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Simulations Plus Inc pbpk model commercial software gastroplus
<t> PBPK </t> model of lacidipine based on the literature data.
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<t> PBPK </t> model of lacidipine based on the literature data.
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<t> PBPK </t> model of lacidipine based on the literature data.
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<t> PBPK </t> model of lacidipine based on the literature data.
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Simulations Plus Inc gastroplus pbpk model
Input data used in the <t> GastroPlus </t> PBPK model.
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 PBPK  model of lacidipine based on the literature data.

Journal: Asian Journal of Pharmaceutical Sciences

Article Title: Virtual population pharmacokinetic using physiologically based pharmacokinetic model for evaluating bioequivalence of oral lacidipine formulations in dogs

doi: 10.1016/j.ajps.2016.03.003

Figure Lengend Snippet: PBPK model of lacidipine based on the literature data.

Article Snippet: In this study, all the in vivo PK simulations were conducted in the PBPK model commercial software GastroPlus (Version 8.6.0003; Simulations Plus, Inc., Lancaster, CA, USA).

Techniques: Permeability, Diffusion-based Assay, Solubility, Clinical Proteomics

Input data used in the  GastroPlus  PBPK model.

Journal: Acta Pharmacologica Sinica

Article Title: Preclinical pharmacokinetics of TPN729MA, a novel PDE5 inhibitor, and prediction of its human pharmacokinetics using a PBPK model

doi: 10.1038/aps.2015.118

Figure Lengend Snippet: Input data used in the GastroPlus PBPK model.

Article Snippet: The GastroPlus (version 8.6; Simulations Plus, Inc, Lancaster, CA, USA) PBPK model was used for all intravenous and oral simulations in preclinical species and humans.

Techniques: Molecular Weight, Permeability, Solubility, Clinical Proteomics

Observed and PBPK-model-predicted plasma-concentration-versus-time profiles of TPN729MA after intravenous administration to rats (A) or dogs (B) and oral administration to rats (C) or dogs (D). Open circles represent observed data from individual animals, and solid lines represent the profiles predicted from the PBPK model in GastroPlus. Doses were 1 mg/kg (iv) and 10 mg/kg (po) in rats and 3 mg/kg (iv) and 3 mg/kg (po) in dogs.

Journal: Acta Pharmacologica Sinica

Article Title: Preclinical pharmacokinetics of TPN729MA, a novel PDE5 inhibitor, and prediction of its human pharmacokinetics using a PBPK model

doi: 10.1038/aps.2015.118

Figure Lengend Snippet: Observed and PBPK-model-predicted plasma-concentration-versus-time profiles of TPN729MA after intravenous administration to rats (A) or dogs (B) and oral administration to rats (C) or dogs (D). Open circles represent observed data from individual animals, and solid lines represent the profiles predicted from the PBPK model in GastroPlus. Doses were 1 mg/kg (iv) and 10 mg/kg (po) in rats and 3 mg/kg (iv) and 3 mg/kg (po) in dogs.

Article Snippet: The GastroPlus (version 8.6; Simulations Plus, Inc, Lancaster, CA, USA) PBPK model was used for all intravenous and oral simulations in preclinical species and humans.

Techniques: Clinical Proteomics, Concentration Assay