3D hepatic mimics - the need for a multicentric approach

被引:6
|
作者
Sasikumar, Shyama [1 ,2 ]
Chameettachal, Shibu [1 ]
Kingshott, Peter [2 ,3 ]
Cromer, Brett [2 ]
Pati, Falguni [1 ]
机构
[1] Indian Inst Technol Hyderabad, Dept Biomed Engn, Sangareddy 502285, Telangana, India
[2] Swinburne Univ Technol, Sch Sci, Dept Chem & Biotechnol, Hawthorn, Vic 3122, Australia
[3] Swinburne Univ Technol, Sch Engn, ARC Training Ctr Surface Engn Adv Mat SEAM, Hawthorn, Vic 3122, Australia
关键词
liver tissue engineering; 3D bioprinting; liver bioprinting; drug screening; in vitromodels; SALT EXPORT PUMP; IN-VITRO MODEL; METABOLIC ZONATION; RAT HEPATOCYTES; LIVER; DRUG; SPHEROIDS; CULTURE; CELLS; TOXICITY;
D O I
10.1088/1748-605X/ab971c
中图分类号
R318 [生物医学工程];
学科分类号
0831 ;
摘要
The liver is a center of metabolic activity, including the metabolism of drugs, and consequently is prone to drug-induced liver injury. Failure to detect hepatotoxicity of drugs during their development will lead to the withdrawal of the drugs during clinical trials. To avoid such clinical and economic consequences,in vitroliver models that can precisely predict the toxicity of a drug during the pre-clinical phase is necessary. This review describes the different technologies that are used to developin vitroliver models and the different approaches aimed at mimicking different functional aspects of the liver at the fundamental level. This involves mimicking of the functional and structural units like the sinusoid, the bile canalicular system, and the acinus.
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收藏
页数:13
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