Internal quality control samples for hair testing

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Standard

Internal quality control samples for hair testing. / Nielsen, Marie Katrine Klose; Johansen, Sys Stybe.

I: Journal of Pharmaceutical and Biomedical Analysis, Bind 188, 113459, 05.09.2020.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Nielsen, MKK & Johansen, SS 2020, 'Internal quality control samples for hair testing', Journal of Pharmaceutical and Biomedical Analysis, bind 188, 113459. https://doi.org/10.1016/j.jpba.2020.113459

APA

Nielsen, M. K. K., & Johansen, S. S. (2020). Internal quality control samples for hair testing. Journal of Pharmaceutical and Biomedical Analysis, 188, [113459]. https://doi.org/10.1016/j.jpba.2020.113459

Vancouver

Nielsen MKK, Johansen SS. Internal quality control samples for hair testing. Journal of Pharmaceutical and Biomedical Analysis. 2020 sep. 5;188. 113459. https://doi.org/10.1016/j.jpba.2020.113459

Author

Nielsen, Marie Katrine Klose ; Johansen, Sys Stybe. / Internal quality control samples for hair testing. I: Journal of Pharmaceutical and Biomedical Analysis. 2020 ; Bind 188.

Bibtex

@article{20d117d16a584bfba893ddb86e23aa1e,
title = "Internal quality control samples for hair testing",
abstract = "For quality assurance, soaked quality hair samples can serve as good substitutes for the detection of chronic drug use and single-dose intake in the hair testing of multi-analytes when authentic hair samples containing the relevant substances are not available as reference material. In this study, we investigated the soaking technique for 29 common pharmaceuticals and drugs of abuse by exposing drug-free hair to reference standard solutions for a few hours. The incorporated amount had a range of 0.27–4.5 ng/mg (unwashed) following 1 h of exposure in an aqueous standard solution. Following the general washing procedures, 27 %–70 % of the incorporated amount remained in the hair, indicating that the drugs penetrated into the hair cells to some extent and were not only deposited on the surface of the hair. Thus, swelling agents such as water and methanol could allow drugs to diffuse from the solution into the hair cells, similar to the incorporation of drugs from the sebum and sweat coating the growing hair. Following the routine analysis of soaked quality samples at two levels for a one-year period, the samples were proved to be homogenous within a batch, with method imprecision less than 20 % (mean: 12 %) at a low level and less than 17 % (mean: 11 %) at a high level. Furthermore, the monitoring of aliquots of the soaked quality samples in control charts showed that the soaked samples were stable within a year except for the unstable analytes chlordiazepoxide and zopiclone, in which a decline of up to 20 % was observed.",
keywords = "Drugs of abuse, Method imprecision, Pharmaceuticals, Quality assurance, Soaked hair, Validation",
author = "Nielsen, {Marie Katrine Klose} and Johansen, {Sys Stybe}",
year = "2020",
month = sep,
day = "5",
doi = "10.1016/j.jpba.2020.113459",
language = "English",
volume = "188",
journal = "Journal of Pharmaceutical and Biomedical Analysis",
issn = "0731-7085",
publisher = "Elsevier",

}

RIS

TY - JOUR

T1 - Internal quality control samples for hair testing

AU - Nielsen, Marie Katrine Klose

AU - Johansen, Sys Stybe

PY - 2020/9/5

Y1 - 2020/9/5

N2 - For quality assurance, soaked quality hair samples can serve as good substitutes for the detection of chronic drug use and single-dose intake in the hair testing of multi-analytes when authentic hair samples containing the relevant substances are not available as reference material. In this study, we investigated the soaking technique for 29 common pharmaceuticals and drugs of abuse by exposing drug-free hair to reference standard solutions for a few hours. The incorporated amount had a range of 0.27–4.5 ng/mg (unwashed) following 1 h of exposure in an aqueous standard solution. Following the general washing procedures, 27 %–70 % of the incorporated amount remained in the hair, indicating that the drugs penetrated into the hair cells to some extent and were not only deposited on the surface of the hair. Thus, swelling agents such as water and methanol could allow drugs to diffuse from the solution into the hair cells, similar to the incorporation of drugs from the sebum and sweat coating the growing hair. Following the routine analysis of soaked quality samples at two levels for a one-year period, the samples were proved to be homogenous within a batch, with method imprecision less than 20 % (mean: 12 %) at a low level and less than 17 % (mean: 11 %) at a high level. Furthermore, the monitoring of aliquots of the soaked quality samples in control charts showed that the soaked samples were stable within a year except for the unstable analytes chlordiazepoxide and zopiclone, in which a decline of up to 20 % was observed.

AB - For quality assurance, soaked quality hair samples can serve as good substitutes for the detection of chronic drug use and single-dose intake in the hair testing of multi-analytes when authentic hair samples containing the relevant substances are not available as reference material. In this study, we investigated the soaking technique for 29 common pharmaceuticals and drugs of abuse by exposing drug-free hair to reference standard solutions for a few hours. The incorporated amount had a range of 0.27–4.5 ng/mg (unwashed) following 1 h of exposure in an aqueous standard solution. Following the general washing procedures, 27 %–70 % of the incorporated amount remained in the hair, indicating that the drugs penetrated into the hair cells to some extent and were not only deposited on the surface of the hair. Thus, swelling agents such as water and methanol could allow drugs to diffuse from the solution into the hair cells, similar to the incorporation of drugs from the sebum and sweat coating the growing hair. Following the routine analysis of soaked quality samples at two levels for a one-year period, the samples were proved to be homogenous within a batch, with method imprecision less than 20 % (mean: 12 %) at a low level and less than 17 % (mean: 11 %) at a high level. Furthermore, the monitoring of aliquots of the soaked quality samples in control charts showed that the soaked samples were stable within a year except for the unstable analytes chlordiazepoxide and zopiclone, in which a decline of up to 20 % was observed.

KW - Drugs of abuse

KW - Method imprecision

KW - Pharmaceuticals

KW - Quality assurance

KW - Soaked hair

KW - Validation

UR - http://www.scopus.com/inward/record.url?scp=85087725623&partnerID=8YFLogxK

U2 - 10.1016/j.jpba.2020.113459

DO - 10.1016/j.jpba.2020.113459

M3 - Journal article

C2 - 32659675

AN - SCOPUS:85087725623

VL - 188

JO - Journal of Pharmaceutical and Biomedical Analysis

JF - Journal of Pharmaceutical and Biomedical Analysis

SN - 0731-7085

M1 - 113459

ER -

ID: 246673972