2012
DOI: 10.1016/j.jconrel.2012.07.041
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Bone repair: New developments in growth factor delivery systems and their mathematical modeling

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Cited by 53 publications
(30 citation statements)
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References 124 publications
(271 reference statements)
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“…20 Theoretical modeling Existing literatures offer various kinds of mathematical (analytical), computational (numerical), and theoretical models of drug release from polymeric microspheres. [21][22][23][24][25] With differ-ent transport phenomena, one can classify these into diffusion-, swelling-, and erosion-based models. 21,23 Because PLGA is a bulk erosion copolymer and its swelling phenomenon is not obvious, not all available models can be applied to PLGA-based drug delivery systems including swellingbased and surface erosion-based models.…”
Section: Theoretical and Computational Modelsmentioning
confidence: 99%
“…20 Theoretical modeling Existing literatures offer various kinds of mathematical (analytical), computational (numerical), and theoretical models of drug release from polymeric microspheres. [21][22][23][24][25] With differ-ent transport phenomena, one can classify these into diffusion-, swelling-, and erosion-based models. 21,23 Because PLGA is a bulk erosion copolymer and its swelling phenomenon is not obvious, not all available models can be applied to PLGA-based drug delivery systems including swellingbased and surface erosion-based models.…”
Section: Theoretical and Computational Modelsmentioning
confidence: 99%
“…rhBMP-2 helps to grow bones better than any other rhBMP; therefore, it is considerably more widely used clinically. BMPs could promote and accelerate the new bone formation and maturation in the implant-bone interface [53,54]. Therefore, the use of the exogenous BMP bone tissue may improve the local content and the activity of BMP, and improve the implant survival rate after radiotherapy.…”
Section: Strategies For Improving the Survival Rate Of Implants In Irmentioning
confidence: 99%
“…The KDF release from the hydrogels was studied by applying an affinity‐based kinetic model that considers the drug release as a result of a partitioning between the solvent phase and the hydrogel . The occurrence of the partition effect is determined by a α factor, called partition activity, and may be obtained by normalα=Fnormalmnormalanormalx1Fnormalmnormalanormalx where F max is the maximum fractional releases of the drug and α is defined as the ratio of the concentrations of solute between the solvent and the hydrogel phases.…”
Section: Resultsmentioning
confidence: 99%