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The cytotoxicity of the formulation was evaluated via MTT assay34.
Furthermore, the designed formulation was evaluated for protein adsorption, hemo˗cytocompatibility and stability.
The optimal formulation was evaluated in various release media and agitation rates.
Dendrimer formulation was evaluated for in vitro drug release and haemolytic studies under various pH conditions.
Finally, the optimal formulation was evaluated in an air-lift bioreactor performing a fed-batch culture.
The optimized formulation was evaluated in LPS-stimulated RAW 264.7 macrophages to investigate its anti-inflammatory activity.
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The drug release properties of the formulation were evaluated under real-time and accelerated test conditions.
The accuracy and effectiveness of the aforementioned formulation are evaluated using four comprehensive examples.
The morphology, size, physicochemical characterization and in vitro release behavior of the optimized formulation were evaluated.
The prediction capability of the new formulation is evaluated under different dominant effects governing interface motion.
In this paper, the current EN1993-1-5 formulation is evaluated and some peculiarities concerning the treatment of hybrid girders subjected to patch loading are pinpointed.
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