Evidence map›Paper›PMID 40012384›Full record

ArticleAnti-cancer agents in medicinal chemistry2025

A Path to the Formation Mechanism of Propolis Nanoparticles, their Cytotoxicity on 3T3 Fibroblasts, Metastatic Murine B16F10 Cells, and their

Jeimmy Gonzalez-Masis, Rodolfo J Gonzalez-Paz, Yendry Regina Corrales Urena, Simon Guerrero, Sara Gonzalez-Camacho, Nohelia Mora-Ugalde, Monica Baizan-Rojas, Randall Loaiza, Jose Roberto Vega-Baudrit, Jorge M Cubero-Sesin

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Article in Anti-cancer agents in medicinal chemistry, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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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

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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

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Jeimmy Gonzalez-MasisCentro de Investigación y Extensión en Materiales, Escuela de Ciencia e Ingeniería de los Materiales, Instituto Tecnológico de Costa Rica, Cartago 159-7050, Costa Rica.ORCID 0000-0003-4282-5230
Rodolfo J Gonzalez-PazNational Nanotechnology Laboratory, National Center of High Technology (LANOTEC-CeNAT- CONARE), 1174-1200 Pavas, San José, Costa Rica.ORCID 0000-0001-8614-0773
Yendry Regina Corrales UrenaNational Nanotechnology Laboratory, National Center of High Technology (LANOTEC-CeNAT- CONARE), 1174-1200 Pavas, San José, Costa Rica.ORCID 0000-0002-1819-2915
Simon GuerreroFacultad de Medicina, Universidad de Atacama, Los Carrera 1579, 1533601 Copiapó, Chile.ORCID 0000-0002-3003-0337
Sara Gonzalez-CamachoBiological Assay Laboratory (LEBi), Universidad de Costa Rica, San José, Costa Rica.ORCID 0000-0002-7278-548X
Nohelia Mora-UgaldeNational Center for Biotechnological Innovations (CENIBiot), National Center of High Technology (CeNAT-CONARE), Pavas 1174-1200 San José, Costa Rica.ORCID 0000-0003-2549-6471
Monica Baizan-RojasNational Center for Biotechnological Innovations (CENIBiot), National Center of High Technology (CeNAT-CONARE), Pavas 1174-1200 San José, Costa Rica.ORCID 0000-0001-9175-6644
Randall LoaizaNational Center for Biotechnological Innovations (CENIBiot), National Center of High Technology (CeNAT-CONARE), Pavas 1174-1200 San José, Costa Rica.ORCID 0000-0002-7037-1902
Jose Roberto Vega-BaudritNational Nanotechnology Laboratory, National Center of High Technology (LANOTEC-CeNAT- CONARE), 1174-1200 Pavas, San José, Costa Rica.ORCID 0000-0002-2002-1744
Jorge M Cubero-SesinCentro de Investigación y Extensión en Materiales, Escuela de Ciencia e Ingeniería de los Materiales, Instituto Tecnológico de Costa Rica, Cartago 159-7050, Costa Rica.ORCID 0000-0002-2201-9736

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundNatural products, such as propolis, are an important source of biologically active compounds with the potential to treat health disorders. Propolis is a well-known waxy resin recognized for its antimicrobial, immunomodulatory, and cytotoxic effects.

objectiveIn this study, we aimed to clarify the formation mechanism of propolis nanoparticles from the perspective of their stability and chemical composition. By evaluating the light absorption behaviour of the nanoparticles formed in different media and quantifying the polyphenols, we show that they are superficially hydrophobic nanoparticles with the capacity to encapsulate some polar compounds.

methodsBiological activity was evaluated by

resultsThe results show that nanoparticles are cytocompatible, with a proliferation effect. In contrast, the results of the viability of metastatic murine B16F10 cells indicate that a dose with a concentration of 5 μg/mL in the cell culture media is sufficient to stop the abnormal cell growth, having an antitumor effect. This effect might be related to the flavonoids present in the propolis nanoparticles. In vivo dermal irritability tests on New Zealand rabbits show that propolis nanoparticles' aqueous dissolution was non-irritant.

conclusionAccording to the results obtained from this study, reducing the size of raw propolis down to nanoparticles and dispersing them in water solvents enhance its positive effects. The superficially hydrophobic propolis nanoparticles encapsulate active compounds such as polyphenols and flavonoids, which also confirms their ability to generate selective effects on the cells, depending on their nature.

Indexed as

Antineoplastic AgentsFibroblastsMelanoma, ExperimentalNanoparticlesPropolisAnimalsCell ProliferationCell SurvivalDose-Response Relationship, DrugDrug Screening Assays, AntitumorMiceMolecular StructureNIH 3T3 CellsParticle SizeRabbitsStructure-Activity RelationshipAntineoplastic AgentsPropoliscancer cellserythema.fibroblastsflavonoidsnanoparticlesPropolis

Identifiers

PMID40012384

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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.