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- W4213447289 endingPage "1148" @default.
- W4213447289 startingPage "1137" @default.
- W4213447289 abstract "Cells and tissues are routinely cultured in vitro for biological research with findings being extrapolated to their host organ and tissue function. However, most samples are cultured and studied in unphysiological environments, without temporal variation in the biochemical cues that are ubiquitous in vivo. The artificiality of these conditions undermines the predictive value of cell culture studies. We ascribe the prevalence of this suboptimal culture methodology to the lack of practical continuous flow systems that are economical and robust. Here, we design and implement an expandable multiplexed flow system for cell culture superfusion. By expanding on the concept of the planar peristaltic pump, we fabricated a highly compact and multiplexed pump head with up to 48 active pump lines. The pump is incorporated into a custom, open-top superfusion system configured for conventional multi-well culture plates. We then demonstrated the utility of the system for in vitro circadian entrainment using a daily cortisol pulse, generating a sustained circadian amplitude that is essential for physiological emulation and chrono-pharmacological studies. The multiplexed pump is complemented by a package of fluidic interconnection and management methods enabling user-friendly and scalable operation. Collectively, the suite of technologies provides a much-needed improvement in physiological emulation to support the predictive value of in vitro biomedical and biological research." @default.
- W4213447289 created "2022-02-25" @default.
- W4213447289 creator A5010376459 @default.
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- W4213447289 date "2022-01-01" @default.
- W4213447289 modified "2023-09-26" @default.
- W4213447289 title "Comprehensive multiplexed superfusion system enables physiological emulation in cell culture: exemplification by persistent circadian entrainment" @default.
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- W4213447289 doi "https://doi.org/10.1039/d1lc00841b" @default.
- W4213447289 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/35199811" @default.
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