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1.
J Anal Toxicol ; 28(7): 593-8, 2004 Oct.
Article in English | MEDLINE | ID: mdl-15516319

ABSTRACT

A new generation of ONLINE assays has been developed that offers improved performance and enhanced ease of use. This family of assays is being applied to both the COBAS INTEGRA and Roche/Hitachi line of analyzers. The four ONLINE DAT II assays that were evaluated included cocaine (benzoylecgonine) (BE), methadone (MDN), opiates (OP), and tetrahydrocannabinol (THC). The BE assay has a dual cutoff (150/300 ng/mL) with a dynamic range from 0 to 5000 ng/mL. The MDN assay has a cutoff of 300 ng/mL with a dynamic range from 0 to 2000 ng/mL. The opiates assay has a 300 ng/mL cutoff with a 0 to 2000 ng/mL range and a 2000 ng/mL cutoff with a 0 to 8000 ng/mL range. The THC assay has 20, 50, and 100 ng/mL cutoffs with 0 to 100, 0 to 300, and 0 to 300 ng/mL dynamic ranges, respectively. The ranges of the intra-assay precision (coefficients of variation for n = 20) run in the semiquantitative mode are 2.3-7.5% for BE, 2.0-3.8% for MDN, 1.9-4.2% for OP, and 3.9-5.2% for THC. The intra-assay qualitative precision for all of the assays as calculated from absorbance values is generally higher than that of the intra-assay semiquantitative precision at the cutoff. The qualitative precision ranges between 0.4% and 3.1%. The standard curve stability defined for the COBAS INTEGRA systems for these reagents ranges from 35 to 68 days. The clinical sensitivity and specificity were compared to the OnLine generation I and CEDIA immunoassays, as well as gas chromatography-mass spectrometry (GC-MS). The results indicate that for each assay, the sensitivity and specificity were the same or greater when compared to the other two immunoassay technologies. The results of each assay also correlated very well (> 99%) when compared with GC-MS.


Subject(s)
Immunoassay/methods , Substance Abuse Detection/methods , Automation , Cocaine/urine , Dronabinol/urine , Gas Chromatography-Mass Spectrometry , Humans , Immunoassay/instrumentation , Methadone/urine , Narcotics/urine , Substance Abuse Detection/instrumentation
2.
J Forensic Sci ; 46(2): 335-40, 2001 Mar.
Article in English | MEDLINE | ID: mdl-11305436

ABSTRACT

The catalytic rates of hydrolysis of lorazepam-glucuronide, oxazepam-glucuronide, and temazepam-glucuronide when catalyzed by E. Coli. beta-glucuronidase both in phosphate buffer and buffered drug-free urine were compared as well as the pH dependence of enzyme activity. In 50 mM phosphate buffer pH 6.4, lorazepam-glucuronide has the highest turnover rate of 3.7 s(-1) with an associated Km of about 100 microM, followed by oxazepam-glucuronide, which has a turnover rate of 2.4 s(-1) with an associated Km of 60 microM. Temazepam-glucuronide has the lowest rate of 0.94 s(-1) with an associated Km of 34 microM. In buffered drug-free urine, a similar trend was observed. In addition, an optimal pH for beta-glucuronidase was determined to be between 6 and 7 when the enzyme hydrolyzes the benzodiazepine conjugates in buffered drug-free urine. Effects of temperature and incubation time were also examined. It can be concluded that the electron donating or withdrawing of the individual benzodiazepine structure may play an important role in the reactivity of the lorazepam-glucuronide, oxazepam-glucuronide and temazepam-glucuronide catalyzed by beta-glucuronidase. This is consistent with other observations made for monosubstituted phenyl-beta-glucuronides by Wang et al. (1).


Subject(s)
Anti-Anxiety Agents/metabolism , Escherichia coli/enzymology , Lorazepam/metabolism , Oxazepam/metabolism , Temazepam/metabolism , Anti-Anxiety Agents/pharmacokinetics , Forensic Medicine/methods , Glucuronidase/metabolism , Glucuronides/analysis , Glucuronides/chemistry , Humans , Hydrogen-Ion Concentration , Hydrolysis , Immunoassay , Lorazepam/pharmacokinetics , Oxazepam/pharmacokinetics , Temazepam/pharmacokinetics , Temperature , Urinalysis
3.
Child Health Care ; 12(3): 122-9, 1984.
Article in English | MEDLINE | ID: mdl-10264990

ABSTRACT

A comprehensive model for child life programming for young children integrating cognitive and affective theories is described. Continual assessment of the cognitive and affective states of children provides the basis for programming. Degree of structure facilitated by the child life worker through his or her physical and/or verbal interaction and type of activities selected and implemented varies with children's cognitive-affective states.


Subject(s)
Child, Hospitalized/psychology , Child , Child, Preschool , Humans , Models, Psychological
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