Nanoantioxidant-Based Silica Particles as Flavonoid Carrier for Drug Delivery Applications

Nanosystems used in pharmaceutical formulations have shown promising results in enhancing the administration of drugs of difficult formulations. In particular, porous silica nanoparticles have demonstrated excellent properties for application in biological systems; however, there are still several c...

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Main Authors: Francisco Arriagada (Author), Germán Günther (Author), Javier Morales (Author)
Format: Book
Published: MDPI AG, 2020-03-01T00:00:00Z.
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001 doaj_4d6dd4ded20b4e29ba4ab2a8b6c8fbb4
042 |a dc 
100 1 0 |a Francisco Arriagada  |e author 
700 1 0 |a Germán Günther  |e author 
700 1 0 |a Javier Morales  |e author 
245 0 0 |a Nanoantioxidant-Based Silica Particles as Flavonoid Carrier for Drug Delivery Applications 
260 |b MDPI AG,   |c 2020-03-01T00:00:00Z. 
500 |a 1999-4923 
500 |a 10.3390/pharmaceutics12040302 
520 |a Nanosystems used in pharmaceutical formulations have shown promising results in enhancing the administration of drugs of difficult formulations. In particular, porous silica nanoparticles have demonstrated excellent properties for application in biological systems; however, there are still several challenges related to the development of more effective and biocompatible materials. An interesting approach to enhance these nanomaterials has been the development of nanoantioxidant carriers. In this work, a hybrid nanoantioxidant carrier based on porous silica nanoplatform with rosmarinic acid antioxidant immobilized on its surface were developed and characterized. Techniques such as dynamic light scattering (DLS), zeta potential, transmission electron microscopy (TEM), N<sub>2</sub> adsorption−desorption measurements, differential scanning calorimetry (DSC), Fourier transform−infrared spectroscopy (FT-IR), and 2,2-diphenyl-1-picrylhydrazyl (DPPH<sup>●</sup>) assay were used to characterize and evaluate the antioxidant activity of nanocarriers. In addition, drug release profile was evaluated using two biorelevant media. The antioxidant activity of rosmarinic acid was maintained, suggesting the correct disposition of the moiety. Kinetic studies reveal that more morin is released in the simulated intestinal fluid than in the gastric one, while an anomalous non−Fickian release mechanism was observed. These results suggest a promising antioxidant nanocarrier suitable for future application in drug delivery. 
546 |a EN 
690 |a drug delivery 
690 |a flavonoid 
690 |a silica nanoparticles 
690 |a nanocarrier 
690 |a nanoantioxidant 
690 |a morin 
690 |a rosmarinic acid 
690 |a Pharmacy and materia medica 
690 |a RS1-441 
655 7 |a article  |2 local 
786 0 |n Pharmaceutics, Vol 12, Iss 4, p 302 (2020) 
787 0 |n https://www.mdpi.com/1999-4923/12/4/302 
787 0 |n https://doaj.org/toc/1999-4923 
856 4 1 |u https://doaj.org/article/4d6dd4ded20b4e29ba4ab2a8b6c8fbb4  |z Connect to this object online.