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Simultaneous Determination of Benzidine, Acetylbenzidine and di-Acetylbenzidine in Rat Urine
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  • Simultaneous Determination of Benzidine, Acetylbenzidine and di-Acetylbenzidine in Rat Urine
  • Simultaneous Determination of Benzidine, Acetylbenzidine and di-Acetylbenzidine in Rat Urine
저자명
신호상,이진현,안혜실,홍춘표,최석남,Sin. Ho Sang,Lee. Jin Hyeon,An. Hye Sil,Hong. Chun Pyo,Choe. Seok Nam
간행물명
Bulletin of the Korean Chemical Society
권/호정보
2001년|22권 7호|pp.685-688 (4 pages)
발행정보
대한화학회
파일정보
정기간행물|ENG|
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이 논문은 한국과학기술정보연구원과 논문 연계를 통해 무료로 제공되는 원문입니다.
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기타언어초록

A gas chromatography/mass spectrometric assay method has been developed for the simultaneous determination of benzidine (BZ), N-acetyl benzidine (ABZ) and N,N-diacetyl benzidine (DABZ) in rat urine. BZ, ABZ and DABZ were extracted from urine at pH 8 with ethyl ether. Conjugated urinary metabolites were extracted at pH 8 after hydrolysis with 1 M HCl for 30 min at 100 $^{circ}C.$ The dried extract was dissolved in 100 ${mu}{ell}$ of ethylacetate and then injected in gas chromatography-mass spectrometric (GC-MS) system without further purification or modification. BZ, ABZ and DABZ have good chromatographic properties and offer very sensitive response for the EI-MS (SIM) without any derivatization. The recoveries for BZ, ABZ and DABZ were about 98.0, 81.8 and 71.4%, respectively, at pH 8.0 and the concentration of 5.0 ng/mL. The coefficients of variation of BZ and ABZ were less than 9.5% from 0.1 to 100 ng/mL and that of DABZ was less than 13% in the same concentration range. The detection limits of the assay were 0.01 ng/mL for both BZ and ABZ, and 0.05 ng/mL for DABZ in urine or plasma 1.0 mL.