Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/17052
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dc.titleIn Vitro and In Vivo Evaluation of Customized Polycaprolactone Tricalcium Phosphate Scaffolds for Bone Tissue Engineering
dc.contributor.authorERVI SJU
dc.date.accessioned2010-05-13T19:29:16Z
dc.date.available2010-05-13T19:29:16Z
dc.date.issued2010-01-21
dc.identifier.citationERVI SJU (2010-01-21). In Vitro and In Vivo Evaluation of Customized Polycaprolactone Tricalcium Phosphate Scaffolds for Bone Tissue Engineering. ScholarBank@NUS Repository.
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/17052
dc.description.abstractDegradation studies of scaffolds play an important role in bone tissue engineering. After initially being subjected to hydrolytic and enzymatic treatment, the degradation kinetics of untreated, sodium hydroxide-treated, and lipase-treated polycaprolactone-20% tricalcium phosphate (PCL-TCP) scaffolds at similar porosity (85%) were conducted in vitro when immersed in culture medium, and in vivo when implanted in the subcutaneous back of rats for up to 24 weeks. At selected time points, samples were retrieved and characterized. Histology was also performed for the in vivo group. Overall the results demonstrated that the NaOH-treated scaffolds achieved the most favorable mechanical properties when higher porosity values were targeted. PCL-TCP scaffolds and sheets were then further studied in a micropig mandibular defect model and analyzed for up to 6 months. Greater bone formation was detected in defect sites augmented with autografts and collagen membranes as compared to PCL-TCP scaffolds which were about 64% efficient.
dc.language.isoen
dc.subjectScaffold; polycaprolactone; tri-calcium phosphate; degradation; bone; surface modification
dc.typeThesis
dc.contributor.departmentMECHANICAL ENGINEERING
dc.contributor.supervisorTEOH SWEE HIN
dc.contributor.supervisorYEO BOON KENG, ALVIN
dc.description.degreeMaster's
dc.description.degreeconferredMASTER OF ENGINEERING
dc.identifier.isiutNOT_IN_WOS
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