Microparticles Loaded with Bursera microphylla A. Gray Fruit Extract with Anti-Inflammatory and Antimicrobial Activity

<b>Background</b>: <i>Bursera microphylla</i> (B) A. Gray, a plant native to northwest Mexico, has long been utilized in traditional medicine for its anti-inflammatory effects. Previous studies have highlighted the bioactivity of <i>B. microphylla</i> fruit extract. Chitosan (Cs), a biopolymer known for its favorable physicochemical properties, has proven effective in encapsulating bioactive compounds. This study aimed to synthesize and characterize Cs-based microparticles containing <i>B. microphylla</i> fruit extract and evaluate their in vitro anti-inflammatory activity. <b>Methods:</b> Cs-based three-dimensional hydrogels were synthesized using physical cross-linking with ammonium hydroxide, incorporating <i>B. microphylla</i> fruit extract. The hydrogels were freeze-dried and mechanically ground into microparticles. The physicochemical properties of the microencapsulates were analyzed through scanning electron microscopy (SEM), optical microscopy (OM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and moisture absorption tests. Anti-inflammatory activity was assessed by measuring nitric oxide (NO) reduction in LPS-activated RAW 264.7 cells. Antimicrobial activity was evaluated against <i>Staphylococcus aureus</i>. <b>Results:</b> SEM and OM analyses revealed irregular morphologies with rounded protuberances, with particle sizes ranging from 135 to 180 µm. FTIR spectra indicated that no new chemical bonds were formed, preserving the integrity of the original compounds. TGA confirmed that the encapsulated extract was heat-protected. The moisture absorption test indicated the microparticles' hydrophilic nature. In vitro, the microencapsulated extract reduced NO production by 46%, compared to 32% for the non-encapsulated extract. The microencapsulated extract was effective in reducing the microbial load of <i>S. aureus</i> between 15-24%. <b>Conclusions:</b> Cs-based microencapsulates containing <i>B. microphylla</i> fruit extract exhibited no chemical interactions during synthesis and demonstrated significant anti-inflammatory and antimicrobial activity. These results suggest that the Cs-based system is a promising candidate for managing inflammatory conditions.

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Publication Details

Journal
Pharmaceuticals
Published
2024-11-21
DOI
https://doi.org/10.3390/ph17121565
Citations
4
Primary Topic
Phytochemical compounds biological activities
Type
article
Field-Weighted Citation Impact
0.94

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article

Microparticles Loaded with Bursera microphylla A. Gray Fruit Extract with Anti-Inflammatory and Antimicrobial Activity

Marlén Alexis González-Reyna, Ramón Enrique Robles‐Zepeda, Víctor Alonso Reyna-Urrutia, Heriberto Torres‐Moreno et al.
4 citations
Pharmaceuticals
Phytochemical compounds biological activities
0.94
article

Microparticles Loaded with Bursera microphylla A. Gray Fruit Extract with Anti-Inflammatory and Antimicrobial Activity

Marlén Alexis González-Reyna, Ramón Enrique Robles‐Zepeda, Víctor Alonso Reyna-Urrutia, Heriberto Torres‐Moreno, Miriam Estévez, Julio César López-Romero, Grecia Vianney Alonso-Martínez, Juan Ramón Cáñez-Orozco
article en
4 citations

Abstract

<b>Background</b>: <i>Bursera microphylla</i> (B) A. Gray, a plant native to northwest Mexico, has long been utilized in traditional medicine for its anti-inflammatory effects. Previous studies have highlighted the bioactivity of <i>B. microphylla</i> fruit extract. Chitosan (Cs), a biopolymer known for its favorable physicochemical properties, has proven effective in encapsulating bioactive compounds. This study aimed to synthesize and characterize Cs-based microparticles containing <i>B. microphylla</i> fruit extract and evaluate their in vitro anti-inflammatory activity. <b>Methods:</b> Cs-based three-dimensional hydrogels were synthesized using physical cross-linking with ammonium hydroxide, incorporating <i>B. microphylla</i> fruit extract. The hydrogels were freeze-dried and mechanically ground into microparticles. The physicochemical properties of the microencapsulates were analyzed through scanning electron microscopy (SEM), optical microscopy (OM), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and moisture absorption tests. Anti-inflammatory activity was assessed by measuring nitric oxide (NO) reduction in LPS-activated RAW 264.7 cells. Antimicrobial activity was evaluated against <i>Staphylococcus aureus</i>. <b>Results:</b> SEM and OM analyses revealed irregular morphologies with rounded protuberances, with particle sizes ranging from 135 to 180 µm. FTIR spectra indicated that no new chemical bonds were formed, preserving the integrity of the original compounds. TGA confirmed that the encapsulated extract was heat-protected. The moisture absorption test indicated the microparticles' hydrophilic nature. In vitro, the microencapsulated extract reduced NO production by 46%, compared to 32% for the non-encapsulated extract. The microencapsulated extract was effective in reducing the microbial load of <i>S. aureus</i> between 15-24%. <b>Conclusions:</b> Cs-based microencapsulates containing <i>B. microphylla</i> fruit extract exhibited no chemical interactions during synthesis and demonstrated significant anti-inflammatory and antimicrobial activity. These results suggest that the Cs-based system is a promising candidate for managing inflammatory conditions.

PharmaceuticalsVol. 17(12)
Universidad de Sonora (MX), Universidad Nacional Autónoma de México (MX)
Consejo Nacional de Ciencia y Tecnología, Universidad de Sonora
Openalex Percentile: Top 25%
Phytochemical compounds biological activities
0.94
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