LC-MS/MS를 이용한 소의 식용조직 중 세팔렉신의 잔류검사법Analytical Method for Determination of Cephalexin in Bovine Edible Tissues using Liquid Chromatography Coupled to Tandem Mass Spectrometry
- Other Titles
- Analytical Method for Determination of Cephalexin in Bovine Edible Tissues using Liquid Chromatography Coupled to Tandem Mass Spectrometry
- Authors
- 채원석; 이성중; 손송이; 김석; 이후장
- Issue Date
- 2018
- Publisher
- 한국식품위생안전성학회
- Keywords
- Cephalexin; Bovine edible tissues; LC-MS/MS
- Citation
- 한국식품위생안전성학회지, v.33, no.1, pp 58 - 64
- Pages
- 7
- Indexed
- KCI
- Journal Title
- 한국식품위생안전성학회지
- Volume
- 33
- Number
- 1
- Start Page
- 58
- End Page
- 64
- URI
- https://scholarworks.gnu.ac.kr/handle/sw.gnu/12899
- DOI
- 10.13103/JFHS.2018.33.1.58
- ISSN
- 1229-1153
2465-9223
- Abstract
- An analytical method for the determination of cephalexin (CEX) in bovine tissues (muscle, liver, kidney and fat tissues) was developed and validated using liquid chromatography coupled to tandem mass spectrometry (LC-MS/MS). Tissue samples were extracted by the liquid-liquid extraction based on 5% trichloroacetic acid (TCA). The chromatographic separation was achieved on a reverse phase C18 column with gradient elution using a mobile phase of 20 mM hexafluroacetylacetone (HFAC)/50% acetonitrile (40:60). The procedure was validated according to the Ministry of Food and Drug Safety guideline determining accuracy, precision, and limit of detection.
Mean recoveries of CEX from spiked edible tissues (6~1,500 μg/kg) were 83.9~106.8%, and the relative standard deviation was between 2.3 and 14.8%. Linearities were obtained with the correlation coefficient (r2) of > 0.999. Limit of detection and limit of quantification for the investigated CEX were 2~10 and 6~30 μg/kg, respectively. This method was reliable, sensitive, economical and suitable for routine monitoring of CEX residues in bovine edible tissues.
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Collections - 수의과대학 > Department of Veterinary Medicine > Journal Articles

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