simultaneous repair (SM). The states of MS-FDE systems are represented by Markov models according to repair policies and the main purpose of this paper is to derive the system availabilities of the Markov models. Analytical solutions of the stationary equations are derived for the Markov models and the system availabilities are immediately determined using the stationary solutions. A simple illustrative example is discussed for the comparison of availability values of the repair policies considered in this paper.

• 천문학회지
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• 제45권2호
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• pp.25-29
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• 2012

New methods are developed to estimate the effective temperature (Te), surface gravity (log g), and metallicity ([A/H]) simultaneously with the spectral line depth ratios. Using the model atmosphere grids, depth values are calculated for the wavelength range of $4000{\AA}-5600{\AA}$ for various temperatures, gravities, and metallicities. All possible different combinations of line depth ratios for different pairs of ratios are investigated. A graphical 3D figure is produced with X, Y, and Z axes corresponding to Te, log g, and [A/H], respectively. By reading a cross point of two curves plotted by a connection of three parameters obtained from spectral line depth ratio pairs on each of the three projected planes, Te, log g, and [A/H] are determined simultaneously. In addition, an analytical method is devised based on the similar algorithm developed for the graphical method. Our methods were applied to estimate the fundamental atmospheric parameters of the Sun and Arcturus.

• 대한화학회지
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• 제53권6호
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• pp.717-726
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• 2009

Triton X-100이 함유된 상태에서 정색시약인 1-(2-thiazolylazo)-2-naphthol이 첨가된 물에서 구리 (II), 니켈(II)과 아연(II)의 동시 분광광도법적 정량을 위한 다변량 모델들이 개발되었다. 분광학적 간섭의 단점을 극복하기 위해서, 주성분회귀분석법(PCR)과 부분최소자승법(PLS) 다변량 분석법적 접근이 적용되었다. 다양한 시험 세트를 사용하여 본 방법의 수행이 입증되었고 그 결과들이 비교되었다. 일반적으로 PLS와 PCR 모델들 사이에 분석적 수행에서의 심각한 차이가 없었다. $Cu^{2+}$, $Ni^{2+}$ and $Zn^{2+}$ 의 세 성분들을 사용한 예측의 제곱근 평균 제곱 오차(RMSEP)들은 각각 0.018, 0.010, 0.011 ppm이었다. 또한 감도, 분석감도, 검출한계(LOD)와 같은 가치들의 측면들이 평가되었다. 본 논문에서 제안하는 과정이 화합물 혼합용액과 수돗물 속의 $Cu^{2+}$, $Ni^{2+}$ and $Zn^{2+}$의 동시 검출에 적용되었을 때에 높은 신뢰도가 성취되었다.

• 한국식품위생안전성학회지
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• 제30권2호
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• pp.143-149
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• 2015

건강기능식품 등 중 수용성 비타민 B군 (비타민 $B_1$, 비타민 $B_2$, 나이아신, 비타민 $B_6$)의 동시분석 방법을 확립하기 위하여 본 연구를 실시하였다. HPLC에 의한 수용성 비타민 B군의 분석 방법은 기기분석조건을 확립하고, 국내외 시험법 및 논문을 참고하여 시험 데이터를 분석하였다. 수용성 비타민 B군의 HPLC 분석은 270 nm에서 Capcell Pak C18 UG 120 컬럼을 사용하여 진행되었다. 분석법 검증은 수용성 비타민 B군의 직선성, 정확성, 정량한계, 정밀성에 대해 수행되었다. 직선성은 비타민 $B_1$, 비타민 $B_2$, 나이아신(nicotinic acid, nicotinamide), 비타민 $B_6$ 모두 $0.1{\sim}2{\mu}m/mL$의 농도범위에서 $R^2=0.999$ 이상의 우수한 직선성을 확인할 수 있었다. 회수율을 검토한 결과, 비타민 $B_1$ 100~103%, 비타민 $B_2$ 104~112%, nicotinic acid 82~85%, nicotinamide 121~124%, 비타민 $B_6$ 95~104%의 양호한 회수율을 확인할 수 있었다. LOQ는 비타민 $B_1$ $0.04{\mu}m/mL$, 비타민 $B_2$ $0.05{\mu}m/mL$, nicotinic acid $0.15{\mu}m/mL$, nicotinamide $0.08{\mu}m/mL$, 비타민 $B_6$ $0.63{\mu}m/mL$ 이었다. 정밀성을 검토한 결과, $B_1$ 0.4%, 비타민 $B_2$ 0.4%, nicotinic acid 0.5%, nicotinamide 0.7%, 비타민 $B_6$ 0.4%로 1% 이내로 양호한 재현성을 확인할 수 있었다. 또한 동시분석법의 정확성을 검증하기 위하여 어린이 기호식품 및 건강기능식품의 표시함량 모니터링을 수행한 결과, 모두 표시기준에 적합함을 확인할 수 있었다.

• 분석과학
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• 제24권3호
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• pp.159-167
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• 2011

식물 체중에 포함되어 있는 항산화제로서 주목받고 있는 게르마늄과 셀레늄의 극미량 분석에 있어서의 재현성 있는 분석방법을 제시하고자 수소화물생성장치와 유도결합플라스마질량분석기를 이용하여 분석하였다. 유도결합플라스마질량분석기에 일반적으로 사용되는 torch 대신 에너지 밀도를 높여 이온 간섭, 분자이온 생성 등의 간섭현상을 줄일 수 있는 mini torch를 사용하여 산 종류와 농도의 영향, 수소화물의 생성을 위한 환원조건, 시료 전처리 방법의 차이 등 다양한 조건하에서 상추 중의 게르마늄과 셀레늄을 분석하였다. 분석의 정확성을 평가하기 위하여 회수율 검증과 셀레늄의 표준시료인 SRM-1547, 1570a을 분석하여 기준 값과 비교함으로서 분석의 정확성을 평가하여 다음과 같은 결론을 얻었다.

• 분석과학
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• 제8권4호
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• pp.759-770
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• 1995

By extensive studies with the quantitative status of the mineral constituents of thousands of water samples, it was found that almost in all natural waters irrespective of the surface or sub-surface sources, minimum 99.5% of the total amount of the cationic constituents are generally the contributions of 3 commonly present parameters viz. Ca, Mg and Na and that of the anionic species are same and contributed by $HCO_3$, Cl and $SO_4$ only. In the field of water works, all these major mineral substances are conventionally measured as their individual ions. But till now, no reliable and generalised methods or rules have been developed for the determination of the exact kinds of the individual salt components and their amounts from these ionic constituents normally present in water. As salt content, only the TDS (Total Dissolved Solids) parameter is frequently measured by evaporation of the water sample. But TDS can tell nothing about the kinds and amounts of the individual salts present in it. Considering the analytical importance of the estimation of the mineral substances as their individual salts, some generalised mathematical models have been developed by this research which are based on the 'hypothetical order of chemical combinations' as may occur among the ionic constituents. With the help of these models, one can easily assume the most probable salts with approximate quantities derived from the ionic constituents. In addition, approximate amount of Na content can also be estimated mathematically with simultaneous verification of the correctness of the water analysis results. The models are stated in this paper with practical illustrations and descriptions of the method of applications.

• 약학회지
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• 제57권4호
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• pp.272-281
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• 2013

In this study, we developed and validated the HPLC method using the isolated components from Erycibae caulis. Their structures were elucidated by spectroscopic methods including UV, $^1H$-NMR, $^{13}C$-NMR, FAB-Mass and ESI-Mass as Compound 1 (crypto-chlorogenic acid), Compound 2 (scopolin), Compound 3 (neochlorogenic acid) and Compound 4 (3,4-di-O-caffeoylquinic acid). Major three compounds and scopoletin were decided as representative components of Erycibae caulis. We established HPLC analytical method by using the representative components and 20 commercial samples which were collected considering to various cultivated area. The HPLC fingerprinting was successfully achieved with an AKZO NOBEL Kromasil 100-5C18 column. The mobile phase consisted of 0.5% acetic acid in water (A) and methanol (B) using gradient method of 85(A) to 50(A) for 35min. The fingerprints of chromatograms were recorded at an optimized wavelength of 330 nm. This developed analytical method was validated with specificity, selectivity, accuracy and precision. And it is suggested that scopolin, scopoletin, neochlorogenic acid, 3,4-di-O-caffeoylquinic acid were more than 0.162%, 0.133%, 0.057%, 0.044%, respectively. In addition, principal component analysis (PCA) was performed on the analytical data of 20 different Erycibae caulis samples in order to classify samples collected from different regions. We hope that this assay can be readily utilized as quality control method for Erycibae caulis.

• 분석과학
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• 제32권4호
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• pp.147-154
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• 2019

Ampicillin and Sulbactam (2:1, w/w) are combined in formulation to provide broader antibacterial action in treatment of many infections. The development of analytical method for simultaneouly determine these two compounds was difficult because of the differences in their chemical structures and ratio in the formulation. Current published methods still have some limitations. In this study, we developed an alternative high-performance liquid chromatography (HPLC) assay method for simultaneously determination of ampicillin sodium and sulbactam sodium in powder for injection. Method validation of HPLC method was conducted to determine linearity, precision, accuracy, system suitability, robustness. The linearity of the calibration curves in the desired concentration range was good ($r^2$> 0.9994). RSDs of intra-day and inter-day precision obtained were less than 2.00 %. Accuracy was obtained with the recoveries in range of 98.42 % and 101.36 %. As a result of system suitability, RSD of both retention time and the peak area obtained were not more than 1.0 %. The values of plate number were more than 7000 and symmetric factors obtained were 0.8. As intermediate-precision and robustness of the developed assay, it could be expected to become valuable tools for revising the Korean Pharmacopoeia (KP XI).

• 환경위생공학
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• 제5권2호
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• pp.63-80
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• 1990

A sensitive and simple analytical system for the simultaneous determination of residual oxytetracycline, tetracycline, and doxycycline in honey was described, and that the analytical method for determination of residual propionic acid in honey was established. Experimental subjects were purchased four kinds of honey, native kind honey, acaccia honey, mixed floral honey, chestnut honey in Kyung Sang Nam Do. Several microbiological methods are available to determine tetracycline antibiotecs(TCs) in foods but their precision apears to be variable and the specificity is questionable. These methods are considered to be not suitable for analysis of tetracycline antibiotics in honey because honey itself has bacteriostatic action. For determination of tetracycline antibiotics in honey, therefore the High Performance Liquid Chromatography(HPLC) method was applied, and the propionic acid were determined by Gas Chromatography(5.C). Ethylacetate, as an extract solvent, was found to be suitable for seperation of TCs in honey, but methanol and acetone were not. The recoverly rate of Oxytetracycline(OTC), Tetracycline(TC), Doxycycline(DC) from honey spiked at a level of 10 $\mu $g/g were 97%, 89%, and 91%, respectively. The cailbration curve in TCs was linear expression from 2$\mu $g/ml to 10$\mu $g/ml. As the results of analysis, the residual tetracycline antibiotics were not detected in the 100 samples of honey. The recovery rate of propionic acid from honey spiked at level of 10$\mu $g/g was 98.3% , and the calibra lion curves were linear expression from 21$\mu $g/ml to 101$\mu $g/ml. As the results of analysis, the residual propionic acid was not detected in the 100 samples of honey. Retention time(min) of OTC, DC, and TC were 3.35, 4.61, and 5.30 minutes at the conditions of table 2, respectively, and retention time(min) of propionic acid was 3.50 minutes at the conditions of table 3. The residual TCs and propionic acid were not detected in the 100 samples of honey, but there is a possibility that antibiotics or propionic acid will be to remain in honey if they are used during product period in order to prevent putrefaction of honey-bee.

• 환경위생공학
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• 제23권4호
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• pp.37-44
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• 2008

In this study we developed the analytical methods for the determination of three neurotoxin; anatoxin-a, saxitoxin and neosaxitoxin using HPLC/FLD system and this analytical methods were applied to real sample; algae culture and algae extracts. For the HPLC/FLD analysis of anatoxin-a samples were concentrated on WCX(Weak Cation Exchanger) SPE and then anatoxin-a in concentrate was derivatized with NBD-F solution. Supernatant was injected on HPLC system. For the HPLC/FLD analysis of saxitoxin and neosaxitoxin samples were separated on the column and then derivatizied by post column reactor for fluorescen detection. For post column reaction of saxitoxin we feed two kinds of reaction solution; Oxidizing Reagent of which composition was periodic acid(7mM) in 50mM potassium phosphate buffer, pH 9 and acidifying reagent of which Composition was 0.5M acetic acid. The LOD value for anatoxin-a, saxitoxin and neosaxitoxin in HPLC/FLD method was 24.3 ng. $35{\mu}g/L$, $27{\mu}g/L$ respectively. We determined the anatoxin-a content of lyophilized anabaena flos-aquae and $20{\mu}g/g$ d.w. of anatoxin-a was detected. We analyzed saxitoxin and neosaxitoxin in algae culture media and extracts of lypopyllized algal cell cultured and that of Deachung reservior. Saxitoxin and neosaxitoxin in real sample were below the limit of detection. Although there are various water treatment processes for removing neurotoxins were suggested no process give simultaneous and complete removal of neurotoxins. It was cocluded that nanofiltration which reject material by size can be a process for removal of neurotoxins.