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| Farmakokinetyka leku zależna od wiązania z celem molekularnym× | Modelowanie farmakodynamiczne populacyjne× | |
|---|---|---|
| Dziedzina | Farmakologia | Farmakologia |
| Rodzina | Process / pipeline | Process / pipeline |
| Rok powstania≠ | 2001 | 1992 |
| Twórca≠ | Donald Mager and William Jusko | Lewis Sheiner and Stephen Roush |
| Typ≠ | nonlinear PK modeling | dose-response modeling |
| Źródło pierwotne≠ | Mager, D. E., & Jusko, W. J. (2001). General pharmacokinetic model for drugs exhibiting target-mediated drug disposition. Journal of Pharmacokinetics and Pharmacodynamics, 28(6), 507-532. DOI ↗ | Dahlström, B., & Nyberg, L. (1993). Population pharmacokinetics and pharmacodynamics. Clinical Pharmacokinetics, 24(1), 45-57. link ↗ |
| Inne nazwy≠ | TMDD, target-driven clearance | PopPD, population PD, hierarchical PD modeling |
| Pokrewne | 3 | 3 |
| Podsumowanie≠ | Target-mediated drug disposition (TMDD) is a mechanistic framework describing nonlinear pharmacokinetics arising from drug binding to a target receptor or protein. Developed by Mager and Jusko in 2001, TMDD explains saturable clearance, dose-dependent half-lives, and time-dependent changes in plasma concentrations observed with protein therapeutics and some small-molecule drugs. | 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. |
| ScholarGateZbiór danych ↗ |
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