Evidence map›Paper›PMID 40507809›Full record

ArticleInternational journal of molecular sciences2025

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

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

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors.

Ana Isabel Rodríguez-CendalUniversidade 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.ORCID 0009-0006-6728-7036
José Señarís-RodríguezUniversidade 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.
María Piñeiro-RamilUniversidade 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.ORCID 0000-0002-6202-1865
Loreto Cabarcos-MouzoUniversidade da Coruña, Grupo de Investigación en Bioingeniería Ambiental y Control de Calidad (BIOENGIN), Centro Interdisciplinar de Química y Biología (CICA), 15071 A Coruña, Spain.ORCID 0009-0001-0026-2276
María Del Carmen Veiga-BarbazánUniversidade da Coruña, Grupo de Investigación en Bioingeniería Ambiental y Control de Calidad (BIOENGIN), Centro Interdisciplinar de Química y Biología (CICA), 15071 A Coruña, Spain.
Rosa María Mejide-FaíldeUniversidade 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.ORCID 0000-0001-8516-9419
Francisco Javier de Toro-SantosUniversidade 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.ORCID 0000-0001-6131-1273
Isaac Manuel Fuentes-BoqueteUniversidade 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.
Silvia María Díaz-PradoUniversidade 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.ORCID 0000-0001-9776-2180

Funding

Ayudas para proyectos Semilla-Disruptivos entre grupos del CICA 2021 (Universidade da Coruña) POLIBIOMEDGrupos con Potencial de Crecemento (Xunta de Galicia) ED431B 2020/55Grupos con Potencial de Crecemento (Xunta de Galicia) ED431B 2023/58Grupos de Referencia Competitiva (Xunta de Galicia) ED431C 2021/55Instituto de Salud Carlos III - General Subdirection of Assessment and Promotion of Research - European Regional Development Fund (FEDER) "A way of making Europe" PI20/00933Proyectos de Desarrollo y Transferencia (Fundación Pública Gallega de Investigación Biomédica) 2022Proyectos de Desarrollo y Transferencia (Fundación Pública Gallega de Investigación Biomédica) 2024Spanish Ministry of Economy and Competitiveness (MINECO) through European FEDER funds PID2023-151067OB-I00
6 · The paper itself

Abstract

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.

Indexed as

CartilageNanoparticlesPolyestersTissue EngineeringTransforming Growth Factor beta3AnimalsCell DifferentiationCell ProliferationCell SurvivalChondrogenesisExtracellular MatrixHumansHydroxybutyratesMesenchymal Stem CellsPolyhydroxybutyratesPolymersHydroxybutyratespoly(3-hydroxybutyrate)-co-(3-hydroxyvalerate)Polyesterspoly(hydroxybutyrate-co-hydroxyvalerate)PolyhydroxybutyratesPolymersTransforming Growth Factor beta3drug delivery system (DDS)nanoparticles (NPs)polyhydroxyalkanoate (PHA)poly(hydroxybutyrate-co-hydroxyvalerate) (PHBV)regenerative therapy

Identifiers

PMID40507809
PMCPMC12154055

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.