Agarose has been used as thickeners in foods, cosmetics, and other conventional uses [5, 6], and can be used for pharmaceutical and cell encapsulation [7, 8].
Aberrant activation of metabolic pathways has emerged as an hallmark of proliferating cancer cells and pharmaceutical approaches targeting cell metabolism hold potential for treating cancer [ 1].
Basically, the triggering process and transition should not damage the incorporated elements, including pharmaceuticals, and cells, including stem cells.
RMS can also provide an invaluable platform for further fundamental studies on stem cells and the effect of various stimuli on their differentiation (eg. mechanical stimulation for osteoblasts), as well as in-vitro testing of new pharmaceuticals on cell models.
Moreover, liposomes provide a unique characteristic to deliver pharmaceuticals into cells or even inside individual compartments [4 7].
Conventional pharmaceutical processes involving cell culture growth are generally taken under control with expensive and long laboratory tests performed by direct sampling to evaluate quality.
Myocardial perfusion is one of the key parameters to e.g., determine the area-at-risk in the infarction model (ligature of left anterior descending coronary artery) and to assess therapeutic effects such as after interventional, pharmaceutical, or stem cell therapies.
Generation and/or enrichment of stage-specific neural cells, such as multipotential neuroepithelial cells, lineage committed neural progenitors, and post-mitotic neuronal and glial subtypes will serve as an invaluable tool for pharmaceutical screening and cell therapy.
Magnetohydrodynamic (MHD) boundary layer flow over wedge shaped bodies in the presence of suspended nanoparticles plays an important role in several engineering applications, such as, microelectronics, drug delivery, heat exchangers, pharmaceutical processes, magnetic cell separation and the storage of nuclear waste.
We confirm their identity and specificity of their localization by bioinformatics, pharmaceutical experiments, live cell imaging of their dynamics and co-staining with established cellular dyes.
