<HashMap><database>biostudies-literature</database><scores/><additional><submitter>Gomez-Archila LG</submitter><funding>Universidad de Antioquia</funding><pagination>e0247668</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7906414</full_dataset_link><repository>biostudies-literature</repository><omics_type>Unknown</omics_type><volume>16(2)</volume><pubmed_abstract>Human peripheral blood mononuclear cells (PBMCs) are part of the innate and adaptive immune system, and form a critical interface between both systems. Studying the metabolic profile of PBMC could provide valuable information about the response to pathogens, toxins or cancer, the detection of drug toxicity, in drug discovery and cell replacement therapy. The primary purpose of this study was to develop an improved processing method for PBMCs metabolomic profiling with nuclear magnetic resonance (NMR) spectroscopy. To this end, an experimental design was applied to develop an alternative method to process PBMCs at low concentrations. The design included the isolation of PBMCs from the whole blood of four different volunteers, of whom 27 cell samples were processed by two different technique</pubmed_abstract><journal>PloS one</journal><pubmed_title>Development of an optimized method for processing peripheral blood mononuclear cells for 1H-nuclear magnetic resonance-based metabolomic profiling.</pubmed_title><pmcid>PMC7906414</pmcid><funding_grant_id>ES84170186</funding_grant_id><pubmed_authors>Zapata-Builes W</pubmed_authors><pubmed_authors>Galeano E</pubmed_authors><pubmed_authors>Palomino-Schatzlein M</pubmed_authors><pubmed_authors>Gomez-Archila LG</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of an optimized method for processing peripheral blood mononuclear cells for 1H-nuclear magnetic resonance-based metabolomic profiling.</name><description>Human peripheral blood mononuclear cells (PBMCs) are part of the innate and adaptive immune system, and form a critical interface between both systems. Studying the metabolic profile of PBMC could provide valuable information about the response to pathogens, toxins or cancer, the detection of drug toxicity, in drug discovery and cell replacement therapy. The primary purpose of this study was to develop an improved processing method for PBMCs metabolomic profiling with nuclear magnetic resonance (NMR) spectroscopy. To this end, an experimental design was applied to develop an alternative method to process PBMCs at low concentrations. The design included the isolation of PBMCs from the whole blood of four different volunteers, of whom 27 cell samples were processed by two different technique</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021</publication><modification>2026-05-08T15:24:48.465Z</modification><creation>2021-03-06T08:11:57Z</creation></dates><accession>S-EPMC7906414</accession><cross_references><pubmed>33630921</pubmed><doi>10.1371/journal.pone.0247668</doi></cross_references></HashMap>