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Analisi mediante Citometria a Flusso×Elettrofisiologia patch-clamp×Modellizzazione Farmacodinamica di Popolazione×
CampoFarmacologiaFarmacologiaFarmacologia
FamigliaProcess / pipelineProcess / pipelineProcess / pipeline
Anno di origine197619761992
IdeatoreLeonard HerzenbergErwin Neher and Bert SakmannLewis Sheiner and Stephen Roush
Tipocell analysis and sortingion channel screeningdose-response modeling
Fonte seminaleHerzenberg, L. A., Parks, D., Sahaf, B., Perez, O., Roederer, M., & Herzenberg, L. A. (2002). The history and future of the fluorescence-activated cell sorter and flow cytometry: a view from Stanford. Clinical Chemistry, 48(10), 1819-1827. DOI ↗Neher, E., & Sakmann, B. (1976). Single-channel currents recorded from membrane of denervated frog muscle fibres. Nature, 260(5554), 799-802. DOI ↗Dahlström, B., & Nyberg, L. (1993). Population pharmacokinetics and pharmacodynamics. Clinical Pharmacokinetics, 24(1), 45-57. link ↗
AliasFACS, fluorescence-activated cell sorting, cell analysispatch clamp, whole-cell recording, ion channel assayPopPD, population PD, hierarchical PD modeling
Correlati333
SintesiFlow cytometry is a laser-based technology for analyzing and sorting individual cells based on fluorescent markers. Developed by Leonard Herzenberg in the 1970s, flow cytometry enables rapid assessment of cell phenotype, drug effects on cell populations, and therapeutic cell characterization in immunology and hematology.Patch-clamp electrophysiology is a technique for measuring ionic currents through ion channels in cell membranes, developed by Neher and Sakmann in 1976. It enables direct observation of single-channel and whole-cell currents at millisecond resolution, making it essential for characterizing drug effects on ion channels and cardiac safety assessment.Population pharmacodynamic (PopPD) modeling integrates pharmacokinetics with individual dose-response relationships across patient populations to characterize drug efficacy and tolerability. Pioneered by Lewis Sheiner and colleagues, PopPD accounts for inter-individual variability in drug effects and enables rational dose optimization and response prediction.
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ScholarGateConfronta i metodi: Flow Cytometry · Patch-Clamp · Population Pharmacodynamics. Consultato il 2026-06-18 da https://scholargate.app/it/compare