Multifunction Mechanisms

Leonard SN, Rybak MJ Telavancin An antimicrobial with a multifunctional mechanism of action for the treatment of serious gram-positive infections. Pharmacotherapy 2008 28 458. [PMID 18363530]... 

Wei et al. studied the separation of amines (aniline, ephedrine, codeine, cocaine, thebaine) and quaternary ammonium compounds (berberine, jatrorrhi-zine) on a bare silica stationary phase [44], A thorough study of the separation mechanism revealed a complex multifunctional mechanism. Contributions from differential electrophoretic migration were superimposed on hydrophobic, cation-exchange, and normal-phase interactions. Retention was highly dependent on the pH (optimal pH 8.3), ionic strength, and the amount of organic modifier. As the content of acetonitrile exceeded 80%, retention was consistent with a normal-phase mechanism. 

Tumor-Speckle MAbs or Fragments. In recent years, MAbs have been identified as effective anticancer agents. Several MAbs have been approved for clinical uses since 1997, and many more are in clinical trials. MAbs are believed to have multifunctional mechanisms. Their high selectivity toward tumors makes them ideal targeting ligands for actively tumor-targeted drug delivery systems. 

The major factors limiting prosAeses to tools are practical ones due to the severe weight, power, and size constraints of hand/atm systems as well as the difficulty in finding a sufficient number of appropriate control sources to control the requisite number of degrees of freedom. Of these, it is the lack of independent control sources that imposes the most severe impediment to the development of today s prosthetic hand/atm systems. As a result, upper-limb prosthetics research is somewhat dominated by considerations of control. Still, the importance of better actuators and better multifunctional mechanisms must not be ignored. Control is useless if effective hand and arm mechatusms are not available. 

For prosthetic arms to be more than just position controllers for portable vices, multifunctional mechanisms that have the ability to have multiple degrees of freedom controlled simultaneously (in parallel) in a subconscious manner need to be developed. Current commercially available multifunctional controllers are generally sequential in nature and take the form of two site, three state multifunctional controllers. Motion Control, Inc., in the ProControl hand-wrist controller, uses rapid cocontraction of the forearm extensors and flexors to switch control between hand opening and closing to wrist rotation. Otto Bock uses a similar control strategy in its wrist-hand controller. Motion Control, Inc., in its elbow controller, uses dwell time (parking) to switch from elbow flexion and extension to hand opening and closure and cocontraction of biceps and triceps to switch control from the hand back to elbow. 

Comparing the above SPE method using P-CD polymer to Oasis FILE method [30] as a representative SPE method based on hydrophobic interaction, it was shown that in the case of the former, the extraction efficiency of polar steroids was higher. This new SPE method gives better selectivity and extraction efficiency than the conventionally used SPE methods based on hydrophobic interaction. These properties are due to the multifunctional mechanism derived from molecular inclusion and chemical interaction of the new SPE method. 

There are difficulties of detecting defects in axial canal because of solid sediment layer of 1. 2 mm thick on the canal surface. When using known defectoscope devices a preliminary labor-intensive mechanical treatment of the axial canal surface is needed. The experience of application of different methods of rotor axial canal control in multifunction automatic device ROTOR - K has pointed to the fact that the most effective method is eddy current one [1]. All the dangerous cracks were just detected by the eddy current method, the part of the cracks were not... 

Resin-modified glass—ionomer lining and restorative materials add a multifunctional acidic monomer to the poly(acryhc acid) [9003-01 Hquid component of the system. Once the glass powder and Hquid are mixed, setting can proceed by the acid—glass—ionomer reaction or the added monomer can be polymerized by a free-radical mechanism to rapidly fix the material in place (74,75). The cured material stiH retains the fluoride releasing capabiHties of a glass—ionomer. 

The (I)-(III)-samples sorption ability investigation for cationic dyes microamounts has shown that for DG the maximum rate of extraction is within 70-90 % at pH 3. The isotherm of S-type proves the physical character of solution process and a seeming ionic exchange. Maximal rate of F extraction for all samples was 40-60 % at pH 8 due to electrostatic forces. The anionic dyes have more significant affinity to surface researching Al Oj-samples comparatively with cationic. The forms of obtained soi ption isotherms atpH have mixed character of H,F-type chemosorption mechanism of fonuation of a primary monolayer with the further bilayers formation due to H-bonds and hydrophobic interactions. The different values of pH p for sorbents and dyes confirm their multifunctional character and distinctions in the acid-base properties of adsoi ption centers. 

It should be noted that many practically important catalytic transformations (such as isomerization of or hydrocracking of paraffins), which are presumed to proceed via consecutive mechanisms, are performed on multifunctional catalysts, with which the coupling of reactions in the sense just discussed may not necessarily occur. The problem of the selectivity of some models of polystep reactions on these catalysts has been discussed in detail by Weisz (56). 

The success of the multifunctional initiators in the preparation of block and graft copolymers depends critically on the kinetics and mechanism of radical production. In particular, the initiator efficiency, the susceptibility to and mechanism of transfer to initiator, and the relative stability of the various radical generating functions. Each of these factors has a substantial influence on the nature and homogeneity of the polymer formed. Features of the kinetics of polymerizations initiated by multifunctional initiators have been modeled by O Driscoll and Bevington 64 and Choi and Lei.265... 

As an organic polymer, poly(tetramethylene oxide) was also used for the preparation of ceramers. The mechanical properties in these cases were much improved in comparison with those for hybrids from polysiloxanes. In these poly (tetramethylene oxide)-silica hybrids, the effect of the number of functional triethoxysilyl groups was examined [13]. As shown in Fig. 2, more multifunctional organic polymer produced more crosslinked hybrid networks. This means that the more rigid the structure in the hybrids is, the higher the modulus and the lower swelling property. 

Recent demands for polymeric materials request them to be multifunctional and high performance. Therefore, the research and development of composite materials have become more important because single-polymeric materials can never satisfy such requests. Especially, nanocomposite materials where nanoscale fillers are incorporated with polymeric materials draw much more attention, which accelerates the development of evaluation techniques that have nanometer-scale resolution." To date, transmission electron microscopy (TEM) has been widely used for this purpose, while the technique never catches mechanical information of such materials in general. The realization of much-higher-performance materials requires the evaluation technique that enables us to investigate morphological and mechanical properties at the same time. AFM must be an appropriate candidate because it has almost comparable resolution with TEM. Furthermore, mechanical properties can be readily obtained by AFM due to the fact that the sharp probe tip attached to soft cantilever directly touches the surface of materials in question. Therefore, many of polymer researchers have started to use this novel technique." In this section, we introduce the results using the method described in Section 21.3.3 on CB-reinforced NR. 

In order to simplify the experimental problems involved in unravelling the mechanisms of UV protection by the piperidines, we have concentrated on the use of the simpler monopiperidine compounds. Although our findings are relevant to the photoprotection by the more complex multifunctional, commercial additives, some major differences may exist, and will be emphasized together with the very significant effects of the solid state on photo-stabilization. 

Additional reports of multifunctional kalihinols implicate a polar and stepwise biosynthetic cationic mechanism [21, 45]. 

Crosslinked polymer networks formed from multifunctional acrylates are completely insoluble. Consequently, solid-state nuclear magnetic resonance (NMR) spectroscopy becomes an attractive method to determine the degree of crosslinking of such polymers (1-4). Solid-state NMR spectroscopy has been used to study the homopolymerization kinetics of various diacrylates and to distinguish between constrained and unconstrained, or unreacted double bonds in polymers (5,6). Solid-state NMR techniques can also be used to determine the domain sizes of different polymer phases and to determine the presence of microgels within a poly multiacrylate sample (7). The results of solid-state NMR experiments have also been correlated to dynamic mechanical analysis measurements of the glass transition (1,8,9) of various polydiacrylates. 

In this paper, we report efforts to find donor/acceptor systems, comprised of at least one multifunctional monomer, capable of sustaining rapid free-radical polymerization without the need for external photoinitiators. Although we will include in this report comonomer systems which form ground state CT complexes, we stress that the primary mechanism for generating free-radical in each case may not be via excitation of ground state CT complexes. 

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