Epithelial cell biocompatibility of silica nanospheres for contrast-enhanced ultrasound molecular imaging

被引:23
作者
Chiriaco, Fernanda [1 ]
Conversano, Francesco [1 ]
Soloperto, Giulia [1 ]
Casciaro, Ernesto [1 ]
Ragusa, Andrea [2 ]
Sbenaglia, Enzo Antonio [1 ]
Dipaola, Lucia [1 ]
Casciaro, Sergio [3 ]
机构
[1] CNR, Inst Clin Physiol, Bioengn Div, I-73100 Lecce, Italy
[2] CNR NANO, Natl Nanotechnol Lab, I-73100 Lecce, Italy
[3] CNR, IFC, I-73100 Lecce, Italy
关键词
Biological techniques; Biomedical materials; Cancer detection; Cells (biology); Medical diagnostic imaging; Molecular imaging; Nanobiotechnology; Nanoparticles; Toxicity; IRON-OXIDE NANOPARTICLES; IN-VITRO EVALUATION; AGENTS; SIZE; PERMEABILITY; RETENTION; PARTICLES;
D O I
10.1007/s11051-013-1779-y
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Nanosized particles are receiving increasing attention as future contrast agents (CAs) for ultrasound (US) molecular imaging, possibly decorated on its surface with biological recognition agents for targeted delivery and deposition of therapeutics. In particular, silica nanospheres (SiNSs) have been demonstrated to be feasible in terms of contrast enhancement on conventional US systems. In this work, we evaluated the cytotoxicity of SiNSs on breast cancer (MCF-7) and HeLa (cervical cancer) cells employing NSs with sizes ranging from 160 to 330 nm and concentration range of 1.5-5 mg/mL. Cell viability was evaluated in terms of size, dose and time dependence, performing the MTT reduction assay with coated and uncoated SiNSs. Whereas uncoated SiNSs caused a variable significant decrease in cell viability on both cell lines mainly depending on size and exposure time, PEGylated SiNSs (SiNSs-PEG) exhibit a high level of biocompatibility. In fact, after 72-h incubation, viability of both cell types was above the cutoff value of 70 % at concentration up to 5 mg/mL. We also investigated the acoustical behavior of coated and uncoated SiNSs within conventional diagnostic US fields in order to determine a suitable configuration, in terms of particle size and concentration, for their employment as targetable CAs. Our results indicate that the employment of SiNSs with diameters around 240 nm assures the most effective contrast enhancement even at the lowest tested concentration, coupled with the possibility of targeting all tumor tissues, being the SiNSs still in a size range where reticuloendothelial system trapping effect is relatively low.
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页数:13
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[11]   In Vitro Evaluation and Theoretical Modeling of the Dissolution Behavior of a Microbubble Contrast Agent for Ultrasound Imaging [J].
Conversano, Francesco ;
Franchini, Roberto ;
Lay-Ekuakille, Aime ;
Casciaro, Sergio .
IEEE SENSORS JOURNAL, 2012, 12 (03) :496-503
[12]   Molecular ultrasound imaging using microbubble contrast agents [J].
Dayton, Paul A. ;
Rychak, Joshua J. .
FRONTIERS IN BIOSCIENCE-LANDMARK, 2007, 12 :5124-5142
[13]   Application of ultrasound to selectively localize nanodroplets for targeted imaging and therapy [J].
Dayton, Paul A. ;
Zhao, Shukui ;
Bloch, Susannah H. ;
Schumann, Pat ;
Penrose, Kim ;
Matsunaga, Terry O. ;
Zutshi, Reena ;
Doinikov, Alexander ;
Ferrara, Katherine W. .
MOLECULAR IMAGING, 2006, 5 (03) :160-174
[14]  
Dipaola L, 2011, P IEEE SENS C OCT 28
[15]   Thermal stability of silica-coated magnetite nanoparticles prepared by an electrochemical method [J].
Fajaroh, Fauziatul ;
Setyawan, Heru ;
Nur, Adrian ;
Lenggoro, I. Wuled .
ADVANCED POWDER TECHNOLOGY, 2013, 24 (02) :507-511
[16]   Control of the in vivo Biodistribution of Hybrid Nanoparticles with Different Poly(ethylene glycol) Coatings [J].
Faure, Anne-Charlotte ;
Dufort, Sandrine ;
Josserand, Veronique ;
Perriat, Pascal ;
Coll, Jean-Luc ;
Roux, Stephane ;
Tillement, Olivier .
SMALL, 2009, 5 (22) :2565-2575
[17]   Pulsatile flow phantom for ultrasound image-guided hifu treatment of vascular injuries [J].
Greaby, Robyn ;
Zderic, Vesna ;
Vaezy, Shahram .
ULTRASOUND IN MEDICINE AND BIOLOGY, 2007, 33 (08) :1269-1276
[18]   Nanoparticles as contrast agents for in-vivo bioimaging: current status and future perspectives [J].
Hahn, Megan A. ;
Singh, Amit K. ;
Sharma, Parvesh ;
Brown, Scott C. ;
Moudgil, Brij M. .
ANALYTICAL AND BIOANALYTICAL CHEMISTRY, 2011, 399 (01) :3-27
[19]   Regulation of transport pathways in tumor vessels: Role of tumor type and microenvironment [J].
Hobbs, SK ;
Monsky, WL ;
Yuan, F ;
Roberts, WG ;
Griffith, L ;
Torchilin, VP ;
Jain, RK .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1998, 95 (08) :4607-4612
[20]   Exploiting the enhanced permeability and retention effect for tumor targeting [J].
Iyer, Arun K. ;
Khaled, Greish ;
Fang, Jun ;
Maeda, Hiroshi .
DRUG DISCOVERY TODAY, 2006, 11 (17-18) :812-818