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Physiologically Based Pharmacokinetics×इन विट्रो-इन विवो सहसंबंध×
क्षेत्रऔषध विज्ञानऔषध विज्ञान
परिवारProcess / pipelineProcess / pipeline
उद्भव वर्ष19971995
प्रवर्तकIvan NestorovGordon Amidon
प्रकारpredictive modelingbioavailability prediction
मौलिक स्रोतNestorov, I. (1997). Sensitivity analysis of pharmacokinetic and pharmacodynamic systems. Journal of Pharmacokinetics and Biopharmaceutics, 25(4), 529-543. link ↗Amidon, G. L., Lennernäs, H., Shah, V. P., & Crison, J. R. (1995). A theoretical basis for a biopharmaceutic drug classification: the correlation of in vitro drug product dissolution and in vivo bioavailability. Pharmaceutical Research, 12(3), 413-420. DOI ↗
उपनामPBPK, PBPK modelingIVIVC
संबंधित33
सारांशPBPK is a mechanistic modeling framework that uses physiological parameters, tissue properties, and drug-specific attributes to predict drug concentration time profiles in the body. Developed rigorously in the 1990s by researchers including Nestorov, PBPK integrates anatomy, biochemistry, and kinetics to enable rational drug development, bridging in vitro data to clinical outcomes.IVIVC is a mathematical relationship between in vitro and in vivo properties of a drug, developed to predict oral bioavailability from dissolution data. Introduced by Amidon and colleagues in the 1995 Biopharmaceutics Classification System, it bridges laboratory measurements and clinical outcomes to streamline drug development.
ScholarGateडेटासेट
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  2. 2 स्रोत
  3. PUBLISHED
  1. v1
  2. 2 स्रोत
  3. PUBLISHED

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