Determination of amphetamines, ketamine and their metabolites in hair with high-speed grinding and solid-phase microextraction followed by LC-MS

A novel hair sample pre-treatment method based on high-speed grinding and solid-phase microextraction (SPME) had been applied for the determination of amphetamines, ketamine and their metabolites in hair samples by liquid chromatography-mass spectrometry (LC-MS). A 20 mg sample of hair was ground wi...

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Main Authors: Liang Meng (Author), Yong Dai (Author), Chen Chen (Author), Jun Zhang (Author)
Format: Book
Published: Oxford University Press, 2021-07-01T00:00:00Z.
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001 doaj_d51b7564dffc4d73ba71eb9a8ec24e86
042 |a dc 
100 1 0 |a Liang Meng  |e author 
700 1 0 |a Yong Dai  |e author 
700 1 0 |a Chen Chen  |e author 
700 1 0 |a Jun Zhang  |e author 
245 0 0 |a Determination of amphetamines, ketamine and their metabolites in hair with high-speed grinding and solid-phase microextraction followed by LC-MS 
260 |b Oxford University Press,   |c 2021-07-01T00:00:00Z. 
500 |a 2096-1790 
500 |a 2471-1411 
500 |a 10.1080/20961790.2020.1838403 
520 |a A novel hair sample pre-treatment method based on high-speed grinding and solid-phase microextraction (SPME) had been applied for the determination of amphetamines, ketamine and their metabolites in hair samples by liquid chromatography-mass spectrometry (LC-MS). A 20 mg sample of hair was ground with 2 mL of saturated sodium carbonate solution using a high-efficiency hair grinder with 70 Hz oscillation for 2 min at 4 °C. After centrifuging, 1.5 mL of the supernatant was transferred and treated with SPME by direct immersion (DI-SPME). The target analytes extracted by fibre were desorbed and analysed using LC-MS. Under the optimum conditions, a recovery of 90.2%-95.8% was obtained for all analytes. The analytical method was linear for all analytes in the range from 0.2 to 10 ng/mg with the correlation coefficient ranging from 0.9985 to 0.9993. The detection limits for all analytes were estimated to be 0.067 ng/mg. The accuracy (mean relative error) was within ±6.9% and the precision (relative standard error) was less than 6.8%. The combination of high-speed grinding of hair and SPME had the advantages of being easy to perform, environment-friendly and high in detection sensitivity. The proposed method offered an alternative analytical approach for the sensitive detection of drugs in hair samples for forensic purposes.Key Points The SPME was involved for the determination of drugs in hair with LC-MS. The hair high-speed grinding combined with SPME was firstly developed. Good linearity, sensitivity, recovery and precision were achieved. 
546 |a EN 
690 |a forensic sciences 
690 |a forensic toxicology 
690 |a drugs of abuse 
690 |a high-speed grinding 
690 |a hair analysis 
690 |a liquid chromatography-mass spectrometry 
690 |a solid-phase microextraction 
690 |a Criminal law and procedure 
690 |a K5000-5582 
690 |a Public aspects of medicine 
690 |a RA1-1270 
655 7 |a article  |2 local 
786 0 |n Forensic Sciences Research, Vol 6, Iss 3, Pp 273-280 (2021) 
787 0 |n http://dx.doi.org/10.1080/20961790.2020.1838403 
787 0 |n https://doaj.org/toc/2096-1790 
787 0 |n https://doaj.org/toc/2471-1411 
856 4 1 |u https://doaj.org/article/d51b7564dffc4d73ba71eb9a8ec24e86  |z Connect to this object online.