LCLoreto Cabarcos-Mouzo

Loreto Cabarcos-Mouzo

*This is an algorithmically generated author record based on publicly available information.

Current Organizations / Institutes

The organizations/institutes from the scholar's latest article


Loreto Cabarcos-Mouzo has a total of 8 co-authors. Here are the top co-authors by number of shared publications:

  • Ana Isabel Rodríguez-Cendal

    Universidade da Coruña, Grupo de Investigación en Terapia Celular y Medicina Regenerativa, Departamento de Fisioterapia, Medicina y Ciencias Biomédicas, Facultad de Ciencias de la Salud, 15071 A Coruña, Spain

    1 shared publication
  • Francisco Javier de Toro-Santos

    Departamento de Fisioterapia, Medicina y Ciencias Biomédicas, área de Anatomía y Embriología Humana, Universidad de A Coruña, A Coruña, España

    1 shared publication
  • Isaac Fuentes-Boquete

    Universidade da Coruña, Grupo de Investigación en Terapia Celular y Medicina Regenerativa, Departamento de Fisioterapia, Medicina y Ciencias Biomédicas, Facultad de Ciencias de la Salud, 15071 A Coruña, Spain

    1 shared publication
  • José Señarís-Rodríguez

    Universidade da Coruña, Grupo de Investigación en Terapia Celular y Medicina Regenerativa, Departamento de Fisioterapia, Medicina y Ciencias Biomédicas, Facultad de Ciencias de la Salud, 15071 A Coruña, Spain

    1 shared publication
  • Maria Carmen Veiga

    Chemical Engineering Laboratory, Faculty of Sciences and Interdisciplinary Center for Chemistry and Biology (CICA), University of Coruña, Rúa da Fraga 10, 15008 A Coruña, Spain

    1 shared publication
  • María Piñeiro-Ramil

    Musculoskeletal Pathology Group, Health Research Institute of Santiago de Compostela (IDIS), Santiago University Clinical Hospital, SERGAS, 15706 Santiago de Compostela, Spain

    1 shared publication

Latest Publications

  • Open Access

    Encapsulation of Transforming Growth Factor-β3 in Poly(hydroxybutyrate-co-hydroxyvalerate) Nanoparticles for Enhanced Cartilage Tissue Engineering

    by Ana Isabel Rodríguez-Cendal, José Señarís-Rodríguez, María Piñeiro-Ramil, Loreto Cabarcos-Mouzo, María del Carmen Veiga-Barbazán, Rosa María Mejide-Faílde, Francisco Javier de Toro-Santos, Isaac Manuel Fuentes-Boquete, Silvia María Díaz-Prado

    Poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV) is a naturally occurring biopolymer belonging to the polyhydroxyalkanoate (PHA) family. Due to its excellent properties (biocompatible, biodegradable, and non-toxic), this biopolymer is presented as a very suitable option for use in regenerative therapy as a drug delivery system (DDS). The protein encapsulated in this study is transforming growth factor β3 (TGF-β3), which plays a key role in the chondrogenic differentiation of mesenchymal stem cells (MSCs). The main objective of this work is to evaluate the efficacy of PHBV nanoparticles (NPs) produced from a dairy by-product (whey) as a DDS of TGF-β3 for cartilage regeneration and extracellular matrix (ECM) synthesis and to reduce the complications associated with multiple high doses of TGF-β3 in its free form. For this purpose, biopolymer cytotoxicity, factor release, cell viability, cell proliferation, and differentiation were analyzed. The results showed that the biomaterial purified with chloroform and ethanol, either by single or double precipitation, was not toxic to cells. A sustained release profile was observed, reaching its maximum around day 4. The TGF-β3 NPs promoted the differentiation of MSCs into chondrocytes and the formation of ECM. In conclusion, PHBV demonstrated its potential as an optimal material for DDSs in cartilage regenerative therapy, effectively addressing the key challenge of the need for a single delivery method to reduce complications associated with multiple high doses of TGF-β3.