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Title: Adsorption and Recovery of Polyphenolic Flavonoids Using TiO2-Functionalized Mesoporous Silica Nanoparticles

Journal Article · · ACS Applied Materials and Interfaces

Exploiting specific interactions with titania (TiO2) has been proposed for the separation and recovery of a broad range of biomolecules and natural products, including therapeutic polyphenolic flavonoids which are susceptible to degradation, such as quercetin. Functionalizing mesoporous silica with TiO2 has many potential advantages over bulk and mesoporous TiO2 as an adsorbent for natural products, including robust synthetic approaches leading to high surface area, stable separation platforms. Here, TiO2 surface functionalized mesoporous silica nanoparticles (MSNPs) are synthesized and characterized as a function of TiO2 content (up to 636 mg TiO2/g). The adsorption isotherms of two polyphenolic flavonoids, quercetin and rutin, were determined (0.05-10 mg/ml in ethanol), and a 100-fold increase in the adsorption capacity was observed relative to functionalized nonporous particles with similar TiO2 surface coverage. An optimum extent of functionalization (approximately 440 mg TiO2/g particles) is interpreted from characterization techniques including grazing incidence x-ray scattering (GIXS), high resolution transmission electron microscopy (HRTEM) and nitrogen adsorption, which examined the interplay between the extent of TiO2 functionalization and the accessibility of the porous structures. The recovery of flavonoids is demonstrated using ligand displacement in ethanolic citric acid solution (20% w/v), in which greater than 90% recovery can be achieved in a multistep extraction process. The radical scavenging activity (RSA) of the recovered and particle-bound quercetin as measured by 2,2-diphenyl-1-picrylhydrazyl (DPPH) radical scavenging assay demonstrates greater than 80% retention of antioxidant activity by both particle-bound and recovered quercetin. In conclusion, these mesoporous titanosilicate materials can serve as a synthetic platform to isolate, recover, and potentially deliver degradation-sensitive natural products to biological systems.

Research Organization:
Argonne National Lab. (ANL), Argonne, IL (United States)
Sponsoring Organization:
National Institutes of Health (NIH); USDOE Office of Science (SC), Basic Energy Sciences (BES) (SC-22), Scientific User Facilities Division
Grant/Contract Number:
AC02-06CH11357
OSTI ID:
1395148
Journal Information:
ACS Applied Materials and Interfaces, Vol. 9, Issue 37; ISSN 1944-8244
Publisher:
American Chemical Society (ACS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 51 works
Citation information provided by
Web of Science

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Cited By (9)

Synthesis of phosphorylated raw sawdust for the removal of toxic metal ions from aqueous medium: Adsorption mechanism for clean approach journal November 2018
Kinetic, Isotherm, and Thermodynamic Studies for Ag(I) Adsorption Using Carboxymethyl Functionalized Poly(glycidyl methacrylate) journal October 2018
Secondary Metabolites in the Green Synthesis of Metallic Nanoparticles journal June 2018
Layer-by-Layer Synthesis of Thick Mesoporous TiO 2 Films with Vertically Oriented Accessible Nanopores and Their Application for Lithium-Ion Battery Negative Electrodes journal July 2018
Mesoporous silica nanoparticles as diagnostic and therapeutic tools: how can they combat bacterial infection? journal March 2018
A neutral Cu-based MOF for effective quercetin extraction and conversion from natural onion juice journal January 2019
Antioxidant Nanomaterial Based on Core–Shell Silica Nanospheres with Surface-Bound Caffeic Acid: A Promising Vehicle for Oxidation-Sensitive Drugs journal February 2019
Evaluation of the superparamagnetic and biological properties of microwave assisted synthesized Zn & Cd doped CoFe2O4 nanoparticles via Pechini sol–gel method journal January 2018
Recovery of Polyphenols from Grape Pomace Using Polyethylene Glycol (PEG)-Grafted Silica Particles and PEG-Assisted Cosolvent Elution journal June 2019

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