TY - JOUR
T1 - Biology-inspired microphysiological system approaches to solve the prediction dilemma of substance testing
AU - Marx, Uwe
AU - Andersson, Tommy B
AU - Bahinski, Anthony
AU - Beilmann, Mario
AU - Beken, Sonja
AU - Cassee, Flemming R
AU - Cirit, Murat
AU - Daneshian, Mardas
AU - Fitzpatrick, Susan
AU - Frey, Olivier
AU - Gaertner, Claudia
AU - Giese, Christoph
AU - Griffith, Linda
AU - Hartung, Thomas
AU - Heringa, Minne B
AU - Hoeng, Julia
AU - de Jong, Wim H
AU - Kojima, Hajime
AU - Kuehnl, Jochen
AU - Leist, Marcel
AU - Luch, Andreas
AU - Maschmeyer, Ilka
AU - Sakharov, Dmitry
AU - Sips, Adrienne J A M
AU - Steger-Hartmann, Thomas
AU - Tagle, Danilo A
AU - Tonevitsky, Alexander
AU - Tralau, Tewes
AU - Tsyb, Sergej
AU - van de Stolpe, Anja
AU - Vandebriel, Rob
AU - Vulto, Paul
AU - Wang, Jufeng
AU - Wiest, Joachim
AU - Rodenburg, Marleen
AU - Roth, Adrian
PY - 2016
Y1 - 2016
N2 - The recent advent of microphysiological systems - microfluidic biomimetic devices that aspire to emulate the biology of human tissues, organs and circulation in vitro - is envisaged to enable a global paradigm shift in drug development. An extraordinary US governmental initiative and various dedicated research programs in Europe and Asia have led recently to the first cutting-edge achievements of human single-organ and multi-organ engineering based on microphysiological systems. The expectation is that test systems established on this basis would model various disease stages, and predict toxicity, immunogenicity, ADME profiles and treatment efficacy prior to clinical testing. Consequently, this technology could significantly affect the way drug substances are developed in the future. Furthermore, microphysiological system-based assays may revolutionize our current global programs of prioritization of hazard characterization for any new substances to be used, for example, in agriculture, food, ecosystems or cosmetics, thus, replacing laboratory animal models used currently. Thirty-six experts from academia, industry and regulatory bodies present here the results of an intensive workshop (held in June 2015, Berlin, Germany). They review the status quo of microphysiological systems available today against industry needs, and assess the broad variety of approaches with fit-for-purpose potential in the drug development cycle. Feasible technical solutions to reach the next levels of human biology in vitro are proposed. Furthermore, key organ-on-a-chip case studies, as well as various national and international programs are highlighted. Finally, a roadmap into the future is outlined, to allow for more predictive and regulatory-accepted substance testing on a global scale.
AB - The recent advent of microphysiological systems - microfluidic biomimetic devices that aspire to emulate the biology of human tissues, organs and circulation in vitro - is envisaged to enable a global paradigm shift in drug development. An extraordinary US governmental initiative and various dedicated research programs in Europe and Asia have led recently to the first cutting-edge achievements of human single-organ and multi-organ engineering based on microphysiological systems. The expectation is that test systems established on this basis would model various disease stages, and predict toxicity, immunogenicity, ADME profiles and treatment efficacy prior to clinical testing. Consequently, this technology could significantly affect the way drug substances are developed in the future. Furthermore, microphysiological system-based assays may revolutionize our current global programs of prioritization of hazard characterization for any new substances to be used, for example, in agriculture, food, ecosystems or cosmetics, thus, replacing laboratory animal models used currently. Thirty-six experts from academia, industry and regulatory bodies present here the results of an intensive workshop (held in June 2015, Berlin, Germany). They review the status quo of microphysiological systems available today against industry needs, and assess the broad variety of approaches with fit-for-purpose potential in the drug development cycle. Feasible technical solutions to reach the next levels of human biology in vitro are proposed. Furthermore, key organ-on-a-chip case studies, as well as various national and international programs are highlighted. Finally, a roadmap into the future is outlined, to allow for more predictive and regulatory-accepted substance testing on a global scale.
KW - microphysiological systems
KW - organ-on-a-chip
KW - in vitro models
KW - predictive toxicology
KW - ådrug testing
U2 - 10.14573/altex.1603161
DO - 10.14573/altex.1603161
M3 - Article
C2 - 27180100
SN - 1868-596X
VL - 33
SP - 272
EP - 321
JO - Altex
JF - Altex
IS - 3
ER -