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. Author manuscript; available in PMC: 2014 May 28.
Published in final edited form as: J Control Release. 2013 Mar 6;168(1):88–102. doi: 10.1016/j.jconrel.2013.02.020

Table 4. Design Parameters for Nanoparticle vehicles for Photosensitizer Delivery to Solid Tumors.

Criteria Rationale
Size and Shape
  • Facilitate vascular margination and extravasation into tumor

Plasma Half-Life
  • Increase circulation time for tumor-selective passive accumulation

Drug Encapsulation Efficiency
  • Limit partitioning of drug in plasma and reduce nonspecific uptake

    Ensure that drug is not in a highly aggregated form

Surface Charge (zeta potential)
  • Minimize aggregation of nanoparticle vehicles in suspension

Controlled Release Kinetics
  • Maintain desirable therapeutic action specifically at the target site

Active Cell-Targeting Ability
  • Facilitate receptor- or membrane-mediated intracellular uptake

Ease of Formulation and Scale Up
  • Facilitate translation into large-scale clinical use

Possible Imaging Component
  • Enable image-guided therapy and image-assisted evaluation