Generic placeholder image

Current Pharmaceutical Design

Editor-in-Chief

ISSN (Print): 1381-6128
ISSN (Online): 1873-4286

Review Article

Human-Derived Organ-on-a-Chip for Personalized Drug Development

Author(s): Yasamin A. Jodat , Min G. Kang, Kiavash Kiaee, Gyeong J. Kim, Angel F.H. Martinez, Aliza Rosenkranz, Hojae Bae * and Su R. Shin*

Volume 24, Issue 45, 2018

Page: [5471 - 5486] Pages: 16

DOI: 10.2174/1381612825666190308150055

Price: $65

Abstract

To reduce the required capital and time investment in the development of new pharmaceutical agents, there is an urgent need for preclinical drug testing models that are predictive of drug response in human tissues or organs. Despite tremendous advancements and rigorous multistage screening of drug candidates involving computational models, traditional cell culture platforms, animal models and most recently humanized animals, there is still a large deficit in our ability to predict drug response in patient groups and overall attrition rates from phase 1 through phase 4 of clinical studies remain well above 90%. Organ-on-a-chip (OOC) platforms have proven potential in providing tremendous flexibility and robustness in drug screening and development by employing engineering techniques and materials. More importantly, in recent years, there is a clear upward trend in studies that utilize human-induced pluripotent stem cell (hiPSC) to develop personalized tissue or organ models. Additionally, integrated multiple organs on the single chip with increasingly more sophisticated representation of absorption, distribution, metabolism, excretion and toxicity (ADMET) process are being utilized to better understand drug interaction mechanisms in the human body and thus showing great potential to better predict drug efficacy and safety. In this review, we summarize these advances, highlighting studies that took the next step to clinical trials and research areas with the utmost potential and discuss the role of the OOCs in the overall drug discovery process at a preclinical and clinical stage, as well as outline remaining challenges.

Keywords: Organ-on-a-chip, microfluidic technology, drug development, personalized medicine, human-derived induced pluripotent stem cells, tissue engineering.

« Previous
[1]
DiMasi JA, Grabowski HG, Hansen RWJ. Johe. Innovation in the pharmaceutical industry: new estimates of R and D costs. J Health Econ 2016; 47: 20-33.
[2]
Smith TJ. Challenges in Orphan Drug Development: Identification of Effective Therapy for Thyroid-Associated Ophthalmopathy. Ann Rev Pharmacol Toxicol 2018.
[3]
Mehta D, Jackson R, Paul G, Shi J, Sabbagh M. Why do trials for Alzheimer’s disease drugs keep failing? A discontinued drug perspective for 2010-2015., Why do trials for Alzheimer’s disease drugs keep failing? A discontinued drug perspective for 2010–2015. Expert Opin Investig Drugs 2017; 26(6): 735-9.
[4]
Berry-Kravis EM, Lindemann L, Jønch AE, et al. Drug development for neurodevelopmental disorders: lessons learned from fragile X syndrome. Nat Rev Drug Discov 2018; 17(4): 280-99.
[5]
Begley CG, Ellis LM. Drug development: Raise standards for preclinical cancer research. Nature 2012; 483(7391): 531-3.
[6]
Kantarjian HM, Prat F, Steensma DP, et al. Cancer research in the United States: A critical review of current status and proposal for alternative models. Cancer 2018; 124(14): 2881-9.
[7]
Kantarjian H, Patel Y. High cancer drug prices 4 years later-Progress and prospects. Cancer 2017; 123(8): 1292-7.
[8]
Nixon NA, Khan OF, Imam H, et al. Drug development for breast, colorectal, and non-small cell lung cancers from 1979 to 2014. Cancer 2017; 123(23): 4672-9.
[9]
Stewart DJ, Stewart AA, Wheatley-Price P, et al. The importance of greater speed in drug development for advanced malignancies. Cancer Med 2018; 7(5): 1824-36.
[10]
Clark M, Steger-Hartmann T. A big data approach to the concordance of the toxicity of pharmaceuticals in animals and humans. Regul Toxicol Pharmacol 2018; 96: 94-105.
[11]
Arrowsmith J, Miller P. Trial watch: phase II and phase III attrition rates 2011-2012. Nat Rev Drug Discov 2013; 12(8): 569.
[12]
Seok J, Warren HS, Cuenca AG, et al. Genomic responses in mouse models poorly mimic human inflammatory diseases 2013 110(9): 3507-12.
[13]
Mestas J, Hughes CC. Of mice and not men: Differences between mouse and human immunology. Proc Natl Acad Sci USA 2004; 172(5): 2731-8.
[14]
Cabrera O, Berman DM, Kenyon NS, Ricordi C, Berggren P-O, Caicedo A. The unique cytoarchitecture of human pancreatic islets has implications for islet cell function. Proc Natl Acad Sci USA 2006; 103(7): 2334-9.
[15]
Masjosthusmann S, Becker D, Petzuch B, et al. A transcriptome comparison of time-matched developing human, mouse and rat neural progenitor cells reveals human uniqueness. Toxicol Appl Pharmacol 2018; 354: 40-55.
[16]
Olson H, Betton G, Robinson D, et al. Concordance of the toxicity of pharmaceuticals in humans and in animals. Regul Toxicol Pharmacol 2000; 32(1): 56-67.
[17]
Waxman HA. The lessons of Vioxx--drug safety and sales. N Engl J Med 2005; 352(25): 2576-8.
[18]
Horton R. Vioxx, the implosion of Merck, and aftershocks at the FDA. Lancet 2004; 364(9450): 1995-6.
[19]
Attarwala H. TGN1412: From discovery to disaster. J Young Pharm 2010; 2(3): 332.
[20]
Nayak TR, Andersen H, Makam VS, et al. Graphene for controlled and accelerated osteogenic differentiation of human mesenchymal stem cells. ACS Nano 2011; 5(6): 4670-8.
[21]
Benmira S, Bhattacharya V, Schmid ML. An effective HIV vaccine: A combination of humoral and cellular immunity? Curr HIV Res 2010; 8(6): 441-9.
[22]
Neurology Parkinson Study Group PRECEPT Investigators. Mixed lineage kinase inhibitor CEP-1347 fails to delay disability in early Parkinson disease. Neurology 2007; 69(15): 1480-90.
[23]
Bai H, Li C, Shi G. Functional composite materials based on chemically converted graphene. Adv Mater 2011; 23(9): 1089-115.
[24]
Bai H, Li C, Shi G. Functional composite materials based on chemically converted graphene. Adv Mater 2011; 23(9): 1089-115.
[25]
Fujiwara R, Nguyen N, Chen S, Tukey RH. Developmental hyperbilirubinemia and CNS toxicity in mice humanized with the UDP glucuronosyltransferase 1 (UGT1) locus. Proc Natl Acad Sci USA 2010; 107(11): 5024-9.
[26]
Fujiwara S. Humanized mice: A brief overview on their diverse applications in biomedical research. J Cell Physiol 2018; 233(4): 2889-901.
[27]
Satoh D, Abe S, Kobayashi K, Nakajima Y, Oshimura M, Kazuki Y. Human and mouse artificial chromosome technologies for studies of pharmacokinetics and toxicokinetics. Drug Metab Pharmacokinet 2018; 33(1): 17-30.
[28]
Naritomi Y, Sanoh S, Ohta S. Chimeric mice with humanized liver: Application in drug metabolism and pharmacokinetics studies for drug discovery. Drug Metab Pharmacokinet 2018; 33(1): 31-9.
[29]
Devoy A, Bunton-Stasyshyn RKA, Tybulewicz VLJ, Smith AJH, Fisher EMC. Genomically humanized mice: technologies and promises. Nat Rev Genet 2011; 13(1): 14-20.
[30]
Brehm MA, Shultz LD, Luban J, Greiner DL. Overcoming current limitations in humanized mouse research. J Infect Dis 2013; 208(Suppl. 2): S125-30.
[31]
Akkina RJV. New generation humanized mice for virus research: comparative aspects and future prospects. Virology 2013; 435(1): 14-28.
[32]
Walsh NC, Kenney LL, Jangalwe S, et al. Humanized mouse models of clinical disease. Annu Rev Pathol 2017; 12: 187-215.
[33]
Lagunas A, Martínez E, Samitier J. Surface-Bound Molecular Gradients for the High-Throughput Screening of Cell Responses. Front Bioeng Biotechnol 2015; 3: 132.
[34]
Kimura H, Sakai Y, Fujii T. Organ/body-on-a-chip based on microfluidic technology for drug discovery. Drug Metab Pharmacokinet 2018; 33(1): 43-8.
[35]
Dittrich PS, Manz A. Lab-on-a-chip: microfluidics in drug discovery. Nat Rev Drug Discov 2006; 5(3): 210.
[36]
Kang L, Chung BG, Langer R, Khademhosseini A. Microfluidics for drug discovery and development: from target selection to product lifecycle management. Drug Discov Today 2008; 13(1-2): 1-13.
[37]
Bhatia SN, Ingber DE. Microfluidic organs-on-chips. Nat Biotechnol 2014; 32(8): 760-72.
[38]
Huh D, Torisawa YS, Hamilton GA, Kim HJ, Ingber DE. Microengineered physiological biomimicry: organs-on-chips. Lab Chip 2012; 12(12): 2156-64.
[39]
Kim J, Lee H, Selimović Š, Gauvin R, Bae H. Organ-on-a-chip: development and clinical prospects toward toxicity assessment with an emphasis on bone marrow. Drug Saf 2015; 38(5): 409-18.
[40]
Whitesides GM. The origins and the future of microfluidics. Nature 2006; 442: 368.
[41]
Duffy DC, McDonald JC, Schueller OJA, Whitesides GM. Rapid Prototyping of Microfluidic Systems in Poly(dimethylsiloxane). Anal Chem 1998; 70(23): 4974-84.
[42]
Sackmann EK, Fulton AL, Beebe DJ. The present and future role of microfluidics in biomedical research. Nature 2014; 507: 181.
[43]
Zhang YS, Aleman J, Shin SR, et al. Multisensor-integrated organs-on-chips platform for automated and continual in situ monitoring of organoid behaviors. Proc Natl Acad Sci USA 2017; 114(12): E2293-302.
[44]
Łopacińska JM, Emnéus J, Dufva MJPO. Poly (dimethylsiloxane)(PDMS) affects gene expression in PC12 cells differentiating into neuronal-like cells. PLoS One 2013; 8(1): e53107.
[45]
Hong TF, Ju WJ, Wu MC, et al. Rapid prototyping of PMMA microfluidic chips utilizing a CO2 laser 2010; 9(6): 1125-33.
[46]
Ma L, Zhou C, Lin B. Li WJBm. A porous 3D cell culture micro device for cell migration study. Biomed Microdevices 2010; 12(4): 753-60.
[47]
Sung JH, Esch MB, Prot JM, et al. Microfabricated mammalian organ systems and their integration into models of whole animals and humans. Lab Chip 2013; 13(7): 1201-12.
[48]
Lee SH, Shim KY, Kim B, Sung JH. Hydrogel-based three-dimensional cell culture for organ-on-a-chip applications. Biotechnol Prog 2017; 33(3): 580-9.
[49]
Chang R, Nam J, Sun W. Direct cell writing of 3D microorgan for in vitro pharmacokinetic model. Tissue Eng Part C Methods 2008; 14(2): 157-66.
[50]
Kim J, Lee H, Selimović Š, Gauvin R, Bae H. Organ-on-a-chip: development and clinical prospects toward toxicity assessment with an emphasis on bone marrow. Drug Saf 2015; 38(5): 409-18.
[51]
Luni C, Serena E, Elvassore N. Human-on-chip for therapy development and fundamental science. Curr Opin Biotechnol 2014; 25: 45-50.
[52]
Sayed N, Liu C, Wu JC. Translation of human-induced pluripotent stem cells: From clinical trial in a dish to precision medicine. J Am Coll Cardiol 2016; 67(18): 2161-76.
[53]
Yamanaka SJC. iPS Cells 10 Years Later 2016; 166.
[54]
Zhao T, Zhang Z-N, Rong Z, Xu Y. Immunogenicity of induced pluripotent stem cellsNature 2011 474(7350): 212-5.
[55]
Esch EW, Bahinski A, Huh D. Organs-on-chips at the frontiers of drug discovery. Nat Rev Drug Discov 2015; 14: 248.
[56]
Scott CW, Peters MF, Dragan YP. Human induced pluripotent stem cells and their use in drug discovery for toxicity testing. Toxicol Lett 2013; 219(1): 49-58.
[57]
Ho CT, Lin RZ, Chang WY, Chang HY, Liu CH. Rapid heterogeneous liver-cell on-chip patterning via the enhanced field-induced dielectrophoresis trap. Lab Chip 2006; 6(6): 724-34.
[58]
Lee SA, No Y, Kang E, Ju J, Kim DS, Lee SH. Spheroid-based three-dimensional liver-on-a-chip to investigate hepatocyte-hepatic stellate cell interactions and flow effects. Lab Chip 2013; 13(18): 3529-37.
[59]
Kostrzewski T, Cornforth T, Snow SA, et al. Three-dimensional perfused human in vitro model of non-alcoholic fatty liver disease. World J Gastroenterol 2017; 23(2): 204-15.
[60]
Freyer N, Greuel S, Knöspel F, et al. Microscale 3D Liver Bioreactor for In Vitro Hepatotoxicity Testing under Perfusion Conditions. Bioengineering (Basel) 2018; 5(1): E24.
[61]
Bavli D, Prill S, Ezra E, et al. Real-time monitoring of metabolic function in liver-on-chip microdevices tracks the dynamics of mitochondrial dysfunction. Proc Natl Acad Sci USA 2016; 113(16): E2231-40.
[62]
Ware BR, Berger DR, Khetani SR. Prediction of Drug-Induced Liver Injury in Micropatterned Co-cultures Containing iPSC-Derived Human Hepatocytes. Toxicol Sci 2015; 145(2): 252-62.
[63]
Ma X, Qu X, Zhu W, et al. Deterministically patterned biomimetic human iPSC-derived hepatic model via rapid 3D bioprinting. Proc Natl Acad Sci USA 2016; 113(8): 2206-11.
[64]
Paoli R, Samitier J. Mimicking the Kidney: A Key Role in Organ-on-Chip Development. Micromachines (Basel) 2016; 7(7): E126.
[65]
Jang KJ, Mehr AP, Hamilton GA, et al. Human kidney proximal tubule-on-a-chip for drug transport and nephrotoxicity assessment. Integr Biol 2013; 5(9): 1119-29.
[66]
Musah S, Dimitrakakis N, Camacho DM, Church GM, Ingber DE. Directed differentiation of human induced pluripotent stem cells into mature kidney podocytes and establishment of a Glomerulus Chip. Nat Protoc 2018; 13(7): 1662-85.
[67]
Musah S, Mammoto A, Ferrante TC, et al. Mature induced-pluripotent-stem-cell-derived human podocytes reconstitute kidney glomerular-capillary-wall function on a chip Nat Biomed Eng 2017; 1(5): 0069.
[68]
Homan KA, Kolesky DB, Skylar-Scott MA, et al. Bioprinting of 3D Convoluted Renal Proximal Tubules on Perfusable Chips. Sci Rep 2016. Oct 11; 6: 34845.
[69]
Chang SY, Weber EJ, Sidorenko VS, et al. Human liver-kidney model elucidates the mechanisms of aristolochic acid nephrotoxicity. JCI Insight 2017; 2(22): 95978.
[70]
Kim HJ, Huh D, Hamilton G, Ingber DE. Human gut-on-a-chip inhabited by microbial flora that experiences intestinal peristalsis-like motions and flow. Lab Chip 2012; 12(12): 2165-74.
[71]
Kim HJ, Li H, Collins JJ, Ingber DE. Contributions of microbiome and mechanical deformation to intestinal bacterial overgrowth and inflammation in a human gut-on-a-chip. Proc Natl Acad Sci USA 2016; 113(1): E7-E15.
[72]
Jalili-Firoozinezhad S, Prantil-Baun R, Jiang A, et al. Modeling radiation injury-induced cell death and countermeasure drug responses in a human Gut-on-a-Chip. Cell Death Dis 2018; 9(2): 223.
[73]
Guo X, Das M, Rumsey J, Gonzalez M, Stancescu M, Hickman J. Neuromuscular junction formation between human stem-cell-derived motoneurons and rat skeletal muscle in a defined system. Tissue Eng Part C Methods 2010; 16(6): 1347-55.
[74]
Taylor AM, Blurton-Jones M, Rhee SW, Cribbs DH, Cotman CW, Jeon NL. A microfluidic culture platform for CNS axonal injury, regeneration and transport. Nat Methods 2005; 2(8): 599-605.
[75]
Nierode GJ, Perea BC, McFarland SK, et al. High-Throughput Toxicity and Phenotypic Screening of 3D Human Neural Progenitor Cell Cultures on a Microarray Chip Platform. Stem Cell Reports 2016; 7(5): 970-82.
[76]
Woodruff G, Reyna SM, Dunlap M, et al. Defective Transcytosis of APP and Lipoproteins in Human iPSC-Derived Neurons with Familial Alzheimer’s Disease Mutations. Cell Reports 2016; 17(3): 759-73.
[77]
Booth R, Kim H. Characterization of a microfluidic in vitro model of the blood-brain barrier (μBBB). Lab Chip 2012; 12(10): 1784-92.
[78]
Wang YI, Abaci HE, Shuler ML. Microfluidic blood-brain barrier model provides in vivo-like barrier properties for drug permeability screening. Biotechnol Bioeng 2017; 114(1): 184-94.
[79]
Qi D, Wu S, Lin H, et al. Establishment of a Human iPSC- and Nanofiber-Based Microphysiological Blood-Brain Barrier System. ACS Appl Mater Interfaces 2018; 10(26): 21825-35.
[80]
Grosberg A, Alford PW, McCain ML, Parker KK. Ensembles of engineered cardiac tissues for physiological and pharmacological study: heart on a chip. Lab Chip 2011; 11(24): 4165-73.
[81]
Christoffersson J, Meier F, Kempf H, et al. A Cardiac Cell Outgrowth Assay for Evaluating Drug Compounds Using a Cardiac Spheroid-on-a-Chip Device. Bioengineering (Basel) 2018; 5(2): E36.
[82]
Qian F, Huang C, Lin YD, et al. Simultaneous electrical recording of cardiac electrophysiology and contraction on chip. Lab Chip 2017; 17(10): 1732-9.
[83]
Mathur A, Loskill P, Shao K, et al. Human iPSC-based cardiac microphysiological system for drug screening applications. Sci Rep 2015; 5: 8883.
[84]
Ellis BW, Acun A, Can UI, Zorlutuna P. Human iPSC-derived myocardium-on-chip with capillary-like flow for personalized medicine. Biomicrofluidics 2017; 11(2): 024105.
[85]
Tzatzalos E, Abilez OJ, Shukla P, Wu JC. Engineered heart tissues and induced pluripotent stem cells: Macro- and microstructures for disease modeling, drug screening, and translational studies. Adv Drug Deliv Rev 2016; 96: 234-44.
[86]
Madden L, Juhas M, Kraus WE, Truskey GA, Bursac N. Bioengineered human myobundles mimic clinical responses of skeletal muscle to drugs. eLife 2015; 4: e04885. [PubMed.].
[87]
McCain ML, Agarwal A, Nesmith HW, Nesmith AP, Parker KK. Micromolded gelatin hydrogels for extended culture of engineered cardiac tissues. Biomaterials 2014; 35(21): 5462-71.
[88]
Serena E, Zatti S, Zoso A, et al. Skeletal Muscle Differentiation on a Chip Shows Human Donor Mesoangioblasts’ Efficiency in Restoring Dystrophin in a Duchenne Muscular Dystrophy Model. Stem Cells Transl Med 2016; 5(12): 1676-83.
[89]
van Engeland NCA, Pollet AMAO, den Toonder JMJ, Bouten CVC, Stassen OMJA, Sahlgren CM. A biomimetic microfluidic model to study signalling between endothelial and vascular smooth muscle cells under hemodynamic conditions. Lab Chip 2018; 18(11): 1607-20.
[90]
Schuhmacher A, Gassmann O, Hinder M. Changing R and D models in research-based pharmaceutical companies. J Transl Med 2016; 14(1): 105.
[91]
Drews J. Drug discovery: A historical perspective. Science 2000; 287(5460): 1960-4.
[92]
Giri S, Bader A. A low-cost, high-quality new drug discovery process using patient-derived induced pluripotent stem cells. Drug Discov Today 2015; 20(1): 37-49.
[93]
Hajba L, Guttman A. Continuous-flow-based microfluidic systems for therapeutic monoclonal antibody production and organ-on-a-chip drug testing. J Flow Chem 2017; 7(3-4): 118-23.
[94]
Materne E-M, Ramme AP, Terrasso AP, et al. A multi-organ chip co-culture of neurospheres and liver equivalents for long-term substance testing. J Biotechnol 2015; 205: 36-46.
[95]
Abaci HE, Shuler ML. Human-on-a-chip design strategies and principles for physiologically based pharmacokinetics/pharmacodynamics modeling. Integr Biol 2015; 7(4): 383-91.
[96]
Bai H, Li C, Shi G. Functional composite materials based on chemically converted graphene. Adv Mater 2011; 23(9): 1089-115.
[97]
Mol PG, Arnardottir AH, Motola D, et al. Post-approval safety issues with innovative drugs: A European cohort study. Drug Saf 2013; 36(11): 1105-15.
[98]
Minotti G. Cardiotoxicity of non-cardiovascular drugs 2010.
[99]
Bhise NS, Manoharan V, Massa S, et al. A liver-on-a-chip platform with bioprinted hepatic spheroids. Biofabrication 2016; 8(1): 014101.
[100]
Wilmer MJ, Ng CP, Lanz HL, Vulto P, Suter-Dick L, Masereeuw RJ. Kidney-on-a-chip technology for drug-induced nephrotoxicity screening. Trends Biotechnol 2016; 34(2): 156-70.
[101]
Schimek K, Hsu HH, Boehme M, et al. Bioengineering of a fullthickness skin equivalent in a 96-well insert format for substance permeation studies and organ-on-a-chip applications. Bioengineer 2018; 5(2).
[102]
Skardal A, Murphy SV, Devarasetty M, et al. Multi-tissue interactions in an integrated three-tissue organ-on-a-chip platform. Sci Rep 2017; 7(1): 8837.
[103]
Khetani SR, Berger DR, Ballinger KR, Davidson MD, Lin C, Ware BR. Microengineered liver tissues for drug testing. J Lab Autom 2015; 20(3): 216-50.
[104]
Jung Y, Ji H, Chen Z, et al. Scaffold-free, human mesenchymal stem cell-based tissue engineered blood vessels. Sci Rep 2015; 5: 15116.
[105]
Miller PG, Shuler ML. Design and demonstration of a pumpless 14 compartment microphysiological system. Biotechnol Bioeng 2016; 113(10): 2213-27.
[106]
Kimmelman J, Tannock IJNRCO. The paradox of precision medicine. Nat Rev Clin Oncol 2018; 15(6): 341.
[107]
Polypharmacy in the older patient with cancer. Cancer Contr 1997; 4(5): 419-28.
[108]
Guthrie B, Makubate B, Hernandez-Santiago V. Dreischulte TJBm. The rising tide of polypharmacy and drug-drug interactions: population database analysis 1995–2010. BMC Med 2015; 13(1): 74.
[109]
Riechelmann RP, Zimmermann C, Chin SN, et al. Potential drug interactions in cancer patients receiving supportive care exclusively. J Pain Symptom Manage 2008; 35(5): 535-43.
[110]
Fede A, Miranda M, Antonangelo D, et al. Use of unnecessary medications by patients with advanced cancer: cross-sectional survey. Support Care Cancer 2011; 19(9): 1313-8.
[111]
Holmes A, Bonner F, Jones D. Assessing drug safety in human tissues—what are the barriers? Nat Rev Drug Discov 2015; 14(8): 585.
[112]
Esch EW, Bahinski A, Huh D. Organs-on-chips at the frontiers of drug discovery. Nat Rev Drug Discov 2015; 14(4): 248-60.
[113]
Freyer N, Greuel S, Knöspel F, et al. Effects of Co-culture media on hepatic differentiation of hiPSC with or without HUVEC Co-Culture. Int J Mol Sci 2017; 18(8): 1724.
[114]
Calejo I, Costa-Almeida R, Reis R, Gomes M, Eds. Optimization and establishment of a co-culture model to study cellular interactions in tendon-to-bone interface. Orthopaedic Proceedings 2018.
[115]
Wikswo JP, Curtis EL, Eagleton ZE, et al. Scaling and systems biology for integrating multiple organs-on-a-chip. Lab Chip 2013; 13(18): 3496-511.
[116]
Sung JH, Shuler ML. A micro cell culture analog (microCCA) with 3-D hydrogel culture of multiple cell lines to assess metabolism-dependent cytotoxicity of anti-cancer drugs. Lab Chip 2009; 9(10): 1385-94.
[117]
Sung JH, Kam C, Shuler ML. A microfluidic device for a pharmacokinetic-pharmacodynamic (PK-PD) model on a chip. Lab Chip 2010; 10(4): 446-55.
[118]
Moraes C, Labuz JM, Leung BM, Inoue M, Chun TH, Takayama S. On being the right size: scaling effects in designing a human-on-a-chip. Integr Biol 2013; 5(9): 1149-61.
[119]
Wikswo JP, Curtis EL, Eagleton ZE, et al. Scaling and systems biology for integrating multiple organs-on-a-chip. Lab Chip 2013; 13(18): 3496-511.
[120]
Prantil-Baun R, Novak R, Das D, et al. Physiologically based pharmacokinetic and pharmacodynamic analysis enabled by microfluidically linked organs-on-chips. Annu Rev Pharmacol Toxicol 2018; 58: 37-64.
[121]
Bovard D, Iskandar A, Luettich K, Hoeng J, Peitsch MCJTR. Application Organs-on-a-chip: A new paradigm for toxicological assessment and preclinical drug development. Toxicol Res App 2017; 1: 2397847317726351.
[122]
Hassell BA, Goyal G, Lee E, et al. Human organ chip models recapitulate orthotopic lung cancer growth, therapeutic responses, and tumor dormancy in vitro 2017; 21(2): 508-16.
[123]
Vernetti LA, Senutovitch N, Boltz R, et al. A human liver microphysiology platform for investigating physiology, drug safety, and disease models. Exp Biol Med (Maywood) 2016; 241(1): 101-14.
[124]
Pocock K, Delon L, Bala V, et al. Intestine-on-a-Chip Microfluidic Model for Efficient in Vitro Screening of Oral Chemotherapeutic Uptake. ACS Biomater Sci Eng 2017; 3(6): 951-9.
[125]
Workman MJ, Gleeson JP, Troisi EJ, et al. Enhanced Utilization of Induced Pluripotent Stem Cell–Derived Human Intestinal Organoids Using Microengineered Chips. Cell Mol Gastroenterol Hepatol 2018; 5(4): 669-77.
[126]
Osaki T, Sivathanu V, Kamm RD. Engineered 3D vascular and neuronal networks in a microfluidic platform. Sci Rep 2018; 8(1): 5168.
[127]
Brown JA, Codreanu SG, Shi M, et al. Metabolic consequences of inflammatory disruption of the blood-brain barrier in an organ-on-chip model of the human neurovascular unit. J Neuroinflam 2016; 13(1): 306.
[128]
Oleaga C, Bernabini C, Smith AST, et al. Multi-Organ toxicity demonstration in a functional human in vitro system composed of four organs. Sci Rep 2016; 6: 20030.
[129]
Miller PG, Shuler ML. Design and demonstration of a pumpless 14 compartment microphysiological system. Biotechnol Bioeng 2016; 113(10): 2213-27.
[130]
Bauer S, Wennberg Huldt C, Kanebratt KP, et al. Functional coupling of human pancreatic islets and liver spheroids on-a-chip: Towards a novel human ex vivo type 2 diabetes model. Sci Rep 2017; 7(1): 14620.
[131]
Esch MB, Ueno H, Applegate DR. Shuler MLJLoaC. Modular, pumpless body-on-a-chip platform for the co-culture of GI tract epithelium and 3D primary liver tissue. Lab Chip 2016; 16(14): 2719-29.
[132]
Kim J-Y, Fluri DA, Marchan R, et al. 3D spherical microtissues and microfluidic technology for multi-tissue experiments and analysis. J Biotechnol 2015; 205: 24-35.
[133]
Oleaga C, Bernabini C, Smith AS, et al. Multi-Organ toxicity demonstration in a functional human in vitro system composed of four organs. Sci Rep 2016; 6: 20030.
[134]
Nawroth J, Rogal J, Weiss M, Brucker SY. Loskill PJAhm. Organ‐on‐a‐chip Systems for Women’s Health Applications. Adv Healthc Mater 2018; 7(2): 1700550.
[135]
Xiao S, Coppeta JR, Rogers HB, et al. A microfluidic culture model of the human reproductive tract and 28-day menstrual cycle. Nat Commun 2017; 8: 14584.
[136]
Andersson TB. Evolution of novel 3D culture systems for studies of human liver function and assessments of the hepatotoxicity of drugs and drug candidates. Basic Clin Pharmacol Toxicol 2017; 121(4): 234-8.
[137]
Ewart L, Dehne E-M, Fabre K, et al. Application of microphysiological systems to enhance safety assessment in drug discovery. Annu Rev Pharmacol Toxicol 2018; 58: 65-82.
[138]
Lal MA, Young KW, Andag U. Targeting the podocyte to treat glomerular kidney disease. Drug Discov Today 2015; 20(10): 1228-34.
[139]
Barrile R, van der Meer AD, Park H, et al. Organ‐on‐Chip Recapitulates Thrombosis Induced by an anti‐CD154 Monoclonal Antibody: Translational Potential of Advanced Microengineered Systems. Clin Pharmacol Ther 2018; 104(6): 1240-8.
[140]
Ilic D. Latest developments in the field of stem cell research and regenerative medicine compiled from publicly available information and press releases from nonacademic institutions 1 January–28 February 28 2018. Regen Med 2018; 13(4): 361-70.
[141]
Jain A, Barrile R, van der Meer AD, et al. Primary Human Lung Alveolus‐on‐a‐chip Model of Intravascular Thrombosis for Assessment of Therapeutics. Clin Pharmacol Ther 2018; 103(2): 332-40.
[142]
van Duinen V, van den Heuvel A, Trietsch SJ, et al. 96 perfusable blood vessels to study vascular permeability in vitro. Sci Rep 2017; 7(1): 18071.
[143]
Lanz HL, Saleh A, Kramer B, et al. Therapy response testing of breast cancer in a 3D high-throughput perfused microfluidic platform. BMC Cancer 2017; 17(1): 709.
[144]
Trietsch SJ, Naumovska E, Kurek D, et al. Membrane-free culture and real-time barrier integrity assessment of perfused intestinal epithelium tubes. Nat Commun 2017; 8(1): 262.
[145]
Junaid A, Mashaghi A, Hankemeier T, Vulto P. An end-user perspective on Organ-on-a-Chip: Assays and usability aspects. Curr Opin Biomed Eng 2017; 1: 15-22.
[146]
Wevers NR, van Vught R, Wilschut KJ, et al. High-throughput compound evaluation on 3D networks of neurons and glia in a microfluidic platform. Sci Rep 2016; 6: 38856.
[147]
Marx U, Andersson TB, Bahinski A, et al. Biology-inspired microphysiological system approaches to solve the prediction dilemma of substance testing. ALTEX 2016; 33(3): 272-321.
[148]
Wilmer MJ, Ng CP, Lanz HL, Vulto P, Suter-Dick L, Masereeuw R. Kidney-on-a-chip technology for drug-induced nephrotoxicity screening. Trends Biotechnol 2016; 34(2): 156-70.
[149]
Moreno EL, Hachi S, Hemmer K, et al. Differentiation of neuroepithelial stem cells into functional dopaminergic neurons in 3D microfluidic cell culture. Lab Chip 2015; 15(11): 2419-28.
[150]
van Duinen V, Trietsch SJ, Joore J, Vulto P, Hankemeier T. Microfluidic 3D cell culture: from tools to tissue models. Curr Opin Biotechnol 2015; 35: 118-26.
[151]
Jang M, Manz A, Volk T, Kleber A. Study of melatonin-mediated effects on various hepatic inflammatory responses stimulated by IL-6 in a new HepG2-on-a-chip platform. Biomed Microdevices 2018; 20(3): 54.
[152]
Jang M, Neuzil P, Volk T, Manz A, Kleber A. On-chip three-dimensional cell culture in phaseguides improves hepatocyte functions in vitro. Biomicrofluidics 2015; 9(3): 034113.
[153]
Koo Y, Hawkins BT, Yun Y. Three-dimensional (3D) tetra-culture brain on chip platform for organophosphate toxicity screening. Sci Rep 2018; 8(1): 2841.
[154]
Pradhan S, Smith AM, Garson CJ, et al. A Microvascularized Tumor-mimetic Platform for Assessing Anti-cancer Drug Efficacy. Sci Rep 2018; 8(1): 3171.
[155]
Tang Y, Soroush F, Sheffield JB, Wang B, Prabhakarpandian B. Kiani MFJSr. A biomimetic microfluidic tumor microenvironment platform mimicking the EPR effect for rapid screening of drug delivery systems 2017; 7(1): 9359.
[156]
Terrell-Hall TB, Ammer AG, Griffith JI, Lockman PRJF, Bot CNS. Permeability across a novel microfluidic blood-tumor barrier model. Fluids Barriers CNS 2017; 4(1): 3.
[157]
Soroush F, Zhang T, King DJ, et al. A novel microfluidic assay reveals a key role for protein kinase C δ in regulating human neutrophil–endothelium interaction. J Leukoc Biol 2016; 100(5): 1027-35.
[158]
Deosarkar SP, Prabhakarpandian B, Wang B, Sheffield JB, Krynska B, Kiani MF. A novel dynamic neonatal blood-brain barrier on a chip 2015 10(11): e0142725.
[159]
Prabhakarpandian B, Shen M-C, Nichols JB, et al. Synthetic tumor networks for screening drug delivery systems. J Control Release 2015; 201: 40-55.
[160]
Grosberg A, Nesmith AP, Goss JA, et al. Muscle on a chip: in vitro contractility assays for smooth and striated muscle. J Pharmacol Toxicol Methods 2012; 65(3): 126-35.
[161]
Laureen Martz. Pulmonary edema on a chip. Sci Bus Exch 2012; 5(48): 1251.
[162]
Sieber S, Wirth L, Cavak N, et al. Bone marrow-on-a-chip: Long-term culture of human haematopoietic stem cells in a three-dimensional microfluidic environment. J Tissue Eng Regen Med 2018; 12(2): 479-89.
[163]
Schimek K, Hsu H-H, Boehme M, et al. Bioengineering of a full-thickness skin equivalent in a 96-well insert format for substance permeation studies and organ-on-a-chip applications. Bioengineering (Basel) 2018; 5(2): 43.
[164]
Materne E-M, Ramme AP, Terrasso AP, et al. A multi-organ chip co-culture of neurospheres and liver equivalents for long-term substance testing. J Biotechnol 2015; 205: 36-46.
[165]
Materne E-M, Maschmeyer I, Lorenz AK, et al. The multi-organ chip-a microfluidic platform for long-term multi-tissue coculture Journal of visualized experiments: JoVE 2015; (98).
[166]
Hasenberg T, Mühleder S, Dotzler A, et al. Emulating human microcapillaries in a multi-organ-chip platform. J Biotechnol 2015; 216: 1-10.
[167]
Maschmeyer I, Lorenz AK, Schimek K, et al. A four-organ-chip for interconnected long-term co-culture of human intestine, liver, skin and kidney equivalents. Lab Chip 2015; 15(12): 2688-99.
[168]
Vernetti LA, Senutovitch N, Boltz R, et al. A human liver microphysiology platform for investigating physiology, drug safety, and disease models. Exp Biol Med (Maywood) 2016; 241(1): 101-14.
[169]
Kim J-Y, Fluri DA, Kelm JM, Hierlemann A, Frey O. 96-well format-based microfluidic platform for parallel interconnection of multiple multicellular spheroids. J Lab Autom 2015; 20(3): 274-82.
[170]
Frey O, Misun PM, Fluri DA, Hengstler JG, Hierlemann A. Reconfigurable microfluidic hanging drop network for multi-tissue interaction and analysis. Nat Commun 2014; 5: 4250.
[171]
Wang YI, Oleaga C, Long CJ, et al. Self-contained, low-cost Body-on-a-Chip systems for drug development. Exp Biol Med (Maywood) 2017; 242(17): 1701-13.
[172]
Wang YI, Carmona C, Hickman JJ, Shuler ML. Multiorgan Microphysiological Systems for Drug Development: Strategies, Advances, and Challenges. Adv Healthc Mater 2018; 7(2): 1701000.
[173]
Abaci HE, Gledhill K, Guo Z, Christiano AM, Shuler ML. Pumpless microfluidic platform for drug testing on human skin equivalents. Lab Chip 2015; 15(3): 882-8.
[174]
Esch MB, Prot JM, Wang YI, et al. Multi-cellular 3D human primary liver cell culture elevates metabolic activity under fluidic flow. Lab Chip 2015; 15(10): 2269-77.
[175]
Chandorkar P, Posch W, Zaderer V, et al. Fast-track development of an in vitro 3D lung/immune cell model to study Aspergillus infections. Sci Rep 2017; 7(1): 11644.
[176]
Martin KC, Yuan X, Stimac G, et al. Symmetry-breaking in branching epithelia: cells on micro-patterns under flow challenge the hypothesis of positive feedback by a secreted autocrine inhibitor of motility. J Anat 2017; 230(6): 766-74.

Rights & Permissions Print Cite
© 2024 Bentham Science Publishers | Privacy Policy