Rifampicin/Quercetin Nanoemulsions: Co-Encapsulation and In Vitro Biological Assessment Toward Tuberculosis Therapy

<b>Background</b>: Tuberculosis (TB) remains a leading cause of global mortality, with 1.25 million deaths reported in 2023. Extended treatment duration contributes to poor patient adherence and treatment failure. Innovative drug delivery platforms are needed to improve therapeutic outcomes. <b>Objective</b>: This study aimed to develop nanoemulsions co-encapsulating quercetin and rifampicin and evaluate their physicochemical properties and in vitro biological activity relevant to TB therapy. <b>Methods</b>: Nanoemulsions (NEs) were prepared via hot solvent diffusion and phase inversion temperature techniques. Physicochemical characterization, stability, anti-inflammatory effects in BEAS-2B cells, and antimycobacterial activity against <i>Mycobacterium tuberculosis</i> H37Rv and resistant strains were assessed in vitro. <b>Results</b>: The quercetin-rifampicin nanoemulsion (QUE-RIF-NE) showed an average size of 24 nm, zeta potential of -27 mV, and drug recovery rates of 77% (quercetin) and 75% (rifampicin). The formulation was stable and non-cytotoxic at 10<sup>-8</sup> M, reducing IFN-γ production by half and reactive oxygen species production by almost 75% in BEAS-2B cells. It also exhibited antimycobacterial activity against both susceptible and resistant <i>M. tuberculosis</i> strains (MIC ≤ 0.015 µg/mL). <b>Conclusions</b>: QUE-RIF-NE exhibits promising physicochemical stability and dual anti-inflammatory and antimicrobial activity in vitro, demonstrating potential for optimized pulmonary or systemic TB therapy that integrates both anti-inflammatory and antimicrobial effects.

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Publication Details

Journal
Pharmaceuticals
Published
2025-12-01
DOI
https://doi.org/10.3390/ph18121829
Primary Topic
Inhalation and Respiratory Drug Delivery
Type
article
Field-Weighted Citation Impact
0.00

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article

Rifampicin/Quercetin Nanoemulsions: Co-Encapsulation and In Vitro Biological Assessment Toward Tuberculosis Therapy

Wanessa Maria dos Santos, Pedro Eduardo Almeida da Silva, Gabriela Alves Felício da Costa, Sergiane Souza Caldas et al.
Pharmaceuticals
Inhalation and Respiratory Drug Delivery
article

Rifampicin/Quercetin Nanoemulsions: Co-Encapsulation and In Vitro Biological Assessment Toward Tuberculosis Therapy

Wanessa Maria dos Santos, Pedro Eduardo Almeida da Silva, Gabriela Alves Felício da Costa, Sergiane Souza Caldas, Cristiana Lima Dora, Beatriz Sodré Matos, Virginia Campello Yurgel, Marcelle Oliveira Garcia, Gabriela Hädrich, Gustavo Richter Vaz, Daniela Fernandes Ramos, FRANCISCO NECY ALVES JÚNIOR, Ednei Gilberto Prímel, Daniela Pastorim Vaiss, Camila de Oliveira Vian, D Teixeira, Alexandre de Paula Rogério, João Victor Villa Real, Lara Cristina dos Santos Teodoro
article en

Abstract

<b>Background</b>: Tuberculosis (TB) remains a leading cause of global mortality, with 1.25 million deaths reported in 2023. Extended treatment duration contributes to poor patient adherence and treatment failure. Innovative drug delivery platforms are needed to improve therapeutic outcomes. <b>Objective</b>: This study aimed to develop nanoemulsions co-encapsulating quercetin and rifampicin and evaluate their physicochemical properties and in vitro biological activity relevant to TB therapy. <b>Methods</b>: Nanoemulsions (NEs) were prepared via hot solvent diffusion and phase inversion temperature techniques. Physicochemical characterization, stability, anti-inflammatory effects in BEAS-2B cells, and antimycobacterial activity against <i>Mycobacterium tuberculosis</i> H37Rv and resistant strains were assessed in vitro. <b>Results</b>: The quercetin-rifampicin nanoemulsion (QUE-RIF-NE) showed an average size of 24 nm, zeta potential of -27 mV, and drug recovery rates of 77% (quercetin) and 75% (rifampicin). The formulation was stable and non-cytotoxic at 10<sup>-8</sup> M, reducing IFN-γ production by half and reactive oxygen species production by almost 75% in BEAS-2B cells. It also exhibited antimycobacterial activity against both susceptible and resistant <i>M. tuberculosis</i> strains (MIC ≤ 0.015 µg/mL). <b>Conclusions</b>: QUE-RIF-NE exhibits promising physicochemical stability and dual anti-inflammatory and antimicrobial activity in vitro, demonstrating potential for optimized pulmonary or systemic TB therapy that integrates both anti-inflammatory and antimicrobial effects.

PharmaceuticalsVol. 18(12)
Universidade Federal do Rio Grande (BR), University of Vienna (AT), Universidade Federal do Rio Grande do Sul (BR), Universidade Federal do Triângulo Mineiro (BR)
Coordenação de Aperfeiçoamento de Pessoal de Nível Superior, Universität Wien, Conselho Nacional de Desenvolvimento Científico e Tecnológico, Fundação de Amparo à Pesquisa do Estado do Rio Grande do Sul, Fundação de Amparo à Pesquisa do Estado de Minas Gerais
Openalex Percentile: Top 44%
Inhalation and Respiratory Drug Delivery
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