Cargando…
Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model
Vitreous humor (VH) is an alternative matrix for drug analysis in forensic toxicology. However, little is known about the distribution of xenobiotics, such as opioids, into VH in living organisms. The aim of this study was to simultaneously measure heroin and metabolite concentrations in blood and V...
Autores principales: | , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Japan
2016
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018035/ https://www.ncbi.nlm.nih.gov/pubmed/27660664 http://dx.doi.org/10.1007/s11419-016-0315-z |
_version_ | 1782452849461952512 |
---|---|
author | Gottås, André Arnestad, Marianne Halvorsen, Per Steinar Bachs, Liliana C. Høiseth, Gudrun |
author_facet | Gottås, André Arnestad, Marianne Halvorsen, Per Steinar Bachs, Liliana C. Høiseth, Gudrun |
author_sort | Gottås, André |
collection | PubMed |
description | Vitreous humor (VH) is an alternative matrix for drug analysis in forensic toxicology. However, little is known about the distribution of xenobiotics, such as opioids, into VH in living organisms. The aim of this study was to simultaneously measure heroin and metabolite concentrations in blood and VH after injection of heroin in a living pig model. Six pigs were under non-opioid anesthesia during the surgical operation and experiment. Ocular microdialysis was used to acquire dialysate from VH, and a venous catheter was used for blood sampling. Twenty milligrams of heroin was injected intravenously with subsequent sampling of blood and dialysate for 6 h. The samples were analyzed by ultra-performance liquid chromatography–tandem mass spectrometry. Heroin was not detected in VH; 6-monoacetylmorphine (6-MAM) and morphine were first detected in VH after 60 min. The morphine concentration in VH thereafter increased throughout the experimental period. For 6-MAM, C(max) was reached after 230 min in VH. In blood, 6-MAM reached C(max) after 0.5 min, with a subsequent biphasic elimination phase. The blood and VH 6-MAM concentrations reached equilibrium after 2 h. In blood, morphine reached C(max) after 4.3 min, with a subsequent slower elimination than 6-MAM. The blood and VH morphine concentrations were in equilibrium about 6 h after injection of heroin. In conclusion, both 6-MAM and morphine showed slow transport into VH; detection of 6-MAM in VH did not necessarily reflect a recent intake of heroin. Because postmortem changes are expected to be small in VH, these experimental results could assist the interpretation of heroin deaths. |
format | Online Article Text |
id | pubmed-5018035 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Springer Japan |
record_format | MEDLINE/PubMed |
spelling | pubmed-50180352016-09-20 Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model Gottås, André Arnestad, Marianne Halvorsen, Per Steinar Bachs, Liliana C. Høiseth, Gudrun Forensic Toxicol Original Article Vitreous humor (VH) is an alternative matrix for drug analysis in forensic toxicology. However, little is known about the distribution of xenobiotics, such as opioids, into VH in living organisms. The aim of this study was to simultaneously measure heroin and metabolite concentrations in blood and VH after injection of heroin in a living pig model. Six pigs were under non-opioid anesthesia during the surgical operation and experiment. Ocular microdialysis was used to acquire dialysate from VH, and a venous catheter was used for blood sampling. Twenty milligrams of heroin was injected intravenously with subsequent sampling of blood and dialysate for 6 h. The samples were analyzed by ultra-performance liquid chromatography–tandem mass spectrometry. Heroin was not detected in VH; 6-monoacetylmorphine (6-MAM) and morphine were first detected in VH after 60 min. The morphine concentration in VH thereafter increased throughout the experimental period. For 6-MAM, C(max) was reached after 230 min in VH. In blood, 6-MAM reached C(max) after 0.5 min, with a subsequent biphasic elimination phase. The blood and VH 6-MAM concentrations reached equilibrium after 2 h. In blood, morphine reached C(max) after 4.3 min, with a subsequent slower elimination than 6-MAM. The blood and VH morphine concentrations were in equilibrium about 6 h after injection of heroin. In conclusion, both 6-MAM and morphine showed slow transport into VH; detection of 6-MAM in VH did not necessarily reflect a recent intake of heroin. Because postmortem changes are expected to be small in VH, these experimental results could assist the interpretation of heroin deaths. Springer Japan 2016-04-07 2016 /pmc/articles/PMC5018035/ /pubmed/27660664 http://dx.doi.org/10.1007/s11419-016-0315-z Text en © Japanese Association of Forensic Toxicology and Springer Japan 2016 |
spellingShingle | Original Article Gottås, André Arnestad, Marianne Halvorsen, Per Steinar Bachs, Liliana C. Høiseth, Gudrun Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
title | Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
title_full | Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
title_fullStr | Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
title_full_unstemmed | Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
title_short | Pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
title_sort | pharmacokinetics of heroin and its metabolites in vitreous humor and blood in a living pig model |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5018035/ https://www.ncbi.nlm.nih.gov/pubmed/27660664 http://dx.doi.org/10.1007/s11419-016-0315-z |
work_keys_str_mv | AT gottasandre pharmacokineticsofheroinanditsmetabolitesinvitreoushumorandbloodinalivingpigmodel AT arnestadmarianne pharmacokineticsofheroinanditsmetabolitesinvitreoushumorandbloodinalivingpigmodel AT halvorsenpersteinar pharmacokineticsofheroinanditsmetabolitesinvitreoushumorandbloodinalivingpigmodel AT bachslilianac pharmacokineticsofheroinanditsmetabolitesinvitreoushumorandbloodinalivingpigmodel AT høisethgudrun pharmacokineticsofheroinanditsmetabolitesinvitreoushumorandbloodinalivingpigmodel |