2000
DOI: 10.1016/s0168-3659(99)00268-0
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Active growth factor delivery from poly(d,l-lactide-co-glycolide) foams prepared in supercritical CO2

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Cited by 191 publications
(111 citation statements)
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“…Natural materials include gelatin [31,32], collagen [33], fibrin [34], heparin [35] and alginate. [36] Synthetic matrices have been generated from poly(ethylene glycol)-g-poly(lactic acid) [37], poly(lactic acid) [38], poly(lactic-co-glycolic acid) [39,40], and methylidene malonate polymers. [41] From a mechanical perspective, these scaffolds have ranged from relatively weak materials (e.g.…”
Section: Discussionmentioning
confidence: 99%
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“…Natural materials include gelatin [31,32], collagen [33], fibrin [34], heparin [35] and alginate. [36] Synthetic matrices have been generated from poly(ethylene glycol)-g-poly(lactic acid) [37], poly(lactic acid) [38], poly(lactic-co-glycolic acid) [39,40], and methylidene malonate polymers. [41] From a mechanical perspective, these scaffolds have ranged from relatively weak materials (e.g.…”
Section: Discussionmentioning
confidence: 99%
“…A bFGF loaded PLGA scaffold fabricated using supercritical CO 2 exhibited 45% initial burst release in one day. [39,40] The release of bFGF from methylidene malonate polymer films had over 30% initial burst release in the first day. [41] In both of these studies the bioactivity of the released bFGF was verified with cellular mitogenicity assays similar to those employed in this study.…”
Section: Discussionmentioning
confidence: 99%
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“…These methods can achieve certain slow release characteristics, but the control over release kinetics is limited. The gas foaming process can entrap PLGA microspheres in a porous scaffold [138,139]. In addition to the lack of control over pore size and shape, the release kinetics of imbedded microspheres in the matrix walls are uncontrollably changed from that by the microspheres.…”
Section: Bioactive Molecule Deliverymentioning
confidence: 99%
“…Moreover, open frames are designed with defined parameters to improve the osteoconductivity, such as porosity, pore size, and connectivity, as well as enhanced mechanical properties [3]. Furthermore, this technique allows producing biocompatible samples without the use of potentially toxic organic solvents [4,5]. These structures were recently tested in vivo for host tissue induced reactions as well as for their osteoconductive properties [6].…”
Section: Introductionmentioning
confidence: 99%