• 정보보호학회논문지
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• 제27권4호
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• pp.831-841
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• 2017

본 논문에서는 콘텐츠 중심 네트워크(CCN, Content-Centric Networking)를 위한 안전한 패킷 단편화(fragmentation) 기술을 제안한다. 제안하는 기술은 패킷조각(fragment)들에 대한 불법적인 위변조 가능성을 차단하고, 패킷조각 수신 시 높은 확률로 즉각적인 신뢰성 검증을 제공함으로써 검증 지연을 악용한 DoS 공격으로부터 높은 안전성을 제공한다. 본 논문의 성능 분석 결과는 약간의 부하 증가만으로 제안하는 기술이 기존 기술보다 훨씬 더 높은 안전성을 제공함을 보여준다.

• 대한약학회:학술대회논문집
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• 대한약학회 2003년도 Proceedings of the Convention of the Pharmaceutical Society of Korea Vol.2-2
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• pp.157.2-157.2
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• 2003

Panax ginseng is one of the most important medicinal plant in the Orient. The international trade of ginseng is increasing yearly. The disguise of Chinese and American ginseng into Korean ginseng became a problem in recent years in Korea and an abroad. Obviously, an effective method of authentication of Korean ginseng from others at a DNA level, is necessary for the healthy development of the ginseng market. In order to develop convenient and reproducible methods for the identification of Korean ginseng, amplified fragment length polymorphism (AFLP) analysis was applied within Panax species (Korean cultivatied and wild ginseng, Chinese wild ginseng, American cultivatied and wild ginseng). (omitted)

• Fisheries and Aquatic Sciences
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• 제11권3호
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• pp.133-139
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• 2008

Molecular techniques, including restriction fragment length polymorphism(RFLP) and polymerase chain reaction-single strand conformational polymorph isms(PCR-SSCP), were developed to identify salted, dried threadfin(Eleutheronema tetradactylum) and white herring(Ilisha elongata) fish. Using PCR with universal primers, conserved 367-bp fragments of the cytochrome b gene were amplified from fresh fish samples and sequenced. The sequences were then searched for specific restriction sites. The digestion of the PCR products with the endonucleases AvaI, FokI, MboII, and MspI generated RFLP, which was used to identify the commercial products. Similarly, the amplified PCR-SSCP products were developed and the products tested. Overall, similar patterns were found in the majority of the fresh and processed products. Based on the results, both RFLP and PCR-SSCP were useful in determining and validating the authenticity of the fish species used to prepare the commercial salted, dried products. A similar approach can be applied to other species.

• Journal of Dairy Science and Biotechnology
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• 제33권4호
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• pp.253-262
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• 2015

The authentication and implications of misleading labeling in milk and dairy products is important to protect against cheating consumers from adulteration and to alert sensitive consumers to any undeclared potential allergens. This need to support milk and dairy products labeling has led to the development of specific analytical techniques for the analysis of milk and dairy products ingredients. Recently, several methods based on polymerase chain reaction (PCR), including restriction fragment length polymorphism (PCR-RFLP), multiplex PCR, species-specific PCR, and real-time PCR, have been proposed as useful means for identifying species of origin in milk and dairy products, as well as quantifying and detecting any adulteration. These methods have particular advantages owing to their high specificity and sensitivity, as well as rapid processing time. In this review, we provide an updated and extensive overview of the PCR-based methods used for milk and dairy products authentication with a particular focus on the application of PCR methods to detect adulteration.

• Journal of Plant Biotechnology
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• 제7권2호
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• pp.81-86
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• 2005

Panax ginseng is one of the most important medicinal plants in the world. The international trade of ginseng is increasing yearly. The disguise of Chinese and American ginseng into Korean ginseng became a problem in recent years in abroad and Korea. An effective method to authenticate the Korean Panax ginseng from others at a DNA level is necessary for the healthy development of the ginseng market. Amplified fragment length polymorphism (AFLP) analysis was applied to develop a method for the identification of Korean ginseng between Chinese ginseng and American ginseng. It is very difficult to detect the different polymorphic bands among Korean field cultivated ginseng, and between field and wild-cultivated ginseng. The genetic distance coefficient by AFLP analysis between field- and wild cultivated Korean ginseng was very low, 0.056. Whereas, polymorphic bands between Korean and Chinese wild-cultivated ginseng was significantly different. The genetic distance coefficient between wild-cultivated Korean and Chinese ginseng was 0.149. The genetic distance coefficients between the P. ginseng and P. quinquefolius were ranging from 0.626 to 0.666. These results support that the AFLP analysis could be applied to authenticate Korean P. ginseng from others Chinese P. ginseng and American ginseng (P. quinquefolius).

• 한국식품과학회지
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• 제41권6호
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• pp.609-614
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• 2009

참기름은 높은 항산화활성 및 항암작용 등의 우수한 영양학적 가치를 지니는 반면 비싼 가격으로 인하여 가짜 참기름의 유통이 범람함에 따라 이를 판별할 수 있는 분석 방법의 확립이 요구되는 실정이다. 질량분석기를 바탕으로 한 전자코를 이용하여 들기름이 혼합된 참기름을 제조하여 진위 판별을 시도하였다. 각각의 유지를 전자코를 이용하여 분석, 통계처리하였다. 혼합 참기름의 휘발성 향기성분으로부터 생성되는 ion fragment 중 40-160 amu에서 각 시료 간에 차별성이 높은 fragment(m/z)를 선택하여 해당 intensity값을 판별 분석한 결과, 참기름 및 들기름은 뚜렷하게 구분되었다. 미량의 들기름이 혼합된 참기름은 첨가된 들기름의 농도에 비례하여 제1판별함수값(DF1)과 높은 상관관계를 나타내었다. 참기름의 볶음온도 및 시간 등의 제조조건 및 재배환경, 재배 산지, 제조회사 등의 요인에 의하여 순수한 참기름의 향기패턴이 달라지는 것을 인도산과 국산 참기름을 이용하여 분석하였다. 향후 참기름의 위조 여부를 검증하는 방법에 하나로 활용될 수 있을 것이다.

• 한국식품과학회지
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• 제43권1호
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• pp.105-109
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• 2011

본 연구는 유채유에 타기름이 혼합되었을 때 그 혼합 비율에 따른 차이를 전자코로 분석하였다. 대두유와 옥수수유를 0, 3, 6, 9, 12, 15, 20%를 유채유에 각각 혼입하여 전자코로 분석한 결과 DF1의 영향을 주로 받아 혼합 비율이 증가함에 따라 DF1이 음의방향으로 일정한 경향을 보이며 이동하여 나타났다. 이를 혼합비율에 따른 DF1값을 막대그래프로 나타낸 결과 혼합비율이 증가함에 따라 DF1값이 감소하여 뚜렷한 차이를 보였다. 유채유에 대두유를 혼합할 경우 DF1= $-0.170{\times}conc.$(대두유 혼합비율)+0.431 ($r^2=0.989$)과 같은 상관관계식을 얻어 유채유에 타 기름이 혼합될 경우 그 함량의 예측이 가능하였다. 이러한 결과를 통해 전자코를 이용하여 유채유의 위조판별이 가능함을 확인하였으며 다른유지를 비롯한 다양한 식품에 적용 가능할 것이다.

• 산업식품공학
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• 제15권2호
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• pp.122-129
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• 2011

오징어 젓갈과 한치 젓갈의 차이를 질량분석기를 기반으로 한 전자코를 이용하여 분석한 결과 두 시료의 mass spectrum은 뚜렷한 차이를 보였다. 판별함수분석을 통해 휘발성분의 패턴을 분석한 결과 오징어 젓갈과 한치 젓갈이 뚜렷이 구분되었으며 젓갈의 양념을 제거한 후 분석하였을 때 구분이 더 잘되었다. 결과적으로 전자코를 이용하여 유사 식품 간의 차이를 충분히 구분 가능하였으며 이러한 결과는 추후 젓갈뿐 아니라 다양한 방면에 적용 가능할 것으로 보여 EMA 식품을 선별하는 데에도 도움이 될 것으로 기대된다.

• 대한본초학회지
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• 제36권1호
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• pp.9-17
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• 2021

Objectives : Tetrapanacis Medulla and Akebiae Caulis are one of the most frequently adulterated herbal medicines because of their confusability of terms in the ancient writings and the similarity of morphological features of dried herbal products. The major adulterant is Aristolochia manshuriensis (Guanmutong) which has a serious safety concern with its toxicity. To ensure the safety and quality of the two herbal medicines, it is necessary to discriminate the toxic adulterant from authentic species. The aim of this study is to develop SCAR markers and to establish the multiplex-SCAR assay for discrimination of four plant species related to Tetrapanacis Medulla and Akebiae Caulis. Methods : ITS regions of fifteen samples of four species (Tetrapanax papyrifer, Fatsia japonica, Aristolochia manshuriensis, and Akebia quinata) collected from different sites were amplified and sequenced. Fifteen obtained ITS sequences were aligned and analysed for the detection of species-specific sequence variations. The SCAR markers were designed based on the sequence alignments and then, multiplex-SCAR assay enhancing rapidity was optimized. Results : ITS sequences clearly distinguished the four species at the species level. The developed SCAR markers and multiplex-SCAR assay were successfully discriminated four species and detected the adulteration of commercial product samples by comparison of the amplified DNA fragment sizes. Conclusions : These SCAR markers and multiplex-SCAR assay are a rapid, simple, and reliable method to identify the authentic Tetrapanacis Medulla and Akebiae Caulis from adulterants. These genetic tools will be useful to ensure the safety and to standardize the quality of the two herbal medicines.