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In-Vitro Sorbent-Mediated Removal of Edoxaban from Human Plasma and Albumin Solution.
Angheloiu, Alexandra A; Tan, Yanglan; Ruse, Cristian; Shaffer, Scott A; Angheloiu, George O.
Affiliation
  • Angheloiu AA; Temple University, Philadelphia, PA, USA.
  • Tan Y; Mass Spectrometry Facility, University of Massachusetts Medical School, Shrewsbury, MA, USA.
  • Ruse C; Biochemistry and Molecular Pharmacology, University of Massachusetts Medical School, Worcester, MA, USA.
  • Shaffer SA; New England Biolabs, Ipswich, MA, USA.
  • Angheloiu GO; Mass Spectrometry Facility, University of Massachusetts Medical School, Shrewsbury, MA, USA.
Drugs R D ; 20(3): 217-223, 2020 Sep.
Article de En | MEDLINE | ID: mdl-32415538
BACKGROUND AND OBJECTIVE: Based on previous experience of sorbent-mediated ticagrelor, dabigatran, and radiocontrast agent removal, we set out in this study to test the effect of two sorbents on the removal of edoxaban, a factor Xa antagonist direct oral anticoagulant. METHODS: We circulated 100 mL of edoxaban solution during six first-pass cycles through 40-mL sorbent columns (containing either CytoSorb in three passes or Porapak Q 50-80 mesh in the remaining three passes) during experiments using human plasma and 4% bovine serum albumin solution as drug vehicles. Drug concentration was measured by liquid chromatography-tandem mass spectrometry. RESULTS: Edoxaban concentration in two experiments performed with human plasma dropped from 276.8 to 2.7 ng/mL and undetectable concentrations, respectively, with CytoSorb or Porapak Q 50-80 mesh (p = 0.0031). The average edoxaban concentration decreased from 407 ng/mL ± 216 ng/mL to 3.3 ng/mL ± 7 ng/mL (p = 0.017), for a removal rate of 99% across all six samples of human plasma (two samples) and bovine serum albumin solution (four samples). In four out of the six adsorbed samples, the drug concentrations were undetectable. CONCLUSION: Sorbent-mediated technology may represent a viable pathway for edoxaban removal from human plasma or albumin solution.
Sujet(s)

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Pyridines / Thiazoles / Inhibiteurs du facteur Xa Limites: Humans Langue: En Journal: Drugs R D Sujet du journal: TERAPIA POR MEDICAMENTOS Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Nouvelle-Zélande

Texte intégral: 1 Collection: 01-internacional Base de données: MEDLINE Sujet principal: Pyridines / Thiazoles / Inhibiteurs du facteur Xa Limites: Humans Langue: En Journal: Drugs R D Sujet du journal: TERAPIA POR MEDICAMENTOS Année: 2020 Type de document: Article Pays d'affiliation: États-Unis d'Amérique Pays de publication: Nouvelle-Zélande