Paula A. A. P. Marques

Graphene oxide modified with PMMA via ATRP as a reinforcement filler

Graphene is a two-dimensional new allotrope of carbon, which is stimulating great curiosity due to its superior mechanical, electrical, thermal and optical properties. Particularly attractive is the availability of bulk quantities of graphene (G) which can be easily processed by chemical exfoliation, yielding graphene oxide (GO). The resultant oxygenated graphene sheets covered with hydroxyl, epoxy and carboxyl groups offer tremendous opportunities for further functionalization opening plenty of opportunities for the preparation of advanced composite materials. In this work poly(methyl methacrylate) (PMMA) chains have been grafted from the GO surface via atom transfer radical polymerization (ATRP), yielding a nanocomposite which was soluble in chloroform. The surface of the PMMA grafted GO (GPMMA) was characterized by AFM, HRTEM, Raman, FTIR and contact angle. The interest of these novel nanocomposites lies in their potential to be homogenously dispersed in polymeric dense matrices and to promote good interfacial adhesion, of particular relevance in stress transfer to the fillers. PMMA composite films were prepared using different percentages of GPMMA and pristine GO. Mechanical analysis of the resulting films showed that loadings as low as 1% (w/w) of GPMMA are effective reinforcing agents, yielding tougher films than pure PMMA films and even than composite films of PMMA prepared with GO. In fact, addition of 1% (w/w) of GPMMA fillers led to a significant improvement of the elongation at break, yielding a much more ductile and therefore tougher material. Thermal analysis showed an increase of the thermal stability properties of these films providing evidence that strong interfacial interactions between PMMA and GPMMA are achieved. In addition, AFM analysis, in friction force mode, is demonstrated to be an effective tool to analyse the surface filler distribution on polymer matrices.

Antibacterial activity of nanocomposites of silver and bacterial or vegetable cellulosic fibers.

Cellulose/Ag nanocomposites were prepared using two distinct methodologies and two cellulose substrates: vegetable and bacterial cellulose. These nanocomposites were characterized in terms of their morphology and chemical composition. Detailed studies on the antibacterial activity of these materials were carried out for Bacillus subtilis, Staphylococcus aureus and Klebsiella pneumoniae. Silver nanoparticles present in the cellulosic fibers in concentrations as low as 5.0x10(-4)wt.% make these nanocomposites effective antibacterial materials. We anticipate that the versatile use of these cellulose-based nanocomposites can bring a promising strategy to produce a wide range of interesting materials where antibacterial properties are crucial.

Superhydrophobic cellulose nanocomposites

Superhydrophobic cellulose nanocomposites were prepared using a multi-step nanoengineering process. The combination of different techniques made it possible to construct novel features at the ensuing surface, characterized by both an increase in its roughness induced by amorphous silica particles and a reduction in its energy insured by perfluoro moieties, giving rise to water contact angles approaching 150 degrees . The modification calls upon an aqueous LbL system followed by siloxane hydrolysis, both conducted at room temperature in air. Each modification was followed by scanning electron microscopy (SEM) and atomic force microscope (AFM). These original cellulose-silica-silane composite materials open the way to further valorisations of a ubiquitous renewable resource in applications such as water repellence and self-cleaning.

Nano‐Graphene Oxide: A Potential Multifunctional Platform for Cancer Therapy

Nano-GO is a graphene derivative with a 2D atomic layer of sp² bonded carbon atoms in hexagonal conformation together with sp³ domains with carbon atoms linked to oxygen functional groups. The supremacy of nano-GO resides essentially in its own intrinsic chemical and physical structure, which confers an extraordinary chemical versatility, high aspect ratio and unusual physical properties. The chemical versatility of nano-GO arises from the oxygen functional groups on the carbon structure that make possible its relatively easy functionalization, under mild conditions, with organic molecules or biological structures in covalent or non-covalent linkage. The synergistic effects resulting from the assembly of well-defined structures at nano-GO surface, in addition to its intrinsic optical, mechanical and electronic properties, allow the development of new multifunctional hybrid materials with a high potential in multimodal cancer therapy. Herein, a comprehensive review of the fundamental properties of nano-GO requirements for cancer therapy and the first developments of nano-GO as a platform for this purpose is presented.

WET SYNTHESIS AND CHARACTERIZATION OF MODIFIED HYDROXYAPATITE POWDERS

Hydroxyapatite powders with reproducibly different Ca/P ratios and powders with varying amounts of co-precipitated magnesium, sodium and potassium were synthesized by a wet method. Solids composition, particle size and morphology, crystalline structure, sintering behaviour and microstructure were investigated in order to understand the effect of composition in the properties of the powders. Under the present conditions of synthesis, it was concluded that magnesium, sodium and potassium will enter the hydroxyapatite lattice in vestigial amounts. Magnesium gives rise to a co-precipitated amorphous phase which crystallizes as β-whitlockite on calcining. A relationship was found between the Ca/P ratio in hydroxyapatite and its sinterability. The sintering process of pure and alkali-containing hydroxyapatites is completed at 1300 °C and leads to dense ceramics in the case of pure and sodium-containing hydroxyapatites but not in potassium-containing material.

Endocytic Mechanisms of Graphene Oxide Nanosheets in Osteoblasts, Hepatocytes and Macrophages

Nano-graphene oxide (GO) has attracted great interest in nanomedicine due to its own intrinsic properties and its possible biomedical applications such as drug delivery, tissue engineering and hyperthermia cancer therapy. However, the toxicity of GO nanosheets is not yet well-known and it is necessary to understand its entry mechanisms into mammalian cells in order to avoid cell damage and human toxicity. In the present study, the cellular uptake of pegylated GO nanosheets of ca. 100 nm labeled with fluorescein isothiocyanate (FITC-PEG-GOs) has been evaluated in the presence of eight inhibitors (colchicine, wortmannin, amiloride, cytochalasin B, cytochalasin D, genistein, phenylarsine oxide and chlorpromazine) that specifically affect different endocytosis mechanisms. Three cell types were chosen for this study: human Saos-2 osteoblasts, human HepG2 hepatocytes and murine RAW-264.7 macrophages. The results show that different mechanisms take part in FITC-PEG-GOs uptake, depending on the characteristics of each cell type. However, macropinocytosis seems to be a general internalization process in the three cell lines analyzed. Besides macropinocytosis, FITC-PEG-GOs can enter through pathways dependent on microtubules in Saos-2 osteoblasts, and through clathrin-dependent mechanisms in HepG2 hepatocytes and RAW-264.7 macrophages. HepG2 cells can also phagocytize FITC-PEG-GOs. These findings help to understand the interactions at the interface of GO nanosheets and mammalian cells and must be considered in further studies focused on their use for biomedical applications.

The fluorapatite–anorthite system in biomedicine

Glasses and glass ceramics of fluorapatite-anorthite (eutectic composition) were produced and characterized in order to evaluate their potential application in biomedicine. Bio-reactivity was determined by in vitro tests by immersion of powders in simulated plasma liquids as well as by in vivo experiments by implantation in rabbits. According to the results, the investigated materials are bio-acceptable since no toxic or other harmful evidence was detected. Glass-ceramics showed remarkable inertness, whereas glasses spontaneously dissolved in SBF and after 1 week moderate formation of apatite was observed, that however ceased within a month.

Breakdown into nanoscale of graphene oxide: Confined hot spot atomic reduction and fragmentation

Nano-graphene oxide (nano-GO) is a new class of carbon based materials being proposed for biomedical applications due to its small size, intrinsic optical properties, large specific surface area, and easy to functionalize. To fully exploit nano-GO properties, a reproducible method for its production is of utmost importance. Herein we report, the study of the sequential fracture of GO sheets onto nano-GO with controllable lateral width, by a simple, and reproducible method based on a mechanism that we describe as a confined hot spot atomic fragmentation/reduction of GO promoted by ultrasonication. The chemical and structural changes on GO structure during the breakage were monitored by XPS, FTIR, Raman and HRTEM. We found that GO sheets starts breaking from the defects region and in a second phase through the disruption of carbon bonds while still maintaining crystalline carbon domains. The breaking of GO is accompanied by its own reduction, essentially by the elimination of carboxylic and carbonyl functional groups. Photoluminescence and photothermal studies using this nano-GO are also presented highlighting the potential of this nanomaterial as a unique imaging/therapy platform.

Inorganic plasma with physiological CO2/HCO3 buffer

The substitution of tris/HCl buffer by CO(2)/HCO(3)(-) buffer in inorganic plasma was studied. An appropriate gas mixture of CO(2)/N(2) was continuously bubbled in Kokubos SBF solution prepared without addition of Tris/HCl. This method enables buffering the solution within the 7.3-7.4 pH interval and, at the same time, reaching a HCO(3)(-) concentration between 24 and 27 mmol dm(-3), which are the normal concentrations reported for blood plasma. Mineralisation studies on calcium phosphate ceramics using this solution showed that, in the presence of such hydrogencarbonate concentrations, the formation of a mineralisation layer on the ceramic occurs via a carbonated octacalcium phosphate, that evolves to carbonated hydroxyapatite. The results suggest that mineralisation studies in this new carbonate-containing simulated inorganic plasma mimic biomineralisation more closely than traditional SBF.

Mineralisation of two phosphate ceramics in HBSS: role of albumin

The role of albumin in the mineralisation process of commercial hydroxyapatite (HAp) and synthesised biphasic (HAp-tricalcium phosphate) ceramics in a bufferless simulated inorganic plasma (HBSS) was investigated by conventional in vitro tests and static and dynamic wettability measurements. Albumin was either pre-adsorbed or solubilised in HBSS. It was found that calcium complexation by albumin plays a key role in early mineralisation kinetics, so that mineralisation is favoured when albumin is pre-adsorbed and hindered when it is dissolved in HBSS. In the biphasic ceramic this picture is complicated by the fact that albumin, in solution, seems to promote the dissolution of tricalcium phosphate, and simultaneously compete for calcium with the ceramic. It also appears that albumin has a stabilising effect of octacalcium phosphate present in deposits on commercial HAp. The same effect may be present in the case of the biphasic ceramic, at earlier mineralisation times, when octacalcium phosphate appears as a precursor of HAp. Octacalcium phosphate formation on commercial apatite is accompanied by carbonate substitution in phosphate positions.