80 research outputs found

    Electrically induced tunable cohesion in granular systems

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    Experimental observations of confined granular materials in the presence of an electric field that induces cohesive forces are reported. The angle of repose is found to increase with the cohesive force. A theoretical model for the stability of a granular heap, including both the effect of the sidewalls and cohesion is proposed. A good agreement between this model and the experimental results is found. The steady-state flow angle is practically unaffected by the electric field except for high field strengths and low flow rates.Comment: accepted for publication in "Journal of Statistical Mechanics: Theory and Experiment

    On px2+q2n=yppx^2 + q^{2n}= y^p and related Diophantine equations

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    The title equation, where p>3p>3 is a prime number ≢7(mod8)\not\equiv 7 \pmod 8, qq is an odd prime number and x,y,nx,y,n are positive integers with x,yx,y relatively prime, is studied. When p3(mod8)p\equiv 3\pmod 8, we prove (Theorem 2.3) that there are no solutions. For p≢3(mod8)p\not\equiv 3\pmod 8 the treatment of the equation turns out to be a difficult task. We focus our attention to p=5p=5, by reason of an article by F. Abu Muriefah, published in this journal, vol. 128 (2008), 1670-1675. Our main result concerning this special equation is Theorem 1.1, whose proof is based on results around the Diophantine equation 5x24=yn5x^2-4=y^n (integer solutions), interesting in themselves, which are exposed in Sections 3 and 4. These last results are obtained by using tools such as Linear Forms in Two Logarithms and Hypergeometric Series.Comment: 23 pages, second version with minor revision

    Release kinetics of 5-fluorouracil-loaded microspheres on an experimental rat glioma.

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    BACKGROUND: Biodegradable loaded systems are promising devices for controlled and sustained release of anticancer drugs to brain tumours. We investigated the influence of drug-release profiles of 5-fluorouracil-loaded microspheres designed for the treatment of malignant gliomas. MATERIALS AND METHODS: 2.5 mg 5-FU delivered by either fast. (1 formulation) or slow-(2 formulations) 5-FU release microspheres (MS) were tested in C6-glioma rat brains. Tumor response was assessed by T2-weighted MRI. RESULTS: All treated animals, whatever the release profile considered, displayed a comparable 50% increase in life span versus controls. Delays in C6-glioma development appeared to correspond to the in vitro release periods of MS. In terms of curative prospect, complete remission was only observed in 11% of 5-FU-treated animals (4 out of 38). CONCLUSION: Formulation was unambiguously implicated in the response observed after local delivery of 5-FU to glioma

    Nanofibrous Scaffolds Incorporating PDGF-BB Microspheres Induce Chemokine Expression and Tissue Neogenesis In Vivo

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    Platelet-derived growth factor (PDGF) exerts multiple cellular effects that stimulate wound repair in multiple tissues. However, a major obstacle for its successful clinical application is the delivery system, which ultimately controls the in vivo release rate of PDGF. Polylactic-co-glycolic acid (PLGA) microspheres (MS) in nanofibrous scaffolds (NFS) have been shown to control the release of rhPDGF-BB in vitro. In order to investigate the effects of rhPDGF-BB release from MS in NFS on gene expression and enhancement of soft tissue engineering, rhPDGF-BB was incorporated into differing molecular weight (MW) polymeric MS. By controlling the MW of the MS over a range of 6.5 KDa–64 KDa, release rates of PDGF can be regulated over periods of weeks to months in vitro. The NFS-MS scaffolds were divided into multiple groups based on MS release characteristics and PDGF concentration ranging from 2.5–25.0 µg and evaluated in vivo in a soft tissue wound repair model in the dorsa of rats. At 3, 7, 14 and 21 days post-implantation, the scaffold implants were harvested followed by assessments of cell penetration, vasculogenesis and tissue neogenesis. Gene expression profiles using cDNA microarrays were performed on the PDGF-releasing NFS. The percentage of tissue invasion into MS-containing NFS at 7 days was higher in the PDGF groups when compared to controls. Blood vessel number in the HMW groups containing either 2.5 or 25 µg PDGF was increased above those of other groups at 7d (p<0.01). Results from cDNA array showed that PDGF strongly enhanced in vivo gene expression of the CXC chemokine family members such as CXCL1, CXCL2 and CXCL5. Thus, sustained release of rhPDGF-BB, controlled by slow-releasing MS associated with the NFS delivery system, enhanced cell migration and angiogenesis in vivo, and may be related to an induced expression of chemokine-related genes. This approach offers a technology to accurately control growth factor release to promote soft tissue engineering in vivo

    Designing Bioactive Delivery Systems for Tissue Regeneration

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    The direct infusion of macromolecules into defect sites generally does not impart adequate physiological responses. Without the protection of delivery systems, inductive molecules may likely redistribute away from their desired locale and are vulnerable to degradation. In order to achieve efficacy, large doses supplied at interval time periods are necessary, often at great expense and ensuing detrimental side effects. The selection of a delivery system plays an important role in the rate of re-growth and functionality of regenerating tissue: not only do the release kinetics of inductive molecules and their consequent bioactivities need to be considered, but also how the delivery system interacts and integrates with its surrounding host environment. In the current review, we describe the means of release of macromolecules from hydrogels, polymeric microspheres, and porous scaffolds along with the selection and utilization of bioactive delivery systems in a variety of tissue-engineering strategies

    Amidons resistants : caracterisations structurales de l'amidon non digere en fin d'intestin grele de l'homme et effets physiologiques

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    * CR de Nantes. Laboratoire de Technologie Appliquee a la Nutrition. BP 527, 44026 Nantes Cedex 03 Diffusion du document : CR de Nantes. Laboratoire de Technologie Appliquee a la Nutrition. BP 527, 44026 Nantes Cedex 03 Diplôme : Dr. d'Universit

    Resistant starch

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    International audienc

    Technologies et qualites nutritionnelles des amidons

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    46 ref.National audienc

    Francisco Javier Sánchez Cantón (1891-1971)

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