Biomedical subjects

C C Perry

Publications and source records attributed to C C Perry.

10 recordsLinked to original sources

PubMed2005

Wetting and wetting transitions on copper-based super-hydrophobic surfaces.

Rough and patterned copper surfaces were produced using etching and, separately, using electrodeposition. In both of these approaches the roughness can be varied in a controlled manner and, when hydrophobized, these surfaces show contact angles that increase with increasing roughness to above 160 degrees . We show transitions from a Wenzel mode, whereby the liquid follows the contours of the copper surface, to a Cassie-Baxter mode, whereby the liquid bridges between features on the surface. Measured contact angles on etched samples could be modeled quantitatively to within a few degrees by the Wenzel and Cassie-Baxter equations. The contact angle hysteresis on these surfaces initially increased and then decreased as the contact angle increased. The maximum occurred at a surface area where the equilibrium contact angle would suggest that a substantial proportion of the surface area was bridged.

Journal Article↗

PubMed2004

Kinetics of electron-induced decomposition of CF2Cl2 coadsorbed with water (ice): a comparison with CCl4.

The kinetics of decomposition and subsequent chemistry of adsorbed CF(2)Cl(2), activated by low-energy electron irradiation, have been examined and compared with CCl(4). These molecules have been adsorbed alone and coadsorbed with water ice films of different thicknesses on metal surfaces (Ru; Au) at low temperatures (25 K; 100 K). The studies have been performed with temperature programmed desorption (TPD), reflection absorption infrared spectroscopy (RAIRS), and x-ray photoelectron spectroscopy (XPS). TPD data reveal the efficient decomposition of both halocarbon molecules under electron bombardment, which proceeds via dissociative electron attachment (DEA) of low-energy secondary electrons. The rates of CF(2)Cl(2) and CCl(4) dissociation increase in an H(2)O (D(2)O) environment (2-3x), but the increase is smaller than that reported in recent literature. The highest initial cross sections for halocarbon decomposition coadsorbed with H(2)O, using 180 eV incident electrons, are measured (using TPD) to be 1.0+/-0.2 x 10(-15) cm(2) for CF(2)Cl(2) and 2.5+/-0.2 x 10(-15) cm(2) for CCl(4). RAIRS and XPS studies confirm the decomposition of halocarbon molecules codeposited with water molecules, and provide insights into the irradiation products. Electron-induced generation of Cl(-) and F(-) anions in the halocarbon/water films and production of H(3)O(+), CO(2), and intermediate compounds COF(2) (for CF(2)Cl(2)) and COCl(2), C(2)Cl(4) (for CCl(4)) under electron irradiation have been detected using XPS, TPD, and RAIRS. The products and the decomposition kinetics are similar to those observed in our recent experiments involving x-ray photons as the source of ionizing irradiation.

Journal Article↗

PubMed2004

Topography driven spreading.

Roughening a hydrophobic surface enhances its nonwetting properties into superhydrophobicity. For liquids other than water, roughness can induce a complete rollup of a droplet. However, topographic effects can also enhance partial wetting by a given liquid into complete wetting to create superwetting. In this work, a model system of spreading droplets of a nonvolatile liquid on surfaces having lithographically produced pillars is used to show that superwetting also modifies the dynamics of spreading. The edge speed-dynamic contact angle relation is shown to obey a simple power law, and such power laws are shown to apply to naturally occurring surfaces.

Hydrophobic and Hydrophilic Interactions↗

PubMed2001

The systematic study of aluminium speciation in medium concentrated aqueous solutions.

Industrial applications and environmental problems involving the aqueous chemistry of aluminium require an understanding of the speciation of this metal ion at a wide range of concentrations. The formation of polynuclear species is of special interest due to the complexity of the hydrolysis mechanisms and the diversity of the hydrolysis products. Kinetic aspects of speciation are also important considering the different stability ranges of polycationic species formed during the hydrolysis process. In the present paper we report results of systematic studies on the formation of aluminium polycations at room temperature. Automated potentiometric titrations have been used to study the hydrolysis of aluminium-ions in solutions (0.01-0.2 M) on a short time scale (2 min between titrant additions). (27)Al NMR spectroscopy and dynamic light scattering have been used for investigations on a longer time scale (24 h). The effects of alkali strength (KOH, NH(4)OH and KHCO(3)) and concentration (0.45-2.0 M), counterion identity (Cl(-), NO(3)(-), SO(4)(2-)) and ionic strength have been investigated. Optimum conditions for the generation of Al(13)-mer are proposed on short and long time scales. On a short time scale, aluminium chloride and nitrate should be used as starting materials, KOH and KHCO(3) should be used for hydrolysis and experiments conducted at low ionic strength. For solutions that have been left to age, there is a considerable hydrolysis window that can be used to generate significant quantities of the Al(13)-mer that vary little with the alkali used. Al(13)-mer species are not generated from alum as the precursor. The presence of sulphate ions alters the pathway of aluminium polymerisation to form polymeric and solid materials. On the basis of the potentiometric titration data, dynamic light scattering and (27)Al NMR measurements evidence is provided for the detrimental role of sulphate-ions in the formation of Al(13)-mer and an alternative mechanism of aluminium ion polycondensation is proposed, based on the increased stability of monomeric and oligomeric species (dimer and trimer) in the presence of sulphate-ions.

Alkalies↗

PubMed2000

Biosilicification: the role of the organic matrix in structure control.

Silicon (although never in the elemental form) is present in all living organisms and is required for the production of structural materials in single-celled organisms through to higher plants and animals. Hydrated amorphous silica is a mineral of infinite functionality and yet it is formed into structures with microscopic and macroscopic form. Research into the mechanisms controlling the process have highlighted proteins and proteoglycans as possible control molecules. Such molecules are suggested to play a critical role in the catalysis of silica polycondensation reactions and in structure direction. This article reviews information on silica form and function, silica condensation chemistry, the role of macromolecules in structure control and in vitro studies of silica formation using biomolecules extracted from biological silicas. An understanding of the mechanisms by which biological organisms regulate mineral formation will assist in our understanding of the essentiality of silicon to life processes and in the generation of new materials with specific form and function for industrial application in the 21st century.

Animals↗

PubMed2000

Model studies of the precipitation of silica in the presence of aluminium; implications for biology and industry.

The unique chemical affinity between the oxides of silicon and aluminium has been cited as a potential route for the amelioration of the detrimental effects of aluminium in the environment and in biological systems. A greater understanding of silicon-aluminium interactions may assist in this endeavour and also provide a means of overcoming silica fouling problems encountered by industry which are exacerbated by the presence of aluminium. It is also conceivable that this increased knowledge may demonstrate a positive use for aluminium in the processing of the silicon dioxide phase. In this study we report the effect of aluminium ions, derived from aluminium chloride, on silicic acid species obtained from potassium catecholato complexes of silicon at circumneutral pH at the molar ratios 1000Si:Al, 100Si:Al and 50Si:Al. Silica and low levels of aluminium-rich silica materials were formed with Si:Al ratios of about 3.5:1 comparable with the element ratios detected in senile plaques and aluminium-rich scale. A kinetic study showed that aluminium in the reaction medium slowed down the rate of formation of one of the silica species formed early in the condensation process, e.g. trimers, but increased the rate at which silicic acid was removed from sub 1 nm diameter particles. The materials precipitated in the presence of aluminium were composed of smaller particles and aggregates with smaller pores (Si100:Al and Si50:Al systems) or larger pores (Si1000:Al) compared to the control. The nature of the interactions responsible for these differences is discussed. The effects described here demonstrate the ability of silica and aluminium to interact under conditions such as those found in biological systems. That silica reacts with aluminium in the presence of catechol supports the protective role assigned to silicon.

Aluminum↗

PubMed1998

Aspects of the bioinorganic chemistry of silicon in conjunction with the biometals calcium, iron and aluminium.

Silicon, in its various forms (silicic acid (Si(OH)4) through to hydrated amorphous silica (SiOn(OH)4-2n, n = 2-4) is important in geological and biological processes. Silicon is considered to be an 'essential' element for some plants and higher animals and when present as silica imparts structural, defensive and photosynthetic advantages to many plants. For the majority of essential elements specific molecular binding sites have been identified, but this is not the case for silicon. This has lead to the proposal that silicon may not act directly on biological systems but may exert its influence via interactions with biometals. Metals for which this may be a viable option include aluminium, iron and calcium, all of which can be found co-located with silicon in both minerals and living organisms. This article briefly reviews the pertinent solution and solid state chemistry of silicon in relation to aluminium, iron and calcium. Examples where silicon and an additional metal are found in solid state phases are described. The biological systems where these deposits are found are extremely complex and preliminary results from a model system designed to study silicon-biometal interactions are described.

Aluminum↗

PubMed1998

Evaluation of the osteoblast response to a silica gel in vitro.

Many bioactive glasses and glass ceramics contain silica, yet the effect of silica on the osteoblast is not well understood. The osteoblast cell response to a silica surface, without the interference of the other ions present in glasses and glass ceramics has been investigated. A silica sol-gel was prepared which gave a molar ratio of 1:4:4 tetraethyl orthosilicate (TEOS): ethanol:acidified water 0.2 M HCl) and spin cast on to thermanox discs. The gel was characterized in terms of bioactivity and release of silicic acid. Primary human osteoblasts (HOBs) were seeded on the surface of upright or inverted silica discs. Cell activity (alamar blue reduction), number (DNA content) and differentiation (alkaline phosphatase activity, nodule formation and mineralization) were measured. There was no apparant difference in cell number, activity or alkaline phosphatase activity between silica discs and controls. Nodules formed much earlier on the silica surfaces and these eventually mineralized. Nodule formation was reproducibly enhanced on the silica surface and less markedly on the inverted discs. It is likely that both the surface characteristics of the silica gel and silicic acid release from the disc affect osteoblast behaviour.

Journal Article↗

PubMed1988

A physico-chemical approach to morphogenesis: the roles of inorganic ions and crystals.

We consider morphogenesis with special references to the development of mineral frameworks, organic filamentous structures and the location of enzymes, including ion-pumps, in membranes. Starting from a description of the morphology of inorganic crystals we analyse so-called equilibrium growth, i.e. growth at constant shape, both outside and inside biological systems. It is shown that an initial small spherical cell in which linear, ordered, inorganic or organic features are built will become distorted. The distortion is due to stresses which affect membrane curvature and consequently rearrange enzymes in membranes. The cell system can rapidly attain a steady-state of development, ('equilibrium') growth, of fixed morphology. After a considerable growth period the cell may cease to grow or the steady state may be broken and a transition can then occur to a quite new morphology. Examples are taken mostly from unicellular organisms but the ideas apply to multi-cellular systems.

Animals↗

PubMed1986

Structural aspects of biogenic silica.

The objectives of this paper are to discuss the characterization of biogenic silica in terms of structural properties, and to elucidate the mechanisms of structural organization within biological systems. The scale of organization is a critical factor in the characterization of biosilicification processes, and order at the nanometre, micrometre and macroscopic levels is described. Molecular order is discussed in the light of high-resolution transmission electron microscopy and solid-state NMR results obtained from samples of biogenic silica. Microscopic organization is expressed in a range of structural motifs, e.g. gels, sheets, fibres, tubes and globular assemblies, and reflects the infinitely adaptive morphology of biogenic silica. Macroscopic structures such as curved rods, spicules, perforated plates, teeth and reticular frameworks can be assembled from these microscopic motifs. The mechanisms of structural organization involve spatial (scalar and vectorial) constraints, ordered particle aggregation and chemical regulation. The possible importance of organic surfaces is discussed.

Eukaryota↗