@article {2450,
	title = {Quantitative analysis of propofol in whole blood using capillary electrophoresis},
	journal = {Journal of Chromatography B-Analytical Technologies in the Biomedical and Life Sciences},
	volume = {877},
	number = {8-9},
	year = {2009},
	note = {ISI Document Delivery No.: 424NVTimes Cited: 2Cited Reference Count: 19Hui, Yu Raedschelders, Koen Zhang, Hong Ansley, David M. Chen, David D. Y.},
	month = {Mar},
	pages = {703-709},
	type = {Article},
	abstract = {We have developed a straightforward capillary electrophoresis method capable of quantifying clinically relevant propofol concentrations in whole blood from patients undergoing aortocoronary bypass grafting with cardiopulmonary bypass. The method utilizes 400 mu L of whole blood and is capable of detecting propofol in the ng/mL range. Factors affecting reproducibility and reliability of analytical results for clinically relevant samples are discussed. The method was used to evaluate propofol concentrations in blood samples from 30 patients. The distribution in the whole blood concentration achieved in patients advocates the need for target-achieved monitoring techniques. (C) 2009 Elsevier B.V. All rights reserved.},
	keywords = {Aortocoronary bypass, BIOPHARMACEUTICAL INDUSTRY, BREATH, capillary electrophoresis, Cardiopulmonary bypass, CHROMATOGRAPHY-MASS-SPECTROMETRY, grafting, HUMAN, Method development, PLASMA, POPULATION, Propofol, Whole blood},
	isbn = {1570-0232},
	url = {<Go to ISI>://000264574300006},
	author = {Hui, Y. and Raedschelders, K. and Zhang, H. and Ansley, D. M. and Chen, D. D. Y.}
}
@article {4584,
	title = {Immunochemical extraction and detection of LSD in whole blood},
	journal = {Journal of Immunological Methods},
	volume = {224},
	number = {1-2},
	year = {1999},
	note = {ISI Document Delivery No.: 195AQTimes Cited: 10Cited Reference Count: 19},
	month = {Apr},
	pages = {11-18},
	type = {Article},
	abstract = {Polyclonal antibodies raised against the hallucinogenic drug, lysergic acid diethylamide (LSD), were used to detect and extract drug from whole blood samples. An indirect ELISA was used to detect as little as 1 pg of total drug in 25 mu l blood. The limit of detection of the immunoassay, calculated from the mean - 3 SD was 39 pg/ml. The analytical recovery of LSD (2.5-0.2 ng/ml) from whole blood was 102-113\%. Within-run CVs for LSD spiked in blood at 1.25, 0.16 and 0.04 ng/ml were 5.6, 3.1, and 8.9\%, respectively (n = 4). There was an overall decrease in precision when whole blood was used in place of urine, due to the increased complexity of the matrix. However, using this technique LSD was calibrated in blood in the sub-ng/ml region of forensic interest. Immunoaffinity extraction was used to isolate LSD from blood and urine samples. The affinity support was prepared by covalently attaching anti-LSD antibodies to Protein A-coated agarose beads. No pre-treatment of the sample was required other than the addition of neutral buffer. Sub-ng/ml concentrations of LSD were routinely extracted from blood and urine samples with greater than 80\% recovery of drug. This technique, which could be used to extract LSD from blood and urine samples prior to confirmatory drug analysis, could be completed in about 10 min. (C) 1999 Elsevier Science B.V. All rights reserved.},
	keywords = {BLOOD, CHROMATOGRAPHY-MASS-SPECTROMETRY, CONFIRMATION, ELISA, HUMAN URINE, immunoaffinity extraction, IMMUNOASSAY, LSD, LYSERGIC-ACID DIETHYLAMIDE, N-DEMETHYL-LSD, RADIOIMMUNOASSAY, SERUM},
	isbn = {0022-1759},
	url = {<Go to ISI>://000080227300002},
	author = {Kerrigan, S. and Brooks, D. E.}
}
