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. Author manuscript; available in PMC: 2009 Feb 26.
Published in final edited form as: Biomaterials. 2005 Oct 21;27(7):947–954. doi: 10.1016/j.biomaterials.2005.09.036

Table 2.

Functional groups incorporated into the vector for regulating environmental interactions

Targeting ligands Target Cell types Refs.
Folate Folate receptor Malignant cells e.g. ovarian carcinomas [22]
Transferrin Transferrin receptor Malignant cells e.g. leukemia cells [23]
RGD Integrin Broad range of cells e.g. endothelial cells [24]
EGF (epidermal growth factor) EGF receptor Malignant cells e.g. epidermal carcinoma cells [25]
Anti-CD3 CD3 T-cells [26]

Vector stabilization Mechanism Refs.

PEG (poly(ethylene glycol)) Provides stability against serum components [22]
Polysaccharides (e.g. β-cyclodextrin, chitosan, polyglucaramidoamine) Reduces toxicity and inflammation, provides stability against serum components [17,19,52]
Biomaterial immobilization Material Refs.

Biotin Neutravidin modified hyaluronic acid [36]
Non-specific interactions (e.g. charge) Poly(lactide-co-glycolide) (PLG) [30]