A modified method for the determination of tobacco specific nitrosamine 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol in human urine by solid phase extraction using a molecularly imprinted polymer and liquid chromatography tandem mass spectrometry
被引:22
作者:
Shah, Kumar A.
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机构:
Virginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USAVirginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USA
Shah, Kumar A.
[1
]
Halquist, Matthew S.
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Virginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USAVirginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USA
Halquist, Matthew S.
[1
]
Karnes, H. Thomas
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Virginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USAVirginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USA
Karnes, H. Thomas
[1
]
机构:
[1] Virginia Commonwealth Univ, Dept Pharmaceut, Richmond, VA 23298 USA
来源:
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
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2009年
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877卷
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14-15期
The work described in this paper represents an improvement over a previously published method for the determination of 4-(methylnitrosamino)-1-(3-pyridyl)-1-butanol (NNAL) in human urine by solid phase extraction on a molecularly imprinted polymer column coupled with HPLC and -MS/MS detection. The influence of ion Suppression due to sample matrix effect was evaluated, and found to influence the response of NNAL. By changing the liquid chromatography conditions, the response for this method was enhanced approximately 25-fold through avoidance of ionization suppression that was found with a previously published method and sample throughput has been improved. The dynamic range of the assay extends from 20 to 2500 pg/mL with a mean r(2) > 0.998. The lower limit of quantitation for the assay was 20 pg/mL despite the use of an inherently lower sensitivity instrument. The method was validated according to current FDA guidelines for bioanalytical method validations. (C) 2009 Elsevier B.V. All rights reserved.