Loughborough University
Leicestershire, UK
LE11 3TU
+44 (0)1509 263171
Loughborough University

Loughborough University Institutional Repository

Please use this identifier to cite or link to this item: https://dspace.lboro.ac.uk/2134/24977

Title: Use of ultrathin shell microcapsules of hepatocytes in bioartificial liver-assist device
Authors: Sun, Tao
Chan, Melinda Ling Hou
Zhou, Yi
Xu, Xi
Zhang, Jing
Lao, Xuejun
Wang, Xianwei
Quek, Chai-Hoon
Chen, Jia-Ping
Leong, Kam W.
Yu, Hanry
Issue Date: 2003
Publisher: © Mary Ann Liebert, Inc.
Citation: SUN, T. ... et al, 2003. Use of ultrathin shell microcapsules of hepatocytes in bioartificial liver-assist device. Tissue Engineering, 9 (supplement 1), pp.65-75
Abstract: We previously encapsulated hepatocytes in ultrathin shell microcapsules and showed them to have enhanced differentiated functions over cells cultured in monolayer. Here we have used these microencapsulated hepatocytes in a bioartificial liver-assisted device (BLAD) with a rat hepatectomy model. Primary rat hepatocytes were encapsulated in 150- to 200-μm microcapsules, using an electrostatic droplet generator. The microencapsulated hepatocytes exhibited good in vitro urea synthesis activity in plasma from rats with fulminant hepatic failure (FHF). The ex vivo hemoperfusion was conducted in FHF rats by perfusing plasma at a rate of 1-2 mL/min through 1.5-2 × 108 encapsulated hepatocytes packed into a packed-bed bioreactor. Hemoperfusion with the bioreactor was initiated 5 h after operative induction of liver failure and continued for 7 h. The BLAD-treated rats showed improvements over the control groups in survival time and metabolic indicators, including ammonia and total bilirubin levels. Furthermore, expanded bed adsorption (EBA) detoxification technology using Streamline-SP resin was explored to complement the bioreactor with microencapsulated hepatocytes. In vitro experiments indicated that serum ammonia could be specifically removed in dose-dependent manner, whereas the total serum proteins were unaffected by the resin. In ex vivo experiments, hemoperfusion with the resin was initiated 3 h after operative induction of liver failure and continued for 7 h. The resin-treated rats showed obvious serum ammonia removal with no observable total blood protein and blood cell adsorption. Therefore, Streamline-SP resin can potentially be integrated into a BLAD for improved efficacy.
Description: This paper is closed access.
Version: Closed access
DOI: 10.1089/10763270360696987
URI: https://dspace.lboro.ac.uk/2134/24977
Publisher Link: http://dx.doi.org/10.1089/10763270360696987
ISSN: 1076-3279
Appears in Collections:Closed Access (Chemical Engineering)

Files associated with this item:

File Description SizeFormat
12.pdfPublished version52.21 kBAdobe PDFView/Open

 

SFX Query

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