TY - JOUR
T1 - Prediction of caco-2 cell permeability using bilinear indices and multiple linear regression
AU - Le-Thi-Thu, Huong
AU - Canizares-Carmenate, Yudith
AU - Marrero-Ponce, Yovani
AU - Torrens, Francisco
AU - Castillo-Garit, Juan A.
N1 - Publisher Copyright:
© 2016 Bentham Science Publishers.
PY - 2016/1/1
Y1 - 2016/1/1
N2 - The qualitative relationship between in vitro Caco-2 cellular transport and in vivo drug permeability allow using Caco-2 cell assay for intestinal absorption studies. In this work, atom-based bilinear indices and multiple linear regression (MLR) are applied to obtain models useful for the prediction of Caco-2 cell absorption. Making use of a previously reported database, we obtain four statistically significant MLR models, the best models shown R2=0.72 (s=0.435) for nonstochastic indices and R2=0.66 (s=0.464) for stochastic indices. No significant difference was found when comparing to previous reported studies. The models were internally validated using leave-one-out cross-validation, bootstrapping, as well as Y-scrambling experiments. Additionally, we performed an external validation using a test set, which yields significant values of R2ext of 0.70 and 0.72 for stochastic models, showing a better predictive power. Furthermore, we define a domain of applicability for our models. These results suggest that our approach could offer an appropriate tool as an alternative to predict the absorption in Caco-2 cells in a short time and decrease experimental costs.
AB - The qualitative relationship between in vitro Caco-2 cellular transport and in vivo drug permeability allow using Caco-2 cell assay for intestinal absorption studies. In this work, atom-based bilinear indices and multiple linear regression (MLR) are applied to obtain models useful for the prediction of Caco-2 cell absorption. Making use of a previously reported database, we obtain four statistically significant MLR models, the best models shown R2=0.72 (s=0.435) for nonstochastic indices and R2=0.66 (s=0.464) for stochastic indices. No significant difference was found when comparing to previous reported studies. The models were internally validated using leave-one-out cross-validation, bootstrapping, as well as Y-scrambling experiments. Additionally, we performed an external validation using a test set, which yields significant values of R2ext of 0.70 and 0.72 for stochastic models, showing a better predictive power. Furthermore, we define a domain of applicability for our models. These results suggest that our approach could offer an appropriate tool as an alternative to predict the absorption in Caco-2 cells in a short time and decrease experimental costs.
KW - ADME
KW - Bilinear indices
KW - Caco-2 cell
KW - QSAR
KW - TOMOCOMD-CARDD
UR - http://www.scopus.com/inward/record.url?scp=84959572109&partnerID=8YFLogxK
U2 - 10.2174/1570180812666150630183511
DO - 10.2174/1570180812666150630183511
M3 - Artículo
AN - SCOPUS:84959572109
SN - 1570-1808
VL - 13
SP - 161
EP - 169
JO - Letters in Drug Design and Discovery
JF - Letters in Drug Design and Discovery
IS - 2
ER -