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Imaging Probes (imaging + probe)
Selected AbstractsGdIII -Functionalized Fluorescent Quantum Dots as Multimodal Imaging Probes,ADVANCED MATERIALS, Issue 21 2006H. Yang Multimodal probes of GdIII -functionalized silica-coated CdS:Mn/ZnS quantum dots (see figure) that exhibit yellow fluorescence and strong paramagnetism are reported. High magnetic resonance imaging (MRI) contrast is exhibited by these quantum dots. These properties make for a probe that can operate in multiple modes, which is highly desirable for in,vivo bioimaging applications. [source] Chlorin,Bacteriochlorin Energy-transfer Dyads as Prototypes for Near-infrared Molecular Imaging Probes: Controlling Charge-transfer and Fluorescence Properties in Polar MediaPHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 4 2009Hooi Ling Kee The photophysical properties of two energy-transfer dyads that are potential candidates for near-infrared (NIR) imaging probes are investigated as a function of solvent polarity. The dyads (FbC-FbB and ZnC-FbB) contain either a free base (Fb) or zinc (Zn) chlorin (C) as the energy donor and a free base bacteriochlorin (B) as the energy acceptor. The dyads were studied in toluene, chlorobenzene, 1,2-dichlorobenzene, acetone, acetonitrile and dimethylsulfoxide (DMSO). In both dyads, energy transfer from the chlorin to bacteriochlorin occurs with a rate constant of ,(5,10 ps),1 and a yield of >99% in nonpolar and polar media. In toluene, the fluorescence yields (,f = 0.19) and singlet excited-state lifetimes (,,5.5 ns) are comparable to those of the benchmark bacteriochlorin. The fluorescence yield and excited-state lifetime decrease as the solvent polarity increases, with quenching by intramolecular electron (or hole) transfer being greater for FbC-FbB than for ZnC-FbB in a given solvent. For example, the ,f and , values for FbC-FbB in acetone are 0.055 and 1.5 ns and in DMSO are 0.019 and 0.28 ns, whereas those for ZnC-FbB in acetone are 0.12 and 4.5 ns and in DMSO are 0.072 and 2.4 ns. The difference in fluorescence properties of the two dyads in a given polar solvent is due to the relative energies of the lowest energy charge-transfer states, as assessed by ground-state redox potentials and supported by molecular-orbital energies derived from density functional theory calculations. Controlling the extent of excited-state quenching in polar media will allow the favorable photophysical properties of the chlorin,bacteriochlorin dyads to be exploited in vivo. These properties include very large Stokes shifts (85 nm for FbC-FbB, 110 nm for ZnC-FbB) between the red-region absorption of the chlorin and the NIR fluorescence of the bacteriochlorin (,f = 760 nm), long bacteriochlorin excited-state lifetime (,5.5 ns), and narrow (,20 nm) absorption and fluorescence bands. The latter will facilitate selective excitation/detection and multiprobe applications using both intensity- and lifetime-imaging techniques. [source] Imparting Multivalency to a Bifunctional Chelator: A Scaffold Design for Targeted PET Imaging Probes,ANGEWANDTE CHEMIE, Issue 40 2009Wei Liu Zwei sind besser als einer: Mehrbindige Gerüste für Imaging-Sonden für die zielgerichtete Positronenemissionstomographie enthalten Chelatliganden, die stabile, neutrale Komplexe mit Radiometallen bilden und funktionelle Gruppen zum Anbringen mehrerer Targeting-Moleküle tragen. Die Synthese eines zweibindigen Gerüsts und dessen Kupplung mit einem Targeting-Liganden ergab eine Sonde, mit deren Hilfe sich effizient Tumoren in vivo abbilden lassen (siehe Bild). [source] Tetraamine-Derived Bifunctional Chelators for Technetium-99m Labelling: Synthesis, Bioconjugation and Evaluation as Targeted SPECT Imaging Probes for GRP-Receptor-Positive Tumours,CHEMISTRY - A EUROPEAN JOURNAL, Issue 7 2010Keelara Abiraj Dr. Abstract Owing to its optimal nuclear properties, ready availability, low cost and favourable dosimetry, 99mTc continues to be the ideal radioisotope for medical-imaging applications. Bifunctional chelators based on a tetraamine framework exhibit facile complexation with Tc(V)O2 to form monocationic species with high in vivo stability and significant hydrophilicity, which leads to favourable pharmacokinetics. The synthesis of a series of 1,4,8,11-tetraazaundecane derivatives (01,06) containing different functional groups at the 6-position for the conjugation of biomolecules and subsequent labelling with 99mTc is described herein. The chelator 01 was used as a starting material for the facile synthesis of chelators functionalised with OH (02), N3 (04) and O -succinyl ester (05) groups. A straightforward and easy synthesis of carboxyl-functionalised tetraamine-based chelator 06 was achieved by using inexpensive and commercially available starting materials. Conjugation of 06 to a potent bombesin-antagonist peptide and subsequent labelling with 99mTc afforded the radiotracer 99mTc-N4-BB-ANT, with radiolabelling yields of >97,% at a specific activity of 37,GBq,,mol,1. An IC50 value of (3.7±1.3),nM was obtained, which confirmed the high affinity of the conjugate to the gastrin-releasing-peptide receptor (GRPr). Immunofluorescence and calcium mobilisation assays confirmed the strong antagonist properties of the conjugate. In vivo pharmacokinetic studies of 99mTc-N4-BB-ANT showed high and specific uptake in PC3 xenografts and in other GRPr-positive organs. The tumour uptake was (22.5±2.6),% injected activity per gram (%,IA,g,1) at 1,h post injection (p.i.). and increased to (29.9±4.0),%,IA,g,1 at 4,h p.i. The SPECT/computed tomography (CT) images showed high tumour uptake, clear background and negligible radioactivity in the abdomen. The promising preclinical results of 99mTc-N4-BB-ANT warrant its potential candidature for clinical translation. [source] Scanning Electrochemical Microscopy as an In Vitro Technique for Measuring Convective Flow Rates Across Dentine and the Efficacy of Surface Blocking TreatmentsELECTROANALYSIS, Issue 3 2005Julie Abstract Scanning electrochemical microscopy (SECM) is shown to be a powerful technique for both the measurement of local solution velocities through human dentine slices, in vitro, and for assessing quantitatively the effect of surface treatments on the flow process. SECM employs a small ultramicroelectrode (micron dimensions) as an imaging probe to provide information on the topography and transport characteristics of dentine, with high spatial resolution. In these studies the dentine sample is a membrane in a two compartment cell, which contains solutions of identical composition, including a redox active mediator (Fe(CN). In the absence of an applied pressure, the transport-limited current response at the probe electrode is due to diffusion of Fe(CN) to the UME, which depends on the probe to sample separation. Under an applied hydrostatic pressure, hydrodynamic flow across the sample enhances mass transport to the UME. With this methodology it was possible to accurately measure effective fluid velocities, by recording tip currents with and without pressure, and assess the efficacy of potential flow retarding agents for the treatment of dentinal hypersensitivity. For native dentine, the solution velocity was found to vary dramatically with location on the sample. The application of a glycerol monooleate - base paste treatment to the surface of dentine was found to lower local flow velocities significantly. This electroanalytical methodology is simple to implement and is generally applicable to assessing the efficacy and mode of action of a wide variety of potential fluid flow retarding agents. [source] Nonblinking and Nonbleaching Upconverting Nanoparticles as an Optical Imaging Nanoprobe and T1 Magnetic Resonance Imaging Contrast AgentADVANCED MATERIALS, Issue 44 2009Yong Il Park Core/shell upconverting nanoparticles (UCNPs) of NaGdF4:Er3+,Yb3+/NaGdF4 (see figure) are shown to serve as a multimodal imaging probe that works for both background-free optical imaging and magnetic resonance imaging (MRI). The nonblinking and nonbleaching properties of UCNPs can contribute to minimization of possible artifacts in long-term imaging experiments. Owing to Gd3+ ions in the host matrix, contrast is enhanced in T1 -weighted MRI. [source] Catheter-based intracardiac echocardiography in the interventional cardiac laboratoryCATHETERIZATION AND CARDIOVASCULAR INTERVENTIONS, Issue 1 2004Zheng Liu MD Abstract Recent advances in technology have engendered a renewed enthusiasm in the use of intracardiac echocardiography (ICE) to guide and assess cardiac interventions. AcuNav is a phased-array sector imaging probe equipped with color and spectral Doppler capabilities. Previous-generation imaging catheters yielded unfamiliar limited-depth radial images with no flow information. Current imaging technology such as the AcuNav has not only consolidated the role of ICE but opened newer applications in the interventional laboratory. ICE has clear advantages over transesophageal echocardiography as the imaging modality of choice in the cardiac catheterization and electrophysiological laboratories. We review the technical evolution of ICE and describe the expanded utility of the AcuNav imaging catheter during cardiac interventions. Catheter Cardiovasc Interv 2004;63:63,71. © 2004 Wiley-Liss, Inc. [source] Fluorescence lifetime imaging of activatable target specific molecular probesCONTRAST MEDIA & MOLECULAR IMAGING, Issue 1 2010Raphael Alford Abstract In vivo optical imaging using fluorescently labeled self-quenched monoclonal antibodies, activated through binding and internalization within target cells, results in excellent target-to-background ratios. We hypothesized that these molecular probes could be utilized to accurately report on cellular internalization with fluorescence lifetime imaging (FLI). Two imaging probes were synthesized, consisting of the antibody trastuzumab (targeting HER2/neu) conjugated to Alexa Fluor750 in ratios of either 1:8 or 1:1. Fluorescence intensity and lifetime of each conjugate were initially determined at endosomal pHs. Since the 1:8 conjugate is self-quenched, the fluorescence lifetime of each probe was also determined after exposure to the known dequencher SDS. In vitro imaging experiments were performed using 3T3/HER2+ and BALB/3T3 (HER2,) cell lines. Changes in fluorescence lifetime correlated with temperature- and time-dependent cellular internalization. In vivo imaging studies in mice with dual flank tumors [3T3/HER2+ and BALB/3T3 (HER2,)] detected a minimal difference in FLI. In conclusion, fluorescence lifetime imaging monitors the internalization of target-specific activatable antibody,fluorophore conjugates in vitro. Challenges remain in adapting this methodology to in vivo imaging. Copyright © 2010 John Wiley & Sons, Ltd. [source] Fluorescent Gold Nanoprobe Sensitive to Intracellular Reactive Oxygen SpeciesADVANCED FUNCTIONAL MATERIALS, Issue 12 2009Hyukjin Lee Abstract Gold nanoprobes immobilized with fluorescein-hyaluronic acid (HA) conjugates are fabricated and utilized for monitoring intracellular reactive oxygen species (ROS) generation in live cells via nanoparticle surface energy transfer. A bio-inspired adhesive molecule, dopamine, is used to robustly end-immobilize HA onto the surface of gold nanoparticles (AuNPs) for securing intracellular stability against glutathione. ROS induces cleavage and fragmentation of the HA chains immobilized on the surface of the AuNPs allows rapid and specific detection of intracellular ROS by emitting strong fluorescence-recovery signals. In particular, fluorescence-quenched gold nanoprobes exhibit selective and dose-dependent fluorescence-recovery signals upon exposure to certain oxygen species such as superoxide anion () and hydroxyl radical (·OH). The fluorescent gold nanoprobe is usefully exploited for real-time intracellular ROS detection and antioxidant screening assay, and has exciting potential for various biomedical applications as a new class of ROS imaging probes. [source] New Generation of Multifunctional Nanoparticles for Cancer Imaging and TherapyADVANCED FUNCTIONAL MATERIALS, Issue 10 2009Kyeongsoon Park Abstract Advances in nanotechnology have contributed to the development of novel nanoparticles that enable the tumor-specific delivery of imaging probes and therapeutic agents in cancer imaging and therapy. Nanobiotechnology combines nanotechnology with molecular imaging, which has led to the generation of new multifunctional nanoparticles for cancer imaging and therapy. Multifunctional nanoparticles hold great promise for the future of cancer treatment because they can detect the early onset of cancer in each individual patient and deliver suitable therapeutic agents to enhance therapeutic efficacy. The combination of tumor-targeted imaging and therapy in an all-in-one system provides a useful multimodal approach in the battle against cancer. Novel multifunctional nanoparticles thus offer a new avenue in the application of personalized medicine in the near future. Herein, new trends and the significance of novel multifunctional nanoparticles in cancer imaging and therapy are reviewed. [source] Chlorin,Bacteriochlorin Energy-transfer Dyads as Prototypes for Near-infrared Molecular Imaging Probes: Controlling Charge-transfer and Fluorescence Properties in Polar MediaPHOTOCHEMISTRY & PHOTOBIOLOGY, Issue 4 2009Hooi Ling Kee The photophysical properties of two energy-transfer dyads that are potential candidates for near-infrared (NIR) imaging probes are investigated as a function of solvent polarity. The dyads (FbC-FbB and ZnC-FbB) contain either a free base (Fb) or zinc (Zn) chlorin (C) as the energy donor and a free base bacteriochlorin (B) as the energy acceptor. The dyads were studied in toluene, chlorobenzene, 1,2-dichlorobenzene, acetone, acetonitrile and dimethylsulfoxide (DMSO). In both dyads, energy transfer from the chlorin to bacteriochlorin occurs with a rate constant of ,(5,10 ps),1 and a yield of >99% in nonpolar and polar media. In toluene, the fluorescence yields (,f = 0.19) and singlet excited-state lifetimes (,,5.5 ns) are comparable to those of the benchmark bacteriochlorin. The fluorescence yield and excited-state lifetime decrease as the solvent polarity increases, with quenching by intramolecular electron (or hole) transfer being greater for FbC-FbB than for ZnC-FbB in a given solvent. For example, the ,f and , values for FbC-FbB in acetone are 0.055 and 1.5 ns and in DMSO are 0.019 and 0.28 ns, whereas those for ZnC-FbB in acetone are 0.12 and 4.5 ns and in DMSO are 0.072 and 2.4 ns. The difference in fluorescence properties of the two dyads in a given polar solvent is due to the relative energies of the lowest energy charge-transfer states, as assessed by ground-state redox potentials and supported by molecular-orbital energies derived from density functional theory calculations. Controlling the extent of excited-state quenching in polar media will allow the favorable photophysical properties of the chlorin,bacteriochlorin dyads to be exploited in vivo. These properties include very large Stokes shifts (85 nm for FbC-FbB, 110 nm for ZnC-FbB) between the red-region absorption of the chlorin and the NIR fluorescence of the bacteriochlorin (,f = 760 nm), long bacteriochlorin excited-state lifetime (,5.5 ns), and narrow (,20 nm) absorption and fluorescence bands. The latter will facilitate selective excitation/detection and multiprobe applications using both intensity- and lifetime-imaging techniques. [source] Isomeric Squaraine-Based [2]Pseudorotaxanes and [2]Rotaxanes: Synthesis, Optical Properties, and Their Tubular Structures in the Solid StateCHEMISTRY - A EUROPEAN JOURNAL, Issue 28 2010Min Xue Abstract On the basis of formation of [2]pseudorotaxane complexes between triptycene-derived tetralactam macrocycles 1,a and 1,b and squaraine dyes, construction of squaraine-based [2]rotaxanes through clipping reactions were studied in detail. As a result, when two symmetrical squaraines 2,d and 2,e were utilized as templates, two pairs of isomeric [2]rotaxanes 3,a,b and 4,a,b as diastereomers were obtained, owing to the two possible linking modes of triptycene derivatives. It was also found, interestingly, that when a nonsymmetrical dye 2,g was involved, there existed simultaneously three isomers of [2]rotaxanes in one reaction due to the different directions of the guest threading. The 1H,NMR and 2D NOESY NMR spectra were used to distinguish the isomers, and the yield of [2]rotaxane 5,a with the benzyl group in the wider rim of the host 1,a was found to be higher than that of another isomer 5,b with an opposite direction of the guest, which indicated the partial selection of the threading direction. The X-ray structures of 3,b and 4,a showed that, except for the standard hydrogen bonds between the amide protons of the hosts and the carbonyl oxygen atoms of the guests, multiple ,,,,, stacking and CH,,,, interactions between triptycene subunits and aromatic rings of the guests also participated in the complexation. Crystallographic studies also revealed that the [2]rotaxane molecules 3,b and 4,a further self-assembled into tubular structures in the solid state with the squaraine dyes inside the channels. In the case of 4,a, all the nonsymmetrical macrocyclic molecules pointed in one direction, which suggests the formation of oriented tubular structures. Moreover, it was also found that the squaraines encapsulated in the triptycene-derived macrocycles were protected from chemical attack, and subsequently have potential applications in imaging probes and other biomedical areas. [source] | ||||||||||||||||