Title of article :
Hydrophilic interaction liquid chromatography-solid phase extraction directly combined with protein precipitation for the determination of triptorelin in plasma
Author/Authors :
Wang، نويسنده , , Jixia and Kong، نويسنده , , Song Xiao-yan، نويسنده , , Jingyu and Jin، نويسنده , , Gaowa and Guo، نويسنده , , Zhimou and Shen، نويسنده , , Aijin and Xu، نويسنده , , Junyan and Zhang، نويسنده , , Xiuli and Zou، نويسنده , , Lijuan and Liang، نويسنده , , Xinmiao، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2014
Pages :
8
From page :
214
To page :
221
Abstract :
Peptide drugs play a critical role in therapeutic treatment. However, as the complexity of plasma, determination of peptide drugs using liquid chromatography–tandem mass spectrometry (LC–MS/MS) is a daunting task. To solve this problem, hydrophilic interaction liquid chromatography-solid phase extraction (HILIC-SPE) directly combined with protein precipitation (PPT) was developed for the selective extraction of triptorelin from plasma. The extracts were analyzed by reversed-phase liquid chromatography (RPLC). Proteins, phospholipids and highly polar interferences could be removed from plasma by the efficient combination of PPT, HILIC-SPE and RPLC–MS/MS. This method was evaluated by matrix effect, recovery and process efficiency at different concentration levels (50, 500 and 5000 ng/mL) of triptorelin. Furthermore, the performance of HILIC-SPE was compared with that of reversed-phase C18 SPE and hydrophilic lipophilic balance (Oasis HLB) SPE. Among them, HILIC-SPE provided the minimum matrix effect (ranging from 96.02% to 103.41%), the maximum recovery (ranging from 80.68% to 90.54%) and the satisfactory process efficiency (ranging from 82.83% to 92.95%). The validated method was successfully applied to determine triptorelin in rat plasma.
Keywords :
PPT , Triptorelin , RPLC–MS/MS , PLASMA , HILIC-SPE
Journal title :
Journal of Chromatography B
Serial Year :
2014
Journal title :
Journal of Chromatography B
Record number :
1472290
Link To Document :
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