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1.
Thomas R. Gengenbach Zoran R. Vasic Sheng Li Ronald C. Chatelier Hans J. Griesser 《Plasmas and Polymers》1997,2(2):91-114
The properties and composition of plasma polymer surfaces stored in air can change considerably over time, especially as a
result of oxidative reactions. When plasma polymers contain an element other than O, it is possible to probe for mechanisms
in addition to oxidation that contribute to the aging of the surface. Plasma polymers containing N were fabricated from either
1,3-diaminopropane (DAP),n-heptylamine (nHA), or allylamine (AA), and studied by X-ray photo-electron spectroscopy (XPS) and air/water contact angles
(CA). For each of the plasma polymers, a multiexponential increase in the O/C ratio was observed over time using XPS. The
N/C ratios remained constant (AA) or decreased somewhat (nHA and DAP). In contrast, the trends in CA values differed, declining
for the nHA surfaces, rising for the AA, and changing little for the DAP. Surface roughness, assessed by scanning tunnelling
or atomic force microscopy, did not change over time. The diverse adjustments in the polarity of each surface and the similar
compositional changes between them are reconcilable if the aging of the plasma polymer surface is a manifestation of the superposition
of concurrent oxidative reactions and partial surface reorientation; the former introduce polar groups and the latter transports
then from the surface to deeper regions beyond the CA probe depth but within the XPS analysis depth. These processes vary
between different plasma polymers. Data for the alkylamine plasma polymers is also compared with that for two plasma polymers
fabricated from methanol. The change in composition, but not polarity, of the DAP surface after 4 days of storage demonstrates
the importance of using multiple techniques to characterize the aging of plasma polymer surfaces. 相似文献
2.
A method of analysing steady-state fluorescence quenching in compartmentalized systems is proposed which allows the evaluation of partition and binding constants where both association processes occur simultaneosly. The number of binding sites is shown to be dependent on the nature of the quencher. 相似文献
3.
Method of immobilization of carboxymethyl-dextran affects resistance to tissue and cell colonization 总被引:1,自引:0,他引:1
McLean KM Johnson G Chatelier RC Beumer GJ Steele JG Griesser HJ 《Colloids and surfaces. B, Biointerfaces》2000,18(3-4):221-234
Coatings from carboxymethylated dextrans (CMDs) were fabricated, analyzed by XPS, and investigated for their ability to inhibit corneal epithelial tissue outgrowth and bovine corneal epithelial cell attachment and growth. CMDs with differing degrees of carboxymethyl substitution and various molecular weights were synthesized by the solution reaction of dextrans with bromoacetic acid under different reactant ratios. The CMD compounds thus obtained were attached onto aminated surfaces produced in two ways: by the plasma deposition of a coating from n-heptylamine vapour, and by the plasma deposition of an acetaldehyde coating onto whose surface aldehyde groups the polyamine compounds polylysine, polyethyleneimine and polyallylamine were immobilized to provide platforms for CMD immobilization. XPS spectra showed that the latter route produced thicker coatings than the former approach. CMD molecules attached directly onto the plasma-fabricated amine surface supported some tissue migration; the extent of carboxymethyl substitution and the molecular weight of the CMDs had little influence. For CMDs immobilized via polyamine spacers, on the other hand, tissue outgrowth was completely inhibited, and again there were no discernible effects from the extent of carboxymethyl substitution and the molecular weight of the CMDs. In assays involving cell attachment and growth, analogous observations were found. Thus, the mode of immobilization of these polysaccharide coatings is the dominant factor in their anti-fouling performance, suggesting that optimization of the architecture of polysaccharide coatings may be an important factor for maximizing their cell-repellent abilities. 相似文献
4.
R Bonfiglio RC King TV Olah K Merkle 《Rapid communications in mass spectrometry : RCM》1999,13(12):1175-1185
A post-column infusion system was developed in order to analyze suppression of electrospray ionization (ESI) tandem mass spectrometry response in the presence of endogenous plasma interferences. By enabling direct detection of these interfering components, this experimental system was used to analyze the ability of several common extraction procedures to remove endogenous plasma components that cause changes in the ESI response of model drug substances. Methyl-t-butyl ether (MTBE) liquid-liquid, Oasis and Empore solid-phase, and acetonitrile (ACN) protein precipitation sample preparation methods were tested using the post-column infusion system. In all cases, ACN protein precipitation samples showed the greatest amount of ESI response suppression while liquid-liquid extracts demonstrated the least. In addition, the three test compounds, phenacetin, caffeine, and a representative Merck compound, demonstrated that ESI response suppression is compound dependent. Suppression was greatest with caffeine, the most polar analyte, and the smallest for the Merck compound, the least polar analyte. Copyright 1999 John Wiley & Sons, Ltd. 相似文献
5.
Samit Mandal J Gerl H Geissel K Hauschild M Hellström Z Janas I Kojouharov Y Kopatch RC Lemmon P Mayet Z Podolyak PH Regan H Schaffner C Schlegel J Simpson HJ Wollersheim 《Pramana》2001,57(1):161-164
Feasibility of gamma-ray spectroscopy at relativistic energies with exotic heavy-ions and new generation of germanium detectors
(segmented Clover) is discussed. An experiment with such detector array and radioactive is discussed. 相似文献
6.
7.
We report measurements of non-linear charge transport in epitaxial (La1−x
Pr
x
)0.7Ca0.3MnO3 thin films fabricated on (100) oriented SrTiO3 single crystals by pulsed laser deposition. The end members of this series, namely Pr0.7Ca0.3MnO3 and La0.7Ca0.3MnO3 are canonical charge-ordered (CO) and ferromagnetic manganites, respectively. The onset of the CO state in Pr0.7Ca0.3MnO3 is manifested by a pronounced insulating behavior below ∼ 200 K. The CO state remains stable even when a large (∼ 2×105 V/cm) electric field is applied across the thin film samples. However, on substitution of Pr with La, a crossover from the
highly resistive CO state to a state of metallic character is observed at relatively low electric fields. The current-voltage
characteristics of the samples at low temperatures show hysteretic and history dependent effects. The electric field driven
charge transport in the system is modelled on the basis of an inhomogeneous medium consisting of ferromagnetic metallic clusters
dispersed in a CO background. 相似文献
8.
Thomas R. Gengenbach Zoran R. Vasic Ronald C. Chatelier Hans J. Griesser 《Plasmas and Polymers》1996,1(3):207-228
Angle-dependent XPS and air/water contact angle (CA) measurements were performed on specimens of n-hexane plasma polymers
at various times after fabrication in order to monitor the aging of the surfaces in contact with air. XPS revealed incorporation
of oxygen over extended periods of time. The depth distribution of O changed in the course of aging. CAs decreased over the
first 3 weeks, then increased again, and finally stabilized at 5 weeks. These results were interpreted in terms of two concurrent
processes: spontaneous oxidation (initiated by trapped radicals), which increased the surface polarity, and surface restructuring,
which caused the partial removal of polar groups from the interface with air. The former process made a larger contribution
to the overall aging of the surfaces but the latter process also contributed measurably. Over the first 3 weeks, oxidation
was rapid and surface restructuring was not competitive. Subsequently, the oxygen uptake slowed down markedly, and the outermost
surface layers became oxygen depleted relative to the deeper layers, due to partial surface reorientation. The surface topography,
assessed by STM, did not change on aging. The aging of n-hexane plasma polymer surfaces thus is due to superimposed effects
arising from post-deposition oxidative processes and partial surface reorientation. 相似文献
9.
10.
H. Kahle M. Nikiel A. Tian M. Trautz Elisabeth Triebel E. H. Riesenfeld T. Hamburger Doemens H. C. Parker Elisabeth W. Parker H. Le Chatelier F. Bogitch A. Damiens A. W. Francis E. P. Oxnard S. E. Berkenblit A. Hutchinson R. Ruer und J. Kuschmann 《Fresenius' Journal of Analytical Chemistry》1930,82(1-3):70-76
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