TY - JOUR
T1 - Dried blood spots combined to an UPLC–MS/MS method for the simultaneous determination of drugs of abuse in forensic toxicology
AU - Sadler Simões, Susana
AU - Castañera Ajenjo, Antonio
AU - Dias, Mário João
N1 - Publisher Copyright:
© 2017 Elsevier B.V.
PY - 2018/1/5
Y1 - 2018/1/5
N2 - A method for the simultaneous determination of 11 illicit drugs, using the dried blood spot (DBS) sampling technique combined with the UPLC–MS/MS technology was developed to study its applicability within the forensic toxicology. The DBS samples, prepared from a blood volume of 50 μL and using the Whatman® BFC 180 bloodstain cards, were extracted with a methanol/acetonitrile mixture. The chromatographic separation was performed using an Acquity UPLC® HSS T3 column (100 mm × 2.1 mm, 1.8 μm) and an acetonitrile/2 mM ammonium formate (0.1% formic acid) gradient. The detection was accomplished with a TQ Detector, operating in the ESI+ and MRM modes. The method was validated in terms of selectivity, matrix effect, extraction recovery (42%–91%), carryover, LOD and LOQ (0.5–1 ng/mL and 1–5 ng/mL, respectively), linearity (LOQ to 500 ng/mL), intraday and interday precision (3.8–14% and 5.3–13%, respectively), accuracy (−9.3% to 7.9%) and dilution integrity. An eight months stability study at room temperature, 2–8 °C and −10 °C, was also performed, with the best results obtained at −10 °C. The procedure was applied to 64 real samples (92 positive results for substances included in this study). The results were compared with the methodologies routinely applied in the laboratory and the statistical analysis allowed to establish an acceptable correlation. This study permitted to determine that the DBS can represent an alternative or a complement to conventional analytical and sampling techniques, responding to some of the present issues concerning the different forensic toxicology applications.
AB - A method for the simultaneous determination of 11 illicit drugs, using the dried blood spot (DBS) sampling technique combined with the UPLC–MS/MS technology was developed to study its applicability within the forensic toxicology. The DBS samples, prepared from a blood volume of 50 μL and using the Whatman® BFC 180 bloodstain cards, were extracted with a methanol/acetonitrile mixture. The chromatographic separation was performed using an Acquity UPLC® HSS T3 column (100 mm × 2.1 mm, 1.8 μm) and an acetonitrile/2 mM ammonium formate (0.1% formic acid) gradient. The detection was accomplished with a TQ Detector, operating in the ESI+ and MRM modes. The method was validated in terms of selectivity, matrix effect, extraction recovery (42%–91%), carryover, LOD and LOQ (0.5–1 ng/mL and 1–5 ng/mL, respectively), linearity (LOQ to 500 ng/mL), intraday and interday precision (3.8–14% and 5.3–13%, respectively), accuracy (−9.3% to 7.9%) and dilution integrity. An eight months stability study at room temperature, 2–8 °C and −10 °C, was also performed, with the best results obtained at −10 °C. The procedure was applied to 64 real samples (92 positive results for substances included in this study). The results were compared with the methodologies routinely applied in the laboratory and the statistical analysis allowed to establish an acceptable correlation. This study permitted to determine that the DBS can represent an alternative or a complement to conventional analytical and sampling techniques, responding to some of the present issues concerning the different forensic toxicology applications.
KW - Dried blood spots
KW - Drugs of abuse
KW - UPLC–MS/MS
KW - Validation
UR - http://www.scopus.com/inward/record.url?scp=85014802506&partnerID=8YFLogxK
U2 - 10.1016/j.jpba.2017.02.046
DO - 10.1016/j.jpba.2017.02.046
M3 - Article
C2 - 28292561
AN - SCOPUS:85014802506
SN - 0731-7085
VL - 147
SP - 634
EP - 644
JO - Journal of Pharmaceutical and Biomedical Analysis
JF - Journal of Pharmaceutical and Biomedical Analysis
ER -