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Stratum corneum permeabilization with photoacoustic waves generated by piezophotonic materials.Spectroscopic properties and photodynamic effects of new lipophilic porphyrin derivatives: efficacy, localisation and cell death pathways.Photoacid for extremely long-lived and reversible pH-jumps.Analytical solution for time-resolved photoacoustic calorimetry data and applications to two typical photoreactions.Biodistribution and photodynamic efficacy of a water-soluble, stable, halogenated bacteriochlorin against melanoma.Irradiation- and sensitizer-dependent changes in the lifetime of intracellular singlet oxygen produced in a photosensitized process.The role of strong hypoxia in tumors after treatment in the outcome of bacteriochlorin-based photodynamic therapy.Intravenous Single-Dose Toxicity of Redaporfin-Based Photodynamic Therapy in Rodents.Photodynamic therapy (PDT) of cancer: from local to systemic treatment.Phthalocyanine Labels for Near-Infrared Fluorescence Imaging of Solid Tumors.Pro-oxidant and Antioxidant Effects in Photodynamic Therapy: Cells Recognise that Not All Exogenous ROS Are Alike.Elimination of primary tumours and control of metastasis with rationally designed bacteriochlorin photodynamic therapy regimens.Photodynamic therapy efficacy enhanced by dynamics: the role of charge transfer and photostability in the selection of photosensitizers.New halogenated water-soluble chlorin and bacteriochlorin as photostable PDT sensitizers: synthesis, spectroscopy, photophysics, and in vitro photosensitizing efficacy.Assessment of lifetime resolution limits in time-resolved photoacoustic calorimetry vs. transducer frequencies: setting the stage for picosecond resolution.Properties of halogenated and sulfonated porphyrins relevant for the selection of photosensitizers in anticancer and antimicrobial therapiesMechanisms of singlet-oxygen and superoxide-ion generation by porphyrins and bacteriochlorins and their implications in photodynamic therapy.Calculation of triplet-triplet energy transfer rates from emission and absorption spectra. The quenching of hemicarcerated triplet biacetyl by aromatic hydrocarbons.The triplet state of indigo.A comparative study of water soluble 5,10,15,20-tetrakis(2,6-dichloro-3-sulfophenyl)porphyrin and its metal complexes as efficient sensitizers for photodegradation of phenols.Excited-state proton transfer in gas-expanded liquids: the roles of pressure and composition in supercritical CO2/methanol mixtures.Modulation of biodistribution, pharmacokinetics, and photosensitivity with the delivery vehicle of a bacteriochlorin photosensitizer for photodynamic therapy.Absolute rate calculations for atom abstractions by radicals: energetic, structural and electronic factors.Ultrafast Dynamics of Manganese(III), Manganese(II), and Free-Base Bacteriochlorin: Is There Time for Photochemistry?On the singlet states of porphyrins, chlorins and bacteriochlorins and their ability to harvest red/infrared light.Synthesis, photophysical studies and anticancer activity of a new halogenated water-soluble porphyrin.Intracellular singlet oxygen photosensitizers: on the road to solving the problems of sensitizer degradation, bleaching and relocalization.One Peptide Reveals the Two Faces of α-Helix Unfolding-Folding Dynamics.Design of Pluronic-Based Formulation for Enhanced Redaporfin-Photodynamic Therapy against Pigmented Melanoma.Electron Transfer in Supercritical Carbon Dioxide: Ultraexothermic Charge Recombination at the End of the “Inverted Region”Temperature Dependence of Ultra-Exothermic Charge RecombinationsS1∼>T1 intersystem crossing in π-conjugated organic polymersMolecular factor analysis in atom-transfer reactionsCombined effects of singlet oxygen and hydroxyl radical in photodynamic therapy with photostable bacteriochlorins: Evidence from intracellular fluorescence and increased photodynamic efficacy in vitroHigher activation barriers can lift exothermic rate restrictions in electron transfer and enable faster reactionsPhotoacoustic transfection of DNA encoding GFPDramatic pressure-dependent quenching effects in supercritical CO2 assessed by the fluorescence of 4'-dimethylamino-3-hydroxyflavone. Thermodynamic versus kinetics control of excited-state intramolecular proton transferAbsolute rate calculations. Proton transfers in solutionThe rates of S(N)2 reactions and their relation to molecular and solvent propertiesUnderstanding chemical reactivity: the case for atom, proton and methyl transfers
P50
Q31111296-B423862E-40A2-4E55-A025-6C8F93F10CF1Q33234518-4FDEE2ED-E66B-48BC-AA21-44E21F8235B9Q33466246-D7164D14-E7C4-4B43-9558-A9147C47DF4BQ33576978-CDA2BC89-BFAE-48CF-8391-C6A42DBBBBD4Q33803055-CBE93D30-31F8-45B0-B2B9-4842E8F82AABQ34083867-CA205D14-D73F-4C68-9587-49C6549E03BAQ34083867-FB683C54-0547-4C68-96B1-C181E2EB5ADFQ35170075-11AE17C3-0A6E-446F-9956-BB2D35F37F7FQ36404170-7F8D4421-5C5E-41EC-964B-7BD1BB0234ECQ38556357-173B0AC1-2053-47B3-8349-73E20BCA0F01Q38778852-0F6377C9-B871-4407-A9D2-966306A7714AQ38792932-9DE3AB6D-F8E9-4672-9750-02EE59077083Q38857046-00461164-B8CD-41B4-86BE-4DB83C4C8EBEQ39014037-35FF3D75-2100-4B24-BEB5-73AD5BC952C2Q39666666-866A50BE-C7A0-4FFA-94B7-A98E63BAA3DEQ40175181-73A5A1A9-717D-4A70-9B14-BC4203BE0A32Q42706711-8C0BF044-1E7F-4FAA-983A-7A77C9FA8FB1Q43008074-5EF1B02D-BE9F-4164-9344-DD07200AFA19Q44475887-7E67E1DA-286D-4706-BC93-CA855FD617EBQ44677933-E191C06B-B043-4184-BE02-CFAC7767E9A6Q46624986-D8F60560-622E-4752-AB83-2F41D3925255Q46665194-AE2E4532-8476-4970-906B-0AF3AF558AEAQ46953154-C015EAA9-8A69-4022-88FB-5BAF0FB14775Q47958714-9B24FED0-52C1-431A-8F48-04806F50D6C1Q48229553-DEB07E53-DF51-4CCC-B5CB-BB56E98EE124Q50511761-826AA207-B566-497D-9A37-51311D159615Q50687340-4508B020-EF0D-4109-B046-02D5C7469C56Q51522742-A54F196F-648B-4AED-B2EB-BDB5C36C2083Q52689890-CFFD5FAF-8186-4666-B76A-60D35E26344CQ53775120-25072A49-9400-404B-A3D6-337AA426F5EDQ57595792-02FE003D-4BDE-4E68-B08E-86EE40A9E68EQ57595807-9BFE5A68-F225-4BF4-A235-766B7B0523E3Q57595888-BE4AB358-C151-4B7D-A532-099B4A42179AQ60216110-0DD8EE0B-9D19-4B8A-9BFF-45206E6DBABDQ60640373-DF629786-2335-4BAF-AD94-B2CD833A1FE1Q61135636-2D77A3E3-1987-4163-AABE-B6E2FC7666E2Q64116455-A98970A1-0B76-4E97-8B55-061F6E848722Q79430232-C9E350E9-D798-468A-9912-139A4988BA73Q79650159-85828D09-2343-45CC-B949-09587CC299E2Q80580503-3B5FD1C6-CA81-460C-BD25-8DBC2A7C8BEB
P50
description
hulumtues
@sq
researcher
@en
wetenschapper
@nl
հետազոտող
@hy
name
Luis G. Arnaut
@ast
Luis G. Arnaut
@en
Luis G. Arnaut
@es
Luis G. Arnaut
@nl
Luis G. Arnaut
@pt
Luis G. Arnaut
@sl
type
label
Luis G. Arnaut
@ast
Luis G. Arnaut
@en
Luis G. Arnaut
@es
Luis G. Arnaut
@nl
Luis G. Arnaut
@pt
Luis G. Arnaut
@sl
prefLabel
Luis G. Arnaut
@ast
Luis G. Arnaut
@en
Luis G. Arnaut
@es
Luis G. Arnaut
@nl
Luis G. Arnaut
@pt
Luis G. Arnaut
@sl
P1053
Q-4135-2016
P106
P1153
7003494940
P21
P31
P3829
P496
0000-0002-3223-4819