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For instance, the activated monomer mechanism (AMM) in cationic ring-opening polymerization allows fine-tuning of network stability, hydrophilicity, and crosslink densityparameters essential for synchronizing scaffold degradation with tissue remodeling kinetics

Potential neuroprotective mechanisms

Abstract Background: For many drugs, steady-state concentration-time profiles are often not optimally characterised by the intrinsic terminal elimination half-life for various reasons, including multiexponential disposition with minimal contribution of the terminal phase to steady-state exposure or use of controlled-release formulations with extended zero- or mixed zero-/first-order absorption

Florez H, Luo J, Castillo-Florez S, et al