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Showing papers by "Aránzazu del Campo published in 2015"


Journal ArticleDOI
TL;DR: This Review highlights the large number of methods to exploit colloidal assembly of comparably simple particles with nano- to micrometer dimensions in order to access complex structural hierarchies from nanoscopic over microscopic to macroscopic dimensions.
Abstract: This Review highlights the large number of methods to exploit colloidal assembly of comparably simple particles with nano- to micrometer dimensions in order to access complex structural hierarchies from nanoscopic over microscopic to macroscopic dimensions

609 citations


Journal ArticleDOI
TL;DR: It is demonstrated that non-invasive, transdermal time-regulated activation of cell-adhesive RGD peptide on implanted biomaterials regulates in vivo cell adhesion, inflammation, fibrous encapsulation, and vascularization of the material.
Abstract: Transdermal light-triggered activation of cell-adhesive peptides on the surface of implanted hydrogels alters cell–material interactions, such as cell adhesion and spatial patterning, and fibrous encapsulation and vascularization of the material.

355 citations


Journal ArticleDOI
TL;DR: It is shown how bacteria attachment is altered in the presence of nanosized topographies and optimum designs for preventing it without compromising biocompatibility and applicability in terms of nanostructure robustness or tissue friction are identified.

105 citations


Journal ArticleDOI
TL;DR: In this paper, the authors compared the friction properties of a hexagonal array of polydimethylsiloxane (PDMS) pillars (elongated and regular) in the presence of water.
Abstract: Anatomic differences on the toe pad epithelial cells of torrent and tree frogs (elongated versus regular geometry) are believed to account for superior ability of torrent frogs to attach to surfaces in the presence of running water. Here, the friction properties of artificial hexagonal arrays of polydimethylsiloxane (PDMS) pillars (elongated and regular) in the presence of water are compared. Elongated pillar patterns show significantly higher friction in a direction perpendicular to the long axis. A low bending stiffness of the pillars and a high edge density of the pattern in the sliding direction are the key design criteria for the enhanced friction. The elongated patterns also favor orientation-dependent friction. These findings have important implications for the development of new reversible adhesives for wet conditions.

104 citations


01 Jan 2015
TL;DR: In this paper, the authors compared the friction properties of a hexagonal array of polydimethylsiloxane (PDMS) pillars (elongated and regular) in the presence of water.
Abstract: Anatomic differences on the toe pad epithelial cells of torrent and tree frogs (elongated versus regular geometry) are believed to account for superior ability of torrent frogs to attach to surfaces in the presence of running water. Here, the friction properties of artificial hexagonal arrays of polydimethylsiloxane (PDMS) pillars (elongated and regular) in the presence of water are compared. Elongated pillar patterns show significantly higher friction in a direction perpendicular to the long axis. A low bending stiffness of the pillars and a high edge density of the pattern in the sliding direction are the key design criteria for the enhanced friction. The elongated patterns also favor orientation-dependent friction. These findings have important implications for the development of new reversible adhesives for wet conditions.

95 citations


Journal ArticleDOI
TL;DR: The morphology of the toe epithelium of the rock frog, Staurois parvus, was investigated using a variety of microscopical techniques, indicating evolutionary convergence and a common evolutionary design for reversible attachment in climbing frogs.
Abstract: The morphology of the toe epithelium of the rock frog, Staurois parvus (Family Ranidae), was investigated using a variety of microscopical techniques. The toe pad epithelium is stratified (four to five cell layers), the apical parts of the cells of the outermost layer being separated by fluid-filled channels. The surface of these cells is covered by a dense array of nanopillars, which also cover the surface of subarticular tubercles and unspecialized ventral epithelium of the toes, but not the dorsal epithelium. The apical portions of the outer two layers contain fibrils that originate from the nanopillars and are oriented approximately normal to the surface. This structure is similar to the pad structure of tree frogs of the families Hylidae and Rhacophoridae, indicating evolutionary convergence and a common evolutionary design for reversible attachment in climbing frogs. The main adaptation to the torrent habitat seems to be the straightness of the channels crossing the toe pad, which will assist in drainage of excess water. The presence of nanopillar arrays on all ventral surfaces of the toes resembles that on clingfish suckers and may be a specific adaptation for underwater adhesion and friction. The relevance of these findings to the development of new biomimetically inspired reversible adhesives is discussed.

59 citations


Journal ArticleDOI
TL;DR: This work explores the possibility of tuning the polymerization kinetics and final mechanical properties of tissue-adhesive PEG gels formed by polymerization of end-functionalized star-PEGs with catecholamines with varying substituents with strong differences in cross-linking time and cohesiveness.

27 citations


Journal ArticleDOI
TL;DR: It is believed the QCM-D strategy can be extended to other photoactivatable ligands to characterize cell membrane receptors activity, a relevant issue for cancer diagnosis (and prognosis) as well as other several pathologies.
Abstract: The Quartz Crystal Microbalance with dissipation (QCM-D) technique was applied to monitor and quantify integrin-RGD recognition during the early stages of cell adhesion. Using QCM-D crystals modified with a photo-activatable RGD peptide, the time point of presentation of adhesive ligand at the surface of the QCM-D crystal could be accurately controlled. This allowed temporal resolution of early integrin-RGD binding and the subsequent cell spreading process, and their separate detection by QCM-D. The specificity of the integrin-RGD binding event was corroborated by performing the experiments in the presence of soluble cyclicRGD as a competitor, and cytochalasin D as inhibitor of cell spreading. Larger frequency change in the QCM-D signal was observed for cells with larger spread area, and for cells overexpressing integrin αvβ3 upon stable transfection. This strategy enables quantification of integrin activity which, in turn, may allow discrimination among different cell types displaying distinct integrin subtypes and expression levels thereof. On the basis of these findings, we believe the strategy can be extended to other photoactivatable ligands to characterize cell membrane receptors activity, a relevant issue for cancer diagnosis (and prognosis) as other several pathologies.

26 citations