کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
5130737 | 1490853 | 2017 | 6 صفحه PDF | دانلود رایگان |

- Separate analyses of metabolite groups are often needed for optimally assessing the patients metabolic status.
- Quantification of these different markers has a long turnaround time.
- Chip-based nanoESI HRMS is a good alternative for current methods.
- CChip-based nanoESI HRMS is extremely fast (with analytical run times of 4.5 min per sample).
- Chip-based nanoESI HRMS is very efficient (many different markers in one run).
Diagnosis and treatment of inborn errors of metabolism (IEM) require the analysis of a variety of metabolites. These compounds are usually quantified by targeted platforms. High resolution mass spectrometry (HRMS) has the potential to detect hundreds to thousands of metabolites simultaneously. A chip-based nanoelectrospray source (chip-based nanoESI) enables the direct infusion of biological samples. Major advantages of this system include high sample throughput, no sample carryover, and low sample consumption. The combination, chip-based nanoESI-HRMS enables untargeted metabolomics of biological samples but its potential for quantification of metabolites has not been reported.We investigated whether chip-based nanoESI-HRMS is suitable for quantification of metabolites in dried blood spots (DBS). After addition of internal standards, metabolites were extracted with methanol. Aliquots of each extract were analysed by chip-based nanoESI-HRMS operating in both positive and negative mode with an m/z window of 70-600 and a resolution of 140,000. Total run time was 4.5Â min per sample and a full report could be generated within 40Â min. Concentrations of all 21 investigated diagnostic metabolites in DBS as quantified by chip-based nanoESI-HRMS correlated well with those obtained by targeted liquid chromatography-tandem mass spectrometry. We conclude that chip-based nanoESI-HRMS is suitable for quantification.
Journal: Analytica Chimica Acta - Volume 979, 1 August 2017, Pages 45-50