TY - JOUR
T1 - Microchip Liquid-Phase Ion Trap for Online Mass Spectrometry Analysis
AU - Dai, Guoxin
AU - Li, Lan
AU - Meng, Xianshuang
AU - Jiang, Ting
AU - Xu, Wei
N1 - Publisher Copyright:
© 2024 American Chemical Society
PY - 2024/8/13
Y1 - 2024/8/13
N2 - Liquid-phase ion trapping (LPIT) was proposed recently for ion manipulations in liquid channels. When coupled with mass spectrometry, LPIT exhibits considerable potential in applications such as target enrichment and bottom-up proteomics. However, further evolution of LPIT techniques requires flexible field designs including electric and fluid fields. In this study, LPIT was constructed and implemented on microfluidic chips. Utilizing conductive polymers, nonlinear potential distribution was achieved in the liquid channel, enabling the focusing of ions at distinct locations based on their effective charges and hydrodynamic radii. The integration of an electrospray ionization source facilitated coupling of the LPIT chip with a mass spectrometer. The working mechanism and parameter optimizations were explored through a combination of theoretical analysis and numerical simulations. Experiments showcased the LIPT chip’s proficiency in enrichment and separation capabilities. The detection sensitivity of the following mass spectrometer could be improved by ∼10-fold. A good linearity (R2 > 0.99) was obtained for reserpine in the range of 1-100 ng/mL. The separation capability was demonstrated using a mixture of 11 amino acids.
AB - Liquid-phase ion trapping (LPIT) was proposed recently for ion manipulations in liquid channels. When coupled with mass spectrometry, LPIT exhibits considerable potential in applications such as target enrichment and bottom-up proteomics. However, further evolution of LPIT techniques requires flexible field designs including electric and fluid fields. In this study, LPIT was constructed and implemented on microfluidic chips. Utilizing conductive polymers, nonlinear potential distribution was achieved in the liquid channel, enabling the focusing of ions at distinct locations based on their effective charges and hydrodynamic radii. The integration of an electrospray ionization source facilitated coupling of the LPIT chip with a mass spectrometer. The working mechanism and parameter optimizations were explored through a combination of theoretical analysis and numerical simulations. Experiments showcased the LIPT chip’s proficiency in enrichment and separation capabilities. The detection sensitivity of the following mass spectrometer could be improved by ∼10-fold. A good linearity (R2 > 0.99) was obtained for reserpine in the range of 1-100 ng/mL. The separation capability was demonstrated using a mixture of 11 amino acids.
UR - http://www.scopus.com/inward/record.url?scp=85200465106&partnerID=8YFLogxK
U2 - 10.1021/acs.analchem.4c01078
DO - 10.1021/acs.analchem.4c01078
M3 - Article
AN - SCOPUS:85200465106
SN - 0003-2700
VL - 96
SP - 13025
EP - 13032
JO - Analytical Chemistry
JF - Analytical Chemistry
IS - 32
ER -