We studied the migration pattern, morphology and viability of cells suspended in five different fibrin glues.
Compared to untreated cells, the Epo-treated cardiac myoblasts exhibited better morphology and viability.
These results suggest that cardiac microtissues respond in terms of morphology and viability following clinical structural cardiotoxins, signifying they are a suitable model system to detect changes in cardiac structure at the morphological level.
Keratinocytes and fibroblasts were exposed to the dusts for different durations of time and their effects on morphology and viability of the cells were determined.
Moreover, the morphology and viability of osteoblast-like cells (MG63) on composite scaffolds were analysed using scanning electron microscopy and MTT assays.
The biocompatibility assay and SEM imaging reveal that the nanofibrous structure promotes the attachment and maintained characteristic cell morphology and viability up to 72 h.
3T3 cell morphology and viability assessed using the live/dead cell staining protocol show a significant enhancement of cell affinity on the surface of Z-P-Ti.
Cell morphology and viability tests indicated that the drug-loaded G5-PC conjugate could effectively enter the cancer cells and inhibit the growth of cancer cells.
Experimental results from cell stain assay and SEM imaging showed that the nanofibrous structure promoted the attachment of human osteoblasts and chondrocytes and maintained characteristic cell morphology and viability throughout the period of study.
In order to evaluate the impact of S-layer functionalization on the degradation of NPCs, S-Layer functionalized NPCs were characterized in vitro in terms of cell morphology and viability.
The morphology and viability of human acini were evaluated.
