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New ureteral scaffold constructed with composite poly(L-lactic acid)-collagen and urothelial cells by new centrifugal seeding system
A tissue‐engineered ureteral scaffold was constructed with composited poly L‐lactic acid (PLLA)–collagen endoluminal stent and uroepithelial cells (UECs) using a new seeding system. The electrospun PLLA–collagen nanofibrous mesh was seeded efficiently with human ureteral epithelial cells using a mod...
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Published in: | Journal of biomedical materials research. Part A 2012-07, Vol.100A (7), p.1725-1733 |
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Main Authors: | , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | A tissue‐engineered ureteral scaffold was constructed with composited poly L‐lactic acid (PLLA)–collagen endoluminal stent and uroepithelial cells (UECs) using a new seeding system. The electrospun PLLA–collagen nanofibrous mesh was seeded efficiently with human ureteral epithelial cells using a modified centrifugal seeding device. The cellular nanofibrous mesh was then wound around a spiral endoluminal stent to form a cellular composited PLLA–collagen ureteral scaffold. The cellular ureteral scaffold was subcutaneously implanted into nude mice. Cell attachment, distribution, and viability in vitro were investigated along with the cell fate in vivo. (3‐(4,5‐dimethylthiazol‐2‐yl)‐2,5‐diphenyltetrazolium bromide) assay showed that scaffolds seeded with centrifugal method had higher cellular activity than scaffolds seeded with static method (p < 0.05), and the metabolic activity per cell had no significant differences between the two methods (p > 0.05). Histologic analysis showed that the entrapped UECs remained in the scaffolds after 2 wk of implantation. The results of the study indicated that the composited PLLA–collagen endoluminal stent could serve as alternative cell carrier for tissue engineering ureter. In addition, the new modified centrifugal seeding system allowed rapid homogeneous distribution of cells onto the nanofibrous mesh, which will be useful to ureteral reconstruction. © 2012 Wiley Periodicals, Inc. J Biomed Mater Res Part A, 2012. |
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ISSN: | 1549-3296 1552-4965 |
DOI: | 10.1002/jbm.a.34134 |