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1.
J Inorg Biochem ; 209: 111119, 2020 08.
Article in English | MEDLINE | ID: mdl-32485479

ABSTRACT

Luminescence monitoring of DNA intercalator complexes is important for assessing their localisation and targeting: We report herein a luminescent hetero-trimetallic complex with europium as a luminescent reporter and two attached platinum acetylide terpyridyl units as the DNA recognition units. The ligand, based on a bisamide derivative of diethylenetriaminepentaacetic acid functionalized with two ethynyl groups, provides a backbone to anchor two platinum terpyridyl units, Pt-tpy, leading to the hairpin-shaped heterometallic complex 1. We also prepared a related mono-nuclear platinum complex 2 to compare its intercalation properties with 1. Linear dichroism, UV-visible and melting experiments show the ability of both complexes to interact with calf thymus DNA, with linear dichroism confirming intercalation and demonstrating the expected greater DNA stiffening by the bis-intercalator 1. Importantly, the tri-metallic complex 1 shows a three-fold enhancement in europium luminescence upon addition of calf thymus DNA; other mono-intercalator lanthanide designs have commonly shown a decrease in emission on binding. The ability of the complex to monitor DNA interactions gives the potential use as a luminescence switch in sensing experiments and highlights the design of heterometallic bis-intercalator complexes as an effective approach for DNA-responsive sensitisation of a lanthanide luminescence signal.


Subject(s)
Coordination Complexes/chemistry , DNA/chemistry , Europium/chemistry , Intercalating Agents/chemistry , Luminescent Agents/chemistry , Animals , Lanthanoid Series Elements/chemistry , Luminescence , Luminescent Measurements/methods , Pentetic Acid/chemistry , Photosensitizing Agents/chemistry , Platinum/chemistry , Spectrometry, Mass, Electrospray Ionization/methods , Spectrometry, Mass, Matrix-Assisted Laser Desorption-Ionization/methods
2.
J Dent ; 56: 112-120, 2017 01.
Article in English | MEDLINE | ID: mdl-27884720

ABSTRACT

OBJECTIVES: Functionalised silica sub-micron particles are being investigated as a method of delivering antimicrobials and remineralisation agents into dentinal tubules. However, their methods of application are not optimised, resulting in shallow penetration and aggregation. The aim of this study is to investigate the impact of cavitation occurring around ultrasonic scalers for enhancing particle penetration into dentinal tubules. METHODS: Dentine slices were prepared from premolar teeth. Silica sub-micron particles were prepared in water or acetone. Cavitation from an ultrasonic scaler (Satelec P5 Newtron, Acteon, France) was applied to dentine slices immersed inside the sub-micron particle solutions. Samples were imaged with scanning electron microscopy (SEM) to assess tubule occlusion and particle penetration. RESULTS: Qualitative observations of SEM images showed some tubule occlusion. The particles could penetrate inside the tubules up to 60µm when there was no cavitation and up to ∼180µm when there was cavitation. CONCLUSIONS: The cavitation bubbles produced from an ultrasonic scaler may be used to deliver sub-micron particles into dentine. This method has the potential to deliver such particles deeper into the dentinal tubules. CLINICAL SIGNIFICANCE: Cavitation from a clinical ultrasonic scaler may enhance penetration of sub-micron particles into dentinal tubules. This can aid in the development of novel methods for delivering therapeutic clinical materials for hypersensitivity relief and treatment of dentinal caries.


Subject(s)
Dental Scaling/methods , Dentin/chemistry , Dentin/ultrastructure , Silicon Dioxide/chemistry , Ultrasonic Therapy/methods , Ultrasonics , Acetone , Bicuspid , Biomechanical Phenomena , Dental Occlusion , Dental Pulp Cavity/chemistry , Dental Pulp Cavity/ultrastructure , Drug Delivery Systems , Humans , Hypersensitivity/prevention & control , Microscopy, Electron, Scanning , Molar , Nanoparticles/chemistry , Particle Size , Silicon Dioxide/therapeutic use , Surface Properties , Water
3.
Inorg Chem ; 40(16): 3912-21, 2001 Jul 30.
Article in English | MEDLINE | ID: mdl-11466049

ABSTRACT

Cyclodextrin cups have been employed to build supramolecular systems consisting of metal and organic photoactive/redox-active components; the photoinduced communication between redox-active units assembled in water via noncovalent interactions is established. The functionalization of a beta-cyclodextrin with a terpyridine unit, ttp-beta-CD, is achieved by protection of all but one of the hydroxyl groups by methylation and attachment of the ttp unit on the free primary hydroxyl group. The metalloreceptors [(beta-CD-ttp)Ru(ttp)][PF(6)](2), [(beta-CD-ttp)Ru(tpy)][PF(6)](2), and [Ru(beta-CD-ttp)(2)][PF(6)](2) are synthesized and fully characterized. The [(beta-CD-ttp)Ru(ttp)][PF(6)](2) metalloreceptor exhibits luminescence in water, centered at 640 nm, from the (3)MLCT state with a lifetime of 1.9 ns and a quantum yield of Phi = 4.1 x 10(-)(5). Addition of redox-active quinone guests AQS, AQC, and BQ to an aqueous solution of [(beta-CD-ttp)Ru(ttp)](2+) results in quenching of the luminescence up to 40%, 20%, and 25%, respectively. Measurement of the binding strength indicates that, in saturation conditions, 85% for AQS and 77% for AQC are bound. The luminescence quenching is attributed to an intercomponent electron transfer from the appended ruthenium center to the quinone guest inside the cavity. Control experiments demonstrate no bimolecular quenching at these conditions. A photoactive osmium metalloguest, [Os(biptpy)(tpy)][PF(6)], is designed with a biphenyl hydrophobic tail for insertion in the cyclodextrin cavity. The complex is luminescent at room temperature with an emission band maximum at 730 nm and a lifetime of 116 ns. The osmium(III) species are formed for the study of photoinduced electron transfer upon their assembly with the ruthenium cyclodextrin, [(beta-CD-ttp)Ru(ttp)](2+). Time-resolved spectroscopy studies show a short component of 10 ps, attributed to electron transfer from Ru(II) to Os(III) giving an electron transfer rate 9.5 x 10(9) s(-)(1).


Subject(s)
Cyclodextrins/chemistry , Organometallic Compounds/chemistry , Ruthenium/chemistry , beta-Cyclodextrins , Catalysis , Electrochemistry , Glucose/chemistry , Magnetic Resonance Spectroscopy , Molecular Structure , Structure-Activity Relationship
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