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Development of fibrous balloon for facilitating the use of calcium phosphate cement in vertebral augmentation procedures

Authors
Padalhin, Andrew R.Kim, BoramVentura, Reiza D.Lee, Hyun JungLee, Seung JinLee, Byong-Taek
Issue Date
15-Nov-2018
Publisher
Elsevier BV
Keywords
Electrospinning; Calcium phosphate cement; Cement encapsulation; Simulated body fluid apatite
Citation
Materials & Design, v.158, pp 172 - 183
Pages
12
Journal Title
Materials & Design
Volume
158
Start Page
172
End Page
183
URI
https://scholarworks.bwise.kr/sch/handle/2021.sw.sch/5495
DOI
10.1016/j.matdes.2018.08.029
ISSN
0264-1275
1873-4197
Abstract
Bone loss and fractures are becoming a common problem due to the aging of the global population. To aid such cases, less invasive procedures for bone regeneration have been developed using injectable bone substitutes. However, injectable materials for bone are commonly composed of inert materials that only provide structural support and still pose a risk of leakage, which contributes to morbidity. This study attempts to address this problem through evaluation of different types of electrospun fibers and their potential for facilitating the use of calcium phosphate-based cement in vertebral augmentation procedure. Thin (0.83 +/- 0.31 mu m fiber diameter) and thick (5.25 +/- 1.22 mu m fiber diameter) electrospun polycaprolactone (PCL) membranes were fabricated and surface modified through hydrolysis and simulated body fluid (SBF) apatite deposition. Samples composed of thin fibers generally retain most of their relevant properties following surface modification, while a significant change was observed in samples composed of thick fibers. The results show that thin electrospun fibers possess desirable mechanical properties for injectable cement encapsulation, while thick electrospun fibers provide a better substrate for pre-osteoblast cells. Balloon samples fabricated from both fiber types were used to test inflation capacity, encapsulation of injectable cement, and bone tissue development in an animal model. (C) 2018 Published by Elsevier Ltd.
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