How to Choose In Vitro Systems to Predict In Vivo Drug Clearance: A System Pharmacology Perspective

被引:5
作者
Wang, Lei [1 ,2 ]
Chiang, ChienWei [3 ,4 ]
Liang, Hong [1 ,2 ]
Wu, Hengyi [3 ,4 ]
Feng, Weixing [1 ,5 ]
Quinney, Sara K. [3 ,6 ]
Li, Jin [1 ,2 ]
Li, Lang [3 ,7 ]
机构
[1] Harbin Engn Univ, Coll Automat, Bioinformat Res Ctr, Harbin 150001, Heilongjiang, Peoples R China
[2] Harbin Engn Univ, Inst Biomed Engn, Coll Automat, Harbin 150001, Heilongjiang, Peoples R China
[3] Indiana Univ, Sch Med, Ctr Computat Biol & Bioinformat, Indianapolis, IN 46202 USA
[4] Indiana Univ, Sch Informat & Comp, Indianapolis, IN 46202 USA
[5] Harbin Engn Univ, Coll Automat, Pattern Recognit & Intelligent Syst Inst, Harbin 150001, Heilongjiang, Peoples R China
[6] Indiana Univ, Sch Med, Dept Obstet & Gynecol, Indianapolis, IN 46202 USA
[7] Indiana Univ, Sch Med, Dept Med & Mol Genom, Indianapolis, IN 46202 USA
基金
中国国家自然科学基金;
关键词
PHYSIOLOGICALLY-BASED PHARMACOKINETICS; INTRINSIC CLEARANCE; HEPATIC-CLEARANCE; METABOLISM; HEPATOCYTES; HUMANS; MODEL; ADME; PHARMACODYNAMICS; DEXTROMETHORPHAN;
D O I
10.1155/2015/857327
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
The use of in vitro metabolism data to predict human clearance has become more significant in the current prediction of large scale drug clearance for all the drugs. The relevant information (in vitro metabolism data and in vivo human clearance values) of thirty-five drugs that satisfied the entry criteria of probe drugs was collated from the literature. Then the performance of different in vitro systems including Escherichia coli system, yeast system, lymphoblastoid system and baculovirus system is compared after in vitro-in vivo extrapolation. Baculovirus system, which can provide most of the data, has almost equal accuracy as the other systems in predicting clearance. And in most cases, baculovirus system has the smaller CV in scaling factors. Therefore, the baculovirus system can be recognized as the suitable system for the large scale drug clearance prediction.
引用
收藏
页数:9
相关论文
共 50 条
[1]   Deciding on Success Criteria for Predictability of Pharmacokinetic Parameters from In Vitro Studies: An Analysis Based on In Vivo Observations [J].
Abduljalil, Khaled ;
Cain, Theresa ;
Humphries, Helen ;
Rostami-Hodjegan, Amin .
DRUG METABOLISM AND DISPOSITION, 2014, 42 (09) :1478-1484
[2]   Assessment of the absorption, metabolism and absolute bioavailability of maraviroc in healthy male subjects [J].
Abel, Samantha ;
Russell, Deborah ;
Whitlock, Lyndsey A. ;
Ridgway, Caroline E. ;
Nedderman, Angus N. R. ;
Walker, Donald K. .
BRITISH JOURNAL OF CLINICAL PHARMACOLOGY, 2008, 65 :60-67
[3]   Pharmacokinetics and safety of single oral doses of sirolimus (rapamycin) in healthy male volunteers [J].
Brattström, C ;
Säwe, J ;
Jansson, B ;
Lönnebo, A ;
Nordin, J ;
Zimmerman, JJ ;
Burke, JT ;
Groth, CG .
THERAPEUTIC DRUG MONITORING, 2000, 22 (05) :537-544
[4]  
Brynne N, 1997, INT J CLIN PHARM TH, V35, P287
[5]   The role of translational bioinformatics in drug discovery [J].
Buchan, Natalie S. ;
Rajpal, Deepak K. ;
Webster, Yue ;
Alatorre, Carlos ;
Gudivada, Ranga Chandra ;
Zheng, Chengyi ;
Sanseau, Philippe ;
Koehler, Jacob .
DRUG DISCOVERY TODAY, 2011, 16 (9-10) :426-434
[6]   Use of intrinsic clearance for prediction of human hepatic clearance [J].
Chao, Piyun ;
Uss, Annette S. ;
Cheng, K. C. .
EXPERT OPINION ON DRUG METABOLISM & TOXICOLOGY, 2010, 6 (02) :189-198
[7]   Utility of Intersystem Extrapolation Factors in Early Reaction Phenotyping and the Quantitative Extrapolation of Human Liver Microsomal Intrinsic Clearance Using Recombinant Cytochromes P450 [J].
Chen, Yuan ;
Liu, Liling ;
Khanh Nguyen ;
Fretland, Adrian J. .
DRUG METABOLISM AND DISPOSITION, 2011, 39 (03) :373-382
[8]   Oral pharmacokinetics of the anti-HIV efavirenz encapsulated within polymeric micelles [J].
Chiappetta, Diego A. ;
Hocht, Christian ;
Taira, Carlos ;
Sosnik, Alejandro .
BIOMATERIALS, 2011, 32 (09) :2379-2387
[9]   Prediction of Hepatic Clearance in Human From In Vitro Data for Successful Drug Development [J].
Chiba, Masato ;
Ishii, Yasuyuki ;
Sugiyama, Yuichi .
AAPS JOURNAL, 2009, 11 (02) :262-276
[10]   DemQSAR: predicting human volume of distribution and clearance of drugs [J].
Demir-Kavuk, Ozgur ;
Bentzien, Joerg ;
Muegge, Ingo ;
Knapp, Ernst-Walter .
JOURNAL OF COMPUTER-AIDED MOLECULAR DESIGN, 2011, 25 (12) :1121-1133