2009
DOI: 10.1021/ac901960d
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High Contrast Upconversion Luminescence Targeted Imaging in Vivo Using Peptide-Labeled Nanophosphors

Abstract: Fluorescence targeted imaging in vivo has proven useful in tumor recognition and drug delivery. In the process of in vivo imaging, however, a high autofluorescence background could mask the signals from the fluorescent probes. Herein, a high contrast upconversion luminescence (UCL) imaging protocol was developed for targeted imaging of tumors based on RGD-labeled upconversion nanophosphors (UCNPs) as luminescent labels. Confocal Z-scan imaging of tissue slices revealed that UCL imaging showed no autofluorescen… Show more

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Cited by 384 publications
(340 citation statements)
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“…11,12 The use of near-infrared (NIR) light in PDT can afford greater penetration depths than that of VIS light because the absorbance for most biomolecules reaches a minimum in the NIR window (700-1,100 nm), 13 and the usefulness of the upconversion nanoparticles (UCNPs) that can convert NIR light to VIS light for noninvasive imaging of deep tissues, drug delivery, and PDT has been shown. [14][15][16][17][18][19][20] In this study, we loaded a commonly used second-generation photosensitizer, chlorin e6 (Ce6), onto silica-coated upconversion nanoparticles to form a supramolecular UCNPs-Ce6 complex used for NIR light-induced PDT of THP-1 macrophages, and we subsequently determined whether UCNPs-Ce6-mediated PDT induced apoptosis through the mitochondrial caspase pathway via ROS bursts, mitochondrial permeability transition pore (MPTP) opening, mitochondrial membrane potential (MMP) depolarization, and mitochondrial dysfunction in vitro.…”
Section: Introductionmentioning
confidence: 99%
“…11,12 The use of near-infrared (NIR) light in PDT can afford greater penetration depths than that of VIS light because the absorbance for most biomolecules reaches a minimum in the NIR window (700-1,100 nm), 13 and the usefulness of the upconversion nanoparticles (UCNPs) that can convert NIR light to VIS light for noninvasive imaging of deep tissues, drug delivery, and PDT has been shown. [14][15][16][17][18][19][20] In this study, we loaded a commonly used second-generation photosensitizer, chlorin e6 (Ce6), onto silica-coated upconversion nanoparticles to form a supramolecular UCNPs-Ce6 complex used for NIR light-induced PDT of THP-1 macrophages, and we subsequently determined whether UCNPs-Ce6-mediated PDT induced apoptosis through the mitochondrial caspase pathway via ROS bursts, mitochondrial permeability transition pore (MPTP) opening, mitochondrial membrane potential (MMP) depolarization, and mitochondrial dysfunction in vitro.…”
Section: Introductionmentioning
confidence: 99%
“…As noted above, the narrow line luminescence, long ES lifetimes and photostability of Ln III -doped UCNPs make these particularly well suited for biological imaging. In this context, there have been some really exciting developments in cellular imaging [103][104][105][106][107] and in vivo imaging with small animals [103,104,[108][109][110][111]. For example, strongly fluorescent core : shell β-NaYF 4 :Yb,Er UCNPs, coated with a thin layer of SiO 2 and modified with amino groups, were covalently linked to rabbit anti-CEA8 antibodies.…”
Section: Uncaging Using Upconversion Nanoparticles (A) Introduction Tmentioning
confidence: 99%
“…Then, the MA-UCNPs were linked with the thiolated cyclopeptide (Arg-Gly-Asp-Phe-Lys(mpa)) for targeted imaging. 67,70 Maeda team 71 structured a MAfunctionalized Er-Y 2 O 3 by reacting MA-PEG-NHS with APTES-Er-Y 2 O 3 . So the MA-functionalized UCNPs could be linked with cyclic RGD peptide to speci¯cally target to integrin v 3 which is highly expressed in the tumor cell surface.…”
Section: Ma Group Modi¯cationmentioning
confidence: 99%