Search results for " co-polymers"

showing 4 items of 4 documents

Amphiphilic inulin graft co-polymers as self assembling micelles for doxorubicin delivery

2020

This paper reports the synthesis and characterization of a new amphiphilic inulin graft copolymer able to self-assemble in water into a micelle type structure and to deliver the anticancer model drug doxorubicin. For this aim, inulin was chemically modified in the side chain with primary amine groups (INU-EDA) and these were used as reactive moieties for the conjugation of poly ethylene glycol 2000 and succinyl-ceramide. The CMC of obtained amphiphilic inulin derivatives (INU-ceramide and INU-ceramide-PEG2000) was measured by means of fluorescence analysis using pyrene as the fluorescent probe. The obtained micelles were characterized by DLS and AFM analysis and the ability to release the l…

Materials sciencemicellesInulinBiomedical EngineeringMicelledoxorubicinchemistry.chemical_compoundPolymer chemistryAmphiphileCopolymermedicineSide chainGeneral Materials ScienceDoxorubicininulin micelles drug delivery doxorubicin graft co-polymersgraft co-polymersinulinGeneral ChemistryGeneral MedicinechemistrySettore CHIM/09 - Farmaceutico Tecnologico ApplicativoDrug deliverydrug deliveryPyrenemedicine.druginulin; micelles; drug delivery; doxorubicin; graft co-polymers
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mPEG-PLGA Nanoparticles Labelled with Loaded or Conjugated Rhodamine-B for Potential Nose-to-Brain Delivery

2021

Nowdays, neurodegenerative diseases represent a great challenge from both the therapeutic and diagnostic points of view. Indeed, several physiological barriers of the body, including the blood brain barrier (BBB), nasal, dermal, and intestinal barriers, interpose between the development of new drugs and their effective administration to reach the target organ or target cells at therapeutic concentrations. Currently, the nose-to-brain delivery with nanoformulations specifically designed for intranasal administration is a strategy widely investigated with the goal to reach the brain while bypassing the BBB. To produce nanosystems suitable to study both in vitro and/or in vivo cells traffickin…

Pharmaceutical Scienceolfactory ensheathing cellsBlood–brain barrierArticlefluorescent dye olfactory ensheathing cells PC12 cell line co-polymers nanomedicine imagingchemistry.chemical_compoundPharmacy and materia medicaIn vivomedicineRhodamine BPC12 cell lineCytotoxicityfluorescent dye; olfactory ensheathing cells; PC12 cell line; co-polymers; nanomedicine; imagingChemistrytechnology industry and agricultureimagingnanomedicineRS1-441medicine.anatomical_structureSettore CHIM/09 - Farmaceutico Tecnologico ApplicativoBiophysicsNanomedicineco-polymersNasal administrationfluorescent dyeDrug carrierEthylene glycolPharmaceutics
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Cyclodextrin–calixarene co-polymers as a new class of nanosponges

2014

Hyper-reticulated co-polymers jointly formed by cyclodextrin and calixarene units, which can be considered as a new class of nanosponges, were easily obtained by means of a click chemistry approach. In particular, we succeeded in preparing our materials by exploiting the copper-catalyzed 1,3-dipolar cycloaddition (CuAAC) reaction between heptakis-(6-deoxy)-(6-azido)-beta-cyclodextrin and (5,11,17,23-tetra-tert-butyl)-(25,26,27,28-tetra-propargyloxy)-calix-[4]-arene, mixed in different proportions. These materials were fully characterized by means of combined FT-IR, thermogravimetric, C-13 {H-1} CP-MAS NMR and nitrogen adsorption/desorption techniques. In particular, C-13 {H-1} CP-MAS spectr…

chemistry.chemical_classificationThermogravimetric analysisPolymers and PlasticsCyclodextrinOrganic ChemistryBioengineeringSettore CHIM/06 - Chimica OrganicaPolymerBiochemistryCombinatorial chemistryCycloadditionchemistryDesorptionCalixareneClick chemistryOrganic chemistryCyclodextrins calixarenes CuAAC reaction co-polymersAbsorption (chemistry)Polym. Chem.
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Binding abilities of new cyclodextrin-cucurbituril supramolecular hosts

2015

Various combined techniques (UV–vis spectrophotometry, isothermal titration calorimetry, thermogravimetry, ESI-MS mass spectrometry, polarimetry and 1H NMR spectroscopy) were used in order to study the interaction between a new combined supramolecular host, namely a bow-tie-structured cyclodextrin–cucurbituril association solely held by non-covalent interactions, and a suitably selected guest, namely the N-(p-nitrophenyl)-1,8-diaminooctane hydrochloride. In particular, the use of different techniques highlighted the peculiar features of the possible host–guest supramolecular interactions under different concentration conditions.

chemistry.chemical_classificationcucubiturilCyclodextrinsmedicine.diagnostic_testCyclodextrinHydrochloridecucurbiturilsSupramolecular chemistryIsothermal titration calorimetryGeneral ChemistrySettore CHIM/06 - Chimica OrganicaMass spectrometrycucurbiturilThermogravimetryCrystallographychemistry.chemical_compoundcyclodextrinchemistryComputational chemistryCucurbiturilSpectrophotometrymedicinecucurbiturils; Cyclodextrins; supramolecular co-polymerssupramolecular co-polymerscyclodextrins; cucurbiturils; supramolecular co-polymers
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