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Polyglycolides

Hollinger JO. Preliminary report on the osteogenic potential of a biodegradable copolymer of polyactide (PLA) and polyglycolide (PGA). J Biomed Mater Res, 1983, 17, 71-82. [Pg.249]

Occasionally in the synthesis of the copolymers, insoluble material is produced. This results from polymer containing blocks of polyglycolide rather than the desired random structure. Obviously, such compositions would have considerable effect on the performance of controlled release formulations utilizing those polymers. This problem is particularly evident when one is seeking to utilize the 50 50 glycolide/lactide copolymer as a biodegradable excipient. However, with carefully controlled polymerization conditions, useful 50 50 polymer is readily produced. [Pg.4]

Various studies have been made on the effects of radiation on lactide/glycolide polymers (24,38,58). Gilding and Reed (24) reported the effect of y rays on Dexon sutures. Those results confirmed that deterioration of the sutures occurs but that random chain scission is not the primary mechanism. Number average-molecular weight Mn showed a dramatic decrease at doses above 1.0 Mrad. Thus, unzipping of the polymer chain appeared to be the more dominant process, at least in the case of polyglycolide. [Pg.13]

The use of polylactides for delivery of insect hormone analogs and other veterinary compounds (115,116) has been studied. Microspheres, pellets, and reservoir devices based on polyglycolide, poly-(DL-Iactide), poly(L-lactide), and various copolymers have been used to deliver methoprene and a number of juvenile hormone analogs. ... [Pg.24]

Bioerodible polymers offer a unique combination of properties that can be tailored to suit nearly any controlled drug delivery application. By far the most common bioerodible polymers employed for biomedical applications are polyesters and polyethers (e.g., polyethylene glycol), polylactide, polyglycolide and their copolymers). These polymers are biocompatible, have good mechanical properties, and have been used in... [Pg.169]

An interesting legal case ensued in the English High Court [87], where Ethicon (Johnson Johnson) maintained, among other things, that the formation and hydrolytic behaviour of polyglycolide fibres were already known and that it was therefore obvious to use the material as an absorbable suture. The outcome was basically favourable to American Cyanamid. [Pg.22]

Meanwhile Ethicon (and others) developed alternative absorbable surgical sutures, based, for example, on copolymers of polyglycolide with poly-L-lactide or poly(trimethylene carbonate), and on polydioxanone, and on poly(e-oxycaproate), and also on copolymers of these with polyglycolide or with each other. These different structures made it possible to provide fibres with different rates of absorption, with different degrees of stiffness or flexibility, and for use in monofilaments, braided multifilaments, and other yam structures, as required for different surgical operations. [Pg.23]

Recent Developments in Metal-Catalyzed Ring-Opening Polymerization of Lactides and Glycolides Preparation of Poly lactides, Polyglycolide, and Poly(lactide-co-glycolide)... [Pg.219]

True solid-state reactions without liquids are exothermically obtained upon heating of halogenoacetate salts (212) to 100-200 °C. Quantitative yields of polyglycolide matrices (213) with cubic holes after washing with water (when the MX dissolved away) were obtained [93] (Scheme 27). [Pg.132]

Keywords chlorocarboxylic acid, oligomerization, polymerization, polyglycolide... [Pg.308]

Polyglycolide was one of the first synthetic polymers used as a degradable surgical suture [122]. Fig. 8 shows the glycolide monomer and polymer structures. This aliphatic polyester is biodegradable and exhibits negligible toxicity when implanted in tissue. It is also possible to fabricate a strong fiber of this polyester with satisfactory mechanical properties. [Pg.59]

Studies using polyglycolide-made sutures have shown that the material loses half of its strength after two weeks and 100% after four weeks. The polymer is completely reabsorbed by the organism within four to six months. [Pg.137]


See other pages where Polyglycolides is mentioned: [Pg.785]    [Pg.785]    [Pg.191]    [Pg.296]    [Pg.228]    [Pg.8]    [Pg.234]    [Pg.65]    [Pg.67]    [Pg.69]    [Pg.22]    [Pg.140]    [Pg.163]    [Pg.168]    [Pg.785]    [Pg.785]    [Pg.308]    [Pg.308]    [Pg.224]    [Pg.274]    [Pg.420]    [Pg.59]    [Pg.433]    [Pg.42]    [Pg.58]    [Pg.59]    [Pg.67]    [Pg.80]    [Pg.114]    [Pg.136]    [Pg.137]    [Pg.137]    [Pg.201]   
See also in sourсe #XX -- [ Pg.168 ]

See also in sourсe #XX -- [ Pg.351 ]

See also in sourсe #XX -- [ Pg.168 ]

See also in sourсe #XX -- [ Pg.152 ]




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Glycolic acids and polyglycolides

Poly polyglycolide copolymers

Polyglycolide

Polyglycolide microspheres

Polyglycolide synthetic polymers

Polyglycolide-<?0-caprolactone

Polyglycolide-<?0-caprolactone polymers

Polyglycolide-lactide

Polyglycolides (PGA)

Polyglycolides and polylactides

Polyglycolides block copolymers

Polylactide/polyglycolide

Polylactide/polyglycolide polymers

Polymer blends polyglycolide

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