Synthesis, characterization, and biodistribution studies of 99mTc-labeled SBA-16 mesoporous silica nanoparticles

被引:43
作者
Branco de Barros, Andre Luis [1 ,2 ]
de Oliveira Ferraz, Karina Silva [1 ]
Soares Dantas, Thais Cristina [1 ]
Andrade, Gracielle Ferreira [1 ]
Cardoso, Valbert Nascimento [2 ]
Barros de Sousa, Edesia Martins [1 ]
机构
[1] Ctr Desenvolvimento Tecnol Nucl, Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Fac Farm, Belo Horizonte, MG, Brazil
来源
MATERIALS SCIENCE & ENGINEERING C-MATERIALS FOR BIOLOGICAL APPLICATIONS | 2015年 / 56卷
关键词
Mesoporous silica nanoparticles; Scintigraphic imaging; Diagnosis; Radiolabeled nanoparticles; Technetium-99m; SBA-16; RECEPTOR;
D O I
10.1016/j.msec.2015.06.030
中图分类号
TB3 [工程材料学]; R318.08 [生物材料学];
学科分类号
0805 ; 080501 ; 080502 ;
摘要
Along with anti-cancer drug delivery researches, many efforts have been done to develop new tracers for diagnostic applications. Based on advances in molecular imaging, nanoparticles can be used to visualize, characterize and measure biological process at molecular and cellular level. Therefore, the purpose of this study was to synthesize, characterize and radiolabeled mesoporous silica nanoparticles (MSNs) for in vivo applications. The nanoparticles were synthesized, functionalized with 3-aminopropyltriethoxysilane (APTES) and then, anchored with diethylenetriaminepentaacetic acid (DTPA). Particles were physicochemical characterized by elemental analysis (CHN), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), and zeta potential, and were morphologically characterized by scanning electron microscopy (SEM), low-angle X-ray diffraction (XRD) and transmission electron microscopy (TEM) techniques. Results indicate that functionalization process was successfully achieved. Next, functionalized silica nanoparticles were radiolabeled with technetium-99m showing high radiochemical yields and high radiolabeled stability. These findings allow the use of the particles for in vivo applications. Biodistribution and scintigraphic images were carried out in healthy mice in order to determine the fate of the particles. Results from in vivo experiments showed high uptake by liver, as expected due to phagocytosis. However, particles also showed a significant uptake in the lungs, indicated by high lung-to-nontarget tissue ratio. In summary, taking into account the great potential of these silica mesoporous structures to carry molecules this platform could be a good strategy for theranostic purposes. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:181 / 188
页数:8
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