کد مقاله کد نشریه سال انتشار مقاله انگلیسی نسخه تمام متن
4760847 1422472 2017 20 صفحه PDF دانلود رایگان
عنوان انگلیسی مقاله ISI
Rapid and highly sensitive analysis of benzodiazepines and tandospirone in human plasma by automated on-line column-switching UFLC-MS/MS
موضوعات مرتبط
مهندسی و علوم پایه شیمی شیمی آنالیزی یا شیمی تجزیه
پیش نمایش صفحه اول مقاله
Rapid and highly sensitive analysis of benzodiazepines and tandospirone in human plasma by automated on-line column-switching UFLC-MS/MS
چکیده انگلیسی


- A new, rapid, sensitive and selective high-throughput method was developed for analysis of 31 benzodiazepines and tandospirone.
- Only a 100-μl of plasma was requires in the assay.
- The present study provided a short analysis time and high sensitivity with lower LLOQs.
- This method can be applied to clinical and toxicological analyses.

A high-throughput method was developed for the detection of 31 benzodiazepine drugs and tandospirone in human plasma by on-line column-switching ultra-fast liquid chromatography-tandem mass spectrometry. Plasma samples (100 μl) spiked with the 32 drugs and oxazepam-d5 (internal standard) were diluted with 300 μl of 13.3 mM ammonium acetate/acetonitrile (33:67, v/v). After centrifugation and filtration, the clear supernatant was injected directly onto the extraction column (Oasis HLB cartridge column). The following procedure was fully automated. The analytes retained on the extraction column were eluted by backflushing of the extraction column and introduced into an analytical column (SUMIPAX ODS D-Swifter column, 30 mm × 3.0 mm i.d.; particle size 2 μm) by column switching. Quantification was performed by multiple reaction monitoring with positive-ion electrospray ionization. Distinct peaks appeared for each drug and the internal standard on each channel within 7 min, including the extraction time. All drugs spiked into plasma showed recoveries of 83-95%. The regression equations for the 32 drugs showed excellent linearities in the range of 50-2000 pg/ml of plasma and the limits of detection ranged from 20 to 50 pg/ml. The lower and upper limits of quantitation were 50-100 ng/ml and 2000 pg/ml, respectively. Intra- and interday coefficients of variation for none of the drugs were greater than 13.6%. The accuracies of quantitation were 87-112%. The multiple reaction monitoring information-dependent acquisition of enhanced product ions method enabled the quantification and confirmation of diazepam, triazolam, and lorazepam obtained from actual plasma.

ناشر
Database: Elsevier - ScienceDirect (ساینس دایرکت)
Journal: Legal Medicine - Volume 24, January 2017, Pages 36-55
نویسندگان
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