A novel stop-flow two-dimensional liquid chromatography–mass spectrometry method for lipid analysis

•A novel 2D HILIC–RPLC–MS system was developed with the stop-flow mode.•A new stop-flow interface with trap column and make-up flow was designed.•The stop-flow 2D LC can avoid sensitivity decrease caused by dilution effect.•Peak capacity of the stop-flow 2D LC is similar to comprehensive 2D LC.•This...

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Published inJournal of Chromatography A Vol. 1321; pp. 65 - 72
Main Authors Wang, Shuangyuan, Li, Jia, Shi, Xianzhe, Qiao, Lizhen, Lu, Xin, Xu, Guowang
Format Journal Article
LanguageEnglish
Published Amsterdam Elsevier B.V 20.12.2013
Elsevier
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Abstract •A novel 2D HILIC–RPLC–MS system was developed with the stop-flow mode.•A new stop-flow interface with trap column and make-up flow was designed.•The stop-flow 2D LC can avoid sensitivity decrease caused by dilution effect.•Peak capacity of the stop-flow 2D LC is similar to comprehensive 2D LC.•This system was powerful for qualitative and quantitative analysis of lipids. A novel on-line two dimensional liquid chromatography (2D LC) based on stop-flow mode coupled with electrospray ionization mass spectrometry (ESI–MS) method was established to separate lipids in human plasma. Hydrophilic interaction liquid chromatography (HILIC) in the first dimension and reversed-phase liquid chromatography (RP LC) in the second dimension were used to separate the lipids into six fractions based on their polar head groups and further into peaks based on aliphatic chains, respectively. A new stop-flow interface with a trap column and an extra make-up flow was designed to construct this system and trap the components eluted from the first dimension. Moreover, the same length of analytical columns and similar flow rates were used in the first and second dimensions. Therefore, the new stop-flow 2D LC system can avoid the sensitivity decrease caused by the dilution effect, which is the shortcoming of comprehensive 2D LC. Three hundred and seventy-two lipids were identified from plasma extract using this 2D LC coupled with ESI–MS in positive mode, and 88 more lipids were detected than one-dimensional RP LC analysis. Peak capacity of this stop-flow 2D LC was 415, which is similar to that of comprehensive 2D LC. The linearity, repeatability and sensitivity of this method were satisfactory, which demonstrated that this method was also suitable for quantitative analysis. All these results indicated that this on-line 2D LC method is powerful for qualitative and quantitative analysis of complex lipids
AbstractList A novel on-line two dimensional liquid chromatography (2D LC) based on stop-flow mode coupled with electrospray ionization mass spectrometry (ESI–MS) method was established to separate lipids in human plasma. Hydrophilic interaction liquid chromatography (HILIC) in the first dimension and reversed-phase liquid chromatography (RP LC) in the second dimension were used to separate the lipids into six fractions based on their polar head groups and further into peaks based on aliphatic chains, respectively. A new stop-flow interface with a trap column and an extra make-up flow was designed to construct this system and trap the components eluted from the first dimension. Moreover, the same length of analytical columns and similar flow rates were used in the first and second dimensions. Therefore, the new stop-flow 2D LC system can avoid the sensitivity decrease caused by the dilution effect, which is the shortcoming of comprehensive 2D LC. Three hundred and seventy-two lipids were identified from plasma extract using this 2D LC coupled with ESI–MS in positive mode, and 88 more lipids were detected than one-dimensional RP LC analysis. Peak capacity of this stop-flow 2D LC was 415, which is similar to that of comprehensive 2D LC. The linearity, repeatability and sensitivity of this method were satisfactory, which demonstrated that this method was also suitable for quantitative analysis. All these results indicated that this on-line 2D LC method is powerful for qualitative and quantitative analysis of complex lipids.
•A novel 2D HILIC–RPLC–MS system was developed with the stop-flow mode.•A new stop-flow interface with trap column and make-up flow was designed.•The stop-flow 2D LC can avoid sensitivity decrease caused by dilution effect.•Peak capacity of the stop-flow 2D LC is similar to comprehensive 2D LC.•This system was powerful for qualitative and quantitative analysis of lipids. A novel on-line two dimensional liquid chromatography (2D LC) based on stop-flow mode coupled with electrospray ionization mass spectrometry (ESI–MS) method was established to separate lipids in human plasma. Hydrophilic interaction liquid chromatography (HILIC) in the first dimension and reversed-phase liquid chromatography (RP LC) in the second dimension were used to separate the lipids into six fractions based on their polar head groups and further into peaks based on aliphatic chains, respectively. A new stop-flow interface with a trap column and an extra make-up flow was designed to construct this system and trap the components eluted from the first dimension. Moreover, the same length of analytical columns and similar flow rates were used in the first and second dimensions. Therefore, the new stop-flow 2D LC system can avoid the sensitivity decrease caused by the dilution effect, which is the shortcoming of comprehensive 2D LC. Three hundred and seventy-two lipids were identified from plasma extract using this 2D LC coupled with ESI–MS in positive mode, and 88 more lipids were detected than one-dimensional RP LC analysis. Peak capacity of this stop-flow 2D LC was 415, which is similar to that of comprehensive 2D LC. The linearity, repeatability and sensitivity of this method were satisfactory, which demonstrated that this method was also suitable for quantitative analysis. All these results indicated that this on-line 2D LC method is powerful for qualitative and quantitative analysis of complex lipids
A novel on-line two dimensional liquid chromatography (2D LC) based on stop-flow mode coupled with electrospray ionization mass spectrometry (ESI-MS) method was established to separate lipids in human plasma. Hydrophilic interaction liquid chromatography (HILIC) in the first dimension and reversed-phase liquid chromatography (RP LC) in the second dimension were used to separate the lipids into six fractions based on their polar head groups and further into peaks based on aliphatic chains, respectively. A new stop-flow interface with a trap column and an extra make-up flow was designed to construct this system and trap the components eluted from the first dimension. Moreover, the same length of analytical columns and similar flow rates were used in the first and second dimensions. Therefore, the new stop-flow 2D LC system can avoid the sensitivity decrease caused by the dilution effect, which is the shortcoming of comprehensive 2D LC. Three hundred and seventy-two lipids were identified from plasma extract using this 2D LC coupled with ESI-MS in positive mode, and 88 more lipids were detected than one-dimensional RP LC analysis. Peak capacity of this stop-flow 2D LC was 415, which is similar to that of comprehensive 2D LC. The linearity, repeatability and sensitivity of this method were satisfactory, which demonstrated that this method was also suitable for quantitative analysis. All these results indicated that this on-line 2D LC method is powerful for qualitative and quantitative analysis of complex lipids
Author Qiao, Lizhen
Li, Jia
Shi, Xianzhe
Lu, Xin
Wang, Shuangyuan
Xu, Guowang
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Keywords On-line
Two-dimensional liquid chromatography
Stop-flow
MS
Lipid
Human
Biological fluid
Tandem mass spectrometry
Chemical analysis
On line
Two dimensional chromatography
Healthy subject
Coupled method
Hydrophilic Interaction Liquid chromatography
HPLC chromatography
Lipids
Electrospray
Blood
Blood plasma
Reversed phase chromatography
Stopped flow method
Clinical biology
Qualitative analysis
Quantitative analysis
Language English
License CC BY 4.0
Copyright © 2013 Elsevier B.V. All rights reserved.
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Snippet •A novel 2D HILIC–RPLC–MS system was developed with the stop-flow mode.•A new stop-flow interface with trap column and make-up flow was designed.•The stop-flow...
A novel on-line two dimensional liquid chromatography (2D LC) based on stop-flow mode coupled with electrospray ionization mass spectrometry (ESI–MS) method...
A novel on-line two dimensional liquid chromatography (2D LC) based on stop-flow mode coupled with electrospray ionization mass spectrometry (ESI-MS) method...
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StartPage 65
SubjectTerms Biological and medical sciences
Chromatography, Liquid - methods
electrospray ionization mass spectrometry
Humans
hydrophilic interaction chromatography
Hydrophobic and Hydrophilic Interactions
Investigative techniques, diagnostic techniques (general aspects)
Limit of Detection
Lipid
lipids
Lipids - blood
Medical sciences
Miscellaneous. Technology
On-line
Pathology. Cytology. Biochemistry. Spectrometry. Miscellaneous investigative techniques
quantitative analysis
Reference Standards
Reproducibility of Results
reversed-phase liquid chromatography
Spectrometry, Mass, Electrospray Ionization - methods
Stop-flow
Two-dimensional liquid chromatography
Title A novel stop-flow two-dimensional liquid chromatography–mass spectrometry method for lipid analysis
URI https://dx.doi.org/10.1016/j.chroma.2013.10.069
https://www.ncbi.nlm.nih.gov/pubmed/24238711
https://www.proquest.com/docview/1635029586
https://www.proquest.com/docview/1694493826
Volume 1321
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