71 research outputs found

    Human Platelet-Rich Plasma- and Extracellular Matrix-Derived Peptides Promote Impaired Cutaneous Wound Healing In Vivo

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    Previous work in our laboratory has described several pro-angiogenic short peptides derived from endothelial extracellular matrices degraded by bacterial collagenase. Here we tested whether these peptides could stimulate wound healing in vivo. Our experiments demonstrated that a peptide created as combination of fragments of tenascin X and fibrillin 1 (comb1) applied into cranial dermal wounds created in mice treated with cyclophosphamide to impair wound healing, can improve the rate of wound closure. Furthermore, we identify and characterize a novel peptide (UN3) created and modified from two naturally-occurring peptides, which are present in human platelet-rich plasma. In vitro testing of UN3 demonstrates that it causes a 50% increase in endothelial proliferation, 250% increase in angiogenic response and a tripling of epithelial cell migration in response to injury. Results of in vivo experiments where comb1 and UN3 peptides were added together to cranial wounds in cyclophosphamide-treated mice leads to improvement of wound vascularization as shown by an increase of the number of blood vessels present in the wound beds. Application of the peptides markedly promotes cellular responses to injury and essentially restores wound healing dynamics to those of normal, acute wounds in the absence of cyclophosphamide impairment. Our current work is aimed at understanding the mechanisms underlying the stimulatory effects of these peptides as well as identification of the cellular receptors mediating these effects.National Institutes of Health (U.S.) (Grant EY15125)National Institutes of Health (U.S.) (Grant EY19533)Wound Care Partners, LL

    Exchange Reactions between Alkanethiolates and Alkaneselenols on Au{111}

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    When alkanethiolate self-assembled monolayers on Au{111} are exchanged with alkaneselenols from solution, replacement of thiolates by selenols is rapid and complete, and is well described by perimeter-dependent island growth kinetics. The monolayer structures change as selenolate coverage increases, from being epitaxial and consistent with the initial thiolate structure to being characteristic of selenolate monolayer structures. At room temperature and at positive sample bias in scanning tunneling microscopy, the selenolate-gold attachment is labile, and molecules exchange positions with neighboring thiolates. The scanning tunneling microscope probe can be used to induce these place-exchange reactions

    Influence of the media granular size of small pilot subsurface flow wetlands on axial dispersion and the hydraulic behaviour

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    peer reviewedThe objective of this paper is to evaluate using tracer tests, the role of the granular media size on the hydraulic behaviour of small -scale pilot horizontal subsurface flow (HSSF) gravel beds. The non-ideal flow was modelled by the tank-in-series model (TIS) using the moment analysis and Gamma distribution fitting using the Solver™ routine in Microsoft Excel™; the Plug Flow with Dispersion (PFD) model was also assessed. Tests were performed under a greenhouse in four identical pilot-scale gravel beds of 9:1:1 ratio, which received an equal, inflow of clear water. The influent flow rate was 40 L/day and the surface area of the pilot cells was 0.8 m². The pea gravel media used in the four beds were as follows: 3-5 mm, 6-8 mm, 8-10 mm and 10-12 mm. The tracer used was Potassium Bromide (KBr) with a concentration of 1 g Br/L, using a single-shot injection into the inlet distribution tubes. Tests were repeated three times, with identical materials and methods. Statistical differences were observed between replications. Water loss by evaporation of the unplanted gravel beds was of 11% for the smaller media size (3-5 mm) which is significantly different than the 4 to 5% obtained for the other media sizes. Tracer detention time, tracer peak time, volumetric and hydraulic efficiencies show all the same tendency which is a significant reduction with larger particles sizes. The two methods of calculation for the number NTIS by moment analysis and Gamma distribution fitting (using Solver™) are significantly different. The Gamma model increases the number of TIS with significantly higher values for smaller media sizes
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