Culturing, Freezing, Processing, and Imaging of Entire Organoids and Spheroids While Still in a Hydrogel.

Organoids and spheroids, three-dimensional growing structures in cell culture labs, are becoming increasingly recognized as superior models compared to two-dimensional culture models, since they mimic the human body better and have advantages over animal studies. However, these studies commonly face problems with reproducibility and consistency. During the long experimental processes - with transfers of organoids and spheroids between different cell culture vessels, pipetting, and centrifuging - these susceptible and fragile 3D growing structures are often damaged or lost. Ultimately, the results are significantly affected, since the 3D structures cannot maintain the same characteristics and quality. The methods described here minimize these stressful steps and ensure a safe and consistent environment for organoids and spheroids throughout the processing sequence while they are still in a hydrogel in a multipurpose device. The researchers can grow, freeze, thaw, process, stain, label, and then examine the structure of organoids or spheroids under various high-tech instruments, from confocal to electron microscopes, using a single multipurpose device. This technology improves the studies' reproducibility, reliability, and validity, while maintaining a stable and protective environment for the 3D growing structures during processing. In addition, eliminating stressful steps minimizes handling errors, reduces time taken, and decreases the risk of contamination.

Effect of biogas sparging with different membrane modules on membrane fouling in anaerobic submerged membrane bioreactor (AnSMBR).

This study focused on the effect of biogas sparging and different membrane modules such as cylinder shaped, funnel-shaped, and U-shaped on the membrane fouling behavior in a lab-scale submerged anaerobic membrane bioreactor (AnSMBR) which was operated for over 60 days. In order to investigate the membrane fouling behavior, a series of analysis such as SMP, EPS, scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDX), particle size distribution, and filtration resistances were performed. Although the rapid generation of cake layer took placed in case of the absence of biogas sparging, the membrane module design mostly influenced the membrane resistance when biogas sparging was applied. Total resistance was the highest for U-shaped module. The permeate fluxes with biogas sparging were higher about one half and two times than those without biogas sparging. Cylinder-shaped module had the lowest SMP and EPS concentrations followed by U-shaped and funnel-shaped modules under both cases with and without biogas sparging. The total resistances of all membrane modules without biogas sparging were found to be very high compared the pore blocking resistances (Rp).

Kinetics of Remazol Black B adsorption onto carbon prepared from sugar beet pulp.

Dried sugar beet pulp, an agricultural solid waste, was used for the production of carbon. Carbonised beet pulp was tested in the adsorption of Remazol Black B dye, and adsorption studies with real textile wastewater were also performed. Batch kinetic studies showed that an equilibrium time of 180 min was needed for the adsorption. The maximum dye adsorption capacity was obtained as 80.0 mg g(-1) at the temperature of 25 °C at pH = 1.0. The Langmuir and Freundlich adsorption models were used for the mathematical description of the adsorption equilibrium, and it was reported that experimental data fitted very well to the Langmuir model. Mass transfer and kinetic models were applied to the experimental data to examine the mechanisms of adsorption and potential rate-controlling steps. It was found that both external mass transfer and intraparticle diffusion played an important role in the adsorption mechanisms of dye, and adsorption kinetics followed the pseudo-second-order type kinetic model. The thermodynamic analysis indicated that the sorption process was exothermic and spontaneous in nature.