Gold and silver nanoparticle-based colorimetric sensors: New trends and applications

Gold and Silver nanoparticles (AuNPs and AgNPs) are perfect platforms for developing sensing colorimetric devices thanks to their high surface to volume ratio and distinctive optical properties, particularly sensitive to changes in the surrounding environment. These characteristics ensure high sensitivity in colorimetric devices. Au and Ag nanoparticles can be capped with suitable molecules that can act as specific analyte receptors, so highly selective sensors can be obtained. This review aims to highlight the principal strategies developed during the last decade concerning the preparation of Au and Ag nanoparticle-based colorimetric sensors, with particular attention to environmental and health monitoring applications

Current trends in polymer based sensors

This review illustrates various types of polymer and nanocomposite polymeric based sensors used in a wide variety of devices. Moreover, it provides an overview of the trends and challenges in sensor research. As fundamental components of new devices, polymers play an important role in sensing applications. Indeed, polymers offer many advantages for sensor technologies: their manufacturing methods are pretty simple, they are relatively low-cost materials, and they can be functionalized and placed on different substrates. Polymers can participate in sensing mechanisms or act as supports for the sensing units. Another good quality of polymer-based materials is that their chemical structure can be modified to enhance their reactivity, biocompatibility, resistance to degradation, and flexibility

Biodegradable hydrogels as scaffolds for nerve regeneration

Biodegradable hydrogels as scaffolds for nerve regeneration Valerio Magnaghi 1, Elisabetta Ranucci 2, Fabio Fenili 2, Patrizia Procacci 3, Giorgio Pivato 4, Paolo Cortese 4 and Paolo Ferruti 2 1 Department of Endocrinology, Physiopathology, Applied biology, Via Balzaretti 9, University of Milan, 20133 Milan, Italy 2 Department of Organic and Industrial Chemistry, University of Milan, Via Venezian 21, 20133 Milan, Italy 3 Department of Human Morphology and Biomedical Sciences - Citta' Studi, University of Milan, Via Mangiagalli 31, 20133 Milan, Italy 4 Hand Surgery Unit, IRCCS Multimedica, Via Milanese 300, 20099 Sesto San Giovanni, Italy Transected peripheral nerves are typically reconnected by direct end-to-end surgery or by autologous nerve graft. However, artificial synthetic guide are a successful alternative which may prevent neuroma formation (1). Among biodegradable conduits a novel approach is represented by use of tuneable polyamidoamine (PAA)-based hydrogels, with specific diameters, different shapes and/or dimensions. Depending by their crosslinking degree, hydrogels made by PAAs are tough material which may absorb large amounts of water. PAA hydrogels are biocompatible and biodegradable in vitro to non-toxic low molecular weight products over a period of time varying from few weeks to months (2). In order to evaluate their ability to promote nerve regeneration, PAA hydrogels scaled as scaffold conduits (10mm lenght, 1mm internal diameter) were studied by using an experimental model of rat nerve transection. A conduit was used to join a gap of 4-5 mm in the sciatic nerve, and a longitudinal analysis was made at 30, 45, 60, 90 days post-surgery. We performed the gait analysis to evaluate locomotor coordination, the plantar test to study nociception and pain sensitivity, and the morphological-morphometric analysis to evaluate the nerve recovery. Preliminary results indicate that nerve ends can be successfully joined by these PAA-based hydrogel conduits. One month after surgery, in fact, the regeneration is appreciable inside the conduit and the nerve is resistant to mechanical traction, without signs of inflammation or serum infiltrate. In the implanted rats 45 days after surgery the footprints analysis reveals a trail similar to sham-operated animals, while the thermal hypersensitivity tend to normalize to the control levels at later times. The morphological evaluation of the explanted conduit at 90 days after surgery shows normal myelin structures, confirming nerve regeneration and complete scaffold re-absorption. In conclusion, our results demonstrate that PAA hydrogels might be a promising scaffold tube for nerve regeneration. Further studies on the hydrogels functionalization for drug delivery, with growth factors or hormones, are in progress in our labs. References 1. Yannas, I.V., Hill, B.J., 2004. Selection of biomaterials for peripheral nerve regeneration using data from the nerve chamber model. Biomaterials 25, 1593-1600. 2. Jacchetti, E., Elimitri, E., Rodighiero, S., Indrieri, M., Gianfelice, A., Lenardi, C., Podest\ue0, A., Ranucci, E., Ferruti, P. Milani, P., 2008. P. Biomimetic poly(amidoamine) hydrogels as synthetic materials for cell culture. J. Biothecnol. 6, 1

Tumor suppressor Nf2/merlin drives Schwann cell changes following electromagnetic field exposure through Hippo-dependent mechanisms

Previous evidence showed mutations of the neurofibromin type 2 gene (Nf2), encoding the tumor suppressor protein merlin, in sporadic and vestibular schwannomas affecting Schwann cells (SC). Accordingly, efforts have been addressed to identify possible factors, even environmental, that may regulate neurofibromas growth. In this context, we investigated the exposure of SC to an electromagnetic field (EMF), which is an environmental issue modulating biological processes. Here we show that SC exposed to 50 Hz EMFs change their morphology, proliferation, migration and myelinating capability. In these cells merlin is downregulated, leading to activation of two intracellular signaling pathways, ERK/AKT and Hippo. Interestingly, SC change their phenotype toward a proliferative/migrating state, which in principle may be pathologically relevant for schwannoma development

Effects of caloric restriction on neuropathic pain, peripheral nerve degeneration and inflammation in normometabolic and autophagy defective prediabetic Ambra1 mice

There is a growing interest on the role of autophagy in diabetes pathophysiology, where development of neuropathy is one of the most frequent comorbidities. We have previously demonstrated that neuropathic pain after nerve damage is exacerbated in autophagy-defective heterozygous Ambra1 mice. Here, we show the existence of a prediabetic state in Ambra1 mice, characterized by hyperglycemia, intolerance to glucose and insulin resistance. Thus, we further investigate the hypothesis that prediabetes may account for the exacerbation of allodynia and chronic pain and that counteracting the autophagy deficit may relieve the neuropathic condition. We took advantage from caloric restriction (CR) able to exert a double action: a powerful increase of autophagy and a control on the metabolic status. We found that CR ameliorates neuropathy throughout anti-inflammatory and metabolic mechanisms both in Ambra1 and in WT animals subjected to nerve injury. Moreover, we discovered that nerve lesion represents, per se, a metabolic stressor and CR reinstates glucose homeostasis, insulin resistance, incomplete fatty acid oxidation and energy metabolism. As autophagy inducer, CR promotes and anticipates Schwann cell autophagy via AMP-activated protein kinase (AMPK) that facilitates remyelination in peripheral nerve. In summary, we provide new evidence for the role of autophagy in glucose metabolism and identify in energy depletion by dietary restriction a therapeutic approach in the fight against neuropathic pain

Bloom’s Syndrome and PICH Helicases Cooperate with Topoisomerase IIα in Centromere Disjunction before Anaphase

Centromeres are specialized chromosome domains that control chromosome segregation during mitosis, but little is known about the mechanisms underlying the maintenance of their integrity. Centromeric ultrafine anaphase bridges are physiological DNA structures thought to contain unresolved DNA catenations between the centromeres separating during anaphase. BLM and PICH helicases colocalize at these ultrafine anaphase bridges and promote their resolution. As PICH is detectable at centromeres from prometaphase onwards, we hypothesized that BLM might also be located at centromeres and that the two proteins might cooperate to resolve DNA catenations before the onset of anaphase. Using immunofluorescence analyses, we demonstrated the recruitment of BLM to centromeres from G2 phase to mitosis. With a combination of fluorescence in situ hybridization, electron microscopy, RNA interference, chromosome spreads and chromatin immunoprecipitation, we showed that both BLM-deficient and PICH-deficient prometaphase cells displayed changes in centromere structure. These cells also had a higher frequency of centromeric non disjunction in the absence of cohesin, suggesting the persistence of catenations. Both proteins were required for the correct recruitment to the centromere of active topoisomerase IIα, an enzyme specialized in the catenation/decatenation process. These observations reveal the existence of a functional relationship between BLM, PICH and topoisomerase IIα in the centromere decatenation process. They indicate that the higher frequency of centromeric ultrafine anaphase bridges in BLM-deficient cells and in cells treated with topoisomerase IIα inhibitors is probably due not only to unresolved physiological ultrafine anaphase bridges, but also to newly formed ultrafine anaphase bridges. We suggest that BLM and PICH cooperate in rendering centromeric catenates accessible to topoisomerase IIα, thereby facilitating correct centromere disjunction and preventing the formation of supernumerary centromeric ultrafine anaphase bridges

Synthesis and Characterization of Thermally and Chemically Gelling Injectable Hydrogels for Tissue Engineering

Novel, injectable hydrogels were developed that solidify through a dual-gelation, physical and chemical, mechanism upon preparation and elevation of temperature to 37°C. A thermogelling, poly(N-isopropylacrylamide)-based macromer with pendant epoxy rings and a hydrolyticallydegradable polyamidoamine-based diamine crosslinker were synthesized, characterized, and combined to produce in situ forming hydrogel constructs. Network formation through the epoxyamine reaction was shown to be rapid and facile, and the progressive incorporation of the hydrophilic polyamidoamine crosslinker into the hydrogel was shown to mitigate the often problematic tendency of thermogelling materials to undergo significant post-formation gel syneresis. The results suggest that this novel class of injectable hydrogels may be attractive substrates for tissue engineering applications due to the synthetic versatility of the component materials and beneficial hydrogel gelation kinetics and stability