In vivo performance of polymer nanocarriers dually-targeted to epitopes of the same or different receptors.

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TitleIn vivo performance of polymer nanocarriers dually-targeted to epitopes of the same or different receptors.
Publication TypeJournal Article
Year of Publication2013
AuthorsPapademetriou, IT, Garnacho, C, Schuchman, EH, Muro, S
JournalBiomaterials
Volume34
Issue13
Pagination3459-66
Date Published2013 Apr
ISSN1878-5905
KeywordsAnimals, Antibodies, Brain, Drug Carriers, Drug Delivery Systems, Epitopes, Intercellular Adhesion Molecule-1, Male, Mice, Mice, Inbred C57BL, Nanoparticles, Organ Specificity, Polymers, Receptors, Transferrin, Sphingomyelin Phosphodiesterase, Tissue Distribution
Abstract

Modification of drug delivery nanomaterials with affinity molecules that facilitate targeting, has rendered a new class of ligands for cell receptors, which often possess valency and dimensions different from natural counterparts. Designing strategies to target multiple receptors or, never explored, multiple epitopes on the same receptor may modulate the biodistribution properties of these nanomaterials. We examined this using antibody-directed targeting of polymer nanocarriers to transferrin receptor (TfR) and intercellular adhesion molecule 1 (ICAM-1). Regarding epitopes on one receptor, nanocarriers addressed with anti-TfR-R17 maintained brain and lung targeting in mice, compared with "free" antibody, while anti-TfR-8D3 nanocarriers lost specificity. Coating nanocarriers with both antibodies decreased targeting in brain and liver, not lungs, modulating biodistribution. Regarding different receptors, nanocarriers coated with both anti-ICAM and anti-TfR displayed intermediate specific accumulation in lungs and higher in liver, compared to single-targeted nanocarriers, while brain targeting was comparable to TfR- and lower than ICAM-1-targeted nanocarriers. Tracing a model therapeutic cargo, acid sphingomyelinase (enzyme replacement for Niemann-Pick Disease A-B), showed that combined-targeted anti-ICAM/TfR nanocarriers enhanced enzyme delivery versus "free" enzyme, with biodistribution patterns different from single-targeted nanocarriers. Hence, targeting nanocarriers to multiple epitopes or receptors holds promise to control distribution of drug delivery nanomaterials in the body.

DOI10.1016/j.biomaterials.2013.01.069
Alternate JournalBiomaterials
PubMed ID23398883
PubMed Central IDPMC3607514
Grant ListR01 HL098416 / HL / NHLBI NIH HHS / United States
R01 HL098416 / HL / NHLBI NIH HHS / United States