Search results for "combinatorial"

showing 10 items of 1208 documents

Water-soluble hyperbranched polyglycerol photosensitizer for enhanced photodynamic therapy

2020

Porphyrin and its derivatives as promising photosensitizers have been widely utilized in photodynamic therapy (PDT). However, the water-solubility and biocompatibility of porphyrins are the typical bottlenecks in clinical PDT processes. Herein, we successfully fabricated a new type of water-soluble, hyperbranched polyglycerol photosensitizer through one-step esterification between water-soluble hyperbranched polyglycerol (hbPG) and fluorophenylporphyrin (FP). Compared with the linear control polymer, i.e., FP covalently connected with linear polyethylene glycol (LPEG), the hyperbranched structures bearing multiple porphyrin units generated more singlet oxygen and exhibited higher cytotoxici…

chemistry.chemical_classificationPolymers and PlasticsBiocompatibilitySinglet oxygenmedicine.medical_treatmentOrganic ChemistryBioengineeringPhotodynamic therapyPolymerBiochemistryCombinatorial chemistryPorphyrinchemistry.chemical_compoundchemistryCovalent bondpolycyclic compoundsmedicinePhotosensitizerCytotoxicityPolymer Chemistry
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Synthesis and characterisation of novel chemical conjugates based on alpha, beta-polyaspartylhydrazide and beta-cyclodextrins

2006

A new family of supramolecular systems based on a synthetic polyaminoacid and cyclic oligosaccharides such as beta-cyclodextrins (beta-CDs) was synthesised. The pharmaceutical potential of these systems arises from the proper combination between the complexing properties of cyclodextrins and the particular pharmacokinetic profile that can be obtained by using macromolecular conjugates with a biocompatible backbone. Five supramolecular conjugates were synthesised by using alpha,beta-polyaspartylhydrazide (PAHy) as a polymeric component and various amounts of two P-CD derivatives. In particular, by reaction of PAHy with beta-CD monoaldehyde, samples named as A(1), A(2) and A(3), bearing, resp…

chemistry.chemical_classificationPolymers and PlasticsCyclodextrinsupramolecular systemsOrganic ChemistrySupramolecular chemistryGeneral Physics and AstronomyChemical modificationConjugated systemCombinatorial chemistryInclusion compoundbeta-cyclodextrinchemistry.chemical_compoundchemistryMaterials ChemistryProton NMROrganic chemistryPAHyMacromoleculeConjugate
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Topology-Dependent Swichability of Peptide Secondary Structures in Bioconjugates with Complex Architectures

2013

Peptide sequences, which exhibit a reversible pH-responsive coil to α-helix secondary structure transition, are conjugated to polymer precursors to yield linear AB and graft ABA peptide-poly(ethylene oxide) conjugates. While the PEO B-block is comparable, the conjugates differ in topologies of the peptide bearing A-blocks. The influences of topology on the structure transitions in the peptide segments are investigated, comparing linear AB-bioconjugates with graft ABA-bioconjugates having multiple peptide segments combined in star or pom-pom topologies.

chemistry.chemical_classificationPolymers and PlasticsEthylene oxideOrganic ChemistryPeptidePolymerConjugated systemMicroscopy Atomic ForceTopologyCombinatorial chemistryProtein Structure SecondaryPolyethylene Glycolschemistry.chemical_compoundchemistryMaterials ChemistrySelf-assemblyPeptidesProtein secondary structureTopology (chemistry)ConjugateMacromolecular Rapid Communications
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Evaluating chemical ligation techniques for the synthesis of block copolypeptides, polypeptoids and block copolypept(o)ides: a comparative study

2015

In this work, we describe the synthesis of block copolypeptides, polypeptoids and block copolypept(o)ides by chemical ligation techniques. Polysarcosine (PSar), poly(N-e-trifluoroacetyl-L-lysine) (PLys(TFA)) and poly(γ-benzyl-L-glutamate) (PGlu(OBzl)) homopolymers of different polarities and end group functionalities but with similar average degrees of polymerization (Xn = 50 and 100) could be obtained by ring opening polymerization (ROP) of α-amino acid N-carboxyanhydrides (NCA) and postpolymerization modification reactions. In the next step, these polymers were applied to copper(I)-catalyzed azide–alkyne coupling (CuAAC), strain-promoted azide–alkyne coupling (SPAAC) and native chemical l…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryBioengineeringPolymerNative chemical ligationBiochemistryCombinatorial chemistryRing-opening polymerizationchemistry.chemical_compoundEnd-groupPolymerizationchemistryPeptide synthesisChemical ligationLigationPolymer Chemistry
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Pencil Lead as a Matrix for MALDI-ToF Mass Spectrometry of Sensitive Functional Polymers

2007

With the increase in complexity of functional polymers in recent years, MALDI-ToF has become an important tool for gaining precise information on polymer functionality, end groups, and, in special cases, molecular weights. Here we describe how pencil lead, deposited by simply drawing with a regular pencil onto conventional MALDI-ToF targets, can be used as a very attractive matrix for MALDI-ToF mass spectrometry of synthetic polymers. Highly sensitive polymers such as silyl hydride functional poly(styrene), poly(butadiene), and poly(isoprene) have been investigated using conventional MALDI-ToF matrices as well as pencil lead. In all cases, the use of pencil lead prevented oxidation of the h…

chemistry.chemical_classificationPolymers and PlasticsOrganic ChemistryMatrix isolationPolymerMass spectrometryCombinatorial chemistryPencil (optics)Inorganic Chemistrychemistry.chemical_compoundEnd-groupchemistryMaterials ChemistryOrganic chemistryMoleculeFunctional polymersSilyl hydrideMacromolecules
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Translocation of enzymes into a mesoporous MOF for enhanced catalytic activity under extreme conditions

2019

Translocation of protease into mesoporous MIL-101-NH2 results in enhanced catalytic activity, excellent recyclability and tolerance to competing enzymes.

chemistry.chemical_classificationProtease010405 organic chemistrymedicine.medical_treatmenteducationfungiQuímica organometàl·licaGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryhumanities0104 chemical sciencesEnzyme catalysisCatalysisChemistryEnzymechemistryBiocatalysismedicineBiocompositeMesoporous material
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Fluorogenic Enzyme-Triggered Domino Reactions Producing Quinoxalin-2(1H)-one-based Heterocycles

2020

International audience; A simple and effective biocompatible domino reaction triggered by a model protease and leading to formation of strongly fluorescent quinoxalin-2(1H)-one N-heterocycles is described. Some positive attributes including versatility and ability to provide outstanding fluorescence "OFF-ON" responses were revealed by this work. They open the way for practical applications of this novel type of "covalent-assembly" based fluorescent probes in the fields of sensing and bioimaging. Among the myriad of synthetic transformations and catalysts currently available for concise and efficient synthesis of organic molecules, bioinspired approaches based on the use of enzymes often int…

chemistry.chemical_classificationProtease[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistrymedicine.medical_treatmentOrganic Chemistry010402 general chemistryBiocompatible material01 natural sciencesBiochemistryCombinatorial chemistryFluorescenceDomino0104 chemical sciencesEnzymeCascade reactionmedicinePhysical and Theoretical ChemistryOrganic Letters
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Bistetrazine-Cyanines as Double-Clicking Fluorogenic Two-Point Binder or Crosslinker Probes

2018

Fluorogenic probes can be used to minimize the background fluorescence of unreacted and nonspecifically adsorbed reagents. The preceding years have brought substantial developments in the design and synthesis of bioorthogonally applicable fluorogenic systems mainly based on the quenching effects of azide and tetrazine moieties. The modulation power exerted by these bioorthogonal motifs typically becomes less efficient on more conjugated systems; that is, on probes with redshifted emission wavelength. To reach efficient quenching, that is, fluorogenicity, even in the red range of the spectrum, we present the synthesis, fluorogenic, and conjugation characterization of bistetrazine-cyanine pro…

chemistry.chemical_classificationQuenching (fluorescence)010405 organic chemistryChemistryOrganic ChemistryPeptideGeneral ChemistryConjugated system010402 general chemistry01 natural sciencesFluorescenceCombinatorial chemistryCatalysis0104 chemical sciencesTetrazinechemistry.chemical_compoundCovalent bondAzideBioorthogonal chemistryChemistry - A European Journal
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On the Nature of the Enzyme–Substrate Complex and the Reaction Mechanism in Human Arginase I. A Combined Molecular Dynamics and QM/MM Study

2020

We present here a detailed theoretical analysis of L-arginine hydrolysis catalyzed by Human Arginase I (HARGI). Our study combines classical molecular dynamic simulations of different model for the...

chemistry.chemical_classificationReaction mechanism010405 organic chemistryChemistrySubstrate (chemistry)General Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysis0104 chemical sciencesCatalysisArginaseQM/MMMolecular dynamicsHydrolysisEnzymeACS Catalysis
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Electrochemical monitoring of ROS generation by anticancer agents: the case of chartreusin

2017

Solution phase and solid-sate electrochemical techniques centered in the voltammetry of microparticles approach are applied for testing the cytotoxic activity of anticancer drugs. The possibility of electrochemical generation of reactive oxygen species (ROS) is exploited for evaluating their contribution to cellular damage. The described methodology is applied to the case of chartreusin (Ch) whose electrochemistry in non-aqueous solutions and in the solid state in contact with aqueous electrolytes is described in the absence (experimental data were confirmed by theoretical calculations) and in the presence of double-stranded DNA (dsDNA). In parallel, scanning electrochemical microscopy (SEC…

chemistry.chemical_classificationReactive oxygen speciesChartreusinGeneral Chemical EngineeringIntercalation (chemistry)Nanotechnology02 engineering and technologyGeneral Chemistry010402 general chemistry021001 nanoscience & nanotechnologyElectrochemistry01 natural sciencesCombinatorial chemistrySolution phase0104 chemical scienceschemistry.chemical_compoundScanning electrochemical microscopychemistry0210 nano-technologyVoltammetryDNARSC Advances
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