Novel intra-tissue perfusion system for culturing thick liver tissue

被引:28
作者
Khong, Yuet Mei
Mang, Jing
Zhou, Sibo
Cheung, Christine
Doberstein, Kai
Samper, Victor
Yu, Hanry
机构
[1] ASTAR, Inst Bioengn & Nanotechnol, Singapore, Singapore
[2] Natl Univ Singapore, NUS Sch Integrat Sci & Engn, NUS Grad Programme Bbioengn, Singapore 117548, Singapore
[3] Natl Univ Singapore, Inst Med, Confocal Microscopy Unit, Singapore 117548, Singapore
[4] Univ London Imperial Coll Sci Technol & Med, Dept Bioengn, London SW7 2AZ, England
[5] Univ Mannheim, Dept Biotechnol, D-6800 Mannheim 1, Germany
[6] Natl Univ Singapore, Dept Physiol, Singapore 117548, Singapore
[7] Singapore MIT Alliance, Singapore, Singapore
[8] Natl Univ Singapore, NUS Tissue Engn Programme, DSO Labs, Singapore 117548, Singapore
[9] Natl Univ Singapore, Dept Haematol Oncol, Singapore 117548, Singapore
来源
TISSUE ENGINEERING | 2007年 / 13卷 / 09期
关键词
D O I
10.1089/ten.2007.0040
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Innovative scaffold fabrication, angiogenesis promotion, and dynamic tissue culture techniques have been utilized to improve delivery of media into the core of large tissue constructs in tissue engineering. We have developed here an intra-tissue perfusion (ITP) system, which incorporates an array of seven micron-sized needles as a delivery conduit, to improve mass transfer into the core of thick liver tissues slices (> > 300 mu m mass transport limit). The ITP system improves the uniformity and distribution of media throughout the tissue, resulting in improved cell viability over the static-cultured controls. The ITP-cultured thick liver slices also exhibit improved phase I and phase II metabolic functions and albumin and urea synthetic functions after 3-day culture, which is the minimal period required by the U.S. Food and Drug Administration (FDA) for studying drug-drug interaction. This ITP system can also be used for culturing other thick tissue constructs of larger dimensions for various in vitro and in vivo applications, including bridging integration of the in vitro cultured constructs into living host tissues.
引用
收藏
页码:2345 / 2356
页数:12
相关论文
共 56 条
[1]  
Bach PH, 1996, ATLA-ALTERN LAB ANIM, V24, P893
[2]   Design of a flow perfusion bioreactor system for bone tissue-engineering applications [J].
Bancroft, GN ;
Sikavitsas, VI ;
Mikos, AG .
TISSUE ENGINEERING, 2003, 9 (03) :549-554
[3]   Extended rat liver slice survival and stability monitored using clinical biomarkers [J].
Behrsing, HP ;
Vickers, AEM ;
Tyson, CA .
BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS, 2003, 312 (01) :209-213
[4]   Bioreactors for tissue engineering: Focus on mechanical constraints. A comparative review [J].
Bilodeau, Katia ;
Mantovani, Diego .
TISSUE ENGINEERING, 2006, 12 (08) :2367-2383
[5]   Hepatocyte encapsulation for enhanced cellular functions [J].
Chia, SM ;
Leong, KW ;
Li, J ;
Xu, X ;
Zeng, KY ;
Er, PN ;
Gao, SJ ;
Yu, H .
TISSUE ENGINEERING, 2000, 6 (05) :481-495
[6]   IMPLANTABLE BIOHYBRID ARTIFICIAL ORGANS [J].
COLTON, CK .
CELL TRANSPLANTATION, 1995, 4 (04) :415-436
[7]  
DOGTEROM P, 1993, DRUG METAB DISPOS, V21, P699
[8]   Development of technologies aiding large-tissue engineering [J].
Eiselt, P ;
Kim, BS ;
Chacko, B ;
Isenberg, B ;
Peters, MC ;
Greene, KG ;
Roland, WD ;
Loebsack, AB ;
Burg, KJL ;
Culberson, C ;
Halberstadt, CR ;
Holder, WD ;
Mooney, DJ .
BIOTECHNOLOGY PROGRESS, 1998, 14 (01) :134-140
[9]   Present and future in vitro approaches for drug metabolism [J].
Ekins, S ;
Ring, BJ ;
Grace, J ;
McRobie-Belle, DJ ;
Wrighton, SA .
JOURNAL OF PHARMACOLOGICAL AND TOXICOLOGICAL METHODS, 2000, 44 (01) :313-324
[10]   Cytochrome P450 isoenzyme activities in cultured rat and mouse liver slices [J].
Gokhale, MS ;
Bunton, TE ;
Zurlo, J ;
Yager, JD .
XENOBIOTICA, 1997, 27 (04) :341-355