Identification of a new metabolite of GHB: gamma-hydroxybutyric acid glucuronide

Research output: Contribution to journalJournal articleResearchpeer-review

Standard

Identification of a new metabolite of GHB : gamma-hydroxybutyric acid glucuronide. / Petersen, Ida Nymann; Tortzen, Christian; Kristensen, Jesper Langgaard; Pedersen, Daniel Sejer; Breindahl, Torben.

In: Journal of Analytical Toxicology, Vol. 37, No. 5, 06.2013, p. 291-7.

Research output: Contribution to journalJournal articleResearchpeer-review

Harvard

Petersen, IN, Tortzen, C, Kristensen, JL, Pedersen, DS & Breindahl, T 2013, 'Identification of a new metabolite of GHB: gamma-hydroxybutyric acid glucuronide', Journal of Analytical Toxicology, vol. 37, no. 5, pp. 291-7. https://doi.org/10.1093/jat/bkt027

APA

Petersen, I. N., Tortzen, C., Kristensen, J. L., Pedersen, D. S., & Breindahl, T. (2013). Identification of a new metabolite of GHB: gamma-hydroxybutyric acid glucuronide. Journal of Analytical Toxicology, 37(5), 291-7. https://doi.org/10.1093/jat/bkt027

Vancouver

Petersen IN, Tortzen C, Kristensen JL, Pedersen DS, Breindahl T. Identification of a new metabolite of GHB: gamma-hydroxybutyric acid glucuronide. Journal of Analytical Toxicology. 2013 Jun;37(5):291-7. https://doi.org/10.1093/jat/bkt027

Author

Petersen, Ida Nymann ; Tortzen, Christian ; Kristensen, Jesper Langgaard ; Pedersen, Daniel Sejer ; Breindahl, Torben. / Identification of a new metabolite of GHB : gamma-hydroxybutyric acid glucuronide. In: Journal of Analytical Toxicology. 2013 ; Vol. 37, No. 5. pp. 291-7.

Bibtex

@article{0eaf89d706ec4ee4962c0aef9479cce5,
title = "Identification of a new metabolite of GHB: gamma-hydroxybutyric acid glucuronide",
abstract = "Gamma-hydroxybutyric acid (GHB) is an important analyte in clinical and forensic toxicology with a narrow detection window of 3-6 h. In the search of improved detection methods, the existence in vivo of a glucuronated GHB metabolite (GHB-GLUC) was hypothesized. Chemically pure standards of GHB-GLUC and a deuterated analogue for chromatography were synthesized. Liquid chromatography and tandem mass spectrometry were used for targeted analysis in anonymous clinical urine samples (n = 50). GHB-GLUC was found in concentrations ranging from 0.11 to 5.0 µg/mL (mean: 1.3 ± 1.2 µg/mL). Thus far, this is the first report of a GHB glucuronide detected in biological samples. Given that glucuronides generally have longer half-life values than their corresponding free drugs, GHB-GLUC should theoretically be a biomarker of GHB intoxication. It is also proposed that the hitherto unexplained reports of elevated GHB concentrations in some biological samples, which has caused the setting of a relatively high cutoff value (10 µg/mL), represent total GHB measurements (sum of free GHB and actively chemically hydrolyzed GHB-GLUC). To address these challenges, the present study must be followed by comprehensive pharmacokinetic and stability studies after the controlled administration of GHB.",
author = "Petersen, {Ida Nymann} and Christian Tortzen and Kristensen, {Jesper Langgaard} and Pedersen, {Daniel Sejer} and Torben Breindahl",
year = "2013",
month = jun,
doi = "10.1093/jat/bkt027",
language = "English",
volume = "37",
pages = "291--7",
journal = "Journal of Analytical Toxicology",
issn = "0146-4760",
publisher = "Oxford University Press",
number = "5",

}

RIS

TY - JOUR

T1 - Identification of a new metabolite of GHB

T2 - gamma-hydroxybutyric acid glucuronide

AU - Petersen, Ida Nymann

AU - Tortzen, Christian

AU - Kristensen, Jesper Langgaard

AU - Pedersen, Daniel Sejer

AU - Breindahl, Torben

PY - 2013/6

Y1 - 2013/6

N2 - Gamma-hydroxybutyric acid (GHB) is an important analyte in clinical and forensic toxicology with a narrow detection window of 3-6 h. In the search of improved detection methods, the existence in vivo of a glucuronated GHB metabolite (GHB-GLUC) was hypothesized. Chemically pure standards of GHB-GLUC and a deuterated analogue for chromatography were synthesized. Liquid chromatography and tandem mass spectrometry were used for targeted analysis in anonymous clinical urine samples (n = 50). GHB-GLUC was found in concentrations ranging from 0.11 to 5.0 µg/mL (mean: 1.3 ± 1.2 µg/mL). Thus far, this is the first report of a GHB glucuronide detected in biological samples. Given that glucuronides generally have longer half-life values than their corresponding free drugs, GHB-GLUC should theoretically be a biomarker of GHB intoxication. It is also proposed that the hitherto unexplained reports of elevated GHB concentrations in some biological samples, which has caused the setting of a relatively high cutoff value (10 µg/mL), represent total GHB measurements (sum of free GHB and actively chemically hydrolyzed GHB-GLUC). To address these challenges, the present study must be followed by comprehensive pharmacokinetic and stability studies after the controlled administration of GHB.

AB - Gamma-hydroxybutyric acid (GHB) is an important analyte in clinical and forensic toxicology with a narrow detection window of 3-6 h. In the search of improved detection methods, the existence in vivo of a glucuronated GHB metabolite (GHB-GLUC) was hypothesized. Chemically pure standards of GHB-GLUC and a deuterated analogue for chromatography were synthesized. Liquid chromatography and tandem mass spectrometry were used for targeted analysis in anonymous clinical urine samples (n = 50). GHB-GLUC was found in concentrations ranging from 0.11 to 5.0 µg/mL (mean: 1.3 ± 1.2 µg/mL). Thus far, this is the first report of a GHB glucuronide detected in biological samples. Given that glucuronides generally have longer half-life values than their corresponding free drugs, GHB-GLUC should theoretically be a biomarker of GHB intoxication. It is also proposed that the hitherto unexplained reports of elevated GHB concentrations in some biological samples, which has caused the setting of a relatively high cutoff value (10 µg/mL), represent total GHB measurements (sum of free GHB and actively chemically hydrolyzed GHB-GLUC). To address these challenges, the present study must be followed by comprehensive pharmacokinetic and stability studies after the controlled administration of GHB.

U2 - 10.1093/jat/bkt027

DO - 10.1093/jat/bkt027

M3 - Journal article

C2 - 23612681

VL - 37

SP - 291

EP - 297

JO - Journal of Analytical Toxicology

JF - Journal of Analytical Toxicology

SN - 0146-4760

IS - 5

ER -

ID: 45842261