Despite the complexity and structural sophistication that 3D organoid models provide, their lack of vascularization and perfusion limit the capability of these models to recapitulate organ physiology effectively. A microfluidic platform named IFlowPlate is engineered, which can be used to culture up to 128 independently perfused and vascularized colon organoids in vitro. Unlike traditional microfluidic devices, the vascularized organoid‐on‐chip device with an “open‐well” design does not require any external pumping systems and allows tissue extraction for downstream analyses, such as histochemistry or even in vivo transplantation. By optimizing both the extracellular matrix (ECM) and the culture media formulation, patient‐derived colon organoids are co‐cultured successfully within a self‐assembled vascular network, and it is found that the colon organoids grow significantly better in the platform under constant perfusion versus conventional static condition. Furthermore, a colon inflammation model with an innate immune function where circulating monocytes can be recruited from the vasculature, differentiate into macrophage, and infiltrate the colon organoids in response to tumor necrosis factor (TNF)‐ inflammatory cytokine stimulation is developed using the platform. With the ability to grow vascularized colon organoids under intravascular perfusion, the IFlowPlate platform could unlock new possibilities for screening potential therapeutic targets or modeling relevant diseases.
The wet strength of cellulose-cellulose joints, reinforced with PAE-loaded microgels, was decreased by nearly a factor of two when the labile disulfide crosslinks on the supporting microgels were exposed to a reducing agent. The supporting microgels were temperature and pH sensitive poly(N-isopropylmethacrylamide-co-acrylic acid) microgels, prepared with a disulfide crosslinker. The level of PAE loading increased with the microgel carboxyl content. This work illustrates a new approach to increasing the recyclability and compostability of wet-strength papers made with PAE wet-strength resin.
Three-dimensional (3D) tissue models such as epithelial spheroids or organoids have become popular for pre-clinical drug studies. However, different from 2D monolayer culture, the characterization of 3D tissue models from...
Human stem‐cell‐derived organoids have provided new opportunities to model biological processes and recapitulate organ development. However, organoid systems lack perfusable vascular networks to deliver nutrients and drugs. In article number 2002974, Boyang Zhang and co‐workers introduce IFlowPlate—a microfluidic system with an “open‐well” design in a 384‐well plate format that can be used to vascularize and intravascularly perfuse organoids. This image shows three independently perfused microvascular networks in an IFlowPlate.
Organ-on-a-chip systems that recapitulate tissue-level functions have been proposed to improve in vitro–in vivo correlation in drug development. Significant progress has been made to control the cellular microenvironment with mechanical...
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