Sentence examples for vitro model designed from inspiring English sources

To investigate material density, flow, and viscosity effects on microsphere distribution within an in vitro model designed to simulate hepatic arteries.

Using an in vitro model designed to recapitulate cellular events implicated in mycobacterial infection and dissemination in vivo (i.e., phagocytosis of apoptotic macrophages containing mycobacteria), we demonstrated reduced recovery of viable mycobacteria within Cd36 -/- macrophages.

To our knowledge, this is the first study, which compares sCUR and nCUR in an in vitro model designed to mimic the pro-inflammatory action of bacteria on human pharyngeal cells.

Native vascular extracellular matrices (vECM) consist of elastic fibers that impart varied topographical properties, yet most in vitro models designed to study the effects of topography on cell behavior are not representative of native architecture.

In vitro models designed to mimic the physiology of Mtb in the dormant state are based on hypoxia, nutrient starvation, and exposure to acid pH and nitric oxide as these conditions are speculated to prevail in the lesion of latent infection [8], [9], [10], [11], [12].

In vitro models designed to assess tumor cell metastatic potential vary considerably and typically possess both advantages and disadvantages.

Similar examples can be found in in vitro models designed to detect enrichment of resistance during treatment of bacterial infections and models reflecting the stage specificity of the action of antimalarial drugs which have helped to explain patterns of parasite clearance observed in clinical studies of quinine and artemisinin-based compounds.

Using an in-vitro model designed to mimic the transport-permissive brain microvasculature, we demonstrate size-dependent permeation properties with respect to core particle size and PEG chain length.

MATERIALS AND METHODS: An in vitro perfusion model designed to mimic arterial flow conditions was created.

Thus, we obtained a useful in vitro experimental model designed to monitor the cytotoxic potential of the natural peptide called magainin II.

We separately simulated the effects of two metabolic inhibitors, 3-NP and sAMS, on the growth of M. tuberculosis cells, using an in vitro media model designed to mimic the limited nutritional environment in a host cell.