Please use this identifier to cite or link to this item:
DC FieldValue
dc.titleDistinctive degradation behaviors of electrospun polyglycolide, poly(dl-Lactide-co-Glycolide), and poly(l-Lactide-co-E-Caprolactone) nanofibers cultured with/without porcine smooth muscle cells
dc.contributor.authorDong, Y.
dc.contributor.authorYong, T.
dc.contributor.authorLiao, S.
dc.contributor.authorChan, C.K.
dc.contributor.authorStevens, M.M.
dc.contributor.authorRamakrishna, S.
dc.identifier.citationDong, Y., Yong, T., Liao, S., Chan, C.K., Stevens, M.M., Ramakrishna, S. (2010-01-01). Distinctive degradation behaviors of electrospun polyglycolide, poly(dl-Lactide-co-Glycolide), and poly(l-Lactide-co-E-Caprolactone) nanofibers cultured with/without porcine smooth muscle cells. Tissue Engineering - Part A 16 (1) : 283-298. ScholarBank@NUS Repository.
dc.description.abstractBiodegradable nanofibers have become a popular candidate for tissue engineering scaffolds because of their biomimetic structure that physically resembles the extracellular matrix. For certain tissue regeneration applications, prolonged in vitro culture time for cellular reorganization and tissue remodeling may be required. Therefore, extensive understanding of cellular effects on scaffold degradation is needed. There are only few studies on the degradation of nanofibers, and also the studies on degradation throughout cell culture are rare. In this study, polyglycolide (PGA), poly(dl-lactide-co- glycolide) (PLGA) and poly(l-lactide-co-E-caprolactone) [P(LLA-CL)] were electrospun into nanofibrous meshes. The nanofibers were cultured with porcine smooth muscle cells for up to 3 months to evaluate their degradation behavior and cellular response. The results showed that the degradation rates are in the order of PGA>>PLGA>P(LLA-CL). PGA nanofibers degraded in 3 weeks and supported cell growth only in the first few days. PLGA nanofiber scaffolds facilitated cell growth during the first 30 days after seeding, but cell growth was slow thereafter. P(LLA-CL) nanofibers facilitated long-term (1-3 months) cell growth. mRNA quantification using real-time polymerase chain reaction revealed that some smooth muscle cell markers (α-actinin and calponin) and extracellular matrix genes (collagen and integrin) seemed to be downregulated with increased cell culture time. Cell culture significantly increased the degradation rate of PGA nanofibers, whereas the effect on PLGA and P(LLA-CL) nanofibers was limited. We found that the molecular weight of P(LLA-CL) and PLGA nanofibers decreased linearly for up to 100 days. Half lives of PLGA and P(LLA-CL) nanofibers were shown to be 80 and 110 days, respectively. In summary, this is the first study to our knowledge to evaluate long-term polymeric nanofiber degradation in vitro with cell culture. Cell culture accelerated the nanofibrous scaffold degradation to a limited extent. P(LLA-CL) nanofibers could be a good choice as scaffolds for long-term smooth muscle cell culture. © Copyright 2009, Mary Ann Liebert, Inc. 2009.
dc.contributor.departmentMECHANICAL ENGINEERING
dc.contributor.departmentORTHOPAEDIC SURGERY
dc.description.sourcetitleTissue Engineering - Part A
Appears in Collections:Staff Publications

Show simple item record
Files in This Item:
There are no files associated with this item.


checked on May 16, 2022


checked on May 9, 2022

Page view(s)

checked on May 12, 2022

Google ScholarTM



Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.