Gelatin has been widely used to develop tissue engineering scaffolds because it has many attractive properties. Dendrimer provides a versatile, compositionally and structurally controlled architecture to construct nanomedicine. This study was aimed at developing a novel electrospun dendrimer-gelatin nanofiber scaffold to best mimic natural extracellular matrix (ECM) to promote tissue formation and serve as a reservoir for controlled drug delivery. Starburst™ polyamidoamine (PAMAM) dendrimer G3.5 was covalently bonded to the gelatin backbone and electrospun into nanofibers. Doxycycline (DC), which is an effective antibiotic that has the ability to inhibit matrix metalloproteinase, was encapsulated into the nanofiber scaffold. The electrospun DC-gelatin scaffold provides a bacterial free environment for cell growth and tissue regeneration. The resulting dendrimer-gelatin nanofiber scaffold achieved a unique structural configuration where covalently bound three-dimensional dendritic nanospheres were evenly distributed along the elongated dimension of the nanofiber, and both dendrimer and gelatin had numerous functional groups suitable for accommodating multiple functional entities and high payload of drugs. The development of this new scaffold with the capability of delivering multiple functional entities was an important step towards the use of bioactive nanofibers to facilitate tissue regeneration and controlled drug release.

We studied the potential applications of Portland cement and Portland cement-Metakaolin blends as scaffolding materials for load bearing bone tissue engineering. Cementitious pastes were prepared by mixing Portland cement and Metakaolin at different ratios (100:0, 85:15), and hydrated under a concentrated CO2 atmosphere (carbonated pastes). Pastes fabricated similarly, but hydrated under normal atmospheric conditions were used for comparison (non-carbonated pastes). Compressive tests were run to evaluate the mechanical properties of the pastes. The bioactivity of the samples was tested in a simulated body fluid (SBF) solution for 1 and 4 days. Sample morphology and chemistry were characterized via scanning electron microscopy (SEM) and energy dispersive spectroscopy (EDS), respectively. The cytocompatibility was studied using human osteosarcoma (HOS) cell cultures and the direct contact assay. Mechanical characterization did not show significant differences in the compressive strength of the blends compared to pure cement controls. The bioactivity test revealed that the pastes induced surface precipitation of calcium phosphate (CaP) when exposed to the SBF solution (as confirmed by SEM and EDS). Non-carbonated pastes induced early CaP precipitation. Cytocompatibility experiments showed that the carbonated blends allowed adequate cell growth. Non-carbonated blends presented a highly cytotoxic behavior. The introduction of Metakaolin did not affect the cytocompatibility of the samples. These results show that Portland cement and Portland cement-Metakaolin blends could present suitable characteristics for applications as scaffolding materials in load bearing bone tissue engineering.

Electrospun composite scaffolds were prepared by mixing gelatin with nanoparticles of hydroxyapatite (nanoHA) in 2,2,2-trifluoroethanol (TFE) solution. The fibrous composite scaffolds with nanoHA content from 0 to 40 wt% were compared in terms of structure and morphology via x-ray diffraction (XRD) and scanning electron microscopy (SEM). Results show that dispersion of nanoHA in the scaffolds is uniform for 0%, 10%, 20%, and 30% nanoHA content, but significant nanoHA agglomeration can be observed for scaffolds with 40% nanoHA. In order to study the effect of nanoHA content on mechanical properties at the nanoscale level, the fibrous scaffolds were pressed into dense pellets and tested by nanoindentation to determine Young's modulus. Young's modulus was found to increase linearly with nanoHA content, reaching unexpectedly high values of 10.2 ± 0.8 GPa. Results are compared with other polymer/HA composites including those made with polycaprolactone or collagen.

We have investigated coaxial electrospinning to produce core-sheath fibers for tissue engineering. We have successfully produced core-sheath structured fibers of poly(ε-caprolactone) (PCL) and gelatin using the coaxial electrospinning technique. The core-sheath scaffold exhibits better mechanical properties compared to gelatin scaffold. We have characterized the resulting core and core-sheath fiber diameters and the scaffold porosity, etc.

A simple and versatile procedure was developed for synthesizing biomorphic mesoporous Ce1-xZrxO2. Aqueous cerium nitrate and zirconium nitrate solutions, and paper were used as the starting materials. Under the structure-directed effect offered by the active hydroxyl radicals of the cellulose in the paper templates, porous and fibrous structures of paper were replicated by the self-assembly of Ce1-xZrxO2 nanocrystallites after the paper underwent chemical infiltration and calcinations. The product, composing of interwoven network of fibers with diameter ranging from 10 to 20 <mu>m, was a replica of the original paper structure only that each fiber was assembled by Ce1-xZrxO2 nanocrystallites with grain size of 3-10 nm. The templating function of cellulose and the mechanism in the formation of nanocrystallites were proposed.

We have observed the assembly of a chemically adsorbed monomolecularlayer (CAM) into microwires, connections, and an electric path according to the location within field regions of a lithographically patterned array of two platinum (Pt) electrodes. A Pt electrode/monolayer/Pt electrode junction was fabricated by the self-assembly of a rigid monomolecular, namely 3-{6-{11-(Trichlorosilyl) undecanoyl} hexyl} thiophene (TEN) with thiophen groups, in the lateral direction between the Pt gap electrodes. The technique of a conductive probe AFM (CP-AFM) has been used to investigate the forward bias conduction properties of a TEN film grown by a wet process deposition on a glass substrate. The self-assembly depends on: (1) the ideal rigidity of the chemically adsorptive monomolecular layer (CAM) and (2) the strong affinity of the thiophen end groups of the CAM for the Pt electrode. The current–voltage (I–V) characteristics of the conjugated thiophen junction exhibited stepwise features at room temperature. From the results in the atmosphere, the conductivity of a lateral conjugated polythiophen group was calculated to be 5.0E4 S/cm.

We have successfully produced biomorphic SiC ceramics from silica-infiltrated wood samples of balsa (Ochroma pyramidale) and flame tree (Delonix regia). This conversion of wood sample to a structure of SiC was performed by a sol-gel technique and a carbothermal reduction process. The biomorphic products were confirmed containing β-SiC and their structures were replica of the original structures of the raw wood samples. The biomorphic products from the denser flame tree (C-SiC) had higher specific strength than that from the biomorphic product from balsa (SiC).

Because of its significant potential in controlling key steps of apatite mineralization, recombinant amelogenin has been applied in different in vitro systems for the synthesis of uniquely ordered composite material similar to enamel. Here we summarize the results of a series of experiments, in which mineral deposition took place on the exposed surface of enamel from extracted human third molars soaked in calcium phosphate solution, in the presence of amelogenin and fluoride. Analysis of crystal size and morphology revealed that in the presence of both amelogenin (50-100 μg/mL) and fluoride (1 ppm), bundles of oriented rod- like fluoridated apatite crystals were formed creating a dense coating on the enamel substrate. Such organized bundles were not formed at low concentrations of rP172 (< 30 μg/mL). Preparation of such ordered nanocomposites provides a promising approach for development of new generation of dental restorative materials with improved esthetic and mechanical properties.

Highly porous carbon-doped anatase was produced by a simple and time-saving method. The product was prepared by using sea wool sponges and a titanium-contained organic solution. The intermediate product was pyrolyzed sponges coated with amorphous anatase. When further annealed, the final product was an entirely carbon – anatase product with the original structure of sea wool sponges. The struts in the carbon – anatase product were hollow with wall thickness less than 300 nm. Cathodoluminescence measurement showed that this C-TiO2 product was sensitive to visible light.

Magnetic particles are used for various biomedical applications because they are easy to both handle and separate from biological samples. Nano-sized bacterial magnetic particles (BacMPs) that display the human estrogen receptor ligand binding domain (ERLBD) on their surfaces were successfully produced by the magnetotactic bacterium, Magnetospirillum magneticum AMB-1. A receptor assay for endocrine-disrupting chemicals using ERLBD-displaying BacMPs was developed. A BacMP membrane-specific protein, Mms16 or Mms13, was used as an anchor protein to localize the ERLBD on the surfaces of BacMPs. ERLBD-BacMP complexes were assayed for competitive binding of alkaline phosphatase-conjugated 17β-estradiol (ALP-E2). Inhibition curve of ALP-E2 to the powerful antagonist, tamoxifen was generated by measuring decreases in luminescence intensity that resulted from the enzymatic reaction of alkaline phosphatase. The overall simplicity of this receptor-binding assay results in a method that can be easily adapted to a high-throughput format.

The sequence of formation of the organic and inorganic components of nacre in bivalves and gastropods is re-studied. We reach the conclusion that interlamellar membranes are formed well in advance of the other elements. In this way, we support and refine the compartment theory for the formation of nacre. We explain the arrangement of chitin crystallites within a single interlamellar membrane and the layering of interlamellar membranes as a process of formation of a liquid crystal.

Collagen fiber orientation plays an important role in many cell properties and actions in vivo. Collagen and other matrix proteins are aligned in many tissues during normal functioning. For example, cardiomyocytes align in the heart to produce a synchronously beating tissue. The extra-cellular matrix environment, including collagen, is aligned along the cells. This matrix helps with cell adhesion and the alignment of the fibers also contributes to the anisotropic mechanical property of the tissue. While it is easy to replicate randomly oriented collagen in vitro, it is much more difficult to create aligned collagen matrices for cell culture. In this work, a novel inkjet printer-based collagen alignment technique was established. A 1 mg/ml rat tail collagen type I solution was printed, using a modified HP DeskJet 500 printer, onto plasma cleaned and UV sterilized glass slides. The collagen was printed in an eight line pattern, designed in Microsoft Word with 87.5 μm by 23.1 mm lines. The pattern was printed three successive times on each slide to complete the alignment. Immunofluorescence imaging of primary antibodies specific to collagen type I indicated that the heat involved in the printing process was not great enough to denature the collagen. The extent of collagen alignment was quantified using atomic force microscopy and compared to random collagen films and collagen films aligned using a mechanical scraping method. Additionally, neonatal rat cardiomyocytes were cultured on the aligned matrices. These cells require extracellular matrix alignment to maintain their in vivo-like phenotype during in vitro culture. The cells grew along the lines of collagen and coordinated beating, indicating the success of the aligned matrix. This collagen alignment technique is cheap, fast, precise, and easy to use in comparison to other current techniques. It can be used to align collagen on any type of substrate, such as a gel, which makes it a useful tool in many applications. This technique may also be used to align other extra-cellular matrix proteins and could even be used to create a three dimensional construct with varying fiber orientations.

Sol-gel thin films and nanoparticles can be functionalized by imprinting strategies based on self-organization of the polymer precursors around a template compound. The resulting rugged layers are highly suitable for operating as sensor layers in harsh environments, such as engine oils. By adding e.g. dimethyl formamide or polyethylene glycol to titanate sols, the resulting layers show substantially increased sensitivity due to higher porosity and accessibility of the recognition sites. The same is true for nanoparticles, where the sensor effects are directly correlated to particle dimensions. Furthermore, also imprinted ZrO2 nanoparticles show very appreciable selectivity.

Biotinylated magnetic nanoparticles were constructed by displaying biotin acceptor peptide (BAP) on the surfaces of bacterial magnetic particles (BacMPs) synthesized by Magnetospirillum magneticum AMB-1. Both BAP and green fluorescent protein (GFP) were fused to Mms13 that was isolated from BacMP membranes. The localization of the fusion protein, BAP-Mms13-GFP, was confirmed by fluorescence analysis. BacMPs that expressed BAP-Mms13-GFP (BAP/GFP-BacMPs) were extracted from bacterial cells and incubated with biotin and Escherichia coli biotin ligase. The in vitro biotinylation of BAP/GFP-BacMPs was confirmed using alkaline phosphatase (ALP)-streptavidin detection. The conjugation system developed in this study provides a method for producing biotin- or streptavidin-labeled magnetic nanoparticles without the use of a crosslinker reagent. Various functional materials can be immobilized site-selectively onto these uniquely designed BacMPs. By combining this site-selective biotinylation technology and protein display methodology, increasingly innovative and attractive magnetic nano-materials can be constructed.

In this paper, a new and simple method for the synthesis of ZnO nanowires under very mild conditions is presented. The nanowire preparation is based on mineralization from alkaline aqueous zinc nitrate solution in the presence of fish sperm DNA as a structure-directing agent. The morphological features of the obtained structures were investigated by scanning electron microscopy (SEM) and transmission electron microscopy (TEM), while the structural characterization of ZnO was done by X-ray diffraction.

A vapor diffusion sol-gel method is reviewed for the preparation of high-quality BaTiO3 nanocrystals on the gram scale at very low temperatures. The synthesis is based on the kinetically controlled introduction of water into a solution of the bimetallic alkoxide, BaTi(O2C4H9)6, where slow hydrolysis then occurs at the vapor-solution interface followed by nucleation and nanocrystal growth at 16 °C. The resulting 6-nm, quasi-spherical nanocrystals are both monodisperse (without stabilizing agents or size selecting purification) and highly crystalline (without any post-synthesis heat treatment), and are isolated in yields near 100%. Based on new permittivity and calorimetry data, the crystal structure of the nanocrystals is most likely in the paraelectric cubic phase (space group Pm3m) at room temperature, which corroborates previous diffraction data. It was also demonstrated that the BaTiO3 nanocrystals can be doped with trivalent lanthanum cations using the same low-temperature vapor diffusion sol-gel method to yield donor-doped Ba1−xLaxTiO3, which exhibits a considerable PTCR effect.

Here we report the nucleic acid/cationic amphiphile based-materials in which we exchange the counter-ions of the polyanionic backbone of the nucleic acids with the cationic amphiphiles to form self-assembled transparent films with the thickness of several microns. Predominantly, single stranded poly(A), poly(U) and double stranded poly(AU) were employed for these studies. Small-angle X-ray scattering (SAXS) experiments suggested lamellar-like structure for all the film samples. However, the molecule length as well as the molecular structure of nucleic acids can affect the topology and mechanical properties of these films. Complementary base-paring of poly(AU) is reported here with comparison to poly(A) and poly(U) complexes.

Organisms can precipitate a wide array of minerals which they use to build calcified tissues (i.e., bone, mollusk shell, eggshell, coccolith) having highly sophisticated microstructures. The disposition of organic and mineral components building these materials is highly organized from the nano- to the millimeter scale. Their ordered assembly implies self-organization processes accorded in space and time, giving rise to highly sophisticated textured materials. The objective of our work is the study of fundamental processes in biomineralization such as self-organization processes and texture control in biomineral crystal aggregates. To study the order in the arrangement of shell making crystals we used area detectors available today in modern X-ray diffractometers. The 2D diffraction patterns, collected using such detectors, contain detailed information not only about the mineralogy but also about the microstructure characteristics of polycrystalline materials – crystal size, stress, crystallinity and crystallographic-texture. For instance, to understand microstructure development in mollusk shells, we use this type of detector to do microdiffraction analyses combined with high resolution SEM in order to follow the ordering mechanisms of crystals making these biomaterials.

Magnetic separation of target cells from mixtures, such as peripheral blood and bone marrow, has considerable practical potential in research and medical applications. Among the current cell separation techniques, magnetic cell separation using immunomagnetic particles has been routinely applied and has proven rapidness and simplicity. Magnetospirillum magneticum AMB-1 synthesizes intracellular nano-sized bacterial magnetic particles (BacMPs) that are individually enveloped by a stable lipid bilayer membrane. BacMPs, which exhibit strong ferrimagnetism, can be collected easily with commercially available permanent magnets. In this study, a novel magnetic nanoparticle displaying protein G (protein G-BacMPs) was fabricated, and one-step cell separation for direct cell separation from whole blood was performed using the protein G-BacMPs. B lymphocytes (CD20+ cells), which cover less than 0.3×10−2 % of whole blood cells, were separated with 93% purity using protein G-BacMPs binding with anti-CD20 monoclonal antibodies. The results of this study demonstrate the utility of protein G-BacMPs and the magnetic cell separation approach based on protein G-BacMPs in numerous applications.