Establishing the Bioequivalence Safe Space for Immediate-Release Oral Dosage Forms Using Physiologically Based Biopharmaceutics Modeling (PBBM): Case Studies
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Title
Establishing the Bioequivalence Safe Space for Immediate-Release Oral Dosage Forms Using Physiologically Based Biopharmaceutics Modeling (PBBM): Case Studies
Authors
Keywords
Bioavailability, Bioequivalence, Dissolution model(s), In Vitro-In Vivo Correlation(s) (IVIVC), Particle size, Physiologically Based Pharmacokinetic (PBPK) modeling, Biopharmaceutics
Journal
JOURNAL OF PHARMACEUTICAL SCIENCES
Volume -, Issue -, Pages -
Publisher
Elsevier BV
Online
2021-09-21
DOI
10.1016/j.xphs.2021.09.017
References
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Related references
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- In vitro dissolution methodology, mini-Gastrointestinal Simulator (mGIS), predicts better in vivo dissolution of a weak base drug, dasatinib
- (2015) Yasuhiro Tsume et al. EUROPEAN JOURNAL OF PHARMACEUTICAL SCIENCES
- Application of Absorption Modeling to Predict Bioequivalence Outcome of Two Batches of Etoricoxib Tablets
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- Pharmacokinetic Drug Interactions with Vandetanib during Coadministration with Rifampicin or Itraconazole
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