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Nanocolloidal albumin-IRDye 800CW: a near-infrared fluorescent tracer with optimal retention in the sentinel lymph node
Authors
AA Dünne
AC Leeuwen Van
+38 more
BE Schaafsma
C Hirche
C Tsopelas
C. René Leemans
D Murawa
DA Heuveling
Derrek A. Heuveling
EA Velde Te
G Binnig
Gerard W. M. Visser
Gijs J. L. Wuite
GL Ross
Guus A. M. S. van Dongen
H Abe
HG Hansma
HG Poel Van der
Johannes F. de Boer
JS Mieog
JV Frangioni
K Rurack
LM Crane
LW Alkureishi
M Baclayon
M Hutteman
MA Broglie
Marian Baclayon
Mattijs de Groot
MG Bredell
MV Marshall
N Tagaya
Remco de Bree
RJ Es Van
S Ohnishi
SL Troyan
T Buckle
T Hojo
T Kitai
Wouter H. Roos
Publication date
1 January 2012
Publisher
Springer-Verlag
Doi
Cite
View
on
PubMed
Abstract
Purpose: At present, the only approved fluorescent tracer for clinical near-infrared fluorescence-guided sentinel node (SN) detection is indocyanine green (ICG), but the use of this tracer is limited due to its poor retention in the SN resulting in the detection of higher tier nodes. We describe the development and characterization of a next-generation fluorescent tracer, nanocolloidal albumin-IRDye 800CW that has optimal properties for clinical SN detection Methods: The fluorescent dye IRDye 800CW was covalently coupled to colloidal human serum albumin (HSA) particles present in the labelling kit Nanocoll in a manner compliant with current Good Manufacturing Practice. Characterization of nanocolloidal albumin-IRDye 800CW included determination of conjugation efficiency, purity, stability and particle size. Quantum yield was determined in serum and compared to that of ICG. For in vivo evaluation a lymphogenic metastatic tumour model in rabbits was used. Fluorescence imaging was performed directly after peritumoral injection of nanocolloidal albumin-IRDye 800CW or the reference ICG/HSA (i.e. ICG mixed with HSA), and was repeated after 24 h, after which fluorescent lymph nodes were excised. Results: Conjugation of IRDye 800CW to nanocolloidal albumin was always about 50% efficient and resulted in a stable and pure product without affecting the particle size of the nanocolloidal albumin. The quantum yield of nanocolloidal albumin-IRDye 800CW was similar to that of ICG. In vivo evaluation revealed noninvasive detection of the SN within 5 min of injection of either nanocolloidal albumin-IRDye 800CW or ICG/HSA. No decrease in the fluorescence signal from SN was observed 24 h after injection of the nanocolloidal albumin-IRDye 800CW, while a strong decrease or complete disappearance of the fluorescence signal was seen 24 h after injection of ICG/HSA. Fluorescence-guided SN biopsy was very easy. Conclusion: Nanocolloidal albumin-IRDye 800CW is a promising fluorescent tracer with optimal kinetic features for SN detection. © The Author(s) 2012
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