journal article·2023-04

The synthesis and anti-cancer efficacy of endoperoxide modified copper sulfide-ferritin nanocages as PDT and PTT agents

Merve Kucukoflaz, Sakine Ulusoy, Bekir Korkmaz, Suleyman Can Ozturk, Melih Akyol, Sibel Berksoy Hayta, Omer Fahrettin Goze, Gunes Esendagli, Fazli Sozmen

Journal of Nanoparticle Research· Volume 25· Issue 4
Publisher page

Abstract

Photodynamic therapy (PDT) using endoperoxides is to produce toxic singlet oxygen of reactive oxygen species through heat from the endoperoxides present in the medium. Compared with conventional PDT, PDT using endoperoxides has some advantages, for instance, in the presence of endoperoxide, singlet oxygen efficiency is not affected by hypoxic environment, because endoperoxides are the source of singlet oxygen. On the other hand, the kinetic stabilities of endoperoxides are important in the body temperature. Another advantage of endoperoxides is that they can produce singlet oxygen upon warming, so regardless of the wavelength of the emitted light, they can selectively produce singlet oxygen in the heated region. The aim of this study is to synthesize core-shell nanocages (10-Aft-CuS) with the synergistic effect of both photothermal therapy (PTT) and PDT by functionalizing the surface of the Apoferritin (Aft) nanocage platform with an endoperoxide derivative and forming ultra-small CuS nanoparticles in its inner cavity for the first time. So, first of all, Aft-CuS nanoparticles were obtained by the synthesis of ultra-small CuS nanoparticles in the inner cavity of Aft nanocages. Then, the surfaces of these nanocages have been functionalized with the Compound 10, an endoperoxide anthracene derivative. While the synthesized nanoparticles in this way have the synergistic effects of PTT and PDT therapies, achieving this with a natural nanoparticle has also been tested in cell cultures in vitro and in mice with progressed melanoma in vivo by increasing the effectiveness against cancer cells. 10-Aft-CuS nanocages showed high anti-tumor efficacy against malignant melanoma in vitro and in vivo.
Source: openaire · Quality: candidate unverified · Source record ↗

Research context

OpenAlex topics: Nanoplatforms for cancer theranostics · Gold and Silver Nanoparticles Synthesis and Applications · Advanced Photocatalysis Techniques

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

References (31)

Show source-provided references
1. Kolemen S, Ozdemir T, Lee D, Kim G, Karatas T, Yoon J, Akkaya E (2016) Remote-controlled release of singlet oxygen by the plasmonic heating of endoperoxide-modified gold nanorods: towards a paradigm change in photodynamic therapy. Angew Chem Int Ed 55:3606–361010.1002/anie.201510064 ↗
2. Dolmans DE, Fukumura D, Jain RK (2003) Photodynamic therapy for cancer. Nat Rev Cancer 3(5):380–38710.1038/nrc1071 ↗
3. Sharman WM, Allen CM, Van Lier JE (1999) Photodynamic therapeutics: basic principles and clinical applications. Drug Discov 4(11):507–517
4. Bertout JA, Patel SA, Simon MC (2008) The impact of O2 availability on human cancer. Nat Rev Cancer 8(12):967–97510.1038/nrc2540 ↗
5. Sullivan R, Graham CH (2007) Hypoxia-driven selection of the metastatic phenotype. Cancer Metastasis Rev 26(2):319–33110.1007/s10555-007-9062-2 ↗
6. Aubry J-M, Pierlot C, Rigaudy J, Schmidt R (2003) Reversible binding of oxygen to aromatic compounds. Acc Chem Res 36(9):668–67510.1021/ar010086g ↗
7. Lee J-J, Gonçalves A, Smith BA, Palumbo R, White AG, Smith BD (2011) Singlet oxygen release and cell toxicity of a chemiluminescent squaraine rotaxane dye: implications for molecular imaging. Aust J Chem 64(5):604–61010.1071/CH11038 ↗
8. Wang L, Tang L, Liu Y, Wu H, Liu Z, Li J, Pan Y, Akkaya EU (2022) Prostate-specific membrane antigen (PSMA) targeted singlet oxygen delivery via endoperoxide tethered ligands. Chem Comm 58(12):1902–190510.1039/D1CC05810J ↗
9. Wu H, Liu Z, Shao Y, Li G, Pan Y, Wang L, Akkaya EU (2022) Degradation of amyloid peptide aggregates by targeted singlet oxygen delivery from a benzothiazole functionalized naphthalene endoperoxide. Chem Comm 58(23):3747–375010.1039/D1CC07133E ↗
10. Li Y, Lu W, Huang Q, Li C, Chen W (2010) Copper sulfide nanoparticles for photothermal ablation of tumor cells. Nanomedicine 5(8):1161–117110.2217/nnm.10.85 ↗
11. Tian Q, Jiang F, Zou R, Liu Q, Chen Z, Zhu M, Yang S, Wang J, Wang J, Hu J (2011) Hydrophilic Cu9S5 nanocrystals: a photothermal agent with a 25.7% heat conversion efficiency for photothermal ablation of cancer cells in vivo. ACS nano 5(12):9761–977110.1021/nn203293t ↗
12. Tian Q, Tang M, Sun Y, Zou R, Chen Z, Zhu M, Yang S, Wang J, Wang J, Hu J (2011) Hydrophilic flower-like CuS superstructures as an efficient 980 nm laser-driven photothermal agent for ablation of cancer cells. Adv Mater 23(31):3542–354710.1002/adma.201101295 ↗
13. Zhou M, Zhang R, Huang M, Lu W, Song S, Melancon MP, Tian M, Liang D, Li C (2010) A chelator-free multifunctional [64Cu] CuS nanoparticle platform for simultaneous micro-PET/CT imaging and photothermal ablation therapy. J Am Chem Soc 132(43):15351–1535810.1021/ja106855m ↗
14. Wang Z, Huang P, Jacobson O, Wang Z, Liu Y, Lin L, Lin J, Lu N, Zhang H, Tian R (2016) Biomineralization-inspired synthesis of copper sulfide−ferritin nanocages as cancer theranostics. ACS nano 10(3):3453–346010.1021/acsnano.5b07521 ↗
15. Arosio P, Ingrassia R, Cavadini P (2009) Ferritins: a family of molecules for iron storage, antioxidation and more. Biochim Biophys Acta-Gen Subj 1790 7:589–59910.1016/j.bbagen.2008.09.004 ↗
16. Bellini M, Mazzucchelli S, Galbiati E, Sommaruga S, Fiandra L, Truffi M, Rizzuto MA, Colombo M, Tortora P, Corsi F (2014) Protein nanocages for self-triggered nuclear delivery of DNA-targeted chemotherapeutics in cancer cells. J Control Release 196:184–19610.1016/j.jconrel.2014.10.002 ↗
17. Thompson KJ, Fried MG, Ye Z, Boyer P, Connor JR (2002) Regulation, mechanisms and proposed function of ferritin translocation to cell nuclei. J Cell Sci 115(10):2165–217710.1242/jcs.115.10.2165 ↗
18. Zhang L, Li L, Di Penta A, Carmona U, Yang F, Schöps R, Brandsch M, Zugaza JL, Knez M (2015) H-Chain Ferritin, A natural nuclei targeting and bioactive delivery nanovector. Adv Healthc Mater 4(9):1305–131010.1002/adhm.201500226 ↗
19. Domınguez-Vera JM (2004) Iron(III) complexation of Desferoxamine B encapsulated in apoferritin. J Inorg Biochem 98(3):469–47210.1016/j.jinorgbio.2003.12.015 ↗
20. Falvo E, Tremante E, Fraioli R, Leonetti C, Zamparelli C, Boffi A, Morea V, Ceci P, Giacomini P (2013) Antibody-drug conjugates: targeting melanoma with cisplatin encapsulated in protein-cage nanoparticles based on human ferritin. Nanoscale 5(24):12278–1228510.1039/c3nr04268e ↗
21. He D, Marles-Wright J (2015) Ferritin family proteins and their use in bionanotechnology. N Biotechnol 32(6):651–65710.1016/j.nbt.2014.12.006 ↗
22. Jääskeläinen A, Soukka T, Lamminmäki U, Korpimäki T, Virta M (2009) Development of a denaturation/renaturation-based production process for ferritin nanoparticles. Biotechnol Bioeng 102(4):1012–102410.1002/bit.22140 ↗
23. Geninatti Crich S, Bussolati B, Tei L, Grange C, Esposito G, Lanzardo S, Camussi G, Aime S (2006) Magnetic resonance visualization of tumor angiogenesis by targeting neural cell adhesion molecules with the highly sensitive gadolinium-loaded apoferritin probe. Cancer Res 66(18):9196–920110.1158/0008-5472.CAN-06-1728 ↗
24. Sun C, Yang H, Yuan Y, Tian X, Wang L, Guo Y, Xu L, Lei J, Gao N, Anderson GJ (2011) Controlling assembly of paired gold Clusters within apoferritin nanoreactor for in vivo kidney targeting and biomedical imaging. J Am Chem Soc 133(22):8617–862410.1021/ja200746p ↗
25. Yamashita I, Hayashi J, Hara M (2004) Bio-template synthesis of uniform CdSe nanoparticles using cage-shaped protein apoferritin. Chem Lett 33(9):1158–115910.1246/cl.2004.1158 ↗
26. Yang Z, Wang X, Diao H, Zhang J, Li H, Sun H, Guo Z (2007) Encapsulation of platinum anticancer drugs by apoferritin. Chem Comm 33:3453–345510.1039/b705326f ↗
27. Chen L, Bai G, Yang S, Yang R, Zhao G, Xu C, Leung W (2014) Encapsulation of curcumin in recombinant human H-chain ferritin increases its water-solubility and stability. Int Food Res J 62:1147–115310.1016/j.foodres.2014.05.054 ↗
28. Kim M, Rho Y, Jin KS, Ahn B, Jung S, Kim H, Ree M (2011) pH-dependent structures of ferritin and apoferritin in solution: disassembly and reassembly. Biomacromolecules 12(5):1629–164010.1021/bm200026v ↗
29. Lin X, Xie J, Niu G, Zhang F, Gao H, Yang M, Quan Q, Aronova MA, Zhang G, Lee S (2011) Chimeric ferritin nanocages for multiple function loading and multi modal imaging. Nano letters 11(2):814–81910.1021/nl104141g ↗
30. International Organization for Standardization (2009) ISO 10993-5: 2009-biological evaluation of medical devices-part 5: tests for in vitro cytotoxicity, p 13
31. Timur SS, Yöyen-Ermiş D, Esendağlı G, Yonat S, Horzum U, Esendağlı G, Gürsoy RN (2019) Efficacy of a novel LyP-1-containing self-microemulsifying drug delivery system (SMEDDS) for active targeting to breast cancer. European Journal of Pharmaceutics and Biopharmaceutics 136:138–14610.1016/j.ejpb.2019.01.017 ↗