Development of Magnetite-Graphene Oxide Nanoplatforms for pH-Sensitive Doxorubicin Delivery and Cytotoxicity Evaluation
Abstract
Objective: This study aimed to develop and characterize a magnetite-graphene oxide (m-GO) nanoplatform for the controlled, pH-sensitive delivery of doxorubicin (DOX), with an emphasis on improving targeted anticancer activity and minimizing systemic toxicity. The potential application of this system in both human and veterinary oncology was also considered. Materials and Methods: Magnetite-functionalized graphene oxide (m-GO) nanoparticles were synthesized by decorating graphene oxide with Fe₃O₄ nanoparticles. DOX was loaded onto the m-GO system, and the loading was confirmed by UV-Vis and FTIR spectroscopy. The nanoparticles were characterized for particle size and zeta potential. In vitro drug release studies were conducted at pH 5.5 and 7.4 to assess pH sensitivity. Cytotoxic effects were evaluated using the MTT assay on MCF-7 human breast cancer cells. Drug release kinetics were also analyzed to determine the release mechanism. Results: The synthesized nanoparticles had a mean particle size of 42.18 ± 4.22 nm and a zeta potential of −19.3 ± 1.54 mV. Drug release studies showed enhanced DOX release at acidic pH (5.5), indicating pH sensitivity. The MTT assay demonstrated dose-dependent cytotoxicity, with free DOX showing immediate higher toxicity, while DOX-loaded m-GO provided controlled cytotoxic effects. Release kinetics analysis revealed a Fickian diffusion-controlled mechanism. Conclusion: DOX-loaded m-GO nanoparticles exhibited favorable physicochemical properties and pH-sensitive drug release behavior. Their ability to provide controlled drug delivery with sustained cytotoxicity suggests that they may serve as promising nanocarrier systems for targeted cancer therapy, with potential applications in both human and veterinary medicine.
Keywords
Supporting Institution
Project Number
Ethical Statement
Thanks
References
- Bakirel T, Alkan FU, Üstüner O, et al. Synergistic growth inhibitory effect of deracoxib with doxorubicin against a canine mammary tumor cell line, CMT U27. J Vet Med Sci. 2016; 78:657-668.
- Depan D, Shah J, Misra RDK. Controlled release of drug from folate decorated and graphene mediated drug delivery system: synthesis, loading efficiency, and drug release response. Mater Sci Eng C. 2011; 31:1305-1312.
- Foroozandeh P, Aziz AA. Insight into cellular uptake and intracellular trafficking of nanoparticles. Nanoscale Res Lett. 2018; 13:339.
- Fullerton E. Doxorubicin: an overview. Todays Vet Tech. 2017; May/June:25-34.
- Geyik G, Işıklan N. pH controlled doxorubicin release from Fe₃O₄@κ carrageenan graft PDMAEMA magnetic nanoparticles. Eurasian J Biol Chem Sci. 2022a; 5:9-14.
- Geyik G, Işıklan N. Multi stimuli sensitive superparamagnetic κ carrageenan based nanoparticles for controlled 5 fluorouracil delivery. Colloids Surf A Physicochem Eng Asp. 2022b; 634:127960.
- Gherman ML, Zanoaga O, Budisan L, Raduly L, Berindan Neagoe I. Doxorubicin as a potential treatment option in canine mammary tumors. Vet Sci. 2023; 10:654.
- He Y, Yi C, Zhang X, Zhao W, Yu D. Magnetic graphene oxide: synthesis approaches, physicochemical characteristics, and biomedical applications. TrAC Trends Anal Chem. 2021; 136:116191.
Details
Primary Language
English
Subjects
Veterinary Pharmacology
Journal Section
Research Article
Authors
Nizamudin Hussien
0000-0003-0110-0444
Türkiye
Enes Güncüm
0000-0001-8127-8730
Türkiye
Nuran Işiklan
*
0000-0002-4051-6533
Türkiye
Mustafa Türk
0000-0001-8202-090X
Türkiye
Publication Date
March 29, 2026
Submission Date
December 30, 2025
Acceptance Date
March 9, 2026
Published in Issue
Year 2026 Volume: 10 Number: 1
