Fluorescent silicon nanoparticle-based gene carriers featuring strong photostability and feeble cytotoxicity

Safe fluorescent gene-transfection vectors are in great demand for basic biological applications and for gene-therapy research. Here, we introduce a new type of luminescent silicon nanoparticle (SiNP)-based gene carrier suitable for determining the intracellular fate of the gene vehicle in a long-term and real-time manner. The presented SiNP-based nanocarriers simultaneously feature strong and stable fluorescence, high DNA-loading capacity and gene-transfection efficiency, as well as favorable biocompatibility. Taking advantage of these unique benefits, we were able to readily observe the behavior of the gene carriers in live cells (e.g. cellular uptake, intracellular trafficking, and endosomal escape) in a long-term and real-time manner. The results demonstrate the potential usability of these fluorescent SiNP-based gene vectors as powerful tools in the field of gene therapy, and provide invaluable information for understanding the intracellular behavior of gene carriers.

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Structural Effects on the Adhesive Properties of Butadiene/Styrene Radial Teleblock Copolymers

The effects of butadiene/styrene ratio, monomer distribution, and molecular weight distribution and branching on the pressure sensitive adhesive properties of butadiene/ styrene radial teleblock copolymers are reported. Styrene content of polymers with varying structures shows a close relation with tack response, and styrene content and structure affect solution viscosity and shear adhesion. When part of the styrene is incorporated into the polybutadiene segment to yield a block progressively enriched in styrene (tapered block), solution viscosity and shear adhesion are reduced. When the butadiene segment is replaced by a block of randomly copolymerized butadiene and styrene, the polymers provide lower solution viscosities and shear adhesion but unchanged tack.

The molecular weight distribution of the radial teleblock polymers can vary from broad, highly branched compositions to narrow molecular weight distributions of almost Iinear polymers. The latter have relatively high solution viscosity and low shear adhesion, whereas the former polymers produce moderate solution viscosity but high shear adhesion. Tack is generally unaffected.     

Swelling behavior and biocompatibility of Carbopol‐containing superporous hydrogel composites

Carbopol‐containing superporous hydrogel composites (SPHCc) with fast swelling and high swelling ratio were prepared using free radical copolymerization. Swelling behavior of the SPHCc was studied in various salt and pH solutions and their biocompatibility was evaluated using tissue damage and cytotoxicity studies. The swelling ratio of the SPHCc decreased with the increase of Carbopol/monomer ratio and was sensitive to pH and ionic strength of the swelling medium. The release of insulin from the SPHCc was rapid in 0.01M phosphate buffered saline (PBS, pH 7.4). In the jejunum mucosal membrane toxicity studies in rat, no significant morphological damage was observed after application of SPHCc. Besides, no damage of the Caco‐2 monolayers was detected after incubation with SPHCc in the trypan blue and propidium iodide tests. On the basis of these results, it was concluded that the SPHCc might be a safe and effective carrier for peroral delivery of peptide and protein drugs. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Cell Culture on MEMS Platforms: A Review

Microfabricated systems provide an excellent platform for the culture of cells, and are an extremely useful tool for the investigation of cellular responses to various stimuli. Advantages offered over traditional methods include cost-effectiveness, controllability, low volume, high resolution, and sensitivity. Both biocompatible and bio-incompatible materials have been developed for use in these applications. Biocompatible materials such as PMMA or PLGA can be used directly for cell culture. However, for bio-incompatible materials such as silicon or PDMS, additional steps need to be taken to render these materials more suitable for cell adhesion and maintenance. This review describes multiple surface modification strategies to improve the biocompatibility of MEMS materials. Basic concepts of cell-biomaterial interactions, such as protein adsorption and cell adhesion are covered. Finally, the applications of these MEMS materials in Tissue Engineering are presented.     

Hydrogels as smart biomaterials

Hydrogels were the first biomaterials rationally designed for human use. Beginning with the pioneering work of Wichterle and Lím on three‐dimensional polymers that swell in water, we review the design, synthesis, properties, and applications of hydrogels. The field of hydrogels has moved forward at a dramatic pace. The development of suitable synthetic methods encompassing traditional chemistry to molecular biology has been used in the design of hydrogels mimicking basic processes of living systems. Stimuli‐sensitive hydrogels, hydrogels with controlled degradability, genetically engineered poly(amino acid) polymers reversibly self‐assembling in precisely defined three‐dimensional structures, and hybrid polymers composed of two distinct classes of molecules are just some examples of these exciting novel biomaterials. The biocompatibility of hydrogels and their applications from implants to nanomaterials are also reviewed. Copyright © 2007 Society of Chemical Industry     

Phospholipid polymer hydrogel formed by the photodimerization of cinnamoyl groups in the polymer side chain

We synthesized new polymers with both photocrosslinkability and biocompatibility by a random copolymerization of 4‐(4‐methoxycinnamoyl)phenyl methacrylate and 2‐methacryloyloxyethyl phosphorylcholine. These polymers were used as prepolymers to make a hydrogel by photoirradiation. Gelation began with 5 s of photoirradiation and reached an equilibrium state after 360 s of photoirradiation. The absorption maximum at 347 nm, attributed to the cinnamoyl group, disappeared with the photoirradiation time. That is, dimerization between cinnamoyl groups in the polymer proceeded and formed a hydrogel. The equilibrium water concentration of the hydrogels was more than 90%. Moreover, we succeeded in making a microshape hydrogel on glass by photoirradiation through a photomask. The window shape of the photomask was transferred to the hydrogel that was formed. We concluded that these photocrosslinkable polymers could be useful in preparing microfluidic devices for separating or immobilizing biomolecules and cells. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 104: 44–50, 2007     

Plasma surface modification and characterization of collagen‐based artificial cornea for enhanced epithelialization

Argon plasma treatment enhanced the attachment of epithelial cells to a collagen‐based artificial cornea crosslinked using glutaraldehyde (GA) and glutaraldehyde‐polyethylene oxide dialdehyde (GA‐PEODA) systems. The epithelialization of untreated and treated surfaces was evaluated by the seeding and growth of human corneal epithelial cells. Characterization of polymer surface properties such as surface hydrophilicity and roughness was also made by contact angle measurement and atomic force microscopy, respectively. Contact angle analysis revealed that the surface hydrophilicity significantly increased after the treatment. In addition, AFM characterization showed an increase in surface roughness through argon plasma treatment. Based on the biological and surface analysis, argon plasma treatment displays promising potential for biocompatibility enhancement of collagen‐based artificial corneas. It was also found that the cell attachment to artificial cornea surfaces was influenced by the combined effects of surface chemistry (i.e., surface energy), polymer surface morphology (i.e., surface roughness), and polar interactions between functional groups at the polymer surface and cell membrane proteins. © 2007 Wiley Periodicals, Inc. J Appl Polym Sci 2007     

Cell Adhesion and Interactions with Biomaterials

The related phenomena of biocompatibility and biodegradation are of major concern in the selection of synthetic polymers for use as implantable biomedical devices. These properties are largely determined by the consequences of the cellular interactions that occur at the polymer/tissue interface during inflammation. Using an in vivo cage implant system, in conjunction with surface analysis techniques, we have investigated the variation in the cellular events that occurred on a polyetherure-thaneurea and a cytotoxic polyvinyl chloride). Quantitative and qualitative information that describe the cellular response to polymer implantation will be presented. From the results, a chronological sequence has been established which suggests that the important events follow cellular adhesion, and include cell spreading over a polymer surface accompanied by lysosomal degranulation of the adherent cells.     

The Role of Bloom Index of Gelatin on the Interaction with Retinal Pigment Epithelial Cells

Biocompatible materials are of considerable interest in the development of cell/drug delivery carriers for therapeutic applications. This paper investigates the effects of the Bloom index of gelatin on its interaction with retinal pigment epithelial (RPE) cells. Following two days of culture of ARPE-19 cells with gelatin samples G75-100, G175, and G300, the in vitro biocompatibility was determined by cell proliferation and viability assays, and glutamate uptake measurements, as well as cytokine expression analyses. The mitochondrial dehydrogenase activity in the G300 groups was significantly lower than that of G75-100 and G175 groups. The Live/Dead assays also showed that the gelatin samples G300 induced mild cytotoxicity. In comparison with the treatment of gelatins with low Bloom index, the exposure to high Bloom strength gelatins markedly reduced the glutamate uptake capacity of ARPE-19 cells. One possible explanation for these observations is that the presence of gelatin samples G300 with high viscosity in the medium may affect the nutrient availability to cultured cells. The analyses of pro-inflammatory cytokine IL-6 expression at both mRNA and protein levels showed that the gelatins with low Bloom index caused less cellular inflammatory reaction and had more acceptable biocompatibility than their high Bloom strength counterparts. These findings suggest that the Bloom index gives influence on cellular responses to gelatin materials.