Lopez-Viota Gallardo

Dr. Lopez-Viota Gallardo


Research Focus & Metrics

Academic Career Length

10Years (2017-Present)

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

Representative Publications

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6 March 2025 in Pharmaceuticals
Verified
Journal Article
Open access
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RGRafael Jesús Giménez-Martínez
Rafael Jesús Giménez-Martínez
Francisco Rivas GarcíaFrancisco Rivas García
Francisco Rivas García
JCJoan Carles March Cerdá
Joan Carles March Cerdá
Ángela Hernández-RuizÁngela Hernández-Ruiz
Ángela Hernández-Ruiz
MCMartha Irene González Castro
Martha Irene González Castro
LGLopez-Viota Gallardo
Lopez-Viota Gallardo
The skin is one of the largest and most important organs of our body. There are numerous factors that are related to skin health, including lifestyle factors, nutrition, or skin care. Bioactive substances from plant and marine extracts play a key role in skin health. The aim of this research was to compile the main evidence on skin and bioactive substances. An integrative review was performed, reporting the main findings according to PRISMA (2020). Thirteen search equations were developed. After the applications of the equations and the process of screening and selection of articles, 95 references were compiled. The main results related to bioactive compounds were classified into food-derived components, nutraceuticals, symbiotics, active substances of marine origin, and substances from plant extracts). There are several factors that indicate that the use of bioactive compounds are interesting for skin health, highlighting some dietary nutrients, substances obtained from plant extracts and metabolites of marine origin that, showing anti-inflammatory and antimicrobial effects, are related to the improvement of some skin conditions or are active principles for cosmetics.

15 May 2017 in AAPS PharmSciTech
Verified
Journal Article
Closed access
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LGLopez-Viota Gallardo
Lopez-Viota Gallardo
MEMazen El-Hammadi
Mazen El-Hammadi
LCLaura Cabeza
Laura Cabeza
JPJosé Prados
José Prados
CMConsolación Melguizo
Consolación Melguizo
Angel V. DelgadoAngel V. Delgado
Angel V. Delgado

7 October 2022 in Animals
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Journal Article
Open access
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VCVictoriano Corpas-López
Victoriano Corpas-López
VDVictoriano Diaz-Saez
Victoriano Diaz-Saez
FMFrancisco Morillas-Márquez
Francisco Morillas-Márquez
FFFrancisco Franco-Montalbán
Francisco Franco-Montalbán
MGMonica Diaz Gavilan
Monica Diaz Gavilan
JSJoaquina Martín Sánchez
Joaquina Martín Sánchez
Canine leishmaniosis is a challenge in veterinary medicine and no drug to date has achieved parasite clearance in dogs. Histone deacetylase inhibitors are a drug class widely used in cancer chemotherapy. We have successfully used O-alkyl hydroxamates (vorinostat derivatives) in the treatment of a laboratory model of visceral leishmaniasis without showing toxicity. In order to test the effectiveness of a particular compound, MTC-305, a parallel-group, randomized, single-centre, exploratory study was designed in naturally infected dogs. In this clinical trial, 18 dogs were allocated into 3 groups and were treated with either meglumine antimoniate (104 mg SbV/kg), MTC-305 (3.75 mg/kg) or a combination of both using a lower MTC-305 dose (1.5 mg/kg) through a subcutaneous route for 2 treatment courses of 30 days, separated by a 30-day rest period. After treatment, a follow-up time of 4 months was established. Parasite burden in bone marrow, lymph node and peripheral blood were quantified through qPCR. Antibody titres were determined through an immunofluorescence antibody test, and cytokine expression values were calculated through RT-qPCR. Treatment safety was evaluated through the assessment of haematological and biochemical parameters in blood, weight, and gastrointestinal alterations. Assessment was carried out before, between and after treatment series. Treatment with MTC-305 was effective at reducing parasite burdens and improving the animals’ clinical picture. Dogs treated with this compound did not present significant toxicity signs. These results were superior to those obtained using the reference drug, meglumine antimoniate, in monotherapy. These results would support a broader clinical trial, optimised dosage, and an expanded follow-up stage to confirm the efficacy of this drug.

30 December 2023 in Pharmaceuticals
Verified
Journal Article
Open access
PDF file
Francisco Rivas GarcíaFrancisco Rivas García
Francisco Rivas García
RGRafael Jesús Giménez-Martínez
Rafael Jesús Giménez-Martínez
FCFelipe José Huertas Camarasa
Felipe José Huertas Camarasa
JCJoan Carles March Cerdá
Joan Carles March Cerdá
FMFuensanta Lloris Messeguer
Fuensanta Lloris Messeguer
LGLopez-Viota Gallardo
Lopez-Viota Gallardo
“End of life” is a stage defined by the existence of an irreversible prognosis that ends with a person’s death. One of the aspects of interest regarding end of life focuses on parenteral nutrition, which is usually administered in order to avoid malnutrition and associated complications. However, parenteral nutrition can be adapted to specific circumstances and evolve in its functionality through supplementation with certain nutrients that can have a beneficial effect. This narrative review aims to carry out a situation analysis of the role that could be adopted by supplemental parenteral nutrition in attenuating alterations typical of end of life and potential improvement in quality of life.