» Articles » PMID: 24072264

The Use of ROC Analysis for the Qualitative Prediction of Human Oral Bioavailability from Animal Data

Overview
Journal Pharm Res
Specialties Pharmacology
Pharmacy
Date 2013 Sep 28
PMID 24072264
Citations 15
Authors
Affiliations
Soon will be listed here.
Abstract

Purpose: To develop and evaluate a tool for the qualitative prediction of human oral bioavailability (Fhuman) from animal oral bioavailability (Fanimal) data employing ROC analysis and to identify the optimal thresholds for such predictions.

Methods: A dataset of 184 compounds with known Fhuman and Fanimal in at least one species (mouse, rat, dog and non-human primates (NHP)) was employed. A binary classification model for Fhuman was built by setting a threshold for high/low Fhuman at 50%. The thresholds for high/low Fanimal were varied from 0 to 100 to generate the ROC curves. Optimal thresholds were derived from 'cost analysis' and the outcomes with respect to false negative and false positive predictions were analyzed against the BDDCS class distributions.

Results: We successfully built ROC curves for the combined dataset and per individual species. Optimal Fanimal thresholds were found to be 67% (mouse), 22% (rat), 58% (dog), 35% (NHP) and 47% (combined dataset). No significant trends were observed when sub-categorizing the outcomes by the BDDCS.

Conclusions: Fanimal can predict high/low Fhuman with adequate sensitivity and specificity. This methodology and associated thresholds can be employed as part of decisions related to planning necessary studies during development of new drug candidates and lead selection.

Citing Articles

Unraveling the Omega-3 Puzzle: Navigating Challenges and Innovations for Bone Health and Healthy Aging.

Ali Z, Al-Ghouti M, Abou-Saleh H, Rahman M Mar Drugs. 2024; 22(10).

PMID: 39452854 PMC: 11509197. DOI: 10.3390/md22100446.


Therapeutic, and pharmacological prospects of nutmeg seed: A comprehensive review for novel drug potential insights.

Al-Rawi S, Ibrahim A, Ahmed H, Khudhur Z Saudi Pharm J. 2024; 32(6):102067.

PMID: 38690209 PMC: 11059288. DOI: 10.1016/j.jsps.2024.102067.


Use of ROC curve analysis for prediction gives fallacious results: Use predictivity-based indices.

Indrayan A, Malhotra R, Pawar M J Postgrad Med. 2024; 70(2):91-96.

PMID: 38668827 PMC: 11160993. DOI: 10.4103/jpgm.jpgm_753_23.


Molecular docking-based virtual screening, drug-likeness, and pharmacokinetic profiling of some anti- cephalosporin derivatives.

Ameji P, Uzairu A, Shallangwa G, Uba S J Taibah Univ Med Sci. 2024; 18(6):1417-1431.

PMID: 38162870 PMC: 10757315. DOI: 10.1016/j.jtumed.2023.05.021.


The Bioavailability of Drugs-The Current State of Knowledge.

Stielow M, Witczynska A, Kubryn N, Fijalkowski L, Nowaczyk J, Nowaczyk A Molecules. 2023; 28(24).

PMID: 38138529 PMC: 10745386. DOI: 10.3390/molecules28248038.


References
1.
Chiou W, Barve A . Linear correlation of the fraction of oral dose absorbed of 64 drugs between humans and rats. Pharm Res. 1998; 15(11):1792-5. DOI: 10.1023/a:1011981317451. View

2.
Grass G, Sinko P . Physiologically-based pharmacokinetic simulation modelling. Adv Drug Deliv Rev. 2002; 54(3):433-51. DOI: 10.1016/s0169-409x(02)00013-3. View

3.
Metz C . Basic principles of ROC analysis. Semin Nucl Med. 1978; 8(4):283-98. DOI: 10.1016/s0001-2998(78)80014-2. View

4.
Broccatelli F, Cruciani G, Benet L, Oprea T . BDDCS class prediction for new molecular entities. Mol Pharm. 2012; 9(3):570-80. PMC: 3295927. DOI: 10.1021/mp2004302. View

5.
Zhao Y, Abraham M, Le J, Hersey A, Luscombe C, Beck G . Evaluation of rat intestinal absorption data and correlation with human intestinal absorption. Eur J Med Chem. 2003; 38(3):233-43. DOI: 10.1016/s0223-5234(03)00015-1. View