scholarly journals Industrial lab-on-a-chip: Design, applications and scale-up for drug discovery and delivery

2013 ◽  
Vol 65 (11-12) ◽  
pp. 1626-1663 ◽  
Author(s):  
Goran T. Vladisavljević ◽  
Nauman Khalid ◽  
Marcos A. Neves ◽  
Takashi Kuroiwa ◽  
Mitsutoshi Nakajima ◽  
...  
2017 ◽  
Author(s):  
S. Grünzner ◽  
F. V. Reddavide ◽  
C. Steinfelder ◽  
M. Cui ◽  
M. Busek ◽  
...  

2006 ◽  
Vol 5 (3) ◽  
pp. 210-218 ◽  
Author(s):  
Petra S. Dittrich ◽  
Andreas Manz
Keyword(s):  

Lab on a Chip ◽  
2014 ◽  
Vol 14 (10) ◽  
pp. 1678-1685 ◽  
Author(s):  
Herbert Ryan ◽  
Alison Smith ◽  
Marcel Utz

Microfluidic high-resolution NMR is possible in spite of magnetic susceptibility mismatches if appropriately shaped compensation structures are included in the chip design.


2021 ◽  
Vol 12 ◽  
Author(s):  
Aya Shanti ◽  
Nicholas Hallfors ◽  
Georg A Petroianu ◽  
Lourdes Planelles ◽  
Cesare Stefanini

Organs-on-chip are gaining increasing attention as promising platforms for drug screening and testing applications. However, lymph nodes-on-chip options remain limited although the lymph node is one of the main determinants of the immunotoxicity of newly developed pharmacological drugs. In this review, we describe existing biomimetic lymph nodes-on-chip, their design, and their physiological relevance to pharmacology and shed the light on future directions associated with lymph node-on-chip design and implementation in drug discovery and development.


2015 ◽  
Vol 20 (9) ◽  
pp. 1101-1111 ◽  
Author(s):  
Markus Kaufmann ◽  
Ansgar Schuffenhauer ◽  
Isabelle Fruh ◽  
Jessica Klein ◽  
Anke Thiemeyer ◽  
...  

Fragile X syndrome (FXS) is the most common form of inherited mental retardation, and it is caused in most of cases by epigenetic silencing of the Fmr1 gene. Today, no specific therapy exists for FXS, and current treatments are only directed to improve behavioral symptoms. Neuronal progenitors derived from FXS patient induced pluripotent stem cells (iPSCs) represent a unique model to study the disease and develop assays for large-scale drug discovery screens since they conserve the Fmr1 gene silenced within the disease context. We have established a high-content imaging assay to run a large-scale phenotypic screen aimed to identify compounds that reactivate the silenced Fmr1 gene. A set of 50,000 compounds was tested, including modulators of several epigenetic targets. We describe an integrated drug discovery model comprising iPSC generation, culture scale-up, and quality control and screening with a very sensitive high-content imaging assay assisted by single-cell image analysis and multiparametric data analysis based on machine learning algorithms. The screening identified several compounds that induced a weak expression of fragile X mental retardation protein (FMRP) and thus sets the basis for further large-scale screens to find candidate drugs or targets tackling the underlying mechanism of FXS with potential for therapeutic intervention.


F1000Research ◽  
2018 ◽  
Vol 7 ◽  
pp. 517 ◽  
Author(s):  
Makeda Stephenson ◽  
Warren Grayson

Bioreactors have become indispensable tools in the cell-based therapy industry. Various forms of bioreactors are used to maintain well-controlled microenvironments to regulate cell growth, differentiation, and tissue development. They are essential for providing standardized, reproducible cell-based products for regenerative medicine applications or to establish physiologically relevant in vitro models for testing of pharmacologic agents. In this review, we discuss three main classes of bioreactors: cell expansion bioreactors, tissue engineering bioreactors, and lab-on-a-chip systems. We briefly examine the factors driving concerted research endeavors in each of these areas and describe the major advancements that have been reported in the last three years. Emerging issues that impact the commercialization and clinical use of bioreactors include (i) the need to scale up to greater cell quantities and larger graft sizes, (ii) simplification of in vivo systems to function without exogenous stem cells or growth factors or both, and (iii) increased control in the manufacture and monitoring of miniaturized systems to better capture complex tissue and organ physiology.


2016 ◽  
Vol 222 ◽  
pp. 721-727 ◽  
Author(s):  
An-Bang Wang ◽  
Po-Hsuan Fang ◽  
Yu Chu Su ◽  
Yu-Wen Hsieh ◽  
Chii-Wann Lin ◽  
...  

Author(s):  
Nauman Khalid ◽  
Sania Arif ◽  
Isao Kobayashi ◽  
Mitsutoshi Nakajima

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