Evidence map›Paper›PMID 35745711›Full record

ArticlePharmaceutics2022

Multifunctional PLA/Gelatin Bionanocomposites for Tailored Drug Delivery Systems.

Carmen Moya-Lopez, Alberto Juan, Murillo Donizeti, Jesus Valcarcel, José A Vazquez, Eduardo Solano, David Chapron, Patrice Bourson, Ivan Bravo, Carlos Alonso-Moreno and 8 more

Open access · goldAbstract read
In one paragraph

Article in Pharmaceutics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed
1.3field-weighted citation impact, top 24% of its field
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

6 citing papers in PubMed, 17 citations in OpenAlex.

  1. Review
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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

18 authors at 9 institutions in 5 countries.

Carmen Moya-LopezLaboratoire Matériaux Optiques Photonique et Systèmes (LMOPS), Centrale Supélec, Université de Lorraine, 57000 Metz, France.ORCID 0000-0002-6210-1443
Alberto JuanCentro Regional de Investigaciones Biomédicas, Unidad NanoCRIB, 02008 Albacete, Spain.ORCID 0000-0002-4159-9772
Murillo DonizetiLaboratoire Matériaux Optiques Photonique et Systèmes (LMOPS), Centrale Supélec, Université de Lorraine, 57000 Metz, France.
Jesus ValcarcelGroup of Recycling and Valorization of Waste Materials (REVAL), Marine Research Institute (IIM-CSIC), 36208 Vigo, Spain.ORCID 0000-0001-7336-4049
José A VazquezGroup of Recycling and Valorization of Waste Materials (REVAL), Marine Research Institute (IIM-CSIC), 36208 Vigo, Spain.ORCID 0000-0002-1122-4726
Eduardo SolanoNCD-SWEET Beamline, ALBA Synchrotron Light Source, 08290 Cerdanyola del Vallès, Spain.ORCID 0000-0002-2348-2271
David ChapronLaboratoire Matériaux Optiques Photonique et Systèmes (LMOPS), Centrale Supélec, Université de Lorraine, 57000 Metz, France.
Patrice BoursonLaboratoire Matériaux Optiques Photonique et Systèmes (LMOPS), Centrale Supélec, Université de Lorraine, 57000 Metz, France.ORCID 0000-0002-3541-3257
Ivan BravoCentro Regional de Investigaciones Biomédicas, Unidad NanoCRIB, 02008 Albacete, Spain.ORCID 0000-0003-1589-5399
Carlos Alonso-MorenoCentro Regional de Investigaciones Biomédicas, Unidad NanoCRIB, 02008 Albacete, Spain.ORCID 0000-0002-7588-0781
Pilar Clemente-CasaresFacultad de Farmacia de Albacete, Universidad de Castilla-La Mancha, 02008 Albacete, Spain.
Carlos Gracia-FernándezTA Instruments Waters Chromatography, Tres Cantos, 28760 Madrid, Spain.
Alessandro LongoID20, ESRF, 71 Avenue des Martyrs, 38000 Grenoble, France.
Georges Salloum-Abou-JaoudeConstellium C-TEC Technology Center, Parc Economique Centr'alp, 725 Rue Aristide Bergès CS10027, 38341 Voreppe, France.ORCID 0000-0003-0499-413X
Alberto OcañaExperimental Therapeutics Unit, Hospital Clínico San Carlos, IdISSC and CIBERONC, 28040 Madrid, Spain.ORCID 0000-0002-1067-9630
Manuel M PiñeiroDepartamento de Física Aplicada, CINBIO, Universidade de Vigo, Campus Lagoas-Marcosende, 36310 Vigo, Spain.ORCID 0000-0002-3955-3564
Carolina Hermida-MerinoDepartamento de Física Aplicada, CINBIO, Universidade de Vigo, Campus Lagoas-Marcosende, 36310 Vigo, Spain.ORCID 0000-0002-9298-3889
Daniel Hermida-MerinoLaboratoire Matériaux Optiques Photonique et Systèmes (LMOPS), Centrale Supélec, Université de Lorraine, 57000 Metz, France.
CentraleSupélec · FRUniversidade de Vigo · ESUniversity of Castilla-La Mancha · ESALBA Synchrotron (Spain) · ESConstellium (France) · FRDutch Research Council · NLHospital Clínico San Carlos · ESInstitute of Nanostructured Materials · ITIS Instruments (United Kingdom) · GB

Funding

Ministerio de Ciencia e Innovación y Agencia Estatal de la Investigación CTQ2017-84131-RMinisterio de Ciencia e Innovación y Agencia Estatal de la Investigación PID2020- 117788RB-I00Ministerio de Ciencia e Innovación y Agencia Estatal de la Investigación RED2018-102387-T Programa Redes Consolider
6 · The paper itself

Abstract

A series of bionanocomposites composed of shark gelatin hydrogels and PLA nanoparticles featuring different nanostructures were designed to generate multifunctional drug delivery systems with tailored release rates required for personalized treatment approaches. The global conception of the systems was considered from the desired customization of the drug release while featuring the viscoelastic properties needed for their ease of storage and posterior local administration as well as their biocompatibility and cell growth capability for the successful administration at the biomolecular level. The hydrogel matrix offers the support to develop a direct thermal method to convert the typical kinetic trapped nanostructures afforded by the formulation method whilst avoiding the detrimental nanoparticle agglomeration that diminishes their therapeutic effect. The nanoparticles generated were successfully formulated with two different antitumoral compounds (doxorubicin and dasatinib) possessing different structures to prove the loading versatility of the drug delivery system. The bionanocomposites were characterized by several techniques (SEM, DLS, RAMAN, DSC, SAXS/WAXS and rheology) as well as their reversible sol-gel transition upon thermal treatment that occurs during the drug delivery system preparation and the thermal annealing step. In addition, the local applicability of the drug delivery system was assessed by the so-called "syringe test" to validate both the storage capability and its flow properties at simulated physiological conditions. Finally, the drug release profiles of the doxorubicin from both the PLA nanoparticles or the bionanocomposites were analyzed and correlated to the nanostructure of the drug delivery system.

Indexed as

bionanocompositedrug deliverygelatinhydrogelnanoparticlespolylactidestereocomplex

Identifiers

PMID35745711
PMCPMC9227928
OpenAlexW4281927105

What OpenQuestion 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 OpenQuestion graph.