TY - JOUR
T1 - Estimation of ADME properties in drug discovery
T2 - Predicting Caco-2 cell permeability using atom-based stochastic and non-stochastic linear indices
AU - Castillo-Garit, Juan A.
AU - Marrero-Ponce, Yovani
AU - Torrens, Francisco
AU - García-Domenech, Ramón
N1 - Funding Information:
Juan A. Castillo-Garit acknowledges to the program ‘Becas para la formación especializada de jóvenes investigadores de países en vías de desarrollo’ for a fellowship to work at Valencia University (2007). Yovani Marrero-Ponce (M-P. Y) acknowledges the Valencia University for kind hospitality during the second semester of 2006. M-P. Y thanks are given to the Generalitat Valenciana, (Spain) for partial financial support as well as the program ‘Estades Temporals per an Investigadors Convidats’ for a fellowship to work at Valencia University (2006–2007). M-P. Y also thanks support from Spanish MEC (Project Reference: SAF2006-04698). F. T. acknowledges financial support from the Spanish MEC DGI (Project No.CTQ2004-07768-C02-01/BQU) and Generalitat Valenciana (DGEUI INF01-051 and INFRA03-047, and OCYT GRUPOS03-173). R.G.D Acknowledges financial support from spanish ministry of health (Projet Fis No. SAF2005/PI052128).
PY - 2008/5
Y1 - 2008/5
N2 - The in vitro determination of the permeability through cultured Caco-2 cells is the most often-used in vitro model for drug absorption. In this report, we use the largest data set of measured Pcaco-2, consisting of 157 structurally diverse compounds. Linear discriminant analysis (LDA) was used to obtain quantitative models that discriminate higher absorption compounds from those with moderate-poorer absorption. The best LDA model has an accuracy of 90.58% and 84.21% for training and test set. The percentage of good correlation, in the virtual screening of 241 drugs with the reported values of the percentage of human intestinal absorption (HIA), was greater than 81%. In addition, multiple linear regression models were developed to predict Caco-2 perme ability with determination coefficients of 0.71 and 0.72. Our method compares favorably with other approaches implemented in the Dragon software, as well as other methods from the international literature. These results suggest that the proposed method is a good tool for studying the oral absorption of drug candidates.
AB - The in vitro determination of the permeability through cultured Caco-2 cells is the most often-used in vitro model for drug absorption. In this report, we use the largest data set of measured Pcaco-2, consisting of 157 structurally diverse compounds. Linear discriminant analysis (LDA) was used to obtain quantitative models that discriminate higher absorption compounds from those with moderate-poorer absorption. The best LDA model has an accuracy of 90.58% and 84.21% for training and test set. The percentage of good correlation, in the virtual screening of 241 drugs with the reported values of the percentage of human intestinal absorption (HIA), was greater than 81%. In addition, multiple linear regression models were developed to predict Caco-2 perme ability with determination coefficients of 0.71 and 0.72. Our method compares favorably with other approaches implemented in the Dragon software, as well as other methods from the international literature. These results suggest that the proposed method is a good tool for studying the oral absorption of drug candidates.
KW - 'in silico' modeling
KW - Atom-based linear indices
KW - Caco-2 cells
KW - Computational ADME
KW - Dragon software
KW - Human intestinal absorption
KW - QSAR
KW - Virtual screening
UR - http://www.scopus.com/inward/record.url?scp=48549086653&partnerID=8YFLogxK
U2 - 10.1002/jps.21122
DO - 10.1002/jps.21122
M3 - Artículo
C2 - 17724669
AN - SCOPUS:48549086653
SN - 0022-3549
VL - 97
SP - 1946
EP - 1976
JO - Journal of Pharmaceutical Sciences
JF - Journal of Pharmaceutical Sciences
IS - 5
ER -