| Literature DB >> 26154069 |
Asish C Misra, Kathryn E Luker, Hakan Durmaz, Gary D Luker, Joerg Lahann1.
Abstract
CXCR4 is a cell membrane receptor that is overexpressed in triple-negative breast cancers and implicated in growth and metastasis of this disease. Using electrohydrodynamic cojetting, we prepared multicompartmental drug delivery carriers for CXCR4 targeting. The particles are comprised of a novel poly(lactide-co-glycolide) derivative that allows for straightforward immobilization of 1,1'-[1,4-phenylenebis(methylene)]bis[1,4,8,11-tetraazacyclotetradecane] (Plerixafor), a small molecule with affinity for CXCR4. Targeted nanocarriers are selectively taken up by CXCR4-expressing cells and effectively block CXCR4 signaling. This study suggests that CXCR4 may be an effective target for nanocarrier-based therapies.Entities:
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Year: 2015 PMID: 26154069 PMCID: PMC5474759 DOI: 10.1021/acs.biomac.5b00653
Source DB: PubMed Journal: Biomacromolecules ISSN: 1525-7797 Impact factor: 6.988