Salīdzināt metodes
Apskatiet izvēlētās metodes blakus; rindas, kas atšķiras, ir izceltas.
| Analīze pēc Šilda (Schild Analysis)× | Populācijas farmakodinamiskā modelēšana× | |
|---|---|---|
| Nozare | Farmakoloģija | Farmakoloģija |
| Saime | Process / pipeline | Process / pipeline |
| Izcelsmes gads≠ | 1947 | 1992 |
| Autors≠ | Henry Schild | Lewis Sheiner and Stephen Roush |
| Tips≠ | antagonism quantification | dose-response modeling |
| Pirmavots≠ | Schild, H. O. (1947). pA, a new scale for the measurement of drug antagonism. Journal of Physiology, 106(3), 337-357. DOI ↗ | Dahlström, B., & Nyberg, L. (1993). Population pharmacokinetics and pharmacodynamics. Clinical Pharmacokinetics, 24(1), 45-57. link ↗ |
| Citi nosaukumi≠ | Schild plot, pA2 | PopPD, population PD, hierarchical PD modeling |
| Saistītās | 3 | 3 |
| Kopsavilkums≠ | Schild analysis is a quantitative method for characterizing competitive receptor antagonism developed by Henry Schild in 1947. It uses dose-response curves in the presence and absence of antagonist to estimate the antagonist affinity constant (pA2), enabling standardized comparison of antagonist potency across drugs and experimental systems. | 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. |
| ScholarGateDatu kopa ↗ |
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