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Quantitative analysis of lab-to-lab variability in Caco-2 permeability assays.
Lee, Jong Bong; Zgair, Atheer; Taha, Dhiaa A; Zang, Xiaowei; Kagan, Leonid; Kim, Tae Hwan; Kim, Min Gi; Yun, Hwi-Yeol; Fischer, Peter M; Gershkovich, Pavel.
Affiliation
  • Lee JB; School of Pharmacy, University of Nottingham, Nottingham, UK.
  • Zgair A; School of Pharmacy, University of Nottingham, Nottingham, UK; College of Pharmacy, University of Anbar, Anbar, Iraq.
  • Taha DA; School of Pharmacy, University of Nottingham, Nottingham, UK.
  • Zang X; Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
  • Kagan L; Department of Pharmaceutics, Ernest Mario School of Pharmacy, Rutgers, The State University of New Jersey, Piscataway, NJ, USA.
  • Kim TH; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
  • Kim MG; School of Pharmacy, Sungkyunkwan University, Suwon, Republic of Korea.
  • Yun HY; College of Pharmacy, Chungnam National University, Daejeon, Republic of Korea.
  • Fischer PM; School of Pharmacy, University of Nottingham, Nottingham, UK.
  • Gershkovich P; School of Pharmacy, University of Nottingham, Nottingham, UK. Electronic address: pavel.gershkovich@nottingham.ac.uk.
Eur J Pharm Biopharm ; 114: 38-42, 2017 May.
Article in En | MEDLINE | ID: mdl-28088633
In this study, Caco-2 permeability results from different laboratories were compared. Six different sets of apparent permeability coefficient (Papp) values reported in the literature were compared to experimental Papp obtained in our laboratory. The differences were assessed by determining the root mean square error (RMSE) values between the datasets, which reached levels as high as 0.581 for the training set compounds, i.e. ten compounds with known effective human permeability (Peff). The consequences of these differences in Papp for prediction of oral drug absorption were demonstrated by introducing the Papp into the absorption and pharmacokinetics simulation software application GastroPlus™ for prediction of the fraction absorbed (Fa) in humans using calibrated "user-defined permeability models". The RMSE were calculated to assess the differences between the simulated Fa and experimental values reported in the literature. The RMSE for Fa simulated with the permeability model calibrated using experimental Papp from our laboratory was 0.128. When the calibration was performed using Papp from literature datasets, the RMSE values for Fa were higher in all cases except one. This study shows quantitative lab-to-lab variability of Caco-2 permeability results and the potential consequences this can have in the use of these results for predicting intestinal absorption of drugs.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Membrane Permeability / Caco-2 Cells Type of study: Prognostic_studies Limits: Humans Language: En Journal: Eur J Pharm Biopharm Journal subject: FARMACIA / FARMACOLOGIA Year: 2017 Document type: Article Country of publication:

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Cell Membrane Permeability / Caco-2 Cells Type of study: Prognostic_studies Limits: Humans Language: En Journal: Eur J Pharm Biopharm Journal subject: FARMACIA / FARMACOLOGIA Year: 2017 Document type: Article Country of publication: