Peer-reviewed research advancing the understanding of drug sequestration, adsorption phenomena and molecule–membrane interactions in critical care and extracorporeal therapies.
Peer-reviewed publications
Journals represented
Years of research
international collaborations
These innovations provide the scientific foundation for broad rangee of applications designed to anticipate, assess, and solve complex molecule-materiel interaction challenges.
Understanding the impact of polyacrylonitrile-derived filters on antifungal drug exposure during CRRT.
Investigating the elimination and sequestration of aminoglycosides, vancomycin, cefepime and cefotaxime in extracorporeal circuits.
Advancing predictive approaches to characterize interactions between therapeutic molecules and filtration materials.
Optimizing drug administration strategies during continuous renal replacement therapy and extracorporeal support.
Integrated solutions to understand, predict, and remove harmful interactions for better health and a cleaner environment.
Letter to the Editor regarding “Impact of Continuous Renal Replacement
Therapy with Polyacrylonitrile-Derived Filter on Caspofungin Concentration: A
Retrospective Study
In vitro assessment of cefepime adsorption in filters used during renal
replacement therapy
Is Caspofungin Efficient to Treat Invasive Candidiasis Requiring Continuous
Veno-Venous Hemofiltration? A Case Report.
Elimination of Cefotaxime Using Polysulfone and Polyacrylonitrile-Derived
Filters: An in Vitro Assessment.
Is Preloading with Amikacin a Measure Able to Mitigate Sequestration? A
Preliminary in Vitro Study
Continuous Renal Replacement Therapy in the Treatment of Severe
Hyperkalemia: An in Vitro Study.
Are We Correctly Treating Invasive Candidiasis under Continuous Renal
Replacement Therapy with Echinocandins? Preliminary in Vitro Assessment
Caspofungin Sequestration in a Polyacrylonitrile-Derived Filter. Increasing the
Dose Does Not Mitigate Sequestration.
Vancomycin Sequestration in ST Filters: An In Vitro Study.
Alteration of the Pharmacokinetics of Aminoglycosides by Adsorption in a
Filter during Continuous Renal Replacement Therapy. An in Vitro Assessment.
Disposition of Gentamicin and Amikacin in Extracorporeal Membrane
Oxygenation Using a Heparin-Coated Filter: An in Vitro Assessment.
Elimination of Voriconazole during Continuous Renal Replacement Therapy.
An in Vitro Assessment.
Elimination of Three Doses of Gentamicin over Three Consecutive Days Using
a Polyacrylonitrile-Derived Filter: An in Vitro Assessment.
Elimination of Fluconazole during Continuous Renal Replacement Therapy.
An in Vitro Assessment.
Diafiltration Flowrate Is a Determinant of the Extent of Adsorption of
Amikacin in Renal Replacement Therapy Using the ST150((R))-AN69 Filter: An
in Vitro Study.
Does Pharmacokinetics in the Central Compartment Evidence Routes of
Elimination During Continuous Renal Replacement Therapy in Ex Vivo
Model?
Should In Vitro and In Vivo Studies on Antimicrobial Agents during
Continuous Renal Replacement Therapy Comply with General Principles of
Pharmacokinetics?