Factors and dosage formulations affecting the solubility and bioavailability of P-glycoprotein substrate drugs
Author:
Affiliation:
1. Hiroshima International University, Hiroshima, Japan
2. Bodor Laboratories, Miami, Florida, USA
3. College of Pharmacy, University of Florida, Gainesville, Florida, USA
Publisher
Informa UK Limited
Subject
Pharmacology,Toxicology,General Medicine
Link
https://www.tandfonline.com/doi/pdf/10.1080/17425255.2021.1902986
Reference176 articles.
1. Overlapping substrate specificities and tissue distribution of cytochrome P450 3A and P-glycoprotein: Implications for drug delivery and activity in cancer chemotherapy
2. Transporter-Enzyme Interactions: Implications for Predicting Drug-Drug Interactions from In Vitro Data
3. Intestinal efflux transporters and drug absorption
4. Segmental Dependent Transport of Low Permeability Compounds along the Small Intestine Due to P-Glycoprotein: The Role of Efflux Transport in the Oral Absorption of BCS Class III Drugs
5. The Prediction of the Relative Importance of CYP3A/P-glycoprotein to the Nonlinear Intestinal Absorption of Drugs by Advanced Compartmental Absorption and Transit Model
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