Virginia Merino

Dr. Virginia Merino

Department of Pharmacy and Pharmaceutical Technology and Parasitology, School of Pharmacy, University of Valencia, Valencia, Spain
orcid

Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 February 2000 in Journal of Controlled Release
Verified
Journal Article
Closed access
RGRichard H. Guy
Richard H. Guy
Yogeshvar KaliaYogeshvar Kalia
Yogeshvar Kalia
M. Begoña Delgado-CharroM. Begoña Delgado-Charro
M. Begoña Delgado-Charro
VMVirginia Merino
Virginia Merino
Alicia López-CastellanoAlicia López-Castellano
Alicia López-Castellano
DMDiego Marro
Diego Marro

1 March 2004 in European Journal of Pharmaceutical Sciences
Verified
Journal Article
Closed access
Marival BermejoMarival Bermejo
Marival Bermejo
AAAlex Avdeef
Alex Avdeef
ARAna Ruiz
Ana Ruiz
Ricardo Nalda-MolinaRicardo Nalda-Molina
Ricardo Nalda-Molina
JRJeffrey A. Ruell
Jeffrey A. Ruell
VMVirginia Merino
Virginia Merino

Verified
Journal Article
Open access
PDF file
ATAdrian H. Teruel
Adrian H. Teruel
Isabel Gonzalez-AlvarezIsabel Gonzalez-Alvarez
Isabel Gonzalez-Alvarez
Marival BermejoMarival Bermejo
Marival Bermejo
VMVirginia Merino
Virginia Merino
MMM. Dolores Marcos
M. Dolores Marcos
RMRamón Martínez-Máñez
Ramón Martínez-Máñez
Colonic Drug Delivery Systems (CDDS) are especially advantageous for local treatment of inflammatory bowel diseases (IBD). Site-targeted drug release allows to obtain a high drug concentration in injured tissues and less systemic adverse effects, as consequence of less/null drug absorption in small intestine. This review focused on the reported contributions in the last four years to improve the effectiveness of treatments of inflammatory bowel diseases. The work concludes that there has been an increase in the development of CDDS in which pH, specific enzymes, reactive oxygen species (ROS), or a combination of all of these triggers the release. These delivery systems demonstrated a therapeutic improvement with fewer adverse effects. Future perspectives to the treatment of this disease include the elucidation of molecular basis of IBD diseases in order to design more specific treatments, and the performance of more in vivo assays to validate the specificity and stability of the obtained systems.

1 February 2015 in Acta Biomaterialia
Verified
Journal Article
Closed access
ICInes Castangia
Ines Castangia
ANAmparo Nacher
Amparo Nacher
CCCarla Caddeo
Carla Caddeo
VMVirginia Merino
Virginia Merino
ODOctavio Díez-Sales
Octavio Díez-Sales
Maria ManconiMaria Manconi
Maria Manconi

1 June 2012 in Colloids and Surfaces B: Biointerfaces
Verified
Journal Article
Closed access
CMC. Mura
C. Mura
ANAmparo Nacher
Amparo Nacher
VMVirginia Merino
Virginia Merino
MMMatilde Merino-Sanjuán
Matilde Merino-Sanjuán
Maria ManconiMaria Manconi
Maria Manconi
ODO. Díez-Sales
O. Díez-Sales

1 September 2005 in European Journal of Pharmaceutics and Biopharmaceutics
Verified
Journal Article
Closed access
AFA. Femenía-Font
A. Femenía-Font
CBC. Balaguer-Fernández
C. Balaguer-Fernández
VMVirginia Merino
Virginia Merino
Vicent RodillaVicent Rodilla
Vicent Rodilla
Alicia López-CastellanoAlicia López-Castellano
Alicia López-Castellano