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WIREs Nanomed Nanobiotechnol
2010 Impact Factor: 2.189

High‐resolution light microscopy using luminescent nanoparticles

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This review presents recent progress in the development of the luminescent nanoparticles for confocal and multiphoton microscopy. Four classes of nanomaterials are discussed: (1) silica‐based nanoparticles doped with fluorescent molecules, (2) gold nanoparticles, (3) semiconductor nanocrystals (quantum dots/rods), and (4) nanophosphors. Special considerations are given to recently developed imaging nanoprobes, such as (1) organically modified silica (ORMOSIL) nanoparticles doped with two‐photon absorbing fluorophores, which exhibit aggregation‐enhanced fluorescence (AEF), and (2) nanophosphors (ceramic nanoparticles containing luminescent lanthanoid ions). Advantages and disadvantages of every class of nanomaterials and their specific applications are briefly discussed. WIREs Nanomed Nanobiotechnol 2010 2 162–175

Figure 1.

Confocal images of MiaPaCa (upper row) and COS-1 (lower row) cells, treated with nontargeted (a, d), and transferrin (b, e) and anti-claudin-4-conjugated (c and f) organically modified silica (ORMOSIL) nanoparticles.

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Figure 2.

Pseudocolor donor (green)-acceptor (red) channel-merged two-photon fluorescence images of HeLa cells treated with NP-AD for 1 h, before (left panel) and after (central panel) acceptor bleaching in the areas indicated by boxes. Right panel shows transmission image of cells. (Reprinted with permission from Ref 42. Copyright 2007 ACS).

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Figure 3.

Two-photon-excited luminescence image of live pancreatic cancer cells targeted with CdSe/CdS/ZnS quantum dots (QDs). Autofluorescence from the cells is shown as green pseudocolor and QDs are shown as red.

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Figure 4.

Confocal microscopy images of HeLa cell labeled with transferrin-conjugated CdSe/CdS/ZnS quantum rods. The luminescence (a) and transmission (b) images are shown.

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Figure 5.

Confocal microscopy images of (a) MiaPaCa cells treated with anti-claudin-4-conjugated InP/ZnS quantum dots (QDs) and (b) KB (human nasopharyngeal epidermal carcinoma cell line) cells treated with anti-claudin-4-conjugated InP/ZnS QDs. A nucleus staining dye, Hoechst 33342, is seen as blue and red shows emission from InP/ZnS QDs.

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Figure 6.

Confocal images of the pancreatic cancer cells (Panc-1) treated with upconverting nanophosphors (UCNPs) (NaYF4: Er3+, Yb3+, Gd3+). Left panel shows cells treated with nonbioconjugated nanophosphors and right panel shows cells targeted with nanophosphors conjugated with anti-claudin-4. (Reprinted with permission from Ref 112. Copyright 2009 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim).

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Figure 7.

Photoluminescence image of Panc-1 cells treated with NIR-to-NIR upconverting nanophosphors (UCNPs). (Reproduced with permission from Ref 106. Copyright 2008 ACS).

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works at the interface of biotechnology and materials science. His lab is researching many topics, such as investigating the mechanism of release from polymeric delivery systems with concomitant microstructural analysis and mathematical modeling; studying applications of these systems including the development of effective long-term delivery systems for insulin, anti-cancer drugs, growth factors, gene therapy agents and vaccines; developing controlled release systems that can be magnetically, ultrasonically, or enzymatically triggered to increase release rates; synthesizing new biodegradable polymeric delivery systems which will ultimately be absorbed by the body; creating new approaches for delivering drugs such as proteins and genes across complex barriers such as the blood-brain barrier, the intestine, the lung and the skin; stem cell research including controlling growth and differentiation; and creating new biomaterials with shape memory or surface switching properties.

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