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الارتباط المختبري-الحيوي (In Vitro-In Vivo Correlation)×معامل التشابه بالذوبان f1/f2×
المجالعلم الأدويةعلم الأدوية
العائلةProcess / pipelineProcess / pipeline
سنة النشأة19951996
صاحب الطريقةGordon AmidonJames Moore and Hector Flanner
النوعbioavailability predictionsimilarity testing
المصدر التأسيسيAmidon, 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 ↗Moore, J. W., & Flanner, H. H. (1996). Mathematical comparison of dissolution profiles. Pharmaceutical Technology, 20(6), 64-74. link ↗
الأسماء البديلةIVIVCf1, f2, similarity factor
ذات صلة33
الملخصIVIVC 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.The f1 and f2 factors are dimensionless statistical measures developed by Moore and Flanner to quantify the similarity between two dissolution profiles. Adopted by regulatory agencies (FDA, EMA) as the gold standard for comparing dissolution curves, these factors enable rapid assessment of whether formulation changes significantly impact drug release.
ScholarGateمجموعة البيانات
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  1. v1
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ScholarGateقارن الطرق: In Vitro-In Vivo Correlation · Dissolution f1/f2 Similarity. استُرجع بتاريخ 2026-06-20 من https://scholargate.app/ar/compare