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31.
Cheng-Chun Peng Colin Cerretani Richard J. Braun C.J. Radke 《Advances in colloid and interface science》2014
Tear-film instability is widely believed to be a signature of eye health. When an interblink is prolonged, randomly distributed ruptures occur in the tear film. “Black spots” and/or “black streaks” appear in 15 to 40 s for normal individuals. For people who suffer from dry eye, tear-film breakup time (BUT) is typically less than a few seconds. To date, however, there is no satisfactory quantitative explanation for the origin of tear rupture. 相似文献
32.
Cross-coupling reaction of N-t-Boc-4-iodo-L-phenylalanine with t-BuSH proceeded efficiently in the presence of Pd2dba3.CHCl3/DPPF as the catalyst system. However, Pd2dba3.CHCl3/DPPB was found to be more effective for coupling with t-BuSNa. 相似文献
33.
placement of a soft contact lens onto the cornea, the upper eyelid deforms and settles the lens by squeezing fluid out of the post-lens tear film or POLTF (i.e., the tear fluid layer sandwiched between the lens and the cornea). This paper studies the physical mechanisms that control the dynamic state of the contact lens during blinking, i.e., its shape and its distance from the cornea, especially a long time after insertion. We model the lens as a deformable elastic shell and the cornea as a flat nondeformable body. The tear fluid is assumed to be Newtonian, and the lens is characterized by an elastic modulus and a Poisson ratio. Lubrication equations under creeping flow are used to solve the fluid problem, while the thin-shell approximation is applied to the solid lens. The solid and fluid mechanics problems are coupled by maintaining continuity of stress and velocity at the solid/liquid interface. Lid applied pressure causes the lens to approach the cornea by squeezing tear fluid out and also leads to the deformation of the lens. Subsequently, in the interblink period, since there is no applied force, the elastic energy stored in the lens due to its deformation is released causing it to move away from the cornea by imbibing tear fluid into the POLTF. If the POLTF thickness is large, the inward motion of the lens in the blink is more than the outward motion during interblink, and this causes the lens to settle closer to the cornea. Eventually, there may be a balance of the inward motion during the blink and the outward motion during the interblink. If so, the lens subsequently exhibits periodic steady-state motion. However, it is also possible that a balance of inward and outward motion is never achieved, and the lens continues to settle endlessly. If this happens, then the thinfilm interactions between the mucin-covered corneal surface and the lens material determine whether the lens actually touches the cornea and possibly adheres. Our elastohydrodynamic analysis serves as a useful tool to elucidate the effects of various lens parameters on the final settled state of the lens. In particular, we are concerned about eventual adherence and/or mechanical abrasion to the cornea, which is very important to the ocular health of soft contact lens wearers. 相似文献
34.
A new model describing the retention in temperature gradient interaction chromatography of polymers is developed. The model predicts that polymers might elute in temperature gradient interaction chromatography in either an increasing or decreasing order or even nearly independent of molar mass, depending on the rate of the temperature increase relative to the flow rate. This is in contrast to solvent gradient elution, where polymers elute either in order of increasing molar mass or molar mass independent. The predictions of the newly developed model were verified with the literature data as well as new experimental data. 相似文献
35.
Roshmi Thomas Aswathi P. Nair Soumya KR Jyothis Mathew Radhakrishnan EK 《Applied biochemistry and biotechnology》2014,173(2):449-460
Silver nanoparticles form promising template for designing antimicrobial agents against drug resistant pathogenic microorganisms. Thus, the development of a reliable green approach for the synthesis of nanoparticles is an important aspect of current nanotechnology research. In the present investigation, silver nanoparticles synthesized by a soil Bacillus sp. were characterized using UV–vis spectroscopy, FTIR, SEM, and EDS. The antibacterial potential of biosynthesized silver nanoparticles, standard antibiotics, and their conjugates were evaluated against multidrug-resistant biofilm-forming coagulase-negative S. epidermidis strains, S. aureus, Salmonella Typhi, Salmonella Paratyphi, and V. cholerae. Interestingly, silver nanoparticles (AgNPs) showed remarkable antibacterial activity against all the test strains with the highest activity against S. epidermidis strains 145 and 152. In addition, the highest synergistic effect of AgNPs was observed with chloramphenicol against Salmonella typhi. The results of the study clearly indicate the promising biomedical applications of biosynthesized AgNPs. 相似文献
36.
Tran VB Sung YS Fleiszig SM Evans DJ Radke CJ 《Journal of colloid and interface science》2011,362(1):58-66
Binding of bacteria to solid surfaces is complex with many aspects incompletely understood. We investigate Pseudomonas aeruginosa uptake kinetics onto hydrogel surfaces representative of soft-contact lenses made of nonionic poly(2-hydroxyethylmethacrylate) (p-HEMA), anionic poly(methacrylic acid) (p-MAA), and anionic poly(acrylic acid) (p-AA). Using a parallel-plate flow cell under phase-contrast microscopy, we document a kinetic "burst" at the anionic hydrogel surface: dilute aqueous P. aeruginosa first rapidly accumulates and then rapidly depletes. Upon continuing flow, divalent cations in the suspending solution sorb into the hydrogel network causing the previously surface-accumulated bacteria to desorb. The number of bacteria eventually bound to the surface is low compared to the nonionic p-HEMA hydrogel. We propose that the kinetic burst is due to reversible divalent-cation bridging between the anionic bacteria and the negatively charged hydrogel surface. The number of surface bridging sites diminishes as divalent cations impregnate into and collapse the gel. P. aeruginosa association with the surface then falls. Low eventual binding of P. aeruginosa to the anionic hydrogel is ascribed to increased surface hydrophilicity compared to the counterpart nonionic p-HEMA hydrogel. 相似文献
37.
A gradient ranging from methanol to tetrahydrofuran (THF) was applied to a series of poly(methyl methacrylate) (PMMA) standards, using the recently developed concept of SEC-gradients. Contrasting to conventional gradients the samples eluted before the solvent, i.e. within the elution range typical for separations by SEC, however, the high molar mass PMMAs were retarded as compared to experiments on the same column using pure THF as the eluent. The molar mass dependence on retention volume showed a complex behaviour with a nearly molar mass independent elution for high molar masses. This molar mass dependence was explained in terms of solubility and size exclusion effects. The solubility based SEC-gradient was proven to be useful to separate PMMA and poly(n-butyl crylate) (PnBuA) from a poly(t-butyl crylate) (PtBuA) sample. These samples could be separated neither by SEC in THF, due to their very similar hydrodynamic volumes, nor by an SEC-gradient at adsorbing conditions, due to a too low selectivity. The example shows that SEC-gradients can be applied not only in adsorption/desorption mode, but also in precipitation/dissolution mode without risking blocking capillaries or breakthrough peaks. Thus, the new approach is a valuable alternative to conventional gradient chromatography. 相似文献
38.
39.
Leonhard K Prausnitz JM Radke CJ 《Langmuir : the ACS journal of surfaces and colloids》2006,22(7):3265-3272
Lattice Monte Carlo simulations describe the adsorption of protein-like heteropolymer chains at an oil/water interface. The heteropolymers are designed sequences of 27 and 64 amino acid-type lattice sites taken from a 20-letter alphabet. We use our recently suggested energy scale to model oil and water. We investigate the effect of the oil parameters on adsorption properties of a single chain and on the aggregation of adsorbed chains while keeping the water parameters fixed to their optimum values found previously. By varying the oil parameters, we can cause a large range of adsorption behavior: from no adsorption to reversible adsorption to irreversible adsorption. We compare adsorption at a liquid/solid interface to that at a liquid/liquid interface. A liquid interface leads to stronger adsorption and denaturation than a solid interface with the same water and oil interaction parameters. We propose "optimal" oil parameters and use them to study multichain adsorption at a liquid interface. 相似文献
40.