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traditional methods for design are compounded as requirements for human safety and structural integrity become more stringent. This chapter provides an outline to an alternative design process for blast mitigation, which utilizes a combination of design experience, empirical data and computer modelling. The methodology is based around three aspects: Prediction of the blast and the developed pressures on nearby structures; Subsequent kinematic response and deformation of the structure; Response of any occupants associated with the structure. This chapter concentrates on the primary aspect, namely the prediction of the blast, however, typical examples of subsequent analyses are presented. The blast modelling methodology developed and validated by Frazer-Nash Consultancy Limited (FNC) has been based on a variety of simple test-cases, for example, normal and angled shock reflection. The predictions have been compared to empirical and analytical results and subsequent blast simulations have been undertaken on more complex structures. The basis of the CFD modelling involves the conversion of the blast source into a transient input within the model. This can be achieved in one of two ways; namely a pressure/ temperature source or a burn model. This transient input can be correlated to a known blast magnitude. Once the blast has been enabled the developed pressures in the flow domain can be monitored and the subsequent response of a given structure predicted.

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@W @W ; T > @x @y > >0 :

where P k is the relative phase of array element k to the centre of the array, K is equal to 27r/X, X is the wavelength, 4 is the azimuth angle of the signal impinging on the array and R is the array radius.

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groups (eg, OH or CO2H) that interact with GC columns Derivatization is necessary to convert the samples into a suitable form for analysis Prederivatization and postderivatization clean-up yields simple chromatograms Quantitation employs stable-isotope-labeled forms of the markers (eg, 13C-labeled Mur derived from labeled blue-green algae) The 3-OH FAs have had great utility in the determination of LPS levels in indoor air However, in tissues and body uids it has been determined that 3-OH FAs are naturally present at low levels as products of mammalian metabolism (mitochondrial fatty acid oxidation) Due to this background GC MS/MS for 3-OH FAs is not recommended as a general marker to determine trace LPS levels in clinical samples [14] However, in certain situations the assessment of 3-OH FAs has been successfully used, for example, in the diagnosis of chronic peridontitis [15].

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There is great potential for the utility of 3-OH FAs as markers for LPS contamination in pharmaceutical products, where often the background matrix would be anticipated to be much less complex Chemical analysis of Mur levels has proved effective in both clinical and environmental samples, since Mur is not synthesized by eukaryotic cells For example, it is readily detected in infected human body uids, for example, synovial uids from patients with staphylococcal arthritis and spinal uids from those with pneumococcal pneumonia [7, 16] However, the most widely used method for its analysis, as an alditol acetate, is time consuming A large number of derivatives have been tested in order to develop a simpler alternative Unfortunately the limit of detection for these alternative approaches has not been optimal [17, 18] The marker monomer is chemically converted into a volatile form suitable of passage through a gas chromatograph.

Because the availability of three-dimensional protein crystals is a prerequisite for structure determination of proteins by X-ray diffraction, membrane-bound proteins are not directly accessible to the technique. Notwithstanding the fact that approximately 30% of eukaryotic genes encode integral membrane-bound proteins, the high-resolution structures of only a handful have been determined to date compared with tens of thousands nonmembrane protein structures. Multi-

The samples then pass into the tandem mass spectrometer where the ionized molecules are detected GC MS/MS employs GC separation coupled with the exquisite selectivity of MS/MS In MS (monitoring/ quantitation mode), background peaks are screened out MS/MS screens out background a second time, thus dramatically lowering the detection limit Alternatively, in the identi cation mode (MS/MS), a chemical ngerprint of the compound of interest allows de nitive identi cation The analysis of Mur serves as an example: natural 12C muramic acid is rst released from PG polymers (present as a minor component in a complex sample matrix) by hydrolysis Conversion of 12C muramic acid to a volatile derivative, muramicitol lactam pentaacetate molecular weight (MW) 445, is essential for GC MS/MS analysis Maximal selectivity, in GC MS analysis, requires selected ion monitoring (SIM).

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