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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

The ability to bypass most cellular barriers to gain access to intracellular compartments has great potential in cell biology. The possibilities range from efficient delivery of macromolecules such as plasmids to small proteins and oligonucleotides that are sensitive to degradation. In biomedicine, easy access means enhanced cellular imaging and delivery of many therapeutics currently hampered by poor stability and cellular uptake. Carbon Nanotubes (CNTs) are attractive in these applications due to their efficient cellular uptake. While mode of entry of CNTs into cells is debatable, possibly their natural shape allows for their selective penetration across biological barriers in a non-destructive way, making them versatile as membrane permeating particles. The present study explores the diverse functionalities of CNTs including: 1) Efficient delivery of DNA into HeLa cells using vertically aligned MWNT arrays, 2) The use of Single Walled Carbon Nanotubes (SWNTs) as nano detoxifiers and 3) the design of SWNTs for efficient cellular uptake. Generally, vertically aligned nanoneedles have been used to influence the behavior and differentiation of various cell types. In the first work described in chapter 2, periodic high-density array MWNT nanoneedles is shown to support cell growth and penetrate into HeLa cells, making it ideal for use in cellular imaging and the efficient delivery of plasmid DNA into cells. Most importantly, we show that transfection with the MWNT substrate exhibited more uniformity in comparison to the commercially available lipofection procedure. Lipofection involves the formation of a complex of DNA and cationic lipids that interact with the cell via electrostatic interactions, leading to internalization, DNA escape into the cytosol, and the eventual transport into the nucleus. Functionalized CNTS have demonstrated great biocompatibility and potential for drug delivery in vitro. In the work described in chapter 3, we synthesized acid-oxidized and non-covalently PEGlyated SWNTs, which were reported previously for drug delivery purposes, and explored their potential for detoxification in the bloodstream. We investigated the binding of SWNTs to a pore-forming toxin pyolysin. The SWNTs were found to prevent toxin-induced pore formation in the cell membrane of human red blood cells. Quantitative hemolysis assay and scanning electron microscopy were used to evaluate the inhibition of hemolytic activity of pyolysin. Unlike HeLa cells, human red blood cells did not internalize oxidized SWNTs according to Raman spectroscopy data. Molecular modeling and circular dichroism measurements were used to predict the 3D structure of pyolysin (domain 4) and its interaction with SWNTs. The Tryptophan-rich hydrophobic motif in the membrane-binding domain of pyolysin, a common construct in a large family of cholesterol-dependent cytolysins (CDCs), showed high affinity for SWNTs. In the final two chapters, chapters 4 and 5, we focused on shorter CNTs (<70 nm) that have less length variations. This enabled the determination of several length related characteristics such as cellular uptake and distribution of SWNTs within between cells. Here, cellular uptake of two water-soluble SWNTs, Short SWNTs (S_SWNTs) and Ultra-Short SWNTs (US_SWNTs), was evaluated against various mammalian cells. Cellular entry of S_SWNTs (chapter 4), similar in dimensions to those reported in the literature, is shown to be affected by their hydrophilic corona and exhibit time-dependent nuclear accumulation. In contrast, US_SWNTs show no dependence of cellular entry on their hydrophilic exterior (chapter 5). Furthermore, intracellular localization and excretion of the US_SWNTs is observed to be cell type-dependent. Results presented in this work show the potential of CNTs as nano detoxifiers. We also use CNTs as vertically aligned nanoneedles and as colloids to efficiently traverse the plasma membrane. While CNTs as nanoneedles show the potential as an efficient means of transfecting mammalian cells, the use of S_SWNTs and US_SWNTs highlight some key observations including the physical and chemical properties (size, surface functionality) and cell type influence on cellular uptake and intracellular trafficking. These findings contribute to the interpretation of SWNT-cell interactions by providing a correlation between CNT length and cellular uptake and also cell type on trafficking of internalized SWNTs. With the realization of the enhanced permeability and retention effects, tumor vascular leakiness resulting from increased angiogenesis and vasoactive factors enhancing permeability at the diseased site, nanoparticles that have long circulation time have higher chance of accumulating at the diseased sites.

京都大学 / 新制・課程博士 / 博士(人間・環境学) / 甲第23533号 / 人博第1012号 / 新制||人||239(附属図書館) / 2021||人博||1012(吉田南総合図書館) / 京都大学大学院人間・環境学研究科相関環境学専攻 / (主査)教授 小松 直樹, 教授 津江 広人, 准教授 土屋 徹 / 学位規則第4条第1項該当 / Doctor of Human and Environmental Studies / Kyoto University / DFAM

Narrowly dispersed amino-functionalised polystyrene microspheres, with a range of diameters, were successfully synthesised via emulsion and dispersion polymerisation. Fluorescent labelling allowed cellular translocation to be assessed in a variety of cell lines and was found to be very high, but controllable, whilst exhibiting no detrimental effect on cellular viability. In order to fully determine the mode of microsphere uptake, “beadfected” melanoma (B16F10) cells were studied using both chemical and microscopic methods. Uptake was found to be wholly unreliant upon energetic processes, with microspheres located cytoplasmically and not encapsulated within endosomes, an important characteristic for delivery devices. In order to demonstrate the effective delivery of exogenous cargo mediated by microspheres, short interfering (si)-RNAs were conjugated to beads and investigated for the gene silencing of enhanced green fluorescent protein (EGFP) in cervical cancer (HeLa) and embryonic (E14) stem cells. EGFP knockdown was found to be highly efficient after 48 – 72 hours. Dual-functionalised microspheres displaying a fluorophore (Cy5) and siRNA allowed only those cells beadfected with the delivery vehicle (and thus containing siRNA) to be assessed for EGFP expression, yielding an accurate assessment of microsphere-mediated gene silencing. In addition, by manipulation of the microsphere preparation conditions, micro-doughnuts and paramagnetic microspheres were produced and their cellular uptake assessed. Paramagnetic microspheres were found to enter cells efficiently and were subsequently used to bias the movement of beadfected cells in response to an externally applied magnet, while micro-doughnuts were found to exhibit cell selective properties and were noted to traffic specifically to the liver in vivo.

Although nano-sized metal colloids are used in industrial and medicinal applications, little is known about the potential liver toxicity of these materials after occupational or intentional exposures. To begin to resolve some outstanding hepatotoxicity concerns, the inflammatory response of hepatocytes after exposure to metal colloids was assessed. Four ~30-nm-sized metal colloids, including silver (nano-Ag), copper (nano-Cu) and nickel (nano-Ni) were examined in an effort to understand the induced cytokine expression in a murine liver cell line (AML12). Here we also utilized another system, co-cultures of hepatocytes, Kupffer’s cells, and lymphocytes isolated from C57BL6 mice. Cells were exposed to the materials over dose-response (0.1mg/L to 1000mg/L) and time-dependent (4 h, 48 h, and 1-week) studies. Cytotoxicity was measured via metabolism of resazurin and validated via MTT assay and cell counts. Inflammatory response was determined by cytokine profiles (TNF-a and IL-6), as well as by mRNA and protein expression of heat shock protein (Hsp70). Results from cells exposed to nano-Ag to doses of up to 100mg/L exhibited no significant changes in cytotoxicity, IL-6, or TNF-a production, or Hsp70 expression. Both nano-Cu and nano-Ni exposed cells exhibited decreased metabolism, increased Hsp70 induction, and increased inflammatory responses (IL-6 and TNF-a). Dynamic light scattering and electron microscopy were used to characterize particle size and surface charge. All three metal colloidal systems demonstrated different particle size distributions, agglomerated sizes, and surface zeta potentials. Furthermore, each metal colloid system elicited different inflammatory biomarker responses and stress protein expression.

An outstanding challenge in modern medicine is the safe and efficient delivery of drugs. One approach to improve drug delivery yield and increase specificity towards diseased cells, is to employ a drug carrier to facilitate transport. Promising steps towards developing such a carrier have been taken by the nascent field of nanomedicine: nanometer-sized particles designed to evade premature excretion, non-specific absorption, and the body’s immune response, can reduce undesired drug loss, while also increasing specific drug uptake into diseased cells through targeting surface modifications. However, progress is limited by incomplete knowledge of the ‘ideal’ nanoparticle design as well as a lack of appropriate high resolution construction methods for its implementation. DNA origami, a modular, nanometer-precise assembly method that would enable the rapid testing of particle properties as well as massively parallel fabrication, could provide an avenue to address these needs. In this thesis, I employed the DNA origami method to investigate how nanoscale shape and ligand functionalization affect nanoparticle uptake into cultured endothelial cells. In the first part, I evaluated the uptake yield of a series of eight shapes that ranged from 7.5 nm to 400 nm in their individual dimensions. The best performing shape of that study, a 15 × 100 nm DNA origami nanocylinder, was internalized 18-fold better than a dsDNA control of the same molecular weight. In a follow up study, I decorated this nanocylinder with integrin-targeting cyclic RGD peptides. This surface functionalization increased cellular uptake another 13-fold. In addition, uptake yield and the ratio of internalized versus surface-bound particles depended on the number of ligands present on the nanoparticle surface. This work represents a significant first step towards attaining the ability to design and implement an 'ideal' nanoparticle drug carrier. In the future, the DNA origami method can be used as a platform technology to further expand our understanding of transport properties of drug carriers and achieve safer and more efficient drug delivery.

>Magister Scientiae - MSc / Silver nanoparticles (AgNPs) apart from being chemically significant, have shown a lot of health benefits, the most studied being their anti-bacterial and anti-inflammatory properties. These biological properties can be further enhanced by adding compounds with known medical properties giving rise to even more desired potent materials. Anti-bacterial and cytotoxicity studies show that these AgNPs can kill bacteria, prevent infections and regenerate skin cells. On the other hand, previous studies have reported dimethyl sulfoxide (DMSO) with attractive wound healing abilities specifically cell growth promotion. It was then envisaged that the combination of DMSO and AgNPs could lead to a potent wound healing agent. It is a well-known fact that non-healing wounds pose a socioeconomic threat to a large population worldwide. / 2023

Antioxidant liposomes provide a unique means of delivering both water and/or lipid soluble antioxidants to tissues thereby affecting disease states or signal transduction pathways modulated by oxidative stress. Considerable evidence suggests that liposome-encapsulated antioxidants can be superior to the corresponding free antioxidants in this regard. This chapter will provide practical details on the preparation, characterization, and use of antioxidant liposomes. Methods will be described for the small-scale preparation (1 ml) and large-scale (100 ml/hour) preparation of antioxidant liposomes as well as the techniques for characterizing their size distribution and their physical and chemical stability. The use of antioxidant liposomes in an in vitro situation will also be detailed.

The growing epidemic of antimicrobial resistance has caused significant morbidity rates worldwide as well as increasing probabilities of cancer recurrence. Efforts to address this epidemic have turned to immunomodulators, a class of molecules which modify the immune system in order to fight off infection. Muramyl dipeptide (MDP) is an immunomodulator of interest due to its specificity for NOD2, a primary receptor involved in immunoregulation. However, use of MDP in vivo causes an overly strong immunostimulatory effect; furthermore, MDP is rapidly cleared from the body due to high solubility and low molecular weight. In order to improve the clinical outlook of MDP, multiple analogues and delivery methods have been explored, with mixed success. MDP analogues have found the most success as adjuvants, although strict FDA approval guidelines limit this approach. Delivery methods for MDP are costly and also induce cytotoxicity, thereby emphasizing the clinical challenges of MDP. Introduced in 1996, Spherical Nucleic Acids (SNAs) are radially oriented oligonucleotides on a nanoparticle surface. SNAs have been shown to readily enter cells with little to no cytotoxicity and in fact, they have found clinical success in a variety of gene delivery and vaccine applications, making them a versatile platform for drug delivery. Herein, we demonstrate that SNAs can be applied as cellular delivery vehicles for MDP. To achieve this, we synthesized dual-layer SNAs whereby two unique oligonucleotides were functionalized onto a gold nanoparticle core. We show that by modulating the surface charge of the SNAs, faster cellular uptake can be achieved, which presents promise for increasing drug delivery and reaching cell compartments of interest. Additionally, we show early evidence that conjugation of MDP to the SNA corona retains MDP activity. Taken together, this work proposes effective SNA designs to deliver muramyl-based immunostimulants, which show promise in the expansion of SNA utility into immunomodulation. / Thesis / Master of Science (MSc) / The growing epidemic of antimicrobial resistance has been linked to deaths, weakened immune systems, and even cancer recurrence. To address this, immunomodulators have become an area of interest. Immunomodulators are capable of modifying the immune system to restore its normal function and fight off infection. Muramyl dipeptide (MDP) is a well-known immunomodulator, however, free MDP is too potent for clinical use. Attempts to modify or deliver MDP have had mixed success. Spherical Nucleic Acids (SNAs) are a 3D orientation of short DNA strands, SNAs are able to readily enter cells with little harmful effects on the cell. Herein, we demonstrate the development of SNAs for MDP delivery. We incorporate two unique DNA strands onto the SNA and leverage charge to enhance cellular uptake. Furthermore, we show early efforts in using the modified SNA as a delivery vehicle for MDP.