Characterization of drug metabolites and cytotoxicity assay simultaneously using an integrated microfluidic device

被引:95
作者
Ma, Bo [1 ,2 ]
Zhang, Guohao [1 ,2 ]
Qin, Jianhua [1 ]
Lin, Bingcheng [1 ]
机构
[1] Chinese Acad Sci, Dalian Inst Chem Phys, Dalian 116023, Peoples R China
[2] Chinese Acad Sci, Grad Sch, Beijing, Peoples R China
关键词
UV ABSORBENCY DETECTION; UDP-GLUCURONOSYLTRANSFERASES; INDUCED HEPATOTOXICITY; TOXICITY; CHIP; MICROREACTOR; HEPATOCYTES; KINETICS; ARRAYS; PHASE;
D O I
10.1039/b809117j
中图分类号
Q5 [生物化学];
学科分类号
071010 ; 081704 ;
摘要
An integrated microfluidic device was developed for the characterization of drug metabolites and a cytotoxicity assay simultaneously. The multi-layer device was composed of a quartz substrate with embedded separation microchannels and a perforated three-microwell array containing sol-gel bioreactors of human liver microsome (HLM), and two PDMS layers. By aligning the microwell array on the quartz substrate with cell culture chambers on the bottom PDMS layer, drug metabolism studies related to functional units, including metabolite generation, detection and incubation with cultured cells to assess metabolism induced cytotoxicity, were all integrated into the microfluidic device. To validate the feasibility of drug metabolism study on the microfluidic chip, UDP-glucuronosyltransferase (UGT) metabolism of acetaminophen (AP) and its effect on hepG2 cytotoxicity were studied first. Then metabolism based drug-drug interaction between AP and phenytoin (PH), which resulted in increased hepG2 cytotoxicity, was proved on this device. All this demonstrated that the developed microfluidic device could be a potential useful tool for drug metabolism and metabolism based drug-drug interaction research.
引用
收藏
页码:232 / 238
页数:7
相关论文
共 28 条
[21]   Drug metabolite profiling and elucidation of drug-induced hepatotoxicity [J].
Tang, Wei .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2007, 3 (03) :407-420
[22]   An in vitro approach to detect metabolite toxicity due to CYP3A4-dependent bioactivation of xenobiotics [J].
Vignati, L ;
Turlizzi, E ;
Monaci, S ;
Grossi, P ;
de Kanter, R ;
Monshouwer, M .
TOXICOLOGY, 2005, 216 (2-3) :154-167
[23]   High-density microfluidic arrays for cell cytotoxicity analysis [J].
Wang, Zhanhui ;
Kim, Min-Cheol ;
Marquez, Manuel ;
Thorsen, Todd .
LAB ON A CHIP, 2007, 7 (06) :740-745
[24]   Process analytical chemistry [J].
Workman, Jerome, Jr. ;
Koch, Mel ;
Veltkamp, Dave .
ANALYTICAL CHEMISTRY, 2007, 79 (12) :4345-4363
[25]   Cell-based high content screening using an integrated microfluidic device [J].
Ye, Nannan ;
Qin, Jianhua ;
Shi, Weiwei ;
Liu, Xin ;
Lin, Bingcheng .
LAB ON A CHIP, 2007, 7 (12) :1696-1704
[26]   Characterizing doxorubicin-induced apoptosis in HepG2 cells using an integrated microfluidic device [J].
Ye, Nannan ;
Qin, Jianhua ;
Shi, Weiwei ;
Lin, Bingcheng .
ELECTROPHORESIS, 2007, 28 (07) :1146-1153
[27]   Fabrication of a bio-MEMS based cell-chip for toxicity monitoring [J].
Yoo, Sung Keun ;
Lee, Jin Hyung ;
Yun, Sung-Sik ;
Gu, Man Bock ;
Lee, Jong Hyun .
BIOSENSORS & BIOELECTRONICS, 2007, 22 (08) :1586-1592
[28]   Microreactor microfluidic systems with human microsomes and hepatocytes for use in metabolite studies [J].
Zguris, JC ;
Itle, LJ ;
Hayes, D ;
Pishko, MV .
BIOMEDICAL MICRODEVICES, 2005, 7 (02) :117-125