• 분석과학
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• 제35권1호
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• pp.1-7
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• 2022

This study suggests a new one-step fluorescent cyanoacylate-fuming method for developing fingerprints by using a CAB mixed with dimethylaminobenzalde (DMAB) and cyanoacylate (CA) in a specific ratio. CAB is prepared by mixing 2.5 % (w/w) DMAB with CA and fumigated at 180 ℃. Under these conditions, developing fingerprints showed the best results. The fuming method using CAB develops latent fingerprints into fluorescence and has a higher sensitivity than CA, and it showed comparable or better contrast to existing fluorescence enhancement methods. It was also applicable on a variety of non-porous surfaces that can be encountered at ordinary times. This method is more useful than conventional fluorescent dyeing methods in that it minimizes damage to fingerprints or samples, makes it easy to manufacture, saves time, and can use existing current equipment as it is.

• 과학수사학회지
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• 제11권3호
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• pp.210-217
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• 2017

법미생물 검사실에서는 식품의 미생물 분석이 요구되는 경우들이 있다. 국립과학수사연구원에 식품 미생물분석이 의뢰된 샘플들 중에서 Bacillus cereus 균이 분리되었던 일부 증례가 있었다. B. cereus는 식중독을 일으킬 수 있는 중요한 병원성 세균이다. 따라서 우리는 최근 미생물 검사를 위해 의뢰된 멸치액젓에서 B. cereus를 분리한 후, 16S rDNA 서열을 기반으로 하는 MSId 방법 및 real-time PCR 법에 따라 균을 동정 하였다. 또한 설사 독소 유전자 및 구토 독소 유전자 검출을 위한 PCR을 실시하고 B. cereus 분리 균주에서 nheABC, bceT 및 entFM 설사 독소 유전자의 존재를 확인하였다. 임상적으로 중요한 몇 가지 식중독 세균들은 식품 미생물 검사 시 주목해야 할 필요가 있다. 특히, 이러한 식중독 세균들 중에서 B. cereus는 환경저항성 및 내열성이 강한 내생포자를 형성하고, 내열성 독소를 형성할 수도 있기 때문에 조리된 음식을 섭취해도 식중독을 일으킬 수 있다. 본 연구를 통해서 B. cereus등의 임상적으로 중요한 세균을 구별하는 것이 식품미생물 검사 시 중요함을 강조하고, 또한 법미생물 검사실에 앞으로 의뢰될 식품미생물 분석 사례들을 위해 B. cereus의 식별 및 세균의 독소 유전자 검출을 위한 지침을 제공 하고자 한다.

• 대한의생명과학회지
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• 제17권2호
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• pp.151-155
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• 2011

Short tandem repeats (STRs) loci are the genetic markers used for forensic human identity test. With multiplex polymerase chain reaction (PCR) assays, STRs are examined and measured PCR product length relative to sequenced allelic ladders. In the repeat region and the flanking region of the commonly-used STR may have DNA sequence variation. A mismatch due to sequence variation in the DNA template may cause allele drop-out (i.e., a "null" or "silent" allele) when it falls within PCR primer binding sites. The STR markers were co-amplified in a single reaction by using commercial PowerPlex$^{(R)}$ 16 system and AmpFlSTR$^{(R)}$ Identifiler$^{(R)}$ PCR amplification kits. Separation of the PCR products and fluorescence detection were performed by ABI PRISM$^{(R)}$ 3100 Genetic Analyzer with capillary electrophoresis. The GeneMapper$^{TM}$ ID software were used for size calling and analysis of STR profiles. Here, this study described a forensic human identity test in which allelic drop-out occurred in the STR system D18S51. During the course of human identity test, two samples with a homozygous (16, 16 and 21, 21) genotype at D18S51 locus were discovered using the PowerPlex$^{(R)}$ 16 system. The loss of alleles was confirmed when the samples were amplified using AmpFlSTR$^{(R)}$ Identifiler$^{(R)}$ PCR amplification kit and resulted in a heterozygous (16, 20 and 20, 21) genotype at this locus each other. This discrepancy results suggest that appropriate measures should be taken for database comparisons and that allele should be further investigated by sequence analysis and be reported to the forensic community.

• 약학회지
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• 제60권3호
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• pp.112-117
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• 2016

A liquid chromatography-tandem mass spectrometry (LC-MS/MS) method was developed and validated for the determination of caffeine in forensic aqueous sample. The centrifuged sample ($100{\mu}l$) was diluted 50-fold with distilled water. The diluted sample ($400{\mu}l$) was then diluted further with $200{\mu}l$ of 0.1% formic acid solution and $400{\mu}l$ of acetonitrile containing 500 ng of caffeine-(3-methyl-$^{13}C_3$) prior to LC-MS/MS analysis. The mobile phase was composed of 0.1% formic acid in distilled water (A) and acetonitrile (B). Chromatographic separation was performed by using a Zorbax SB-C18 ($100mm{\times}2.1mm$ i.d., $3.5{\mu}m$) column and caffeine was eluted within 1.1 min. Linear least-squares regression with a 1/x weighting factor was used to generate a calibration curve with the coefficients of determination ($r^2=0.9983$). The lower limit of quantification was $25ng/ml$ for the analyte. The process efficiency was 98.6~100.1%. Intra- and inter-day precisions were not more than 2.1% and 1.7%, while intra- and inter-day accuracies were ranged from -6.8 to 4.5%, respectively. The suitability of the method was examined by analyzing unknown forensic aqueous samples.

• The Journal of Asian Finance, Economics and Business
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• 제8권3호
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• pp.807-819
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• 2021

This study aims to determine the availability of forensic accounting application factors sought by auditors' representatives of Jordanian Certified Public Accounting and auditors working in the Audit Bureau. The study identifies as well the role of these application factors in enhancing the efficiency of auditors due to the increased responsibility on them in the face of various fraud cases on the one hand, and their appearance in the courts as financial experts supporting the judiciary to adjudicate financial cases on the other hand. To achieve the objectives of the study, the researchers used the descriptive analytical method because of its suitability for the nature of the research. The population of the study consisted of 433 Jordanian certified public accountants and 520 auditors working in the Audit Bureau, from which a sample of 426 was constructed. A questionnaire was developed to collect data and the Statistical Package for Social Sciences was utilized to analyze data and test hypotheses. The study found that there is a statistical difference between the responses of the two samples of the study, and it concluded a set of recommendations, which are hoped to help legislators in strengthening and developing the forensic accounting profession in Jordan.

• 분석과학
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• 제34권6호
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• pp.259-266
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• 2021

대마는 전 세계적으로 가장 많이 남용되고 있는 물질 중의 하나이며, 우리나라에서는 메트암페타민 다음으로 많이 남용되고 있으며, 1976년부터 국내에서 마약류관리법에 의해 규제되고 있다. 소변 중 대마성분의 검출을 위하여는 대마의 유효 성분인 Δ⁹-tetrahydrocannabinol (THC)의 생체내 주된 대사체인 11-nor-Δ⁹-carboxy-tetrahydrocannabinol (THCCOOH)을 확인하는 것이 일반적이며, 이는 과학수사 및 사법처리와 관련된 법과학 분야에서 중요한 증거로 받아들여지고 있다. 본 연구에서는 소변 중 대마 대사체의 분석을 위하여 분석법이 간단하고 단시간이 소요되는 분석방법으로 THCCOOH 및 THCCOOH-glucuronide를 액상 추출하고 액체크로마토그라피/질량분석법(LC-MS/MS)을 사용하여 동시 분석하는 방법을 확립하였다. 내부표준물질로는 THCCOOH-D₃ 및 THCCOOH-glucuronide-D₃를 사용하였다. 시험방법의 유효화를 위하여 매질 효과, 회수율, 직선성, 정밀도, 정확도, 시험과정의 효율성 및 안정성 등을 시험하였고, 모든 결과가 적합함을 알 수 있었다. 실험 과정에서의 carryover는 나타나지 않았으며, 선택성 및 간섭성도 우수하였다. THCCOOH 및 THCCOOH-glucuronide의 검출 한계는 각각 0.3 및 0.2 ng/mL 이었다. 확립된 분석방법을 면역시험법과 가스크로마토그라피/질량분석법(GC/MS)법에서 대마 양성으로 최종 판정된 28개의 실제 소변에 적용하여 분석법의 적합성을 검토하였다. 28개 소변 중 THCCOOH 및 THCCOOH-glucuronide의 농도는 각각 정량 한계 미만~226.90 ng/mL 및 6.43~2133.03 ng/mL이었고, 모든 시료에서 THCCOOH-glucuronide가 THCCOOH 보다 많이 검출되었다. 본 분석법을 소변 중 대마의 흡연여부를 판정하는 감정시험에 적용함으로써 단시간에 효율적인 분석을 실시할 수 있게 되어 과학수사 발전에 기여할 수 있을 것으로 사료된다.

• Archives of Pharmacal Research
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• 제28권9호
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• pp.1086-1091
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• 2005

An analytical method was developed for evaluating the cannabidiol (CBO), cannabinol (CBN), ${\Delta}^9-tetrahydrocannabinol$ $({\Delta}^9-THC)$ level in human hair using gas chromatography-mass spectrometry (GC-MS). Hair samples (50mg) were washed with isopropyl alcohol and cut into small fragments (< 1mm). After adding a deuterated internal standard, the hair samples were incubated in 1.0M NaOH for 10 min at $95^{\circ}C$. The analytes from the resulting hydrolyzed samples were extracted using a mixture of n-hexane-ethyl acetate (75:25, v/v). The extracts were then evaporated, derivatized, and injected into the GC-MS. The recovery ranges of CBD, CBN, and ${\Delta}^9-THC$ at three concentration levels were $37.9-94.5\%$ with good correlation coefficients $(r^2>0.9989)$. The intra-day precision and accuracy ranged from $-9.4\%\;to\;17.7\%$, and the inter-day precision and accuracy ranged from $-15.5\%\;to\;14.5\%$, respectively. The limits of detection (LOD) for CBD, CBN, and ${\Delta}^9-THC$ were 0.005, 0.002, and 0.006 ng/mg, respectively. The applicability of this method of analyzing the hair samples from cannabis abusers was demonstrated.

• 분석과학
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• 제17권3호
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• pp.271-277
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• 2004

The aim of this study was to investigate questioned documents written with blue or black ballpoint pen on paper by nondestructive technique. In this work, 21 blue and 22 black ballpoint pen inks which were purchased on different brands were analyzed by using Microspectrophotometry (MSP). The reflectance spectra were obtained from these ink samples and their shapes and the wavelength of the maximum intensity were compared. In the blue and black ballpoint pen inks, the discriminating powers (DP) were 0.85 and 0.61, respectively. The changes of the reflectance intensity at their wavelength of maximum intensity and their shapes appeared according to the exposure time to sunshine in a laboratory, especially in the blue ballpoint pen inks. Therefore it is possible to distinguish ink entries on the same paper with the relative age in case of questioned letters written with blue ballpoint pen.

• 약학회지
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• 제55권4호
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• pp.289-294
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• 2011

Illegal addition of steroids into cosmetics, ointments or drugs have been increased and their careless usage induced detrimental effect on health. We developed simultaneous analytical method using TLC, HPLC and LC/MS for the identification of 40 corticosteroids. 34 corticosteroids were well separated in HPLC with isocratic mode and remaining 6 drugs were also separated with gradient mode. All of the 40 corticosteroids were detected in negative mode in LC/MS. Halcinonide, prednisolone, triamcinolone acetonide and methylprednisolone hemisuccinate were detected in real samples.

• Mass Spectrometry Letters
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• 제5권4호
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• pp.104-109
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• 2014

Nonmedical use of prescription stimulants such as methylphenidate (MPH) and amphetamine (AP) by normal persons has been increased to improve cognitive functions. Due to high potential for their abuse, reliable analytical methods were required to detect these prescription stimulants in biological samples. A direct injection liquid chromatography-tandem mass spectrometric (LC-MS/MS) method was developed and implemented for simultaneous determination of MPH, AP and their metabolites ritalinic acid (RA) and 4-hydroxyamphetamine (HAP) in human urine. Urine sample was centrifuged and the upper layer ($100{\mu}L$) was mixed with $800{\mu}L$ of distilled water and $100{\mu}L$ of internal standards ($0.2{\mu}g/mL$ in methanol). The mixture was then directly injected into the LC-MS/MS system. The mobile phase was composed of 0.2% formic acid in distilled water (A) and acetonitrile (B). Chromatographic separation was performed by using a Capcell Pak MG-II C18 ($150mm{\times}2.0mm$ i.d., $5{\mu}m$, Shiseido) column and all analytes were eluted within 5 min. Linear least-squares regression with a 1/x weighting factor was used to generate a calibration curve and the assay was linear from 20 to 1500 ng/mL (HAP), 40-3000 ng/mL (AP and RA) and 2-150 ng/mL (MPH). The intra- and inter-day precisions were within 16.4%. The intra- and inter-day accuracies ranged from -15.6% to 10.8%. The limits of detection for all the analytes were less than 4.7 ng/mL. The suitability of the method was examined by analyzing urine samples from drug abusers.