Targeting pancreatic cancer with magneto-fluorescent theranostic gold nanoshells

We report a magneto-fluorescent theranostic nanocomplex targeted to neutrophil gelatinase-associated lipocalin (NGAL) for imaging and therapy of pancreatic cancer. Gold nanoshells resonant at 810 nm were encapsulated in silica epilayers doped with iron oxide and the near-infrared (NIR) dye indocyani...

Full description

Saved in:
Bibliographic Details
Published inNanomedicine (London, England) Vol. 9; no. 8; pp. 1209 - 1222
Main Authors Chen, Wenxue, Ayala-Orozco, Ciceron, Biswal, Nrusingh C, Perez-Torres, Carlos, Bartels, Marc, Bardhan, Rizia, Stinnet, Gary, Liu, Xian-De, Ji, Baoan, Deorukhkar, Amit, Brown, Lisa V, Guha, Sushovan, Pautler, Robia G, Krishnan, Sunil, Halas, Naomi J, Joshi, Amit
Format Journal Article
LanguageEnglish
Published London Future Medicine Ltd 01.06.2014
Future Medicine
Subjects
MRI
MRI
Online AccessGet full text

Cover

Loading…
More Information
Summary:We report a magneto-fluorescent theranostic nanocomplex targeted to neutrophil gelatinase-associated lipocalin (NGAL) for imaging and therapy of pancreatic cancer. Gold nanoshells resonant at 810 nm were encapsulated in silica epilayers doped with iron oxide and the near-infrared (NIR) dye indocyanine green, resulting in theranostic gold nanoshells (TGNS), which were subsequently conjugated with antibodies targeting NGAL in AsPC-1-derived xenografts in nude mice. Anti-NGAL-conjugated TGNS specifically targeted pancreatic cancer cells and providing contrast for both NIR fluorescence and T -weighted MRI with higher tumor contrast than can be obtained using long-circulating, but nontargeted, PEGylated nanoparticles. The nanocomplexes also enabled highly specific cancer cell death via NIR photothermal therapy . TGNS with embedded NIR and magnetic resonance contrasts can be specifically targeted to pancreatic cancer cells with expression of early disease marker NGAL, and enable molecularly targeted imaging and photothermal therapy. Original submitted 6 November 2012; Revised submitted 25 March 2013
Bibliography:ObjectType-Article-2
SourceType-Scholarly Journals-1
ObjectType-Feature-1
content type line 23
Equal contributing first authors
ISSN:1743-5889
1748-6963
DOI:10.2217/nnm.13.84