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									<identifier>oai:www.peertechzpublications.org:10.17352/abse.000003</identifier>
									<datestamp>2015-09-28</datestamp>
									<setSpec>PTZ.ABSE:VOL1</setSpec>
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										<dc:title>
										Fabrication and Characterization of HER2 Cell Receptor-Targeted Indocyanine Green-Encapsulated Poly (Lactic-co-Glycolic Acid) Nanoparticles
										</dc:title><dc:creator>Yu-Hsiang Lee</dc:creator><dc:creator> Yun-Han Lai</dc:creator><dc:description>&lt;p&gt;&lt;strong&gt;Introduction:&lt;/strong&gt; The aim of this study is to fabricate and characterize human epidermal growth
factor receptor 2 (HER2)-targeted indocyanine green (ICG)-loaded poly (lactic-co-glycolic acid (PLGA)
nanoparticles (HIPNPs).&lt;/p&gt;&lt;p&gt;&lt;strong&gt;&amp;nbsp;Methods: &lt;/strong&gt;The HIPNPs were fabricated by a modified emulsification in association with solvent
evaporation approach. The size and surface charge of the manufactured&amp;nbsp; &amp;nbsp;anoparticles were
determined by dynamic light scattering technique. The morphology of the HIPNPs was detected by
SEM. The activity of surface anchored anti-HER2 antibodies was detected by spectro fluorometry
and fluorescent microscopy. The encapsulation rate of ICG, percentage of ICG content, and the
degradation efficiencies of entrapped ICG under different temperatures were measured through UVVis
spectrometry.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Results:&lt;/strong&gt; All HIPNPs exhibited particulate morphology with size of 302 ± 1.8 nm and surface charge
of -15 ± 0.15 mV where the polydispersity index was in the range of 0.02 - 0.07. The encapsulation rate
of ICG and percentage of ICG content in the HIPNPs were 70% and 23%, respectively. The stability
of ICG can be improved after encapsulated into the PLGA nanoparticles, by which the degradation
rates of entrapped ICG in 4 o
C and 37 o
C aqueous medium significantly reduced about 6- and 3-fold,
respectively, as compared to the freely dissolved ICG within 48 h.&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Conclusions:&lt;/strong&gt; We have successfully fabricated and characterized the HIPNPs in this study.
Based on the enhanced stability, bioavailability, biocompatibility, and target-ability of the HIPNPs, the
developed ICG Nano-carriers exhibited a high potential for use in near infrared-based diagnostics and
therapeutics in vitro and/or in vivo for HER2-expressing cells.&amp;nbsp;&lt;br&gt;&lt;/p&gt;</dc:description>
										<dc:publisher>Archive of Biomedical Science and Engineering - Peertechz Publications</dc:publisher>
										<dc:date>2015-09-28</dc:date>
										<dc:type>Research Article</dc:type>
										<dc:identifier>https://doi.org/10.17352/abse.000003</dc:identifier>
										<dc:language>en</dc:language>
										<dc:rights>Copyright © Yu-Hsiang Lee et al.</dc:rights>
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