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


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Background: Natural 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.

Objective: In 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.

Methods: Biological activity was evaluated by in vitro cell viability performed on NIH/3T3 fibroblasts incubated with 10, 100, and 1000 μg/mL of propolis nanoparticles for 48 hours.

Results: The 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.

Conclusion: According 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.

Sobre autores

Jeimmy Gonzalez-Masis

Centro de Investigación y Extensión en Materiales, Escuela de Ciencia e Ingeniería de los Materiales, Instituto Tecnológico de Costa Rica

Email: info@benthamscience.net

Rodolfo Gonzalez-Paz

National Nanotechnology Laboratory, National Center of High Technology ((LANOTEC-CeNAT- CONARE)

Autor responsável pela correspondência
Email: info@benthamscience.net

Yendry Urena

National Nanotechnology Laboratory, National Center of High Technology ((LANOTEC-CeNAT- CONARE)

Email: info@benthamscience.net

Simon Guerrero

Facultad de Medicina, Universidad de Atacama

Email: info@benthamscience.net

Sara Gonzalez-Camacho

Biological Assay Laboratory (LEBi), University of Costa Rica

Email: info@benthamscience.net

Nohelia Mora-Ugalde

National Center for Biotechnological Innovations (CENIBiot), National Center of High Technology (CeNAT-CONARE)

Email: info@benthamscience.net

Monica Baizan-Rojas

National Center for Biotechnological Innovations (CENIBiot), National Center of High Technology (CeNAT-CONARE)

Email: info@benthamscience.net

Randall Loaiza

National Center for Biotechnological Innovations (CENIBiot), National Center of High Technology (CeNAT-CONARE)

Email: info@benthamscience.net

Jose Vega-Baudrit

National Nanotechnology Laboratory, National Center of High Technology ((LANOTEC-CeNAT- CONARE)

Email: info@benthamscience.net

Jorge Cubero-Sesin

Centro de Investigación y Extensión en Materiales, Escuela de Ciencia e Ingeniería de los Materiales, Instituto Tecnológico de Costa Rica

Email: info@benthamscience.net

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