1993
DOI: 10.1016/0009-8981(93)90160-6
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Comparison of a mechanized version of the ‘König’ reaction and a fluorescence polarization immunoassay for the determination of nicotine metabolites in urine

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Cited by 9 publications
(10 citation statements)
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“…However, a study has shown that trans-3¢-hydroxycotinine crossreacts by about 30% with the polyclonal rabbit anticotinine antiserum commonly used to determine cotinine levels by enzyme-linked immunosorbent assay (ELISA) [82], which does not seem to be the case for monoclonal antibodies [44]. Besides this possible cross-reactivity, immunoassays require the use of costly reagents [70]. The principal advantages of immunological methods are low sample-volume requirements, little sample manipulation, and rapidity of analysis [97].…”
Section: Analytical Aspectsmentioning
confidence: 99%
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“…However, a study has shown that trans-3¢-hydroxycotinine crossreacts by about 30% with the polyclonal rabbit anticotinine antiserum commonly used to determine cotinine levels by enzyme-linked immunosorbent assay (ELISA) [82], which does not seem to be the case for monoclonal antibodies [44]. Besides this possible cross-reactivity, immunoassays require the use of costly reagents [70]. The principal advantages of immunological methods are low sample-volume requirements, little sample manipulation, and rapidity of analysis [97].…”
Section: Analytical Aspectsmentioning
confidence: 99%
“…This method must therefore be considered a reliable index of smoking status, provided that blanks are included to take into account the coloration of each urine sample [41,94]. However, interferences due, for example, to the presence of drugs with a pyridine ring (nicotinic acid, isoniazid, nicotinamide) are important [70,94]. Moreover, the high detection threshold makes this method inappropriate for monitoring of ETS exposure (see below) [41].…”
Section: Analytical Aspectsmentioning
confidence: 99%
“…A range of 1.003 to 1.03 was used to indicate good hydration [21]. Total nicotine metabolites were determined using a colorimetric assay adapted for an automatic chemistry analyser (Cobass Bio, Roche, Australia) [22]. Urinary methyl histidines were determined by a high performance liquid chromatography (HPLC) assay which was adapted from the method of Simons and Johnson [23].…”
Section: Activity Measurementsmentioning
confidence: 99%
“…The remaining 17 subjects did not complete the diaries and were excluded from further analyses. In a previous study (Pickert et al 1992) we found that self reported cigarette consumption was correlated highly with urinary cotinine level. In order to evaluate whether the smoker groups differed on important data regarding the cardiovascular system, data from the daily records (systolic and diastolic blood pressure, heart rate, athletic activity, 339 coffee consumption, tobacco consumption) and the blood lipid data (total cholesterol, HDL, LDL, LDL/HDL) were subjected to oneway ANOVAs containing the factor Group (non-smoker or light, medium and heavy smokers).…”
Section: Subjectsmentioning
confidence: 92%