<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>196</volume><submitter>Xing Y</submitter><pubmed_abstract>To administer vitamin C (VC) with precision to patients with the coronavirus disease (COVID-19), we developed an ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method to assess plasma VC concentrations. 31 patients with COVID-19 and 51 healthy volunteers were enrolled. VC stability was evaluated in blood, plasma, and precipitant-containing stabilizers. A proportion of 7.7 % of VC was degraded in blood at room temperature (RT) (approximately 20-25 °C) at 1.5 h post administration with respect to the proportion degraded at 0.5 h, but without statistical difference. VC was stable in plasma for 0.75 h at RT, 2 h at 4 °C, 5 days at -40 °C, and 4 h in precipitant-containing stabilizer (2 % oxalic acid) at RT. The mean plasma concentration of VC in patients wit</pubmed_abstract><journal>Journal of pharmaceutical and biomedical analysis</journal><pagination>113927</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC7839397</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Vitamin C supplementation is necessary for patients with coronavirus disease: An ultra-high-performance liquid chromatography-tandem mass spectrometry finding.</pubmed_title><pmcid>PMC7839397</pmcid><pubmed_authors>Guo M</pubmed_authors><pubmed_authors>Zhu Z</pubmed_authors><pubmed_authors>Ling Y</pubmed_authors><pubmed_authors>Gao M</pubmed_authors><pubmed_authors>Zhao B</pubmed_authors><pubmed_authors>He J</pubmed_authors><pubmed_authors>Lu H</pubmed_authors><pubmed_authors>Xing Y</pubmed_authors><pubmed_authors>Mao E</pubmed_authors><pubmed_authors>Zhang L</pubmed_authors><pubmed_authors>Yin L</pubmed_authors><pubmed_authors>Shi H</pubmed_authors></additional><is_claimable>false</is_claimable><name>Vitamin C supplementation is necessary for patients with coronavirus disease: An ultra-high-performance liquid chromatography-tandem mass spectrometry finding.</name><description>To administer vitamin C (VC) with precision to patients with the coronavirus disease (COVID-19), we developed an ultra-high-performance liquid chromatography-tandem mass spectrometry (UPLC-MS/MS) method to assess plasma VC concentrations. 31 patients with COVID-19 and 51 healthy volunteers were enrolled. VC stability was evaluated in blood, plasma, and precipitant-containing stabilizers. A proportion of 7.7 % of VC was degraded in blood at room temperature (RT) (approximately 20-25 °C) at 1.5 h post administration with respect to the proportion degraded at 0.5 h, but without statistical difference. VC was stable in plasma for 0.75 h at RT, 2 h at 4 °C, 5 days at -40 °C, and 4 h in precipitant-containing stabilizer (2 % oxalic acid) at RT. The mean plasma concentration of VC in patients wit</description><dates><release>2021-01-01T00:00:00Z</release><publication>2021 Mar</publication><modification>2026-05-07T19:22:08.215Z</modification><creation>2026-04-07T23:13:29.429Z</creation></dates><accession>S-EPMC7839397</accession><cross_references><pubmed>33549875</pubmed><doi>10.1016/j.jpba.2021.113927</doi></cross_references></HashMap>