Dergiler / Journal of advances in vetbio science and techniques / 2026 / Issue: 2

Comparison of the effects of nano, micro silver particles, and silver nitrate on glioblastoma multiforme (CRL-1690)

Sinem Pehlivan(ANKARA MEDİPOL ÜNİVERSİTESİ)0000-0002-3389-3189
İlker Şimşek(ÇANKIRI KARATEKİN ÜNİVERSİTESİ)0000-0001-9181-9879
Eda Akdağ(CANKIRI KARATEKIN UNIVERSITY)0000-0001-9132-4438
Ali Fatih Yıltırak(CANKIRI KARATEKIN UNIVERSITY)0000-0001-9835-4584
Pınar Arslan Yüce(CANKIRI KARATEKIN UNIVERSITY)0000-0001-5910-2835
Özgür Kuzukıran(CANKIRI KARATEKIN UNIVERSITY)0000-0001-9294-2801
Ayhan Filazi(ANKARA UNIVERSITY, ANKARA FACULTY OF VETERINARY MEDICINE)0000-0002-2800-6215
Sayfa
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Yayın Tarihi
2026-05-06
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Yapay Zeka Hızlı Bakış & Çıkarımlar

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⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Although further research is needed regarding their ability to cross the blood-brain barrier, AgNPs can be considered as potential agents that can be effectively used in GBM treatment due to their potent inhibitory effects.

📌 3 Maddede Bu Makale

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Amaç & Hipotez:Glioblastoma multiforme (GBM) constitutes a significant majority of glial-derived tumors.
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Temel Bulgular & Veri:It has a poor prognosis.
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Sonuç & Katkı:Although further research is needed regarding their ability to cross the blood-brain barrier, AgNPs can be considered as potential agents that can be effectively used in GBM treatment due to their potent inhibitory effects.
🔬Tür:Research Article
📍Kapsam:Genişletilmiş Akademik Örneklem
⚙️Değişkenler:Blood–brain barrier · Brain tumor treatment · Cytotoxicity

Abstract

Glioblastoma multiforme (GBM) constitutes a significant majority of glial-derived tumors. It has a poor prognosis. It is highly aggressive and malignant. In this disease, where treatment methods can be used alone or in combination, localization and, consequently, accessibility are among the most important factors affecting treatment. Nanoparticle-based approaches, such as silver-based nanoparticles containing different silver forms like AgNO₃, AgMP, and AgNP, are emerging as potential agents in tumor treatment. This study aimed to determine the effects of silver nanoparticles of different sizes on GBM cell viability. The results obtained revealed that AgNP exposure produced a highly cytotoxic effect and that the cytotoxic properties of AgMPs were lower compared to the other silver forms examined in our study. Although further research is needed regarding their ability to cross the blood-brain barrier, AgNPs can be considered as potential agents that can be effectively used in GBM treatment due to their potent inhibitory effects.

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Bu Makaleye Atıf Yap

Pehlivan, S., Şimşek, İ., Akdağ, E., Yıltırak, A. F., Yüce, P. A., Kuzukıran, Ö., Filazi, A. (2026). Comparison of the effects of nano, micro silver particles, and silver nitrate on glioblastoma multiforme (CRL-1690). Journal of advances in vetbio science and techniques, Issue: 2. https://doi.org/10.31797/vetbio.1863533

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Kaynakça (24)

  1. Al-Khedhairy, A. A. & Wahab, R. (2022). Silver nanoparticles: An instantaneous solution for anticancer activity against human liver (HepG2) and breast (MCF-7) cancer cells. Metals, 12(1), 148. https://doi.org/10.3390/met12010148
  2. Avalos Funez, A., Isabel Haza, A., Mateo, D. & Morales, P. (2013). In vitro evaluation of silver nanoparticles on human tumoral and normal cells. Toxicology Mechanisms and Methods, 23(3), 153–160. https://doi.org/10.3109/15376516.2012.762081
  3. Barile, F. A. (1994). Introduction to in vitro cytotoxicology: Mechanisms and methods. In F. A. Barile (Ed.), In vitro cytotoxicology (pp. 33–43). CRC Press.
  4. Butler, M. (2004). Animal cell culture and technology (2nd ed.). Taylor & Francis.
  5. Choi, J. H., Min, W. K., Gopal, J., Lee, Y. M., Muthu, M., Chun, S. & Oh, J. W. (2018). Silver nanoparticle-induced hormesis of astroglioma cells: A Mu-2-related death-inducing protein-orchestrated modus operandi. International Journal of Biological Macromolecules, 117, 1147–1156. https://doi.org/10.1016/j.ijbiomac.2018.05.234
  6. El-Sonbaty, S. M. (2013). Fungus-mediated synthesis of silver nanoparticles and evaluation of antitumor activity. Cancer Nanotechnology, 4(4), 73–79. https://doi.org/10.1007/s12645-013-0038-3
  7. Emanuelsson, I., Wikvall, K., Friman, T. & Norlin, M. (2018). Vitamin D analogues tacalcitol and calcipotriol inhibit proliferation and migration of T98G human glioblastoma cells. Basic & Clinical Pharmacology & Toxicology, 123(2), 130–136. https://doi.org/10.1111/bcpt.13007
  8. Eugenio, M., Campanati, L., Müller, N., Romão, L. F., de Souza, J., Alves-Leon, S., de Souza, W. & Sant’Anna, C. (2018). Silver/silver chloride nanoparticles inhibit the proliferation of human glioblastoma cells. Cytotechnology, 70(6), 1607–1618. https://doi.org/10.1007/s10616-018-0253
  9. Fuster, E., Candela, H., Estévez, J., Arias, A. J., Vilanova, E., & Sogorb, M. A. (2020). Effects of silver nanoparticles on T98G human glioblastoma cells. Toxicology and Applied Pharmacology, 404, 115178. https://doi.org/10.1016/j.taap.2020.115178
  10. Garrido, W., Muñoz, M., San Martín, R. & Quezada, C. (2011). FK506 confers chemosensitivity to anticancer drugs in glioblastoma multiforme cells by decreasing the expression of the multiple resistance-associated protein-1. Biochemical and Biophysical Research Communications, 411(1), 62–68. https://doi.org/10.1016/j.bbrc.2011.06.087
  11. Guo, X., Li, Y., Yan, J., Ingle, T., Jones, M. Y., Mei, N., Boudreau, M. D., Cunningham, C. K., Abbas, M., Paredes, A. M., Zhou, T., Moore, M. M., Howard, P C. & Chen, T. (2016). Size- and coating-dependent cytotoxicity and genotoxicity of silver nanoparticles evaluated using in vitro standard assays. Nanotoxicology, 10(9), 1373–1384. https://doi.org/10.1080/17435390.2016.1214764
  12. Haverkamp, R. G. & Marshall, A. T. (2009). The mechanism of metal nanoparticle formation in plants: Limits on accumulation. Journal of Nanoparticle Research, 11(6), 1453–1463. https://doi.org/10.1007/s11051-008-9533-6
  13. He, Y., Du, Z., Ma, S., Liu, Y., Li, D., Huang H., Jiang S., Cheng, S., Wu, W., Zhang, K. & Zheng, X. (2016). Effects of green-synthesized silver nanoparticles on lung cancer cells in vitro and grown as xenograft tumors in vivo. International Journal of Nanomedicine, 11, 1879–1887. https://doi.org/10.2147/IJN.S103695
  14. Hersh, A. M., Alomari, S., & Tyler, B. M. (2022). Crossing the blood–brain barrier: Advances in nanoparticle technology for drug delivery in neuro-oncology. International Journal of Molecular Sciences, 23(8), 4153
  15. Hodson, L. (2013). Protecting the nanotechnology workforce: NIOSH nanotechnology research and guidance strategic plan, 2013–2016. U.S. Department of Health and Human Services, Centers for Disease Control and Prevention, National Institute for Occupational Safety and Health.
  16. Kaba, S. I. & Egorova, E. M. (2015). In vitro studies of the toxic effects of silver nanoparticles on HeLa and U937 cells. Nanotechnology, Science and Applications, 8, 19–29. https://doi.org/10.2147/NSA.S78134
  17. Kaplan, A., Akalin Ciftci, G. & Kutlu, H. M. (2017). The apoptotic and genomic studies on A549 cell line induced by silver nitrate. Tumor Biology, 39(4), 1010428317695033. https://doi.org/10.1177/10104283176950
  18. Liu, L., An, X., Schaefer, M., Yan, B., de Torre, C., Hillmer, S., Gladkich, J. & Herr, I. (2022). Nanosilver inhibits the progression of pancreatic cancer by inducing a paraptosis-like mixed type of cell death. Biomedicine & Pharmacotherapy, 153, 113511. https://doi.org/10.1016/j.biopha.2022.113511
  19. Muntimadugu, E., Kommineni, N. & Khan, W. (2017). Exploring the potential of nanotherapeutics in targeting tumor microenvironment for cancer therapy. Pharmacological Research, 126, 109–122. https://doi.org/10.1016/j.phrs.2017.05.010
  20. Sriram, M. I., Kanth, S. B. M., Kalishwaralal, K. & Gurunathan, S. (2010). Antitumor activity of silver nanoparticles in Dalton’s lymphoma ascites tumor model. International Journal of Nanomedicine, 5, 753–762. https://doi.org/10.2147/IJN.S11727
  21. Takáč, P., Michalková, R., Čižmáriková, M., Bedlovičová, Z., Balážová, L. & Takáčová, G. (2023). The role of silver nanoparticles in the diagnosis and treatment of cancer: Are there any perspectives for the future? Life, 13(2), 466. https://doi.org/10.3390/life13020466
  22. Vivek, R., Thangam, R., Muthuchelian, K., Gunasekaran, P., Kaveri, K., & Kannan, S. (2012). Green biosynthesis of silver nanoparticles from Annona squamosa leaf extract and its in vitro cytotoxic effect on MCF-7 cells. Process Biochemistry, 47(12), 2405–2410. https://doi.org/10.1016/j.procbio.2012.09.025
  23. Wu, D., Chen, Q., Chen, X., Han, F., Chen, Z., & Wang, Y. (2023). The blood–brain barrier: Structure, regulation and drug delivery. Signal Transduction and Targeted Therapy, 8(1), 217.
  24. Yurdakok-Dikmen, B., Alpay, M., Kismali, G., Filazi, A., Kuzukiran, O. & Sireli, U. T. (2015). In vitro effects of phthalate mixtures on colorectal adenocarcinoma cell lines. Journal of Environmental Pathology, Toxicology and Oncology, 34(2), 101–112. https://doi.org/10.1615/JEnvironPatholToxicolOncol.2015013256