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1.
J Chromatogr Sci ; 47(10): 902-9, 2009.
Article in English | MEDLINE | ID: mdl-19930803

ABSTRACT

In recent years, there has been a rapid proliferation of smokeless products with a wide range of nicotine content and flavoring formulations that may appeal to new users and existing cigarette smokers. The CDC nicotine method, which employs gas chromatography-flame ionization detection (GC-FID), provides a robust means for measuring nicotine in smokeless tobacco. However, several compounds, identified in a few flavored smokeless products, interfere with nicotine quantification using GC-FID. In response, the standard nicotine method (26.7 min run time) was modified to use faster GC ramping (3.7 min run time) and detection with mass spectrometry (GC-MS) in selected ion-monitoring mode to reduce signal interferences that can bias nicotine values. Seven conventional smokeless samples (n = 12) and blank tobacco samples spiked at three nicotine concentration levels (n = 5) were analyzed using the GC-FID and GC-MS methods and found to be in excellent agreement. However, only the GC-MS method provided confirmation of chromatographic peak purity in certain highly flavored products. The GC-MS method is not intended to replace the GC-FID method but to provide a method versatile enough to analyze a wide range of nicotine values in domestic and international samples of varying complexity. Accurate nicotine quantification is important for determining total nicotine content in tobacco and in subsequent calculations of un-protonated nicotine content.


Subject(s)
Gas Chromatography-Mass Spectrometry/methods , Nicotine/analysis , Tobacco, Smokeless/chemistry
2.
Am J Emerg Med ; 24(5): 582-94, 2006 Sep.
Article in English | MEDLINE | ID: mdl-16938598

ABSTRACT

Youth violence is widely recognized as a major public health problem. Adolescent suicidality (ideation, behavior, or both) is disturbingly common in the United States, and homicide remains one of the leading causes of death for young people aged 10 to 24 years. Assessing youth suicidality and homicidality in the emergency department (ED) is a complex and challenging task. Evidence about the value of available ED risk assessments is not encouraging. Attempts to develop models that predict violence have in part been unsuccessful from the fact that ideation is common and the value of depression is hard to determine. The current study presents an empirically based assessment (adolescent and child urgent threat evaluation) and algorithm (violence ideation and suicidality treatment algorithm) evaluating the impact of ideation and nonideation states on attempt among clinical samples, such as serotonin reuptake inhibitor akathisia and acute adjustment disorders. The authors suggest important time-related factors and easy-to-administer procedures when assessing near-future youth violence. A validated suicide-homicide final common pathway model is discussed.


Subject(s)
Adolescent Behavior , Emergency Service, Hospital , Mass Screening/methods , Violence/prevention & control , Violence/psychology , Adolescent , Child , Female , Homicide/prevention & control , Homicide/psychology , Humans , Longitudinal Studies , Male , Mass Screening/standards , Neuropsychological Tests , Practice Guidelines as Topic , Prospective Studies , Psychometrics , Reproducibility of Results , Sensitivity and Specificity , Suicide/psychology , United States , Suicide Prevention
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