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Head stability

Quality Ten topic headings—Stability, Analytical Validation, Impurities, Pharmacopoeias, Quality of Biotechnological Products, Specifications, GMP, Pharmaceutical Development, Quality Risk Management, Pharmaceutical Quality System total of 24 guidelines... [Pg.223]

Propagation, or chain growth, takes place in a head-to-tail configuration as a result of resonance stabilization and steric factors by carbocation (M+) addition to another monomer molecule. The head stabilizes the cation best so it is the growing site while the least sterically... [Pg.137]

Head Stabilization outer protein addition or covalent crosslinks... [Pg.580]

While most vesicles are formed from double-tail amphiphiles such as lipids, they can also be made from some single chain fatty acids [73], surfactant-cosurfactant mixtures [71], and bola (two-headed) amphiphiles [74]. In addition to the more common spherical shells, tubular vesicles have been observed in DMPC-alcohol mixtures [70]. Polymerizable lipids allow photo- or chemical polymerization that can sometimes stabilize the vesicle [65] however, the structural change in the bilayer on polymerization can cause giant vesicles to bud into smaller shells [76]. Multivesicular liposomes are collections of hundreds of bilayer enclosed water-filled compartments that are suitable for localized drug delivery [77]. The structures of these water-in-water vesicles resemble those of foams (see Section XIV-7) with the polyhedral structure persisting down to molecular dimensions as shown in Fig. XV-11. [Pg.549]

The interest in vesicles as models for cell biomembranes has led to much work on the interactions within and between lipid layers. The primary contributions to vesicle stability and curvature include those familiar to us already, the electrostatic interactions between charged head groups (Chapter V) and the van der Waals interaction between layers (Chapter VI). An additional force due to thermal fluctuations in membranes produces a steric repulsion between membranes known as the Helfrich or undulation interaction. This force has been quantified by Sackmann and co-workers using reflection interference contrast microscopy to monitor vesicles weakly adhering to a solid substrate [78]. Membrane fluctuation forces may influence the interactions between proteins embedded in them [79]. Finally, in balance with these forces, bending elasticity helps determine shape transitions [80], interactions between inclusions [81], aggregation of membrane junctions [82], and unbinding of pinched membranes [83]. Specific interactions between membrane embedded receptors add an additional complication to biomembrane behavior. These have been stud-... [Pg.549]

Film stability is a primary concern for applications. LB films of photopoly-merizable polymeric amphiphiles can be made to crosslink under UV radiation to greatly enhance their thermal stability while retaining the ordered layered structure [178]. Low-molecular-weight perfluoropolyethers are important industrial lubricants for computer disk heads. These small polymers attached to a polar head form continuous films of uniform thickness on LB deposi-... [Pg.560]

All Group IV elements form both a monoxide, MO, and a dioxide, MO2. The stability of the monoxide increases with atomic weight of the Group IV elements from silicon to lead, and lead(II) oxide, PbO, is the most stable oxide of lead. The monoxide becomes more basic as the atomic mass of the Group IV elements increases, but no oxide in this Group is truly basic and even lead(II) oxide is amphoteric. Carbon monoxide has unusual properties and emphasises the different properties of the group head element and its compounds. [Pg.177]

For most vinyl polymers, head-to-tail addition is the dominant mode of addition. Variations from this generalization become more common for polymerizations which are carried out at higher temperatures. Head-to-head addition is also somewhat more abundant in the case of halogenated monomers such as vinyl chloride. The preponderance of head-to-tail additions is understood to arise from a combination of resonance and steric effects. In many cases the ionic or free-radical reaction center occurs at the substituted carbon due to the possibility of resonance stabilization or electron delocalization through the substituent group. Head-to-tail attachment is also sterically favored, since the substituent groups on successive repeat units are separated by a methylene... [Pg.23]

During the polymeriza tion process the normal head-to-tad free-radical reaction of vinyl chloride deviates from the normal path and results in sites of lower chemical stabiUty or defect sites along some of the polymer chains. These defect sites are small in number and are formed by autoxidation, chain termination, or chain-branching reactions. Heat stabilizer technology has grown from efforts to either chemically prevent or repair these defect sites. Partial stmctures (3—6) are typical of the defect sites found in PVC homopolymers (2—5). [Pg.544]

Some stabilizers or inhibitors require a certain oxygen concentration in the tank head space atmosphere in order to function. Where inerting is required, careful control is necessary to maintain this minimum oxygen concentration in inerting gas while still staying below the minimum oxygen concentration required for combustion. [Pg.107]

Tail rods are dummy rods that protrude from the head end of the cylinder (see Figure 3-9). The purpose of the rod is to pressure-balance a piston or to stabilize a particular piston design. Because of the personnel hazard, a guard must be specified and provided. In a tandem cylinder arrangement, the outboard cylinders are driven with a rod similar to the tail rod... [Pg.69]

Because of its hardness and ability to be electroplated, together with good dimensional stability, phenolic mouldings are used in the manufacture of golf ball heads for typewriters. [Pg.654]

The extent of head-to-head units in PVC and their effect on stability of the polymer is yet to be conclusively demonstrated, although it would seem that as compared to other structural defects their contribution to polymer instability is a minor one. [Pg.324]

Tray Stability with Varying Liquid Head, Air-Water System... [Pg.187]

Utilizing a forced-draft fan, the burner has a gas head arranged to mix the fuel and air in a blast tube which controls the stability and shape of the flame. Gas exits from nozzles or holes in the head and is mixed partly in the high-velocity air stream and partly allowed to exit into an area downstream of a bluff body. Behind the bluff body, a relatively quiescent zone forms which provides a means for flame stability. Many configurations exist, but the most... [Pg.375]

Most monomers have an asymmetric substitution pattern and the two ends of the double bond are distinct. For mono- and 1,1-disubstituted monomers (Section 4,3.1) it is usual to call the less substituted end "the tail" and the more substituted end "the head". Thus the terminology evolved for two modes of addition head and tail and for the three types of linkages hcad-to-tail, hcad-to-hcad and tail-to-ta.il. For 1,2-di-, tri- and tetrasubstituted monomers definitions of head and tail are necessarily more arbitrary. The term "head" has been used for that end with the most substituents, the largest substituents or the best radical stabilizing substituent (Scheme 4.4). [Pg.176]

NMR studies15 1 1 on polymers prepared with, 3C-labeled BPO have shown that the primary benzoyloxy and phenyl end groups formed by tail addition to monomer are thermally stable under conditions where the polymer degrades. They persist to > 50% weight loss at 300°C under nitrogen. Thus, these groups are unlikely to be directly responsible for the poor thermal stability of PS prepared with BPO as initiator. On the other hand, the secondary benzoate end groups, formed by head addition or transfer to initiator, appear extremely labile under these conditions. Their half life at 300°C is <5 min. [Pg.415]


See other pages where Head stability is mentioned: [Pg.819]    [Pg.819]    [Pg.819]    [Pg.819]    [Pg.2377]    [Pg.219]    [Pg.24]    [Pg.428]    [Pg.431]    [Pg.513]    [Pg.149]    [Pg.167]    [Pg.289]    [Pg.189]    [Pg.441]    [Pg.534]    [Pg.534]    [Pg.2219]    [Pg.32]    [Pg.257]    [Pg.80]    [Pg.642]    [Pg.716]    [Pg.352]    [Pg.226]    [Pg.40]    [Pg.545]    [Pg.62]    [Pg.498]    [Pg.555]    [Pg.7]    [Pg.100]    [Pg.275]    [Pg.434]    [Pg.795]   


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