Enhanced efficiency of samarium-doped TiO2 nanoparticles for targeted imaging: Characterization and in vivo evaluation

Document Type : Research Paper

Authors

1 Physics Department, Faculty of Science, Mansoura University, Mansoura, Egypt

2 Mansoura Urology and Nephrology Center, Mansoura University, Mansoura 35516, Egypt

3 Spectroscopy Department, Physics Division, National Research Center, 33 ElBehouth St., Dokki, 12311, Cairo, Egypt

Abstract

Objective(s): This study aimed to synthesize Samarium-doped TiO2 nanoparticles (Ti(Sm)O2 NPs) using solvothermal synthesis and evaluate their suitability as targeted imaging agents. The objectives were to enhance the stability and biocompatibility of the nanoparticles by coating them with polymeric materials and assess their imaging capabilities and safety. 
Materials and Methods: Ti(Sm)O2 NPs were synthesized using the solvothermal method with TiO2, NaOH, and deionized water. The resulting solution was filtered, dried, and processed in a Teflon-lined stainless steel autoclave. The obtained product was washed, dried, and coated with FDA-approved polymers including polyethylene glycol (PEG), polyvinylpyrrolidone (PVP), and carboxymethyl cellulose (CMC). Coating was achieved through a mixing process and subsequent drying. 
Results: Characterization studies confirmed the desired morphology, crystal structure, optical properties, surface charge, and biocompatibility of the Ti(Sm)O2 NPs. In vivo imaging evaluations demonstrated their excellent imaging capabilities, particularly in distinguishing lung pathologies. Additionally, in vivo toxicity studies confirmed the nanoparticles biocompatibility and safety, with no adverse effects on organ function observed. 
Conclusion: In this study, Samarium-doped TiO2 nanoparticles WERE successfully synthesized and their potential as targeted imaging agents was evaluated. The coating of the nanoparticles with polymeric materials enhanced their stability and biocompatibility. The nanoparticles exhibited excellent imaging capabilities, particularly in distinguishing lung pathologies. Moreover, they demonstrated biocompatibility and safety in vivo. These findings contribute to the development of advanced contrast agents for biomedical applications, providing effective tools for targeted imaging and improving the diagnosis and monitoring of various lung pathologies.

Keywords


1.    Bae KH, Chung HJ, Park TG. Nanomaterials for cancer therapy and imaging. Molecules and cells. 2011;31(4):295-302.
2.    Hallouard F, Anton N, Choquet P, Constantinesco A, Vandamme T. Iodinated blood pool contrast media for preclinical X-ray imaging applications--a review. Biomaterials. 2010;31(24):6249-6268.
3.    Liu Y, Ai K, Lu L. Nanoparticulate X-ray computed tomography contrast agents: from design validation to in vivo applications. Accounts of chemical research. 2012;45(10):1817-1827.
4.    Cormode DP, Naha PC, Fayad ZA. Nanoparticle contrast agents for computed tomography: a focus on micelles. Contrast media & molecular imaging. 2014;9(1):37-52.
5.    Hainfeld JF, Slatkin DN, Focella TM, Smilowitz HM. Gold nanoparticles: a new X-ray contrast agent. Br J Radiol. 2006;79(939):248-253.
6.    Jackson PA, Rahman WN, Wong CJ, Ackerly T, Geso M. Potential dependent superiority of gold nanoparticles in comparison to iodinated contrast agents. EMJ Radiol. 2010;75(1):104-109.
7.    Connor EE, Mwamuka J, Gole A, Murphy CJ, Wyatt MD. Gold nanoparticles are taken up by human cells but do not cause acute cytotoxicity. Small (Weinheim an der Bergstrasse, Germany). 2005;1(3):325-327.
8.    Jakhmola A, Anton N, Vandamme TF. Inorganic nanoparticles based contrast agents for X-ray computed tomography. Advanced healthcare materials. 2012;1(4):413-431.
9.    Rabin O, Manuel Perez J, Grimm J, Wojtkiewicz G, Weissleder R. An X-ray computed tomography imaging agent based on long-circulating bismuth sulphide nanoparticles. Nature materials. 2006;5(2):118-122.
10.    Pan D, Roessl E, Schlomka JP, Caruthers SD, Senpan A, Scott MJ, et al. Computed tomography in color: NanoK‐enhanced spectral CT molecular imaging. Angewandte Chemie. 2010;122(50):9829-9833.
11.    Nadel JA, Wolfe WG, Graf PD, Youker JE, Zamel N, Austin JH, et al. Powdered tantalum. N Engl J Med. 1970;283(6):281-286.
12.    Chakravarty S, Hix JML, Wiewiora KA, Volk MC, Kenyon E, Shuboni-Mulligan DD, et al. Tantalum oxide nanoparticles as versatile contrast agents for X-ray computed tomography. Nanoscale. 2020;12(14):7720-7734.
13.    Xing H, Bu W, Ren Q, Zheng X, Li M, Zhang S, et al. A NaYbF4: Tm3+ nanoprobe for CT and NIR-to-NIR fluorescent bimodal imaging. Biomaterials. 2012;33(21):5384-5393.
14.    Jafari S, Mahyad B, Hashemzadeh H, Janfaza S, Gholikhani T, Tayebi L. Biomedical Applications of TiO(2) Nanostructures: Recent Advances. Int J Nanomed. 2020;15:3447-3470.
15.    Townley HE, Rapa E, Wakefield G, Dobson PJ. Nanoparticle augmented radiation treatment decreases cancer cell proliferation. Nanomedicine: nanotechnology, biology, and medicine. 2012;8(4):526-536.
16.    Michalet X, Pinaud FF, Bentolila LA, Tsay JM, Doose S, Li JJ, et al. Quantum dots for live cells, in vivo imaging, and diagnostics. Science (New York, NY). 2005;307(5709):538-544.
17.    Koudrina A, DeRosa MC. Advances in Medical Imaging: Aptamer- and Peptide-Targeted MRI and CT Contrast Agents. ACS omega. 2020;5(36):22691-22701.
18.    Fahmy HM, Mosleh AM, Elghany AA, Shams-Eldin E, Abu Serea ES, Ali SA, et al. Coated silver nanoparticles: synthesis, cytotoxicity, and optical properties. RSC advances. 2019;9(35):20118-20136.
19.    Abo Gabal R, Osama S, Hanafy N, Oraby A. Micellization thermodynamics as a function of the temperature of a cationic zwitterionic dodecyl phosphocholine and anionic sodium dodecyl sulfate mixed micelles with fluorometry. Appl Phys A. 2023;129(3):201.
20.    Park JY, Daksha P, Lee GH, Woo S, Chang Y. Highly water-dispersible PEG surface modified ultra small superparamagnetic iron oxide nanoparticles useful for target-specific biomedical applications. Nanotechnology. 2008;19(36):365603.
21.    Gaaz TS, Sulong AB, Akhtar MN, Kadhum AA, Mohamad AB, Al-Amiery AA. Properties and Applications of Polyvinyl Alcohol, Halloysite Nanotubes and Their Nanocomposites. Molecules (Basel, Switzerland). 2015;20(12):22833-22447.
22.    Babic M, Horák D, Trchová M, Jendelová P, Glogarová K, Lesný P, et al. Poly(L-lysine)-modified iron oxide nanoparticles for stem cell labeling. Bioconjugate chemistry. 2008;19(3):740-750.
23.    Mano SS, Kanehira K, Sonezaki S, Taniguchi A. Effect of polyethylene glycol modification of TiO₂nanoparticles on cytotoxicity and gene expressions in human cell lines. Int J Mol Sci. 2012;13(3):3703-3717.
24.    Vitha MF. Spectroscopy: Principles and Instrumentation: John Wiley & Sons; 2018;Ch.2:39.
25.    Kannan M. Transmission Electron Microscope -Principle, Components and Applications Illumination system (Electron gun and condenser lenses) Electron gun. 2018. p. 93-101.
26.    Franks GV. Zeta potentials and yield stresses of silica suspensions in concentrated monovalent electrolytes: isoelectric point shift and additional attraction. J Colloid Interface Sci. 2002;249(1):44-51.
27.    De Dios I, Ramudo L, Alonso JR, Recio JS, Garcia-Montero AC, Manso MA. CD45 expression on rat acinar cells: involvement in pro-inflammatory cytokine production. FEBS letters. 2005;579(28):6355-6360.
28.    Gabal RA, Shokeir D, Orabi A. Cytotoxicity and Hemostatic One Step Green Synthesis of Iron Nanoparticles Coated with Green Tea for Biomedical Application. Trends Sci. 2022;19(3):2062.
29.    Pogson EM, McNamara J, Metcalfe P, Lewis RA. Comparing and evaluating the efficacy of the TOR18FG Leeds test X-ray phantom for T-rays. Quantitative imaging in medicine and surgery. 2013;3(1):18-27.
30.    Shi J, Votruba AR, Farokhzad OC, Langer R. Nanotechnology in drug delivery and tissue engineering: from discovery to applications. Nano letters. 2010;10(9):3223-3230.