Revising Pharmacokinetics of Oral Drug Absorption: I Models Based on Biopharmaceutical/Physiological and Finite Absorption Time Concepts-Reference-Cited by-同舟云学术

Revising Pharmacokinetics of Oral Drug Absorption: I Models Based on Biopharmaceutical/Physiological and Finite Absorption Time Concepts

Published:2020-09-04 Issue:10 Volume:37 Page:
ISSN:0724-8741
Container-title:Pharmaceutical Research
language:en
Short-container-title:Pharm Res

Author:

Macheras Panos^ORCID,Chryssafidis Pavlos

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Organic Chemistry,Pharmaceutical Science,Pharmacology,Molecular Medicine,Biotechnology

Link

https://link.springer.com/content/pdf/10.1007/s11095-020-02894-w.pdf

Reference33 articles.

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2. Wu C, Benet L. “Predicting drug disposition via application of BCS: transport/absorption/ elimination interplay and development of a biopharmaceutics drug disposition classification system”. In: Pharm Res 22.1 (2005), pp. 11–23. [Journal Article].

3. Food and Drug Administration. Center for Drug Evaluation and Research (CDER). Waiver of In Vivo Bioavailability and Bioequivalence Studies for Immediate-Release Solid Oral Dosage Forms Based on a Biopharmaceutics Classification System. Guidance for Industry U.S. Department of Health and Human Services. 2017. [Scientific Guideline].

4. European Medicines Agency. Committee for medicinal products for human use (CHMP) Guideline on the investigation of bioequivalence. London, Jan. 2017.[Scientific Guideline].

5. Charalabidis A, Sfouni M, Bergström C, Macheras P. “BCS and BDDCS: Beyond guidelines”. In: International Journal of Pharmaceutics (2019), 566:264–281. [Journal Article].

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