Evaluation of the antimicrobial and anticancer potential of a modified silver nanoparticle-impregnated carrier system

This study aimed to develop silver nanoparticles embedded in poly(ricinoleic acid)-poly(methyl methacrylate)-poly(ethylene glycol) (AgNPsPRici-PMMA-PEG) nanoparticles (NPs) containing caffeic acid (Caff) and tetracycline hydrochloride (TCH) for treating infections and cancer in bone defects. The block copolymers were synthesised via free radical polymerisation. NPs were prepared using the solvent evaporation method and characterised by FTIR, HNMR, SEM, DSC, TGA, and DLS. Drug loading (LE), encapsulation efficiency (EE), antimicrobial activity, cytotoxicity, and <i>in vitro</i> release studies were conducted. The NPs exhibited a size of 198 ± 2.89 nm, a narrow size distribution (PDI < 0.1), and a zeta potential of -27.5 ± 0.13 mV. The EE of Caff were 73 ± 0.09% w/w and 78 ± 0.32% w/w. Caff NPs showed prolonged release (69 ± 0.23% w/w), cytotoxicity with the cell viability of 66.85 ± 10.51% in SaOS cells, and antimicrobial zones ranging from 1.5 ± 0.3 to 4.2 ± 0.2 mm. TCH-Caff-AgNPsPRici-PMMA-PEG NPs exhibited promising therapeutic potential for infection and cancer treatment in bone defects.

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Publication Details

Journal
Journal of Microencapsulation
Published
2024-12-24
DOI
https://doi.org/10.1080/02652048.2024.2443437
Primary Topic
Nanoparticle-Based Drug Delivery
Type
article
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article

Evaluation of the antimicrobial and anticancer potential of a modified silver nanoparticle-impregnated carrier system

Bakí Hazer, Ebru Kılıçay, Ebru Erdal, Ömer Karadağ
Journal of Microencapsulation
Nanoparticle-Based Drug Delivery
article

Evaluation of the antimicrobial and anticancer potential of a modified silver nanoparticle-impregnated carrier system

Bakí Hazer, Ebru Kılıçay, Ebru Erdal, Ömer Karadağ
article en

Abstract

This study aimed to develop silver nanoparticles embedded in poly(ricinoleic acid)-poly(methyl methacrylate)-poly(ethylene glycol) (AgNPsPRici-PMMA-PEG) nanoparticles (NPs) containing caffeic acid (Caff) and tetracycline hydrochloride (TCH) for treating infections and cancer in bone defects. The block copolymers were synthesised via free radical polymerisation. NPs were prepared using the solvent evaporation method and characterised by FTIR, HNMR, SEM, DSC, TGA, and DLS. Drug loading (LE), encapsulation efficiency (EE), antimicrobial activity, cytotoxicity, and <i>in vitro</i> release studies were conducted. The NPs exhibited a size of 198 ± 2.89 nm, a narrow size distribution (PDI < 0.1), and a zeta potential of -27.5 ± 0.13 mV. The EE of Caff were 73 ± 0.09% w/w and 78 ± 0.32% w/w. Caff NPs showed prolonged release (69 ± 0.23% w/w), cytotoxicity with the cell viability of 66.85 ± 10.51% in SaOS cells, and antimicrobial zones ranging from 1.5 ± 0.3 to 4.2 ± 0.2 mm. TCH-Caff-AgNPsPRici-PMMA-PEG NPs exhibited promising therapeutic potential for infection and cancer treatment in bone defects.

Journal of MicroencapsulationVol. 42(2)
Ankara University (TR), Çankırı Karatekin University (TR), Zonguldak Bülent Ecevit University (TR), University of Kara (TG), Advanced Technologies Application Center (CU), Cappadocia University (TR), Ankara Yıldırım Beyazıt University (TR)
Openalex Percentile: Top 88%
Nanoparticle-Based Drug Delivery
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