LC/MS Analysis of Nucleotides on SeQuant ZIC-cHILIC

LC/MS Analysis of Nucleotides on SeQuant ZIC-cHILIC

Conditions

instrument Agilent® 6530 Q-TOF LC/MS
column SeQuant ZIC-cHILIC, 10 cm x 2.1 mm, 3.0 µm
mobile phase [A] acetonitrile; [B] 50 mM ammonium acetate, pH 5.0 with acetic acid in water
gradient 26 to 27% B in 10 min; to 27 to 35% B in 10 min; to 26% B in 0.1 min; hold at 26% B for 9.9 min
flow rate 0.3 mL/min
pressure 1059 psi
column temp. 50 °C
detector Q-TOF (ESI-negative)
detector other XIC of the following m/z values: AMP-346, ADP-426, ATP-506, CMP-322, CDP-402, CTP-482, GMP-362,  GDP-442,  GTP-522, UMP-323, UDP-403, UTP-483  
injection 10 µL

Description

Analysis Note HILIC separation is an alternative that permits sensitive MS detection and without the use of ion-pair reagents. Nucleotides are the building blocks of nucleic acids. They comprise a nitrogenous base, a sugar, and a phosphate group making them highly polar and ionic. This causes a challenge for typical reversed phase chromatography (RPC). These charged polar analytes are poorly retained by RPC, and thus typically chromatographed by either ion-exchange chromatography or RPC in conjunction with an ion-pairing reagent. Nucleotide analysis using ion-pair reagents or high concentration of phosphate buffers cause high background and ion source pollution for MS detection and is undesirable compared to HILIC.
Featured Industry Life Science and Biopharma 
Legal Information SeQuant is a trademark of Merck KGaA, Darmstadt, Germany
LiChrosolv is a trademark of Merck KGaA, Darmstadt, Germany
Application No. ASC140218E

Materials

     
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