Formulación y biodisponibilidad de nuevos medicamentos
Universidad Autónoma de Madrid
Madrid, EspañaPublicaciones en colaboración con investigadores/as de Universidad Autónoma de Madrid (10)
2023
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Promising biomedical subcutaneous delivery system in opioid disaccustom process: In vitro/in vivo evaluation of naloxone microparticles on antagonist effect of morphine
International Journal of Pharmaceutics, Vol. 635
2019
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Investigation on the Existence of Sex-By-Formulation Interaction in Bioequivalence Trials
Clinical Pharmacology and Therapeutics, Vol. 106, Núm. 5, pp. 1099-1112
2015
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Critical attributes of formulation and of elaboration process of PLGA-protein microparticles
International Journal of Pharmaceutics, Vol. 480, Núm. 1-2, pp. 27-36
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Overcoming glucocorticoid resistances and improving antitumor therapies: Lipid and polymers carriers
Pharmaceutical Research, Vol. 32, Núm. 3, pp. 968-985
2012
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Differences in lercanidipine systemic exposure when administered according to labelling: In fasting state and 15 minutes before food intake
European Journal of Clinical Pharmacology, Vol. 68, Núm. 7, pp. 1043-1047
2005
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Biodegradable additives modulate ganciclovir release rate from PLGA microspheres destined to intraocular administration
Letters in Drug Design and Discovery, Vol. 2, Núm. 2, pp. 148-149
1991
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Dissolution kinetics of bezafibrate in two solid forms for oral administration.
European journal of drug metabolism and pharmacokinetics, Vol. Spec No 3, pp. 371-378
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In vitro evaluation of the dissolution rate of crystalline suspensions destined to intramuscular administration.
European journal of drug metabolism and pharmacokinetics, Vol. Spec No 3, pp. 379-384
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Pharmacokinetic study of etodolac after rectal administration; "in vitro" release kinetics.
European journal of drug metabolism and pharmacokinetics, Vol. Spec No 3, pp. 389-396
1980
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INFLUENCIA DE pH Y AGENTES SOLUBILIZANTES EN LA ESTABILIDAD DEL FENOBARBITAL
Bollettino Chimico Farmaceutico, Vol. 119, Núm. 7, pp. 405-416