| Literature DB >> 31544246 |
Ann Lin1,2, Frøydis Sved Skottvoll1,3, Simon Rayner1,4, Stig Pedersen-Bjergaard5, Gareth Sullivan1,6,7,8,9, Stefan Krauss1,10, Steven Ray Wilson1,3, Sean Harrison1.
Abstract
In vitro derived simplified 3D representations of human organs or organ functionalities are predicted to play a major role in disease modeling, drug development, and personalized medicine, as they complement traditional cell line approaches and animal models. The cells for 3D organ representations may be derived from primary tissues, embryonic stem cells or induced pluripotent stem cells and come in a variety of formats from aggregates of individual or mixed cell types, self-organizing in vitro developed "organoids" and tissue mimicking chips. Microfluidic devices that allow long-term maintenance and combination with other tissues, cells or organoids are commonly referred to as "microphysiological" or "organ-on-a-chip" systems. Organ-on-a-chip technology allows a broad range of "on-chip" and "off-chip" analytical techniques, whereby "on-chip" techniques offer the possibility of real time tracking and analysis. In the rapidly expanding tool kit for real time analytical assays, mass spectrometry, combined with "on-chip" electrophoresis, and other separation approaches offer attractive emerging tools. In this review, we provide an overview of current 3D cell culture models, a compendium of current analytical strategies, and we make a case for new approaches for integrating separation science and mass spectrometry in this rapidly expanding research field.Entities:
Keywords: Chromatography; Electrophoresis; Mass spectrometry; Organ on a chip; Organoid
Mesh:
Year: 2019 PMID: 31544246 DOI: 10.1002/elps.201900170
Source DB: PubMed Journal: Electrophoresis ISSN: 0173-0835 Impact factor: 3.535