IDM
Institut d' investigació
Universidad Miguel Hernández de Elche
Elche, EspañaPublikationen in Zusammenarbeit mit Forschern von Universidad Miguel Hernández de Elche (66)
2024
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In Vivo Predictive Dissolution and Biopharmaceutic-Based In Silico Model to Explain Bioequivalence Results of Valsartan, a Biopharmaceutics Classification System Class IV Drug
Pharmaceutics, Vol. 16, Núm. 3
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Pharmaceutical Compounding in Veterinary Medicine: Suspension of Itraconazole
Pharmaceutics, Vol. 16, Núm. 5
2022
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Level A IVIVC for immediate release tablets confirms in vivo predictive dissolution testing for ibuprofen
International Journal of Pharmaceutics, Vol. 614
2020
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Candesartan cilexetil in vitro–in vivo correlation: Predictive dissolution as a development tool
Pharmaceutics, Vol. 12, Núm. 7, pp. 1-21
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New insights of oral colonic drug delivery systems for inflammatory bowel disease therapy
International Journal of Molecular Sciences, Vol. 21, Núm. 18, pp. 1-30
2019
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Covalently crosslinked organophosphorous derivatives-chitosan hydrogel as a drug delivery system for oral administration of camptothecin
European Journal of Pharmaceutics and Biopharmaceutics, Vol. 136, pp. 174-183
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Double Drug Delivery Using Capped Mesoporous Silica Microparticles for the Effective Treatment of Inflammatory Bowel Disease
Molecular Pharmaceutics, Vol. 16, Núm. 6, pp. 2418-2429
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Ion-pair approach coupled with nanoparticle formation to increase bioavailability of a low permeability charged drug
International Journal of Pharmaceutics, Vol. 557, pp. 36-42
2018
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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, Vol. 35, Núm. 1
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Computer simulations for bioequivalence trials: Selection of analyte in BCS class II and IV drugs with first-pass metabolism, two metabolic pathways and intestinal efflux transporter
European Journal of Pharmaceutical Sciences, Vol. 117, pp. 193-203
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Defining level A IVIVC dissolution specifications based on individual in vitro dissolution profiles of a controlled release formulation
European Journal of Pharmaceutical Sciences, Vol. 119, pp. 200-207
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Functional magnetic mesoporous silica microparticles capped with an azo-derivative: A promising colon drug delivery device
Molecules, Vol. 23, Núm. 2
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Ionic Hydrogel Based on Chitosan Cross-Linked with 6-Phosphogluconic Trisodium Salt as a Drug Delivery System
Biomacromolecules, Vol. 19, Núm. 4, pp. 1294-1304
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Long-circulating hyaluronan-based nanohydrogels as carriers of hydrophobic drugs
Pharmaceutics, Vol. 10, Núm. 4
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PLGA nanoparticles are effective to control the colonic release and absorption on ibuprofen
European Journal of Pharmaceutical Sciences, Vol. 115, pp. 119-125
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Preclinical models for colonic absorption, application to controlled release formulation development
European Journal of Pharmaceutics and Biopharmaceutics, Vol. 130, pp. 247-259
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Semi-mechanistic Pharmacokinetic/Pharmacodynamic model of three pegylated rHuEPO and ior®EPOCIM in New Zealand rabbits
European Journal of Pharmaceutical Sciences, Vol. 120, pp. 123-132
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Smart gated magnetic silica mesoporous particles for targeted colon drug delivery: New approaches for inflammatory bowel diseases treatment
Journal of Controlled Release, Vol. 281, pp. 58-69
2017
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Comparison of segmental-dependent permeability in human and in situ perfusion model in rat
European Journal of Pharmaceutical Sciences, Vol. 107, pp. 191-196
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Enhancing Oral Absorption of β-Lapachone: Progress Till Date
European Journal of Drug Metabolism and Pharmacokinetics, Vol. 42, Núm. 1