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Polyhydroxy valerate

Aliphatic polyesters based on monomers other than a-hydroxyalkanoic acids have also been developed and evaluated as drug delivery matrices. These include the polyhydroxybutyrate and polyhydroxy valerate homo- and copolymers developed by Imperial Chemical Industries (ICI) from a fermentation process and the polycaprolactones extensively studied by Pitt and Schindler (14,15). The homopolymers in these series of aliphatic polyesters are hydrophobic and crystalline in structure. Because of these properties, these polyesters normally have long degradation times in vivo of 1-2 years. However, the use of copolymers and in the case of polycaprolactone even polymer blends have led to materials with useful degradation times as a result of changes in the crystallinity and hydrophobicity of these polymers. An even larger family of polymers based upon hydroxyaliphatic acids has recently been prepared by bacteria fermentation processes, and it is anticipated that some of these materials may be evaluated for drug delivery as soon as they become commercially available. [Pg.24]

The two most common PHAs are polyhydroxybutyrate (PHB) and a copolymer of polyhy-droxybutyrate and polyhydroxy valerate (PHBV). PHAs can be used as films, fibers, and coatings for hot beverage cups made of paper. [Pg.1168]

Ahmed, T., Margal, H., Lawless, M., Wanandy, N. S., Chiu, A., Foster, L. J. R., Polyhydroxybutyrate and its copolymer with polyhydroxy-valerate as biomaterials Influence on progression of stem cell cycle. Binmocromoip.cuip.s. 10, 2707-2715 (2010), DOl 10.1021/ bml007579. [Pg.922]

The simplest PHA is polyhydroxybutyrate (PHB), whose formula is shown in Fig. 22.1. This polymer and its copolymer with polyhydroxy valerate seem to be, at present, the only PHAs relevant for practical applications. [Pg.451]

Higher molecular weight PHB and its copolymers with poly(3-hydroxy-valerate) (PHV) can be synthesized from racemic P-butyrolactone and P Valerolactone, using an oligomeric alumoxane catalyst. These polyesters, with only partial stereoregularity, are less susceptible to enzymatic degradation than the bacterial ones. Polyhydroxy-butyrate-valerate (PHBV) is produced by Monsanto as Biopol . [Pg.1155]

Bacterial polyesters (polyhydroxy alkanoates) Poly(3-hydroxy butyrate), poly(3-hydroxy valerate) Some micro-organisms, especially bacteria, can synthesise biocompatible aliphatic polyesters, which have potential in medical applications. [Pg.79]

Comparisons of thermal properties of polymer before and after reinforcement with multiwalled carbon nanotubes have also been reported for polyhydroxy butyrate-co-hydroxy valerate [52] and polycaprolactomy composites [55],... [Pg.158]

Otari SV, Ghosh JS. Production and characterization of the polymer polyhydroxy butyrate-copolyhydroxy valerate by Bacillus megaterium NCIM 2475. Curr Res J Biol Sci 2009 1 23-6. [Pg.602]

FIGURE 16 Representative melting and glass transition temperatures of bio and fossil based polymers (PCL-Str - Polycaprolactone/Starch blends, PC - Polycaprolactone, mcPHA - medium chain Polyhydroxyalkanoates, Ali-coPES - Aliphatic (co)Polyesters, PUBAf -Polyhydroxy Butyrate/valerate, and PEA - Polyester Amides). [Pg.142]

Some specific recent applications of the GC-MS technique to various types of polymers include the following PE [49,50], poly(l-octene) [51], poly(l-decene) [51], poly(l-dodecene) [51], 1-octene-l-decene-l-dodecene terpolymer [51], chlorinated polyethylene [52], polyolefins [53, 54], acrylic acid methacrylic acid copolymers [55], polyacrylates [56], styrene-butadiene and other rubbers [57-59], nitrile rubber [60], natural rubbers [61, 62], chlorinated natural rubber [63, 64], polychloroprene [65], PVC [66-68], silicones [69, 70], polycarbonates [71], styrene-isoprene copolymers [72], substituted PS [73], polypropylene carbonate [74], ethylene-vinyl acetate copolymers [75], Nylon [76], polyisopropenyl cyclohexane a-methyl styrene copolymers [77], m-cresol-novolac epoxy resins [78], polymeric flame retardants [79], poly(4-N-alkyl styrenes) [80], polyvinyl pyrrolidone [81], vinyl pyrrolidone-methyl acryloxysilicone copolymers [82], polybutylcyanoacrylate [83], polysulfide copolymers [84], poly(diethyl-2-methacryloxy)ethyl phosphate [85], ethane-carbon monoxide copolymers [86], polyetherimide [87], bisphenol A [88], ethyl styrene [89], styrene-isoprene block copolymer [89], polyvinyl alcohol-co-vinyl acetate [90], epoxide thiol [91], maleic acid-propylene copolymer [92], P-hydroxy butyrate-P-hydroxy valerate copolymer [93], polycaprolactams [39,94], PS [95,96], polypyrrole [95,96], polyhydroxy alkanoates [97], poly(p-chloromethyl) styrene [81], polybenzooxazines and siloxy substituted polyoxadisila-pentanylenes [98,99] poly benzyl methacrylates [100], polyolefin blends after ageing in soil [101] and polystyrene peroxide [43]. [Pg.150]


See other pages where Polyhydroxy valerate is mentioned: [Pg.195]    [Pg.652]    [Pg.389]    [Pg.505]    [Pg.593]    [Pg.873]    [Pg.195]    [Pg.448]    [Pg.195]    [Pg.652]    [Pg.389]    [Pg.505]    [Pg.593]    [Pg.873]    [Pg.195]    [Pg.448]    [Pg.70]    [Pg.264]    [Pg.67]   
See also in sourсe #XX -- [ Pg.156 ]




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