Pregled bibliografske jedinice broj: 864538
LONG TERM STABILITY OF METHADONE AND EDDP IN CLINICAL BLOOD SAMPLES
LONG TERM STABILITY OF METHADONE AND EDDP IN CLINICAL BLOOD SAMPLES // Abstracts of the 5th Croatian Congress of Toxicology with International Participation CROTOX 2016 / Durgo, Ksenija (ur.).
Zagreb, 2016. str. 63-63 (poster, međunarodna recenzija, sažetak, ostalo)
CROSBI ID: 864538 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
LONG TERM STABILITY OF METHADONE AND EDDP IN CLINICAL BLOOD SAMPLES
Autori
Veršić Bratinčević, Maja ; Sutlović, Davorka
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, ostalo
Izvornik
Abstracts of the 5th Croatian Congress of Toxicology with International Participation CROTOX 2016
/ Durgo, Ksenija - Zagreb, 2016, 63-63
Skup
CROTOX 2016 - 5th Croatian Congress of Toxicology with International Participation
Mjesto i datum
Poreč, Hrvatska, 09.10.2016. - 12.10.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
methadone, EDDP, blood samples, stability, GC/MS, toxicology
Sažetak
Methadone is a synthetic opiate, widely used to help heroin addicts undergoing maintenance programs. Determination of methadone and its metabolites represents a routine procedure in forensic toxicology. Biological samples, according to legislation, should be stored at least six months after the first analysis. Storage conditions, combined with the stability of drugs, can significantly affect the interpretation of results. Due to these reasons, it was necessary to examine the time effect on the stability of methadone and its metabolite 2-ethylidene-1, 5-dimethyl-3, 3-diphenylpyrrolidine (EDDP) in biological blood samples stored for more than six months. The effect of long-term stability of methadone and EDDP was studied by a repeated quantitative analysis of the same samples after long-term storage at -20 °C. A total of 50 clinical blood samples were analysed, and 20 samples, in which the presence of methadone and EDDP was confirmed, were reanalyzed after long-term storage period. The first analysis was performed 1-3 days after sampling, and the repeated analysis was performed after 293-369 days of storage for each sample. GC/MS analysis of clinical blood samples preceded the LLE sample preparation, and results were compared. In the repeated analysis, all blood samples showed lower methadone concentrations (from 2.04% to 80.74%). Contrary to expectations, reanalysis of all blood samples showed absence of EDDP. Further experiments on methadone and EDDP stability in stored biological samples, at different storage conditions and in combination with other factors, should be undertaken to ensure the proper interpretation, reliability and reproducibility of the analysis results.
Izvorni jezik
Engleski
Znanstvena područja
Temeljne medicinske znanosti, Farmacija
POVEZANOST RADA
Ustanove:
KBC Split,
Medicinski fakultet, Split