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A Comprehensive Procedure to Evaluate the In Vivo Performance of Cancer Nanomedicines
Published on: March 4, 2017
The Reality of Active Targeting in Nanomedicine: Promise Versus Performance
1Department of Chemistry, Materials and Chemical Engineering "Giulio Natta", Politecnico di Milano, Milan, Italy.
Chembiochem : a European Journal of Chemical Biology
|July 24, 2026
Summary
Active targeting in nanomedicine shows promise but faces clinical translation challenges. Future nanocarrier design must mimic natural biological targeting for improved drug delivery.
Area of Science:
- Nanomedicine
- Biotechnology
- Materials Science
Background:
- Active targeting in nanomedicine uses ligands on nanocarriers for selective binding to biological targets.
- Clinical translation of targeted nanoparticles is limited, with approved systems often using antibodies or passive delivery.
Purpose of the Study:
- To critically examine the gap between active targeting's promise and its practical performance in nanomedicine.
- To highlight limitations in current nanomedicine targeting strategies compared to natural biological systems.
Main Methods:
- Comparative analysis of active targeting in nanomedicine versus natural biological targeting mechanisms.
- Identification of key factors neglected in current nanomedicine targeting approaches.
Main Results:
- Natural targeting involves dynamic, multi-step, energy-dependent processes, unlike simplified ligand-receptor interactions.
- Current nanomedicine approaches oversimplify targeting, ignoring multivalency, spatial organization, kinetics, and biological barriers.
Conclusions:
- Future nanomedicine requires systems-level design integrating spatiotemporal control, adaptive materials, and computational modeling.
- A design-by-architecture paradigm, encoding targeting into nanomaterial structure, is proposed for programmable, biologically guided delivery.
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