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Characterization of a novel composite scaffold consisting of acellular bladder submucosa matrix, polycaprolactone and Pluronic F127 as a substance for bladder reconstruction

Authors
Jang, YJChun, SYKim, GNKim, JROh, SHLee, JHKim, BSSong, PHYoo, ESKwon, TG
Issue Date
Jul-2014
Publisher
ELSEVIER SCI LTD
Citation
ACTA BIOMATERIALIA, v.10, pp.3117 - 3125
Journal Title
ACTA BIOMATERIALIA
Volume
10
Start Page
3117
End Page
3125
URI
http://scholarworks.bwise.kr/kbri/handle/2023.sw.kbri/890
ISSN
1742-7061
Abstract
The bladder is an organ susceptible to a variety of congenital anomalies, injuries and disorders. To address the clinical limitations of existing scaffolds, we fabricated a novel scaffold that can be applied to morphological and functional bladder reconstruction. As a first step to prove the benefit of the scaffold, intensive in vitro and in vivo analyses were conducted. The novel composite scaffold was fabricated using polycaprolactone/Pluronic F127 (PCL/F127) and variable proportions (1, 3, 5 and 10 wt.%) of porcine acellular bladder submucosa matrix (BSM). Physicochemical properties and biocompatibilities of the scaffolds were characterized. For cell-mediated analysis, upper-urinary-tract-derived urine stem cells were used. Observations of tensile strength, modulus, porosity, cell adhesion, viability and proliferation characteristics of scaffolds indicated that the optimum proportion of BSM in the composite scaffolds was 3 or 5 wt.%. Based on comparison of 3 and 5 wt.% BSM/PCL/F127 scaffolds with respect to degradability, hydrophilicity, surface properties and functional group presence, the 3 wt.% BSM was chosen for in vivo studies. 8 weeks after kidney-subcapsular implantation of the 3 wt.% BSM/PCL/F127 scaffold, cells remained attached to the surface and there was no evidence of teratomas. A BSM content of 3 wt.% was the optimum proportion for fabrication of the neo scaffold. We predict that the 3 wt.% BSM/PCL/F127 composite scaffold could act as an ideal matrix after cystectomy based on its favorable physicochemical properties and biocompatibilities. (C) 2014 Acta Materialia Inc. Published by Elsevier Ltd. All rights reserved.
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연구본부 (뇌발달질환 연구그룹)
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