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Biomedical subjects

Paul F McMillan

Publications and source records attributed to Paul F McMillan.

16 recordsLinked to original sources
PubMed2006

High pressure effects in anaesthesia and narcosis.

There is growing interest in determining the effects of high pressure on biological functions. Studies of brain processes under hyperbaric conditions can give a unique insight into phenomena such as nitrogen narcosis, inert gas anaesthesia, and pressure reversal of the effects of anaesthetic and narcotic agents. Such research may shed light on the action of anaesthetics, which remains poorly understood, and on the nature of consciousness itself. Various studies have established the behavioural response of organisms to hyperbaric conditions, in the presence or absence of anaesthetic agents. At the molecular level, X-ray crystallography has been used to investigate the incorporation of species like Xe in hydrophobic pockets within model ion channels that may account for pressure effects on neuronal transmission. New magnetic resonance imaging techniques are providing tomographic three-dimensional images that detail brain structure and function, and that can be correlated with behavioural studies and psychological test results. Such whole organ techniques are linked to the molecular scale via voltage-sensitive dye (VSD) imaging studies on brain slices that provide time-resolved images of the dynamic formation and interconnection of inter-neuronal complexes. The VSD experiments are readily adapted to in situ studies under high pressure conditions. In this tutorial review we review the current state of knowledge of hyperbaric effects on brain processes: anaesthesia and narcosis, recent studies at the molecular level via protein crystallography at high pressure in a Xe atmosphere, and we also present some preliminary results of VSD imaging of brain slices under hyperbaric conditions.

Anesthesia↗
PubMed2006

Structural studies and polymorphism in amorphous solids and liquids at high pressure.

When amorphous materials are compressed their structures are expected to change in response to densification. In some cases, the changes in amorphous structure can be discontinuous and they can even have the character of first-order phase transitions. This is a phenomenon referred to as polyamorphism. Most evidence for polyamorphic transitions between low and high density liquids or analogous transformations between amorphous forms of the same substance to date has been indirect and based on the changes in thermodynamic and other structure-related properties with pressure. Recent studies using advanced X-ray and neutron scattering methods combined with molecular dynamics simulations are now revealing the details of structural changes in polyamorphic systems as a function of pressure. Various "two state" or "two species" models are used to understand the anomalous densification behaviour of liquids with melting curve maxima or regions of negative melting slope. Thermodynamic analysis of the two state model leads to the possibility of low- to high-density liquid transitions caused by differences in bulk thermodynamic properties between different amorphous forms and on the degree of cooperativity between low- and high-density structural configurations. The potential occurrence of first-order transitions between supercooled liquids is identified as a critical-like phenomenon. In this tutorial review we discuss the background to polyamorphism, incorporating the experimental observations, simulation studies and the two-state models. We also describe work carried on several systems that are considered to be polyamorphic.

Journal Article↗
PubMed2006

High-pressure chemistry of nitride-based materials.

Besides temperature at one atmosphere, the applied pressure is another important parameter for influencing and controlling reaction pathways and final reaction products. This is relevant not only for the genesis of natural minerals, but also for synthetic chemical products and technological materials. The present critical review (316 references) highlights recent developments that utilise high pressures and high-temperatures for the synthesis of new materials with unique properties, such as high hardness, or interesting magnetic or optoelectronic features. Novel metal nitrides, oxonitrides as well as the new class of nitride-diazenide compounds, all formed under high-pressure conditions, are highlighted. Pure oxides and carbides are not considered here. Moreover, syntheses under high-pressure conditions require special equipment and preparation techniques, completely different from those used for conventional synthetic approaches at ambient pressure. Therefore, we also summarize the high-pressure techniques used for the synthesis of new materials on a laboratory scale. In particular, our attention is focused on reactive gas pressure devices with pressures between 1.2 and 600 MPa, multi-anvil apparatus at P < 25 GPa and the diamond anvil cell, which allows work at pressures of 100 GPa and higher. For example, some of these techniques have been successfully upgraded to an industrial scale for the synthesis of diamond and cubic boron nitride.

Journal Article↗
PubMed2006

Size-dependent pressure-induced amorphization in nanoscale TiO2.

We investigated the size-dependent high-pressure phase transition behavior of nanocrystalline anatase TiO2 with synchrotron x-ray diffraction and Raman spectroscopy to 45 GPa at ambient temperature. Pressure-induced amorphization results in a high-density amorphous (HDA) form when the starting crystallite size is < 10 mm. The HDA-TiO2 transforms to a low-density amorphous form at lower pressures. Harnessing the nanometer length scale thus provides a new window for experimental investigation of amorphization in poor glass formers and a synthesis route for new amorphous materials.

Journal Article↗
PubMed2005

A density-driven phase transition between semiconducting and metallic polyamorphs of silicon.

Amorphous and crystalline forms of silicon are well-known, tetrahedrally coordinated semiconductors. High-pressure studies have revealed extensive polymorphism among various metallic crystal structures containing atoms in six-, eight- and 12-fold coordination. Melting silicon at ambient or high pressure results in a conducting liquid, in which the average coordination is greater than four (ref. 3). This liquid cannot normally be quenched to a glass, because of rapid crystallization to the diamond-structured semiconductor. Solid amorphous silicon is obtained by synthesis routes such as chemical or physical vapour deposition that result in a tetrahedrally bonded semiconducting state. It has long been speculated that the amorphous solid and the liquid could represent two polymorphic forms of the amorphous state that are linked by density- or entropy-driven transformations. Such polyamorphic transitions are recognized to occur among several different types of liquid and glassy systems. Here we present experimental evidence for the occurrence of a density-driven polyamorphic transition between semiconducting and metallic forms of solid amorphous silicon. The experiments are combined with molecular dynamics simulations that map the behaviour of the amorphous solid on to that of the liquid state.

Computer Simulation↗
PubMed2005

Pressing on: the legacy of Percy W. Bridgman.

A hundred years ago, Percy Bridgman invented mechanical devices that dramatically expanded the high-pressure range available for carrying out physics and chemistry experiments into an unprecedented regime of high densities. His pioneering work revolutionized condensed matter research. His spirit remains alive today as researchers continue to push back the boundaries of high-pressure science.

Biocompatible Materials↗
PubMed2003

Chemistry of materials under extreme high pressure-high-temperature conditions.

Most of our knowledge of chemistry is derived from experiments carried at the Earth's surface, at pressures near one atmosphere. However, most elements and compounds in the universe exist under conditions of extremely high pressures, often combined with high temperatures, deep within the planets and stars. Under these conditions, new high-density crystal forms occur, species usually known only as molecules become dense covalent or ionic solids, and insulators and semiconductors become metals and even superconductors. Valency states and coordination numbers are changed, and it is expected that chemical bonding and reactivity is modified. Paul McMillan describes how the field of condensed matter chemistry under extreme high pressure conditions now represents a vast new area to be explored.

Journal Article↗
PubMed2003

Crystal-liquid phase relations in silicon at negative pressure.

The stable and metastable melting relations for silicon in the diamond and Si136 clathrate-II structures at positive and negative pressures are calculated by molecular dynamics computer simulation. The simulated liquid and crystalline clathrates undergo cavitation at approximately -3 and -12 GPa. Between these limits a stretched crystal would transform directly to gas in response to a mechanical instability. Most importantly, the clathrate-II crystal becomes thermodynamically stable over the diamond at negative pressure below -1 GPa at the melting point. Si136 should then crystallize from a slightly stretched liquid, which would have the same volume as a diamond-structure crystal.

Journal Article↗
PubMed2002

New materials from high-pressure experiments.

High-pressure synthesis on an industrial scale is applied to obtain synthetic diamonds and cubic boron nitride (c-BN), which are the superhard abrasives of choice for cutting and shaping hard metals and ceramics. Recently, high-pressure science has undergone a renaissance, with novel techniques and instrumentation permitting entirely new classes of high-pressure experiments. For example, superconducting behaviour was previously known for only a few elements and compounds. Under high-pressure conditions, the 'superconducting periodic table' now extends to all classes of the elements, including condensed rare gases, and ionic compounds such as CsI. Another surprising result is the newly discovered solid-state chemistry of light-element 'gas' molecules such as CO2, N2 and N2O. These react to give polymerized covalently bonded or ionic mineral structures under conditions of high pressure and temperature: the new solids are potentially recoverable to ambient conditions. Here we examine innovations in high-pressure research that might be harnessed to develop new materials for technological applications.

Journal Article↗