TY - JOUR
T1 - Receptor-Targeted Luminescent Silver Bionanoparticles
AU - Bunschoten, Anton
AU - Chin, Patrick T.K.
AU - Buckle, Tessa
AU - van der Linden, Marte
AU - Barendregt, Arjan
AU - Verheijen, Marcel A.
AU - van Leeuwen, Fijs W.B.
PY - 2016
Y1 - 2016
N2 - Luminescent Ag nanoclusters (Ag-NC) provide the next generation in bionanoparticles, wherein the luminescence (650 nm) and large Stokes shift of these inorganic nanoclusters are favorable for biological imaging. By combining these characteristics with those of human serum albumin (HSA; a protein capable of binding multiple endo- and exogenous compounds), the Ag nanoclusters can be shielded from the environment and functionalized with (receptor) targeting moieties. Encapsulation of the 1.5 nm Ag nanoclusters by HSA resulted in a threefold increase in luminescence intensity and a twofold increase of the luminescence lifetime (1.7 vs. 3.6 µs). To exemplify the potential of this targeted concept, we functionalized HSA-Ag nanoparticles with chemokine receptor 4 (CXCR4) targeting peptides [Ac-TZ14011(CO2H)]. The resulting Ac-TZ14011-HSA-Ag nanoparticles demonstrated specific binding to CXCR4-overexpressing tumor cells. Upon exposure to (ambient) light, particle-functionalized tumor cells were killed. Combined, these experiments illustrate that HSA-Ag nanoparticles may have a potential in biological imaging and possibly even in targeted theranostic applications.
AB - Luminescent Ag nanoclusters (Ag-NC) provide the next generation in bionanoparticles, wherein the luminescence (650 nm) and large Stokes shift of these inorganic nanoclusters are favorable for biological imaging. By combining these characteristics with those of human serum albumin (HSA; a protein capable of binding multiple endo- and exogenous compounds), the Ag nanoclusters can be shielded from the environment and functionalized with (receptor) targeting moieties. Encapsulation of the 1.5 nm Ag nanoclusters by HSA resulted in a threefold increase in luminescence intensity and a twofold increase of the luminescence lifetime (1.7 vs. 3.6 µs). To exemplify the potential of this targeted concept, we functionalized HSA-Ag nanoparticles with chemokine receptor 4 (CXCR4) targeting peptides [Ac-TZ14011(CO2H)]. The resulting Ac-TZ14011-HSA-Ag nanoparticles demonstrated specific binding to CXCR4-overexpressing tumor cells. Upon exposure to (ambient) light, particle-functionalized tumor cells were killed. Combined, these experiments illustrate that HSA-Ag nanoparticles may have a potential in biological imaging and possibly even in targeted theranostic applications.
KW - Bioinorganic chemistry
KW - Drug delivery
KW - Imaging agents
KW - Medicinal chemistry
KW - Nanoparticles
KW - Silver
U2 - 10.1002/ejic.201501414
DO - 10.1002/ejic.201501414
M3 - Article
AN - SCOPUS:84977103424
SN - 1434-1948
VL - 2016
SP - 3030
EP - 3035
JO - European Journal of Inorganic Chemistry
JF - European Journal of Inorganic Chemistry
IS - 18
ER -