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Low Molecular Weight Protein Enrichment on Mesoporous Silica Thin Films for Biomarker Discovery
Published on: April 17, 2012
Morin loaded mesoporous molecular sieves as novel devices to the potential treatment of tumor pathologies
María Gabriela Montiel Schneider1, María Julia Martín1,2, Natalia Cuello3
1INQUISUR, Departamento de Química, Universidad Nacional del Sur (UNS)-CONICET, Bahía Blanca, Argentina.
Abstract:
Morin is an antioxidant and anticancer flavonoid, extracted from natural sources, that may exert beneficial effects for several pathologies. Despite this, the administration of morin represents a challenge due to its low aqueous solubility. Mesoporous silica materials have emerged as biocompatible tools for drug delivery, as their pore size can be modulated for maximum surface area to volume ratio. In this contribution, we evaluate the ability of iron-modified mesoporous materials, for morin loading and controlled delivery. The SBA-15 and MCM-41 sieves were synthesized and modified with iron (metal content 4.02 and 6.27 % wt, respectivily). Characterization by transmission electron microscopy, XRD and UV-Vis revealed adequate pore size and agglomerates of very small metallic nanospecies (nanoclusters), without larger iron oxide nanoparticles. FT-IR spectra confirmed the presence of silanol groups in the solid hosts, which can interact with different groups present in morin molecules. SBA-15 materials were more efficient in terms of morin loading capacity (LC) due to their larger pore diameter. LC was more than 35% for SBA-15 materials when adsorptions studies were carried out with 9 mg of drug. Antioxidant activity were assayed by using DPPH test. Free iron materials presented a significate improvement as antioxidants after morin incorporation, reaching a scavenging activity of almost a 90%. On the other hand, in iron modified mesoporous materials, the presence of morin did not affect the scavenging activity. The results could be related with the formation of a complex between the flavonoid and the iron. Finally, biosafety studies using normal epithelial cells revealed that neither the loaded nor the unloaded materials exerted toxicity, even at doses of 1 mg/ml. These findings expand knowledge about mesoporous materials as suitable carriers of flavonoids with the aim of improving therapies for a wide range of pathologies.
Insights
Iron-modified mesoporous silica effectively loads morin, enhancing its antioxidant capacity. These biocompatible materials show no toxicity, offering a promising drug delivery system for flavonoids to treat various diseases.
Area of Science:
- Materials Science
- Nanotechnology
- Biomedical Engineering
Background:
- Morin, a natural antioxidant and anticancer flavonoid, faces administration challenges due to poor water solubility.
- Mesoporous silica materials offer biocompatible drug delivery platforms with tunable pore sizes.
- Iron modification of mesoporous silica is explored for enhanced drug loading and delivery.
Purpose of the Study:
- To evaluate iron-modified mesoporous silica (SBA-15 and MCM-41) for morin loading and controlled release.
- To assess the impact of iron modification on morin's antioxidant activity.
- To determine the biosafety of these novel drug delivery systems.
Main Methods:
- Synthesis and characterization of iron-modified SBA-15 and MCM-41 using TEM, XRD, UV-Vis, and FT-IR.
- Morin loading capacity (LC) studies, particularly for SBA-15.
- Antioxidant activity assessment using the DPPH assay.
- Biosafety evaluation with normal epithelial cells.
Main Results:
- SBA-15 exhibited higher morin loading capacity (>35%) due to its larger pore diameter.
- Iron-modified materials showed a significant increase in antioxidant scavenging activity (up to 90%) after morin incorporation.
- No toxicity was observed for loaded or unloaded materials in epithelial cells.
Conclusions:
- Iron-modified mesoporous silica, especially SBA-15, is an efficient carrier for morin, enhancing its antioxidant properties.
- The formation of a morin-iron complex may influence antioxidant activity.
- These biocompatible and non-toxic materials show potential for improved flavonoid-based therapies.
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