Document Detail


Investigation of basic mobile phases with positive ESI LC-MS for metabonomics studies.
MedLine Citation:
PMID:  23216123     Owner:  NLM     Status:  In-Data-Review    
Abstract/OtherAbstract:
Background: Accurate mass based LC-MS combined with statistical analysis is established as a core analytical technology for metabonomic studies. This is primarily due to the specificity, sensitivity and structural elucidation capabilities of the technology. The vast majority of these studies are performed using acidic-based mobile phases in combination with positive ESI mode LC-MS. Recent studies have investigated the use of highly basic pH mobile phases (>10 pH units) in bioanalytical studies that utilize positive ESI mode LC-MS. This non-traditional combination has been shown to improve analyte retention, chromatographic peak shape, and S/N for a variety of probe pharmaceutical compounds in biofluid samples. Results: The incorporation of basic pH mobile phases resulted in increased retention for analytes that where comparatively weakly retained by a traditional acidic-modified mobile phase. Increased resolution of isomers, which otherwise co-eluted under acidic conditions, was observed. Moreover, the implementation of basic pH mobile phases further allowed for the detection of complementary marker ions. Conclusion: Basic pH mobile phases utilized with positive ESI mode LC-MS have the potential for producing increased information from metabonomic studies and could lead to the detection of analytes that may prove to be valid biomarkers.
Authors:
Paul D Rainville; Norman W Smith; David Cowan; Jeremy K Nicholson; Jp Shockcor; St John Skilton; Robert S Plumb
Related Documents :
18376583 - Spectrophotometric and reversed-phase high-performance liquid chromatographic methods f...
24859693 - Hydrophilic interaction liquid chromatography coupled with tandem mass spectrometry for...
23747843 - Application of exogenous mixture of glutathione and stable isotope labeled glutathione ...
Publication Detail:
Type:  Journal Article    
Journal Detail:
Title:  Bioanalysis     Volume:  4     ISSN:  1757-6199     ISO Abbreviation:  Bioanalysis     Publication Date:  2012 Dec 
Date Detail:
Created Date:  2012-12-10     Completed Date:  -     Revised Date:  -    
Medline Journal Info:
Nlm Unique ID:  101512484     Medline TA:  Bioanalysis     Country:  England    
Other Details:
Languages:  eng     Pagination:  2833-42     Citation Subset:  IM    
Affiliation:
King's College London, School of Pharmacy, Stamford St, London, SE1 9NH, UK.
Export Citation:
APA/MLA Format     Download EndNote     Download BibTex
MeSH Terms
Descriptor/Qualifier:

From MEDLINE®/PubMed®, a database of the U.S. National Library of Medicine


Previous Document:  Evaluation of glucuronide metabolite stability in dried blood spots.
Next Document:  Development and validation of an ultra-sensitive method for the measurement of plasma renin activity...