Hydrophilic interaction liquid chromatography (HILIC) coupled to inductively coupled plasma mass spectrometry (ICPMS) utilizing a mobile phase with a low-volatile organic modifier for the determination of cisplatin, and its monohydrolyzed metabolite

2008 ◽  
Vol 23 (7) ◽  
pp. 948 ◽  
Author(s):  
Yvonne Nygren ◽  
Petrus Hemström ◽  
Crister Åstot ◽  
Peter Naredi ◽  
Erik Björn
Keyword(s):  
Mass Spectrometry ◽  
Liquid Chromatography ◽  
Inductively Coupled Plasma ◽  
Mobile Phase ◽  
Organic Modifier ◽  
Hydrophilic Interaction ◽  
Inductively Coupled ◽  
Volatile Organic ◽  
Plasma Mass Spectrometry

scholarly journals Arsenic Species Analysis at Trace Level by High Performance Liquid Chromatography with Inductively Coupled Plasma Mass Spectrometry

2019 ◽  
Vol 2019 ◽  
pp. 1-6 ◽  
Author(s):  
Hongfang Hou ◽  
Wanjing Cui ◽  
Qing Xu ◽  
Zhanhui Tao ◽  
Yafei Guo ◽  
...  
Keyword(s):  
Mass Spectrometry ◽  
High Performance Liquid Chromatography ◽  
Liquid Chromatography ◽  
Inductively Coupled Plasma ◽  
Mobile Phase ◽  
High Performance ◽  
Arsenic Species ◽  
Dimethylarsinic Acid ◽  
Inductively Coupled ◽  
Plasma Mass Spectrometry

A sensitive and accurate simultaneous continuous analysis for six arsenic species including arsenobetaine (AsB), arsenocholine (AsC), monomethylarsonic acid (MMA), dimethylarsinic acid (DMA), arsenite (AsIII), and arsenate (AsV) has been developed by high performance liquid chromatography with inductively coupled plasma mass spectrometry (HPLC-ICP-MS). An anion-exchange column of Hamilton PRP-X100 (Switzerland) was applied for separation of the six arsenic species with gradient elution of 1.25 mmol/L Na2HPO4 and 11.0 mmol/L KH2PO4 as the mobile phase A and 2.5 mmol/L Na2HPO4 and 22.0 mmol/L KH2PO4 as the mobile phase B. The linearity ranges for AsB, AsC, MMA, DMA, AsIII, and AsV were between 0.5 and 50.0 μg/L, and the detection limits of the six arsenic species were all within 0.01–0.35 ng/L. The relative standard deviations (RSDs) were within 2.26–3.68% and the recovery rates of samples ranged from 95 to 103%. The proposed method was applied for the arsenic speciation analysis of sediment pore-water samples, which were taken from the supernatant after centrifugation and filtration.

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