Please use this identifier to cite or link to this item: https://doi.org/10.1002/bit.20538
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dc.titleSimulation of gentamicin delivery for the local treatment of osteomyelitis
dc.contributor.authorLee, C.G.
dc.contributor.authorFu, Y.-C.
dc.contributor.authorWang, C.-H.
dc.date.accessioned2014-06-17T07:49:00Z
dc.date.available2014-06-17T07:49:00Z
dc.date.issued2005-09-05
dc.identifier.citationLee, C.G., Fu, Y.-C., Wang, C.-H. (2005-09-05). Simulation of gentamicin delivery for the local treatment of osteomyelitis. Biotechnology and Bioengineering 91 (5) : 622-635. ScholarBank@NUS Repository. https://doi.org/10.1002/bit.20538
dc.identifier.issn00063592
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/64590
dc.description.abstractIn order to understand the effect of antibiotics delivery to bone tissue, by biodegradable polymeric drug disc, for the treatment of osteomyelitis, a three-dimensional simulation model is developed. The simulation investigates the effect of pressure-induced convection on drug distribution, by taking into account the pressure gradient that exists between capillaries and interstitial space, and also as a result of the surgical opening. The clotting process at the surgical opening is incorporated into the simulation, and the effect of clotting duration is investigated. The clotting duration for the baseline simulation is 2 days and it is observed that increasing this duration depresses the mean drug concentration in the marrow and cortical bone. The effect of double burst release profile is also studied and it is observed that drug concentration drops too rapidly after the first burst to provide any therapeutic effect. However, it is shown that the drug concentration after the second burst stays above the minimum inhibitory concentration of the bacteria for a longer period of time, than would have been observed for a mono-burst release. Inserting non-biodegradable polymethylmethacrylate (PMMA) beads into bone seems to cause a higher average concentration of drug in the marrow. However, this could be brought about by the difference in the geometry between the disc and the bead, and the amount of drug packed in each bead. Further simulations on the management of dead space shows the ineffectiveness of having the void filled up with surgical gel as it becomes an additional barrier to drug delivery to the infected tissues. © 2005 Wiley Periodicals, Inc.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/bit.20538
dc.sourceScopus
dc.subjectComputer simulation
dc.subjectDrug delivery
dc.subjectGentamicin
dc.subjectOsteomyelitis
dc.typeArticle
dc.contributor.departmentCHEMICAL & BIOMOLECULAR ENGINEERING
dc.description.doi10.1002/bit.20538
dc.description.sourcetitleBiotechnology and Bioengineering
dc.description.volume91
dc.description.issue5
dc.description.page622-635
dc.description.codenBIBIA
dc.identifier.isiut000231523600010
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