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. 2020 Nov 26;23(1):6. doi: 10.1208/s12248-020-00535-z

Correction to: Use of Physiologically Based Pharmacokinetic (PBPK) Modeling for Predicting Drug-Food Interactions: an Industry Perspective

Arian Emami Riedmaier 1,, Kevin DeMent 2, James Huckle 3, Phil Bransford 4, Cordula Stillhart 5, Richard Lloyd 6, Ravindra Alluri 7, Sumit Basu 8, Yuan Chen 9, Varsha Dhamankar 10,11, Stephanie Dodd 12, Priyanka Kulkarni 13, Andrés Olivares-Morales 14, Chi-Chi Peng 13,15, Xavier Pepin 16, Xiaojun Ren 17, Thuy Tran 18, Christophe Tistaert 19, Tycho Heimbach 20, Filippos Kesisoglou 21, Christian Wagner 22, Neil Parrott 23
PMCID: PMC7852959  PMID: 33244667

Erratum to: The AAPS Journal volume 22, Article number: 123 (2020)

10.1208/s12248-020-00508-2

The BCS classification for furosemide in Table 3 should read IV (not III).

Table III.

Summary of the Proposed Mechanism of Food Effect and the Associated Confidence Category in the PBPK Prediction of Food Effect. Color Coding Indicates Confidence in the PBPK Food Effect Prediction; Green: High; Yellow: Moderate; Red: Low

Compound Food Effect BCS Confidence in PBPK Prediction Mechanism of Food Effect
Alectinib Positive II Low Changes in microenvironment pH and complex effect of formulation
Amiodarone Positive II Low Salt form
Aprepitant Positive II/IV High (middle-out) Bile acids and phospholipids
Cimetidine None III High (middle-out) No food effect
Clarithromycin None II Moderate No food effect
Dabrafenib Negative II Low Salt form; effect on microenvironment pH
Danazol Positive II Low Uncertainty in solubility (in vivo)
Danirixin Negative II High (bottom-up) Ion-pairing
d-Sotalol None III High (middle-out) No food effect
Etoricoxib Negative II High (bottom-up) GI motility changes in presence of food
Fluoxetine HCl None I High (bottom-up) No food effect
Furosemide Negative IV High (bottom-up/middle-out) GI motility changes in presence of food
Imatinib None II High (middle-out) No food effect
Isoniazid Negative I Moderate Drug-food interaction
Itraconazole Positive II High (middle-out) Buffer capacity alters dissolution
Ivacaftor Positive II/IV High (middle-out) Bile acids and phospholipids
Metoprolol Positive I Moderate Effect of hepatic and splanchnic blood flow
Nefazodone HCl Negative II Moderate Effect of hepatic and splanchnic blood flow
Nelfinavir Mesylate Positive II/IV Moderate Precipitation kinetics affected by food
Nifedipine None II High (bottom-up) No food effect
Oseltamivir None III Moderate No food effect
Panobinostat None II High (bottom-up) No food effect
Pazopanib Positive II/IV Low Impact of biorelevant buffer species on solubilization*; Salt form
Phenytoin Positive II High (middle-out) Bile acids and phospholipids
Telaprevir Positive II Low Impact of biorelevant buffer species on solubilization*
Tezacaftor None II High (middle-out) No food effect
Trospium IR/XR Negative III Low Changes in hydrodynamics (viscosity) in the presence of food
Venetoclax Positive IV Moderate Lymphatic uptake
Zidovudine Negative III High (bottom-up) GI motility changes in presence of food
Ziprasidone HCl Positive II Moderate Salt form

*Specialized biorelevant media required to capture food effect

Footnotes

The online version of the original article can be found at 10.1208/s12248-020-00508-2

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