Synthesis, characterization and in vitro biocompatibility assessment of a novel tripeptide hydrogelator, as a promising scaffold for tissue engineering applications.

We have synthesized and characterized a self-assembling tripeptide hydrogelator Ac-l-Phe-l-Phe-l-Ala-NH2. A series of experiments showed that the hydrogel material could serve as a stabile and biocompatible physical support as it improves the survival of HEK293T cells in vitro, thus being a promising biomaterial for use in tissue engineering applications.

Preparation of biodegradable xanthan-glycerol hydrogel, foam, film, aerogel and xerogel at room temperature.

Polymers, hence hydrogels, pollute waters and soils accelerating environmental degradation. Environmentally benign hydrogels were made in water from biodegradable xanthan (X) and glycerol (G) at 22.5±2.5°C. Molar ratio [G]/[X]<3.0 was used to maximize crosslinking by mono-glycerol instead by poly-glycerol. XG-hydrogels were transformed into: XG-foams, XG-films, and XG-aerogel. Anionic character of XG-materials changes with changing [G]/[X] ratio. XG-films made from XG-hydrogels absorb up to 40 times more water than XG-films made from XG-foams. The films made from XG-foams and HCl do not dissolve in water during 48h. Making XG-materials is a no-waste process which decreases pollution, eliminates waste disposal costs, and minimizes energy expenses. XG-materials are suitable for both industrial and environmental applications including slow release and concentration of cations. XG-materials, made of xanthan, microbial polysaccharide, could also be used in applications targeting populations that do not consume meat or meat based products.

Evaluation of an alginate-gelatine crosslinked hydrogel for bioplotting.

Using additive manufacturing to create hydrogel scaffolds which incorporate homogeneously distributed, immobilized cells in the context of biofabrication approaches represents an emerging and expanding field in tissue engineering. Applying hydrogels for additive manufacturing must consider the material processing properties as well as their influence on the immobilized cells. In this work alginate-dialdehyde (ADA), a partially oxidized alginate, was used as a basic material to improve the physico-chemical properties of the hydrogel for cell immobilization. At first, the processing ability of the gel using a bioplotter and the compatibility of the process with MG-63 osteoblast like cells were investigated. The metabolic and mitochondrial activities increased at the beginning of the incubation period and they balanced at a relatively high level after 14-28 days of incubation. During this incubation period the release of vascular endothelial growth factor-A also increased. After 28 days of incubation the cell morphology showed a spreading morphology and cells were seen to move out of the scaffold struts covering the whole scaffold structure. The reproducible processing capability of alginate-gelatine (ADA-GEL) and the compatibility with MG-63 cells were proven, thus the ADA-GEL material is highlighted as a promising matrix for applications in biofabrication.

Measuring the modulus of silicone hydrogel contact lenses.

PURPOSE: The purpose of this study is to demonstrate a novel method for measuring the modulus of contact lenses in their as-received, variable-thickness form and to determine whether modulus varies with location within commercial lenses and whether it is dependent on lens geometry and temperature. METHODS: The thickness profiles of lenses having powers from -8 diopters (D) to +4 D were measured using a Rehder electronic thickness gauge. Strip-shaped specimens having a width of 5.5 mm were then cut from the lenses. Graphite particles were sprinkled on the specimen surface so that its motions could be tracked using digital image-correlation techniques. The specimens were mounted in a BioTester test system using BioRakes (rather than clamps) and stretched uniaxially until all parts of the lens between the attachment points had elongated by at least 10%. This procedure allowed local modulus values to be determined at 110 locations over the surface of each lens and any property variations within the lenses to be characterized. Tests were performed at 5, 23, and 37°C. RESULTS: Material modulus was found to be essentially constant within any given lens and was independent of the optical power of the lens. Young's Modulus values ranged from 0.3 to 1.9 MPa, depending on the lens manufacturer and product, and some lens materials showed a decrease in modulus with temperature. For the materials tested, those with lower water content had a tendency to exhibit higher moduli. CONCLUSIONS: Testing of the kind reported here is important for assessing the efficacy of current and proposed contact lens materials and designs, especially if such designs make use of variable properties to enhance function or fit.

Antidegenerative effects of partial disc replacement in an animal surgery model.

STUDY DESIGN: In vivo degenerative changes of rabbit intervertebral discs after partial disc replacements were evaluated radiologically and histologically in a controlled trial. OBJECTIVE: To demonstrate the therapeutic effects of partial disc replacement in an animal surgical model. SUMMARY OF BACKGROUND DATA: Although some authors reported that partial disc replacements have beneficial clinical outcomes, there are few controlled animal studies in which the therapeutic effects of this procedure have been demonstrated. METHODS: The implants for partial disc replacements were made of poly (vinyl alcohol) hydrogel and rod-shaped. The L2-L3 or L3-L4 intervertebral discs of Japanese white rabbits were pierced with a 2.0-mm Kirschner wire and implants were inserted into the holes. For comparative purposes, the adjacent discs underwent sham treatments or control treatments in which the disc was pierced but no implant was inserted. Sixty discs from 30 rabbits were analyzed radiologically and histologically for degenerative changes at 1, 3, or 6 months after surgery. RESULTS: Radiologic analysis revealed that significantly less disc height was lost with the replacement treatment than with the control treatment. Change in disc height after the replacement treatment was not significantly different from that after the sham treatment. Histologic degeneration of the replaced discs was delayed in comparison with that of the control discs but progressed with time. CONCLUSIONS: The antidegenerative effects of partial disc replacement surgery were demonstrated by quantitative radiologic and histologic analyses. Degeneration of the anulus fibrosus after the replacement treatment was delayed by preserving disc height and occupying the space of the nucleus pulposus. Properly designed implants and minimally invasive techniques are necessary for long-term success.

In vivo monitoring of extracellular glutamate in the brain with a microsensor.

Recent discoveries have revealed that glutamatergic neurotransmission in the central nervous system is mediated by a dynamic interplay between neurons and astrocytes. To enhance our understanding of this process, the study of extracellular glutamate is crucial. At present, microdialysis is the most frequently used analytical technique to monitor extracellular glutamate levels directly in the brain. However, the neuronal and physiological origin of the detected glutamate levels is questioned as they do not fulfil the classical release criteria for exocytotic release, such as calcium dependency or response to the sodium channel blocker tetrodotoxine (TTX). It is hypothesized that an analytical technique with a higher spatial and temporal resolution is required. Glutamate microsensors provide a promising analytical solution to meet this requirement. In the present study, we applied a 10 micro m diameter hydrogel-coated glutamate microsensor to monitor extracellular glutamate levels in the striatum of anesthetized rats. To explore the potential of the microsensor, different pharmacological agents were injected in the vicinity of the sensor at an approximate distance of 100 micro m. It was observed that KCl, exogenous glutamate, kainate and the reuptake inhibitor DL-threo-beta-benzyloxyaspartate (DL-TBOA) increased the extracellular glutamate levels significantly. TTX decreased the basal extracellular glutamate levels approximately 90%, which indicates that the microsensor is capable of detecting neuronally derived glutamate. This is one of the first studies in which a microsensor is applied in vivo on a routine base, and it is concluded that microsensor research can contribute significantly to improve our understanding of the physiology of glutamatergic neurotransmission in the brain.