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Usefulness of Caco-2/HT29-MTX and Caco-2/HT29-MTX/Raji B Coculture Models To Predict Intestinal and Colonic Permeability Compared to Caco‑2 Monoculture

Molecular pharmaceutics, 2017-04, Vol.14 (4), p.1264-1270

2017

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A preclinical study to model taurine pharmokinetics in the undernourished rat

British journal of nutrition, 2018-04, Vol.119 (7), p.826-835

2018

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Comparison of segmental-dependent permeability in human and in situ perfusion model in rat

European journal of pharmaceutical sciences, 2017-09, Vol.107, p.191-196

2017

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Impact of Time on Parameters for Assessing the Microstructure Equivalence of Topical Products: Diclofenac 1% Emulsion as a Case Study

Pharmaceutics, 2024-06, Vol.16 (6), p.749

2024

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Impact of Pharmacokinetic and Pharmacodynamic Properties of Monoclonal Antibodies in the Management of Psoriasis

Pharmaceutics, 2022-03, Vol.14 (3), p.654

2022

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Influence of Inter- and Intra-Batch Variability on the Sample Size Required for Demonstration of Equivalent Microstructure of Semisolid Dosage Forms

Pharmaceutics, 2020-11, Vol.12 (12), p.1159

2020

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Study of the Influence of Bone Cement Type and Mixing Method on the Bioactivity and the Elution Kinetics of Ciprofloxacin

The Journal of arthroplasty, 2015-07, Vol.30 (7), p.1243-1249

2015

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Assessment of the Inter-Batch Variability of Microstructure Parameters in Topical Semisolids and Impact on the Demonstration of Equivalence

Pharmaceutics, 2019-10, Vol.11 (10), p.503

2019

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Population pharmacokinetics of lenalidomide in multiple myeloma patients

Cancer chemotherapy and pharmacology, 2017-01, Vol.79 (1), p.189-200

2017

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Multi-output Model with Box-Jenkins Operators of Quadratic Indices for Prediction of Malaria and Cancer Inhibitors Targeting Ubiquitin- Proteasome Pathway (UPP) Proteins

Current protein & peptide science, 2016-05, Vol.17 (3), p.220-227

2016

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Quality Improvement Project to Evaluate Discharge Prescriptions in Children With Cystic Fibrosis

Pediatric quality & safety, 2019-09, Vol.4 (5), p.e208-e208

2019

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Segmental-dependent permeability throughout the small intestine following oral drug administration: Single-pass vs. Doluisio approach to in-situ rat perfusion

International journal of pharmaceutics, 2016-12, Vol.515 (1-2), p.201-208

2016

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Investigation of Different Iontophoretic Currents Profiles for Short-Term Applications in Cosmetics

Pharmaceutics, 2018-12, Vol.10 (4), p.266

2018

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Relationship between rheological properties, in vitro release and in vivo equivalency of topical formulations of diclofenac

International journal of pharmaceutics, 2019-12, Vol.572, p.118755, Article 118755

2019

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Investigating drug absorption from the colon: Single-pass vs. Doluisio approaches to in-situ rat large-intestinal perfusion

International journal of pharmaceutics, 2017-07, Vol.527 (1-2), p.135-141

2017

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Characterization of intestinal absorption of C-glycoside flavonoid vicenin-2 from Lychnophora ericoides leafs in rats by nonlinear mixed effects modeling

Revista brasileira de farmacognosia, 2015-05, Vol.25 (3), p.212-218

2015

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Closed-Loop Doluisio (Colon, Small Intestine) and Single-Pass Intestinal Perfusion (Colon, Jejunum) in Rat—Biophysical Model and Predictions Based on Caco-2

Pharmaceutical research, 2018-01, Vol.35 (1), p.2-23, Article 2

2018

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In Situ Perfusion Model in Rat Colon for Drug Absorption Studies: Comparison with Small Intestine and Caco-2 Cell Model

Journal of pharmaceutical sciences, 2015-09, Vol.104 (9), p.3136-3145

2015

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Monitoring the quality of the hospital pharmacoterapeutic process by sentinel patient program

Farmacia Hospitalaria, 2018-03, Vol.42 (2), p.45-52

2018

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Current Evidence, Challenges, and Opportunities of Physiologically Based Pharmacokinetic Models of Atorvastatin for Decision Making

Pharmaceutics, 2021-05, Vol.13 (5), p.709

2021

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Multi-output model with Box–Jenkins operators of linear indices to predict multi-target inhibitors of ubiquitin–proteasome pathway

Molecular diversity, 2015-05, Vol.19 (2), p.347-356

2015

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Erratum: Mangas-Sanjuán, V.; et al. Assessment of the Inter-Batch Variability of Microstructure Parameters in Topical Semisolids and Impact on the Demonstration of Equivalence. Pharmaceutics 2019, 11 , 503

Pharmaceutics, 2020-05, Vol.12 (5), p.436

2020

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In vitro skin penetration of bronidox, bronopol and formaldehyde from cosmetics

Regulatory toxicology and pharmacology, 2021-06, Vol.122, p.104888, Article 104888

2021

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Pharmacometric characterization of entero-hepatic circulation processes of orally administered formulations of amiodarone under complex binding kinetics

European journal of pharmaceutical sciences, 2022-07, Vol.174, p.106198-106198, Article 106198

2022

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Ion-pair approach coupled with nanoparticle formation to increase bioavailability of a low permeability charged drug

International journal of pharmaceutics, 2019-02, Vol.557, p.36-42

2019

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Usefulness of Caco-2/HT29-MTX and Caco-2/HT29-MTX/Raji B Coculture Models To Predict Intestinal and Colonic Permeability Compared to Caco‑2 Monoculture

A preclinical study to model taurine pharmokinetics in the undernourished rat

Comparison of segmental-dependent permeability in human and in situ perfusion model in rat

Impact of Time on Parameters for Assessing the Microstructure Equivalence of Topical Products: Diclofenac 1% Emulsion as a Case Study

Impact of Pharmacokinetic and Pharmacodynamic Properties of Monoclonal Antibodies in the Management of Psoriasis

Influence of Inter- and Intra-Batch Variability on the Sample Size Required for Demonstration of Equivalent Microstructure of Semisolid Dosage Forms

Study of the Influence of Bone Cement Type and Mixing Method on the Bioactivity and the Elution Kinetics of Ciprofloxacin

Assessment of the Inter-Batch Variability of Microstructure Parameters in Topical Semisolids and Impact on the Demonstration of Equivalence

Population pharmacokinetics of lenalidomide in multiple myeloma patients

Multi-output Model with Box-Jenkins Operators of Quadratic Indices for Prediction of Malaria and Cancer Inhibitors Targeting Ubiquitin- Proteasome Pathway (UPP) Proteins

Quality Improvement Project to Evaluate Discharge Prescriptions in Children With Cystic Fibrosis

Segmental-dependent permeability throughout the small intestine following oral drug administration: Single-pass vs. Doluisio approach to in-situ rat perfusion

Investigation of Different Iontophoretic Currents Profiles for Short-Term Applications in Cosmetics

Relationship between rheological properties, in vitro release and in vivo equivalency of topical formulations of diclofenac

Investigating drug absorption from the colon: Single-pass vs. Doluisio approaches to in-situ rat large-intestinal perfusion

Characterization of intestinal absorption of C-glycoside flavonoid vicenin-2 from Lychnophora ericoides leafs in rats by nonlinear mixed effects modeling

Closed-Loop Doluisio (Colon, Small Intestine) and Single-Pass Intestinal Perfusion (Colon, Jejunum) in Rat—Biophysical Model and Predictions Based on Caco-2

In Situ Perfusion Model in Rat Colon for Drug Absorption Studies: Comparison with Small Intestine and Caco-2 Cell Model

Monitoring the quality of the hospital pharmacoterapeutic process by sentinel patient program

Current Evidence, Challenges, and Opportunities of Physiologically Based Pharmacokinetic Models of Atorvastatin for Decision Making

Multi-output model with Box–Jenkins operators of linear indices to predict multi-target inhibitors of ubiquitin–proteasome pathway

Erratum: Mangas-Sanjuán, V.; et al. Assessment of the Inter-Batch Variability of Microstructure Parameters in Topical Semisolids and Impact on the Demonstration of Equivalence. Pharmaceutics 2019, 11 , 503

In vitro skin penetration of bronidox, bronopol and formaldehyde from cosmetics

Pharmacometric characterization of entero-hepatic circulation processes of orally administered formulations of amiodarone under complex binding kinetics

Ion-pair approach coupled with nanoparticle formation to increase bioavailability of a low permeability charged drug

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