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LC-MS/MS determination of d-mannose in human serum as a potential cancer biomarker.


ABSTRACT: Several metabolites in human serum have been identified as potential cancer biomarkers for early detection. This study focuses on the LC-MS/MS method development and validation of d-mannose in human serum. Surrogate blank serum, coupled with stable isotope d-mannose-13C6, as internal standard, was used for generating standard curves ranging from 1 to 50?g/mL. Separation was achieved by an Agilent 1200 series HPLC equipped with a SUPELCOGELTM Pb, 6% Crosslinked column with HPLC water as a mobile phase at flow rate of 0.5mL/min at 80°C. Mass detection was performed under negative ionization electrospray. Inter- and intra-day accuracy and precision were <2%. The extraction recovery and matrix effect were 104.1%-105.5% and 97.0%-100.0%, respectively. This method was successfully applied for the quantification of d-mannose in the serum samples of 320 esophageal cancer patients and 323 healthy volunteers. We report a simple, specific and reproducible LC-MS/MS method for the quantification of d-mannose in human serum as a potential cancer biomarker.

SUBMITTER: White L 

PROVIDER: S-EPMC5924413 | biostudies-literature | 2017 Apr

REPOSITORIES: biostudies-literature

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LC-MS/MS determination of d-mannose in human serum as a potential cancer biomarker.

White Lyndsey L   Ma Jing J   Liang Su S   Sanchez-Espiridion Beatriz B   Liang Dong D  

Journal of pharmaceutical and biomedical analysis 20161228


Several metabolites in human serum have been identified as potential cancer biomarkers for early detection. This study focuses on the LC-MS/MS method development and validation of d-mannose in human serum. Surrogate blank serum, coupled with stable isotope d-mannose-<sup>13</sup>C<sub>6</sub>, as internal standard, was used for generating standard curves ranging from 1 to 50μg/mL. Separation was achieved by an Agilent 1200 series HPLC equipped with a SUPELCOGELTM Pb, 6% Crosslinked column with H  ...[more]

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