Nanostructured biosilica produced by Thalassiosira weissflogii diatoms is covalently functionalized with the cyclic nitroxide 2,6,6-tetramethylpiperidine-N-oxyl (TEMPO), an efficient scavenger of reactive oxygen species (ROS) in biological systems. Drug delivery properties of the TEMPO-functionalized biosilica are studied for Ciprofloxacin, an antimicrobial thoroughly employed in orthopedic or dental implant related infections. The resulting TEMPO-biosilica, combining Ciprofloxacin drug delivery with anti-oxidant properties, is demonstrated to be a suitable material for fibroblasts and osteoblast-like cells growth. Them bones gonna rise again: Covalent functionalization of nanostructured silica shells from diatoms with TEMPO radical endows biosilica with both drug-delivery properties and antioxidant activity. The resulting functional biosilica is demonstrated to be a suitable substrate for bone cell growth.

Chemically Modified Diatoms Biosilica for Bone Cell Growth with Combined Drug-Delivery and Antioxidant Properties

VONA, DANILO;DE GIGLIO, Elvira;COMETA, STEFANIA;RAGNI, ROBERTA;FARINOLA, Gianluca Maria
2015-01-01

Abstract

Nanostructured biosilica produced by Thalassiosira weissflogii diatoms is covalently functionalized with the cyclic nitroxide 2,6,6-tetramethylpiperidine-N-oxyl (TEMPO), an efficient scavenger of reactive oxygen species (ROS) in biological systems. Drug delivery properties of the TEMPO-functionalized biosilica are studied for Ciprofloxacin, an antimicrobial thoroughly employed in orthopedic or dental implant related infections. The resulting TEMPO-biosilica, combining Ciprofloxacin drug delivery with anti-oxidant properties, is demonstrated to be a suitable material for fibroblasts and osteoblast-like cells growth. Them bones gonna rise again: Covalent functionalization of nanostructured silica shells from diatoms with TEMPO radical endows biosilica with both drug-delivery properties and antioxidant activity. The resulting functional biosilica is demonstrated to be a suitable substrate for bone cell growth.
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11586/173038
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