| Literature DB >> 32552084 |
Laís F Azevedo de M Oliveira1, Lais Vanessa de Azevedo Teles da Silva2, Ticiano G do Nascimento2, Lara Mendes de Almeida2, Rodrigo José Nunes Calumby2, Ábner Magalhães Nunes3, Leonardo Mendonça Tenório de Magalhães Oliveira4, Eduardo J da Silva Fonseca1.
Abstract
This work brings the promise of MCM-41 mesoporous silica as a vehicle for red propolis for the development of controlled release drugs and delivery to a specific target site. The synthesis of MCM-41 by the sol-gel method with a pore size of approximately 3.6 nm and the incorporation of red propolis extract by the physical adsorption method in ethanolic medium were easily accomplished with around 15% encapsulation. MCM-41 and MCM-41 with red propolis (MCM-41/Pr) were characterized by Fourier transform infrared spectroscopy, X-ray diffraction, thermal analysis, N2 adsorption-desorption, scanning electron microscopy, and an ultra-high-performance liquid chromatography-diode array detection (UPLC-DAD). In vitro release of encapsulated red propolis was analyzed in phosphate buffer at pH 7.2, 7.4, and 7.6. An in vitro test for MCM-41/Pr antioxidant activity was performed using 2,2-diphenyl-1-picrylhydrazyl as well as analysis of antibacterial activity against Staphylococcus aureus by the well diffusion method. UPLC-DAD analysis showed that the integrity of the red propolis constituents was maintained after the embed process, and the antioxidant and antibacterial activities were preserved.Entities:
Keywords: Synthesis; UPLC-DAD; antibacterial activities; mesoporous; nanostructures; red propolis extract
Year: 2020 PMID: 32552084 DOI: 10.1080/03639045.2020.1782423
Source DB: PubMed Journal: Drug Dev Ind Pharm ISSN: 0363-9045 Impact factor: 3.225