Stuttgart, Univ., Diss., 2003.

Stuttgart, Univ., Diss., 2002.

Techn. Universiẗat, Diss., 1998--Berlin.

A series of well-defined stimuli responsive water soluble [60]fullerene (C₆₀) containing polymers such as polyelectrolytes (polyacids and polybases), polyampholyte and polyzwitterionic polymers were synthesized using atom transfer radical polymerization. The aqueous solution properties of these polymers with respective external stimuli such as pH, temperature and salt were studied using potentiometric and conductivity titration, light transmittance, laser light scattering and transmission electron microscopic techniques. The influence of polymer concentration, temperature, pH and electrolyte on the hydrodynamic radius (Rh), radius of gyration (Rg) and aggregation number (Nagg) of the particles were investigated in detail to elucidate the morphology of the particles. The morphology of the aggregates was further confirmed by the TEM micrographs. The cytotoxicity of the pH responsive C₆₀ containing well-defined polymers (PAA-b-C₆₀, C₆₀-b-PAA-b-C₆₀ and PEO-b-PAA-b-C₆₀) was studied to confirm the suitability of these particles as potential drug delivery vehicles. The binding interaction between the anti-cancer drug (doxorubicin) and C₆₀ containing pH responsive polymers was studied using isothermal titration calorimetry, and the implication of the results will be discussed. / Singapore-MIT Alliance (SMA)

Fullerenes and metallofullerenes have been discovered to have a lot of applications in the biomedical area, for instance, they have been shown to have antioxidant, anti-virus, anti-cancer, immunological properties, etc. However, the hydrophobicity nature of fullerenes and metallofullerenes raises the need for functionalized hydrophilic fullerenes and metallofullerenes. Also, the advancement of the purification techniques of fullerenes and metallofullerenes makes the isolation of new fullerenes and metallofullerenes possible. Therefore, discovering the biomedical applications of these newly found fullerenes and metallofullerenes is also of vital importance. In Chapter 1, we provided a comprehensive background on the history of fullerenes and metallofullerenes, synthesis and purification methods of fullerenes and metallofullerenes, and some of their biological applications, including antioxidant applications and fluorescence applications. Some important fullerene and metallofullerenes and milestones in this area were also discussed. In Chapter 2, we demonstrated the antioxidant and anti-inflammation ability of a conjugate, FIFIFK(Cy5)PEG24K(NH2)CONH2-C60, that consisted of a peptide that binds specifically to a formyl peptide receptor-1 (FPR-1), which expresses on activated macrophages, and a carboxyl-group-functionalized C60, which is the first discovered and most used fullerene is history. We showed that the fullerene-peptide conjugate had great ability as a radical scavenger and to reduce the volume of inflammatory tissue. In Chapter 3, we demonstrated the antioxidant and anti-inflammation ability of several metallofullerene derivatives, including amino-Gd3N@C80, amino-Sc3N@C80, carboxy-Gd3N@C80, and carboxyl-Sc3N@C80. Amino-group-functionalized metallofullerenes were found to have higher radical scavenging ability and anti-inflammation ability. In Chapter 4, we developed fluorescent metallofullerene derivatives, including Tb3N@C80(NH2)9(OH)4NO2 and Tb3N@C80(CH2CH2COOH)21(OH)18. The fluorescence properties of the derivatives of fullerenes or metallofullerenes were normally realized by the addition of fluorescent moieties on the carbon cage of fullerenes or metallofullerenes. However, the fluorescence of our newly developed metallofullerene derivative was realized by the tri-terbium nitride cluster inside the carbon cage. This saved the multi-step synthesis of the fluorescence probe and maintained the simplicity of the structure of the metallofullerene derivative. These derivatives of terbium-containing metallofullerene also showed radical scavenging ability towards hydroxyl radicals. In Chapter 5, we developed another fluorescent Tb3N@C80 derivative, Tb3N@C80[DiPEG2000]. The advantage of this fluorescent metallofullerene derivative was that it was easier to purify compared to small-functional-groups-functionalized Tb3N@C80 derivatives. This newly developed fluorescent Tb3N@C80 derivative also showed great fluorescent ability and radical scavenging ability. In Chapter 6, we provided a summary of the studies on the antioxidant and fluorescent properties of fullerenes and metallofullerenes' derivatives that were discussed in this dissertation. / Doctor of Philosophy / Fullerenes and metallofullerenes' have large carbonaceous outer structures that give them possibilities for a lot of chemical reactions. The conjugated carbonaceous outer structures also endow them with exceptional antioxidant ability by reacting with the oxidant species. Therefore, fullerenes and metallofullerenes can be considered as great antioxidants, which are substances that can prevent or slow damage to cells caused by oxidants, in most cases free radicals or other unstable oxidant molecules that the body produces as reactions to environmental and other pressures. Fullerenes and metallofullerenes are sometimes called "free-radical scavengers". However, fullerenes and metallofullerenes are not soluble in biological systems, therefore, it's necessary to attach functional groups onto the outer cage-like structures of fullerenes and metallofullerenes to make them water-soluble, while maintaining their great antioxidant properties. Fullerenes and metallofullerenes are not limited to antioxidant applications, and with the attachment of specialized moieties, for instance, short peptides, they can be made of additional applications. Different metals in these metallofullerenes also provide them with specialized applications. Herein, we have developed a series of water-soluble fullerenes and metallofullerenes and compared their antioxidant properties. We have also developed a water-soluble C60-peptide conjugate that can specifically bind to inflammatory cells and ease the inflammatory condition. We also synthesized a series of metallofullerene derivatives that had dual modalities fluorescent properties and antioxidant properties.

No description available.

Interactions of engineered nanomaterials (ENMs) with environmental interfaces have become a critical aspect of environmental health and safety evaluations. Carbon fullerene (C₆₀) has emerged at the forefront of nanoscale research and applications due to its unique properties. Although there are concerns associated with the harmful effects of fullerene towards living organisms, the mechanisms of fullerene toxicity are still under debate. A first step toward assessing these mechanisms requires evaluation of the bio-accumulation and bio-uptake of fullerene through lipid membranes which serve as biological barriers in cells. In this dissertation, partitioning of fullerene between water and lipid membranes and cellular uptake of fullerene were investigated to assess bioavailability of this nanoparticle. Traditional methods to estimate the equilibrium partitioning of molecular level chemicals between water and lipid membranes (K[subscript lipw]) cannot be applied to measure K[subscript lipw] of nanoparticles due to the large size of nanoparticle aggregates. In this study, we developed an in vitro method to estimate K[subscript lipw] of fullerene using solid supported lipid membranes (SSLMs) with various membrane compositions. K[subscript lipw] of fullerene increased with increasing acyl chain length and K[subscript lipw] values were higher after creating phase separation in ternary lipid membranes compared to pre-phase separation. In addition, the partitioning values (K[subscript lipw]) were found to depend on the lipid head charges. These results suggest that the lipid membrane composition can be a critical factor for assessing bioaccumulation of fullerene. Evaluation of the partitioning thermodynamics of fullerene demonstrated that the partitioning mechanism of fullerene is different from that of molecular level chemicals. It is generally acknowledged that molecular level chemicals partition into the hydrophobic center of lipid membranes (i.e., absorption), however, the partitioning mechanism of fullerene is a combination of adsorption on the lipid membrane surface and absorption. Caco-2 cellular uptake of fullerene nanoparticles was investigated using an in vitro method developed in this study to distinguish between active and passive transport across cell membranes. Energy dependent endocytosis is hypothesized to be the main cellular transport mechanism based on an observed temperature dependence of cellular uptake and evidence for saturation of the active sites of transport during cellular uptake of fullerene. Metabolic inhibitors decreased the mass of fullerene taken up by the cells, which supports an active transport mechanism of fullerene through the cell membranes. To evaluate bioavilability of fullerene under environmentally relevant conditions, the effects of humic acid and fetal bovine serum (FBS) on the lipid accumulation and cellular uptake were also investigated. Humic acid and FBS changed the surface characteristics of fullerene. The presence of FBS significantly decreased lipid accumulation of fullerene presumably due to higher steric hinderance of FBS coated fullerene as well as the changes in surface energy, water solubility, and lipid solubility of charged FBS coated fullerene relative to that of bare fullerene. Both humic acid and FBS also effectively lowered the cellular uptake of fullerene. These results imply that natural organic matter and biomolecules in natural aquatic and biological environments have significant effects on the bioavilability of fullerene nanoparticles / text

Fullerenes are carbon nanospheres that can be solublized by the addition of polar chemical groups to the carbon cage, forming fullerene derivatives. One specifically derivatized fullerene compound, termed C70-Tetragylocolate (C70-TGA), has been shown to stabilize mast cell responses in vitro thus we hypothesized it may have an effect on mast cell-driven diseases such as asthma and systemic anaphylaxis. To observe the effects of C70-TGA on systemic anaphylaxis, mice were subjected to a model of passive systemic anaphylaxis. In this model, mice were injected with DNP-specific IgE 16 hours prior to challenge, then treated with C70-TGA. Immediately prior to DNP challenge, mice were subjected to a second injection of C70-TGA. Following DNP challenge, body temperature was recorded and blood was collected for quantitation of histamine levels. Treatment with C70-TGA significantly reduced body temperature drop associated with systemic anaphylaxis and serum histamine levels. To observe the effects of C70-TGA on chronic features of asthma in vivo, we utilized a heavily MC influenced model of asthma pathogenesis. Mice were sensitized by intraperitoneal (i.p.) injection of ovalbumin (OVA) in saline, challenged intranasally (i.n.) with OVA, and one of two treatment strategies was pursued. In one, C70-TGA was given i.n. throughout disease development. In the other, C70-TGA was given following an initial set of challenges to allow disease to develop prior to treatment; mice were then re-challenged with OVA to assess the effect on established disease. We found that C70-TGA treatment significantly reduced airway inflammation and eosinophilia and dramatically reduced bronchoconstriction in either model. Cytokines IL-4 and IL-5 and serum IgE levels are significantly reduced in C70-TGA treated animals. Interestingly, we also saw an increase in the anti-inflammatory eicosanoid 11, 12-epoxyeicosatreinoic acid (11,12-EET) in the BAL fluid, suggesting the involvement of this mediator in C70-TGA inhibition. Further experiments utilizing an inhibitor of 11,12-EET formation (6-(2-Propargyloxyphenyl)hexanoic acid) and a structural analog of 14,15-EET (14,15-EE-5(Z)-E) in vivo indicate that these mediators are closely associated with C70-TGA mediated inhibition as their inhibition reverses the anti-inflammatory effects of C70-TGA. Importantly, mice did not exhibit any acute toxicity following C70-TGA treatment and liver and kidney function were normal. Collectively, these results show that the fullerene C70 derivative C70-TGA is capable of dampening severe allergic responses including systemic anaphylaxis, airway inflammation, and bronchoconstriction. The mechanism of inhibition is through the upregulation of the anti-inflammatory EETs, which may dampen mast cell degranulation in vivo, thus contributing to the inhibitory effect of C70-TGA on allergic disease.

Significant improvements in power conversion efficiency (>10%) of emerging thin-film photovoltaics have been achieved in the last 5 years. High efficiencies would not be possible without the development of new selective interfacial layers. However, a complete understanding of how interfacial layers function to improve the selectivity of charge extracting contacts in thin-film photovoltaics is still being sought. The goal of this work is to contribute to the understanding of the operation of selective interfacial layers based on the study of ionically functionalized fullerenes. Just as other ionically functionalized materials have shown promise as electron-selective interfacial layers in organic photovoltaics and mixed organic-inorganic halide perovskites, Chapter II demonstrates the utility of ionically functionalized fullerenes. High performing solar cells necessitate the use of conductive interfacial layers; anomalously high conductivity in ionically functionalized materials, which have been used as interfacial layers, has been ascribed to self-doping. This work demonstrates that less than 1% of an ionically functionalized fullerene is reduced in its highly conductive pristine state and is concurrent with the presence of distinct chemical species. These studies describe how the chemical origin of the high conductivity of ionically functionalized fullerenes does not require the invocation of direct anion reduction or significant chemical transformations such as Hofmann-like elimination reactions occurring to a stoichiometric degree. This work also addresses the question of how the selectivity of a charge extracting contact is improved by the presence of an interfacial layer. The quantification of energy barrier reduction, which is often discussed in terms of work function modification or energy-level alignment, is demonstrated using metal|semiconductor junctions modified with an ionically functionalized fullerene. The barrier height of high work function electrodes was reduced significantly, by as much as 0.45 V, and was correlated to thin (2–5 nm) portions of the film rather than fullerene aggregates. The studies that comprise this work form a coherent model for understanding the key factors that have resulted in the continued use of ionically functionalized interfacial layers, their high conductivity, and energy barrier modification of the charge extracting electrodes. This dissertation contains coauthored, previously published, and unpublished work. / 10000-01-01

This research focuses on device design and process integration of high density nonvolatile memory devices. Research was carried out to improve scaling of floating gate memories by increasing charge density as well as spin-based memories by reducing critical switching current. This work demonstrates fabrication of CMOS-compatible nonvolatile hybrid memory device using fullerene molecules as a floating gate. Molecules have dimensions of several Angstroms resulting in an electron density of ~10¹³ cm⁻² or higher. In hybrid MOSCAPs, fullerenes were encapsulated between inorganic oxides, i.e. SiO₂ as a tunnel oxide and HfO₂ as a control oxide. Introduction of a high-k material as a control oxide improves capacitive coupling between control gate and floating gate as well as the program/erase efficiency. The MOS capacitors demonstrate nonvolatile memory operation at room temperature. The device data infers that program/erase mechanism in fullerene devices is Fowler-Nordheim tunneling; however, retention is determined by trap-assisted tunneling. The next part of the work focused on spin-transfer-torque (STT) based magnetic memory. Spin-based memory has the unique potential to be the universal memory because of its high density, fast switching, and nonvolatility. This work presents STT switching of perpendicular magnetic anisotropy (PMA) spin-valves with tilted magnetization using point contact measurement. The PMA materials have high coercivity resulting in good retention and tilted magnetization induces precessional switching resulting in a lower switching current density. First, micromagnetic simulations were performed for spin-valves with tilted magnetization and precessional switching was observed to reduce the switching current. Then, spin-valve structures were fabricated by e-beam evaporation. The structure consisted of Co/Pt and Co/Ni layers, where the thickness of the layers was optimized to obtain different amount of tilt in magnetization. Point contact measurements of tilted spin-valves show STT switching, where the switching field of the free layer varies with the magnitude and sign of the applied current. The observed STT effect is stronger in a 45° tilted spin-valve compared to a 12° tilted device presumably due to the tilted spin polarization. However, tilting introduces nonuniform effective field and canting of the domains which affect the STT. / text