A novel digitonin/graphene oxide/iron oxide nanocomposite: synthesis, physiochemical characterization and antioxidant activity

In this work, iron oxide (Fe 3 O 4 ) magnetic nanoparticles (MNPs) and graphene oxide (GO) nanosheets were prepared via the co-precipitation technique and the Modified Hummer method. Fe 3 O 4 MNPs and GO nanosheets were combined to prepare Fe 3 O 4 /GO nanocomposite and subsequently conjugated with...

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Published in:Discover nano Vol. 19; no. 1; pp. 15 - 12
Main Authors: Aljawrneh, Bashar, Shawakfeh, Khaled, Albiss, Borhan Aldeen, Alshanableh, Abdelelah, Al-Qudah, Mahmoud A., Bataineh, Tariq T., Shawakfeh, Lona
Format: Journal Article
Language:English
Published: New York Springer US 22-01-2024
Springer Nature B.V
Springer
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Summary:In this work, iron oxide (Fe 3 O 4 ) magnetic nanoparticles (MNPs) and graphene oxide (GO) nanosheets were prepared via the co-precipitation technique and the Modified Hummer method. Fe 3 O 4 MNPs and GO nanosheets were combined to prepare Fe 3 O 4 /GO nanocomposite and subsequently conjugated with Digitonin (DIG) in order to obtain a dual-targeted delivery system based on DIG/Fe 3 O 4 /GO nanocomposite. SEM images reveal the presence of Fe 3 O 4 MNPs at a scale of 100 nm, exhibiting dispersion between the GO nanosheets. Aggregation of the DIG/Fe 3 O 4 /GO nanocomposite was observed at various size scales. The XRD structural analysis confirms the crystal structure of the prepared samples. The Fe 3 O 4 MNPs demonstrated the main XRD-diffracted peaks. Also, GO nanosheets exhibit crystalline characteristics on the (001) and (002) planes. The predominant peaks observed in the DIG/GO/Fe 3 O 4 nanocomposite are attributed to the crystal phases of Fe 3 O 4 MNPs. The FT-IR vibrational modes observed in the GO/DIG/Fe 3 O 4 nanocomposite indicate the presence of crosslinking between GO nanosheet layers and the Fe 3 O 4 MNPs. The antioxidant activity of the prepared samples was measured and the DIG/GO/Fe 3 O 4 nanocomposite demonstrated a significantly high antioxidant activity in both 2-diphenyl-1-picrylhydrazyl (DPPH · ) and 2,2-azino-bis-3-ethylbenzthiazoline-6-sulfonic acid (ABTS ·+ ) tests.
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ISSN:2731-9229
1931-7573
2731-9229
1556-276X
DOI:10.1186/s11671-024-03960-7