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Matrix application

The concentration of the matrix in solution must be carefully considered before matrix application. If the concentration is too low, the analytes may diffuse from its original position before crystallization, or these will not be sufficient to form proper crystals. If the concentration is too high, rapid crystallization could occur, which makes a limited time for analyte extraction and incorporation. An approximate concentration of 50 mg DHB/mL is usually used for IMS of lipids. [Pg.262]

The type of modifier also affects IMS analysis in general as discussed in Chapter 4. For example, mass spectra can be simplified by addition of potassium acetate [57] or LiCl [58] to the matrix solution, which results in the formation of exclusively potassium or lithium adducts of lipids, respectively. By changing the concentration of alkali metal salts in the matrix solution, it is also possible to selectively ionize either polar or nonpolar lipids [59]. [Pg.262]


The solid matrix is used most effectively. Authors elaborated two ways of the polymer matrix application ... [Pg.82]

The pores of the silica template can be filled by carbon from a gas or a liquid phase. One may consider an insertion of pyrolytic carbon from the thermal decomposition of propylene or by an aqueous solution of sucrose, which after elimination of water requires a carbonization step at 900°C. The carbon infiltration is followed by the dissolution of silica by HF. The main attribute of template carbons is their well sized pores defined by the wall thickness of the silica matrix. Application of such highly ordered materials allows an exact screening of pores adapted for efficient charging of the electrical double layer. The electrochemical performance of capacitor electrodes prepared from the various template carbons have been determined and are tentatively correlated with their structural and microtextural characteristics. [Pg.31]

If the sections are not washed, they need to be dried well right after excision. On the other hand, sections that are washed need to be dried well before the matrix application. Not drying them sufficiently may cause the samples to peel off in the vacuum chamber of the mass spectrometer. [Pg.375]

The second method of sample preparation for IMS is a matrix-coating method for MALDI imaging. In this chapter, we review the choices of matrix compound and solvent composition appropriate for IMS of tissue sections. Three kinds of matrix-application methods and examples of their use are illustrated. [Pg.375]

Several methods have been used for the matrix application (1) immersing a tissue section quickly in a matrix solution, (2) spraying matrix solution onto a tissue section with an air brush, (3) putting small droplets of matrix solution onto a tissue section with an automatic pipetting device that can dispense picoliter volumes (lpL = 10 pk) of reagents.4,5,715161819... [Pg.377]

Sugiura Y, Shimma S, Setou M. Two-step matrix application technique to improve ionization efficiency for matrix-assisted laser desorption/ionization in imaging mass spectrometry. Anal. Chem. 2006 78 8227-8235. [Pg.388]

I. Vikholm, W.M. Albers, H. Valimaki, and H. Helle, In situ quartz crystal microbalance monitoring of Fab-fragment binding to hnker lipids in a phosphatidylcholine monolayer matrix application to immunosensors. Thin Solid Films 327, 643-646 (1998). [Pg.278]

Carter, S., and Handy, N. C. (1987), A Method for the Determination of the Eigenvalues of a Very Large Matrix Application to Vibrational Energy Levels, Comput. Phys. Comm. 44, 1. [Pg.224]

Compound Matrix/ application Sample preparation Separation mode Detection method Comments Reference... [Pg.116]

The extracted compounds are collected into a vial that usually has in it a small volume of an organic collection solvent. The choice of collection solvent is important to ensure good recovery. Although there are many variables to consider when developing an extraction method by SFE, manufacturers of SFE instruments will provide information on the most appropriate conditions for a particular compound from a given matrix. Applications range from the extraction of fats and oils from foodstuffs to the... [Pg.114]

Hankin J, Barkley R, Murphy R (2007) Sublimation as a method of matrix application for mass spectrometric imaging. J Am Soc Mass Spectrom 18 1646-1652. doi 10.1016/j. lasms.2007.06.010... [Pg.421]

Detailed performance analysis of the OVPD device again revealed comparable or even slightly better device performance of the OVPD processed device compared with the VTE reference. Figure 9.13 shows the luminous efficiency of the PhOLEDs processed by OVPD and VTE. The OVPD-PhOLED reached 25 cd A-1 and the VTE device approximately 24 cd A-1, equivalent to a maximum external quantum efficiency of 7.0 + 0.1%, which is desirable for active matrix applications. Besides these comparable luminous efficiencies, the spectra differ slightly in their shape... [Pg.216]

Ying L, Edelman R (1986) A novel thermoplastic polyimide for composite matrix applications. 31st International SAMPE Symposium 1131... [Pg.103]

Omont, A. (1977). Irreducible components of the density matrix. Application to optical pumping, Progress in Quantum Electronics, 5, 69-138. [Pg.287]

No loss of reagents to environment, some added selectivity, operational in some added matrices, capable of element removal to low levels SC CO2 moves chelating agent through interstices of solid materials, recovery involves lowering pressure with loss of CO2, promising for solid matrix applications, CO2 is environmentally benign... [Pg.310]

Up until now, Raman spectra of matrix-isolated species have rarely been recorded, due to the low scattering cross-.section inherent to the technique. If the progress in FT-Raman spectroscopy which has been observed over the last years continues (Cutter, 1990), there will be a renaissance of matrix applications. [Pg.299]

The term solid-phase extraction was introduced by personnel of the J. T. Baker Company in 1982. The method consists of retention of the analytes from a liquid or gaseous sample to a solid stationary phase and subsequent removal of analytes using an appropriate eluent. The main purpose of SPE is isolation and preconcentration of compounds of interest or sample clean-up and simplification of the matrix. Application of this sample preparation technique also allows extract fractionation. As a result of significant reduction in the volume of organic solvents used, high recovery, and the possibility of process automation, SPE is a good alternative for conventional liquid-liquid extraction. According to their affinity for the compound of interest, stationary phases are classified as follows ... [Pg.126]

When constructing biosensors, which are to be used continuously in vivo or in situ, maintaining sensor efficiency while increasing sensor lifetime are major issues to be addressed. Researchers have attempted various methods to prevent enzyme inactivation and maintain a high density of redox mediators at the sensor surface. Use of hydrogels, sol-gel systems, PEI and carbon paste matrices to stabilize enzymes and redox polymers was mentioned in previous sections. Another alternative is to use conductive polymers such as polypyrrole [123-127], polythiophene [78,79] or polyaniline [128] to immobilize enzymes and mediators through either covalent bonding or entrapment in the polymer matrix. Application to various enzyme biosensors has been tested. [Pg.361]

For the off-diagonal contributions to the vibronic potential matrix, application of group theory gives ... [Pg.244]

Figure 2 shows pore-size distributiona of silico-aluminates having promise for FCC matrix application. For comparison purposes, the initial kaolinite is included. Modification of the kaolinite increases porosity, and, consequently, pore volume and surface area are increased. A bi-modal pore distribution is created, generating large fractions of pores in the 20 - 70 A and... [Pg.378]


See other pages where Matrix application is mentioned: [Pg.14]    [Pg.604]    [Pg.371]    [Pg.371]    [Pg.377]    [Pg.546]    [Pg.556]    [Pg.26]    [Pg.365]    [Pg.374]    [Pg.407]    [Pg.4]    [Pg.286]    [Pg.301]    [Pg.331]    [Pg.178]    [Pg.68]    [Pg.293]    [Pg.169]    [Pg.170]    [Pg.480]   
See also in sourсe #XX -- [ Pg.131 , Pg.132 , Pg.133 , Pg.134 , Pg.135 , Pg.136 , Pg.137 , Pg.138 , Pg.139 , Pg.140 , Pg.141 , Pg.142 , Pg.143 , Pg.144 , Pg.150 , Pg.155 , Pg.175 , Pg.178 , Pg.190 , Pg.289 , Pg.290 , Pg.291 , Pg.295 , Pg.353 , Pg.374 , Pg.388 , Pg.396 , Pg.398 , Pg.401 , Pg.411 , Pg.434 , Pg.438 , Pg.442 , Pg.447 , Pg.453 , Pg.456 , Pg.457 , Pg.466 , Pg.469 , Pg.472 , Pg.476 ]

See also in sourсe #XX -- [ Pg.537 ]




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