Iron-platinum nanoparticles as multifunctional vehicles in imaging and drug delivery

2016 ◽  
Author(s):  
◽  
Christian Alan Mason

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] In the United States alone, approximately 1.6 million people are diagnosed with cancer and over 500,000 people die of cancer each year. According to the American Cancer Society the probability that a male and female will die of cancer are roughly one in four and one in six, respectively. Though current research and development has reduced the mortality rate, the effectiveness of treatment options are severely limited. There has been a rising interest in the literature focused on developing materials with the ability to selectively treat and diagnose a disease or illness. Iron-platinum nanoparticles have great potential as magnetic resonance imaging (MRI) agents. These superparamagnetic materials have been studied as they may offer a better alternative to current materials. Several different mechanisms for their formation have been described, and multiple parameters have been used to control the size and shape of these nanoparticles. Variables such as the amounts of surfactant, heating rates, and concentration of metal precursors were explored. The synthesis produced nanoparticles with a disordered face-centered cubic (fcc) structure, subsequent annealing could be performed to produce the face-centered tetragonal crystal structure. The nanoparticles size and shape were analyzed using transmission electron microscopy (TEM) along with ImageJ software. The results of these syntheses show that the amount of surfactant used during the synthesis has a significant effect on the size and shape of the nanoparticles. The cubic and spheroid shaped nanoparticles were analyzed for variations in unit cell structure, composition, or magnetic properties. The composition of the nanoparticles was analyzed with energy dispersive X-ray spectroscopy (EDS) and inductively coupled plasma mass spectrometry (ICP-MS). Unit cell structure was analyzed using powder X-ray diffraction (XRD). Magnetic measurements were obtained using a 7T MRI instrument. These analyses have shown that the unit cell structure, composition, and magnetic characteristics are different for the cubic and spheroid shaped nanoparticles. The iron-platinum nanoparticles have been coated by a silicon-dioxide network using a silanization reaction developed from the Stober process. Magnetic characteristics and compositional analysis of the coated iron-platinum nanoparticles were performed again using both MRI and ICP-MS. The surface of the silicon-dioxide coated ironplatinum nanoparticles was functionalized using 3-chloropropyltrimethoxy silane. The chlorine functional groups were then replaced with an azide followed by a click reaction to produce beta-cyclodextrin functionalized silica coated iron-platinum nanoparticle. An inclusion study was performed to analyze the beta-cyclodextrin functionalization reactions. These nanoparticles systems have great potential as cancer therapeutic and diagnostic agents.

2016 ◽  
Author(s):  
◽  
Emilia Ohsone-Zargham Mason

[ACCESS RESTRICTED TO THE UNIVERSITY OF MISSOURI AT AUTHOR'S REQUEST.] Cancer is the second leading cause of death in the United States, exceeded only by heart disease, and it is estimated that one in every four deaths is due to cancer.1 Many therapeutic techniques that are currently used are often severely limited and can cause adverse effects, which prevents the aggressive treatment of late stage cancers. Significant improvements are needed involving early detection and more selective treatment options. Much interest has been shown in the development of materials that are highly selective and capable of being used in both therapeutic and diagnostic applications.2,3 nanoparticles have been shown to passively accumulate in tumors, making them useful materials for developments in cancer research.4 Iron-platinum (FePt) nanoparticles have an excellent potential as delivery agents for medicinal applications. Superparamagnetic FePt nanoparticles were embedded in a surface-functionalized polymeric shell as drug delivery platforms. The FePt core offers improved characteristics for magnetic resonance imaging (MRI) over currently used materials. The FePt nanoparticles were optimized to sizes between 2 to 6 nanometers and their physical and magnetic properties were also analyzed. The amount of surfactants used during the synthesis had a significant effect on the size and shape of the nanoparticles. The altered synthetic parameters resulted in the formation of both cubic and spherical nanoparticles. Face-centered cubic (fcc) unit cell structures were produced, which could also be thermally annealed to form the more ordered face-centered tetragonal (fct) structures. The fcc and fct unit cell structures of the FePt nanoparticles were characterized using powder X-ray diffraction (XRD). The FePt nanoparticle cores were coated using an emulsion polymerization reaction to increase their stability in biological systems.5 The polystyrene coating was optimized to produce an overall size of approximately 12 to 30 nanometers. The magnetic characteristics of the coated FePt nanoparticles were analyzed by MRI. Dynamic light scattering (DLS), transmission electron microscopy (TEM), energy dispersive X-ray spectroscopy (EDS), and inductively coupled plasma mass spectrometry (ICP-MS) were also used to characterize the size and composition of the nanoparticles. The coated nanoparticles were functionalized with azides on the surface and analyzed using both Fourier transform infrared spectroscopy (FTIR) and nuclear magnetic resonance (NMR). beta-cyclodextrin was attached to the surface of the nanoparticles using a click chemistry reaction. The hydrophobic cavity of the beta-cyclodextrin allows for the incorporation of hydrophobic drugs for subsequent delivery. These superparamagnetic FePt coated and functionalized nanoparticles show great potential to selectively treat and diagnosis various types of cancer and diseases.6 Furthermore, there are numerous drugs such as FK866, doxorubicin, gemcitabine, and paclitaxel that are used to treat various types of cancer. Many of these drugs have different mechanisms by which they cause cell death. New derivatives of FK866, considered to be one of the most potent anti-cancer drugs, have been developed through the inclusion of carboranes.7,8 These drugs have shown increased potency and antiproliferative activity against cancer cells in vitro through the use of various cell culture assays.9/11 The inhibitory concentrations on various cells lines were reported through the use of MTT colorimetric assays.12 Drug combinations were also performed and analyzed using CompuSyn to determine the existence of any synergistic effects.


2014 ◽  
Vol 70 (a1) ◽  
pp. C1135-C1135
Author(s):  
Patrik Ahvenainen ◽  
Ritva Serimaa

Cellulose is the most abundant biopolymer on Earth and hence it has enormous potential as a source of renewable energy. The nanoscale properties of cellulose are also import for the wood and papermaking industries. The atomic level structure of naturally occurring cellulose Iβ allomorph is well known [1] and this atomistic model is employed in this study for the cellulose unit cell structure. The cellulose crystallinity cannot be measured directly with scattering methods, but the crystallinity of the sample can be estimated by fitting models of crystalline and amorphous contributions to the sample intensity profile. The crystallinity fitting can be enhanced by improving the cellulose fitting model or the amorphous model. We focus on the cellulose crystallite model. The nanoscale level organization of crystalline cellulose in different plant materials is less well established that the unit cell structure of cellulose Iβ. Information on the texture of the sample is obtained efficiently by measuring the sample with a two-dimensional detector. The two-dimensional diffraction pattern can be used to obtain a wealth of information in one measurement, including the crystallite size, crystallite orientation and the crystallinity of the sample. The small size of cellulose crystallites in the wood cell wall limits the information obtainable from the diffraction pattern as the diffraction peaks widen and overlap. The overlapping of certain diffraction peaks can be studied at least qualitatively by computing the diffraction patterns from crystallite models of varying dimensions. Different models for cellulose crystallite have been suggested in the literature, such as the 36 chain model [2]. We investigate how the crystallinity fitting is influenced by the selected cellulose crystallite model and evaluate the suitability of different models to experimental X-ray scattering data of plant material, wood and highly crystalline cellulose.


2011 ◽  
Vol 82 (3) ◽  
pp. 220-241 ◽  
Author(s):  
Kadir Bilisik ◽  
Nesrin Sahbaz

The aim of this study was to understand the effects of braid pattern and the number of layers on three-dimensional (3D) braided unit cell structures. Various unit cell-based representative 3D braided preforms were developed. Data generated from these structures included unit cell dimensions, yarn angle, and yarn length in the unit cell structures. It was shown that braid patterns affected the 3D braided unit cell structures. The 1 × 1 braid pattern made fully interconnected integral 3D braided unit cell structures, whereas the 2 × 1 braid pattern created disconnected braid layers that were connected to the structures edges. When the number of layers increased, 3D braided unit cell thickness also increased. Braid pattern slightly affected the braider yarn angle, whereas the number of layers did not influence it. It was observed that the number of layers considerably affected the yarn length in the unit cell structure. Increasing the layer number from five to 10 layers created a yarn path in the unit cell edge regions called the ‘multilayer yarn length’. This yarn path was not observed below five-layer 3D braided unit cell structures. In jamming conditions, minimum jamming decreased the width of the unit cell structure, but maximum jamming increased its width. On the other hand, minimum jamming decreased the surface angle of the unit cell structure, whereas maximum jamming increased the surface angle. In addition, it was realized that jamming conditions influenced the density of the unit cell but did not affect the yarn length in the unit cell structures.


2015 ◽  
Vol 2015 ◽  
pp. 1-9 ◽  
Author(s):  
Muhammad Tauseef Asim ◽  
Mushtaq Ahmed

A dual layer periodically patterned metamaterial inspired antenna on a low cost FR4 substrate is designed, simulated, fabricated, and tested. The eigenmode dispersion simulations are performed indicating the left handed metamaterial characteristics and are tunable with substrate permittivity. The same metamaterial unit cell structure is utilized to fabricate a metascreen. This metascreen is applied below the proposed metamaterial antenna and next used as superstrate above a simple patch to study the effects on impedance bandwidth, gain, and radiation patterns. The experimental results of these antennas are very good and closely match with the simulations. More importantly, the resonance for the proposed metamaterial antenna with metascreen occurs at the left handed (LH) eigenfrequency of the metamaterial unit cell structure. The measured −10 dB bandwidths are 14.56% and 22.86% for the metamaterial antenna with single and double metascreens, respectively. The metascreens over the simple patch show adjacent dual band response. The first and second bands have measured −10 dB bandwidths of 9.6% and 16.66%. The simulated peak gain and radiation efficiency are 1.83 dBi and 74%, respectively. The radiation patterns are also very good and could be useful in the UWB wireless applications.


2016 ◽  
Vol 145 (17) ◽  
pp. 174706 ◽  
Author(s):  
Tobias Huempfner ◽  
Martin Hafermann ◽  
Christian Udhardt ◽  
Felix Otto ◽  
Roman Forker ◽  
...  

2017 ◽  
Vol 16 ◽  
pp. 1273-1276 ◽  
Author(s):  
Xiang Gao ◽  
Timothy James Jackson ◽  
Peter Gardner

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